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Merck

Venlafaxine and neuropathic pain.

Pharmacology (2012-11-28)
Krystyna Cegielska-Perun, Magdalena Bujalska-Zadrożny, Jan Tatarkiewicz, Emilia Gąsińska, Helena Elżbieta Makulska-Nowak
摘要

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.

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Sigma-Aldrich
文拉法辛 盐酸盐, ≥98% (HPLC), powder
Supelco
文拉法辛 盐酸盐 溶液, 1.0 mg/mL in methanol (as free base), ampule of 1 mL, certified reference material, Cerilliant®
文拉法辛, European Pharmacopoeia (EP) Reference Standard
文拉法辛 盐酸盐, European Pharmacopoeia (EP) Reference Standard