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

被引:0
作者
Jang, Hisu [1 ,2 ]
Shin, Su-Kyung [1 ,2 ]
Bae, Heekyong R. [1 ,2 ]
Lee, Hangyeol [3 ]
Seo, Hye-Young [3 ]
Seo, Woo Duck [4 ]
Kwon, Eun-Young [1 ,2 ,5 ,6 ]
机构
[1] Kyungpook Natl Univ, Dept Food Sci & Nutr, 80 Daehak Ro, Daegu 41566, South Korea
[2] Kyungpook Natl Univ, Ctr Food & Nutr Genom Res, 80 Daehak Ro, Daegu 41566, South Korea
[3] Rural Dev Adm RDA, Natl Inst Crop Sci NICS, Food Tech Resources Res Div, Wanju 55365, South Korea
[4] Rural Dev Adm RDA, Int Technol Cooperat Ctr ITCC, Cheorwon Branch, Jeonrabug Do 54875, South Korea
[5] Kyungpook Natl Univ, Ctr Beautiful Aging, 80 Daehak Ro, Daegu 41566, South Korea
[6] Kyungpook Natl Univ, Dept Integrat Bioconvergence, 80 Daehak Ro, Daegu 41566, South Korea
关键词
AMPK alpha; Azukisaponin II; Obesity; PPAR alpha; Red bean seedlings extract; White adipose tissue; GAMMA;
D O I
10.1016/j.foodres.2025.116803
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
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 PPAR alpha and AMPK alpha 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 AMPK alpha signaling and upregulating PPAR alpha 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 PPAR alpha-knockdown 3T3-L1 cells with RS and AZ alleviates lipid accumulation by activating PPAR alpha-AMPK alpha signaling. RS supplementation effectively reduces obesity in HFD-induced mice by enhancing lipid metabolism and mitochondrial function through PPAR alpha-AMPK alpha 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.
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页数:12
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