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反式氧化茋及其他结构相关的药物代谢酶诱导剂对磷酸戊糖途径及其他碳水化合物代谢酶的影响。

The effect of trans-stilbene oxide and other structurally related inducers of drug-metabolizing enzymes on the pentose phosphate pathway and other enzymes of carbohydrate metabolism.

作者信息

Seidegård J, DePierre J W

出版信息

Biochem Pharmacol. 1982 May 1;31(9):1717-21. doi: 10.1016/0006-2952(82)90674-8.

DOI:10.1016/0006-2952(82)90674-8
PMID:7104035
Abstract

trans-Stilbene oxide has been found earlier to be a new type of inducer of drug-metabolizing systems. Here we demonstrate that treatment of rats with this xenobiotic results in an increase in the activity of the cytosolic glucose 6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase, the first and third enzymes in th pentose phosphate pathway, to 350% and 170% of the control values, respectively. At the time microsomal glucose 6-phosphate dehydrogenase activity was unaffected by administration of trans-stilbene oxide or benzil. The time course and dose-response of the increases in glucose 6-phosphate and 6-phosphogluconate dehydrogenase activities have been characterized. The activities of ribulose 5-phosphate 3-epimerase and ribose 5-phosphate activities have been characterized. The activities of ribulose 5-phosphate 3-epimerase and ribose 5-phosphate ketol isomerase, enzymes further along in the pentose phosphate pathway, were not significantly affected by trans-stilbene oxide or benzil. An investigation of the effect of treating rats with different metabolites of stilbene and with other structurally related compounds on hepatic cytosolic glucose 6-phosphate dehydrogenase activity revealed the structural features which are important for increasing this activity. Finally, it was found that administration of trans-stilbene oxide did not affect the activities of glucokinase and phosphoglucose isomerase, the two glycolytic enzymes which can produce glucose 6-phosphate, the link between glycolysis and the pentose phosphate shunt.

摘要

反式氧化茋早前被发现是一种新型的药物代谢系统诱导剂。在此我们证明,用这种外源性物质处理大鼠会导致胞质葡萄糖6-磷酸脱氢酶和6-磷酸葡萄糖酸脱氢酶(戊糖磷酸途径中的第一种和第三种酶)的活性分别增加至对照值的350%和170%。同时,微粒体葡萄糖6-磷酸脱氢酶的活性不受反式氧化茋或联苯甲酰给药的影响。已对葡萄糖6-磷酸脱氢酶和6-磷酸葡萄糖酸脱氢酶活性增加的时间进程和剂量反应进行了表征。已对核糖5-磷酸3-表异构酶和核糖5-磷酸的活性进行了表征。戊糖磷酸途径中更靠后的核糖5-磷酸3-表异构酶和核糖5-磷酸酮醇异构酶的活性未受到反式氧化茋或联苯甲酰的显著影响。一项关于用茋的不同代谢产物以及其他结构相关化合物处理大鼠对肝细胞质葡萄糖6-磷酸脱氢酶活性影响的研究揭示了对增加该活性很重要的结构特征。最后,发现反式氧化茋的给药不影响葡萄糖激酶和磷酸葡萄糖异构酶的活性,这两种糖酵解酶可产生葡萄糖6-磷酸,是糖酵解和戊糖磷酸分流之间的联系。

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