Exercise ameliorates adipose tissue insulin resistance by activating the lactate/GPR81 signaling pathway in DIO-IR mice.

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Yihsuan Lin, Ge Song, Yue Chen, Chunyu Liang, Zhen Ni, Lijing Gong, Yi Yan
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引用次数: 0

Abstract

Growing evidence indicates that both exogenous lactate administration and physical exercise improve insulin resistance (IR). This study investigates, from a novel perspective, whether exercise-induced lactate serves as a signaling molecule to ameliorate adipose tissue IR and explores the underlying mechanisms. Using diet-induced obese and insulin-resistant (DIO-IR) mice subjected to high-lactate exercise training, insulin-resistant 3T3-L1 (IR-3T3-L1) adipocytes treated with lactate, and a G protein-coupled receptor 81 (GPR81)-overexpressing cell line, we demonstrate three key findings: first, high-lactate exercise training markedly alleviated adipose tissue and systemic IR in DIO-IR mice. Second, acute high-lactate exercise mirrored the effects of l-lactate injection by elevating circulating and epididymal white adipose tissue (eWAT) lactate concentrations, concomitantly upregulating GPR81 and glucose uptake signaling expression while modulating adipokine secretion. Mechanistically, lactate/GPR81 signaling potentiated glucose uptake in IR-3T3-L1 adipocytes via the insulin receptor substrate 1 (IRS1)-AKT-glucose transporter 4 (GLUT4) pathway. Collectively, these results demonstrate that exercise-induced lactate enhances glucose uptake signaling and rebalances adipokine secretion. It may act as a signaling molecule that upregulates the specific receptor GPR81, thereby alleviating adipose tissue and systemic insulin resistance in DIO-IR mice. Our findings uncover a previously unrecognized link between exercise metabolism and adipose tissue homeostasis, highlighting lactate as a potential therapeutic target for IR-related metabolic disorders.NEW & NOTEWORTHY Exercise-induced lactate as a critical signaling molecule that ameliorates insulin resistance in obesity. Lactate enhances adipose tissue glucose uptake and rebalances adipokine secretion by upregulating the receptor G protein-coupled receptor 81 (GPR81). The findings establish lactate as an essential exercise metabolite with therapeutic potential for metabolic disorders.

运动通过激活DIO-IR小鼠乳酸/GPR81信号通路改善脂肪组织胰岛素抵抗。
越来越多的证据表明,外源性乳酸管理和体育锻炼可以改善胰岛素抵抗(IR)。本研究从一个新的角度探讨运动诱导的乳酸是否作为一种信号分子改善脂肪组织IR,并探讨其潜在的机制。通过高乳酸运动训练的饮食诱导肥胖和胰岛素抵抗(DIO-IR)小鼠、乳酸处理的胰岛素抵抗3T3-L1 (IR-3T3-L1)脂肪细胞和gpr81过表达细胞系,我们展示了三个关键发现:首先,高乳酸运动训练显著减轻DIO-IR小鼠的脂肪组织和全身IR。其次,急性高乳酸运动通过提高循环和附睾白色脂肪组织(eWAT)乳酸浓度,同时上调GPR81和葡萄糖摄取信号表达,同时调节脂肪因子分泌,从而反映l -乳酸注射的作用。在机制上,乳酸/GPR81信号通过IRS1-AKT-GLUT4途径增强IR-3T3-L1脂肪细胞的葡萄糖摄取。总的来说,这些结果表明运动诱导的乳酸增强葡萄糖摄取信号并重新平衡脂肪因子的分泌。它可能作为一种信号分子,上调特异性受体GPR81,从而减轻饮食诱导的肥胖胰岛素抵抗(DIO-IR)小鼠的脂肪组织和全身胰岛素抵抗。我们的研究结果揭示了运动代谢和脂肪组织稳态之间以前未被认识到的联系,突出了乳酸作为ir相关代谢紊乱的潜在治疗靶点。
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来源期刊
CiteScore
9.80
自引率
0.00%
发文量
98
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.
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