Institute of Veterinary Physiology and Biochemistry University of Milan Via Celoria 10 Milan 20133 Italy.
Mediators Inflamm. 1994;3(6):439-44. doi: 10.1155/S0962935194000621.
In anaesthetized paralysed, mechanically ventilated pigs, the vascular and respiratory effects of 80 ppm nitric oxide (NO) inhaled for 6 min were evaluated. To evoke different levels of smooth muscle contraction ET-1 or PAF, mediators involved in pulmonary disorders, were used. In control conditions, inhaled NO caused selective pulmonary vasodilatation without affecting respiratory resistances. This pulmonary vascular activity influenced the distensibility of the respiratory system and decreased inspiratory work. ET-1 administration significantly increased pulmonary arterial pressure and modestly changed mechanical properties of the respiratory system, while PAF caused potent vasoconstriction and bronchoconstriction associated with a marked change in volume-pressure relationship. In both cases, the changes in vascular and mechanical properties of the respiratory system increased inspiratory work. The vascular and respiratory activities of inhaled NO were correlated with preconstriction levels. The data show that the combination of vascular and respiratory effects improves pulmonary function, suggesting that inhalation of NO is a possible therapeutic approach for obstructive and inflammatory pulmonary diseases.
在麻醉且瘫痪的机械通气猪中,评估了吸入 80ppm 一氧化氮(NO) 6 分钟对血管和呼吸的影响。为了诱发不同程度的平滑肌收缩,使用了参与肺部疾病的介质内皮素-1(ET-1)或血小板活化因子(PAF)。在对照条件下,吸入的 NO 引起选择性肺血管舒张,而不影响呼吸阻力。这种肺血管活性影响呼吸系统的顺应性并降低吸气功。ET-1 给药显著增加肺动脉压并适度改变呼吸系统的机械特性,而 PAF 引起强烈的血管收缩和支气管收缩,与体积-压力关系的显著变化相关。在这两种情况下,呼吸系统的血管和机械特性的变化都增加了吸气功。吸入 NO 的血管和呼吸活性与预收缩水平相关。这些数据表明,血管和呼吸效应的结合改善了肺功能,提示吸入 NO 可能是治疗阻塞性和炎症性肺部疾病的一种方法。