NADPH oxidase 1 promotes hepatic steatosis in obese mice and is abrogated by augmented skeletal muscle mass

Author:

Larion Sebastian12,Padgett Caleb A.1ORCID,Mintz James D.1,Thompson Jennifer A.3ORCID,Butcher Joshua T.1ORCID,Belin de Chantemèle Eric. J.12ORCID,Haigh Stephen1,Khurana Sandeep4,Fulton David J.15ORCID,Stepp David W.16ORCID

Affiliation:

1. Vascular Biology Center, Medical College of Georgia, Augusta University, Augusta, Georgia, United States

2. Department of Medicine, Medical College of Georgia, Augusta University, Augusta, Georgia, United States

3. Department of Physiology and Pharmacology, University of Calgary, Calgary, Alberta, Canada

4. Division of Gastroenterology, Geisinger Health System, Danville, Pennsylvania, United States

5. Department of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, Augusta, Georgia, United States

6. Department of Physiology, Medical College of Georgia, Augusta University, Augusta, Georgia, United States

Abstract

This study documents a novel mechanism by which changes in body composition, notably increased muscle mass, protect against fatty liver disease. This mechanism involves NADPH oxidase 1 (NOX1), an enzyme that increases superoxide and increases insulin signaling, leading to increased fat accumulation in the liver. NOX1 may represent a new early target for preventing fatty liver to stave off later liver diseases such as cirrhosis or liver cancer.

Funder

HHS | National Institutes of Health

HHS

Publisher

American Physiological Society

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