Djuric Dragan, Mitrovic Veselin, Jakovljevic Vladimir
Institute of Physiology, Belgrade University School of Medicine, Belgrade, F.R. Yugoslavia.
Arzneimittelforschung. 2002;52(5):365-70. doi: 10.1055/s-0031-1299899.
The aim of the study was to compare the effects of Ca2+ channel antagonists on coronary endothelial L-arginine/NO system in isolated rat heart. The hearts of male Wistar albino rats (n = 36, age 8 weeks, body mass 180-200 g) were perfused according to Langendorff technique at gradually increased coronary perfusion pressure (CPP) which induced flow-dependent NO release (nitrite outflow). The experiments were performed during control condition or in the presence of different Ca2+ channel antagonists: nifedipine (CAS 21829-25-4, 30 nmol/l), diltiazem (CAS 42399-41-7, 3 mumol/l), verapamil (CAS 52-53-9, 0.4 mumol/l) or amlodipine (CAS 88150-42-9, 100 nmol/l) were administered separately. Also, nifedipine or amlodipine were administered in combination with an inhibitor of nitric oxide synthase (NOS), L-NAME (NG-nitro-L-arginine-methylester, 30 mumol/l). Coronary flow (CF) varied in autoregulatory range from 3.93 +/- 0.25 ml/min/g wt at 50 cmH2O to 4.49 +/- 0.31 ml/min/g wt at 90 cmH2O. In autoregulatory range nitrite outflow varied from 1.80 +/- 0.22 nmol/min/g wt at 50 cmH2O to 2.21 +/- 0.25 nmol/min/g wt at 90 cmH2O and was strictly parallel with the CPP-CF (coronary perfusion pressure/coronary flow) curve. The autoregulatory range of CF was significantly extended (40-100 cmH2O) under the influence of nifedipine. Hemodynamic effects were accompanied by significant changes in nitrite outflow in all groups except for the verapamil group. Nifedipine and diltiazem induced statistically significant increases of nitrite outflow in coronary venous effluent, strictly parallel with the CPP-CF curve, from 58% at 120 cmH2O to 190% at 40 cmH2O and from 74% at 120 cmH2O to 166% at 40 cmH2O, respectively. On the contrary, amlodipine induced significant reduction of nitrite outflow which was stronger at the lower value of CPP (44-46% at 40-80 cmH2O), compared to the higher value of CPP (32-37% at 100-120 cmH2O). When L-NAME was applied in combination with nifedipine or amlodipine, CF was significantly reduced with parallel changes in nitrite outflow. The results show that Ca2+ channel antagonists (verapamil, diltiazem, nifedipine and amlodipine) strongly influence the coronary endothelial L-arginine/NO system in isolated rat heart leading to the difference in nitrite outflow.
本研究的目的是比较钙通道拮抗剂对离体大鼠心脏冠状动脉内皮L-精氨酸/一氧化氮系统的影响。雄性Wistar白化大鼠(n = 36,8周龄,体重180 - 200 g)的心脏按照Langendorff技术在逐渐升高的冠状动脉灌注压(CPP)下进行灌注,该压力诱导了流量依赖性一氧化氮释放(亚硝酸盐流出)。实验在对照条件下或在不同钙通道拮抗剂存在的情况下进行:分别给予硝苯地平(CAS 21829 - 25 - 4,30 nmol/L)、地尔硫䓬(CAS 42399 - 41 - 7,3 μmol/L)、维拉帕米(CAS 52 - 53 - 9,0.4 μmol/L)或氨氯地平(CAS 88150 - 42 - 9,100 nmol/L)。此外,硝苯地平或氨氯地平与一氧化氮合酶(NOS)抑制剂L - NAME(NG - 硝基 - L - 精氨酸甲酯,30 μmol/L)联合使用。冠状动脉流量(CF)在自动调节范围内从50 cmH₂O时的3.93±0.25 ml/min/g体重变化到90 cmH₂O时的4.49±0.31 ml/min/g体重。在自动调节范围内,亚硝酸盐流出从50 cmH₂O时的1.80±0.22 nmol/min/g体重变化到90 cmH₂O时的2.21±0.25 nmol/min/g体重,并且与CPP - CF(冠状动脉灌注压/冠状动脉流量)曲线严格平行。在硝苯地平的影响下,CF的自动调节范围显著扩大(40 - 100 cmH₂O)。除维拉帕米组外,所有组的血流动力学效应均伴有亚硝酸盐流出的显著变化。硝苯地平和地尔硫䓬分别使冠状动脉静脉流出液中的亚硝酸盐流出量在统计学上显著增加,与CPP - CF曲线严格平行,从120 cmH₂O时的58%增加到40 cmH₂O时的190%,以及从120 cmH₂O时的74%增加到40 cmH₂O时的166%。相反,氨氯地平导致亚硝酸盐流出量显著减少,在较低的CPP值(40 - 80 cmH₂O时为44 - 46%)时比在较高的CPP值(100 - 120 cmH₂O时为32 - 37%)时更强。当L - NAME与硝苯地平或氨氯地平联合使用时,CF显著降低,同时亚硝酸盐流出量也发生平行变化。结果表明,钙通道拮抗剂(维拉帕米、地尔硫䓬、硝苯地平和氨氯地平)强烈影响离体大鼠心脏的冠状动脉内皮L - 精氨酸/一氧化氮系统,导致亚硝酸盐流出量存在差异。