Pulmonary interstitial pressure and tissue matrix structure in acute hypoxia

被引:63
作者
Miserocchi, G
Passi, A
Negrini, D
Del Fabbro, M
De Luca, G
机构
[1] Univ Milan, Dept Expt & Environm Med & Biotechnol, I-20052 Monza, Italy
[2] Univ Milan, Dept Med Surg & Dent, I-20142 Milan, Italy
[3] Univ Insubria, Dept Expt & Clin Biomed Sci, I-21100 Varese, Italy
关键词
high-altitude pulmonary edema; micropuncture; microvascular permeability; proteoglycans; metalloproteinases;
D O I
10.1152/ajplung.2001.280.5.L881
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Pulmonary interstitial pressure was measured via micropuncture in anesthetized rabbits in normoxia and after breathing 12% O-2. In normoxia [arterial PO2 = 88 +/- 2 (SD) mmHg], pulmonary arterial pressure and pulmonary interstitial pressure were 16 +/- 8 and -9.6 +/- 2 cmH(2)O, respectively. After 6 h of hypoxia (arterial PO2 = 39 +/- 16 mmHg), the corresponding values were 30 +/- 8 and 3.5 +/- 2.5 cmH(2)O (P < 0.05). Pulmonary interstitial proteoglycan extractability, evaluated by hexuronate assay after 0.4 M guanidinium hydrochloride extraction, was 12.3, 32.4, and 60.6 <mu>g/g wet tissue in normoxia and after 3 and 6 h of hypoxia, respectively, indicating a weakening of the noncovalent bonds linking proteoglycans to other extracellular matrix components. Gel filtration chromatography showed an increased fragmentation of chondroitin sulfate- and heparan sulfate-proteoglycans during hypoxic exposure, accounting for a loss of extracellular matrix native architecture and basement membrane structure. Gelatin zymography demonstrated increased amounts of the proteolytically activated form of gelatinase B (matrix metalloproteinase-9) after hypoxic exposure, providing evidence that the activation of proteinases may play a role in hypoxia-induced lung injury.
引用
收藏
页码:L881 / L887
页数:7
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