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阿托伐他汀通过激活内皮型一氧化氮合酶改善对西地那非初始反应不佳的患者的勃起功能障碍。

Atorvastatin improves erectile dysfunction in patients initially irresponsive to Sildenafil by the activation of endothelial nitric oxide synthase.

机构信息

Professor of Pharmacology and Toxicology, Pharmacology Department, Faculty of Pharmacy, Tanta University, Tanta, Egypt.

出版信息

Int J Impot Res. 2013 Jul-Aug;25(4):143-8. doi: 10.1038/ijir.2012.46. Epub 2013 Jan 17.

Abstract

This study aimed at comparing the effects of atorvastatin and vitamin E on erectile dysfunction in patients initially irresponsive to sildenafil, with investigation into the underlying possible mechanisms. Sixty patients were randomly divided into three groups: the atorvastatin group received 80 mg daily, the vitamin E group received 400 IU daily and the control group received placebo capsules. Patients were examined both before and after 6 weeks of treatment for biochemical tests; Superoxide dismutase (SOD), glutathione peroxidase (GPO), C-reactive protein (CRP), interleukin-6 (IL-6), nitric oxide (NO) and endothelial nitric oxide synthase (eNOS) and for erectile function tests; International index of erectile function (IIEF-5) scores and Rigiscan. Both atorvastatin and vitamin E showed a statistically significant GPO increase (P<0.05) and a statistically significant IL-6 decrease (P<0.05). Only atorvastatin showed a statistically significant increase in NO (15.19%, P<0.05), eNOS (20.58%, P<0.01), IIEF-5 score (53.1%, P<0.001) and Rigiscan rigidity parameters (P<0.01), in addition to a statistically significant decrease in CRP (57.9%, P<0.01). However, SOD showed a statistically significant increase only after vitamin E intake (23.1%, P<0.05). Both atorvatstain and vitamin E had antioxidant and anti-inflammatory activities. Although activating eNOS by atorvastatin was the real difference, and expected to be the main mechanism for NO increase and for improving erectile dysfunction. Atorvastatin, but not vitamin E, is a promising drug for sildenafil nonresponders.

摘要

本研究旨在比较阿托伐他汀和维生素 E 对最初对西地那非无反应的患者勃起功能障碍的影响,并探讨潜在的可能机制。将 60 名患者随机分为三组:阿托伐他汀组每天服用 80mg,维生素 E 组每天服用 400IU,对照组服用安慰剂胶囊。患者在治疗 6 周前后进行生化检查;超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GPO)、C 反应蛋白(CRP)、白细胞介素 6(IL-6)、一氧化氮(NO)和内皮型一氧化氮合酶(eNOS);以及勃起功能测试;国际勃起功能指数(IIEF-5)评分和 Rigiscan。阿托伐他汀和维生素 E 均显示 GPO 增加有统计学意义(P<0.05),IL-6 降低有统计学意义(P<0.05)。只有阿托伐他汀显示 NO(15.19%,P<0.05)、eNOS(20.58%,P<0.01)、IIEF-5 评分(53.1%,P<0.001)和 Rigiscan 硬度参数增加有统计学意义(P<0.01),此外 CRP 降低有统计学意义(57.9%,P<0.01)。然而,仅在摄入维生素 E 后 SOD 显示有统计学意义的增加(23.1%,P<0.05)。阿托伐他汀和维生素 E 均具有抗氧化和抗炎活性。虽然阿托伐他汀激活 eNOS 是 NO 增加和改善勃起功能障碍的真正差异,也是预期的主要机制。阿托伐他汀,而不是维生素 E,是西地那非无反应者的一种有前途的药物。

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