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

被引:26
作者
Zhang, Xiangying [1 ,2 ]
Ding, Jianbo [1 ]
Gou, Chunyan [1 ]
Wen, Tao [3 ]
Li, Li [1 ]
Wang, Xiaojun [1 ]
Yang, Huasheng [1 ]
Liu, Dan [1 ]
Lou, Jinli [1 ]
Chen, Dexi [1 ,2 ]
Ren, Feng [1 ,2 ]
Li, Xiuhui [1 ]
机构
[1] Capital Med Univ, Beijing You An Hosp, Beijing 100069, Peoples R China
[2] Beijing Inst Hepatol, Beijing 100069, Peoples R China
[3] Capital Med Univ, Beijing Chao Yang Hosp, Beijing 100043, Peoples R China
基金
中国国家自然科学基金;
关键词
Qingchangligan formula; Acute liver failure; Apoptosis; Inflammation; Autophagy; FULMINANT HEPATIC-FAILURE; GALACTOSAMINE-SENSITIZED MICE; AUTOPHAGY PROTECTS; CELL-DEATH; MECHANISMS; APOPTOSIS; PATHOGENESIS; INJURY; ALPHA; MODEL;
D O I
10.1016/j.jep.2016.11.007
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: 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. Aim of the study: To test the hypothesis that the Qingchangligan formula protects mice against acute liver failure by inhibiting liver inflammation. Materials and methods: Acute liver failure (ALF) was induced by intraperitoneal injection of u-GalN (700 mg/kg) plus LPS (10 mu g/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-GaIN/LPS injection by intragastric administration. The mice in different groups were sacrificed at 6 h after o-GalN/LPS injection, and liver samples and blood Were collected for analysis. Results: 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. Conclusions: 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.
引用
收藏
页码:108 / 116
页数:9
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