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解偶联蛋白 BAM15 可逆转小鼠的饮食诱导肥胖和胰岛素抵抗。

Mitochondrial uncoupler BAM15 reverses diet-induced obesity and insulin resistance in mice.

机构信息

School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW, 2052, Australia.

Sydney Medical School, Charles Perkins Centre, University of Sydney, Sydney, NSW, 2006, Australia.

出版信息

Nat Commun. 2020 May 14;11(1):2397. doi: 10.1038/s41467-020-16298-2.

Abstract

Obesity is a health problem affecting more than 40% of US adults and 13% of the global population. Anti-obesity treatments including diet, exercise, surgery and pharmacotherapies have so far failed to reverse obesity incidence. Herein, we target obesity with a pharmacotherapeutic approach that decreases caloric efficiency by mitochondrial uncoupling. We show that a recently identified mitochondrial uncoupler BAM15 is orally bioavailable, increases nutrient oxidation, and decreases body fat mass without altering food intake, lean body mass, body temperature, or biochemical and haematological markers of toxicity. BAM15 decreases hepatic fat, decreases inflammatory lipids, and has strong antioxidant effects. Hyperinsulinemic-euglycemic clamp studies show that BAM15 improves insulin sensitivity in multiple tissue types. Collectively, these data demonstrate that pharmacologic mitochondrial uncoupling with BAM15 has powerful anti-obesity and insulin sensitizing effects without compromising lean mass or affecting food intake.

摘要

肥胖是一个影响超过 40%美国成年人和 13%全球人口的健康问题。抗肥胖治疗,包括饮食、运动、手术和药物治疗,迄今为止未能逆转肥胖的发病率。在此,我们通过靶向肥胖的药物治疗方法来解决肥胖问题,该方法通过线粒体解偶联来降低热量效率。我们发现,最近鉴定的一种线粒体解偶联剂 BAM15 具有口服生物利用度,可增加营养物质的氧化,减少体脂肪量,而不改变食物摄入、瘦体重、体温或毒性的生化和血液学标志物。BAM15 可减少肝脂肪,减少炎症脂质,具有很强的抗氧化作用。高胰岛素-正常血糖钳夹研究表明,BAM15 可改善多种组织类型的胰岛素敏感性。总的来说,这些数据表明,BAM15 的药物性线粒体解偶联具有强大的抗肥胖和胰岛素增敏作用,而不会损害瘦体重或影响食物摄入。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6eb/7224297/495fa8e26352/41467_2020_16298_Fig1_HTML.jpg

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