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实验动物体内谷胱甘肽的消耗与再合成

Glutathione depletion and resynthesis in laboratory animals.

作者信息

Ecobichon D J

出版信息

Drug Chem Toxicol. 1984;7(4):345-55. doi: 10.3109/01480548408998263.

DOI:10.3109/01480548408998263
PMID:6489190
Abstract

The availability of tissue glutathione (GSH) appears to depend upon a balance between tissue concentrations, the rate of reactive metabolite formation and the re-synthesis of GSH. To test this hypothesis, diethyl maleate (DEM, 5.8 mmol/kg bw) was administered intraperitoneally to male and female mice, hamsters, rats and guinea pigs. The regeneration of hepatic and renal GSH was examined at 0.5, 1, 2, 4, 8 and 24 hr post-treatment. DEM caused a rapid and marked depletion of tissue GSH but re-synthesis began to occur by 4 hr post-treatment in all species with the exception of the guinea pig. By 24 hr after treatment, the mouse, hamster and rat had tissue levels of GSH in excess of usual values but, in the guinea pig, recovery of hepatic GSH was still significantly reduced. Considering the reported species differences in S-alkenetransferases which detoxify DEM, the present results revealed that the conjugation of DEM proceeded rapidly in all four species but that the toxicity elicited in the guinea pig may have arisen from the unavailability of GSH during the slow re-synthesis stage following maximal depletion of this agent.

摘要

组织谷胱甘肽(GSH)的可利用性似乎取决于组织浓度、活性代谢物形成速率与GSH重新合成之间的平衡。为了验证这一假设,对雄性和雌性小鼠、仓鼠、大鼠和豚鼠腹腔注射马来酸二乙酯(DEM,5.8 mmol/kg体重)。在处理后0.5、1、2、4、8和24小时检查肝脏和肾脏GSH的再生情况。DEM导致组织GSH迅速且显著减少,但除豚鼠外,所有物种在处理后4小时开始重新合成。处理后24小时,小鼠、仓鼠和大鼠的组织GSH水平超过正常值,但豚鼠肝脏GSH的恢复仍显著降低。考虑到报道的使DEM解毒的S - 烯烃转移酶的物种差异,目前的结果表明,DEM在所有四个物种中均迅速结合,但豚鼠中引发的毒性可能源于该物质最大程度消耗后缓慢重新合成阶段GSH的不可用。

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