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Long-term effects of a novel phosphorothionate (RPR-Ⅱ) on detoxifying enzymes in brain, lung, and kidney rats

机译:新型硫代硫代磷酸酯(RPR-Ⅱ)对脑,肺和肾大鼠排毒酶的长期影响

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The effects of a phosphorothionate, 2-butenoic acid-3-(diethoxyphosphinothioyl) methyl ester (RPR-Ⅱ), on the activities of glutathione S-transferase (GST) and UDP-glucuronyltransferase (UDPGT) and the level of glutathione (GSH) were evaluated in rats after administration of RPR-Ⅱ at 0.014 (low), 0.028 (medium), and 0.042 (high) mg kg~(-1) day~(-1) for 90 days and also at 28 days (withdrawal) after stopping treatment. Brain GST activity and GSH level decreased significantly at the high dose on the 45th and 90th days of treatment. Dose- and time-dependent decreases in GST activity and GSH was level were observed in lung at medium and high doses and in kidneys at all three doses on both the 45th and 90th days. UDPGT activity increased significantly in kidneys at the medium and high doses at 45 and 90 days. Brain and lung did not display any significant variations in UDPGT activity when compared with the control. Interestingly, the withdrawal study revealed that the effect was reversible within 28 days of cessation of treatment, when enzyme activity reverted to levels close to those of controls. The study revealed that RPR-Ⅱ affected the GSH- and GST-dependent detoxification system of the treated tissues of rat and its potential to modulate the enzymes is in the order kidneys > lung brain. The present subacute study suggests that RPR-Ⅱ may bring about physiological upsets by altering GSH- and GST-dependent events in different tissues of exposed organisms.
机译:硫代磷酸酯2-丁烯酸-3-(二乙氧基膦硫基)甲基酯(RPR-Ⅱ)对谷胱甘肽S-转移酶(GST)和UDP-葡萄糖醛酸基转移酶(UDPGT)的活性以及谷胱甘肽(GSH)含量的影响在RPR-Ⅱ以0.014(低),0.028(中)和0.042(高)mg kg〜(-1)天〜(-1)施用90天和28天(停药)后,对大鼠进行了评估停止治疗后。在治疗的第45天和第90天,高剂量时脑GST活性和GSH水平显着下降。在第45天和第90天,在中等剂量和高剂量下,以及在所有三种剂量下的肾脏中,GST活性和GSH的水平均随时间和时间而降低,在肾脏中也是如此。在45和90天的中高剂量肾脏中,UDPGT活性显着增加。与对照组相比,脑和肺在UDPGT活性方面未显示任何显着变化。有趣的是,戒断研究显示,当酶活性恢复至接近对照水平时,在停药后28天内这种作用是可逆的。研究表明,RPR-Ⅱ影响了大鼠组织中GSH和GST依赖的排毒系统,其调节酶的潜力依次为肾脏>肺脑。目前的亚急性研究表明,RPR-Ⅱ可能通过改变暴露生物体不同组织中的GSH和GST依赖性事件而引起生理不适。

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