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谷胱甘肽耗竭剂马来酸二乙酯、佛尔酮和丁硫氨酸亚砜胺对大鼠胆汁铜排泄的影响。

Effect of the glutathione-depleting agents diethylmaleate, phorone and buthionine sulfoximine on biliary copper excretion in rats.

作者信息

Nederbragt H

机构信息

Department of Pathology, Faculty of Veterinary Science, University of Utrecht, The Netherlands.

出版信息

Biochem Pharmacol. 1989 Oct 15;38(20):3399-406. doi: 10.1016/0006-2952(89)90107-x.

Abstract

The involvement of glutathione (GSH) in the biliary excretion of Cu was investigated in bile-cannulated inbred WAG/Rij and BN rats, pretreated with diethylmaleate (DEM), phorone or buthionine sulfoximine (BSO) and injected with Cu doses of 10 or 30 micrograms/100 g body wt. DEM reduced liver GSH to 27-56% and biliary GSH excretion to 18-38%; phorone reduced GSH in the liver to 55% and increased it in the bile (113%) followed by a slight decrease (79%); BSO reduced liver GSH to 50% and bile GSH to 20%. After injection of Cu to control rats a profile of biliary Cu excretion was found, composed of a slowly (SCuE) and a rapidly (RCuE) disappearing component, the latter only present after the dose of 30 micrograms Cu. DEM had no effect on SCuE after a 10 micrograms dose and a temporary effect on SCuE after a 30 micrograms dose in both WAG/Rij and BN rats. Phorone reduced SCuE after both Cu doses to 50%. Both agents abolished RCuE and reduced endogenous biliary Cu excretion to less than 50%. Release of injected Cu from plasma and uptake by the liver was inhibited by DEM and phorone in both rat strains; in BN rats basal plasma Cu level of DEM-treated rats was increased as well. BSO reduced SCuE after both Cu doses but had no influence on RCuE. Endogenous Cu excretion was reduced by BSO in BN rats but not in WAG/Rij rats. The results show that biliary Cu excretion proceeds by a pattern, the components of which can be affected differently by the various drugs. They also indicate that GSH is not directly involved in biliary Cu excretion but suggest that it may play a role in the metabolism of Cu in the liver.

摘要

在胆管插管的近交系WAG/Rij和BN大鼠中,研究了谷胱甘肽(GSH)在铜的胆汁排泄中的作用。这些大鼠用马来酸二乙酯(DEM)、佛尔酮或丁硫氨酸亚砜胺(BSO)预处理,并注射10或30微克/100克体重的铜剂量。DEM将肝脏GSH降低至27 - 56%,胆汁GSH排泄降低至18 - 38%;佛尔酮将肝脏GSH降低至55%,并使胆汁中的GSH增加(113%),随后略有下降(79%);BSO将肝脏GSH降低至50%,胆汁GSH降低至20%。给对照大鼠注射铜后,发现胆汁铜排泄呈现一种模式,由一个缓慢消失的成分(SCuE)和一个快速消失的成分(RCuE)组成,后者仅在注射30微克铜剂量后出现。在WAG/Rij和BN大鼠中,10微克剂量的铜注射后,DEM对SCuE没有影响,30微克剂量的铜注射后对SCuE有暂时影响。两种铜剂量注射后,佛尔酮都将SCuE降低至50%。两种药物都消除了RCuE,并将内源性胆汁铜排泄降低至不到50%。在两种大鼠品系中,DEM和佛尔酮均抑制了注射铜从血浆中的释放以及肝脏对铜的摄取;在BN大鼠中,DEM处理大鼠的基础血浆铜水平也有所升高。两种铜剂量注射后,BSO均降低了SCuE,但对RCuE没有影响。在BN大鼠中,BSO降低了内源性铜排泄,但在WAG/Rij大鼠中没有。结果表明,胆汁铜排泄遵循一种模式,其各个成分受不同药物的影响不同。它们还表明,GSH并不直接参与胆汁铜排泄,但提示其可能在肝脏铜代谢中发挥作用。

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