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口服酚妥拉明:一种用于治疗勃起功能障碍的α-1、α-2肾上腺素能拮抗剂。

Oral phentolamine: an alpha-1, alpha-2 adrenergic antagonist for the treatment of erectile dysfunction.

作者信息

Goldstein I

机构信息

Department of Urology, Boston University School of Medicine, Boston, MA, USA.

出版信息

Int J Impot Res. 2000 Mar;12(S1):S75-S80.

Abstract

Phentolamine mesylate is an alpha-1 and alpha-2 selective adrenergic receptor antagonist which has undergone clinical trials for erectile dysfunction treatment. Biochemical and physiological studies in human erectile tissue have revealed a high affinity of phentolamine for alpha-1 and alpha-2 adrenergic receptors. Based on pharmacokinetic studies, it is suggested that 30-40 min following oral ingestion of 40 or 80 mg of phentolamine (Vasomax), the mean plasma phentolamine concentrations are sufficient to occupy the alpha-1 and -2 adrenergic receptors in erectile tissue and thereby result in inhibition of adrenergic-mediated physiologic activity. In large multi-center, placebo-controlled pivotal phase III clinical trials, the mean change in the erectile function domain of the International Index of Erectile Function scores (Questions 1-5 and 15) from screening to the end of treatment was significantly higher following use of active drug (40 mg and 80 mg) compared to placebo. Three to four times as many patients receiving phentolamine reported being satisfied or very satisfied compared with those receiving placebo. At doses of 40 mg and 80 mg respectively, 55% and 59% of men were able to achieve vaginal penetration with 51% and 53% achieving penetration on 75% of attempts. The correction of erectile dysfunction or improvement to a less severe category of dysfunction was experienced by 53% of men with the 80 mg dose and 40% with the 40 mg dose of phentolamine. All trends of response were the same regardless of any concomitant medication. There were no severe adverse events. At 40 mg, 7.7% experienced rhinitis and fewer than 3.1% experienced any other side effect of treatment. Phentolamine is safe, well tolerated and efficacious for the treatment of erectile dysfunction. International Journal of Impotence Research (2000) 12, Suppl 1, S75-S80

摘要

甲磺酸酚妥拉明是一种α-1和α-2选择性肾上腺素能受体拮抗剂,已进行过治疗勃起功能障碍的临床试验。对人体勃起组织的生化和生理学研究表明,酚妥拉明对α-1和α-2肾上腺素能受体具有高亲和力。基于药代动力学研究,有人提出,口服40或80毫克酚妥拉明(Vasomax)后30 - 40分钟,平均血浆酚妥拉明浓度足以占据勃起组织中的α-1和α-2肾上腺素能受体,从而抑制肾上腺素能介导的生理活性。在大型多中心、安慰剂对照的关键III期临床试验中,与安慰剂相比,使用活性药物(40毫克和80毫克)后,从筛查到治疗结束,国际勃起功能指数评分(问题1 - 5和15)的勃起功能领域平均变化显著更高。与接受安慰剂的患者相比,接受酚妥拉明治疗的患者报告满意或非常满意的人数多出三到四倍。分别给予40毫克和80毫克剂量时,55%和59%的男性能够实现阴道插入,51%和53%的男性在75%的尝试中实现插入。80毫克剂量的酚妥拉明使53%的男性勃起功能障碍得到纠正或改善为较轻程度的功能障碍,40毫克剂量则使40%的男性如此。无论使用何种伴随药物,所有反应趋势均相同。没有严重不良事件。40毫克剂量时,7.7%的患者出现鼻炎,出现任何其他治疗副作用的患者少于3.1%。酚妥拉明治疗勃起功能障碍安全、耐受性良好且有效。《国际阳痿研究杂志》(2000年)12卷,增刊1,S75 - S80

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