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1 Department of Anesthesia, 2 Department of Physiology/Biophysics, and 3 Department of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana 46202; and 4 Departments of Medicine and of Physiology and Biophysics, University of Washington, Seattle, Washington 98195
Received 22 February 1996; accepted in final form 15 November 1996.
Hillier, Simon C., Jacquelyn A. Graham, Christopher C. Hanger, Patricia S. Godbey, Robb W. Glenny, and Wiltz W. Wagner, Jr.
Hypoxic vasoconstriction in pulmonary arterioles and venules. J. Appl. Physiol. 82(4):
1084-1090, 1997.
Pulmonary microvessels (<70 µm) lack a
complete muscular media. We tested the hypothesis that these
thin-walled vessels do not participate in the hypoxic pressor response.
Isolated canine lobes were pump perfused at precisely known
microvascular pressures. A videomicroscope, coupled to a computerized
image-enhancement system, permitted accurate diameter measurements of
subpleural arterioles and venules, with each vessel serving as its own
control. While vascular pressure was maintained constant throughout the
protocol, hypoxia caused an average reduction of 25% of microvessel
diameters. The constriction was reversed when nitric oxide was added to
the hypoxic gas mixture. The nitric oxide reversal, combined with a
lack of lobar blood flow redistribution as measured by fluorescent
microspheres, shows that the constriction was active. This response
suggests the unexpected potential for active intra-acinar
ventilation-perfusion matching.
pulmonary circulation; nitric oxide; pulmonary microcirculation; videomicroscopy; hypoxic pulmonary vasoconstriction; dogs
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