Seeger W, Róka L, Moser U
J Clin Chem Clin Biochem. 1984 Nov;22(11):711-5. doi: 10.1515/cclm.1984.22.11.711.
A specific method for the detection of organic hydroperoxides in lung lavage fluid (lung surfactant system) and lung tissue homogenate is described. After the inactivation of endogenous GSH peroxidase and GSH reductase and preincubation with catalase, organic hydroperoxides are consumed by addition of GSH and GSH peroxidase. The increase of GSSG, compared to a blank without addition of GSH peroxidase, is measured in a second enzymatic step with GSH reductase. The recoveries of t-butyl hydroperoxide and of peroxidized, free fatty acids added to lavage fluid or to lung homogenate are higher than 85% in each case. The detection limits of this assay for organic hydroperoxides are 0.9 nmol/mg surfactant phospholipid (molar ratio of 0.00066) and 40 nmol/g wet lung weight. The assay detects organic hydroperoxides in the surfactant system of normal rabbit lungs, but not in lung tissue homogenate.
本文描述了一种检测肺灌洗液(肺表面活性物质系统)和肺组织匀浆中有机氢过氧化物的具体方法。在使内源性谷胱甘肽过氧化物酶和谷胱甘肽还原酶失活并与过氧化氢酶预孵育后,通过加入谷胱甘肽和谷胱甘肽过氧化物酶来消耗有机氢过氧化物。在第二步酶促反应中,使用谷胱甘肽还原酶测量与未添加谷胱甘肽过氧化物酶的空白相比氧化型谷胱甘肽(GSSG)的增加量。添加到灌洗液或肺匀浆中的叔丁基氢过氧化物和过氧化游离脂肪酸的回收率在每种情况下均高于85%。该检测方法对有机氢过氧化物的检测限为0.9 nmol/mg表面活性物质磷脂(摩尔比为0.00066)和40 nmol/g湿肺重量。该检测方法可检测正常兔肺表面活性物质系统中的有机氢过氧化物,但不能检测肺组织匀浆中的有机氢过氧化物。