Lobato E B, Beaver T, Muehlschlegel J, Kirby D S, Klodell C, Sidi A
Department of Anaesthesiology and Department of Surgery, University of Florida College of Medicine, FL 32610-0254, USA.
Br J Anaesth. 2006 Mar;96(3):317-22. doi: 10.1093/bja/ael009. Epub 2006 Jan 27.
To evaluate the effects of phosphodiesterase type III and V (PDEIII and PDEV) inhibition on pulmonary and systemic haemodynamics in a porcine model of acute pulmonary hypertension.
Twenty-four adult swine were anaesthetized with 1 MAC isoflurane and mechanically ventilated with an FI(O(2)) of 100%. Micromanometer-tipped catheters were placed in the ascending aorta, pulmonary artery and right ventricle. Pulmonary flow was measured with a perivascular probe using transit time ultrasound. Pulmonary hypertension was induced with a continuous infusion of the thromboxane analogue, U46619. The animals were then randomized to four groups: Group 1 (n=6) received 50 mg of sildenafil (PDEV inhibitor) diluted in water via an orogastric tube; Group 2 (n=6) received 50 microg kg(-1) of i.v. milrinone (PDEIII inhibitor); Group 3 (n=6) received sildenafil followed by milrinone; and Group 4 (n=6) received placebo via an orogastric tube.
Pulmonary hypertension was achieved in all animals. Calculated pulmonary vascular resistance decreased by an average of 36% after sildenafil (P<0.05), 41% after milrinone (P<0.05), and 61% with both drugs combined (P<0.05). Systemic vascular resistance decreased by 37% (P<0.05) with milrinone alone, and 36% (P<0.05) with milrinone and sildenafil combined but it was preserved in the sildenafil group. Cardiac output and right ventricular dP/dT were significantly improved after milrinone or both drugs combined, but not with sildenafil.
Milrinone and sildenafil are effective pulmonary vasodilators, with independent action and additive effect. Both drugs combined achieved a better haemodynamic profile, with greater pulmonary vasodilatation and increased contractility but without additional systemic vasodilatation. The systemic haemodynamic profile (systemic vasodilation, cardiac output, right ventricular dP/dT) is improved with milrinone but not with sildenafil.
在猪急性肺动脉高压模型中评估Ⅲ型和Ⅴ型磷酸二酯酶(PDEⅢ和PDEV)抑制对肺和全身血流动力学的影响。
24只成年猪用1个最低肺泡有效浓度的异氟烷麻醉,并用100%的吸入氧浓度进行机械通气。将微测压导管置于升主动脉、肺动脉和右心室。用经血管探头通过渡越时间超声测量肺血流量。通过持续输注血栓素类似物U46619诱导肺动脉高压。然后将动物随机分为四组:第1组(n = 6)经口胃管给予50mg溶于水的西地那非(PDEV抑制剂);第2组(n = 6)静脉给予50μg/kg米力农(PDEⅢ抑制剂);第3组(n = 6)先给予西地那非,然后给予米力农;第4组(n = 6)经口胃管给予安慰剂。
所有动物均成功诱导出肺动脉高压。西地那非治疗后计算得出的肺血管阻力平均降低36%(P<0.05),米力农治疗后降低41%(P<0.05),两种药物联合使用后降低61%(P<0.05)。单独使用米力农时全身血管阻力降低37%(P<0.05),米力农与西地那非联合使用时降低36%(P<0.05),但西地那非组全身血管阻力保持不变。米力农或两种药物联合使用后心输出量和右心室dp/dt显著改善,但西地那非未使其改善。
米力农和西地那非是有效的肺血管扩张剂,具有独立作用和相加效应。两种药物联合使用可获得更好的血流动力学状态,肺血管扩张作用更强且收缩力增加,但无额外的全身血管扩张作用。米力农可改善全身血流动力学状态(全身血管扩张、心输出量、右心室dp/dt),但西地那非不能。