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他达拉非治疗动脉性 ED 患者后内皮细胞凋亡减少,停药后不会持续。

Endothelial apoptosis decrease following tadalafil administration in patients with arterial ED does not last after its discontinuation.

机构信息

Section of Endocrinology, Andrology and Internal Medicine, Master in Andrological, Human Reproduction and Biotechnology Sciences, Department of Internal Medicine and Systemic Diseases, University of Catania, Catania, Italy.

出版信息

Int J Impot Res. 2011 Sep-Oct;23(5):200-5. doi: 10.1038/ijir.2011.28. Epub 2011 Jun 16.

Abstract

Although it is well known that phosphodiesterase V inhibitors, used to treat patients with ED, can improve the endothelial dysfunction in organic vascular forms, few studies have explored the duration of their effect on the endothelium after discontinuation. Therefore, the purpose of this study was to evaluate the serum concentrations of apoptotic endothelial microparticles (EMPa), selected as a marker of endothelial damage, in patients with arterial ED at baseline, during tadalafil administration and 3 and 6 months after its discontinuation. In all, 50 patients with arterial ED were evaluated at baseline and 1 week after administration of tadalafil 5 mg once daily for 90 days. Clinical (International Index of Erectile Function-5 score), instrumental (dynamic penile echo color Doppler) and flow-cytometric (serum EMPa concentrations) analyses were performed before (T0) and 1 week (T1), 3 months (T2) and 6 months (T3) after tadalafil discontinuation. The events CD45(neg)/CD144(pos)/annexinV(pos) were defined as EMPa. At T0, patients with arterial ED had serum EMPa concentration significantly higher than 20 healthy men (controls). At T1, patients with arterial ED showed a serum EMPa concentration significantly lower than T0. The significant difference was maintained, though reduced, at T2 and completely lost at T3. In conclusion, the administration of tadalafil decreased serum EMPa concentration in patients with arterial ED. This positive effect on the endothelial dysfunction disappeared 6 months after tadalafil discontinuation.

摘要

尽管众所周知,用于治疗 ED 患者的磷酸二酯酶 V 抑制剂可以改善有机血管形式的内皮功能障碍,但很少有研究探讨其在停药后对内皮的作用持续时间。因此,本研究旨在评估动脉性 ED 患者在基线时、他达拉非给药期间以及停药后 3 和 6 个月时的凋亡内皮微颗粒(EMPa)血清浓度,这些微颗粒被选择作为内皮损伤的标志物。总共评估了 50 例动脉性 ED 患者,他们在基线时和每日服用他达拉非 5mg 连续 90 天 1 周后接受了评估。在开始(T0)、1 周(T1)、3 个月(T2)和 6 个月(T3)时进行了临床(国际勃起功能指数-5 评分)、仪器(动态阴茎回声彩色多普勒)和流式细胞术(血清 EMPa 浓度)分析。将 CD45(neg)/CD144(pos)/annexinV(pos) 事件定义为 EMPa。在 T0 时,动脉性 ED 患者的血清 EMPa 浓度明显高于 20 名健康男性(对照组)。在 T1 时,动脉性 ED 患者的血清 EMPa 浓度明显低于 T0。这种差异在 T2 时仍然存在,但有所降低,而在 T3 时完全消失。总之,他达拉非的给药降低了动脉性 ED 患者的血清 EMPa 浓度。这种对内皮功能障碍的积极影响在他达拉非停药 6 个月后消失。

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