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首页> 外文期刊>World Journal of Gastroenterology >Electroacupuncture at ST25 inhibits jejunal motility: Role of sympathetic pathways and TRPV1
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Electroacupuncture at ST25 inhibits jejunal motility: Role of sympathetic pathways and TRPV1

机译:ST25的电针抑制了Jejunal运动:交感神经途径和TRPV1的作用

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AIM: To investigate whether electroacupuncture (EA) at ST25 affects jejunal motility in vivo and if so, whether a sympathetic pathway is involved. METHODS: Jejunal motility was assessed using a manometric balloon placed in the jejunum approximately about 3-5 cm away from the suspensory ligament of the duodenum in anesthetized animals. The effects of EA at ST25 were measured in male Sprague-Dawley rats, some of which were treated with propranolol or clenbuterol (EA intensities: 1, 3, 5, 7, and 9 mA), and in male transient receptor potential vanilloid-1 (TRPV1) (capsaicin receptor) knockout mice (EA intensities: 1, 2, and 4 mA). RESULTS: Anesthetized rats exhibited three types of fasting jejunal motor patterns (types A, B, and C), and only type C rats responded to EA stimulation. In type C rats, EA at ST25 significantly suppressed the motor activity of the jejunum in an intensity-dependent manner. The inhibitory effect of EA was weakened by propranolol (β adrenoceptor antagonist) and disappeared with clenbuterol (β adrenoceptor agonist) induced inhibition of motility, suggesting that the effect of EA on motility is mediated via a sympathetic pathway. Compared with wild-type mice, EA at ST25 was less effective in TRPV1 knockout mice, suggesting that this multi-modal sensor channel participates in the mechanism. CONCLUSION: EA at ST25 was found to inhibit jejunal motility in an intensity-dependent manner, via a mechanism in which sympathetic nerves and TRPV1 receptors play an important role.
机译:目的:调查ST25的电针(EA)是否影响了体内的Jejunal运动,如果是,是否涉及交感神经途径。方法:使用在麻醉动物中大约3-5厘米的Jejunum中放置在Jejunum中的测量球囊评估Jejunal运动性。在雄性Sprague-Dawley大鼠中测量EA在ST25的影响,其中一些用普萘洛尔或亚氯酮(EA强度:1,3,5,7和9mA)处理,并且在阳瞬态受体潜在的香草1中(TRPV1)(辣椒素受体)敲除小鼠(EA强度:1,2和4 mA)。结果:麻醉大鼠表现出三种类型的空腹电机模式(类型A,B和C),只有C型大鼠响应EA刺激。在C型大鼠中,ST25的EA以强度依赖性方式显着抑制了Jejunum的电机活动。 EA的抑制作用被普萘洛尔(β肾上腺素受体拮抗剂)削弱,并与氯丁苯甲醇(β肾上腺素受体激动剂)诱导的运动抑制,表明EA对运动的影响是通过交感神经途径介导的。与野生型小鼠相比,ST25的EA在TRPV1敲除小鼠中效果较低,表明该多模态传感器通道参与该机制。结论:在ST25处发现EA以强度依赖性方式抑制Jejunal运动,通过同情神经和TRPV1受体发挥重要作用的机制。

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