Liver regeneration after hepatectomy is significantly suppressed in a muscular atrophy mouse model

Author:

Hagiwara Kei1,Watanabe Akira1,Harimoto Norifumi1ORCID,Araki Kenichiro1ORCID,Yokobori Takehiko2,Muranushi Ryo1,Hoshino Kouki1,Ishii Norihiro1ORCID,Tsukagoshi Mariko1,Shirabe Ken1

Affiliation:

1. Division of Hepatobiliary and Pancreatic Surgery, Department of General Surgical Science Gunma University Graduate School of Medicine Maebashi Gunma Japan

2. Division of Integrated Oncology Research Gunma University Initiative for Advanced Research (GIAR) Maebashi Gunma Japan

Abstract

AbstractBackgroundSarcopenia is a syndrome characterized by progressive and generalized loss of skeletal muscle mass and strength. As reported in previous studies, the loss of skeletal muscle mass is associated with poor liver regeneration after hepatectomy. It is considered important to clarify the effect of sarcopenia on liver regeneration; however, there are no reports about model animals for sarcopenia. We focused on the peroxisome proliferator‐activated receptor‐gamma coactivator‐1alpha (PGC‐1α) transgenic mice that overexpressed PGC‐1α, specifically for skeletal muscle, and showed significant atrophy of type 2B fiber‐rich muscles like sarcopenia.MethodsWe performed 70% hepatectomy using PGC‐1α transgenic mice and examined the liver regeneration rate and the effects of branched‐chain amino acids (BCAA) after hepatectomy.ResultsLiver regeneration after 70% hepatectomy was significantly suppressed in the PGC‐1α transgenic mice. In addition, a decrease in the blood BCAA concentration and a decrease in the liver glycogen content after 70% hepatectomy were observed in the PGC‐1α transgenic mice. By administering BCAA before and after surgery, it was clarified that a significant increase in the blood BCAA concentration was observed and the liver regeneration rate was improved in the PGC‐1α transgenic mice.ConclusionsBCAA administration may improve the suppression of liver regeneration in patients with sarcopenia.

Funder

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

Hepatology,Surgery

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