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prevents high-fat diet-induced non-alcoholic fatty liver disease in rats by inhibiting expression the TLR4/MyD88 and the phosphorylation of NF-κB. | LitMetric

AI Article Synopsis

  • Franch (Gentianaceae) is explored for its therapeutic effects on non-alcoholic fatty liver disease, particularly in the context of high-fat diets and hypercholesterolaemia.
  • Research involved feeding 32 rats a high-fat diet and administering a water extract of Franch, leading to significant reductions in various lipid and liver enzyme levels compared to control groups.
  • The study suggests that Franch may work as an anti-inflammatory agent by inhibiting the TLR4/MyD88/NF-κB pathway, calling for further research to confirm its clinical potential.

Article Abstract

Context: Franch. (Gentianaceae) is a source of the traditional Tibetan medicine, ZangYinChen, and is used to treat chronic hepatitis and many types of jaundice.

Objective: This study explored the therapeutic effects and mechanism of on non-alcoholic fatty liver disease in diet-induced hypercholesterolaemia.

Materials And Methods: After a week of adaptive feeding, 32 Sprague-Dawley rats were divided into four groups: (1) Control, (2) Control-S, (3) Model, and (4) Model-S. During the 12 experimental weeks, we established the Model using a high-fat diet. Control-S and Model-S were given 1.0 g/kg water extract via gavage starting in the fifth week until the end of experiment.

Results: When compared with Model rats, the water extract led to a reduction in high-density lipoproteins (43.9%) and albumin (13.9%) and a decrease in total cholesterol (54.0%), triglyceride (45.6%), low-density lipoproteins (8.6%), aspartate aminotransferase (11.0%), alanine aminotransferase (15.5%), alkaline phosphatase (19.1%), total protein (6.4%), and glucose (20.8%) in serum. A reduction in three cytokines (IL-1β, IL-6, and TNFα) was detected. Histopathological examination showed that liver steatosis was significantly relieved in -treated high-fat diet rats. also caused a downregulation in the expression of TLR4 (43.2%), MyD88 (33.3%), and a decrease in phosphorylation of NF-κB.

Discussion And Conclusions: Our findings indicate that may act as a potential anti-inflammation drug via inhibition of the TLR4/MyD88/NF-κB pathway. Further and studies are needed to validate its potential in clinical medicine.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9559049PMC
http://dx.doi.org/10.1080/13880209.2022.2127153DOI Listing

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