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肝脏谷胱甘肽-S-转移酶活性与年龄相关的改变。

Age-associated alterations in hepatic glutathione-S-transferase activities.

作者信息

Fujita S, Kitagawa H, Ishizawa H, Suzuki T, Kitani K

出版信息

Biochem Pharmacol. 1985 Nov 1;34(21):3891-4. doi: 10.1016/0006-2952(85)90440-x.

Abstract

Age-associated alterations of hepatic cytosolic glutathione-S-transferase (GST) activities towards sulfobromophthalein sodium tetrahydrate (BSP), styrene oxide (STOX), trans-4-phenyl-3-butene-2-one (PBO), 1,2-dichloro-4-nitrobenzene (DCNB), and 1-chloro-2,4-dinitrobenzene (CDNB) were investigated in Fischer-344 rats of both sexes with ages ranging from 1.5 to 28 months. The GST activities towards PBO and DCNB in male rats increased with age till 6-12 months when maximum values were attained, and then gradually decreased till 28 months when the values became the lowest. The GST activities towards STOX and BSP did not show any significant increase after 1.5 months and stayed at this level till 12 months, followed by a gradual decrease till 28 months when the values were the lowest. In contrast, the GST activity towards CDNB in male rats did not show much of an age-associated alteration. Age-associated alterations in GST activities in females were much smaller than those observed in males. Sex differences in GST activities (significantly higher male values than female values) were observed with all the substrates examined at least at some time of the animal life. The kinetic studies of GST activities indicated that alterations in the relative abundance as well as the total quantity of GST isozymes caused the substrate selective alterations of GST activities with age.

摘要

在年龄范围为1.5至28个月的雌雄Fischer-344大鼠中,研究了肝脏胞质谷胱甘肽-S-转移酶(GST)对四水合磺溴酞钠(BSP)、氧化苯乙烯(STOX)、反式-4-苯基-3-丁烯-2-酮(PBO)、1,2-二氯-4-硝基苯(DCNB)和1-氯-2,4-二硝基苯(CDNB)的活性与年龄相关的变化。雄性大鼠中,GST对PBO和DCNB的活性随年龄增长直至6 - 12个月达到最大值,然后逐渐下降直至28个月降至最低值。GST对STOX和BSP的活性在1.5个月后未显示任何显著增加,并保持在该水平直至12个月,随后逐渐下降直至28个月降至最低值。相比之下,雄性大鼠中GST对CDNB的活性未显示出明显的年龄相关变化。雌性大鼠中GST活性的年龄相关变化比雄性大鼠中观察到的要小得多。在动物生命的至少某些时候,在所检测的所有底物中均观察到GST活性的性别差异(雄性值显著高于雌性值)。GST活性的动力学研究表明,GST同工酶相对丰度以及总量的变化导致了GST活性随年龄的底物选择性变化。

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