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Am J Physiol Heart Circ Physiol 292: H1777-H1781, 2007. First published December 1, 2006; doi:10.1152/ajpheart.01024.2006
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Direct demonstration of 25- and 50-µm arteriovenous pathways in healthy human and baboon lungs

Andrew T. Lovering,1,2 Michael K. Stickland,1 Amy J. Kelso,2 and Marlowe W. Eldridge1,2,3

1John Rankin Laboratory of Pulmonary Medicine; and 2Departments of Pediatrics, and 3Biomedical Engineering, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin

Submitted 19 September 2006 ; accepted in final form 27 November 2006

Postmortem microsphere studies in adult human lungs have demonstrated the existence of intrapulmonary arteriovenous pathways using nonphysiological conditions. The aim of the current study was to determine whether large diameter (>25 and 50 µm) intrapulmonary arteriovenous pathways are functional in human and baboon lungs under physiological perfusion and ventilation pressures. We used fresh healthy human donor lungs obtained for transplantion and fresh lungs from baboons (Papio c. anubis). Lungs were ventilated with room air by using a peak inflation pressure of 15 cmH2O and a positive end-expiratory pressure of 5 cmH2O. Lungs were perfused between 10 and 20 cmH2O by using a phosphate-buffered saline solution with 5% albumin. We infused a mixture of 25- and 50-µm microspheres (0.5 and 1 million total for baboons and human studies, respectively) into the pulmonary artery and collected the entire pulmonary venous outflow. Under these conditions, evidence of intrapulmonary arteriovenous anastomoses was found in baboon (n = 3/4) and human (n = 4/6) lungs. In those lungs showing evidence of arteriovenous pathways, 50-µm microspheres were always able to traverse the pulmonary circulation, and the fraction of transpulmonary passage ranged from 0.0003 to 0.42%. These data show that intrapulmonary arteriovenous pathways >50 µm in diameter are functional under physiological ventilation and perfusion pressures in the isolated lung. These pathways provide an alternative conduit for pulmonary blood flow that likely bypasses the areas of gas exchange at the capillary-alveolar interface that could compromise both gas exchange and the ability of the lung to filter out microemboli.

intrapulmonary arteriovenous anastomoses; shunt; baboon; pulmonary circulation



Address for reprint requests and other correspondence: A. T. Lovering, John Rankin Laboratory of Pulmonary Medicine, Dept. of Pediatrics and Population Health Sciences, Univ. of Wisconsin School of Medicine and Public Health, Rm. 4245 MSC, 1300 Univ. Ave., Madison, WI 53706-1532 (E-mail: atlovering{at}wisc.edu)




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