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内皮素-1对收缩和舒张功能的调节:与冠脉血流的关系

Modulation of systolic and diastolic function by endothelin-1: relation to coronary flow.

作者信息

Offstad J, Tønnessen T, Kirkebøen K A, Ilebekk A, Downing S E

机构信息

Institute for Experimental Medical Research, University of Oslo, Norway.

出版信息

Acta Physiol Scand. 1995 Jun;154(2):103-11. doi: 10.1111/j.1748-1716.1995.tb09892.x.

Abstract

Different conclusions have been reached with regard to the effect of endothelin (ET-1) on cardiac contractility. We examined systolic and diastolic function in response to constant known concentrations of ET-1 with or without ET-1 induced reductions in coronary flow (CF). Rat hearts (n = 21) were buffer-perfused using constant coronary flow (cCF) or constant perfusion pressure (cPP). Left ventricular function was assessed isovolumically. Addition of ET-1 (10(-9) M) in the cCF group caused a gradual increase in PP from 61 +/- 2 to 165 +/- 6 mmHg (mean +/- SE) (P < 0.01). Within 10 min left ventricular systolic pressure (LVSP) increased from 111 +/- 2 to a maximum of 134 +/- 4 mmHg (P < 0.01) and [LVdP/dt] increased from 1640 +/- 81 to a maximum of 2020 +/- 92 mmHg s-1 (P < 0.01). After 15 min left ventricular end diastolic pressure (LVEDP), a measure of diastolic stiffness (DS), also increased. With ET-1 (10(-8) M), similar haemodynamic alterations appeared more rapidly. In the cPP group, ET-1 (10(-9) M) caused a sharp decrease in CF and LVSP fell from 115 +/- 8 to 62 +/- 12 mmHg at 10 min (P < 0.001). Systolic function remained stable at a reduced level for 1 h. DS did not change. Thus, ET-1 possesses positive inotropic effects and increases diastolic stiffness. Both effects may be masked by vasoconstriction-induced ischaemia.

摘要

关于内皮素(ET - 1)对心脏收缩性的影响,已得出不同结论。我们研究了在有或无ET - 1诱导的冠状动脉血流(CF)减少的情况下,对已知恒定浓度ET - 1的收缩和舒张功能反应。使用恒定冠状动脉血流(cCF)或恒定灌注压力(cPP)对大鼠心脏(n = 21)进行缓冲灌注。通过等容方式评估左心室功能。在cCF组中添加ET - 1(10⁻⁹ M)导致灌注压从61±2 mmHg逐渐升高至165±6 mmHg(平均值±标准误)(P < 0.01)。在10分钟内,左心室收缩压(LVSP)从111±2 mmHg升高至最高134±4 mmHg(P < 0.01),[LVdP/dt]从1640±81 mmHg s⁻¹升高至最高2020±92 mmHg s⁻¹(P < 0.01)。15分钟后,左心室舒张末期压力(LVEDP),即舒张硬度(DS)的一个指标,也升高了。使用ET - 1(10⁻⁸ M)时,类似的血流动力学改变出现得更快。在cPP组中,ET - 1(10⁻⁹ M)导致CF急剧下降,LVSP在10分钟时从115±8 mmHg降至62±12 mmHg(P < 0.001)。收缩功能在降低水平保持稳定1小时。DS没有变化。因此,ET - 1具有正性肌力作用并增加舒张硬度。这两种作用可能都被血管收缩诱导的缺血所掩盖。

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