Department of Pharmacology, Faculty of Medicinal Sciences, University of Campinas, State University of Campinas, Campinas, SP, Brazil.
Department of Pharmacology, Faculty of Medicine of Ribeirao Preto, University of Sao Paulo, Av. Bandeirantes, 3900, 14049-900, Ribeirao Preto, SP, Brazil.
Eur J Clin Pharmacol. 2011 Apr;67(4):365-370. doi: 10.1007/s00228-011-1003-x. Epub 2011 Feb 9.
The antihypertensive effects of angiotensin-converting enzyme inhibitors (ACEi) are explained, at least in part, by enhanced bradykinin-dependent nitric oxide (NO) formation and decreased angiotensin II-induced oxidative stress and vasoconstriction. We examined for the first time whether treatment with enalapril increases the plasma levels of markers of NO formation and decreases oxidative stress in mild to moderate hypertensive patients.
Eighteen untreated hypertensive patients were treated with enalapril 10 mg/day (n=10) or 20 mg/day (n=8) for 60 days. Eighteen normotensive healthy controls were followed for the same period. Venous blood samples were collected at baseline and after 30/60 days of treatment with enalapril. Plasma NOx (nitrites + nitrates) concentrations were determined by using the Griess reaction. Plasma nitrite and whole blood nitrite concentrations were determined by using an ozone-based chemiluminescence assay. Plasma thiobarbituric acid-reactive species (TBARS) and 8-isoprostane concentrations were determined by a fluorimetric method and by ELISA, respectively.
Treatment with enalapril decreased blood pressure in hypertensive patients. However, we found no significant changes in plasma NOx, nitrite, whole blood nitrite, and in the levels of markers of oxidative stress in both normotensive controls and hypertensive patients treated with enalapril.
Our data show that enalapril 10-20 mg/day does not affect the concentrations of relevant markers of NO formation or markers of oxidative stress in mild to moderately hypertensive subjects, despite satisfactory blood pressure control. Our findings do not rule out the possibility that ACEi may produce such effects in more severely hypertensive patients treated with higher doses of ACEi.
血管紧张素转换酶抑制剂(ACEi)的降压作用至少部分归因于增强缓激肽依赖性一氧化氮(NO)的形成以及减少血管紧张素 II 诱导的氧化应激和血管收缩。我们首次研究了依那普利治疗是否会增加轻度至中度高血压患者的血浆 NO 形成标志物水平并降低氧化应激。
18 名未经治疗的高血压患者分别接受依那普利 10 mg/天(n=10)或 20 mg/天(n=8)治疗 60 天。18 名血压正常的健康对照者在相同时间内接受随访。在基线时和依那普利治疗 30/60 天后采集静脉血样。通过格里希反应测定血浆 NOx(亚硝酸盐+硝酸盐)浓度。通过基于臭氧的化学发光测定法测定血浆亚硝酸盐和全血亚硝酸盐浓度。通过荧光法和 ELISA 分别测定血浆硫代巴比妥酸反应性物质(TBARS)和 8-异前列腺素浓度。
依那普利治疗可降低高血压患者的血压。然而,我们在血压正常的对照组和依那普利治疗的高血压患者中均未发现血浆 NOx、亚硝酸盐、全血亚硝酸盐以及氧化应激标志物水平有显著变化。
我们的数据表明,依那普利 10-20 mg/天不会影响轻度至中度高血压患者中与 NO 形成相关的标志物或氧化应激标志物的浓度,尽管血压得到了满意的控制。我们的研究结果并不排除 ACEi 在接受更高剂量 ACEi 治疗的更严重高血压患者中可能产生这种作用的可能性。