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施畅, 王和枚, 廖明阳. 异环磷酰胺对大鼠肝脏毒作用及其机理探讨[J]. 中国公共卫生, 2001, 17(5): 388-390. DOI: 10.11847/zgggws2001-17-05-03
引用本文: 施畅, 王和枚, 廖明阳. 异环磷酰胺对大鼠肝脏毒作用及其机理探讨[J]. 中国公共卫生, 2001, 17(5): 388-390. DOI: 10.11847/zgggws2001-17-05-03
SHI Chang, . Hepatotoxicity and its Mechanism(s) Induced by Ifosfamide on Rats[J]. Chinese Journal of Public Health, 2001, 17(5): 388-390. DOI: 10.11847/zgggws2001-17-05-03
Citation: SHI Chang, . Hepatotoxicity and its Mechanism(s) Induced by Ifosfamide on Rats[J]. Chinese Journal of Public Health, 2001, 17(5): 388-390. DOI: 10.11847/zgggws2001-17-05-03

异环磷酰胺对大鼠肝脏毒作用及其机理探讨

Hepatotoxicity and its Mechanism(s) Induced by Ifosfamide on Rats

  • 摘要: 目的 探讨异环磷酰胺(Ifo)对肝脏的毒性和毒作用机理.方法 采用雄性Wistar大鼠Ifo40mg·kg-1·d-1×5dip;200mg·kg-1·d-1×1dip,观察停药后第1、4、7和10天血浆生化指标及肝组织丙二醛、巯基和Cyt-P450含量变化.结果 血浆生化指标和肝组织丙二醛含量没有显着变化,而肝组织总巯基、非蛋白巯基、蛋白巯基和总P450含量呈现时间依赖性下降,第7天降至最低值,第10天有所恢复,其中蛋白巯基的消耗是导致总巯基耗竭的主要原因.重复给药的作用明显强于一次性给药.病理学检查发现Ifo引起肝小叶中央区肝细胞空泡变性,肝细胞点状及小灶性坏死,坏死区及汇管区慢性炎细胞浸润;超微结构病变主要为线粒体肿胀、内质网扩张、胞内溶酶体聚集.结论 Ifo可引起大鼠肝损伤,巯基状态的改变和Cyt-P450的抑制在Ifo的肝损伤中起重要作用.

     

    Abstract: Objective In order to investigate the hepatotoxicity and its mechanism(s) induced by Ifosfamide(Ifo).Mehods Serum biochemical parameters and the contents of malondialdehyde(MDA),sulfhydryl groups and Cyt-P450 in male Wistar rats liver tissue were detected on days 1,4,7,10 after administration of Ifo(40mg·kg-1·d-1×5d ip,200mg·kg-1·d-1 ×1d ip).Results Serum biochemical parameters and ocncentration of MDA in liver tissue didn't change significantly in both treated groups while total、noneprotein、protein bound sulfhydryl and total P450 contents in liver tissue declined time dependently respectively with be lowest contents on day 7 and a little recovery on day 10.The decrease of protein bound sulfhydryl was ascribed to total sulfhydryl's depletion.However,the chages caused by repeated administraiton is more significant than single administration.In the pathologic examination,the hepatocytes in the central zone of the hepatic lobule were found vacuolation,spotty and focal necroses of hepatocytes in the liver were also found with chronic inflammatory cells infiltration in the necrotic and portal areas.The pathologic changes under the ultrastructure level were mitochondrial swelling、endoplasmic reticulum dilation and secondary lysosomes collection.Conclusion The results indicated that Ifo could induce hepatotoxicity on rats.The changes of sulfhydryl states and inhibition of Cyt-P450 were contributed to the liver injury induced by Ifo.

     

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