二甲双胍
餐后
双胍
内科学
内分泌学
代谢物
生物
线粒体
药理学
氧化磷酸化
2型糖尿病
碳水化合物代谢
代谢组学
医学
糖异生
化学
胰高血糖素样肽-1
β氧化
糖尿病
葡萄糖摄取
线粒体呼吸链
精氨酸
呼吸链
葡萄糖转运蛋白
噻唑烷二酮
线粒体生物发生
小肠
2型糖尿病
线粒体ROS
线粒体DNA
胰岛素
丸(消化)
药品
糖耐量试验
新陈代谢
作者
Zachary L. Sebo,Ram P. Chakrabarty,Rogan A. Grant,Karis B. D’Alessandro,Alec Koss,Jenna L. E. Blum,Shawn M. Davidson,Colleen R. Reczek,Navdeep S. Chandel
标识
DOI:10.1038/s42255-026-01530-y
摘要
Metformin is a versatile biguanide drug primarily prescribed for type II diabetes. Despite its extensive use, the mechanisms underlying its clinical effects, including attenuated postprandial glucose excursions and elevated intestinal glucose uptake, remain unclear. Here we map these and other effects of metformin to intestine-specific mitochondrial complex I inhibition. Using human metabolomic data and an orthogonal genetics approach in male mice, we demonstrate that metformin suppresses citrulline synthesis, a metabolite generated exclusively by small intestine mitochondria, and increases GDF15 by inhibiting the mitochondrial respiratory chain at complex I. This inhibition co-opts the intestines to function as a glucose sink, driving the uptake of excess glucose and its conversion to lactate and lactoyl-phenylalanine. We also find that glucose lowering by metformin is due to repeated bolus exposure rather than a cumulative chronic response. Notably, the efficacy of phenformin, another biguanide, and berberine, a structurally unrelated nutraceutical, similarly depends on intestine-specific mitochondrial complex I inhibition, underscoring a shared therapeutic mechanism.
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