Qingchangligan formula attenuates the inflammatory response to protect the liver from acute failure induced by d -galactosamine/lipopolysaccharide in mice

药理学 医学 肝损伤 炎症 体内 脂多糖 腹腔注射 肝细胞 半乳糖胺 丙氨酸转氨酶 免疫学 体外 内科学 化学 生物 生物化学 生物技术 氨基葡萄糖
作者
Xiangying Zhang,Jianbo Ding,Chunyan Gou,Tao Wen,Li Li,Wang Xiao-jun,Huasheng Yang,Dan Liu,Jinli Lou,Dexi Chen,Feng Ren,Xiuhui Li
出处
期刊:Journal of Ethnopharmacology [Elsevier]
卷期号:201: 108-116 被引量:27
标识
DOI:10.1016/j.jep.2016.11.007
摘要

The Qingchangligan formula, a traditional Chinese medicine comprising five herbs, is useful for treatment of patients with liver failure; however, its protective and regulatory mechanisms remain elusive. To test the hypothesis that the Qingchangligan formula protects mice against acute liver failure by inhibiting liver inflammation. Acute liver failure (ALF) was induced by intraperitoneal injection of D-GalN (700 mg/kg) plus LPS (10 μg/kg). The Qingchangligan formula was administered to mice in three doses of 50 mg/kg (on day 1, day 2, and day 3) prior to D-GalN/LPS injection by intragastric administration. The mice in different groups were sacrificed at 6 h after D-GalN/LPS injection, and liver samples and blood were collected for analysis. Administration of the Qingchangligan formula not only ameliorated liver injury, as evidenced by reduced transaminase levels and well-preserved liver architecture, but also decreased the lethality in ALF mice. Moreover, in the ALF model, pretreatment with the Qingchangligan formula alleviated liver inflammation and decreased hepatocyte apoptosis. Further demonstrating the protective effects of the Qingchangligan formula, we found that pretreatment with the Qingchangligan formula reduced the expression of inflammatory cytokines by decreasing the expression of components of the mitogen-activated protein kinase (MAPK) pathway and promoting autophagy in vitro and in vivo. Our findings demonstrated that the Qingchangligan formula exerts a protective effect against the pathophysiology of ALF, especially in regulating liver inflammation, and provide a rationale for using the Qingchangligan formula as a potential therapeutic strategy to ameliorate ALF.
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