Aniotensin-Converting Enzyme (ACE) Activity: Aortic ancf Endocardial Endothelium Compared

D. Lang, A. Shah, M. Lewis
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引用次数: 5

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...
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主动脉内皮与心内膜内皮负压转换酶(ACE)活性比较
血管内皮细胞释放缓激素(BK),它以自分泌的方式提高细胞内钙浓度([Ca2+]i)并释放NO,这种作用可以通过血管紧张素转换酶(ACE)抑制剂来调节。然而,对BK和ACE抑制剂对心内膜内皮的影响知之甚少。在这项研究中,我们研究了ACE抑制剂卡托普利和雷米普利特对牛主动脉内皮(BAE)和右心室心内膜(BRVE)细胞中(a) bk降解活性,(b)静息Ca2+稳态和(c) bk诱导的[Ca2+]i和cGMP变化的影响。卡托普利和雷米普利可抑制两种细胞的bk降解活性。BRVE患者的静息[Ca2+]i和cGMP水平明显高于BAE患者。卡托普利或雷米普利特没有改变静息时的[Ca*+]i,但引起静息时cGMP的显著增加,而cGMP被NO合成酶抑制剂l -硝基精氨酸苄酯和b2 -激肽受体拮抗剂ho140降低。卡托普利和雷米普利……
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