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

Study · human · Nature communications · 2020 · DOI 10.1038/s41467-020-16298-2 · PMID 32409697

Plain-language summary

Paraphrased from the published abstract below — not a verdict on whether anything works.

This mouse study examined whether the mitochondrial uncoupler BAM15 affected diet-induced obesity and insulin resistance, in the context of obesity affecting more than 40% of US adults and 13% of the global population. The authors report that oral BAM15 increased nutrient oxidation and decreased body fat mass without altering food intake, lean body mass, body temperature, or measured biochemical and haematological toxicity markers. BAM15 was also associated with decreased hepatic fat, decreased inflammatory lipids, and antioxidant effects, and hyperinsulinemic-euglycemic clamp studies showed improved insulin sensitivity across multiple tissue types.

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.

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