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5-HT(7) Receptor Is Involved in Electroacupuncture Inhibition of Chronic Pain in the Spinal Cord

Knee osteoarthritis (KOA) is a common and disabling condition characterized by attacks of pain around the joints, and it is a typical disease that develops chronic pain. Previous studies have proved that 5-HT(1), 5-HT(2), and 5-HT(3) receptors in the spinal cord are involved in electroacupuncture (E...

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Detalles Bibliográficos
Autores principales: Yuan, Xiao-Cui, Yan, Xiang-Ji, Tian, Li-Xia, Guo, Yi-Xiao, Zhao, Yu-Long, Baba, Sani Sa’idu, Wang, Yu-Ying, Liang, Ling-Li, Jia, Hong, Xu, Lin-Ping, Li, Li, Lin, Han, Huo, Fu-Quan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484641/
https://www.ncbi.nlm.nih.gov/pubmed/34602973
http://dx.doi.org/10.3389/fnins.2021.733779
Descripción
Sumario:Knee osteoarthritis (KOA) is a common and disabling condition characterized by attacks of pain around the joints, and it is a typical disease that develops chronic pain. Previous studies have proved that 5-HT(1), 5-HT(2), and 5-HT(3) receptors in the spinal cord are involved in electroacupuncture (EA) analgesia. The 5-HT(7) receptor plays antinociceptive role in the spinal cord. However, it is unclear whether the 5-HT(7) receptor is involved in EA analgesia. The 5-HT(7) receptor is a stimulatory G-protein (Gs)-coupled receptor that activates adenylyl cyclase (AC) to stimulate cyclic adenosine monophosphate (cAMP) formation, which in turn activates protein kinase A (PKA). In the present study, we found that EA significantly increased the tactile threshold and the expression of the 5-HT(7) receptor in the dorsal spinal cord. Intrathecal injection of 5-HT(7) receptor agonist AS-19 mimicked the analgesic effect of EA, while a selective 5-HT(7) receptor antagonist reversed this effect. Moreover, intrathecal injection of AC and PKA antagonists prior to EA intervention prevented its anti-allodynic effect. In addition, GABA(A) receptor antagonist bicuculline administered (intrathecal, i.t.) prior to EA intervention blocked the EA effect on pain hypersensitivity. Our data suggest that the spinal 5-HT(7) receptor activates GABAergic neurons through the Gs–cAMP–PKA pathway and participates in EA-mediated inhibition of chronic pain in a mouse model of KOA.