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5-羟色胺能靶点在治疗抗抑郁药所致性功能障碍中的应用:格拉司琼和舒马曲坦的一项初步研究

Serotonergic targets in the treatment of antidepressant induced sexual dysfunction: a pilot study of granisetron and sumatriptan.

作者信息

Berk M, Stein D J, Potgieter A, Maud C M, Els C, Janet M L, Viljoen E

机构信息

Department of Psychiatry, University of the Witwatersrand Medical School, Parktown, Johannesburg, South Africa.

出版信息

Int Clin Psychopharmacol. 2000 Sep;15(5):291-5. doi: 10.1097/00004850-200015050-00006.

Abstract

Antidepressant induced sexual dysfunction is a common adverse event that is particularly evident with serotonergic antidepressants. There is a paucity of clinical trial evidence on the treatment of this problem. While there is some evidence of involvement of the serotonin (5-HT2) receptor subtype in this phenomenon, other serotonergic receptor systems are not well studied. In this trial, 35 patients on maintenance therapy with a variety of serotonergic antidepressants, who reported antidepressant induced sexual dysfunction, were enrolled. Patients were given both granisetron 1 mg, and sumatriptan 100 mg, in a crossover design, to be used 1 h before intercourse. Sexual dysfunction was measured using the Feiger scale. There was a high dropout rate in the trial, reflecting both embarrassment with the pharmacological treatment of sexual dysfunction and difficulties with planning and timing the medication. Nevertheless, there was a significant effect of granisetron in this study, with scores decreasing from 23.7 (SD 2.52) to 16.0 (SD 6.42) on the Feiger scale (n = 14, P = 0.001, Wilcoxon sign rank test). Sumatriptan failed to show a significant change from baseline at the 0.01 level of significance. While the small sample size, high dropout rates and open label design are limitations to this study, it suggests efficacy of the granisetron in antidepressant induced sexual dysfunction and the role of the 5-HT3 receptor in this phenomenon.

摘要

抗抑郁药引起的性功能障碍是一种常见的不良事件,在使用血清素能抗抑郁药时尤为明显。关于该问题的治疗,临床试验证据匮乏。虽然有一些证据表明血清素(5-HT2)受体亚型参与了这一现象,但其他血清素能受体系统尚未得到充分研究。在这项试验中,招募了35名正在接受多种血清素能抗抑郁药维持治疗且报告有抗抑郁药引起的性功能障碍的患者。采用交叉设计,让患者在性交前1小时服用1毫克格拉司琼和100毫克舒马曲坦。使用费格量表来测量性功能障碍。该试验的脱落率很高,这既反映了对性功能障碍进行药物治疗时的尴尬,也反映了药物计划和服用时间安排上的困难。尽管如此,格拉司琼在本研究中产生了显著效果,费格量表评分从23.7(标准差2.52)降至16.0(标准差6.42)(n = 14,P = 0.001,威尔科克森符号秩检验)。在0.01的显著性水平上,舒马曲坦未能显示出与基线相比有显著变化。虽然小样本量、高脱落率和开放标签设计是本研究的局限性,但它表明了格拉司琼在抗抑郁药引起的性功能障碍中的疗效以及5-HT3受体在这一现象中的作用。

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