Suppr超能文献

敌草快和对乙酰氨基酚诱导的大鼠胆汁铁流出改变。

Diquat- and acetaminophen-induced alterations of biliary efflux of iron in rats.

作者信息

Benzick A E, Reddy S L, Gupta S, Rogers L K, Smith C V

机构信息

Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030.

出版信息

Biochem Pharmacol. 1994 Jun 1;47(11):2079-85. doi: 10.1016/0006-2952(94)90084-1.

Abstract

The effects of diquat on the biliary efflux of nonheme iron in rats were studied as a means of examining the possible effects of diquat metabolism on hepatocellular iron metabolism and the association of altered iron metabolism with the initiation of acute hepatic necrosis. Administration of hepatotoxic doses (0.1 mmol/kg) of diquat to male Fischer-344 rats increased biliary iron concentrations from 6 microM to more than 15 microM. However, increases in biliary efflux of iron were not observed during the first 60 min following exposure to diquat, despite the rapid increases in biliary glutathione disulfide concentrations, which increased maximally within 40 min. Biliary efflux of iron was not altered by diquat in Sprague-Dawley rats, which are resistant to hepatic necrosis in response to diquat, despite the marked oxidant stress responses observed in these animals. Conversely, hepatotoxic doses of acetaminophen (1500 mg/kg) caused significant decreases in biliary iron efflux. The rapid decreases in biliary iron caused by acetaminophen and the delay in diquat-induced iron efflux suggested the possibility that some fraction of the biliary iron was being excreted as reversibly formed GS-Fe2+ chelates, with inhibition of export by glutathione disulfide (GSSG) in the case of diquat, or by 3-(glutathion-S-yl)-acetaminophen (GS-AAP) in the case of the acetaminophen-treated animals. However, 50-200 mg/kg doses of acetaminophen showed little effect on biliary iron excretion despite producing biliary GS-AAP conjugate concentrations almost 1000 times the 6 microM concentrations of iron, which would not appear to support the hypothesis of excretion of GS-Fe2+ chelates. The data demonstrate a significant effect of diquat on hepatic iron metabolism in Fischer-344 rats, and the possible importance of this iron redistribution to reactive oxygen-mediated cell damage in vivo is indicated by the absence of similar responses in diquat-treated Sprague-Dawley rats.

摘要

研究了敌草快对大鼠非血红素铁胆汁流出的影响,以此作为考察敌草快代谢对肝细胞铁代谢可能产生的影响以及铁代谢改变与急性肝坏死起始之间关联的一种手段。给雄性Fischer-344大鼠施用肝毒性剂量(0.1 mmol/kg)的敌草快,可使胆汁中铁浓度从6微摩尔/升增加至超过15微摩尔/升。然而,在接触敌草快后的最初60分钟内未观察到铁的胆汁流出增加,尽管胆汁中谷胱甘肽二硫化物浓度迅速升高,在40分钟内达到最大值。在对敌草快诱导的肝坏死具有抗性的Sprague-Dawley大鼠中,敌草快并未改变铁的胆汁流出,尽管在这些动物中观察到了明显的氧化应激反应。相反,肝毒性剂量的对乙酰氨基酚(1500 mg/kg)导致胆汁中铁流出显著减少。对乙酰氨基酚引起的胆汁中铁的快速减少以及敌草快诱导的铁流出延迟表明,胆汁中铁的一部分可能以可逆形成的GS-Fe2+螯合物形式排出,在敌草快的情况下,谷胱甘肽二硫化物(GSSG)抑制其输出,而在对乙酰氨基酚处理的动物中,3-(谷胱甘肽-S-基)-对乙酰氨基酚(GS-AAP)抑制其输出。然而,50 - 200 mg/kg剂量的对乙酰氨基酚对胆汁中铁排泄几乎没有影响,尽管其产生的胆汁中GS-AAP共轭物浓度几乎是6微摩尔/升铁浓度的1000倍,这似乎不支持GS-Fe2+螯合物排泄的假说。数据表明敌草快对Fischer-344大鼠的肝脏铁代谢有显著影响,并且在经敌草快处理的Sprague-Dawley大鼠中未出现类似反应,这表明这种铁重新分布对体内活性氧介导的细胞损伤可能具有重要意义。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验