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ORIGINAL RESEARCH article

Front. Pharmacol.
Sec. Ethnopharmacology
Volume 15 - 2024 | doi: 10.3389/fphar.2024.1528100
This article is part of the Research Topic Herbal Medicine for the Treatment of Chronic Metabolic Diseases, Volume II View all 7 articles

Qizhu Rougan Granules suppress liver fibrosis by inhibiting the expression of the P2Y14 receptor on hepatic stellate cells

Provisionally accepted
Yujing Tao Yujing Tao 1,2Qun Niu Qun Niu 1,2*Yuanqian Yao Yuanqian Yao 1,2*Kaixin Wang Kaixin Wang 1,2*HaiJian Dong HaiJian Dong 1,2Xin Zhao Xin Zhao 1,2*Zeng Zijian Zeng Zijian 1,2Hui Li Hui Li 1,2*
  • 1 Chengdu University of Traditional Chinese Medicine, Chengdu, China
  • 2 Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan Province, China

The final, formatted version of the article will be published soon.

    Liver fibrosis is a globally prevalent chronic liver disease, often representing the advanced stage of various chronic liver conditions. Despite its widespread occurrence, there is currently no widely accepted or effective treatment for liver fibrosis. However, increasing evidence supports the efficacy of Traditional Chinese Medicine (TCM) in inhibiting the progression of fibrosis. In this study, we explored the effects and potential mechanisms of Qizhu-Ruogan-Granules (QZRG), a formulation from the Affiliated Hospital of the Chengdu University of TCM, on carbon tetrachloride (CCl4)-induced liver fibrosis in mice. A total of 40 male C57BL/6J mice were randomly divided into five groups (n=8 per group), with liver fibrosis induced by injecting 10% CCl4 for 15 weeks. From the 7th week onward, QZRG granules were administered orally to the treatment groups at low, medium, and high doses. To assess liver function, serum levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP) were measured. Liver morphology and fibrosis were evaluated using hematoxylin-eosin (H&E) and Masson's trichrome staining, while gene and protein expression levels were analyzed through quantitative reverse transcription polymerase chain reaction (RT-PCR) and western blot techniques. The results showed that QZRG granules significantly reduced serum levels of AST, ALT, and ALP in CCl4treated mice, alleviated liver damage, and reduced collagen accumulation. Furthermore, QZRG granules inhibited the expression of apoptosis-related proteins BAX, Caspase9, Caspase8, and Caspase3, while reducing P2Y14 expression in fibrotic liver tissues.Additionally, QZRG granules suppressed the proliferation of activated hepatic stellate cells. Our findings suggest that QZRG granules may exert anti-fibrotic effects by downregulating P2Y14 expression and effectively slowing the progression of liver fibrosis.

    Keywords: liver fibrosis, Hepatic stellate cells(HSCs), P2Y14, Qizhu-Ruogan-Granules (QZRG), Apoptosis

    Received: 14 Nov 2024; Accepted: 19 Dec 2024.

    Copyright: © 2024 Tao, Niu, Yao, Wang, Dong, Zhao, Zijian and Li. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence:
    Qun Niu, Chengdu University of Traditional Chinese Medicine, Chengdu, China
    Yuanqian Yao, Chengdu University of Traditional Chinese Medicine, Chengdu, China
    Kaixin Wang, Chengdu University of Traditional Chinese Medicine, Chengdu, China
    Xin Zhao, Chengdu University of Traditional Chinese Medicine, Chengdu, China
    Hui Li, Chengdu University of Traditional Chinese Medicine, Chengdu, China

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.