二甲双胍
线粒体
药理学
体内
生物
内科学
内分泌学
化学
医学
生物化学
糖尿病
生物技术
作者
Colleen R. Reczek,Ram Prosad Chakrabarty,Karis B. D’Alessandro,Zachary L. Sebo,Rogan A. Grant,Peng Gao,G. R. Scott Budinger,Navdeep S. Chandel
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2024-12-18
卷期号:10 (51)
被引量:1
标识
DOI:10.1126/sciadv.ads5466
摘要
Metformin is among the most prescribed antidiabetic drugs, but the primary molecular mechanism by which metformin lowers blood glucose levels is unknown. Previous studies have proposed numerous mechanisms by which acute metformin lowers blood glucose, including the inhibition of mitochondrial complex I of the electron transport chain (ETC). Here, we used transgenic mice that globally express the Saccharomyces cerevisiae internal alternative NADH dehydrogenase (NDI1) protein to determine whether the glucose-lowering effect of acute oral administration of metformin requires inhibition of mitochondrial complex I of the ETC in vivo. NDI1 is a yeast NADH dehydrogenase enzyme that complements the loss of mammalian mitochondrial complex I electron transport function and is insensitive to pharmacologic mitochondrial complex I inhibitors including metformin. We demonstrate that NDI1 expression attenuates metformin’s ability to lower blood glucose levels under standard chow and high-fat diet conditions. Our results indicate that acute oral administration of metformin targets mitochondrial complex I to lower blood glucose.
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