Electroacupuncture at ST25 ameliorated gastrointestinal dysmotility via downregulation sympathetic nerve-mediated α2-adrenoceptors in postoperative ileus.

IF 2.3 3区 医学 Q3 PHYSIOLOGY
Yi-Duo Liu, Yue-Jie Li, Jin Huang, Jing-Wen Yang, Cun-Zhi Liu, Guang-Xia Shi, Na-Na Yang
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引用次数: 0

Abstract

Postoperative ileus (POI) is a prevalent complication resulting from an imbalance in sympathetic activity or dysregulation of the intestinal immune system. Research has shown that interactions between the peripheral nervous system and immune system modulate intestinal functions. Electroacupuncture (EA) has been shown to ameliorate gastrointestinal dysmotility in patients with POI; however, the specific pathways and molecular mechanisms underlying its effects remain unclear. Here, we reported the signaling pathways that mediate the regulatory effects of EA in POI. Our findings indicated that EA ameliorated gastrointestinal dysmotility, inhibited celiac sympathetic overactivation, and reduced norepinephrine (NE) release. Notably, NE released by the sympathetic nerve terminals regulates the immune system primarily via its stimulation of α2-adrenoceptors (α2-ARs). α2-ARs could regulate macrophage activation in POI and were the key receptors for macrophages to perform neuroimmunomodulatory functions. Furthermore, sympathectomy and α2-ARs antagonist could mimic the improvement effects of EA on gastrointestinal motility and inflammatory response. Our findings demonstrated the pivotal function of the NE-α2-ARs signaling pathways in the modulation of POI, potentially contributing to the development of EA-based therapeutic interventions for gastrointestinal dysmotility disorders after surgery.NEW & NOTEWORTHY Electroacupuncture (EA) ameliorated gastrointestinal dysmotility and inhibited celiac sympathetic overactivation. The α2-adrenergic signaling pathway was involved in the regulation of gastrointestinal dysmotility and was regulated by EA stimulation. The α2-adrenoceptors (α2-ARs) regulated the activation of macrophages in postoperative ileus (POI). The improvement of EA in gastrointestinal motility was mimicked by sympathectomy and α2-adrenoceptors antagonist.

电针ST25通过下调交感神经介导的α 2-肾上腺素受体改善术后肠梗阻胃肠道运动障碍。
术后肠梗阻(POI)是一种常见的并发症,由交感神经活动失衡或肠道免疫系统失调引起。研究表明,周围神经系统和免疫系统之间的相互作用调节肠道功能。电针(EA)已被证明可以改善POI患者的胃肠运动障碍;然而,其作用的具体途径和分子机制尚不清楚。在这里,我们报道了介导EA在POI中的调节作用的信号通路。我们的研究结果表明,EA改善胃肠运动障碍,抑制乳糜泻交感神经过度激活,减少去甲肾上腺素(NE)的释放。值得注意的是,交感神经末梢释放的NE主要通过刺激α2-肾上腺素受体(α2-ARs)来调节免疫系统。α2-ARs可调节POI中巨噬细胞的活化,是巨噬细胞发挥神经免疫调节功能的关键受体。此外,EA的肠道功能改善作用可以通过交感神经切除和α2-ARs拮抗剂来模拟。我们的研究结果证明了NE-α2-ARs信号通路在POI调节中的关键作用,可能有助于开发基于ea的手术后胃肠动力障碍治疗干预措施。
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来源期刊
CiteScore
5.30
自引率
3.60%
发文量
145
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Regulatory, Integrative and Comparative Physiology publishes original investigations that illuminate normal or abnormal regulation and integration of physiological mechanisms at all levels of biological organization, ranging from molecules to humans, including clinical investigations. Major areas of emphasis include regulation in genetically modified animals; model organisms; development and tissue plasticity; neurohumoral control of circulation and hypertension; local control of circulation; cardiac and renal integration; thirst and volume, electrolyte homeostasis; glucose homeostasis and energy balance; appetite and obesity; inflammation and cytokines; integrative physiology of pregnancy-parturition-lactation; and thermoregulation and adaptations to exercise and environmental stress.
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