Kloner Robert A
Heart Institute, Good Samaritan Hospital, Keck School of Medicine, University of Southern California, Los Angeles, CA 90017, USA.
Am J Cardiol. 2005 Dec 26;96(12B):42M-46M. doi: 10.1016/j.amjcard.2005.07.011. Epub 2005 Dec 5.
Currently, 3 phosphodiesterase 5 (PDE5) inhibitor agents are available worldwide for the treatment of erectile dysfunction (ED): sildenafil, vardenafil, and tadalafil. Each of these agents is effective across a broad range of etiologies, including vasculogenic ED in men. Because PDE5 enzyme is found within the vascular smooth muscle cells in the walls of systemic arteries and veins, PDE5 inhibitors are mild vasodilators associated with small (and in general, clinically insignificant) decreases in blood pressure. However, because of the synergistic decrease in blood pressure (both systolic and diastolic) in the presence of organic nitrates, these 3 agents are contraindicated in patients receiving organic nitrates. The duration of interaction between a PDE5 inhibitor and nitrate administration depends on the specific drug being studied. The interaction between sildenafil or vardenafil and nitroglycerin is no longer observed by 24 hours. A preliminary study with sildenafil and sublingual nitroglycerin suggested the interaction is no longer observable by 4 hours. The interaction between tadalafil and nitroglycerin has dissipated by 48 hours after tadalafil administration. This is consistent with the longer elimination half-life of the drug. When PDE5 inhibitors are administered to patients with hypertension who are taking most antihypertensive agents (eg, beta-blockers, angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, calcium antagonists, diuretics), there are usually small additive decreases in blood pressure without a significant increase of adverse events. Some patients develop orthostatic hypotension when PDE5 inhibitors are used in conjunction with an alpha-blocker (typically for hypertension or for urologic conditions, such as benign prostatic hypertrophy). Precautions are necessary for all 3 of the PDE5 inhibitors regarding this potential interaction. Some studies suggest that the interaction is less relevant clinically if the patient has been undergoing long-term alpha-blocker therapy. Several analyses have suggested that PDE5 inhibitors do not increase myocardial infarction rates or death rates compared with placebo controls or expected rates from age-matched populations. In contrast, recent studies have shown that PDE5 inhibitors may have therapeutic potential for a host of cardiovascular diseases. In general, these agents, when used appropriately, are highly safe and effective.
目前,全球有3种5型磷酸二酯酶(PDE5)抑制剂可用于治疗勃起功能障碍(ED):西地那非、伐地那非和他达拉非。这些药物中的每一种对多种病因都有效,包括男性血管性ED。由于PDE5酶存在于全身动脉和静脉壁的血管平滑肌细胞内,PDE5抑制剂是轻度血管扩张剂,与血压小幅下降(一般在临床上无显著意义)有关。然而,由于在使用有机硝酸盐时会出现协同性血压下降(收缩压和舒张压均下降),这3种药物在接受有机硝酸盐治疗的患者中禁用。PDE5抑制剂与硝酸盐给药之间的相互作用持续时间取决于所研究的具体药物。西地那非或伐地那非与硝酸甘油之间的相互作用在24小时后不再出现。一项关于西地那非和舌下硝酸甘油的初步研究表明,4小时后这种相互作用不再明显。他达拉非与硝酸甘油之间的相互作用在他达拉非给药后48小时消失。这与该药物较长的消除半衰期一致。当PDE5抑制剂用于正在服用大多数抗高血压药物(如β受体阻滞剂、血管紧张素转换酶抑制剂、血管紧张素受体阻滞剂、钙拮抗剂、利尿剂)的高血压患者时,通常血压会有小幅相加性下降,且不良事件无显著增加。当PDE5抑制剂与α受体阻滞剂(通常用于治疗高血压或泌尿系统疾病,如良性前列腺增生)联合使用时,一些患者会出现体位性低血压。对于所有3种PDE5抑制剂,都需要针对这种潜在相互作用采取预防措施。一些研究表明,如果患者长期接受α受体阻滞剂治疗,这种相互作用在临床上的相关性较小。多项分析表明,与安慰剂对照或年龄匹配人群的预期发生率相比,PDE5抑制剂不会增加心肌梗死发生率或死亡率。相比之下,最近的研究表明,PDE5抑制剂可能对多种心血管疾病具有治疗潜力。一般来说,这些药物在适当使用时,安全性和有效性都很高。