Sasa veitchii extract alleviates nonalcoholic steatohepatitis in methionine–choline deficient diet‐induced mice by regulating peroxisome proliferator‐activated receptor alpha

Author:

Yoshioka Hiroki1ORCID,Wu Sixun2,Moriishi Takeshi2,Tsukiboshi Yosuke1,Yokota Satoshi3,Miura Nobuhiko4,Yoshikawa Masae5,Inagaki Naoki1,Matsushita Yuki2,Nakao Makoto5

Affiliation:

1. Faculty of Pharmacy Gifu University of Medical Science Gifu Japan

2. Department Cell Biology Nagasaki University Graduate School of Biomedical Sciences Nagasaki Japan

3. Division of Cellular and Molecular Toxicology, Center for Biological Safety and Research National Institute of Health Sciences Kawasaki Japan

4. Department of Health Science Yokohoma University of Pharmacy Yokohama Japan

5. Department of Pharmacy, College of Pharmacy Kinjo Gakuin University Nagoya Japan

Abstract

AbstractAimNonalcoholic steatohepatitis (NASH) is a pandemic liver disease. This study aimed to explore the protective effects of Sasa veitchii extract (SE) in a mouse model of methionine–choline‐deficient (MCD) diet‐induced NASH.MethodsEight‐week‐old male C57BL/6J mice were fed a normal diet or an MCD diet for 8 weeks (0–8 weeks). SE (0.1 mL) was administered orally once daily for the latter period (4 weeks; 5–8 weeks). Body weight was measured weekly. The mice were euthanized and plasma samples were collected. Livers were collected and weighed.ResultsThe MCD diet decreased the liver/body weight ratio, elevated plasma alanine aminotransferase and aspartate aminotransferase levels, and increased liver oxidative stress, fibrosis, and inflammation. These changes were alleviated by SE administration. We also found that the MCD‐induced increase in triglycerides and lipid droplets in the liver was attenuated by SE. Furthermore, MCD‐induced glutathione peroxidase‐4 and peroxisome proliferator‐activated receptor‐alpha downregulation was sustained by SE administration.ConclusionOur results showed that SE protected mice against MCD‐induced hepatic injury, including oxidative stress and inflammation, by modulating peroxisome proliferator‐activated receptor alpha activation.

Publisher

Wiley

Subject

Environmental Engineering

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