[3-吲哚乙酸酯在喹啉酸引起的小鼠惊厥中的作用]。

Farmakologiia i toksikologiia Pub Date : 1991-09-01
S Mirzaev, I V Ryzhov
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引用次数: 0

摘要

对两系286只小鼠(SHR和C57BL/6)的实验表明,3-吲哚丙酮酸(色氨酸的天然酮类似物,血清素和犬尿酸的前体)对喹啉酸诱发的惊厥具有选择性剂量依赖性(100-500 mg/kg,腹腔注射)保护作用。延长给药时间(50- 100mg /kg,连续10天,每天两次),其效率显著提高。据推测,3-吲哚丙酮酸抗惊厥作用的机制包括增强犬尿酸的合成,犬尿酸是n-甲基- d -天冬氨酸受体的阻滞剂,长期给药也增加了这些受体的敏感性和密度。
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[The action of 3-indolepyruvate in quinolinate-induced convulsions in mice].

The experiments on 286 mice of two lines (SHR and C57BL/6) showed that 3-indoipyruvate, a natural keto analogue of tryptophan and a precursor of serotonin and kynurenic acid) possesses the selective dose-dependent (100-500 mg/kg, intraperitoneally) protective effect against quinolinate-induced convulsions. At prolonged administration (50-100 mg/kg for 10 days twice a day) its efficiency drastically increased. It is supposed that the mechanism of the anticonvulsant action of 3-indolpyruvate involves an enhancement of synthesis of kynurenic acid, a blocker of N-methyl-D-aspartate receptors, and at chronic administration--also an increase of sensitivity and density of these receptors.

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