Electroacupuncture Alleviates Obesity and Insulin Resistance via the GLP-1-VTADA Reward Circuit.

IF 3.2 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM Neuroendocrinology Pub Date : 2024-01-01 Epub Date: 2023-11-21 DOI:10.1159/000535068
Ye Zhu, Jun Tian, Xiali Wei, Shaohui Jia, Qing Shu
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Abstract

Introduction: We investigated the effects of electroacupuncture (EA) on improving obesity and insulin resistance (IR) in high-fat diet-induced (HFDI) obese rats by modulating the nucleus tractus solitarius (NTS) glucagon-like peptide-1 (GLP-1)-ventral tegmental area (VTA) dopamine (DA) neural reward circuit, thereby uncovering a possible central mechanism underlying EA's actions in improving obesity and IR.

Methods: We randomly allocated 45 Wistar male rats to five groups (normal, model, EA, chemogenetic activation, chemogenetic suppression + EA), with 9 rats in each group. All interventions were conducted within 8 weeks after the model was established. We tested rats for obesity phenotypes included body mass, Lee's index, 24-h food intake, and glucose-metabolism parameters. We observed protein and gene expression for GLP-1 in the NTS and tyrosine hydroxylase in the VTA by Western blotting and real-time polymerase chain reaction, as well as their localization by immunofluorescence. We also determined the DA content in the VTA using high-performance liquid chromatography.

Results: Obese rats exhibited marked hyperphagia, accompanied by increased excitability of DA neurons in the VTA region and reduced insulin sensitivity. After EA treatment, obese rats showed augmented excitability of NTS GLP-1 and suppression of VTADA neurons with a diminution in food intake, showing results similar to those in the chemogenetic activation group. After EA treatment and while inhibiting GLP-1 neurons by chemogenetics, the effect of EA on activating GLP-1 neurons and inhibiting VTADA was partially abrogated. The effects of improving obesity and insulin sensitivity were likewise also suppressed.

Conclusion: EA effectively activated GLP-1 neurons in the NTS, thereby inhibited the expression of DA in the VTA and improved obesity and insulin sensitivity in HFDI-obese rats.

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电针通过GLP-1-VTA - DA奖励回路减轻肥胖和胰岛素抵抗。
目的:研究电针(EA)通过调节孤独束核(NTS)胰高血糖素样肽-1 (GLP-1)-腹侧被盖区(VTA)多巴胺(DA)神经奖赏回路改善高脂饮食诱导(HFDI)肥胖大鼠肥胖和胰岛素抵抗(IR)的作用,从而揭示电针(EA)改善肥胖和IR的可能中枢机制。方法:将45只雄性Wistar大鼠随机分为正常组、模型组、EA组、化生激活组、化生抑制组+ EA组,每组9只。所有干预均在模型建立后8周内进行。我们测试了大鼠的肥胖表型,包括体重、李氏指数、24小时食物摄入量和葡萄糖代谢参数。采用western blotting (WB)和实时聚合酶链反应(RT-qPCR)观察NTS中GLP-1和VTA中酪氨酸羟化酶(TH)的蛋白和基因表达,并采用免疫荧光法定位。用高效液相色谱法测定了VTA中DA的含量。结果:肥胖大鼠表现出明显的贪食,并伴有VTA区DA神经元兴奋性升高和胰岛素敏感性降低。在EA治疗后,肥胖大鼠表现出NTS GLP-1的兴奋性增强和VTADA神经元的抑制,同时食物摄入量减少,结果与化学遗传激活组相似。经EA处理后,在化学遗传学抑制GLP-1神经元的同时,EA对GLP-1神经元的激活和对VTADA的抑制作用部分减弱。改善肥胖和胰岛素敏感性的效果也同样受到抑制。结论:EA能有效激活NTS内GLP-1神经元,从而抑制VTA内DA的表达,改善hfdi肥胖大鼠的肥胖和胰岛素敏感性。
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来源期刊
Neuroendocrinology
Neuroendocrinology 医学-内分泌学与代谢
CiteScore
8.30
自引率
2.40%
发文量
50
审稿时长
6-12 weeks
期刊介绍: ''Neuroendocrinology'' publishes papers reporting original research in basic and clinical neuroendocrinology. The journal explores the complex interactions between neuronal networks and endocrine glands (in some instances also immunecells) in both central and peripheral nervous systems. Original contributions cover all aspects of the field, from molecular and cellular neuroendocrinology, physiology, pharmacology, and the neuroanatomy of neuroendocrine systems to neuroendocrine correlates of behaviour, clinical neuroendocrinology and neuroendocrine cancers. Readers also benefit from reviews by noted experts, which highlight especially active areas of current research, and special focus editions of topical interest.
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