Harabin A L, Braisted J C, Flynn E T
Naval Medical Research Institute, Bethesda, Maryland 20814-5055.
J Appl Physiol (1985). 1990 Jul;69(1):328-35. doi: 10.1152/jappl.1990.69.1.328.
Rats and guinea pigs were exposed to O2 at 2.8 ATA (HBO) delivered either continuously or intermittently (repeated cycles of 10 min of 100% O2 followed by 2.5 min of air). The O2 time required to produce convulsions and death was increased significantly in both species by intermittency. To determine whether changes in brain and lung superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GSHPx) correlated with the observed tolerance, enzyme activities were measured after short or long HBO exposures. For each exposure duration, one group received continuous and one intermittent HBO; O2 times were matched. HBO had marked effects on these enzymes: lung SOD increased (guinea pigs 47%, rats 88%) and CAT and GSHPx activities decreased (33%) in brain and lung. No differences were seen in lung GSHPx or brain CAT in rats or brain SOD in either species. In guinea pigs, but less so in rats, the observed changes in activity were usually modulated by intermittency. Increases in hematocrit, organ protein, and lung DNA, which may also reflect ongoing oxidative damage, were also slowed with intermittency in guinea pigs. Intermittency benefited both species by postponing gross symptoms of toxicity, but its modulation of changes in enzyme activities and other biochemical variables was more pronounced in guinea pigs than in rats, suggesting that there are additional mechanisms for tolerance.
将大鼠和豚鼠暴露于2.8个绝对大气压(ATA)的氧气环境中(高压氧),氧气供应方式为持续或间歇供应(100%氧气持续10分钟,随后空气供应2.5分钟,重复此循环)。间歇性供应氧气显著延长了两种动物产生惊厥和死亡所需的氧气暴露时间。为了确定大脑和肺部超氧化物歧化酶(SOD)、过氧化氢酶(CAT)以及谷胱甘肽过氧化物酶(GSHPx)的变化是否与观察到的耐受性相关,在短时间或长时间高压氧暴露后测量了酶活性。对于每种暴露持续时间,一组接受持续高压氧,另一组接受间歇高压氧;两组的氧气暴露时间匹配。高压氧对这些酶有显著影响:肺部SOD活性增加(豚鼠增加47%,大鼠增加88%),大脑和肺部的CAT和GSHPx活性降低(33%)。大鼠肺部的GSHPx、大脑的CAT以及两种动物大脑的SOD活性未见差异。在豚鼠中,观察到的活性变化通常受间歇性供应的调节,在大鼠中则较少。血细胞比容、器官蛋白和肺部DNA的增加(这些也可能反映正在进行的氧化损伤)在豚鼠中也因间歇性供应而减缓。间歇性供应通过推迟毒性的明显症状使两种动物都受益,但它对酶活性和其他生化变量变化的调节在豚鼠中比在大鼠中更明显,这表明存在其他耐受性机制。