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  2. Stress can attenuate hepatic lipid accumulation via elevation of hepatic β-muricholic acid levels in mice with nonalcoholic steatohepatitis

Stress can attenuate hepatic lipid accumulation via elevation of hepatic β-muricholic acid levels in mice with nonalcoholic steatohepatitis

  • Lab Invest. 2021 Feb;101(2):193-203. doi: 10.1038/s41374-020-00509-x.
Sayuri Takada 1 2 Tsutomu Matsubara 3 Hideki Fujii 2 4 Misako Sato-Matsubara 2 5 Atsuko Daikoku 2 Naoshi Odagiri 2 Yuga Amano-Teranishi 2 Norifumi Kawada 2 Kazuo Ikeda 1
Affiliations

Affiliations

  • 1 Department of Anatomy and Regenerative Biology, Osaka City University Graduate School of Medicine, Osaka, Japan.
  • 2 Department of Hepatology, Osaka City University Graduate School of Medicine, Osaka, Japan.
  • 3 Department of Anatomy and Regenerative Biology, Osaka City University Graduate School of Medicine, Osaka, Japan. matsu335@med.osaka-cu.ac.jp.
  • 4 Endowed Department of Liver Cirrhosis Therapeutics, Osaka City University Graduate School of Medicine, Osaka, Japan.
  • 5 Endowed Laboratory of Synthetic Biology, Osaka City University Graduate School of Medicine, Osaka, Japan.
Abstract

Stress can affect our body and is known to lead to some diseases. However, the influence on the development of nonalcohol fatty liver disease (NAFLD) remains unknown. This study demonstrated that chronic restraint stress attenuated hepatic lipid accumulation via elevation of hepatic β-muricholic acid (βMCA) levels in the development of nonalcoholic steatohepatitis (NASH) in mice. Serum cortisol and corticosterone levels, i.e., human and rodent stress markers, were correlated with serum bile acid levels in patients with NAFLD and methionine- and choline-deficient (MCD) diet-induced mice, respectively, suggesting that stress is related to bile acid (BA) homeostasis in NASH. In the mouse model, hepatic βMCA and cholic acid (CA) levels were increased after the stress challenge. Considering that a short stress enhanced hepatic CYP7A1 protein levels in normal mice and corticosterone increased CYP7A1 protein levels in primary mouse hepatocytes, the enhanced Cyp7a1 expression was postulated to be involved in the chronic stress-increased hepatic βMCA level. Interestingly, chronic stress decreased hepatic lipid levels in MCD-induced NASH mice. Furthermore, βMCA suppressed lipid accumulation in mouse primary hepatocytes exposed to palmitic acid/oleic acid, but CA did not. In addition, Cyp7a1 expression seemed to be related to lipid accumulation in hepatocytes. In conclusion, chronic stress can change hepatic lipid accumulation in NASH mice, disrupting BA homeostasis via induction of hepatic Cyp7a1 expression. This study discovered a new βMCA action in the liver, indicating the possibility that βMCA is available for NAFLD therapy.

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