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心内膜内皮是否介导对血管紧张素I和血管紧张素II的正性肌力反应?

Does endocardial endothelium mediate positive inotropic response to angiotensin I and angiotensin II?

作者信息

Meulemans A L, Andries L J, Brutsaert D L

机构信息

University of Antwerp, Belgium.

出版信息

Circ Res. 1990 Jun;66(6):1591-601. doi: 10.1161/01.res.66.6.1591.

Abstract

The positive inotropic response to angiotensin I and II in cardiac tissue of most mammalian species, as well as the exact site in the heart for conversion of local and systemic angiotensin I into angiotensin II, remains to be elucidated. In isolated cat papillary muscles, angiotensin I and angiotensin II (0.1 nM to 1 microM, 35 degrees C, 1.25 mM Ca2+) increased, in a dose-dependent manner, peak twitch tension with typical slight prolongation of twitch duration. This typical response did not necessitate the presence of an intact endocardial endothelium (EE), as a similar response was observed in muscles where the EE had been damaged by a 1-second exposure to 0.5% Triton X-100. After addition of captopril, an angiotensin converting enzyme inhibitor, the positive inotropic response to angiotensin I was completely abolished, both in the presence and the absence of an intact EE. Hence, the heart possesses angiotensin converting enzyme, which mediates the positive inotropic response to angiotensin I. An intact EE was not a prerequisite for this response; thus, myocytes as well as nonmyocytes may be possible locations (in addition to the EE) for angiotensin converting enzyme. In the presence of an intact EE, and after addition of captopril, the positive inotropic response to angiotensin II was significantly diminished (desensitization). By contrast, in the absence of an intact EE, but also after addition of captopril, the positive response to angiotensin II was potentiated (sensitization). Both desensitization and sensitization (in the presence or absence of an intact EE, respectively) of the response to angiotensin II induced by the addition of captopril were inhibited by indomethacin, a cyclooxygenase inhibitor, suggesting a role for prostaglandins.

摘要

大多数哺乳动物心脏组织对血管紧张素I和II的正性肌力反应,以及局部和全身血管紧张素I转化为血管紧张素II在心脏中的确切位点,仍有待阐明。在离体猫乳头肌中,血管紧张素I和血管紧张素II(0.1 nM至1 microM,35℃,1.25 mM Ca2+)以剂量依赖性方式增加了峰值收缩张力,并伴有典型的收缩持续时间轻度延长。这种典型反应并不需要完整的心内膜内皮(EE)存在,因为在EE经0.5% Triton X - 100暴露1秒而受损的肌肉中也观察到了类似反应。添加血管紧张素转换酶抑制剂卡托普利后,无论EE是否完整,对血管紧张素I的正性肌力反应均完全消失。因此,心脏具有血管紧张素转换酶,它介导了对血管紧张素I的正性肌力反应。完整的EE不是这种反应的先决条件;因此,心肌细胞以及非心肌细胞(除EE外)都可能是血管紧张素转换酶的可能存在部位。在EE完整且添加卡托普利后,对血管紧张素II的正性肌力反应显著减弱(脱敏)。相比之下,在EE不完整但添加卡托普利后,对血管紧张素II的正性反应增强(致敏)。添加卡托普利诱导的对血管紧张素II反应的脱敏和致敏(分别在EE完整或不完整的情况下)均被环氧化酶抑制剂吲哚美辛抑制,提示前列腺素发挥了作用。

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