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鞘内注射拟胆碱药物对大鼠和猫的镇痛作用。

Antinociceptive effects of intrathecally injected cholinomimetic drugs in the rat and cat.

作者信息

Yaksh T L, Dirksen R, Harty G J

出版信息

Eur J Pharmacol. 1985 Oct 29;117(1):81-8. doi: 10.1016/0014-2999(85)90474-1.

Abstract

Rats chronically implanted with intrathecal catheters displayed a dose-dependent increase in the hot-plate, tail-flick response latencies, and decreased the magnitude of the writhing response following the injection of certain cholinomimetics into the subarachnoid space through the indwelling catheter. The structure-activity relationship for these agents is oxotremorine greater than carbachol greater than acetylcholine + physostigmine much much greater than acetylcholine = nicotine-HCl = 0. Atropine, but not naloxone, strychnine, picrotoxin, curare or methysergide and phentolamine, reversed the antinociceptive effect. This suggests the involvement of muscarinic cholinergic mechanisms. Experiments with intrathecal injection of carbachol into the spinal subarachnoid space of cats fitted with intrathecal catheters also revealed a potent antinociceptive effect which was completely antagonized by atropine. The effect was somatotopically limited with the skin surfaces innervated by cord segments nearest the catheter tip showing the most significant effect with the shortest latency of onset. This observation, together with the absence of changes in general reflex motor function or postural control further indicated a selective spinal effectiveness of muscarinic agonists after low dose intrathecal administration.

摘要

长期植入鞘内导管的大鼠,在通过留置导管向蛛网膜下腔注射某些拟胆碱药后,热板试验、甩尾反应潜伏期呈剂量依赖性增加,扭体反应幅度降低。这些药物的构效关系为:氧化震颤素>卡巴胆碱>乙酰胆碱+毒扁豆碱>>乙酰胆碱=盐酸尼古丁=0。阿托品可逆转这种抗伤害感受作用,而纳洛酮、士的宁、印防己毒素、箭毒、麦角新碱和酚妥拉明则不能。这表明毒蕈碱胆碱能机制参与其中。在给装有鞘内导管的猫的脊髓蛛网膜下腔注射卡巴胆碱的实验中,也发现了强效的抗伤害感受作用,且该作用完全被阿托品拮抗。这种作用在躯体定位上是有限的,导管尖端附近脊髓节段所支配的皮肤表面显示出最显著的作用,起效潜伏期最短。这一观察结果,以及一般反射运动功能或姿势控制未发生变化,进一步表明低剂量鞘内给药后毒蕈碱激动剂具有选择性脊髓效应。

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