The Hospital for Sick Children Toronto, 555 Univ. Ave., Toronto, Ontario M5G 1X8, Canada.
Am J Physiol Lung Cell Mol Physiol. 2014 Jan;306(2):L207-15. doi: 10.1152/ajplung.00164.2013. Epub 2013 Nov 15.
Inhaled nitric oxide (NO) and other cGMP- or cAMP-dependent pulmonary vasodilators are often used in combination for the treatment of the persistent pulmonary hypertension of the newborn syndrome. There is in vitro evidence to indicate that NO downregulate the pulmonary vascular response to cGMP-dependent agonists raising concern as to whether a synergistic effect is observed when employing a combined strategy in newborns. Hypothesizing that a synergistic effect is absent, we evaluated newborn and juvenile rat pulmonary arteries to determine the individual and combined vasodilatory effect of cGMP- and cAMP-dependent agonists. In precontracted near-resistance pulmonary arteries, the addition of sildenafil reduced vasorelaxation response to NO donor S-nitroso-N-acetyl penicillamine (SNAP). A similar decrease in SNAP-induced vasodilation was observed in arteries pretreated with BAY 41-2272 (10(-9) M), a soluble guanylate cyclase stimulator cGMP, and its downstream protein kinase activator. cGMP also reduced the vasorelaxant response to the cAMP-dependent forskolin. Inhibition of endogenous vascular NO generation enhanced SNAP-induced relaxation. The present data suggest that the mechanism involved in the cGMP desensitization to other relaxant agonists involves downregulation of the small heat shock protein HSP20 and is evident in rat pulmonary and systemic vascular smooth muscle cells. In newborn rats with chronic hypoxia-induced pulmonary hypertension, the combination of sildenafil and inhaled NO resulted in a lesser reduction in pulmonary vascular resistance compared with their individual effect. These data suggest that clinical exposure to one cGMP-dependent pulmonary vasodilator may affect the response to other cGMP- or cAMP-mediated agonists.
吸入一氧化氮(NO)和其他 cGMP 或 cAMP 依赖性肺血管扩张剂通常联合用于治疗新生儿持续性肺动脉高压综合征。有体外证据表明,NO 下调肺血管对 cGMP 依赖性激动剂的反应,这引起了人们的关注,即在新生儿中采用联合策略时是否观察到协同作用。假设不存在协同作用,我们评估了新生和幼年大鼠肺动脉,以确定 cGMP 和 cAMP 依赖性激动剂的单独和联合血管舒张作用。在预收缩的近阻力肺动脉中,添加西地那非可降低一氧化氮供体 S-亚硝基-N-乙酰青霉胺(SNAP)的血管舒张反应。在预先用 BAY 41-2272(10(-9) M)处理的动脉中观察到 SNAP 诱导的血管舒张的类似减少,BAY 41-2272 是一种可溶性鸟苷酸环化酶刺激物 cGMP 及其下游蛋白激酶激活剂。cGMP 还降低了对 cAMP 依赖性 forskolin 的血管舒张反应。内源性血管 NO 生成的抑制增强了 SNAP 诱导的松弛。目前的数据表明,cGMP 对其他松弛激动剂脱敏的机制涉及小热休克蛋白 HSP20 的下调,并且在大鼠肺和全身血管平滑肌细胞中明显。在慢性低氧诱导的肺动脉高压的新生大鼠中,西地那非和吸入 NO 的联合使用导致肺血管阻力的降低小于其单独作用。这些数据表明,临床暴露于一种 cGMP 依赖性肺血管扩张剂可能会影响对其他 cGMP 或 cAMP 介导的激动剂的反应。