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Effects of sildenafil on hypoxic pulmonary vascular function in dogs

¹Department of Internal Medicine, Hôpital Lapeyronie, Montpellier, France; and ²Laboratory of Physiology, Faculty of Medicine, Université Libre de Bruxelles, Brussels, Belgium

Submitted 20 March 2006 ; accepted in final form 29 May 2006

Sildenafil has been shown to be an effective treatment of pulmonary arterial hypertension and is believed to present with pulmonary selectivity. This study was designed to determine the site of action of sildenafil compared with inhaled nitric oxide (NO) and intravenous sodium nitroprusside (SNP), known as selective and nonselective pulmonary vasodilators, respectively. Inhaled NO (40 ppm), and maximum tolerated doses of intravenous SNP and sildenafil, (5 µg·kg^–1·min^–1 and 0.1 mg·kg^–1·h^–1), respectively, were administered to eight dogs ventilated in hypoxia. Pulmonary vascular resistance (PVR) was evaluated by pulmonary arterial pressure (Ppa) minus left atrial pressure (Pla) vs. flow curves, and partitioned into arterial and venous segments by the occlusion method. Right ventricular hydraulic load was defined by pulmonary arterial characteristic impedance (Zc) and elastance (Ea) calculations. Right ventricular arterial coupling was estimated by the ratio of end-systolic elastance (Ees) to Ea. Decreasing the inspired oxygen fraction from 0.4 to 0.1 increased Ppa – Pla at a standardized flow of 3 l·min^–1·m^–2 from 6 ± 1 to 18 ± 1 mmHg (mean ± SE). Ppa – Pla was decreased to 9 ± 1 by inhaled NO, 14 ± 1 by SNP, and 14 ± 1 mmHg by sildenafil. The partition of PVR, Zc, Ea, and Ees/Ea was not affected by the three interventions. Inhaled NO did not affect systemic arterial pressure, which was similarly decreased by sildenafil and SNP, from 115 ± 4 to 101 ± 4 and 98 ± 5 mmHg, respectively. We conclude that inhaled NO inhibits hypoxic pulmonary vasoconstriction more effectively than sildenafil or SNP, and sildenafil shows no more selectivity for the pulmonary circulation than SNP.

pulmonary hypertension; nitric oxide; sodium nitroprusside; right ventricle; pulmonary vascular resistance; pulmonary vascular impedance