Paeoniflorin modulates oxidative stress, inflammation and hepatic stellate cells activation to alleviate CCl4-induced hepatic fibrosis by upregulation of heme oxygenase-1 in mice

Author:

Wang Ting1ORCID,Zhou Xu2,Kuang Ge2,Jiang Rong3,Guo Xinyi2,Wu Shengwang2,Wan Jingyuan1ORCID,Yin Liangjun1

Affiliation:

1. Department of Orthopaedics, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China

2. Department of Pharmacology, Chongqing Medical University, Chongqing, China

3. Laboratory of Stem Cell and Tissue Engineering, Chongqing Medical University, Chongqing, China

Abstract

Abstract Objectives The role of Paeoniflorin on hepatic fibrosis and the specific mechanisms has not yet been elucidated. Therefore, we explored whether Paeoniflorin exerted protective effects on carbon tetrachloride (CCl4)-induced hepatic fibrosis and the underlying mechanisms. Methods A model of hepatic fibrosis was induced by intraperitoneally injecting with CCl4 (10% 5 μl/g) twice a week for 7 weeks. To explore the effects of Paeoniflorin, mice were treated with Paeoniflorin (100 mg/kg) by gavage once a day at 1 week after modeling until they were sacrificed. Key findings Paeoniflorin remarkably improved liver function and histopathological changes of hepatic tissues in CCl4-induced liver injury. Besides, the serum MAO enzyme activity and hydroxyproline contents were notably decreased following the intervention of Paeoniflorin. The decreased expression of Vimentin, α-SMA, Col1a and Desmin manifested the inhibition of the hepatic stellate cells (HSCs) activation. Interestingly, Paeoniflorin intervention significantly upregulated the expression of heme oxygenase-1, and attenuated the inflammatory cytokines production as well as the CCl4-induced oxidative stress imbalance. Conclusions Paeoniflorin could effectively alleviate CCl4-induced hepatic fibrosis by upregulation of heme oxygenase-1, and it might be a new effective option for the comprehensive treatment of hepatic fibrosis.

Funder

Chongqing Science and Technology Commission

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

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