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[急性和亚急性经口实验条件下暴露于除草剂乙草胺的白鼠脑组织中的生化变化]

[Biochemical changes in the brain tissue of white rats exposed to the herbicide acetochlor under acute and subacute oral experimental conditions].

作者信息

Khalkova Zh, Zaĭkov Kh, Buzidi A, Antov G

出版信息

Probl Khig. 1990;15:96-102.

PMID:2099469
Abstract

In the conditions of acute and subacute oral intoxication with acetanilidic preparation acetochlorine applied in doses respectively 1/5 LD50 for acute experiment and 1/20 and 1/100 LD50 for subacute experiment (LD50 for male animals--1063 mg/kg-1, and for females--768 mg/kg-1) are traced the changes in the capacity for methaemoglobin formation, the quantity of sulfhydryl groups in the serum, the activity of LDH, G-6-PhDH, IDH, MDH, SDH, Cyt Oxidasis and the quantity of soluble proteins in brain homogenates and isolated mitochondria of brain. The animals of the acute experiment are examined on the 1, 3, 5, 7, 10 and 14 day of the poisoning, and the animals of the subacute experiment--on the 24th hour after the last administration (42-day treatment with the preparation, 5 days weekly). The herbicide acetochlorine at unrepeated introduction of dose 212 6 mg/kg-1 (1/5 LD50) and multiple administration for a period of 42 days in doses 1/20 and 1/1000 LD50 in the stomach of white rats possess well expressed methaemoglobin formation capacity. In the conditions of acute and subacute experiment the preparation causes one-type changes in the enzymes activity, certifying for a destruction of the mitochondrial apparatus. A suppression of the activity of SDH, IDH, Cyt oxidasis and increase of the LDH, G-6-PhDH activity, could be a result of methaemoglobin formation. The latter is a predispose factor for appearing of chemical hypoxia leading to the inclusion of compensatory anaerobic oxidizing processes. The registered deviations have to be read at the hygiene standardization of the preparation.

摘要

在急性和亚急性经口中毒条件下,使用乙酰苯胺类制剂乙草胺,急性实验剂量分别为1/5 LD50,亚急性实验剂量分别为1/20和1/100 LD50(雄性动物LD50为1063 mg/kg-1,雌性动物LD50为768 mg/kg-1),观察高铁血红蛋白形成能力、血清中巯基数量、乳酸脱氢酶(LDH)、葡萄糖-6-磷酸脱氢酶(G-6-PhDH)、异柠檬酸脱氢酶(IDH)、苹果酸脱氢酶(MDH)、琥珀酸脱氢酶(SDH)、细胞色素氧化酶活性以及脑匀浆和脑分离线粒体中可溶性蛋白质数量的变化。急性实验动物在中毒后第1、3、5、7、10和14天进行检查,亚急性实验动物在最后一次给药后24小时检查(制剂治疗42天,每周5天)。除草剂乙草胺以212.6 mg/kg-1(1/5 LD50)的剂量单次给药以及在大鼠胃内以1/20和1/1000 LD50的剂量多次给药42天,具有明显的高铁血红蛋白形成能力。在急性和亚急性实验条件下,该制剂引起酶活性的单一类型变化,证明线粒体装置遭到破坏。SDH、IDH、细胞色素氧化酶活性的抑制以及LDH、G-6-PhDH活性的增加,可能是高铁血红蛋白形成的结果。后者是化学性缺氧出现的诱发因素,导致代偿性无氧氧化过程的启动。所记录的偏差必须在制剂的卫生标准化时予以考虑。

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