Kariya K, Lee E, Takamura Y
Xenobiotica. 1984 Apr;14(4):349-53. doi: 10.3109/00498258409151421.
Treatment of rats with propylthiouracil for one to two weeks caused an increase in glutathione S-transferase (GST) activity of the liver cytosol, but not of the particulate fraction. Increased GST activity was reversed two weeks after discontinuing PTU administration. Activation of the enzyme was inversely proportional to the decrease in leukocytes. Repeated administration of PTU increased the Vmax of the enzyme without affecting the Km value for the substrate 1-chloro-2,4-dinitrobenzene, whereas both the Km and Vmax for glutathione (GSH) were increased by PTU treatment. GSH content and GSH peroxidase activity were not affected by PTU, but this resulted in an increase in glucose 6-phosphate dehydrogenase activity. PTU treatment caused increase in GST activity using 1-chloro-2,4-dinitrobenzene, 1,2-dichloro-4-nitrobenzene, p-nitrobenzyl chloride, and benzalacetone as substrates; enzyme activity towards chlorodinitrobenzene was the highest.
用丙基硫氧嘧啶治疗大鼠一到两周会导致肝细胞溶质中的谷胱甘肽 S-转移酶(GST)活性增加,但微粒体部分的活性未增加。停止给予丙基硫氧嘧啶两周后,增加的 GST 活性恢复正常。该酶的激活与白细胞数量的减少成反比。重复给予丙基硫氧嘧啶会增加该酶的 Vmax,而不影响底物 1-氯-2,4-二硝基苯的 Km 值,而丙基硫氧嘧啶处理会增加谷胱甘肽(GSH)的 Km 和 Vmax。GSH 含量和 GSH 过氧化物酶活性不受丙基硫氧嘧啶影响,但这导致葡萄糖 6-磷酸脱氢酶活性增加。以 1-氯-2,4-二硝基苯、1,2-二氯-4-硝基苯、对硝基苄基氯和苯亚甲基丙酮为底物时,丙基硫氧嘧啶处理会导致 GST 活性增加;该酶对氯二硝基苯的活性最高。