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作 者:郑曲波[1] 邹越前[1] 程涛[1] 刘惠萍[1]
机构地区:[1]中国人民解放军第458医院,广东广州510600
出 处:《中西医结合肝病杂志》2010年第1期41-43,共3页Chinese Journal of Integrated Traditional and Western Medicine on Liver Diseases
摘 要:目的:制备大鼠肝内胆汁淤积模型,检测熊去氧胆酸干预前后多药耐药相关蛋白2(MRP2)表达的变化。方法:采用Wistar雄性大鼠灌服α-茶基异硫氰酸酯(ANIT)制备肝内胆汁淤积模型,分别以生理盐水、地塞米松、熊去氧胆酸干预大鼠5天后,检测肝功能,并取肝脏,采用实时荧光定量RT-PCR方法检测肝组织MRP2基因mRNA水平,Western-blot检测肝组织内MRP2蛋白水平。结果:与生理盐水组大鼠相比,地塞米松组和熊去氧胆酸组肝功能检测总胆红素、直接胆红素显著降低(P<0.01),肝组织MRP2基因mRNA水平、蛋白水平显著升高(P<0.01)。结论:地塞米松和熊去氧胆酸均能降低胆红素水平,其作用机制可能与两种药物上调MRP2基因表达有关。Objective: To study the effect of ursodeoxycholic acid (UDCA) on expression of multidrug resistance-associated protein 2 ( MRP2 ) in alpha-naphthylisothiocyanare (ANIT) induced cholestatic hepatitis. Methods: Rats were treated 5 days with normal saline, dexamethasone, UDCA respectively after administration of ANIT. The liver function were examined. The expression level of MRP2 on gene and protein were detected by real-time RT-PCR and Western-blot. Results: Compared to the normal saline, dexamethasone and UDCA could significantly decrease the TBil and DBil ( P 〈 0. 01 ), while markedly increasing the expression of mRNA and protein of MRP2 (P 〈 0. 01 ) . Conclusion: The dexamethasone and UDCA can decrease bilirubin by increasing the expression of MRIY2.
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