Volume 2021, Issue 1 6659445
Research Article
Open Access

Gegen Qinlian Decoction Ameliorates Nonalcoholic Fatty Liver Disease in Rats via Oxidative Stress, Inflammation, and the NLRP3 Signal Axis

Yuqi Ying

Yuqi Ying

College of Second Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou 310053, Zhejiang, China zcmu.edu.cn

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Haitao Zhang

Haitao Zhang

Department of Urinary Surgery, Taizhou Municipal Hospital, Taizhou 318000, Zhejiang, China tzhospital.com

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Dian Yu

Dian Yu

College of Second Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou 310053, Zhejiang, China zcmu.edu.cn

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Wei Zhang

Wei Zhang

Department of Endocrinology, Taizhou Municipal Hospital, Taizhou, Zhejiang, China tzhospital.com

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Dongling Zhou

Corresponding Author

Dongling Zhou

Department of Nursing, Taizhou Municipal Hospital, Taizhou, Zhejiang, China tzhospital.com

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Shuangchun Liu

Corresponding Author

Shuangchun Liu

Department of Blood Transfusion Division, Taizhou Municipal Hospital, Taizhou, Zhejiang, China tzhospital.com

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First published: 16 February 2021
Citations: 6
Academic Editor: Vincenzo De Feo

Abstract

Gegen Qinlian Decoction (GQD), a classic Chinese herbal formula, has been widely used in Chinese clinic for centuries and is well defined in treating nonalcoholic fatty liver disease (NAFLD). However, the mechanism action of GQD on NAFLD is still rarely evaluated. The present study aims to investigate the effect of GQD on treatment of NAFLD in rats and to further explore the underlying mechanism. The rat NAFLD model established by high-fat-diet feeding was used in the research. Our results exhibited the liver lesions and steatosis was significantly alleviated in NAFLD rats treated with GQD via Oil Red O and H&E staining. Body weight and liver index in GQD groups were reduced significantly (P < 0.05). Moreover, the biochemical analyzer test results showed that GQD significantly decreased blood lipid levels total cholesterol (TC), triglycerides (TG), low-density lipoprotein cholesterol (LDL-C), and liver injury indicators alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP), while it increased the level of high-density lipoprotein cholesterol (HDL-C) (P < 0.05). The levels of interferon-β (IFN-β), tumor necrosis factor-α (TNF-α), and malondialdehyde (MDA) after the GQD treatment were significantly lower, and then interleukin-2 (IL-2), superoxide dismutase (SOD), and glutathione peroxidase (GSH-Px) levels were lifted significantly (P < 0.05). Further, GQD blocked the expression of NLRP3, ASC, caspase-1 mRNA, and proteins in the liver tissues significantly (P < 0.05). These findings indicated that GQD can ameliorate the hepatic steatosis and injury of NAFLD. Its possible mechanism involves the modulation of inflammatory cytokines and antioxidative stress and the inhibition of NLRP3 signal axis activation. The results support that GQD may be a promising candidate in the treatment of NAFLD.

Conflicts of Interest

All authors declare that there are no conflicts of interest regarding the publication of this article.

Data Availability

The datasets used and/or analyzed during the current study are available from the corresponding author upon reasonable request.

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