Key result
Hugan Qingzhi tablet reduces liver enzymes, lipids, and proinflammatory cytokines in a rat NAFLD model.
Why the study?
Does Hugan Qingzhi tablet improve biochemical and inflammatory markers in a rat model of nonalcoholic fatty liver disease?
Does Hugan Qingzhi tablet improve biochemical and inflammatory markers in a rat model of nonalcoholic fatty liver disease?
Hugan Qingzhi tablet demonstrates anti-inflammatory and antioxidant effects in a rat model of NAFLD, potentially via SIRT1 and Ac-NF-κB-p65 regulation.
Answers are grounded in this paper and cite their sources.
Does not support clinical use in NAFLD; hypothesis-generating for SIRT1-mediated effects in rodent models.
Ethnopharmacological Relevance. The Hugan Qingzhi tablet (HQT) is a traditional Chinese medicine used for treating NAFLD (nonalcoholic fatty liver disease). The present study evaluated the anti-inflammatory effects of HQT in rats with NAFLD. Materials and Methods. HQT was administered daily to the NAFLD experimental groups. Biochemical markers, histopathological data, and oxidative stress/antioxidant biomarkers were determined. Proinflammatory cytokines interleukin-1β (IL-1β), tumor necrosis factor α (TNF-α), and interleukin-6 (IL-6) were detected by enzyme-linked immunoassay. Expressions of silent information regulator 1 (SIRT1) and acetylated-nuclear-factor kappaB-p65 (Ac-NF-κB-p65) were performed by western blotting. Results. At high and moderate doses, HQT was highly effective in decreasing serum alanine aminotransferase (P < 0.01), aspartate aminotransferase (P < 0.01), hepatic total cholesterol (P < 0.01), triglycerides (P < 0.01), and free fatty acid levels (P < 0.01). Moreover, high and moderate doses of HQT reduced hepatic levels of the proinflammatory cytokines TNF-α (P < 0.01), IL-1β (P < 0.01), and IL-6 (P < 0.01), enhanced SIRT1 expression, and depressed Ac-NF-κB-p65 expression at protein level. Conclusions. In our NAFLD rat model, HQT exerted substantial anti-inflammatory and antioxidant activities, possibly involving the regulation of SIRT1 and Ac-NF-κB-p65 expression.
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Tang et al. (2015) studied Nonalcoholic fatty liver disease (NAFLD). Hugan Qingzhi tablet (HQT) was evaluated on Serum alanine aminotransferase, aspartate aminotransferase, hepatic total cholesterol, triglycerides, and free fatty acid levels (p=<0.01). In a rat model of NAFLD, Hugan Qingzhi tablet significantly decreased serum liver enzymes, lipid levels, and proinflammatory cytokines (P<0.01).
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