肝纤维化
MAPK/ERK通路
医学
肝星状细胞
纤维化
内科学
内分泌学
蛋白激酶A
肝硬化
激酶
药理学
生物
生物化学
作者
Hong Cai,Xuegang Sun,Zhi Feng Liu,Ya Wei Liu,Jing Tang,Qiang Liu,Bao Ji,Yu Song,Ying Zhou,Ming Yang,Zhi Lv
标识
DOI:10.1016/j.jep.2010.08.019
摘要
Dahuangzhechong pill (DHZCP), a well-known and canonical Chinese medicine formula from “The Synopsis of Prescriptions of the Golden Chamber”, is officially approved and recommended by Chinese association of integrative medicine for the prevention and treatment of hepatic fibrosis in China. To test the hypothesis that therapeutic effects of DHZCP on hepatic fibrosis are conferred by regulating cytokine profile through a mitogen activated protein kinase (MAPK) pathway. Hepatic fibrosis is inducted by carbon tetrachloride (CCl4) in rats which then were randomly divided into six groups: hepatic fibrosis model group, high dose DHZCP group, low dose DHZCP group, Fufang Biejia Ruangan Pian (FBRP) group, Colchicine group and control group. Pathological, immunohistochemical, multiplex immunoassay and protein expression studies (Western blotting) are performed. DHZCP significantly decreases the levels of alanine aminotransferase, aspartate aminotransferase, hyaluronic acid, laminin, type IV collagen and procollagen III, and reverses hepatic fibrosis in rat model. DHZCP also could reduce the expression of α-smooth muscle actin, and lower the serum level of tumor necrosis factor alpha (TNF-α) and interleukin 13 (IL-13). The expressions of phosphorylated p38 MAPK and extracellular signal-regulated kinase (ERK) are down-regulated, while no significant changes are found in phosphorylation of c-Jun N-terminal kinase (JNK). DHZCP can alleviate hepatic fibrosis induced by CCl4. The anti-fibrotic effects of DHZCP are conferred by decreasing the secretion of TNF-α and IL-13 through down-regulating p38 and ERK phosphorylation.
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