Ziegler J W, Ivy D D, Wiggins J W, Kinsella J P, Clarke W R, Abman S H
Department of Pediatrics, University of Colorado School of Medicine, and Children's Hospital, Denver, Colorado, USA.
Am J Respir Crit Care Med. 1998 Nov;158(5 Pt 1):1388-95. doi: 10.1164/ajrccm.158.5.9710117.
Inhaled nitric oxide (iNO) causes selective pulmonary vasodilation by increasing pulmonary vascular levels of cyclic guanosine monophosphate (cGMP). Dipyridamole, a drug with several putative vasodilator mechanisms, is an inhibitor of cGMP-specific phosphodiesterases (PDE5); it therefore has the potential to increase pulmonary vascular cGMP levels, lower pulmonary vascular resistance, augment iNO-induced pulmonary vasodilation, and attenuate excessive pulmonary vasoreactivity. To test dipyridamole in the pulmonary circulation, we studied pediatric patients undergoing cardiac catheterization who had severe resting pulmonary hypertension (Group 1; n = 11) or exaggerated acute hypoxia-induced pulmonary vasoconstriction (Group 2; n = 4). In Group 1, we compared the effects of iNO (20 ppm), dipyridamole (0.6 mg/kg), and combined treatments (iNO + dipyridamole) on pulmonary and systemic hemodynamics. In Group 2 we measured the pulmonary and systemic effects of dipyridamole while the patients were breathing room air and hypoxic gas mixtures (FIO2 = 0.16). One patient in Group 1 had a hypotensive response to dipyridamole and was exluded from study. In the remaining 12 studies done on 10 patients, iNO caused a selective decrease in mean pulmonary artery pressure (Ppa) and indexed pulmonary vascular resistance (PVRI) without affecting mean aortic pressure (Pao) or indexed systemic vascular resistance (SVRI). Dipyridamole decreased PVRI to similar values as did iNO, but this effect was primarily due to an increase in cardiac index (CI), and was not associated with any change in Ppa, and was associated with a decrease in Pao and SVRI. In comparison with individual treatments, combined therapy (iNO + dipyridamole) did not augment pulmonary vasodilation in the group as a whole; however, in 50% of patients, combined therapy decreased PVRI by 20% more than did iNO or dipyridamole alone. In Group 2, Ppa and the pulmonary-to-systemic resistance ratio (Rp/Rs) increased to suprasystemic levels during acute hypoxia. Pretreatment with dipyridamole blunted the increase in Ppa and Rp/Rs during repeat hypoxia, keeping Ppa at a subsystemic level and Rp/Rs < 1. We conclude that: (1) dipyridamole nonselectively reduces PVRI, primarily through an increase in CI; (2) in combination with iNO, dipyridamole augments the decrease in PVRI in some patients; and (3) dipyridamole blunts the severity of acute hypoxic pulmonary vasoconstriction in children with exaggerated hypoxic pressor responses.
吸入一氧化氮(iNO)通过提高肺血管中环磷酸鸟苷(cGMP)水平来引起选择性肺血管舒张。双嘧达莫是一种具有多种假定血管舒张机制的药物,是cGMP特异性磷酸二酯酶(PDE5)的抑制剂;因此它有潜力提高肺血管cGMP水平、降低肺血管阻力、增强iNO诱导的肺血管舒张,并减轻过度的肺血管反应性。为了在肺循环中测试双嘧达莫,我们研究了接受心导管检查的儿科患者,这些患者患有严重的静息性肺动脉高压(第1组;n = 11)或急性低氧诱导的肺血管收缩过度(第2组;n = 4)。在第1组中,我们比较了iNO(20 ppm)、双嘧达莫(0.6 mg/kg)以及联合治疗(iNO + 双嘧达莫)对肺和全身血流动力学的影响。在第2组中,我们测量了患者在呼吸室内空气和低氧混合气体(FIO2 = 0.16)时双嘧达莫对肺和全身的影响。第1组中有1例患者对双嘧达莫有低血压反应并被排除在研究之外。在对10例患者进行的其余12项研究中,iNO导致平均肺动脉压(Ppa)和肺血管阻力指数(PVRI)选择性降低,而不影响平均主动脉压(Pao)或体循环血管阻力指数(SVRI)。双嘧达莫使PVRI降低至与iNO相似的值,但这种作用主要是由于心指数(CI)增加,与Ppa的任何变化无关,且与Pao和SVRI降低有关。与单独治疗相比,联合治疗(iNO + 双嘧达莫)在整个组中并未增强肺血管舒张;然而,在50%的患者中,联合治疗使PVRI降低的幅度比单独使用iNO或双嘧达莫多20%。在第2组中,急性低氧期间Ppa和肺循环与体循环阻力比值(Rp/Rs)升高至超过体循环水平。双嘧达莫预处理可减轻重复低氧期间Ppa和Rp/Rs的升高,使Ppa维持在低于体循环水平且Rp/Rs < 1。我们得出结论:(1)双嘧达莫主要通过增加CI非选择性地降低PVRI;(2)与iNO联合使用时,双嘧达莫可增强部分患者PVRI的降低;(3)双嘧达莫可减轻低氧加压反应过度的儿童急性低氧性肺血管收缩的严重程度。