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瞬时受体电位香草酸亚型1(TRPV1)在神经内分泌调节中的作用:对抗肥胖的潜在靶点?

Role of TRPV1 in neuroendocrine regulation: a potential target against obesity?

作者信息

Wang Jiexin, Liu Maohui, Wen Lingmiao, Xing Pengfei, Chen Jiawei, Xia Xiuwen, Ding WeiJun

机构信息

School of Basic Medical Sciences, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

出版信息

Front Immunol. 2025 Jul 3;16:1598804. doi: 10.3389/fimmu.2025.1598804. eCollection 2025.

DOI:10.3389/fimmu.2025.1598804
PMID:40677717
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12267016/
Abstract

Obesity is a common metabolic syndrome in which an imbalance between energy intake and consumption is the main cause of excessive accumulation of body fat. The increasing prevalence of obesity and its associated complications poses significant challenges to public health. Activation of the transient receptor potential vanilloid subtype 1 (TRPV1) cascade plays a key role in lipid metabolism and energy intake. TRPV1 is expressed across the central nervous system and peripheral organs is involved in the regulation of hormone secretion, appetite and mitochondrial function, and is recognized as one of the key targets for preventing obesity. The current treatments for obesity exhibit limited efficacy and are associated with numerous side effects. Targeting TRPV1 represents a potentially effective approach for managing obesity. In this work, by combining the recent mechanism of the role of TRPV1 in neuroendocrine regulation, we hope to provide novel approaches to block or even reverse the development of obesity.

摘要

肥胖是一种常见的代谢综合征,其中能量摄入与消耗之间的失衡是体内脂肪过度堆积的主要原因。肥胖及其相关并发症的患病率不断上升,给公共卫生带来了重大挑战。瞬时受体电位香草酸亚型1(TRPV1)级联反应的激活在脂质代谢和能量摄入中起关键作用。TRPV1在中枢神经系统和外周器官中表达,参与激素分泌、食欲和线粒体功能的调节,被认为是预防肥胖的关键靶点之一。目前的肥胖治疗方法疗效有限,且伴有许多副作用。靶向TRPV1是一种潜在有效的肥胖管理方法。在这项工作中,通过结合TRPV1在神经内分泌调节中作用的最新机制,我们希望提供新的方法来阻止甚至逆转肥胖的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3e6/12267016/5df67706dca1/fimmu-16-1598804-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3e6/12267016/36c3bd66d4db/fimmu-16-1598804-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3e6/12267016/5df67706dca1/fimmu-16-1598804-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3e6/12267016/36c3bd66d4db/fimmu-16-1598804-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3e6/12267016/5df67706dca1/fimmu-16-1598804-g002.jpg

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本文引用的文献

1
The β-Adrenergic Receptor: Structure, Physiopathology of Disease, and Emerging Therapeutic Potential.β-肾上腺素能受体:结构、疾病的病理生理学及新兴治疗潜力
Adv Pharmacol Pharm Sci. 2024 Nov 28;2024:2005589. doi: 10.1155/2024/2005589. eCollection 2024.
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TRPV1 Promotes Periodontitis Tissue Inflammation and Oxidative Damage by Regulating STAT3 Signaling Pathway.瞬时受体电位香草酸亚型1通过调节信号转导和转录激活因子3信号通路促进牙周炎组织炎症和氧化损伤。
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One Nervous System: Critical Links Between Central and Peripheral Nervous System Health and Implications for Obesity and Diabetes.一个神经系统:中枢神经系统和周围神经系统健康之间的关键联系及其对肥胖和糖尿病的影响。
Diabetes. 2024 Dec 1;73(12):1967-1975. doi: 10.2337/dbi24-0004.
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Obesity: exploring its connection to brain function through genetic and genomic perspectives.肥胖症:从遗传学和基因组学角度探索其与脑功能的联系。
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TRPV1 Activation Antagonizes High-Fat Diet-Induced Obesity at Thermoneutrality and Enhances UCP-1 Transcription via PRDM-16.瞬时受体电位香草酸亚型1(TRPV1)激活可拮抗热中性条件下高脂饮食诱导的肥胖,并通过PRDM-16增强解偶联蛋白1(UCP-1)转录。
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Obesity-associated Inflammation and Alloimmunity.肥胖相关炎症与同种免疫
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Curr Opin Pharmacol. 2024 Apr;75:102447. doi: 10.1016/j.coph.2024.102447. Epub 2024 Mar 11.
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