Goldenberg M M
The Mount Sinai/NYU Medical Center/Health System, New York 10029, USA.
Clin Ther. 1998 Nov-Dec;20(6):1033-48. doi: 10.1016/s0149-2918(98)80103-3.
Sildenafil citrate, an oral therapy for erectile dysfunction, is a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type 5 (PDE5), the predominant isozyme metabolizing cGMP in the corpus cavernosum. Chemically, it is a compound of the pyrazolo-pyrimidinyl-methylpiperazine class. Sildenafil has no direct relaxant effect on human corpus cavernosum but enhances the relaxant effect of nitric oxide (NO) on the corpus cavernosum by inhibiting PDE5, which is responsible for degradation of cGMP in this tissue. When sexual stimulation causes local release of NO, inhibition of PDE5 by sildenafil increases concentrations of cGMP in the corpus cavernosum, causing smooth muscle relaxation and blood flow into the penis, resulting in an erection. Sildenafil at recommended doses has no effect in the absence of sexual stimulation. The drug is rapidly absorbed after oral administration, with absolute bioavailability of 40%. Its pharmacokinetics are dose proportional over the recommended dosage range. Maximum plasma concentrations are reached within 30 to 120 minutes after oral dosing in the fasting state. Sildenafil is cleared predominantly by the hepatic microsomal isoenzymes CYP3A4 (major route) and CYP2C9 (minor route). Clinical studies assessed the effect of sildenafil on the ability of men with erectile dysfunction to engage in sexual activity and, specifically, to achieve and maintain an erection sufficient for satisfactory sexual intercourse. Sildenafil was evaluated at doses of 25, 50, and 100 mg in randomized, double-masked, placebo-controlled clinical trials of up to 6 months' duration. The drug was administered to hundreds of patients aged 19 to 87 years having erectile dysfunction of various etiologies for a mean duration of 5 years. Sildenafil was associated with statistically significant improvement in erectile function compared with placebo. Adverse effects reported at a rate of >2% were headache, flushing, dyspepsia, nasal congestion, urinary tract infection, abnormal vision, diarrhea, dizziness, and rash. No cases of priapism were reported. The use of sildenafil is contraindicated in men who are taking organic nitrates, because of the potential for a precipitous decrease in blood pressure. Postmarketing reports and surveillance have revealed at least 39 deaths with sildenafil use in men having a history of heart disease, men taking nitrate medications, and men in poor physical health due to lack of exercise. Many of the men who experienced serious adverse effects or death had a variety of concomitant diseases and were taking multiple medications.
枸橼酸西地那非是一种治疗勃起功能障碍的口服药物,是环磷酸鸟苷(cGMP)特异性5型磷酸二酯酶(PDE5)的选择性抑制剂,PDE5是阴茎海绵体中代谢cGMP的主要同工酶。从化学结构上看,它是吡唑并嘧啶基甲基哌嗪类化合物。西地那非对人体阴茎海绵体没有直接的舒张作用,但通过抑制PDE5增强一氧化氮(NO)对阴茎海绵体的舒张作用,PDE5负责该组织中cGMP的降解。当性刺激引起局部释放NO时,西地那非抑制PDE5可增加阴茎海绵体内cGMP的浓度,导致平滑肌松弛和血液流入阴茎,从而产生勃起。在没有性刺激的情况下,推荐剂量的西地那非没有作用。该药物口服后吸收迅速,绝对生物利用度为40%。在推荐剂量范围内,其药代动力学呈剂量正比关系。空腹口服给药后30至120分钟内达到最大血浆浓度。西地那非主要通过肝微粒体同工酶CYP3A4(主要途径)和CYP2C9(次要途径)清除。临床研究评估了西地那非对勃起功能障碍男性进行性活动能力的影响,特别是达到并维持足以进行满意性交的勃起能力。在长达6个月的随机、双盲、安慰剂对照临床试验中,对25毫克、50毫克和100毫克剂量的西地那非进行了评估。该药物被给予数百名年龄在19至87岁之间、患有各种病因勃起功能障碍且平均病程为5年的患者。与安慰剂相比,西地那非在勃起功能方面有统计学上的显著改善。报告发生率>2%的不良反应有头痛、潮红、消化不良、鼻塞、尿路感染、视力异常、腹泻、头晕和皮疹。未报告阴茎异常勃起的病例。正在服用有机硝酸盐的男性禁用西地那非,因为可能会导致血压急剧下降。上市后报告和监测显示,有心脏病史的男性、服用硝酸盐药物的男性以及因缺乏运动而身体健康不佳的男性使用西地那非后至少有39例死亡。许多经历严重不良反应或死亡的男性患有多种伴发疾病且正在服用多种药物。