Tien Yun-Chen, Liao Jung-Chun, Chiu Chuan-Sung, Huang Tai-Hung, Huang Chih-Yang, Chang Wen-Te, Peng Wen-Huang
School of Chinese Pharmaceutical Sciences and Chinese Medicine Resources, College of Pharmacy, China Medical University, 91 Hsueh-Shih road, Taichung 404, Taiwan; E-Mails:
Int J Mol Sci. 2011;12(6):4053-67. doi: 10.3390/ijms12064053. Epub 2011 Jun 16.
Esculetin (ESC) is a coumarin that is present in several plants such as Fraxinus rhynchophylla and Artemisia capillaris. Our previous study found that FR ethanol extract (FR(EtOH)) significantly ameliorated rats' liver function. This study was intended to investigate the protective mechanism of ESC in hepatic apoptosis in rats induced by carbon tetrachloride. Rat hepatic apoptosis was induced by oral administration of CCl(4). All rats were administered orally with CCl(4) (20%, 0.5 mL/rat) twice a week for 8 weeks. Rats in the ESC groups were treated daily with ESC, and silymarin group were treated daily with silymarin. Serum alanine aminotransferase (ALT), aspartate aminotransferase (AST) as well as the activities of the anti-oxidative enzymes glutathione peroxidase (GPx), superoxide dismutase (SOD), and catalase in the liver were measured. In addition, expression of liver apoptosis proteins and anti-apoptotic proteins were detected. ESC (100, 500 mg/kg) significantly reduced the elevated activities of serum ALT and AST caused by CCl(4) and significantly increased the activities of catalase, GPx and SOD. Furthermore, ESC (100, 500 mg/kg) significantly decreased the levels of the proapoptotic proteins (t-Bid, Bak and Bad) and significantly increased the levels of the anti-apoptotic proteins (Bcl-2 and Bcl-xL). ESC inhibited the release of cytochrome c from mitochondria. In addition, the levels of activated caspase-9 and activated caspase-3 were significantly decreased in rats treated with ESC than those in rats treated with CCl(4) alone. ESC significantly reduced CCl(4)-induced hepatic apoptosis in rats.
七叶亭(ESC)是一种香豆素,存在于多种植物中,如白蜡树和茵陈蒿。我们之前的研究发现,白蜡树乙醇提取物(FR(EtOH))能显著改善大鼠的肝功能。本研究旨在探讨ESC对四氯化碳诱导的大鼠肝脏细胞凋亡的保护机制。通过口服给予四氯化碳诱导大鼠肝脏细胞凋亡。所有大鼠每周口服两次四氯化碳(20%,0.5 mL/只),持续8周。ESC组大鼠每天给予ESC治疗,水飞蓟素组大鼠每天给予水飞蓟素治疗。检测血清丙氨酸氨基转移酶(ALT)、天冬氨酸氨基转移酶(AST)以及肝脏中抗氧化酶谷胱甘肽过氧化物酶(GPx)、超氧化物歧化酶(SOD)和过氧化氢酶的活性。此外,检测肝脏凋亡蛋白和抗凋亡蛋白的表达。ESC(100、500 mg/kg)显著降低了四氯化碳引起的血清ALT和AST活性升高,并显著提高了过氧化氢酶、GPx和SOD的活性。此外,ESC(100、500 mg/kg)显著降低了促凋亡蛋白(t-Bid、Bak和Bad)的水平,并显著提高了抗凋亡蛋白(Bcl-2和Bcl-xL)的水平。ESC抑制了细胞色素c从线粒体的释放。此外,与仅用四氯化碳处理的大鼠相比,用ESC处理的大鼠中活化的半胱天冬酶-9和活化的半胱天冬酶-3的水平显著降低。ESC显著减少了四氯化碳诱导的大鼠肝脏细胞凋亡。