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文拉法辛与神经性疼痛。

Venlafaxine and neuropathic pain.

机构信息

Department of Pharmacodynamics, Medical University of Warsaw, Warsaw, Poland.

出版信息

Pharmacology. 2013;91(1-2):69-76. doi: 10.1159/000345035. Epub 2012 Nov 22.

Abstract

The possible mechanisms involved in the antinociceptive effect of venlafaxine (VFX), a selective serotonin and noradrenaline reuptake inhibitor, after a single administration and chronic treatment were investigated in a diabetic neuropathic pain (DNP) model. VFX produced a significant antihyperalgesic effect after a single and repeated administration. This effect was reversed by pretreatment with yohimbine (a relatively selective α(2)-adrenergic antagonist) and p-chloroamphetamine (a neurotoxin which destroys serotonergic neurons). Conversely, naloxone (a nonselective opioid antagonist) did not reverse the effect of VFX in a DNP model. It is concluded that both noradrenergic and serotonergic mechanisms participate in the antinociceptive effect of VFX in the DNP model. However, the noradrenergic mechanism probably plays a more important role.

摘要

文拉法辛(一种选择性 5-羟色胺和去甲肾上腺素再摄取抑制剂)单次给药和慢性治疗后在糖尿病神经病理性疼痛(DNP)模型中产生的抗伤害感受作用的可能机制。文拉法辛在单次和重复给药后产生显著的抗痛觉过敏作用。预先给予育亨宾(一种相对选择性的α2-肾上腺素能拮抗剂)和对氯苯丙胺(一种破坏 5-羟色胺能神经元的神经毒素)可逆转这种作用。相反,纳洛酮(一种非选择性阿片类拮抗剂)不能在 DNP 模型中逆转文拉法辛的作用。结论是,去甲肾上腺素能和 5-羟色胺能机制都参与了文拉法辛在 DNP 模型中的抗伤害感受作用。然而,去甲肾上腺素能机制可能起更重要的作用。

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