{"title":"主动脉内皮与心内膜内皮负压转换酶(ACE)活性比较","authors":"D. Lang, A. Shah, M. Lewis","doi":"10.3109/10623329609024681","DOIUrl":null,"url":null,"abstract":"Vascular endothelial cells release bradykinin (BK), which acts in an autocrine manner to raise intracellular calcium concentrations ([Ca2+]i) and release NO, effects which can be modified by angiotensin-converting enzyme (ACE) inhibitors. Little is known of the effects of BK and ACE inhibitors on endocardial endothelium however. In this study, we investigated the effects of the ACE inhibitors captopril and ramiprilat on (a) BK-degrading activity, (b) resting Ca2+ homeostasis and (c) BK-induced changes in [Ca2+]i and cGMP in bovine aortic endothelial (BAE) and right ventricle endocardial (BRVE) cells. Captopril and ramiprilat inhibited the BK-degrading activity of both cell types. Resting levels of [Ca2+]i and cGMP were significantly higher in BRVE than in BAE. Captopril or ramiprilat did not alter resting [Ca*+]i, but caused significant increases in resting cGMP which were reduced by the NO synthase inhibitor L-nitroarginine benzyl ester and the B2-kinin receptor antagonist HOE 140. Captopril and ramipril...","PeriodicalId":11588,"journal":{"name":"Endothelium-journal of Endothelial Cell Research","volume":"18 1","pages":"51-61"},"PeriodicalIF":0.0000,"publicationDate":"1996-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"Aniotensin-Converting Enzyme (ACE) Activity: Aortic ancf Endocardial Endothelium Compared\",\"authors\":\"D. Lang, A. Shah, M. Lewis\",\"doi\":\"10.3109/10623329609024681\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Vascular endothelial cells release bradykinin (BK), which acts in an autocrine manner to raise intracellular calcium concentrations ([Ca2+]i) and release NO, effects which can be modified by angiotensin-converting enzyme (ACE) inhibitors. Little is known of the effects of BK and ACE inhibitors on endocardial endothelium however. In this study, we investigated the effects of the ACE inhibitors captopril and ramiprilat on (a) BK-degrading activity, (b) resting Ca2+ homeostasis and (c) BK-induced changes in [Ca2+]i and cGMP in bovine aortic endothelial (BAE) and right ventricle endocardial (BRVE) cells. Captopril and ramiprilat inhibited the BK-degrading activity of both cell types. Resting levels of [Ca2+]i and cGMP were significantly higher in BRVE than in BAE. Captopril or ramiprilat did not alter resting [Ca*+]i, but caused significant increases in resting cGMP which were reduced by the NO synthase inhibitor L-nitroarginine benzyl ester and the B2-kinin receptor antagonist HOE 140. Captopril and ramipril...\",\"PeriodicalId\":11588,\"journal\":{\"name\":\"Endothelium-journal of Endothelial Cell Research\",\"volume\":\"18 1\",\"pages\":\"51-61\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1996-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Endothelium-journal of Endothelial Cell Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3109/10623329609024681\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Endothelium-journal of Endothelial Cell Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3109/10623329609024681","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Vascular endothelial cells release bradykinin (BK), which acts in an autocrine manner to raise intracellular calcium concentrations ([Ca2+]i) and release NO, effects which can be modified by angiotensin-converting enzyme (ACE) inhibitors. Little is known of the effects of BK and ACE inhibitors on endocardial endothelium however. In this study, we investigated the effects of the ACE inhibitors captopril and ramiprilat on (a) BK-degrading activity, (b) resting Ca2+ homeostasis and (c) BK-induced changes in [Ca2+]i and cGMP in bovine aortic endothelial (BAE) and right ventricle endocardial (BRVE) cells. Captopril and ramiprilat inhibited the BK-degrading activity of both cell types. Resting levels of [Ca2+]i and cGMP were significantly higher in BRVE than in BAE. Captopril or ramiprilat did not alter resting [Ca*+]i, but caused significant increases in resting cGMP which were reduced by the NO synthase inhibitor L-nitroarginine benzyl ester and the B2-kinin receptor antagonist HOE 140. Captopril and ramipril...