van der Made Flip, Bloemers Jos, van Ham Diana, El Yassem Wadi, Kleiverda Gunilla, Everaerd Walter, Olivier Berend, Tuiten Adriaan
Flevoziekenhuis, Department of Gynecology and Obstetrics, Almere, The Netherlands.
J Sex Med. 2009 Feb;6(2):429-39. doi: 10.1111/j.1743-6109.2008.01103.x. Epub 2008 Dec 2.
Female sexual dysfunction (FSD) may be associated with reduced central sensitivity for sexual cues. A single dose of testosterone might induce an increase in sensitivity for sexual stimuli, which in turn allows a PDE5 inhibitor to be effective in boosting the physiological sexual response. Negative sexual experience-like childhood sexual abuse (CSA)-might be an important intervening factor in these drugs-induced alterations.
To investigate if the combination of testosterone and vardenafil causes an increase in sensitivity for sexual cues and an increase in physiological sexual responding in women suffering from hypoactive sexual desire disorder (HSDD).
Thirteen women with HSDD underwent four different drug treatments: (i) placebo; (ii) vardenafil; (iii) testosterone; and (iv) combination of testosterone and vardenafil. During each treatment, they performed an emotional Stroop task and watched neutral and erotic film clips.
A masked version of the emotional Stroop task, and the vaginal pulse amplitude (VPA).
We found different effects in women who had reported CSA (N = 5) compared with those who had not (N = 8). In women without CSA, testosterone induced an increase in their originally low levels of preconscious attention for sexual cues, while women with CSA showed a decrease in their originally high levels of attention. In these groups, we also found different effects of the combination of testosterone and vardenafil on the VPA: women without CSA revealed a statistically significant increase in their VPA during treatment with the combination of testosterone and vardenafil as compared with placebo. Women with CSA, however, showed no alterations in their physiological sexual responding during this combined drug treatment.
In women without CSA, testosterone appears to activate central sexual mechanisms resulting in higher VPA under the combination of testosterone and vardenafil. This effect did not occur in women with CSA.
女性性功能障碍(FSD)可能与对性暗示的中枢敏感性降低有关。单剂量睾酮可能会增加对性刺激的敏感性,进而使磷酸二酯酶5抑制剂在增强生理性性反应方面发挥作用。负面性经历,如童年性虐待(CSA),可能是这些药物引起的变化中的一个重要干预因素。
研究睾酮和伐地那非联合使用是否会增加患有性欲减退障碍(HSDD)的女性对性暗示的敏感性以及生理性性反应。
13名患有HSDD的女性接受了四种不同的药物治疗:(i)安慰剂;(ii)伐地那非;(iii)睾酮;(iv)睾酮和伐地那非联合使用。在每种治疗期间,她们进行了情绪Stroop任务,并观看了中性和色情电影片段。
情绪Stroop任务的隐蔽版本以及阴道脉搏振幅(VPA)。
我们发现报告有CSA的女性(N = 5)与未报告有CSA的女性(N = 8)存在不同的效果。在没有CSA的女性中,睾酮使她们原本较低的对性暗示的前意识注意力水平有所增加,而有CSA的女性则显示出她们原本较高的注意力水平有所下降。在这些组中,我们还发现睾酮和伐地那非联合使用对VPA有不同的影响:与安慰剂相比,没有CSA的女性在接受睾酮和伐地那非联合治疗期间VPA有统计学意义的增加。然而,有CSA的女性在这种联合药物治疗期间生理性性反应没有变化。
在没有CSA的女性中,睾酮似乎激活了中枢性机制,导致在睾酮和伐地那非联合使用时VPA升高。这种效果在有CSA的女性中未出现。