| Literature DB >> 30638902 |
Yue Li1, Chun-Yue Li1, Wang Xi1, Sen Jin2, Zuo-Hang Wu1, Ping Jiang1, Ping Dong1, Xiao-Bin He2, Fu-Qiang Xu2, Shumin Duan1, Yu-Dong Zhou1, Xiao-Ming Li3.
Abstract
Both the ventral tegmental area (VTA) and dorsal raphe nucleus (DRN) are involved in affective control and reward-related behaviors. Moreover, the neuronal activities of the VTA and DRN are modulated by opioids. However, the precise circuits from the VTA to DRN and how opioids modulate these circuits remain unknown. Here, we found that neurons projecting from the VTA to DRN are primarily GABAergic. Rostral VTA (rVTA) GABAergic neurons preferentially innervate DRN GABAergic neurons, thus disinhibiting DRN serotonergic neurons. Optogenetic activation of this circuit induces aversion. In contrast, caudal VTA (cVTA) GABAergic neurons mainly target DRN serotonergic neurons, and activation of this circuit promotes reward. Importantly, μ-opioid receptors (MOPs) are selectively expressed at rVTA→DRN GABAergic synapses, and morphine depresses the synaptic transmission. Chronically elevating the activity of the rVTA→DRN pathway specifically interrupts morphine-induced conditioned place preference. This opioid-modulated inhibitory circuit may yield insights into morphine reward and dependence pathogenesis.Entities:
Keywords: Circuit; dorsal raphe; morphine; reward; synaptic plasticity; ventral tegmental area
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Year: 2019 PMID: 30638902 DOI: 10.1016/j.neuron.2018.12.012
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173