| Literature DB >> 33887198 |
Deyang Yu1, Nicole E Richardson2, Cara L Green3, Alexandra B Spicer4, Michaela E Murphy5, Victoria Flores5, Cholsoon Jang6, Ildiko Kasza7, Maria Nikodemova4, Matthew H Wakai3, Jay L Tomasiewicz8, Shany E Yang3, Blake R Miller3, Heidi H Pak3, Jacqueline A Brinkman3, Jennifer M Rojas9, William J Quinn9, Eunhae P Cheng3, Elizabeth N Konon3, Lexington R Haider3, Megan Finke3, Michelle Sonsalla3, Caroline M Alexander7, Joshua D Rabinowitz10, Joseph A Baur9, Kristen C Malecki4, Dudley W Lamming11.
Abstract
Low-protein diets promote metabolic health in rodents and humans, and the benefits of low-protein diets are recapitulated by specifically reducing dietary levels of the three branched-chain amino acids (BCAAs), leucine, isoleucine, and valine. Here, we demonstrate that each BCAA has distinct metabolic effects. A low isoleucine diet reprograms liver and adipose metabolism, increasing hepatic insulin sensitivity and ketogenesis and increasing energy expenditure, activating the FGF21-UCP1 axis. Reducing valine induces similar but more modest metabolic effects, whereas these effects are absent with low leucine. Reducing isoleucine or valine rapidly restores metabolic health to diet-induced obese mice. Finally, we demonstrate that variation in dietary isoleucine levels helps explain body mass index differences in humans. Our results reveal isoleucine as a key regulator of metabolic health and the adverse metabolic response to dietary BCAAs and suggest reducing dietary isoleucine as a new approach to treating and preventing obesity and diabetes. Published by Elsevier Inc.Entities:
Keywords: FGF21; GCN2; body mass index; branched-chain amino acids; diabetes; insulin resistance; isoleucine; mTORC1; obesity; valine
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Year: 2021 PMID: 33887198 PMCID: PMC8102360 DOI: 10.1016/j.cmet.2021.03.025
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287