Bakuchiol-induced caspase-3-dependent apoptosis occurs through c-Jun NH2-terminal kinase-mediated mitochondrial translocation of Bax in rat liver myofibroblasts

被引:53
作者
Park, Eun-Jeon [1 ]
Zhao, Yu-Zhe [1 ]
Kim, Youn-Chul [1 ]
Sohn, Dong Hwan [1 ]
机构
[1] Wonkwang Univ, Dept Pharm, Iksan 570749, Jeonbuk, South Korea
关键词
bakuchiol; hepatic stellate cell; myofibroblast; apoptosis; c-Jun NH2-terminal protein kinase; HEPATIC STELLATE CELLS; IN-VITRO; PSORALEA-CORYLIFOLIA; HERBAL MEDICINE; KAPPA-B; FIBROSIS; GLIOTOXIN; RESOLUTION; INHIBITION; EXPRESSION;
D O I
10.1016/j.ejphar.2007.01.024
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Liver fibrosis and cirrhosis may be reversible, possibly through the selective clearance of activated hepatic stellate cells/myofibroblasts by apoptosis. Hepatic stellate cells transdifferentiate into myofibroblast-phenotype cells in culture, a process that recapitulates hepatic stellate cell activation in vivo. Bakuchiol, a prenylated phenolic terpene isolated from the seed of Psoralea corylifolia L. (Leguminosae), reduced activated hepatic stellate cells when treated to rats during liver injury recovery period as demonstrated by a-smooth muscle actin immunostaining in rat liver and induced apoptosis in activated hepatic stellate cells/myofibroblasts as demonstrated by DNA fragmentation, activation of caspase-3, release of cytochrome c into the cytoplasm, translocation of Bax into mitochondria, and the proteolytic cleavage of poly(ADP-ribose) polymerase (PARP) in vitro. Balcuchiol-induced apoptosis was prevented by z-DEVD-fmk, a specific inhibitor of caspase-3, and z-VAD-fmk, a general caspase inhibitor, suggesting that bakuchiol-induced apoptosis occurs through a caspase-3-dependent pathway in vitro. Bakuchiol treatment stimulated the activation of extracellular signal-regulated kinase 1/2 (ERK), c-Jun NH2-terminal protein kinase (JNK), and p38 mitogen-activated protein kinases (MAPK) in vitro. Pretreatment with SP600125 attenuated the bakuchiol-induced translocation of Bax into mitochondria, cytochrome c release into the cytosol, caspase-3 activation, and PARP cleavage. In contrast, preincubation with SB203580, a p38 MAPK inhibitor, and U0126, an ERK inhibitor, had no effect on bakuchiol-induced cell death and caspase-3 activity. Taken together, these findings indicate that bakuchiol induces caspase-3-dependent apoptosis through the activation of JNK, followed by Bax translocation into mitochondria in rat liver myofibroblasts. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:115 / 123
页数:9
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