[PEG 300对三乙基锡中毒的抗脑水肿作用]。

Journal de pharmacologie Pub Date : 1986-10-01
J M Reymann, D Bentué-Ferrer, J van den Driessche, H Bagot, H Allain
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引用次数: 0

摘要

聚乙二醇(PEG)常用作非水溶性分子的溶剂,具有一定的毒性和药效学性质。研究了PEG 300 (10 ml/kg)对大鼠亚慢性三乙基锡盐(TEE)(每天2 mg/kg,连续5天)中毒诱导的中枢神经系统(CNS)变化的影响。记录以下参数:脑水肿测量,四个不同脑区的胺能神经递质浓度,神经状态,行为,死亡率。PEG 300可以对抗或减少TEE的一些影响:水肿,行为障碍,死亡率。相反,胺及其代谢物诱导的修饰没有变化。这种对TEE脑毒性某些成分的选择性拮抗作用为该溶剂的药理学特性提供了更多信息,并开启了神经递质在脑水肿中的作用的讨论。
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[Anti-cerebral edema properties of PEG 300 in triethyltin poisoning].

The polyethylene glycols (PEG) frequently used as solvents of non hydrosoluble molecules present toxic and pharmacodynamic properties. The effect of PEG 300 (10 ml/kg) on the modifications of the central nervous system (CNS) previously induced by a subchronic intoxication with triethyltin salt (TEE) (2 mg/kg p.o. for 5 days) has been studied in rat. The following parameters are recorded: measure of brain edema, concentration of the aminergic neurotransmitters in four different brain areas, neurological status, behaviour, mortality. The PEG 300 antagonizes or reduces some of the effects of the TEE: edema, behavioral disturbances, mortality. On the opposite, no change in the amines and their metabolites induced modifications is observed. This selective antagonism towards some of the components of TEE brain toxicity brings more information on pharmacological properties of this solvent and opens a discussion on the role of neurotransmitters on brain edema.

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[Modification of aminergic neurotransmitters and neurobehavioral correlates in acute cerebral ischemia in the rat]. [Effects of nicergoline on artificially induced micturition in the rabbit with and without prostatic hypertrophy]. [Anti-cerebral edema properties of PEG 300 in triethyltin poisoning]. [Effects of acute and chronic treatment with an adrenergic alpha receptor agonist, LE S3341, on the rate of catecholamine turnover in various peripheral organs and brain structures in the rat]. Incubated or superfused rat lung parenchymal strip: a valid preparation for direct measurement of beta-responses.
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