Domenech R, Macho P, Penna M, Schwarze H, Huidobro-Toro J P, Thumala A
Department of Pathophysiology, Faculty of Medicine, University of Chile, Santiago.
Eur J Pharmacol. 1993 Jul 6;238(1):53-8. doi: 10.1016/0014-2999(93)90504-b.
The endothelium plays a key role in the regulation of vasoreactivity. To assess its importance on coronary flow regulation, we studied the participation of endothelium-derived relaxing factor-nitric oxide (EDRF-NO) on coronary reactive hyperemia and on the hyperemia that occurs secondary to an increase in myocardial oxygen consumption. In 15 dogs, the reactive hyperemic response decreased substantially after inhibition of EDRF-NO synthesis with N-omega-nitro-L-arginine (P < 0.01). In contrast, the hyperemia secondary to an increase in myocardial oxygen consumption, characterized by a linear correlation between myocardial oxygen consumption and coronary flow, did not change significantly after inhibition of EDRF-NO production (regression analysis, P > 0.1). Thus EDRF-NO synthesis by the endothelium is an important mechanism mediating the reactive hyperemic response but it does not seem to be essential for the metabolic regulation of coronary vascular resistance during hyperemia induced by an increased metabolic demand on the myocardium.
内皮细胞在血管反应性调节中起关键作用。为评估其在冠状动脉血流调节中的重要性,我们研究了内皮衍生舒张因子一氧化氮(EDRF-NO)在冠状动脉反应性充血以及继发于心肌耗氧量增加的充血中的作用。在15只犬中,用N-ω-硝基-L-精氨酸抑制EDRF-NO合成后,反应性充血反应显著降低(P<0.01)。相反,以心肌耗氧量与冠状动脉血流呈线性相关为特征的继发于心肌耗氧量增加的充血,在抑制EDRF-NO生成后无明显变化(回归分析,P>0.1)。因此,内皮细胞合成EDRF-NO是介导反应性充血反应的重要机制,但在心肌代谢需求增加引起的充血过程中,它似乎对冠状动脉血管阻力的代谢调节并非必不可少。