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治疗女性性兴趣和唤起障碍的精神药物学方法的最新进展

Recent Developments in Psychopharmaceutical Approaches to Treating Female Sexual Interest and Arousal Disorder.

作者信息

Both Stephanie

机构信息

Department of Psychosomatic Gynecology and Sexology, Leiden University Medical Center, Albinusdreef 2, PO Box 9600, 2300 RC Leiden, The Netherlands.

出版信息

Curr Sex Health Rep. 2017;9(4):192-199. doi: 10.1007/s11930-017-0124-3. Epub 2017 Oct 19.

Abstract

PURPOSE OF REVIEW

This review summarizes the recent literature and empirical studies on psychopharmacological approaches to treating female sexual interest/arousal disorder (FSIAD).

RECENT FINDINGS

Several new drugs for FSIAD that are intended to increase sexual responsiveness by influencing central excitatory and inhibitory neuromodulatory processes are under development. Studies on flibanserin resulted in the first approved medication for the treatment of low sexual desire in premenopausal women. New drugs under development are testosterone combined with sildenafil or buspiron, bremelanotide, BP101, and nasal testosterone (TBS-2).

SUMMARY

Although pharmacological enhancement of sexual responsiveness may be potentially helpful in the treatment of FSIAD, the observed effects of flibanserin and other new drugs under development seem limited in terms of clinical significance. Given the multifactorial character of FSIAD, it may be important to integrate psychopharmacological treatment with sex therapy for optimal treatment efficacy.

摘要

综述目的

本综述总结了近期关于治疗女性性兴趣/唤起障碍(FSIAD)的精神药理学方法的文献和实证研究。

最新发现

几种用于FSIAD的新药正在研发中,旨在通过影响中枢兴奋性和抑制性神经调节过程来提高性反应能力。对氟班色林的研究促成了首个获批用于治疗绝经前女性性欲低下的药物。正在研发的新药有睾酮联合西地那非或丁螺环酮、布雷默浪丹、BP101和鼻用睾酮(TBS - 2)。

总结

尽管通过药物增强性反应能力可能对治疗FSIAD有潜在帮助,但氟班色林和其他正在研发的新药的观察效果在临床意义方面似乎有限。鉴于FSIAD的多因素特性,将精神药物治疗与性治疗相结合以实现最佳治疗效果可能很重要。

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引用本文的文献

本文引用的文献

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BP101 Peptide Promotes Female Sexual Receptivity in the Rat.
J Sex Med. 2017 Mar;14(3):336-346. doi: 10.1016/j.jsxm.2017.01.008. Epub 2017 Feb 8.
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