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可乐定可逆转甲基黄嘌呤诱导的巴氯芬抗伤害感受作用增强。

Clonidine reverses methylxanthine-induced potentiation of baclofen antinociception.

作者信息

Steardo L, Sawynok J

出版信息

Pharmacol Biochem Behav. 1985 May;22(5):905-7. doi: 10.1016/0091-3057(85)90546-5.

Abstract

The effect of clonidine on the antinociceptive effect of methylxanthine/baclofen and dopamine antagonist/baclofen combinations was examined to determine if alterations in noradrenaline turnover might mediate the potentiating effect of these agents. Clonidine alone had intrinsic activity in the tail flick test, so a dose and treatment schedule which produced a plateau effect was chosen. Clonidine pretreatment did not significantly alter the effect of baclofen alone, but reversed the potentiation of the action of baclofen produced by both theophylline and isobutylmethylxanthine. The intrinsic effect of isobutylmethylxanthine also was reversed. Combinations of dopamine antagonists and baclofen were potentiated or unaffected by clonidine. A possible interpretation of these results is that mutual interactions by baclofen and methylxanthines with descending noradrenergic pathways mediate the methylxanthine-induced potentiation of the antinociceptive effect of baclofen. A more specific determination of noradrenergic pathways involved in the action of baclofen will require the use of more specific alternative approaches.

摘要

研究了可乐定对甲基黄嘌呤/巴氯芬和多巴胺拮抗剂/巴氯芬组合的抗伤害感受作用的影响,以确定去甲肾上腺素代谢的改变是否可能介导这些药物的增强作用。单独使用可乐定在甩尾试验中有内在活性,因此选择了产生平台效应的剂量和治疗方案。可乐定预处理并未显著改变单独使用巴氯芬的效果,但逆转了茶碱和异丁基甲基黄嘌呤对巴氯芬作用的增强。异丁基甲基黄嘌呤的内在作用也被逆转。多巴胺拮抗剂和巴氯芬的组合被可乐定增强或不受影响。这些结果的一种可能解释是,巴氯芬和甲基黄嘌呤与下行去甲肾上腺素能通路的相互作用介导了甲基黄嘌呤诱导的巴氯芬抗伤害感受作用的增强。要更具体地确定参与巴氯芬作用的去甲肾上腺素能通路,需要使用更具体的替代方法。

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