- home
- Advanced Search
Filters
Clear All- Energy Research
- 2. Zero hunger
- JP
- Energy Research
- Neuroscience
- Energy Research
- 2. Zero hunger
- JP
- Energy Research
- Neuroscience
description Publicationkeyboard_double_arrow_right Article , Journal 2020Publisher:MDPI AG Keiichi Yokoyama; Yosuke Yamada; Yasunori Akamatsu; Yasuko Yoshinaka; Akiko Yamamoto; Tomonori Koizumi; Kana Ohyama; Katsuya Suzuki; Masaki Hashimoto; Hitoshi Sato; Misaka Kimura;Sedentary/inactive lifestyle leads middle-aged and older adults to metabolic syndrome and frailty. Capsinoids from nonpungent chili pepper cultivar have been reported to reduce body fat mass, promote metabolism, and improve unidentified complaints of chills. Additionally, they have an anti-inflammation effect; therefore, we hypothesized that continuous oral ingestion of capsinoids alleviates age-related inflammation in the brain and improves the physical activity (PA) in middle-aged and older adults. In our double-blind human study, 69 participants (17 male, 52 female; mean age: 74.1 ± 7.7 years; range: 52–87 years) were administered either 9 mg of capsinoids which were extracted from pepper fruit variety CH-19 Sweet (Capsicum anuum L.) (CP group), or a placebo (PL group) daily over a 3 month period. In an animal study, PA and inflammation-related mRNA expression in the brain were examined in 5-week (young) and 53-week (old) aged mice fed a diet with or without 0.3% dihydrocapsiate, a type of capsinoids, for 12 weeks. In a human study, capsinoids intake did not increase the amount of light-to-moderate PA less than 6.0 metabolic equivalents (METs) (CP: 103.0 ± 28.2 at baseline to 108.2 ± 28.3 at 12 weeks; PL: 104.6 ± 19.8 at baseline to 115.2 ± 23.6 at 12 weeks, METs × hour/week); however, in participants exhibiting an inactive lifestyle, it showed significant increase (CP: 84.5 ± 17.2 at baseline to 99.2 ± 24.9 at 12 weeks; PL: 99.7 ± 23.3 at baseline to 103.8 ± 21.9 at 12 weeks). The energy expenditure in physical activity also improved in the inactive CP group (CP: 481.2 ± 96.3 at baseline to 562.5 ± 145.5 at 12 weeks; PL: 536.8 ± 112.2 at baseline to 598.6 ± 127.6 at 12 weeks; kcal/day). In all participants, CP showed reduced waist circumference, percent body fat, and visceral fat volume; in addition, chills were eased in subjects aged 80 years and older. The older mice fed capsinoids showed increased locomotion activity, decreased inflammation, and oxidative stress in the brain. The results suggest that the continuous oral ingestion of capsinoids gains PA through anti-inflammation effect in the brain as well as reduces fat accumulation and chills in inactive and older humans.
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/nu12010212&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 10 citations 10 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/nu12010212&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2006Publisher:American Chemical Society (ACS) Takuya Koseki; Michio Komai; Katsumi Hashizume; Ardiansyah; Kousaku Ohinata; Hitoshi Shirakawa;pmid: 16506853
Effect of dietary supplementation of two types of rice bran fraction on blood pressure (BP), lipid profile, and glucose metabolism in stroke-prone spontaneously hypertensive rats was studied. Male 4-week-old rats were divided into one group fed the AIN-93M-based control (C) diet and two groups fed diet supplemented with 60 g/kg of Driselase and ethanol fractions (DF and EF, respectively) of rice bran. After 8 weeks feeding, the BP decreased in the DF and EF groups in comparison with the C group (p < 0.01). Plasma ACE inhibitory activity, BUN, BUN/creatinine ratio, albumin, triglyceride, and glucose levels were lower in the DF and EF groups than in the C group (p < 0.01). Plasma nitric oxide and urinary 8-hydroxy-2'-deoxyguanosine levels were lower in the DF and EF groups than in the C group (p < 0.01). Rice bran fractions appear to have a beneficial dietary component that improves hypertension, hyperlipidemia, and hyperglycemia.
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1021/jf068016h&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesbronze 87 citations 87 popularity Top 10% influence Top 10% impulse Top 10% Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1021/jf068016h&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2020 CroatiaPublisher:Frontiers Media SA Funded by:HRZZ | Serotonergic modulation o...HRZZ| Serotonergic modulation of obesity: cross-talk between regulatory molecules and pathwaysKesić, Maja; Baković, Petra; Horvatiček, Marina; Proust, Bastien Lucien Jean; Štefulj, Jasminka; Čičin-Šain, Lipa;Central and peripheral pools of biogenic monoamine serotonin (5-hydroxytryptamine [5HT]) exert opposite effects on the body weight regulation: increase in brain 5HT activity is expected to decrease body weight, whereas increase in peripheral 5HT activity will increase body weight and adiposity. In a genetic model of rats with constitutionally high- or low-5HT homeostasis (hyperserotonergic/hyposerotonergic rats), we have studied how individual differences in endogenous 5HT tone modulate net energy balance of the organism. The high-5HT and low-5HT sublines of the model were developed by selective breeding toward extreme platelet activities of 5HT transporter, a key molecule determining 5HT bioavailability/activity. In animals from high-5HT and low-5HT sublines, we assessed physiological characteristics associated with body weight homeostasis and expression profile of a large scale of body weight-regulating genes in hypothalamus, a major brain region controlling energy balance. Results showed that under standard chow diet animals from the high-5HT subline, as compared to low-5HT animals, have lifelong increased body weight (by 12%), higher absolute daily food intake (by 9%), and different pattern of fat distribution (larger amount of white adipose tissue and lower amount of brown adipose tissue). A large number of body weight-regulating hypothalamic genes were analyzed for their mRNA expression: 24 genes by reverse transcription-quantitative polymerase chain reaction (n = 9-10 rats/subline) including neuropeptides and their receptors, growth factors, transcriptional factors, and receptors for peripheral signals, and a total of 84 genes of various classes by polymerase chain reaction array (pools of six rats/subline). Only few genes showed significant differences in mRNA expression levels between 5HT sublines (e.g. neuropeptide Y receptor, fibroblast growth factor 10), but high-5HT animals displayed a clear trend to upregulation of mRNAs for a number of orexigenic signaling peptides, their receptors, and other molecules with orexigenic activity. Receptors for peripheral signals (leptin, insulin) and molecules in their downstream signaling were not altered, indicating no changes in central insulin/leptin resistance. At the protein level, there were no differences in the content of hypothalamic leptin receptor between 5HT sublines, but significant sex and age effects were observed. Results show that higher constitutive/individual 5HT tone favors higher body weight and adiposity probably due to concurrent upregulation of several hypothalamic orexigenic pathways.
Frontiers in Neurosc... arrow_drop_down add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3389/fnins.2020.00219&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 15 citations 15 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
visibility 164visibility views 164 download downloads 141 Powered bymore_vert Frontiers in Neurosc... arrow_drop_down add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3389/fnins.2020.00219&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2021Publisher:MDPI AG Yoshihiro Yoshimura; Hidetaka Wakabayashi; Ryo Momosaki; Fumihiko Nagano; Takahiro Bise; Sayuri Shimazu; Ai Shiraishi;We conducted a retrospective observational study in 170 older, underweight patients after stroke to elucidate whether stored energy was associated with gains in body weight (BW) and skeletal muscle mass (SMM). Energy intake was recorded on admission. The energy requirement was estimated as actual BW (kg) × 30 (kcal/day), and the stored energy was defined as the energy intake minus the energy requirement. Body composition was measured by bioelectrical impedance analysis. The study participants gained an average of 1.0 ± 2.6 kg of BW over a mean hospital stay of 100 ± 42 days with a mean stored energy of 96.2 ± 91.4 kcal per day. They also gained an average of 0.2 ± 1.6 kg of SMM and 0.5 ± 2.3 kg of fat mass (FM). This means about 9600 kcal were needed to gain 1 kg of BW. In addition, a 1 kg increase in body weight resulted in a 23.7% increase in SMM and a 45.8% increase in FM. Multivariate regression analyses showed that the stored energy was significantly associated with gains in BW and SMM. Aggressive nutrition therapy is important for improving nutritional status and function in patients with malnutrition and sarcopenia.
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/nu13093274&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 22 citations 22 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/nu13093274&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 1991Publisher:Elsevier BV Ken-ichi Kato; Nagao Suzuki; Yasuo Gomi; Hideo Kato; Yuji Iwanaga; Kouji Morikawa; Tatsuya Kimura; Yasuo Ito;doi: 10.1254/jjp.61.277 , 10.1254/jjp.61.333 , 10.1254/jjp.62.289 , 10.1254/jjp.61.341 , 10.1254/jjp.62.379 , 10.1254/jjp.62.161 , 10.1254/jjp.62.1 , 10.1254/jjp.62.9 , 10.1254/jjp.62.269 , 10.1254/jjp.61.283 , 10.1254/jjp.62.99 , 10.1254/jjp.62.123 , 10.1254/jjp.61.299 , 10.1254/jjp.61.351 , 10.1254/jjp.61.291 , 10.1254/jjp.61.325 , 10.1254/jjp.62.387 , 10.1254/jjp.62.183 , 10.1254/jjp.61.375 , 10.1254/jjp.62.49 , 10.1254/jjp.62.111 , 10.1254/jjp.62.103 , 10.1016/s0021-5198(19)39119-x , 10.1254/jjp.62.373 , 10.1254/jjp.62.263 , 10.1016/1056-8719(94)90054-x , 10.1254/jjp.62.415 , 10.1254/jjp.62.339 , 10.1254/jjp.62.169 , 10.1254/jjp.62.75 , 10.1254/jjp.62.131 , 10.1254/jjp.62.175 , 10.1254/jjp.62.223 , 10.1016/0921-8696(92)90705-6 , 10.1254/jjp.62.199 , 10.1254/jjp.62.325 , 10.1254/jjp.62.215 , 10.1254/jjp.62.279 , 10.1254/jjp.62.211 , 10.1254/jjp.62.57 , 10.1254/jjp.62.107 , 10.1254/jjp.62.329 , 10.1254/jjp.62.331 , 10.1254/jjp.62.395 , 10.1254/jjp.62.67 , 10.1254/jjp.62.419
pmid: 8105126 , 8391605 , 8341031 , 8371515 , 8320874 , 8101883 , 8101886 , 8320884 , 8230864 , 8320879 , 8391606 , 7693993 , 8230869 , 8411779 , 8101884 , 8230865 , 8411775 , 8371517 , 8371516 , 8230860 , 7901446 , 7688057 , 8411771 , 7688056 , 8103809 , 8411776 , 8371514 , 8230866 , 8105123 , 8105124 , 7690431 , 8320878 , 8411770 , 8341029 , 8320875 , 8100594 , 8320880 , 8341023 , 8230867 , 8341024 , 7688055
doi: 10.1254/jjp.61.277 , 10.1254/jjp.61.333 , 10.1254/jjp.62.289 , 10.1254/jjp.61.341 , 10.1254/jjp.62.379 , 10.1254/jjp.62.161 , 10.1254/jjp.62.1 , 10.1254/jjp.62.9 , 10.1254/jjp.62.269 , 10.1254/jjp.61.283 , 10.1254/jjp.62.99 , 10.1254/jjp.62.123 , 10.1254/jjp.61.299 , 10.1254/jjp.61.351 , 10.1254/jjp.61.291 , 10.1254/jjp.61.325 , 10.1254/jjp.62.387 , 10.1254/jjp.62.183 , 10.1254/jjp.61.375 , 10.1254/jjp.62.49 , 10.1254/jjp.62.111 , 10.1254/jjp.62.103 , 10.1016/s0021-5198(19)39119-x , 10.1254/jjp.62.373 , 10.1254/jjp.62.263 , 10.1016/1056-8719(94)90054-x , 10.1254/jjp.62.415 , 10.1254/jjp.62.339 , 10.1254/jjp.62.169 , 10.1254/jjp.62.75 , 10.1254/jjp.62.131 , 10.1254/jjp.62.175 , 10.1254/jjp.62.223 , 10.1016/0921-8696(92)90705-6 , 10.1254/jjp.62.199 , 10.1254/jjp.62.325 , 10.1254/jjp.62.215 , 10.1254/jjp.62.279 , 10.1254/jjp.62.211 , 10.1254/jjp.62.57 , 10.1254/jjp.62.107 , 10.1254/jjp.62.329 , 10.1254/jjp.62.331 , 10.1254/jjp.62.395 , 10.1254/jjp.62.67 , 10.1254/jjp.62.419
pmid: 8105126 , 8391605 , 8341031 , 8371515 , 8320874 , 8101883 , 8101886 , 8320884 , 8230864 , 8320879 , 8391606 , 7693993 , 8230869 , 8411779 , 8101884 , 8230865 , 8411775 , 8371517 , 8371516 , 8230860 , 7901446 , 7688057 , 8411771 , 7688056 , 8103809 , 8411776 , 8371514 , 8230866 , 8105123 , 8105124 , 7690431 , 8320878 , 8411770 , 8341029 , 8320875 , 8100594 , 8320880 , 8341023 , 8230867 , 8341024 , 7688055
We investigated the subtype of alpha-adrenoceptors participating in central noradrenergic inhibition of gastric motility in urethane-anesthetized rats. Noradrenaline at 10 nmole administered intracisternally (i.c.) significantly decreased gastric motility. Yohimbine at 10 nmole, i.c., but not the same dose of prazosin, abolished this noradrenaline-induced decrease in gastric motility. Clonidine at 10 nmole, i.c., but not phenylephrine at 20 nmole, significantly decreased gastric motility. These results suggest that alpha 2-adrenoceptor-mediated mechanisms in the brain stem are involved in noradrenergic inhibitory regulation of gastric motility.
The Japanese Journal... arrow_drop_down The Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1991 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefJournal of Pharmacological and Toxicological MethodsArticle . 1994 . Peer-reviewedLicense: Elsevier TDMData sources: CrossrefNeuroscience Research SupplementsArticle . 1992 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1254/jjp.61.277&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesgold 521 citations 521 popularity Top 10% influence Top 1% impulse Top 1% Powered by BIP!
more_vert The Japanese Journal... arrow_drop_down The Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1991 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefJournal of Pharmacological and Toxicological MethodsArticle . 1994 . Peer-reviewedLicense: Elsevier TDMData sources: CrossrefNeuroscience Research SupplementsArticle . 1992 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1254/jjp.61.277&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2019Publisher:Japanese Association for Laboratory Animal Science Kenju Shimomura; Yuko Maejima; Rie O’hashi; Masato Aoyama; Shoko Yokota;Basic research on obesity is becoming more important due to an increasing number of obese people. Experiments using obesity-model animals often require surgical interventions, such as gastric operation, and proper selection of anesthesia is important. Avertin, an agent mainly composed of 2,2,2-Tribromoethanol, has been used as general anesthesia for a long time, without the use of narcotic drugs. In the current study, we found that a single injection of avertin can decrease body weight (BW) in male and female C57BL/6J and ICR mice with high fat-diet (HFD)-induced obesity, but not in standard diet-fed nonobese males and females. Because the BW-reducing effect was more prominent in the female mice, we compared the effects of avertin and a mixture of three types of anesthetic agents (3MIX), which was developed in 2011, on BW reduction in HFD-induced obese female mice. Although both avertin and 3MIX decreased food intake and BW, the effects of avertin were significantly more potent than those of 3MIX. C-Fos expression, a neural activation marker, was dramatically increased in the brain regions related to the regulation of both food intake and the autonomic nervous system after avertin injection, but not after 3MIX injection. This suggests that avertin strongly stimulates the center of feeding regulation and the autonomic nervous system and therefore decreases BW. The current study suggests the advantages of using 3MIX for surgical interventions in mice in obesity research, as it is ideal to prevent anesthesia-induced BW decline.
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1538/expanim.17-0145&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 1 citations 1 popularity Average influence Average impulse Average Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1538/expanim.17-0145&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Part of book or chapter of book , Journal 1993Publisher:Elsevier BV Authors: Miyako Omoto; Kumiko Seki; Tsunehiko Imai; Ryoji Nomura;The effects of maternal drinking on offspring have been studied epidemiologically, in human beings, and experimentally, in rats. The physical growth of offspring of female alcoholic rats, including histological growth of brain, lung, thymus gland, liver, and kidney, was previously reported by us. In the present study, we observed the effect of ethanol intake by the mother rat on learning ability and behavior of offspring rats using an eight radical arm maze. At the same time histological observations of the cerebrum were carried out. The mother rat was exposed to ethanol from a young age to delivery (P-DEL) or to weaning (P-NURS). After weaning, the offspring was exposed to ethanol until the tests began (P-WEAN). Experimental groups, classified by length of ethanol exposure, as mentioned above, disclosed the following: (1) Number of trials required for fulfilling learning criterion was significantly large in P-DEL and P-NURS rat groups relative to the controls; that is, P-DEL and P-NURS rats were slow in learning. (2) Numbers of rats which did not fulfill the learning criterion were: Group P-DEL, one male of eight; Group P-NURS, three males of seven. The behavior of the rats in Group P-WEAN differed from those in other groups; while they were receiving acclimation training, they were, unlike ordinary rats, not watchful of the device, slow to find the feed, and indifferent. They seemed to lack carefulness and sometimes failed to eat the feed even though they succeeded in selecting correct arms. Their motion was abrupt and they ran at extraordinarily high speeds. (3) In the observations of correct choices in the first eight choices, groups P-DEL and P-NURS showed significantly low values. This suggested the lowering of their learning ability. (4) In the observations of continuous correct choices, Group P-DEL showed a significantly low value. This suggested the rats did not learn thoroughly enough to retain their acquisition long. (5) Body weight, learning ability, and hippocampal neurons were affected by ethanol exposure more severely in Group P-NURS than in Group P-DEL. An even more severe effect was observed in Group P-WEAN.
Environmental Resear... arrow_drop_down https://doi.org/10.1016/b978-0...Part of book or chapter of book . 1994 . Peer-reviewedData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1006/enrs.1993.1133&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesbronze 14 citations 14 popularity Average influence Average impulse Average Powered by BIP!
more_vert Environmental Resear... arrow_drop_down https://doi.org/10.1016/b978-0...Part of book or chapter of book . 1994 . Peer-reviewedData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1006/enrs.1993.1133&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 1979Publisher:Center for Academic Publications Japan Authors: Yoshinori Itokawa; Tomoko Abe; Eiichi Okamoto;doi: 10.3177/jnsv.25.375
pmid: 396369
Rats were separated into four groups and four different liquid diets were given to each group. Group 1: thiamine-sufficient diet with no ethanol, group 2: thiamine-sufficient diet with ethanol, group 3: thiamine-deficient diet with no ethanol, group 4: thiamine-deficient diet with ethanol. After four weeks, all rats were fasted for 24 hr and then ethanol was given orally to every rat. After one hour, every rat was sacrificed and biochemical and histological analyses were carried out. Transketolase activity in brain and liver decreased in groups 2, 3 and 4. There was significant decrease in transketolase activity in ethanol-fed groups (groups 2 and 4) as compared to control groups (groups 1 and 3). Ethanol concentrations in blood, liver and heart of rats in groups 2 and 4 were higher than in groups 1 and 3. When comparison was made between the thiamine-deficient groups and the corresponding thiamine-sufficient groups, ethanol concentrations in liver and heart were higher in the thiamine-deficient groups. Alcohol dehydrogenase activity in liver decreased significantly in groups 2 and 4. By histological analyses, fatty degeneration was observed in the livers of groups 2 and 4. The degeneration was more prominent in group 4 than group 2. These findings suggest that chronic ethanol administration may impair the ability to metabolize ethanol and the impairment may increase when rats are in the condition of thiamine deficiency.
Journal of Nutrition... arrow_drop_down Journal of Nutritional Science and VitaminologyArticle . 1979 . Peer-reviewedData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3177/jnsv.25.375&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesgold 19 citations 19 popularity Average influence Top 10% impulse Average Powered by BIP!
more_vert Journal of Nutrition... arrow_drop_down Journal of Nutritional Science and VitaminologyArticle . 1979 . Peer-reviewedData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3177/jnsv.25.375&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2013Publisher:Frontiers Media SA Authors: Glenn W. Stevenson; Meredith A. Fox;Ethyl alcohol (ethanol) is produced by the process of fermentation whereby plant sugars are converted to ethanol by yeast. Products of fermentation include mead from honey, wine from grapes, sake from rice, and beer from grains. Fermented products can also be distilled, for example when whisky is distilled from grains (Herbst and Herbst, 2003). The history of voluntary ethanol use by humans dates as far back as 8000 years ago for wine and possibly earlier for beer, as barley may have been the oldest cultivated grain (Pendell, 2010). It is also documented that ethanol was an extremely important staple to ancient civilizations such as the Egyptians and the Maya (Johnson, 1994), as well as more modern societies such as the original American colonies (Pendell, 2010). It seems that modern society's interest in alcohol has certainly not waned, and from the standpoint of neuropharmacology, has probably increased. During the past several decades, there has been a concerted effort to determine the neuropharmacological mechanism of action(s) of ethanol. Ethanol has been reported to produce its effects via modulation of neural cell membrane fluidity as well as modulation of several neurotransmitter systems, including γ-amino butyric acid (GABA), glutamate, dopamine, and opioid systems (for reviews, see Koob et al., 1998; Kumar et al., 2009). GABA is an inhibitory amino acid neurotransmitter that is ubiquitously distributed in the mammalian brain, and ethanol's effects on the GABA system are thought to be mediated primarily by activating the GABAA receptor, a 5-subunit receptor that gates Cl− ions (for a review, see Kumar et al., 2009). Thus, GABA receptor activation produces CNS inhibition via Cl− influx. It has also been reported that specific GABAA receptor subunits mediate specific effects. For example, the α1 subunit is associated with sedation, whereas the α2 and α3 subunits are associated with anti-anxiety effects (Licata and Rowlett, 2008; Ator et al., 2010). Many types of sedative-hypnotic compounds (drugs producing dose-dependent sedation and ultimately sleep), including the benzodiazepines, barbiturates, and ethanol, bind to and activate the GABAA receptor, and it is reasonable to assume that the sedative effects of these agents are mediated, at least in part, by the α1 subunit. It is known that neurotransmitters, including GABA, bind to their receptors as “first messengers,” and initiate a complex cascade of intra-cellular events. In the case of GABA, part of this cellular cascade includes modulation of the “second messenger” systems Ca++ and cAMP that ultimately modulate two protein kinases, PKC and PKA, resulting in myriad effects in the cell, including changes to gene expression (Moss et al., 1992; Diamond and Gordon, 1997; Brandon et al., 2000 for a review, see Kumar et al., 2009). Leslie Morrow and colleagues have been exploring the complex cascade of downstream cellular events mediated by ethanol-induced GABAA receptor activation. In their recent Frontiers in Neuroscience report (Kumar et al., 2012), this research team determined the effects of acute ethanol exposure on PKA-mediated GABAA receptor expression. Although chronic ethanol exposure has been reported to produce down-regulation and/or desensitization of GABAA receptors, Morrow and colleagues reported an interesting finding of acute ethanol exposure. Specifically, acute intracerebroventricular administration of ethanol produced dose-dependent increases in expression of PKA and GABAA receptor α1 subunits. In addition, antagonism studies revealed that blockade of PKA blocked the ethanol-induced increases in GABAA receptor α1 subunit expression, providing further evidence for a PKA-GABAA receptor network communication. An additional manipulation showed that enhancing PKA activity actually enhanced ethanol-induced loss of righting reflex. Together with earlier reports from this research group, these data indicate that PKA (Kumar et al., 2012) and PKC (Kumar et al., 2006) may have antagonistic effects on GABAA receptor α1 subunit expression, thus delineating specific potential pathway(s) for mediation of ethanol effects on cell function and overt organismal behavior. This group's current report represents a comprehensive analysis of the specific effects of ethanol on kinase activity and receptor subunit expression levels, and adds another layer of knowledge about the neuropharmacological mechanisms of ethanol. It is quite possible that further elucidation of the complex molecular “systems level” analysis of ethanol's actions in nerve cells may yield important “systems level” approaches and advances for the treatment of alcohol abuse and dependence.
Frontiers in Neurosc... arrow_drop_down add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3389/fnins.2013.00122&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 2 citations 2 popularity Average influence Average impulse Average Powered by BIP!
more_vert Frontiers in Neurosc... arrow_drop_down add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3389/fnins.2013.00122&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu
description Publicationkeyboard_double_arrow_right Article , Journal 2020Publisher:MDPI AG Keiichi Yokoyama; Yosuke Yamada; Yasunori Akamatsu; Yasuko Yoshinaka; Akiko Yamamoto; Tomonori Koizumi; Kana Ohyama; Katsuya Suzuki; Masaki Hashimoto; Hitoshi Sato; Misaka Kimura;Sedentary/inactive lifestyle leads middle-aged and older adults to metabolic syndrome and frailty. Capsinoids from nonpungent chili pepper cultivar have been reported to reduce body fat mass, promote metabolism, and improve unidentified complaints of chills. Additionally, they have an anti-inflammation effect; therefore, we hypothesized that continuous oral ingestion of capsinoids alleviates age-related inflammation in the brain and improves the physical activity (PA) in middle-aged and older adults. In our double-blind human study, 69 participants (17 male, 52 female; mean age: 74.1 ± 7.7 years; range: 52–87 years) were administered either 9 mg of capsinoids which were extracted from pepper fruit variety CH-19 Sweet (Capsicum anuum L.) (CP group), or a placebo (PL group) daily over a 3 month period. In an animal study, PA and inflammation-related mRNA expression in the brain were examined in 5-week (young) and 53-week (old) aged mice fed a diet with or without 0.3% dihydrocapsiate, a type of capsinoids, for 12 weeks. In a human study, capsinoids intake did not increase the amount of light-to-moderate PA less than 6.0 metabolic equivalents (METs) (CP: 103.0 ± 28.2 at baseline to 108.2 ± 28.3 at 12 weeks; PL: 104.6 ± 19.8 at baseline to 115.2 ± 23.6 at 12 weeks, METs × hour/week); however, in participants exhibiting an inactive lifestyle, it showed significant increase (CP: 84.5 ± 17.2 at baseline to 99.2 ± 24.9 at 12 weeks; PL: 99.7 ± 23.3 at baseline to 103.8 ± 21.9 at 12 weeks). The energy expenditure in physical activity also improved in the inactive CP group (CP: 481.2 ± 96.3 at baseline to 562.5 ± 145.5 at 12 weeks; PL: 536.8 ± 112.2 at baseline to 598.6 ± 127.6 at 12 weeks; kcal/day). In all participants, CP showed reduced waist circumference, percent body fat, and visceral fat volume; in addition, chills were eased in subjects aged 80 years and older. The older mice fed capsinoids showed increased locomotion activity, decreased inflammation, and oxidative stress in the brain. The results suggest that the continuous oral ingestion of capsinoids gains PA through anti-inflammation effect in the brain as well as reduces fat accumulation and chills in inactive and older humans.
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/nu12010212&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 10 citations 10 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/nu12010212&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2006Publisher:American Chemical Society (ACS) Takuya Koseki; Michio Komai; Katsumi Hashizume; Ardiansyah; Kousaku Ohinata; Hitoshi Shirakawa;pmid: 16506853
Effect of dietary supplementation of two types of rice bran fraction on blood pressure (BP), lipid profile, and glucose metabolism in stroke-prone spontaneously hypertensive rats was studied. Male 4-week-old rats were divided into one group fed the AIN-93M-based control (C) diet and two groups fed diet supplemented with 60 g/kg of Driselase and ethanol fractions (DF and EF, respectively) of rice bran. After 8 weeks feeding, the BP decreased in the DF and EF groups in comparison with the C group (p < 0.01). Plasma ACE inhibitory activity, BUN, BUN/creatinine ratio, albumin, triglyceride, and glucose levels were lower in the DF and EF groups than in the C group (p < 0.01). Plasma nitric oxide and urinary 8-hydroxy-2'-deoxyguanosine levels were lower in the DF and EF groups than in the C group (p < 0.01). Rice bran fractions appear to have a beneficial dietary component that improves hypertension, hyperlipidemia, and hyperglycemia.
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1021/jf068016h&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesbronze 87 citations 87 popularity Top 10% influence Top 10% impulse Top 10% Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1021/jf068016h&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2020 CroatiaPublisher:Frontiers Media SA Funded by:HRZZ | Serotonergic modulation o...HRZZ| Serotonergic modulation of obesity: cross-talk between regulatory molecules and pathwaysKesić, Maja; Baković, Petra; Horvatiček, Marina; Proust, Bastien Lucien Jean; Štefulj, Jasminka; Čičin-Šain, Lipa;Central and peripheral pools of biogenic monoamine serotonin (5-hydroxytryptamine [5HT]) exert opposite effects on the body weight regulation: increase in brain 5HT activity is expected to decrease body weight, whereas increase in peripheral 5HT activity will increase body weight and adiposity. In a genetic model of rats with constitutionally high- or low-5HT homeostasis (hyperserotonergic/hyposerotonergic rats), we have studied how individual differences in endogenous 5HT tone modulate net energy balance of the organism. The high-5HT and low-5HT sublines of the model were developed by selective breeding toward extreme platelet activities of 5HT transporter, a key molecule determining 5HT bioavailability/activity. In animals from high-5HT and low-5HT sublines, we assessed physiological characteristics associated with body weight homeostasis and expression profile of a large scale of body weight-regulating genes in hypothalamus, a major brain region controlling energy balance. Results showed that under standard chow diet animals from the high-5HT subline, as compared to low-5HT animals, have lifelong increased body weight (by 12%), higher absolute daily food intake (by 9%), and different pattern of fat distribution (larger amount of white adipose tissue and lower amount of brown adipose tissue). A large number of body weight-regulating hypothalamic genes were analyzed for their mRNA expression: 24 genes by reverse transcription-quantitative polymerase chain reaction (n = 9-10 rats/subline) including neuropeptides and their receptors, growth factors, transcriptional factors, and receptors for peripheral signals, and a total of 84 genes of various classes by polymerase chain reaction array (pools of six rats/subline). Only few genes showed significant differences in mRNA expression levels between 5HT sublines (e.g. neuropeptide Y receptor, fibroblast growth factor 10), but high-5HT animals displayed a clear trend to upregulation of mRNAs for a number of orexigenic signaling peptides, their receptors, and other molecules with orexigenic activity. Receptors for peripheral signals (leptin, insulin) and molecules in their downstream signaling were not altered, indicating no changes in central insulin/leptin resistance. At the protein level, there were no differences in the content of hypothalamic leptin receptor between 5HT sublines, but significant sex and age effects were observed. Results show that higher constitutive/individual 5HT tone favors higher body weight and adiposity probably due to concurrent upregulation of several hypothalamic orexigenic pathways.
Frontiers in Neurosc... arrow_drop_down add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3389/fnins.2020.00219&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 15 citations 15 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
visibility 164visibility views 164 download downloads 141 Powered bymore_vert Frontiers in Neurosc... arrow_drop_down add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3389/fnins.2020.00219&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2021Publisher:MDPI AG Yoshihiro Yoshimura; Hidetaka Wakabayashi; Ryo Momosaki; Fumihiko Nagano; Takahiro Bise; Sayuri Shimazu; Ai Shiraishi;We conducted a retrospective observational study in 170 older, underweight patients after stroke to elucidate whether stored energy was associated with gains in body weight (BW) and skeletal muscle mass (SMM). Energy intake was recorded on admission. The energy requirement was estimated as actual BW (kg) × 30 (kcal/day), and the stored energy was defined as the energy intake minus the energy requirement. Body composition was measured by bioelectrical impedance analysis. The study participants gained an average of 1.0 ± 2.6 kg of BW over a mean hospital stay of 100 ± 42 days with a mean stored energy of 96.2 ± 91.4 kcal per day. They also gained an average of 0.2 ± 1.6 kg of SMM and 0.5 ± 2.3 kg of fat mass (FM). This means about 9600 kcal were needed to gain 1 kg of BW. In addition, a 1 kg increase in body weight resulted in a 23.7% increase in SMM and a 45.8% increase in FM. Multivariate regression analyses showed that the stored energy was significantly associated with gains in BW and SMM. Aggressive nutrition therapy is important for improving nutritional status and function in patients with malnutrition and sarcopenia.
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/nu13093274&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 22 citations 22 popularity Top 10% influence Average impulse Top 10% Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3390/nu13093274&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 1991Publisher:Elsevier BV Ken-ichi Kato; Nagao Suzuki; Yasuo Gomi; Hideo Kato; Yuji Iwanaga; Kouji Morikawa; Tatsuya Kimura; Yasuo Ito;doi: 10.1254/jjp.61.277 , 10.1254/jjp.61.333 , 10.1254/jjp.62.289 , 10.1254/jjp.61.341 , 10.1254/jjp.62.379 , 10.1254/jjp.62.161 , 10.1254/jjp.62.1 , 10.1254/jjp.62.9 , 10.1254/jjp.62.269 , 10.1254/jjp.61.283 , 10.1254/jjp.62.99 , 10.1254/jjp.62.123 , 10.1254/jjp.61.299 , 10.1254/jjp.61.351 , 10.1254/jjp.61.291 , 10.1254/jjp.61.325 , 10.1254/jjp.62.387 , 10.1254/jjp.62.183 , 10.1254/jjp.61.375 , 10.1254/jjp.62.49 , 10.1254/jjp.62.111 , 10.1254/jjp.62.103 , 10.1016/s0021-5198(19)39119-x , 10.1254/jjp.62.373 , 10.1254/jjp.62.263 , 10.1016/1056-8719(94)90054-x , 10.1254/jjp.62.415 , 10.1254/jjp.62.339 , 10.1254/jjp.62.169 , 10.1254/jjp.62.75 , 10.1254/jjp.62.131 , 10.1254/jjp.62.175 , 10.1254/jjp.62.223 , 10.1016/0921-8696(92)90705-6 , 10.1254/jjp.62.199 , 10.1254/jjp.62.325 , 10.1254/jjp.62.215 , 10.1254/jjp.62.279 , 10.1254/jjp.62.211 , 10.1254/jjp.62.57 , 10.1254/jjp.62.107 , 10.1254/jjp.62.329 , 10.1254/jjp.62.331 , 10.1254/jjp.62.395 , 10.1254/jjp.62.67 , 10.1254/jjp.62.419
pmid: 8105126 , 8391605 , 8341031 , 8371515 , 8320874 , 8101883 , 8101886 , 8320884 , 8230864 , 8320879 , 8391606 , 7693993 , 8230869 , 8411779 , 8101884 , 8230865 , 8411775 , 8371517 , 8371516 , 8230860 , 7901446 , 7688057 , 8411771 , 7688056 , 8103809 , 8411776 , 8371514 , 8230866 , 8105123 , 8105124 , 7690431 , 8320878 , 8411770 , 8341029 , 8320875 , 8100594 , 8320880 , 8341023 , 8230867 , 8341024 , 7688055
doi: 10.1254/jjp.61.277 , 10.1254/jjp.61.333 , 10.1254/jjp.62.289 , 10.1254/jjp.61.341 , 10.1254/jjp.62.379 , 10.1254/jjp.62.161 , 10.1254/jjp.62.1 , 10.1254/jjp.62.9 , 10.1254/jjp.62.269 , 10.1254/jjp.61.283 , 10.1254/jjp.62.99 , 10.1254/jjp.62.123 , 10.1254/jjp.61.299 , 10.1254/jjp.61.351 , 10.1254/jjp.61.291 , 10.1254/jjp.61.325 , 10.1254/jjp.62.387 , 10.1254/jjp.62.183 , 10.1254/jjp.61.375 , 10.1254/jjp.62.49 , 10.1254/jjp.62.111 , 10.1254/jjp.62.103 , 10.1016/s0021-5198(19)39119-x , 10.1254/jjp.62.373 , 10.1254/jjp.62.263 , 10.1016/1056-8719(94)90054-x , 10.1254/jjp.62.415 , 10.1254/jjp.62.339 , 10.1254/jjp.62.169 , 10.1254/jjp.62.75 , 10.1254/jjp.62.131 , 10.1254/jjp.62.175 , 10.1254/jjp.62.223 , 10.1016/0921-8696(92)90705-6 , 10.1254/jjp.62.199 , 10.1254/jjp.62.325 , 10.1254/jjp.62.215 , 10.1254/jjp.62.279 , 10.1254/jjp.62.211 , 10.1254/jjp.62.57 , 10.1254/jjp.62.107 , 10.1254/jjp.62.329 , 10.1254/jjp.62.331 , 10.1254/jjp.62.395 , 10.1254/jjp.62.67 , 10.1254/jjp.62.419
pmid: 8105126 , 8391605 , 8341031 , 8371515 , 8320874 , 8101883 , 8101886 , 8320884 , 8230864 , 8320879 , 8391606 , 7693993 , 8230869 , 8411779 , 8101884 , 8230865 , 8411775 , 8371517 , 8371516 , 8230860 , 7901446 , 7688057 , 8411771 , 7688056 , 8103809 , 8411776 , 8371514 , 8230866 , 8105123 , 8105124 , 7690431 , 8320878 , 8411770 , 8341029 , 8320875 , 8100594 , 8320880 , 8341023 , 8230867 , 8341024 , 7688055
We investigated the subtype of alpha-adrenoceptors participating in central noradrenergic inhibition of gastric motility in urethane-anesthetized rats. Noradrenaline at 10 nmole administered intracisternally (i.c.) significantly decreased gastric motility. Yohimbine at 10 nmole, i.c., but not the same dose of prazosin, abolished this noradrenaline-induced decrease in gastric motility. Clonidine at 10 nmole, i.c., but not phenylephrine at 20 nmole, significantly decreased gastric motility. These results suggest that alpha 2-adrenoceptor-mediated mechanisms in the brain stem are involved in noradrenergic inhibitory regulation of gastric motility.
The Japanese Journal... arrow_drop_down The Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1991 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefJournal of Pharmacological and Toxicological MethodsArticle . 1994 . Peer-reviewedLicense: Elsevier TDMData sources: CrossrefNeuroscience Research SupplementsArticle . 1992 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1254/jjp.61.277&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesgold 521 citations 521 popularity Top 10% influence Top 1% impulse Top 1% Powered by BIP!
more_vert The Japanese Journal... arrow_drop_down The Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1991 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefThe Japanese Journal of PharmacologyArticle . 1993 . Peer-reviewedLicense: CC BY NC NDData sources: CrossrefJournal of Pharmacological and Toxicological MethodsArticle . 1994 . Peer-reviewedLicense: Elsevier TDMData sources: CrossrefNeuroscience Research SupplementsArticle . 1992 . Peer-reviewedLicense: Elsevier TDMData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1254/jjp.61.277&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2019Publisher:Japanese Association for Laboratory Animal Science Kenju Shimomura; Yuko Maejima; Rie O’hashi; Masato Aoyama; Shoko Yokota;Basic research on obesity is becoming more important due to an increasing number of obese people. Experiments using obesity-model animals often require surgical interventions, such as gastric operation, and proper selection of anesthesia is important. Avertin, an agent mainly composed of 2,2,2-Tribromoethanol, has been used as general anesthesia for a long time, without the use of narcotic drugs. In the current study, we found that a single injection of avertin can decrease body weight (BW) in male and female C57BL/6J and ICR mice with high fat-diet (HFD)-induced obesity, but not in standard diet-fed nonobese males and females. Because the BW-reducing effect was more prominent in the female mice, we compared the effects of avertin and a mixture of three types of anesthetic agents (3MIX), which was developed in 2011, on BW reduction in HFD-induced obese female mice. Although both avertin and 3MIX decreased food intake and BW, the effects of avertin were significantly more potent than those of 3MIX. C-Fos expression, a neural activation marker, was dramatically increased in the brain regions related to the regulation of both food intake and the autonomic nervous system after avertin injection, but not after 3MIX injection. This suggests that avertin strongly stimulates the center of feeding regulation and the autonomic nervous system and therefore decreases BW. The current study suggests the advantages of using 3MIX for surgical interventions in mice in obesity research, as it is ideal to prevent anesthesia-induced BW decline.
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1538/expanim.17-0145&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 1 citations 1 popularity Average influence Average impulse Average Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1538/expanim.17-0145&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Part of book or chapter of book , Journal 1993Publisher:Elsevier BV Authors: Miyako Omoto; Kumiko Seki; Tsunehiko Imai; Ryoji Nomura;The effects of maternal drinking on offspring have been studied epidemiologically, in human beings, and experimentally, in rats. The physical growth of offspring of female alcoholic rats, including histological growth of brain, lung, thymus gland, liver, and kidney, was previously reported by us. In the present study, we observed the effect of ethanol intake by the mother rat on learning ability and behavior of offspring rats using an eight radical arm maze. At the same time histological observations of the cerebrum were carried out. The mother rat was exposed to ethanol from a young age to delivery (P-DEL) or to weaning (P-NURS). After weaning, the offspring was exposed to ethanol until the tests began (P-WEAN). Experimental groups, classified by length of ethanol exposure, as mentioned above, disclosed the following: (1) Number of trials required for fulfilling learning criterion was significantly large in P-DEL and P-NURS rat groups relative to the controls; that is, P-DEL and P-NURS rats were slow in learning. (2) Numbers of rats which did not fulfill the learning criterion were: Group P-DEL, one male of eight; Group P-NURS, three males of seven. The behavior of the rats in Group P-WEAN differed from those in other groups; while they were receiving acclimation training, they were, unlike ordinary rats, not watchful of the device, slow to find the feed, and indifferent. They seemed to lack carefulness and sometimes failed to eat the feed even though they succeeded in selecting correct arms. Their motion was abrupt and they ran at extraordinarily high speeds. (3) In the observations of correct choices in the first eight choices, groups P-DEL and P-NURS showed significantly low values. This suggested the lowering of their learning ability. (4) In the observations of continuous correct choices, Group P-DEL showed a significantly low value. This suggested the rats did not learn thoroughly enough to retain their acquisition long. (5) Body weight, learning ability, and hippocampal neurons were affected by ethanol exposure more severely in Group P-NURS than in Group P-DEL. An even more severe effect was observed in Group P-WEAN.
Environmental Resear... arrow_drop_down https://doi.org/10.1016/b978-0...Part of book or chapter of book . 1994 . Peer-reviewedData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1006/enrs.1993.1133&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesbronze 14 citations 14 popularity Average influence Average impulse Average Powered by BIP!
more_vert Environmental Resear... arrow_drop_down https://doi.org/10.1016/b978-0...Part of book or chapter of book . 1994 . Peer-reviewedData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1006/enrs.1993.1133&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 1979Publisher:Center for Academic Publications Japan Authors: Yoshinori Itokawa; Tomoko Abe; Eiichi Okamoto;doi: 10.3177/jnsv.25.375
pmid: 396369
Rats were separated into four groups and four different liquid diets were given to each group. Group 1: thiamine-sufficient diet with no ethanol, group 2: thiamine-sufficient diet with ethanol, group 3: thiamine-deficient diet with no ethanol, group 4: thiamine-deficient diet with ethanol. After four weeks, all rats were fasted for 24 hr and then ethanol was given orally to every rat. After one hour, every rat was sacrificed and biochemical and histological analyses were carried out. Transketolase activity in brain and liver decreased in groups 2, 3 and 4. There was significant decrease in transketolase activity in ethanol-fed groups (groups 2 and 4) as compared to control groups (groups 1 and 3). Ethanol concentrations in blood, liver and heart of rats in groups 2 and 4 were higher than in groups 1 and 3. When comparison was made between the thiamine-deficient groups and the corresponding thiamine-sufficient groups, ethanol concentrations in liver and heart were higher in the thiamine-deficient groups. Alcohol dehydrogenase activity in liver decreased significantly in groups 2 and 4. By histological analyses, fatty degeneration was observed in the livers of groups 2 and 4. The degeneration was more prominent in group 4 than group 2. These findings suggest that chronic ethanol administration may impair the ability to metabolize ethanol and the impairment may increase when rats are in the condition of thiamine deficiency.
Journal of Nutrition... arrow_drop_down Journal of Nutritional Science and VitaminologyArticle . 1979 . Peer-reviewedData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3177/jnsv.25.375&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess Routesgold 19 citations 19 popularity Average influence Top 10% impulse Average Powered by BIP!
more_vert Journal of Nutrition... arrow_drop_down Journal of Nutritional Science and VitaminologyArticle . 1979 . Peer-reviewedData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3177/jnsv.25.375&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Journal 2013Publisher:Frontiers Media SA Authors: Glenn W. Stevenson; Meredith A. Fox;Ethyl alcohol (ethanol) is produced by the process of fermentation whereby plant sugars are converted to ethanol by yeast. Products of fermentation include mead from honey, wine from grapes, sake from rice, and beer from grains. Fermented products can also be distilled, for example when whisky is distilled from grains (Herbst and Herbst, 2003). The history of voluntary ethanol use by humans dates as far back as 8000 years ago for wine and possibly earlier for beer, as barley may have been the oldest cultivated grain (Pendell, 2010). It is also documented that ethanol was an extremely important staple to ancient civilizations such as the Egyptians and the Maya (Johnson, 1994), as well as more modern societies such as the original American colonies (Pendell, 2010). It seems that modern society's interest in alcohol has certainly not waned, and from the standpoint of neuropharmacology, has probably increased. During the past several decades, there has been a concerted effort to determine the neuropharmacological mechanism of action(s) of ethanol. Ethanol has been reported to produce its effects via modulation of neural cell membrane fluidity as well as modulation of several neurotransmitter systems, including γ-amino butyric acid (GABA), glutamate, dopamine, and opioid systems (for reviews, see Koob et al., 1998; Kumar et al., 2009). GABA is an inhibitory amino acid neurotransmitter that is ubiquitously distributed in the mammalian brain, and ethanol's effects on the GABA system are thought to be mediated primarily by activating the GABAA receptor, a 5-subunit receptor that gates Cl− ions (for a review, see Kumar et al., 2009). Thus, GABA receptor activation produces CNS inhibition via Cl− influx. It has also been reported that specific GABAA receptor subunits mediate specific effects. For example, the α1 subunit is associated with sedation, whereas the α2 and α3 subunits are associated with anti-anxiety effects (Licata and Rowlett, 2008; Ator et al., 2010). Many types of sedative-hypnotic compounds (drugs producing dose-dependent sedation and ultimately sleep), including the benzodiazepines, barbiturates, and ethanol, bind to and activate the GABAA receptor, and it is reasonable to assume that the sedative effects of these agents are mediated, at least in part, by the α1 subunit. It is known that neurotransmitters, including GABA, bind to their receptors as “first messengers,” and initiate a complex cascade of intra-cellular events. In the case of GABA, part of this cellular cascade includes modulation of the “second messenger” systems Ca++ and cAMP that ultimately modulate two protein kinases, PKC and PKA, resulting in myriad effects in the cell, including changes to gene expression (Moss et al., 1992; Diamond and Gordon, 1997; Brandon et al., 2000 for a review, see Kumar et al., 2009). Leslie Morrow and colleagues have been exploring the complex cascade of downstream cellular events mediated by ethanol-induced GABAA receptor activation. In their recent Frontiers in Neuroscience report (Kumar et al., 2012), this research team determined the effects of acute ethanol exposure on PKA-mediated GABAA receptor expression. Although chronic ethanol exposure has been reported to produce down-regulation and/or desensitization of GABAA receptors, Morrow and colleagues reported an interesting finding of acute ethanol exposure. Specifically, acute intracerebroventricular administration of ethanol produced dose-dependent increases in expression of PKA and GABAA receptor α1 subunits. In addition, antagonism studies revealed that blockade of PKA blocked the ethanol-induced increases in GABAA receptor α1 subunit expression, providing further evidence for a PKA-GABAA receptor network communication. An additional manipulation showed that enhancing PKA activity actually enhanced ethanol-induced loss of righting reflex. Together with earlier reports from this research group, these data indicate that PKA (Kumar et al., 2012) and PKC (Kumar et al., 2006) may have antagonistic effects on GABAA receptor α1 subunit expression, thus delineating specific potential pathway(s) for mediation of ethanol effects on cell function and overt organismal behavior. This group's current report represents a comprehensive analysis of the specific effects of ethanol on kinase activity and receptor subunit expression levels, and adds another layer of knowledge about the neuropharmacological mechanisms of ethanol. It is quite possible that further elucidation of the complex molecular “systems level” analysis of ethanol's actions in nerve cells may yield important “systems level” approaches and advances for the treatment of alcohol abuse and dependence.
Frontiers in Neurosc... arrow_drop_down add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3389/fnins.2013.00122&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 2 citations 2 popularity Average influence Average impulse Average Powered by BIP!
more_vert Frontiers in Neurosc... arrow_drop_down add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.3389/fnins.2013.00122&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu