神经病理性疼痛
嘌呤能受体
医学
止痛药
麻醉
封锁
神经痛
药理学
慢性疼痛
MAPK/ERK通路
神经科学
受体
内科学
信号转导
心理学
化学
物理疗法
生物化学
作者
Juping Xing,Ηongji Wang,Lisha Chen,Hanxi Wang,Huan Huang,Jiabao Huang,Changshui Xu
标识
DOI:10.1016/j.intimp.2022.109506
摘要
Neuropathic pain is a growing concern in the medical community, and studies on new analgesic targets for neuropathic pain have become a new hot spot. Whether Connexin43 (Cx43) has a key role in neuropathic pain mediated by the purinergic 2X4 (P2X4) receptor in rats with chronic constriction injury (CCI) was explored in this study. Our experimental results show that blockade of Cx43 could attenuate neuropathic pain in rats suffering from CCI via the P2X4, p38, ERK, and NF-kB signalling pathways. These results suggest that Cx43 may be a promising therapeutic target for the development of novel pharmacological agents in the management of neuropathic pain.
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