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甘草酸对实验性肝内胆汁郁积大鼠的预防和治疗作用
引用本文:郭继强,丁宇,廖娜,赵营,翟德胜,杨锦南,陈西敬.甘草酸对实验性肝内胆汁郁积大鼠的预防和治疗作用[J].中国临床药理学与治疗学,2006,11(11):1248-1252.
作者姓名:郭继强  丁宇  廖娜  赵营  翟德胜  杨锦南  陈西敬
作者单位:1. 新乡医学院,新乡,453003,河南
2. 新乡医学院,新乡,453003,河南;中国药科大学药学院药物代谢动力学中心,南京,210009,江苏
3. 中国药科大学药学院药物代谢动力学中心,南京,210009,江苏
摘    要:目的:探讨甘草酸(glycyrrhizin,GL)和地塞米松(dexamethasone,DEX)对α-萘异硫氰酸(alphanaphthylisothiocyanate,ANIT)致急性肝内胆汁郁积型肝炎的作用。方法:应用ANIT制造大鼠急性肝内胆汁郁积型肝炎模型,分别应用GL和DEX进行预防性和治疗性给药,观察GL和DEX对大鼠肝功能生化指标、肝组织病理改变、2h胆汁流量和酮洛芬葡萄糖醛酸结合物(ketoprofen glucuroide,KPG)的累计胆排泄率的影响。结果:DEX预防性给药明显减轻胆管损伤,对肝细胞损伤无保护作用。ANIT染毒后3h给予DEX不能减轻胆汁郁积,染毒后12h给予DEX使肝细胞损伤加重。预防性给予GL和染毒后3h给予GL均能明显减轻胆汁郁积和肝细胞损伤。结论:在实验性急性肝内胆汁郁积型肝炎早期,GL具有明显的预防和治疗作用。

关 键 词:甘草酸  地塞米松  肝内胆汁郁积  α-萘异硫氰酸
文章编号:1009-2501(2006)11-1248-05
收稿时间:07 18 2006 12:00AM
修稿时间:08 13 2006 12:00AM

Protective effect of glycyrrhizin on acute cholestasis induced by alpha-naphthylisothiocyanate in rats
GUO Ji-qiang,DING Yu,LIAO Na,ZHAO Ying,ZHAI De-sheng,YANG Jin-nan,CHEN Xi-jing.Protective effect of glycyrrhizin on acute cholestasis induced by alpha-naphthylisothiocyanate in rats[J].Chinese Journal of Clinical Pharmacology and Therapeutics,2006,11(11):1248-1252.
Authors:GUO Ji-qiang  DING Yu  LIAO Na  ZHAO Ying  ZHAI De-sheng  YANG Jin-nan  CHEN Xi-jing
Affiliation:1. Xinxiang Medical College, Xinxiang 453003, Henan, China; 2.Center of Drug Metabolism and Pharmacokinetics, China Pharmaceutical University, Nanjing 210009, Jiangsu, China
Abstract:AIM: To investigate the effects of glycyrrhizin(GL)and dexamethasone(DEX)on alpha-naphthylisothiocyanate(ANIT) induced acute cholestasis in rats. METHODS: Acute cholestasis in rats was induced by ANIT, and the effects of GL and DEX on acute cholestasis were examined by serology determination, histological assessment of hepatic injury and bile excretion experiments. RESULTS: The protection of DEX pretreatment was directed toward cholangiocytes rather than hepatocytes. Rats remedially treated with DEX 3 h after ANIT administration were not resistant to ANIT toxicity. Notably, remedial treatment with DEX 12 h after ANIT enhanced ANIT toxicity. However, GL attenuated both bile duct and hepatocyte damage induced by ANIT in the initial phase of impairment. CONCLUSION: GL exhibited better protection against ANIT-induced acute cholestasis than DEX. In the initial phase of impairment of acute cholestasis, the protection of GL maybe partially due to modifications of metabolism and excretion of ANIT and anti-inflammatory effect.
Keywords:glycyrrhizin  dexamethasone  alphanaphthylisothiocyanate  intrahepatic cholestasis
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