| Literature DB >> 32502461 |
Hao Wang1, Ping Dong2, Chao He2, Xiao-Yang Feng2, Yue Huang2, Wei-Wei Yang2, Hua-Jing Gao2, Xiao-Fan Shen2, Shan Lin2, Shu-Xia Cao2, Hong Lian2, Jiadong Chen2, Min Yan3, Xiao-Ming Li4.
Abstract
Pain is a source of substantial discomfort. Abnormal activity in both the zona incerta (ZI) and posterior complex of the thalamus (Po) are implicated in neuropathic pain, but their exact roles remain unclear. In particular, the precise cell types and molecular mechanisms of the ZI-Po circuit that regulate nociception are largely uncharacterized. Here, we found that parvalbumin (PV)-positive neuronal projections from the ventral ZI (ZIv) to the Po (ZIv-Po) are critical for promoting nocifensive behaviors, whereas selectively inhibiting ZIv-Po activity reduces nocifensive withdrawal responses. Furthermore, cannabinoid type 1 receptors (CB1Rs) are expressed specifically at ZIv-Po axon terminals in this circuit, and cannabinoids attenuate nocifensive responses through presynaptic inhibition. Selective inhibition of the ZIv-Po circuit or administration of cannabinoids into the Po are sufficient to ameliorate pathological pain. These findings identify the critical role of the ZIv-Po circuit and its modulation by endocannabinoids in controlling nocifensive behaviors.Entities:
Keywords: cannabinoid type 1 receptors; nocifensive behavior; posterior complex of the thalamus; zona incerta
Year: 2020 PMID: 32502461 DOI: 10.1016/j.neuron.2020.04.027
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173