血脂异常
内分泌学
内科学
代谢物
脂肪酸合成
肥胖
激素
代谢途径
化学
口服
生物合成
饮食性肥胖
脂肪酸
药理学
下调和上调
色氨酸
医学
β氧化
胰岛素抵抗
生物化学
生物
新陈代谢
胰岛素
脂肪生成
脂质代谢
脂肪变性
体外
胆固醇
信号转导
作者
Yingyu Wang,Yue Wan,Han Wang,Jiai Yan,Jing Ping Sun,Ju Yang,Feng Zhang,Hong Cao,Dan Li
标识
DOI:10.1021/acs.jafc.5c14556
摘要
further confirmed that IAA directly suppresses de novo fatty acid biosynthesis and triacylglycerol assembly. Mechanistically, IAA upregulated hepatic Gpha2 expression, thereby activating the TSH-THR-PGC-1α-PPARγ signaling cascade and concomitantly repressing key lipogenic genes (Fasn, Acaca, and Srebp-1c). Collectively, these findings position IAA as a promising microbiota-derived metabolite with substantial preventive and therapeutic potential for obesity and related metabolic disorders.
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