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首页> 外文期刊>The Internet Journal of Nutrition and Wellness >Improved Ejacultory Control And Sexual Satisfaction In Pilot Study Of Men Taking Hypericum Perforatum Extract
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Improved Ejacultory Control And Sexual Satisfaction In Pilot Study Of Men Taking Hypericum Perforatum Extract

机译:贯叶连翘提取物男性试验研究中改善的射精控制和性满意度

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The most common male sexual dysfunction is premature ejaculation (PE) and yet there are no approved currently effective therapies. Based on research that Hypericum perforatum, a natural supplement has been demonstrated pharmacologically to delay ejaculation in a rat model of PE, we evaluated the effects of hyperforin extract of Hypericum perforatum on the ejaculatory reflex duration by using the intravaginal ejaculatory latency time (IELT) and sexual satisfaction.Sixteen men who desired longer sexual intercourse and without erectile dysfunction were treated with Hypericum perforatum immediately prior to sexual activity. An intercourse diary was used to document baseline data for 2 weeks and throughout the study period of 4 weeks. Partners were asked to measure IELT using a stopwatch as well as complete a sexual function questionnaire both pre and post treatment. All 16 subjects completed the study (average age 35.0 ± 4.6 years old). There was a significant increase in mean IELT times from 246±29 to 331±34 seconds (p<0.002) in subjects taking hyperforin extract. Fourteen of 16 men (87.5%) reported an improvement in IELT. The increase was seen in both the men who reported PE as bothersome and those who did not feel that PE was a problem for them. There was also significant increase in male satisfaction scores from 3.8±0.27 to 4.25 ±0.21 (p<0.03). Female satisfaction scores also showed a significant increase from 4.9±0.27 to 5.2±0.23 (p<0.04). This pilot study was limited by the lack of placebo control. No systemic or adverse effects on erectile function or orgasm were reported.Hyperforin extract of Hypericum perforatum can increase the duration of sexual intercourse and improve sexual satisfaction for men with and without complaints of PE. Background Premature ejaculation (PE) is a common, embarrassing and significantly undertreated medical condition that affects men and their partners. Approximately one third of sexually active men in the United States report this condition. Though, the prevalence of PE is approximately twice that of erectile dysfunction (ED), many healthcare practitioners have few treatment options for most men with PE [1,2]. The neurotransmitter 5-HT has been implicated in the control of many autonomic and behavioral functions including ejaculation. The link between 5-HT and ejaculation is most likely mediated by the medial preoptic area and paraventricular nucleus of the hypothalamus as these regions have been shown to integrate the sexual responses of men [3,4]. Several lines of evidence suggest that an enhanced synaptic availability of 5-HT in the central nervous system results in an inhibition of ejaculation [5,6,7]. From this perspective, PE is associated with an ejaculation reflex that is genetically “set” at a lower point [8,9]. There are currently no pharmacotherapies specifically approved for the treatment of PE, but a number of selective serotonin reuptake inhibitors (SSRIs) such as paroxetine, sertraline and fluoxetine have been prescribed “off label” as a treatment strategy for PE symptoms [2,10]. Placebo controlled clinical trials have shown fluoxetine, paroxetine, and sertraline increase IELT. A randomized, double-blind, placebo-controlled study found that paroxetine significantly improved PE complaints. After 6 weeks of treatment fluoxetine, paroxetine, and sertraline all significantly increased the mean IELT above the placebo group [10]. Daily treatment with SSRIs can lead to the desired delay in the ejaculation, but their use is associated with side effects that include: nausea, drowsiness, cognitive impairments, anticholinergic and sexual side-effects. Specific unintended sexual effects include abnormal ejaculation, decreased libido, reduced sexual desire, and genital anesthesia [11]. Further drawbacks of SSRIs include the slow onset of action of and relatively long half-life of these agents with the risk of accumulation and an exacerbation of SSRI-related adverse events [1,11]. Side effects
机译:男性性功能障碍最常见的是早泄(PE),但目前尚无批准的有效疗法。基于对贯叶连翘的天然补品的药理学研究已证明可以延缓PE大鼠模型中的射精,我们通过使用阴道内射精潜伏时间(IELT)评估了贯叶连翘的贯叶连翘提取物对射精反射持续时间的影响。性满足感。十六名希望性交时间更长且没有勃起功能障碍的男性在性活动开始前立即接受了贯叶连翘的治疗。使用性交日记记录2周和整个4周研究期间的基线数据。要求合作伙伴使用秒表测量IELT,并在治疗前和治疗后填写性功能问卷。所有16名受试者均完成了研究(平均年龄35.0±4.6岁)。服用Hyperforin提取物的受试者的平均IELT时间从246±29秒显着增加至331±34秒(p <0.002)。 16名男性中有14名(87.5%)报告称IELT有所改善。在报告PE令人烦恼的男性和不认为PE对他们来说是一个问题的男性中都可以看到这种增加。男性满意度得分也从3.8±0.27显着提高到4.25±0.21(p <0.03)。女性满意度得分也从4.9±0.27显着提高到5.2±0.23(p <0.04)。由于缺乏安慰剂对照,这项初步研究受到了限制。没有关于勃起功能或性高潮的全身性或不良反应的报道。贯叶连翘的Hyperforin提取物可以增加性交的持续时间,并改善有或没有PE症状的男性的性满足感。背景技术早泄(PE)是一种常见的,令人尴尬且未得到充分治疗的医学疾病,会影响男性及其伴侣。在美国,大约有三分之一的性活跃男性报告这种情况。尽管PE的患病率大约是勃起功能障碍(ED)的两倍,但对于大多数PE男性,许多医疗保健从业者几乎没有治疗选择[1,2]。神经递质5-HT与许多自主神经和行为功能的控制有关,包括射精。 5-HT和射精之间的联系最有可能是由下视丘的内侧视前区和室旁核介导的,因为这些区域已显示出整合了男性的性反应[3,4]。有几条证据表明,5-HT在中枢神经系统中的突触可用性增强,导致射精受到抑制[5,6,7]。从这个角度来看,PE与射精反射相关,而射精反射在遗传上位于较低点[8,9]。目前尚无专门批准用于治疗PE的药物疗法,但已将“选择性的5-羟色胺再摄取抑制剂”(SSRIs)(如帕罗西汀,舍曲林和氟西汀)开出处方,作为治疗PE症状的策略[2,10] 。安慰剂对照的临床试验表明,氟西汀,帕罗西汀和舍曲林可增加IELT。一项随机,双盲,安慰剂对照的研究发现,帕罗西汀可显着改善PE症状。治疗6周后,氟西汀,帕罗西汀和舍曲林均使IELT均值明显高于安慰剂组[10]。 SSRI的每日治疗可导致所需的射精延迟,但其使用会产生副作用,包括:恶心,嗜睡,认知障碍,抗胆碱能和性副作用。特定的意想不到的性影响包括射精异常,性欲降低,性欲降低和生殖器麻醉[11]。 SSRI的其他缺点包括这些药物起效缓慢,半衰期相对较长以及具有积累的风险,并加剧了SSRI相关的不良事件[1,11]。副作用

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