Protective effect of chaige anti-alcoholic granules on acute alcoholic liver injury in rats and acute toxicity in mice

组织病理学 毒性 医学 酒精性肝病 肌酐 肝损伤 内科学 胃肠病学 药理学 急性毒性 谷胱甘肽 病理 化学 生物化学 肝硬化
作者
Ying Chen,Feiyu Zhao,Xing Sang,Rongzhen Zhang,Mengfei Bi,Meimei Tang,RongBin Wang,Hongting Wang,Cunqin Wang
出处
期刊:Frontiers in Pharmacology [Frontiers Media]
卷期号:16: 1595544-1595544
标识
DOI:10.3389/fphar.2025.1595544
摘要

Background and aim Alcoholic liver disease (ALD), caused by consumption of alcohol, with high morbidity and mortality, whose effective interventions is essential. Chinese medicine has a long history of detoxification, and Chaige anti-alcoholic granules (CAG) is an accepted formula including 13 Chinese herbs with definite detoxifying and liver-protecting effects in clinical for acute alcohol intoxication. However, the underlying mechanism is unclear. Methods In this study, mice were selected for acute toxicity experiments with the increasing drug concentration to 0.78 mg⋅mL-1. Body weight changes, organ indices, liver and kidney histological observations were performed after 2 weeks. ALT, AST, BUN, and creatinine in mice serum were detected by the kits. A rat model of alcoholic liver injury (ALI) was established by gavage of Chinese wine with 56% alcohol, which was intragastrically received with CAG at 1575, 3150 and 6300 mg⋅kg⋅day-1 for 2 weeks, respectively, while positive group 100 mg⋅kg⋅day-1 metadoxine. The organ indices were measured, and the protective effect of CAG on ALI was determined using kits, ELISA, histopathology, and western blotting. Results The results of the acute toxicity experiment showed that the mice were alive normally and the organ index, liver and kidney histopathology, and serum biochemical indicators showed no significant difference between the control group and the CAG-treated groups. The results of hepatoprotective effect of CAG in rat showed that compared with the control group, the liver index, ALT, AST, ADH, TC, TG, GSH-Px, SOD, and CYP450 2E1 levels were all increased in the model group ( P < 0.01), while ALDH and MDA were decreased ( P < 0.01). Compared with the model group, the detection indicators in the different dose CAG treatment groups could be reversed, and there was a certain dose-effect relationship, that is, the reversal effect of the high and med-dose groups was better ( P < 0.01). Liver histological observation showed that CAG could alleviate the infiltration of inflammatory cells. Conclusion These indicated that CAG had no acute toxicity and exhibited a large safety range, and was first identified to protect against hepatotoxicity through anti-oxidative stress and anti-inflammation, providing a scientific basis for further research into its clinical applications.
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