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肾上腺素色素诱导大鼠心脏冠状动脉收缩。

Adrenochrome-induced coronary artery constriction in the rat heart.

作者信息

Karmazyn M, Beamish R E, Fliegel L, Dhalla N S

出版信息

J Pharmacol Exp Ther. 1981 Oct;219(1):225-30.

PMID:6793711
Abstract

Adrenochrome, an oxidation product of epinephrine, has been demonstrated to produce cardiotoxic effects. In this study, we have investigated whether this agent can alter coronary resistance in isolated rat hearts. Concentrations of adrenochrome from 1 to 1000 ng/ml increased coronary pressure in a dose- and time-dependent manner. The highest concentration produced a 3-fold elevation in pressure after a 1-hr perfusion. Myocardial contractile force decreased only with either 100 or 1000 ng/ml of adrenochrome and this effect was evident after substantial elevations in coronary pressure. The elevation in coronary pressure was significantly reduced by two calcium antagonists, verapamil and D-600. Furthermore, the degree of constriction by adrenochrome was dependent on the CaCl2 concentration in the perfusion medium. High concentrations of indomethacin or propranolol attenuated the degree of coronary pressure elevation, whereas acetylsalicylic acid and phenoxybenzamine were without effect. Sulfinpyrazone, which has been shown to reduce the arrhythmogenic action of adrenochrome in vivo, significantly reduced the coronary pressure increases. These results suggest that adrenochrome is a potent coronary constricting agent in the rat heart and its action is seemingly dependent on external Ca++ availability.

摘要

肾上腺素色素是肾上腺素的氧化产物,已被证明会产生心脏毒性作用。在本研究中,我们调查了该物质是否会改变离体大鼠心脏的冠状动脉阻力。浓度为1至1000 ng/ml的肾上腺素色素以剂量和时间依赖性方式增加冠状动脉压力。在灌注1小时后,最高浓度使压力升高了3倍。仅在100或1000 ng/ml的肾上腺素色素作用下,心肌收缩力才会下降,且这种作用在冠状动脉压力大幅升高后才明显。两种钙拮抗剂维拉帕米和D - 600可显著降低冠状动脉压力的升高。此外,肾上腺素色素引起的收缩程度取决于灌注液中的氯化钙浓度。高浓度的吲哚美辛或普萘洛尔可减弱冠状动脉压力升高的程度,而乙酰水杨酸和酚苄明则无作用。已证明在体内能降低肾上腺素色素致心律失常作用的磺吡酮,可显著降低冠状动脉压力的升高。这些结果表明,肾上腺素色素是大鼠心脏中一种强效的冠状动脉收缩剂,其作用似乎依赖于细胞外钙离子的可用性。

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