Influence of enalapril on the endothelial function of DOCA-salt hypertensive rats

V.W Nunes , Z.B Fortes , D Nigro , M.H.C Carvalho , T.M.T Zorn , R Scivoletto
{"title":"Influence of enalapril on the endothelial function of DOCA-salt hypertensive rats","authors":"V.W Nunes ,&nbsp;Z.B Fortes ,&nbsp;D Nigro ,&nbsp;M.H.C Carvalho ,&nbsp;T.M.T Zorn ,&nbsp;R Scivoletto","doi":"10.1016/S0306-3623(00)00053-7","DOIUrl":null,"url":null,"abstract":"<div><p>In the present study, we investigated whether the correction of endothelial dysfunction can be independent of the normalization of high blood pressure levels by enalapril in deoxycorticosterone (DOCA-salt) hypertensive rats. Aorta morphology and the response of aortas with (E+) and without (E−) endothelium to noradrenaline, acetylcholine, and sodium nitroprusside were studied. DOCA-salt hypertensive and normotensive (control) rats were or were not treated with enalapril (5 mg/day/rat in the drinking fluid) for 1, 7, or 15 days. Blood pressure was measured before and after 1, 3, 7, and 15 days of enalapril treatment. Enalapril normalized the high blood pressure levels in 50% (responders) of the hypertensive rats after 3 to as many as 15 days but not after 1 day of treatment. Initial blood pressure levels were not different between responders and nonresponders. Blood pressure levels of normotensive control rats were not altered by enalapril treatment. The tunica media of aortas of DOCA-salt hypertensive rats treated or not treated with enalapril for 15 days was thicker than aortas from normotensive rats. Enalapril corrected the reduced response to acetylcholine observed in aorta from hypertensive rats from the first day of treatment. This treatment rendered aortas from normotensive control rats more sensitive (lower EC<sub>50</sub>) to acetylcholine without a change in the maximal responses. The responses to sodium nitroprusside, a nitric oxide donor, were unaltered in aorta E+ or E− from control and hypertensive rats before and after enalapril treatment. Enalapril did not correct the increased responses to noradrenaline observed in aorta E+ of hypertensive rats. These results suggest that the high blood pressure in DOCA-salt hypertension is not correlated with the altered response to endothelium-dependent agents (either dilator or constrictors). The endothelium-dependent vasodilation by antihypertensive agents can be corrected independently of normalization of blood pressure levels or the vascular morphology.</p></div>","PeriodicalId":12607,"journal":{"name":"General Pharmacology-the Vascular System","volume":"34 2","pages":"Pages 117-125"},"PeriodicalIF":0.0000,"publicationDate":"2000-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0306-3623(00)00053-7","citationCount":"13","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"General Pharmacology-the Vascular System","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0306362300000537","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 13

Abstract

In the present study, we investigated whether the correction of endothelial dysfunction can be independent of the normalization of high blood pressure levels by enalapril in deoxycorticosterone (DOCA-salt) hypertensive rats. Aorta morphology and the response of aortas with (E+) and without (E−) endothelium to noradrenaline, acetylcholine, and sodium nitroprusside were studied. DOCA-salt hypertensive and normotensive (control) rats were or were not treated with enalapril (5 mg/day/rat in the drinking fluid) for 1, 7, or 15 days. Blood pressure was measured before and after 1, 3, 7, and 15 days of enalapril treatment. Enalapril normalized the high blood pressure levels in 50% (responders) of the hypertensive rats after 3 to as many as 15 days but not after 1 day of treatment. Initial blood pressure levels were not different between responders and nonresponders. Blood pressure levels of normotensive control rats were not altered by enalapril treatment. The tunica media of aortas of DOCA-salt hypertensive rats treated or not treated with enalapril for 15 days was thicker than aortas from normotensive rats. Enalapril corrected the reduced response to acetylcholine observed in aorta from hypertensive rats from the first day of treatment. This treatment rendered aortas from normotensive control rats more sensitive (lower EC50) to acetylcholine without a change in the maximal responses. The responses to sodium nitroprusside, a nitric oxide donor, were unaltered in aorta E+ or E− from control and hypertensive rats before and after enalapril treatment. Enalapril did not correct the increased responses to noradrenaline observed in aorta E+ of hypertensive rats. These results suggest that the high blood pressure in DOCA-salt hypertension is not correlated with the altered response to endothelium-dependent agents (either dilator or constrictors). The endothelium-dependent vasodilation by antihypertensive agents can be corrected independently of normalization of blood pressure levels or the vascular morphology.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
依那普利对doca盐高血压大鼠内皮功能的影响
在本研究中,我们研究了依那普利对脱氧皮质酮(doca盐)高血压大鼠内皮功能障碍的纠正是否可以独立于高血压水平的正常化。观察(E+)和(E−)内皮对去甲肾上腺素、乙酰胆碱和硝普钠的影响。doca盐高血压和正常(对照)大鼠分别给予或不给予依那普利(5mg /天/只饮水)1、7或15天。测量依那普利治疗1、3、7、15天前后血压。依那普利在治疗3至15天后使50%的高血压大鼠(应答者)的血压水平正常化,但在治疗1天后没有。反应者和无反应者的初始血压水平没有差异。正常血压对照组大鼠的血压水平未因依那普利治疗而改变。依那普利治疗和未治疗15 d的doca盐高血压大鼠主动脉中膜均较正常大鼠主动脉厚。依那普利纠正了从治疗第一天起高血压大鼠主动脉对乙酰胆碱反应的降低。这种治疗使正常血压对照大鼠的主动脉对乙酰胆碱更敏感(EC50更低),但最大反应没有变化。在依那普利治疗前后,对照大鼠和高血压大鼠的主动脉E+或E -对硝普钠(一氧化氮供体)的反应没有改变。依那普利不能纠正高血压大鼠主动脉E+对去甲肾上腺素反应的增加。这些结果表明,doca -盐高血压患者的高血压与内皮依赖性药物(扩张剂或收缩剂)的反应改变无关。抗高血压药物的内皮依赖性血管舒张可以独立于血压水平或血管形态的正常化而得到纠正。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Analysis of moricizine block of sodium current in isolated guinea-pig atrial myocytes Atrioventricular difference of moricizine block Regulation of chemokine expression in atherosclerosis Homocysteine and arterial disease Experimental mechanisms MS general pharmacology—the vascular system Endothelial dysfunction in atherosclerosis Endothelial cell response to hyperlipemia Activation–dysfunction–injury, the protective role of simvastatin
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1