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首页> 外文期刊>Digestive Diseases and Sciences >Electroacupuncture Upregulated Ghrelin in Rats with Functional Dyspepsia via AMPK/TSC2/Rheb-Mediated mTOR Inhibition
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Electroacupuncture Upregulated Ghrelin in Rats with Functional Dyspepsia via AMPK/TSC2/Rheb-Mediated mTOR Inhibition

机译:通过AMPK / TSC2 / RHEB介导的MTOR抑制函数功能性消化不良的大鼠电针上调Ghrelin

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Background Gastrointestinal motility disorder is an important pathological basis for functional dyspepsia (FD). Epigastric ache and discomfort are the main symptoms of FD, and ghrelin deficiency is closely related to the occurrence and development of FD. While electroacupuncture (EA) alleviated the symptoms of FD patients and improved their quality of life, there is a lack of sufficient mechanistic evidence to support these beneficial effects. Methods An in vivo FD model was established in wild-type and mammalian target of rapamycin (mTOR) knockout (-/-) rats. FD rats were subjected to EA with or without mTOR agonists or inhibitors. Gastric emptying and intestinal propulsion were assessed, and pathological changes in the hypothalamus, gastric antrum, and small intestine were examined histologically. In addition, ghrelin expression and AMPK/TSC2/Rheb/mTOR activation were detected by quantitative reverse transcription polymerase chain reaction and western blot. Results EA alone or in combination with mTOR inhibitors improved gastrointestinal function in FD rats by increasing the rates of intestinal propulsion and gastric emptying, and pathological changes in the hypothalamus, gastric antrum, and small intestine were alleviated. This may be related to the significant upregulation of ghrelin expression and the effective activation of the AMPK/TSC2/Rheb/mTOR signaling pathway. Interestingly, EA also improved gastrointestinal function and ghrelin expression in mTOR (-/-) KO FD rats. Conclusion Altering the level of ghrelin by regulating AMPK/TSC2/Rheb-mediated mTOR inhibition is an important way through which EA treats FD. The complex EA-mediated regulatory mechanisms of the brain-gut axis still require further exploration.
机译:背景技术胃肠动力障碍是功能性消化不良(FD)的重要病理基础。 Epigastric Acche和不适是FD的主要症状,Ghrelin缺陷与FD的发生和发展密切相关。虽然电针(EA)缓解了FD患者的症状并提高了他们的生活质量,但缺乏足够的机制证据来支持这些有益效果。方法以野生型和哺乳动物敲击(MTOR)敲除( - / - )大鼠的野生型和哺乳动物靶标建立体内FD模型。在没有MTOR激动剂或抑制剂的情况下对FD大鼠进行EA。评估胃排空和肠道推进,并在组织学上检查下丘脑,胃窦和小肠的病理变化。此外,通过定量逆转录聚合酶链反应和Western印迹检测Ghrelin表达和AMPK / TSC2 / RHEB / mTOR活化。结果EA单独或与MTOR抑制剂组合通过增加肠道推进和胃排空的速率来改善FD大鼠的胃肠功能,并且缓解下丘脑,胃窦和小肠的病理变化。这可能与Ghrelin表达的显着上调和AMPK / TSC2 / RHEB / MTOR信号传导途径的有效激活有关。有趣的是,EA还改善了MTOR( - / - )KO FD大鼠的胃肠功能和Ghrelin表达。结论通过调节AMPK / TSC2 / RHEB介导的MTOR抑制改变GHRELIN水平是EA治疗FD的重要方式。复杂的EA介导的脑齿轴的调节机制仍需要进一步探索。

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