Neurophysiological mechanisms of electroacupuncture in regulating pancreatic function and adipose tissue expansion.

IF 4.6 3区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Yun Liu, Zhi Yu, Xuan Wang, Ming-Qian Yuan, Meng-Jiang Lu, Mei-Rong Gong, Qian Li, You-Bing Xia, Guan-Hu Yang, Bin Xu, Gerhard Litscher, Tian-Cheng Xu
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引用次数: 0

Abstract

Background: Electroacupuncture (EA) has been recognized for its beneficial effects on glucolipid metabolism, potentially through the regulation of sensory nerve coordination. The expandability of peripancreatic adipose tissue (PAT) is implicated in the transition from obesity to type 2 diabetes mellitus (T2DM). However, the specific pancreatic responses to EA require further elucidation.

Aim: To investigate the influence of EA on pancreatic glucolipid reduction level in a high-fat diet (HFD) rat model.

Methods: To delineate the precise pathway through which EA mediates interactions between PAT and islets, we assessed the expression levels of NGF, TRPV1, insulin, as well as other proteins in the pancreas and PAT. This approach enabled us to identify the acupoints that are most conducive to optimizing glycolipid metabolism.

Results: The ST25, LI11 and ST37 groups attenuated HFD-induced obesity and insulin resistance (IR) to distinct degrees, with ST25 group having the greatest effect. EA at ST25 was found to modify the local regulatory influence of PAT on the pancreatic intrinsic nervous system. Specifically, EA at ST25 obviously activated the TRPV1-CGRP-islet beta cell pathway, contributing to the relief of glucolipid metabolic stress. The beneficial effects were abrogated following the chemical silencing of TRPV1 sensory afferents, confirming their indispensable role in EA-mediated regulation of islet and PAT function. Furthermore, in TRPV1 knockout mice, a reduction in PAT inflammation was observed, along with the recovery of islet beta cell function. EA at LI11 and ST37 demonstrated anti-inflammatory properties and helped ameliorate IR.

Conclusion: The PAT ecological niche influenced the progression from obesity to T2DM through various immunometabolic pathways. EA at ST25 could regulate glucolipid metabolism via the TRPV1-CGRP-islet beta cell pathway.

电针调节胰腺功能和脂肪组织扩张的神经生理机制。
背景:电针(EA)已被认为对糖脂代谢有益,可能通过调节感觉神经协调。胰腺周围脂肪组织(PAT)的可扩展性与肥胖症向2型糖尿病(T2DM)的转变有关。然而,胰腺对EA的特异性反应需要进一步阐明。目的:探讨EA对高脂饮食大鼠胰糖脂降低水平的影响。方法:为了描述EA介导PAT与胰岛相互作用的确切途径,我们评估了胰腺和PAT中NGF、TRPV1、胰岛素以及其他蛋白质的表达水平。这种方法使我们能够确定最有利于优化糖脂代谢的穴位。结果:ST25、LI11和ST37组均不同程度地减轻了hfd诱导的肥胖和胰岛素抵抗(IR),其中ST25组效果最大。发现ST25处的EA可改变PAT对胰腺内在神经系统的局部调节作用。其中,ST25 EA明显激活了trpv1 - cgrp -胰岛β细胞通路,有助于缓解糖脂代谢应激。随着TRPV1感觉传入的化学沉默,其有益作用被取消,证实了它们在ea介导的胰岛和PAT功能调节中不可或缺的作用。此外,在TRPV1基因敲除小鼠中,观察到PAT炎症的减少,以及胰岛β细胞功能的恢复。LI11和ST37处的EA显示出抗炎特性,并有助于改善IR。结论:PAT生态位通过多种免疫代谢途径影响肥胖向T2DM的发展。ST25的EA可通过trpv1 - cgrp -胰岛β细胞通路调节糖脂代谢。
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来源期刊
World Journal of Diabetes
World Journal of Diabetes ENDOCRINOLOGY & METABOLISM-
自引率
2.40%
发文量
909
期刊介绍: The WJD is a high-quality, peer reviewed, open-access journal. The primary task of WJD is to rapidly publish high-quality original articles, reviews, editorials, and case reports in the field of diabetes. In order to promote productive academic communication, the peer review process for the WJD is transparent; to this end, all published manuscripts are accompanied by the anonymized reviewers’ comments as well as the authors’ responses. The primary aims of the WJD are to improve diagnostic, therapeutic and preventive modalities and the skills of clinicians and to guide clinical practice in diabetes. Scope: Diabetes Complications, Experimental Diabetes Mellitus, Type 1 Diabetes Mellitus, Type 2 Diabetes Mellitus, Diabetes, Gestational, Diabetic Angiopathies, Diabetic Cardiomyopathies, Diabetic Coma, Diabetic Ketoacidosis, Diabetic Nephropathies, Diabetic Neuropathies, Donohue Syndrome, Fetal Macrosomia, and Prediabetic State.
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