Controlled-release mitochondrial protonophore reverses diabetes and steatohepatitis in rats

Author:

Perry Rachel J.123,Zhang Dongyan1,Zhang Xian-Man2,Boyer James L.24,Shulman Gerald I.123

Affiliation:

1. Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT, USA.

2. Departments of Internal Medicine, Yale University School of Medicine, New Haven, CT, USA.

3. Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, CT, USA.

4. Yale Liver Center, Yale University School of Medicine, New Haven, CT, USA.

Abstract

Special delivery for fatty liver disease Nonalcoholic fatty liver disease is one of many unwelcome consequences of the global rise in obesity rates. Fat accumulation within the liver can lead to inflammation and cirrhosis, a predisposing factor for liver cancer. Treatment options are limited. Perry et al. revisit a mitochondrial uncoupling agent (2,4-dinitrophenol) that was used as a drug for weight loss in the 1930s but was discontinued because of serious toxicities. Encouragingly, an altered formulation of the drug that ensures its controlled release at low levels ameliorated fatty liver and diabetes in rodent models, without side effects. Science , this issue p. 1253

Funder

National Institutes of Health

Novo Nordisk Foundation Center for Basic Metabolic Research

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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