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Bioassay-Guided Evaluation of Antinociceptive Effect of N-Salicyloyltryptamine: A Behavioral and Electrophysiological Approach

机译:生物测定指导的N-水杨酰色胺的镇痛作用评估:行为和电生理方法

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摘要

We investigated the antinociceptive and nerve excitability effects of the N-salicyloyltryptamine (NST) NST-treated mice exhibited a significant decrease in the number of writhes when 100 and 200 mg/kg (i.p.) were administered (i.p.). This effect was not antagonized by naloxone (1.5 mg/kg, i.p.). NST inhibited the licking response of the injected paw when 100 and 200 mg/kg were administered (i.p.) to mice in the first and second phases of the formalin test. Because the antinociceptive effects could be associated with neuronal excitability inhibition, we performed the single sucrose gap technique and showed that NST (3.57 mM) significantly reduced (29.2%) amplitude of the compound action potential (CAP) suggesting a sodium channel effect induced by NST. Our results demonstrated an antinociceptive activity of the NST that could be, at least in part, associated to the reduction of the action potential amplitude. NST might represent an important tool for pain management.
机译:我们研究了N-水杨酰胰色胺(NST)的抗伤害感受性和神经兴奋性作用,当给予100和200μmg/ kg(i.p.)时,经NST处理的小鼠的扭动次数显着减少。纳洛酮(1.5μmg/ kg,腹腔注射)不能拮抗这种作用。当在福尔马林测试的第一阶段和第二阶段对小鼠进行腹腔注射100和200 mg / kg时,NST抑制了注射爪的舔response反应。因为抗伤害性作用可能与神经元兴奋性抑制有关,所以我们进行了单蔗糖缺口技术,结果显示NST(3.57 mM)显着降低了复合动作电位(CAP)的幅度(29.2%),表明NST诱导了钠通道作用。我们的结果表明,NST的抗伤害感受活性可能至少部分与动作电位振幅的降低有关。 NST可能代表疼痛管理的重要工具。

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