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Nicotinic Cholinergic Receptors in VTA Glutamate Neurons Modulate Excitatory Transmission

Authors :
Can Peng
Veronica J. Kim
Xiao Tao Jin
Yijin Yan
Luke D. Lavis
Matthew D. Ramsey
J. Michael McIntosh
David L. Wokosin
Sambashiva Banala
Matthew C. Arvin
Ryan M. Drenan
Yong Wang
Source :
Cell Reports, Vol 23, Iss 8, Pp 2236-2244 (2018), Cell reports
Publication Year :
2018
Publisher :
Elsevier BV, 2018.

Abstract

SUMMARY Ventral tegmental area (VTA) glutamate neurons are important components of reward circuitry, but whether they are subject to cholinergic modulation is unknown. To study this, we used molecular, physiological, and photostimulation techniques to examine nicotinic acetylcholine receptors (nAChRs) in VTA glutamate neurons. Cells in the medial VTA, where glutamate neurons are enriched, are responsive to acetylcholine (ACh) released from cholinergic axons. VTA VGLUT2+ neurons express mRNA and protein subunits known to comprise heteromeric nAChRs. Electrophysiology, coupled with two-photon microscopy and laser flash photolysis of photoactivatable nicotine, was used to demonstrate nAChR functional activity in the somatodendritic subcellular compartment of VTA VGLUT2+ neurons. Finally, optogenetic isolation of intrinsic VTA glutamatergic microcircuits along with gene-editing techniques demonstrated that nicotine potently modulates excitatory transmission within the VTA via heteromeric nAChRs. These results indicate that VTA glutamate neurons are modulated by cholinergic mechanisms and participate in the cascade of physiological responses to nicotine exposure.<br />In Brief Yan et al. examine how functional activity of nicotinic cholinergic receptors is distributed in diverse VTA cell types, revealing nAChR activity in VTA glutamate neurons. These receptors modulate local glutamate transmission in VTA, suggesting mechanisms by which nicotine influences mesolimbic circuitry.

Details

ISSN :
22111247
Volume :
23
Database :
OpenAIRE
Journal :
Cell Reports
Accession number :
edsair.doi.dedup.....097d97dbaa99f47589b29980a441e2b5
Full Text :
https://doi.org/10.1016/j.celrep.2018.04.062