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膳食红豆幼苗提取物通过激活高脂饮食喂养的肥胖小鼠白色脂肪组织中的PPARα - AMPKα信号通路来减轻肥胖。

Dietary red bean seedlings extract alleviates obesity via activation of PPARα - AMPKα signaling in white adipose tissue of high-fat diet-fed obese mice.

作者信息

Jang Hisu, Shin Su-Kyung, Bae Heekyong R, Lee HanGyeol, Seo Hye-Young, Seo Woo Duck, Kwon Eun-Young

机构信息

Department of Food Science and Nutrition, Kyungpook National University, 80, Daehak-ro, Buk-Ku, Daegu 41566, Republic of Korea; Center for Food and Nutritional Genomics Research, Kyungpook National University, 80, Daehak-ro, Buk-Ku, Daegu 41566, Republic of Korea.

Food Tech Resources Research Division, National Institute of Crop Science (NICS), Rural Development Administration (RDA), Wanju, 55365, Republic of Korea.

出版信息

Food Res Int. 2025 Oct;218:116803. doi: 10.1016/j.foodres.2025.116803. Epub 2025 Jun 9.

Abstract

With the global prevalence of obesity rising, there is an increasing need for the development of obesity treatments using natural substances with fewer side effects. The efficacy of germinated red bean extract and its bioactive compound, azukisaponin II (AZ), on anti-obesity has been reported very little to date. This study aims to investigate the anti-obesity effects of red bean seedling extract (RS) and AZ, on PPARα and AMPKα signaling pathways in white adipose tissue. RS supplementation effectively reduced fat mass and improved lipid metabolism in HFD-induced obese mice. RS decreased body weight gain, reduced adipocyte size, and lowered plasma triglyceride, free fatty acids, and total cholesterol. RS also enhanced mitochondrial function and fatty acid oxidation by activating AMPKα signaling and upregulating PPARα expression in white adipose tissue. In particular, the levels of lipolysis-related factors (ATGL, HSL, and PLIN5) and proteins in the mitochondrial electron transport chain (NDUFB8, SDHB, UQCRC2, MTCO1, ATP5A) were increased in the RS200 and RS300 groups. RS and AZ treatments inhibited adipogenesis and promoted lipid metabolism in 3T3-L1 adipocytes. Additionally, we confirmed that treating PPARα-knockdown 3T3-L1 cells with RS and AZ alleviates lipid accumulation by activating PPARα-AMPKα signaling. RS supplementation effectively reduces obesity in HFD-induced mice by enhancing lipid metabolism and mitochondrial function through PPARα-AMPKα signaling. Additionally, RS and AZ decrease lipid accumulation and promote mitochondrial biogenesis in 3T3-L1 cells, indicating their potential for treating obesity and metabolic disorders with a favorable safety profile.

摘要

随着全球肥胖患病率的上升,越来越需要开发使用副作用较少的天然物质的肥胖治疗方法。迄今为止,发芽红豆提取物及其生物活性化合物小豆皂苷II(AZ)的抗肥胖功效报道甚少。本研究旨在探讨红豆幼苗提取物(RS)和AZ对白色脂肪组织中PPARα和AMPKα信号通路的抗肥胖作用。补充RS可有效降低高脂饮食诱导的肥胖小鼠的脂肪量并改善脂质代谢。RS降低了体重增加,减小了脂肪细胞大小,并降低了血浆甘油三酯、游离脂肪酸和总胆固醇。RS还通过激活AMPKα信号和上调白色脂肪组织中PPARα的表达来增强线粒体功能和脂肪酸氧化。特别是,RS200和RS300组中脂解相关因子(ATGL、HSL和PLIN5)以及线粒体电子传递链中的蛋白质(NDUFB8、SDHB、UQCRC2、MTCO1、ATP5A)水平升高。RS和AZ处理抑制3T3-L1脂肪细胞的脂肪生成并促进脂质代谢。此外,我们证实用RS和AZ处理PPARα基因敲低的3T3-L1细胞可通过激活PPARα-AMPKα信号减轻脂质积累。补充RS可通过PPARα-AMPKα信号增强脂质代谢和线粒体功能,有效减轻高脂饮食诱导的小鼠肥胖。此外,RS和AZ减少3T3-L1细胞中的脂质积累并促进线粒体生物发生,表明它们具有以良好的安全性治疗肥胖和代谢紊乱的潜力。

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