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Pulmonary interstitial pressure and tissue matrix structure in acute hypoxia.

机译:急性缺氧时的肺间质压和组织基质结构。

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摘要

Pulmonary interstitial pressure was measured via micropuncture in anesthetized rabbits in normoxia and after breathing 12% O(2). In normoxia [arterial PO(2) = 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 PO(2) = 39 +/- 16 mm Hg), the corresponding values were 30+/-8 and 3.5+/-2.5 cm H(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 microg/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.
机译:在常氧和呼吸12%O(2)后,通过微穿刺在麻醉兔中测量肺间质压力。在常氧[动脉PO(2)= 88 +/- 2(SD)mmHg]中,肺动脉压和肺间质压分别为16 +/- 8和-9.6 +/- 2 cmH(2)O。缺氧6小时后(动脉PO(2)= 39 +/- 16 mm Hg),相应的值为30 +/- 8和3.5 +/- 2.5 cm H(2)O(P <0.05)。肺间质蛋白聚糖的提取能力(在0.4 M盐酸胍提取后,通过己糖酸盐测定评估)在正常氧和缺氧3和6小时后分别为12.3、32.4和60.6 microg / g湿组织,表明连接蛋白聚糖的非共价键减弱其他细胞外基质成分。凝胶过滤色谱显示低氧暴露期间硫酸软骨素和硫酸乙酰肝素蛋白聚糖的碎片增加,说明细胞外基质天然结构和基底膜结构的损失。明胶酶谱显示低氧暴露后明胶酶B(基质金属蛋白酶9)的蛋白水解激活形式增加,提供了蛋白酶激活可能在缺氧诱导的肺损伤中起作用的证据。

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