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Hypoxic vasoconstriction in pulmonary arterioles and venules
被引:74
作者:
Hillier, SC
Graham, JA
Hanger, CC
Godbey, PS
Glenny, RW
Wagner, WW
机构:
[1] INDIANA UNIV,SCH MED,DEPT ANESTHESIA,INDIANAPOLIS,IN 46202
[2] INDIANA UNIV,SCH MED,DEPT PHYSIOL BIOPHYS,INDIANAPOLIS,IN 46202
[3] INDIANA UNIV,SCH MED,DEPT PEDIAT,INDIANAPOLIS,IN 46202
[4] UNIV WASHINGTON,DEPT MED,SEATTLE,WA 98195
[5] UNIV WASHINGTON,DEPT PHYSIOL & BIOPHYS,SEATTLE,WA 98195
关键词:
pulmonary circulation;
nitric oxide;
pulmonary microcirculation;
videomicroscopy;
hypoxic pulmonary vasoconstriction;
dogs;
VENOUS OCCLUSION;
NITRIC-OXIDE;
DOG LUNG;
ENDOTHELIN;
SITES;
FLOW;
D O I:
10.1152/jappl.1997.82.4.1084
中图分类号:
Q4 [生理学];
学科分类号:
071003 ;
摘要:
Pulmonary microvessels (<70 mu m) lack a complete muscular media. We tested the hypothesis that these thin-walled vessels do not participate in the hypoxic presser 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.
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页码:1084 / 1090
页数:7
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