
You have already added 0 works in your ORCID record related to the merged Research product.
You have already added 0 works in your ORCID record related to the merged Research product.
<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=undefined&type=result"></script>');
-->
</script>
α6 subunit‐containing nicotinic receptors mediate low‐dose ethanol effects on ventral tegmental area neurons and ethanol reward

α6 subunit‐containing nicotinic receptors mediate low‐dose ethanol effects on ventral tegmental area neurons and ethanol reward
AbstractDopamine (DA) neuron excitability is regulated by inhibitory GABAergic synaptic transmission and modulated by nicotinic acetylcholine receptors (nAChRs). The aim of this study was to evaluate the role of α6 subunit‐containing nAChRs (α6*‐nAChRs) in acute ethanol effects on ventral tegmental area (VTA) GABA and DA neurons. α6*‐nAChRs were visualized on GABA terminals on VTA GABA neurons, and α6*‐nAChR transcripts were expressed in most DA neurons, but only a minority of VTA GABA neurons from GAD67 GFP mice. Low concentrations of ethanol (1–10 mM) enhanced GABAA receptor (GABAAR)‐mediated spontaneous and evoked inhibition with blockade by selective α6*‐nAChR antagonist α‐conotoxins (α‐Ctxs) and lowered sensitivity in α6 knock‐out (KO) mice. Ethanol suppression of VTA GABA neuron firing rate in wild‐type mice in vivo was significantly reduced in α6 KO mice. Ethanol (5–100 mM) had no effect on optically evoked GABAAR‐mediated inhibition of DA neurons, and ethanol enhancement of VTA DA neuron firing rate at high concentrations was not affected by α‐Ctxs. Ethanol conditioned place preference was reduced in α6 KO mice compared with wild‐type controls. Taken together, these studies indicate that relatively low concentrations of ethanol act through α6*‐nAChRs on GABA terminals to enhance GABA release onto VTA GABA neurons, in turn to reduce GABA neuron firing, which may lead to VTA DA neuron disinhibition, suggesting a possible mechanism of action of alcohol and nicotine co‐abuse.
- University of Utah United States
- Midwestern University United States
- St. Joseph's Hospital and Medical Center United States
- Dignity Health United States
- Utah Valley University United States
Male, Mice, Knockout, Ethanol, Ventral Tegmental Area, Receptors, Nicotinic, Synaptic Transmission, Mice, Inbred C57BL, Mice, Reward, Models, Animal, Animals, GABAergic Neurons
Male, Mice, Knockout, Ethanol, Ventral Tegmental Area, Receptors, Nicotinic, Synaptic Transmission, Mice, Inbred C57BL, Mice, Reward, Models, Animal, Animals, GABAergic Neurons
8 Research products, page 1 of 1
- 2014IsAmongTopNSimilarDocuments
- 2019IsAmongTopNSimilarDocuments
- 2018IsAmongTopNSimilarDocuments
- 2018IsAmongTopNSimilarDocuments
- 2016IsAmongTopNSimilarDocuments
- 2019IsAmongTopNSimilarDocuments
- 2013IsAmongTopNSimilarDocuments
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).16 popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.Top 10% influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).Average impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.Top 10%
