von Ritter C, Grisham M B, Hollwarth M, Inauen W, Granger D N
Department of Physiology and Biophysics, Louisiana State University Medical Center, Shreveport.
Gastroenterology. 1989 Sep;97(3):778-80. doi: 10.1016/0016-5085(89)90654-9.
The effects of several free radical scavengers and antioxidant enzymes on neutrophil-mediated changes in mucosal permeability (measured using blood-to-lumen clearance of 51Cr-labeled ethylene-diaminetetraactate) were assessed using ileal loops perfused with N-formyl-methionyl-leucyl-phenylalanine (FMLP). Neither superoxide dismutase nor catalase reduced the FMLP-induced increase in mucosal permeability. However, manganese-loaded desferrioxamine (a superoxide dismutase mimetic), PZ51 (a glutathione peroxidase analogue), desferrioxamine (an iron chelator), or dimethylsulfoxide (a hydroxyl radical scavenger) significantly attenuated FMLP-induced mucosal damage. The results of our experiments indicate that neutrophilic oxidants are responsible for a major portion of the mucosal permeability changes induced by FMLP.
使用灌注了N-甲酰甲硫氨酰亮氨酰苯丙氨酸(FMLP)的回肠肠袢,评估了几种自由基清除剂和抗氧化酶对中性粒细胞介导的黏膜通透性变化(使用51Cr标记的乙二胺四乙酸从血液到肠腔的清除率来测量)的影响。超氧化物歧化酶和过氧化氢酶均未降低FMLP诱导的黏膜通透性增加。然而,负载锰的去铁胺(一种超氧化物歧化酶模拟物)、PZ51(一种谷胱甘肽过氧化物酶类似物)、去铁胺(一种铁螯合剂)或二甲基亚砜(一种羟自由基清除剂)显著减轻了FMLP诱导的黏膜损伤。我们的实验结果表明,中性粒细胞氧化剂是FMLP诱导的黏膜通透性变化的主要原因。