9-12 No study has reported the effect of sustained

hypoxic ventilation in the isolated perfused rat lung. Phenylephrine (PHE) is an α1 and G protein-coupled receptor agonist which causes pulmonary vasoconstriction in an in vivo cat model.13,14 Pre-constriction of pulmonary artery rings in rat with PHE induces a biphasic increase in tension during hypoxia.7 In contrast, it has been shown that PHE or norepinephrine do not significantly increase pulmonary artery pressure Inhibitors,research,lifescience,medical (PAP) during 3 min of hypoxic ventilation in the isolated perfused rat lung.10 By taking the above research into consideration, we aimed to establish, for the first time, biphasic pulmonary vasoconstriction during alveolar hypoxia in the isolated ventilated perfused rat lung. This study was performed in the presence of PHE as a vasoconstrictor for potentiating the hypoxic response of the rat pulmonary vasculature. Interestingly, we noted Inhibitors,research,lifescience,medical that addition of PHE to pulmonary circulation only after hypoxic ventilation led to biphasic HPV. Materials and Methods Lung

Isolation, Perfusion, and Ventilation Adult Sprague-Dawley male rats (n=30) were obtained from the Laboratory Animal Breeding Center and used following approval Inhibitors,research,lifescience,medical the Ethical Committee for Animal Care, Shiraz University of Medical Sciences. We chose the rat as an experimental model because of its suitable size and accessibility. Additionally, distribution of perfusate flow in the rat lung is approximately PF299804 supplier uniform compared to larger animals. The model of isolated perfused lung was described elsewhere.3-5,9,15 Inhibitors,research,lifescience,medical Briefly, animals (body weight 250-300 g) were each deeply anesthetized with an i.p. injection of pentobarbital (50 mg/kg body weight) and heparinized (150 U/100 g body weight) for prevention of clot formation during lung preparation. The trachea was cannulated and animals

were ventilated with room air (tidal volume 1.2 ml/100 g body weight, respiratory Inhibitors,research,lifescience,medical rate 50 beats/min). The chest was opened, after which we cannulated the pulmonary artery and left atrium. The lungs were perfused with 4°C air bubble-free Krebs-Henseleit solution (perfusate) through the pulmonary artery cannula that was connected to a peristaltic pump with a pulsatile Phosphoprotein phosphatase flow of 2 ml/min. The isolated perfused lung was placed in a temperature equilibrated housing chamber and freely suspended from a force transducer for continued monitoring of lung weight. After rinsing the lungs with the perfusate to remove the blood, the perfusion circuit was closed with a total circuit volume of 40 ml. Meanwhile, the flow rate was slowly increased from 2 to 10 ml/min and the entire system (double glass reservoirs, tubing, and housing chamber) was heated from 4°C to 40°C. Concomitantly, the left atrial pressure (LAP) was set at 2-3 cm H2O by adjusting the height of venous part of the system to have zone 3 blood flow in the lung.