Effect of homotaurine in experimental analgesia tests.

R M Ruiz de Valderas, M I Serrano, J S Serrano, A Fernandez
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引用次数: 10

Abstract

1. The possible antinociceptive action of GABA A receptor agonist homotaurine, has been studied through a battery of chemical (acetic acid) and thermal (hot plate, tail flick and tail immersion) tests in rats and mice. 2. The aminoacid was used at the following doses 22.25; 55.62 and 111.24 mg/kg i.p. and 50-100 micrograms i.c.v.; and measurements were made at the time of and at 5, 15 and 30 min after drug administration. 3. Homotaurine exhibited a significantly antinociceptive effect in all the above mentioned test except hot plate and when administered i.c.v. in the tail flick test. 4. The antinociceptive effect in the chemical test was dose and time dependent. 5. In the tail immersion test, latency time for withdrawal of the tail was significantly increased with the dose of 55.62 mg/kg at 15 min and 111.24 mg/kg at 30 min. 6. In the tail flick test the antinociceptive effect was dose dependent at 15 and 30 min. 7. From the above results the implication of peripheral and spinal mechanisms in the antinociceptive effect of homotaurine may be concluded.

同型牛磺酸在实验性镇痛试验中的作用。
1. 通过化学(醋酸)和热(热板、甩尾和浸尾)试验,研究了氨基丁酸A受体激动剂同型牛磺酸可能的抗痛觉作用。2. 氨基酸的使用剂量为22.25;55.62和111.24 mg/kg i.p.和50-100微克i.c.v.;分别于给药时、给药后5、15、30 min进行测量。3.除热板实验和甩尾实验外,同型牛磺酸在上述所有实验中均表现出显著的抗伤害感受作用。4. 化学试验的抗伤感受作用具有剂量和时间依赖性。5. 在尾浸试验中,15 min剂量为55.62 mg/kg, 30 min剂量为111.24 mg/kg,显著增加了尾退潜伏期。在甩尾实验中,15min和30min的抗伤害感受作用呈剂量依赖性。从以上结果可以推断出同型牛磺酸抗伤害感受作用的外周和脊柱机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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