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暴露于高氧环境的豚鼠肺部循环巨噬细胞的聚集。

Accumulation of circulating macrophages in lungs of guinea pigs exposed to hyperoxia.

作者信息

Baehner R L, Boxer L A, Higgins C, Johnson G S

出版信息

Pediatr Res. 1981 Oct;15(10):1356-8. doi: 10.1203/00006450-198110000-00011.

Abstract

Superoxide dismutase (SOD) and glutathione peroxidase (GPx) key enzymes in alveolar macrophages regulating levels of superoxide anion and hydrogen peroxide, respectively, were observed to fluctuate in response to FIO2 of 50 and 85% for 18 to 90 hr. At the lower oxygen tension, SOD rose two-fold and GPx decreased significantly by 18 hr and throughout the exposure periods compared to a delayed increase in SOD activity which was not sustained beyond 66 hr of exposure and a sustained rise in GPx to an FIO2 of 85%. Peritoneal macrophages containing lower SOD activity and greater GPx activity than resident alveolar macrophages upon injection into the circulation resulted in 10-fold accumulation in the lungs during exposure of animals to FIO2 of 85% but not at 50%. This study indicates that brief exposure to FIO2 of 85% but not 50% resulted in alterations of the vascular integrity of the lungs resulting in the accumulation of circulating macrophages to the alveolar macrophage pool. The delayed rise in SOD activity and the sustained increase in GPx activity in alveolar macrophages from animals exposed to FIO2 of 85% could in part be related to this influx of circulating macrophages with enzymatic characteristics observed for peritoneal macrophages.

摘要

超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GPx)分别是肺泡巨噬细胞中调节超氧阴离子和过氧化氢水平的关键酶,研究发现,在18至90小时内,它们会随50%和85%的吸入氧分数(FIO2)发生波动。在较低的氧分压下,与SOD活性延迟升高(暴露66小时后未持续)和GPx持续升高至85%的FIO2相比,SOD在18小时时升高了两倍,且在整个暴露期间GPx显著下降。与驻留肺泡巨噬细胞相比,腹腔巨噬细胞的SOD活性较低,GPx活性较高,将其注入循环系统后,在动物暴露于85%的FIO2而非50%的FIO2期间,肺部会积累10倍之多。该研究表明,短暂暴露于85%而非50%的FIO2会导致肺血管完整性改变,从而使循环巨噬细胞在肺泡巨噬细胞池中积累。暴露于85%的FIO2的动物肺泡巨噬细胞中SOD活性的延迟升高和GPx活性的持续增加,可能部分与具有腹腔巨噬细胞酶学特征的循环巨噬细胞的流入有关。

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