瘦素和g蛋白偶联受体(GPCR)信号传导:肥胖症的治疗潜力。

IF 4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xun Sun,Lincoln Brueck,Dongming Yang,Patrick L Sheets,Baohua Zhou,Hongxia Ren
{"title":"瘦素和g蛋白偶联受体(GPCR)信号传导:肥胖症的治疗潜力。","authors":"Xun Sun,Lincoln Brueck,Dongming Yang,Patrick L Sheets,Baohua Zhou,Hongxia Ren","doi":"10.1016/j.jbc.2025.110768","DOIUrl":null,"url":null,"abstract":"Leptin, an adipocyte-derived hormone, plays a crucial role in regulating food intake and energy homeostasis. However, individuals with obesity exhibit hyperleptinemia and impaired leptin responsiveness, which contribute to greater food intake, reduced energy expenditure, and metabolic dysregulation, exacerbating weight gain and obesity-related complications. Leptin resistance remains a major challenge in obesity treatment, limiting the efficacy of leptin-based therapies. G-protein coupled receptors (GPCRs) are a large family of seven-transmembrane (7TM) receptors that respond to a variety of ligands, including neuropeptides, gastrointestinal hormones, and metabolites. GPCRs are central regulators of glucose metabolism and energy balance, which have emerged as key drug targets for diabetes and obesity. Combining leptin with GPCR-targeting therapies, such as gut peptides, shows promise in overcoming leptin resistance and improving metabolic outcomes. Understanding the molecular crosstalk between leptin and GPCRs provides valuable insights for expanding leptin's therapeutic potential and developing effective anti-obesity treatments. In this review, we highlight the therapeutic potential of combining molecules targeting GPCR signaling with leptin for obesity treatment.","PeriodicalId":15140,"journal":{"name":"Journal of Biological Chemistry","volume":"1 1","pages":"110768"},"PeriodicalIF":4.0000,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Leptin and G-protein coupled receptor (GPCR) Signaling: Therapeutic Potential in Obesity.\",\"authors\":\"Xun Sun,Lincoln Brueck,Dongming Yang,Patrick L Sheets,Baohua Zhou,Hongxia Ren\",\"doi\":\"10.1016/j.jbc.2025.110768\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Leptin, an adipocyte-derived hormone, plays a crucial role in regulating food intake and energy homeostasis. However, individuals with obesity exhibit hyperleptinemia and impaired leptin responsiveness, which contribute to greater food intake, reduced energy expenditure, and metabolic dysregulation, exacerbating weight gain and obesity-related complications. Leptin resistance remains a major challenge in obesity treatment, limiting the efficacy of leptin-based therapies. G-protein coupled receptors (GPCRs) are a large family of seven-transmembrane (7TM) receptors that respond to a variety of ligands, including neuropeptides, gastrointestinal hormones, and metabolites. GPCRs are central regulators of glucose metabolism and energy balance, which have emerged as key drug targets for diabetes and obesity. Combining leptin with GPCR-targeting therapies, such as gut peptides, shows promise in overcoming leptin resistance and improving metabolic outcomes. Understanding the molecular crosstalk between leptin and GPCRs provides valuable insights for expanding leptin's therapeutic potential and developing effective anti-obesity treatments. In this review, we highlight the therapeutic potential of combining molecules targeting GPCR signaling with leptin for obesity treatment.\",\"PeriodicalId\":15140,\"journal\":{\"name\":\"Journal of Biological Chemistry\",\"volume\":\"1 1\",\"pages\":\"110768\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2025-09-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Biological Chemistry\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1016/j.jbc.2025.110768\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Biological Chemistry","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.jbc.2025.110768","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

瘦素是一种脂肪细胞衍生的激素,在调节食物摄入和能量平衡中起着至关重要的作用。然而,肥胖个体表现出高瘦素血症和瘦素反应受损,这导致更多的食物摄入,减少能量消耗和代谢失调,加剧体重增加和肥胖相关并发症。瘦素抵抗仍然是肥胖治疗的主要挑战,限制了基于瘦素的治疗的疗效。g蛋白偶联受体(gpcr)是一个由7个跨膜(7TM)受体组成的大家庭,它们对多种配体(包括神经肽、胃肠激素和代谢物)有反应。gpcr是葡萄糖代谢和能量平衡的中心调节因子,已成为糖尿病和肥胖症的关键药物靶点。将瘦素与gpcr靶向疗法(如肠肽)结合,有望克服瘦素抵抗并改善代谢结果。了解瘦素和GPCRs之间的分子串扰为扩大瘦素的治疗潜力和开发有效的抗肥胖治疗方法提供了有价值的见解。在这篇综述中,我们强调了靶向GPCR信号的分子与瘦素联合治疗肥胖的治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Leptin and G-protein coupled receptor (GPCR) Signaling: Therapeutic Potential in Obesity.
Leptin, an adipocyte-derived hormone, plays a crucial role in regulating food intake and energy homeostasis. However, individuals with obesity exhibit hyperleptinemia and impaired leptin responsiveness, which contribute to greater food intake, reduced energy expenditure, and metabolic dysregulation, exacerbating weight gain and obesity-related complications. Leptin resistance remains a major challenge in obesity treatment, limiting the efficacy of leptin-based therapies. G-protein coupled receptors (GPCRs) are a large family of seven-transmembrane (7TM) receptors that respond to a variety of ligands, including neuropeptides, gastrointestinal hormones, and metabolites. GPCRs are central regulators of glucose metabolism and energy balance, which have emerged as key drug targets for diabetes and obesity. Combining leptin with GPCR-targeting therapies, such as gut peptides, shows promise in overcoming leptin resistance and improving metabolic outcomes. Understanding the molecular crosstalk between leptin and GPCRs provides valuable insights for expanding leptin's therapeutic potential and developing effective anti-obesity treatments. In this review, we highlight the therapeutic potential of combining molecules targeting GPCR signaling with leptin for obesity treatment.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Biological Chemistry
Journal of Biological Chemistry Biochemistry, Genetics and Molecular Biology-Biochemistry
自引率
4.20%
发文量
1233
期刊介绍: The Journal of Biological Chemistry welcomes high-quality science that seeks to elucidate the molecular and cellular basis of biological processes. Papers published in JBC can therefore fall under the umbrellas of not only biological chemistry, chemical biology, or biochemistry, but also allied disciplines such as biophysics, systems biology, RNA biology, immunology, microbiology, neurobiology, epigenetics, computational biology, ’omics, and many more. The outcome of our focus on papers that contribute novel and important mechanistic insights, rather than on a particular topic area, is that JBC is truly a melting pot for scientists across disciplines. In addition, JBC welcomes papers that describe methods that will help scientists push their biochemical inquiries forward and resources that will be of use to the research community.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信