导水管周围灰质
内大麻素系统
医学
内源性阿片
去抑制
类阿片
加巴能
内生
刺激
增食欲素
内科学
内分泌学
利莫那班
食欲素-A
麻醉
药理学
抑制性突触后电位
神经科学
神经肽
中脑
中枢神经系统
心理学
大麻素受体
兴奋剂
精神科
受体
作者
Yi-Hung Chen,Hsin-Jung Lee,Ming Tatt Lee,Ya-Ting Wu,Yen-Hsien Lee,Ling-Ling Hwang,Ming‐Shiu Hung,Andreas Zimmer,Ken Mackie,Lih‐Chu Chiou
标识
DOI:10.1073/pnas.1807991115
摘要
Significance Pain remains an unmet medical need due to the ineffectiveness or significant side effects of current pain therapies. Peripheral neurostimulation has been used to relieve pain for decades, but its mechanism(s) remain unsettled. Here, we established an animal model of median nerve stimulation by electrically stimulating the PC6 (Neiguan) acupoint of mice (MNS-PC6). We found MNS-PC6 can release an endogenous neuropeptide (orexin) from the hypothalamus to inhibit pain responses in mice through an endocannabinoid (an endogenous lipid functioning like chemicals from cannabis) that reduces the inhibitory (GABAergic) control in a midbrain pain-control region (the periaqueductal gray). Importantly, MNS-PC6–induced pain relief is endogenous opioid independent. Thus, MNS-PC6 may provide an alternative strategy for pain management in opioid-tolerant patients.
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