Watts F L, Bernard G R
Center for Lung Research, Vanderbilt University Medical School, Nashville, TN 37232.
Pulm Pharmacol. 1991;4(1):32-6. doi: 10.1016/0952-0600(91)90036-3.
The effect of the beta-agonist, ritodrine HCl, was studied on cardiac output (CO) and pulmonary lymph flow (QL) in sheep. Increased CO is associated with an increase in pulmonary QL in sheep during exercise. Isoproterenol increases CO but has not been shown to increase pulmonary QL. Ritodrine HCl was chosen because of its association with pulmonary edema when used to halt premature labor in pregnant women. Unanesthetized sheep received an intravenous infusion of ritodrine in increasing doses over 4 h up to a maximum of 6.3 micrograms/kg/min. Pulmonary pressure increased 2 mmHg after 1 h and returned to baseline by hours 3 and 4 with no change in left atrial pressure or lymph to plasma protein ratio. Pulmonary QL increased by 61% and CO by 80% at hour 3 of infusion (ritodrine dose 5.4 micrograms/kg/min) and remained at this level. Pulmonary QL and CO (normalized to baseline) correlated, r = 0.72, p less than 0.001, but there was no correlation between pulmonary QL and calculated microvascular pressure. Although an increase in pulmonary microvascular endothelium permeability with concurrent pulmonary vasodilation can not be completely ruled out, it appears from this study that beta-agonist therapy with ritodrine increases pulmonary QL by a CO related recruitment of microvessels.
研究了盐酸利托君这种β-激动剂对绵羊心输出量(CO)和肺淋巴流量(QL)的影响。在绵羊运动过程中,心输出量增加与肺淋巴流量增加有关。异丙肾上腺素可增加心输出量,但尚未显示能增加肺淋巴流量。选择盐酸利托君是因为它在用于阻止孕妇早产时与肺水肿有关。未麻醉的绵羊在4小时内接受递增剂量的盐酸利托君静脉输注,最大剂量为6.3微克/千克/分钟。1小时后肺压升高2 mmHg,在第3小时和第4小时恢复到基线水平,左心房压力或淋巴与血浆蛋白比值无变化。在输注第3小时(利托君剂量为5.4微克/千克/分钟)时,肺淋巴流量增加61%,心输出量增加80%,并维持在该水平。肺淋巴流量和心输出量(相对于基线进行标准化)相关,r = 0.72,p < 0.001,但肺淋巴流量与计算出的微血管压力之间无相关性。虽然不能完全排除肺微血管内皮通透性增加并伴有肺血管舒张的情况,但从本研究来看,盐酸利托君的β-激动剂治疗通过与心输出量相关的微血管募集增加了肺淋巴流量。