Venlafaxine (Effexor) is an effective antidepressant and has also been approved for the treatment of generalized anxiety disorder. Venlafaxine was initially characterized as an inhibitor of both serotonin (5HT) and norepinephrine (NE) uptake and was therefore termed a "dual uptake inhibitor." This chapter reviews data from both in vitro and in vivo studies regarding its effects on 5HT and NE neurotransmission. In addition, the effects of venlafaxine on other systems that may play a role in its therapeutic efficacy effects are described. The data indicate that venlafaxine is a relatively weak inhibitor of NE transport in vitro. In vivo studies indicate that venlafaxine selectively inhibits 5HT uptake at low therapeutic doses and inhibits both 5HT and NE uptake at higher therapeutic doses. This chapter concludes with a discussion of the effects of venlafaxine on various aspects of physiology.

译文

:Venlafaxine(Effexor)是一种有效的抗抑郁药,也已被批准用于治疗广泛性焦虑症。最初将文拉法辛表征为5-羟色胺(5HT)和去甲肾上腺素(NE)摄取的抑制剂,因此被称为“双重摄取抑制剂”。本章回顾了有关其对5HT和NE神经传递的影响的体内和体外研究数据。另外,描述了文拉法辛对可能在其治疗功效中起作用的其他系统的作用。数据表明文拉法辛是体外NE转运的相对较弱的抑制剂。体内研究表明,文拉法辛在低治疗剂量下选择性抑制5HT摄取,在高治疗剂量下同时抑制5HT和NE摄取。本章最后讨论了文拉法辛对生理学各个方面的影响。

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