Electroacupuncture relieves visceral hypersensitivity through modulation of the endogenous cannabinoid system

医学 单酰甘油脂肪酶 电针 生理盐水 内大麻素系统 脂肪酸酰胺水解酶 TRPV1型 大麻素 内科学 大麻素受体 麻醉 内分泌学 药理学 针灸科 受体 兴奋剂 病理 瞬时受体电位通道 替代医学
作者
Ning Ma,Xiaojing Li,Qiuhua Li,Diqi Yang,Shen Zhuang,Sha Nan,Liu Ai,Mingxing Ding,Yi Ding
出处
期刊:Acupuncture in Medicine [SAGE Publishing]
卷期号:41 (4): 224-234 被引量:2
标识
DOI:10.1177/09645284221107699
摘要

Background: Electroacupuncture (EA) can effectively relieve visceral hypersensitivity (VH). However, its mechanisms are still unclear. Objective: To investigate the impact of EA on VH caused by ileitis, and whether EA relieves VH by modulating the endogenous cannabinoid system (ECS). Methods: Thirty male native goats were randomly divided into a saline-treated control group (Saline, n = 9) and three 2,4,6-trinitro-benzenesulfonic acid (TNBS)-treated VH model groups that underwent injection of TNBS into the ileal wall to induce VH and remained untreated (TNBS, n = 9) or received six sessions of EA (for 30 min every 3 days) (TNBS + EA, n = 6) or sham acupuncture (TNBS + Sham, n = 6). The visceromotor response (VMR) to colorectal distention (CRD) was measured after each EA treatment. Three goats in the Saline/TNBS groups were euthanized after 7 days for histopathological examination; the remaining 24 (n = 6/group) underwent sampling of the ileal wall, T11 spinal cord and brain nuclei/areas related to visceral regulation and ascending pain modulation system on day 22. Expression of cannabinoid receptor 1 (CB1R), fatty acid amide hydrolase (FAAH) and monoacylglycerol lipase (MAGL) was detected by immunohistochemistry. Results: VMR to CRD was greater in TNBS-treated goats than in saline-treated goats (p < 0.01) from day 7 to 22. After day 7, EA-treated goats showed a decreased (p < 0.05) VMR compared with untreated TNBS-exposed goats. TNBS treatment decreased CB1R and increased FAAH and MAGL expression in the ileum and related nuclei/areas; this was reversed by EA. Conclusion: EA ameliorates VH, probably by regulating the ECS in the intestine and nuclei/areas related to visceral regulation and descending pain modulation systems.
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