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用苯并(a)芘处理的怀孕大鼠中谷胱甘肽S-转移酶(GST)活性增强。

Enhanced glutathione S-transferase (GST) activity in pregnant rats treated with benzo(a)pyrene.

作者信息

Cervello I, Lafuente A, Giralt M, Mallol J

机构信息

Department of Pharmacology, School of Medicine (Reus), University of Barcelona, Spain.

出版信息

Placenta. 1992 May-Jun;13(3):273-80. doi: 10.1016/0143-4004(92)90042-r.

Abstract

Administration of Benzo(a)pyrene (BP, 50 mg/kg/d) to pregnant rats significantly increased Glutathione S-transferase (GST) activity in placental tissue-extract (Vmax = 40 nmol/min/mg protein and 69 nmol/min/mg protein in controls versus treated animals respectively; P less than 0.01) and total fetal tissue-extract (Vmax = 51 nmol/min/mg protein and 82 nmol/min/mg protein in controls versus treated animals respectively; P less than 0.01) indicating an induction effect of BP on the GST system. An increase in the Km values was also observed: 1.61 x 10(-3) M and 2.84 x 10(-3) M in control versus treated placentae; 1.38 x 10(-3) M and 2.05 x 10(-3) M in control versus treated fetuses. A competitive effect on the enzyme by the BP present in the sample may also be involved. The glutathione content in both tissues did not show any changes after the treatment with BP. This increase in the GST system was not sufficient to protect the fetus. BP affected the reproductive performance of pregnant rats by significantly increasing the number of resorptions and fetal wastage, and, also, by decreasing the fetal weight.

摘要

给怀孕大鼠注射苯并(a)芘(BP,50毫克/千克/天)可显著提高胎盘组织提取物中的谷胱甘肽S-转移酶(GST)活性(对照组和处理组动物的Vmax分别为40纳摩尔/分钟/毫克蛋白质和69纳摩尔/分钟/毫克蛋白质;P<0.01)以及整个胎儿组织提取物中的GST活性(对照组和处理组动物的Vmax分别为51纳摩尔/分钟/毫克蛋白质和82纳摩尔/分钟/毫克蛋白质;P<0.01),这表明BP对GST系统有诱导作用。还观察到Km值增加:对照组和处理组胎盘的Km值分别为1.61×10⁻³M和2.84×10⁻³M;对照组和处理组胎儿的Km值分别为1.38×10⁻³M和2.05×10⁻³M。样品中存在的BP对该酶可能也有竞争作用。用BP处理后,两种组织中的谷胱甘肽含量均未显示任何变化。GST系统的这种增加不足以保护胎儿。BP通过显著增加吸收和胎儿损耗的数量,以及降低胎儿体重,影响了怀孕大鼠的生殖性能。

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