产热
线粒体生物发生
SIRT3
生物
内分泌学
TFAM公司
褐色脂肪组织
内科学
锡尔图因
产热素
脂解
西妥因1
紫檀
线粒体
肠道菌群
脂肪组织
化学
细胞生物学
生物化学
白藜芦醇
医学
下调和上调
乙酰化
基因
作者
Yen‐Chun Koh,Sze‐Kwan Lin,Kuan-Lun Hsu,Kalyanam Nagabhushanam,Chi‐Tang Ho,Min‐Hsiung Pan
标识
DOI:10.1002/mnfr.202300370
摘要
Sirtuin 1/peroxisome proliferator-activated receptor gamma co-activator 1 alpha (SIRT1/PGC-1α) pathway activation is known to promote thermogenesis and mitochondrial biogenesis. Pterostilbene (PSB) and pinostilbene (PIN), the methylated analogs of resveratrol, are potential candidates to enhance thermogenesis and mitochondrial biogenesis.A model of Western diet-induced obesity in mice is designed. Either PSB or PIN is supplemented in the diet for 16 weeks. Both samples can significantly reduce body weight gain but only PSB can decrease inguinal adipose tissue weight. Besides, both samples can promote lipolysis but only PSB supplementation activates the SIRT1/PGC-1α/SIRT3 pathway to enhance mitochondrial biogenesis and thermogenesis in the inguinal adipose tissue. In addition, although both samples exert a modulatory effect on gut microbiota but significant increments in fecal isobutyric acid, valeric acid, and isovaleric acid are only observed in the PSB group, functioning as gut microbial metabolites.Overall, these findings suggest PSB and PIN as potential candidates for the improvement of obesity and gut microbiota dysbiosis. With its higher stability, PSB exerts a greater effect than PIN by promoting thermogenesis and mitochondrial biogenesis via SIRT1 activation.
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