Bishop M J, Cheney F W
J Cardiovasc Pharmacol. 1983 Mar-Apr;5(2):184-9. doi: 10.1097/00005344-198303000-00003.
We studied the effects of hypoxia on pulmonary hemodynamics and gas exchange before and after minoxidil or nifedipine administration. The studies were carried out in eight normal dogs to determine the relative effects of these two drugs in inhibiting hypoxic pulmonary vasoconstriction. Each dog was studied twice--once with each drug--and exposed repeatedly to hypoxia on each day. Minoxidil raised cardiac output from 2.84 +/- 0.19 to 4.67 +/- 0.29 L/min (mean +/- SE), whereas nifedipine raised it from 3.04 +/- 0.25 to 4.38 +/- 0.38 L/min. Prior to the drugs, hypoxia raised pulmonary vascular resistance 2.4-fold. Minoxidil abolished this pressor response, while nifedipine reduced this response to a 1.6-fold increase. Minoxidil raised venous admixture during normoxia from 6 +/- 1 to 16 +/- 4%, while nifedipine raised it from 7 +/- 1 to 11 +/- 2%. Both drugs are inhibitors of the vasoconstrictive response to hypoxia. At the doses used, minoxidil was a more potent inhibitor of the pressor response to hypoxia than was nifedipine.
我们研究了在给予米诺地尔或硝苯地平前后,缺氧对肺血流动力学和气体交换的影响。研究在8只正常犬身上进行,以确定这两种药物在抑制缺氧性肺血管收缩方面的相对作用。每只犬接受两次研究,每次使用一种药物,并且每天反复暴露于缺氧环境。米诺地尔使心输出量从2.84±0.19升/分钟提高到4.67±0.29升/分钟,而硝苯地平使其从3.04±0.25升/分钟提高到4.38±0.38升/分钟。在使用药物之前,缺氧使肺血管阻力增加2.4倍。米诺地尔消除了这种升压反应,而硝苯地平将这种反应降低至增加1.6倍。在常氧状态下,米诺地尔使静脉混合血从6±1%提高到16±4%,而硝苯地平使其从7±1%提高到11±2%。两种药物都是缺氧性血管收缩反应的抑制剂。在所使用的剂量下,米诺地尔对缺氧升压反应的抑制作用比硝苯地平更强。