Wang Tao, Sun Ning-Ling, Zhang Wei-Dong, Li Hui-Liang, Lu Guo-Cai, Yuan Bo-Jun, Jiang Hua, She Jia-Hong, Zhang Chuan
Center for New Drug Evaluation, Institute of Basic Medical Science, Second Military Medical University, No 800 Xiang Yin Road, Shanghai 200433, PR China.
J Ethnopharmacol. 2008 May 8;117(2):300-8. doi: 10.1016/j.jep.2008.02.010. Epub 2008 Feb 14.
To investigate the protective effects of dehydrocavidine (DC), a main active ingredient of Corydalis saxicola Bunting (Yanhuanglian), on carbon tetrachloride (CCl4)-induced hepatotoxicity and the possible mechanisms involved in male Sprague-Dawley rats.
Acute hepatotoxicity was induced by CCl4 intoxication in rats. Serum biological analysis, lipid peroxides and antioxidants estimation, histopathological studies were carried out.
Both pre-treatment with DC prior to CCl4 administration and post-treatment with DC after CCl4 administration significantly prevented increases in serum enzymatic activities of alanine aminotransferase (ALT), aspartate aminotransferase (AST), lactate dehydrogenase (LDH), alkaline phosphatase (ALP) and total bilirubin (TBIL). In addition, pre- and post-treatment with DC also significantly prevented formation of hepatic malondialdehyde (MDA), depletion of glutathione peroxidase (GPx) and depression of superoxide dismutase (SOD) in the liver of CCl4-intoxicated rats. ALT, AST, LDH, ALP and TBILL levels, as well as MDA, SOD and GPx activities were unaffected in normal rats by treatment with DC alone. GST, a phase II enzyme, had no significant changes during our experiments. Histopathological changes induced by CCl4 were also significantly attenuated by DC treatment in both preventive and curative experiments.
DC has a potent hepatoprotective effect on CCl4-induced liver injury in rats through its antioxidant activity.
探讨岩黄连主要活性成分脱氢卡维丁(DC)对雄性斯普拉格-道利大鼠四氯化碳(CCl4)诱导的肝毒性的保护作用及其可能机制。
通过CCl4中毒诱导大鼠急性肝毒性。进行血清生物学分析、脂质过氧化物和抗氧化剂评估以及组织病理学研究。
在给予CCl4之前用DC预处理以及在给予CCl4之后用DC后处理均显著预防了血清丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)、乳酸脱氢酶(LDH)、碱性磷酸酶(ALP)和总胆红素(TBIL)酶活性的升高。此外,DC预处理和后处理还显著预防了CCl4中毒大鼠肝脏中丙二醛(MDA)的形成、谷胱甘肽过氧化物酶(GPx)的消耗和超氧化物歧化酶(SOD)的降低。单独用DC处理对正常大鼠的ALT、AST、LDH、ALP和TBILL水平以及MDA、SOD和GPx活性没有影响。在我们的实验中,II相酶谷胱甘肽S-转移酶(GST)没有显著变化。在预防和治疗实验中,DC处理也显著减轻了CCl4诱导的组织病理学变化。
DC通过其抗氧化活性对CCl4诱导的大鼠肝损伤具有强大的肝保护作用。