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电子顺磁共振自旋捕获技术在检测大鼠吸入臭氧暴露期间体内产生的自由基中的应用。

Application of the EPR spin-trapping technique to the detection of radicals produced in vivo during inhalation exposure of rats to ozone.

作者信息

Kennedy C H, Hatch G E, Slade R, Mason R P

机构信息

Laboratory of Molecular Biophysics, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina 27709.

出版信息

Toxicol Appl Pharmacol. 1992 May;114(1):41-6. doi: 10.1016/0041-008x(92)90094-9.

Abstract

Ozone is known to induce lipid peroxidation of lung tissue, although no direct evidence of free radical formation has been reported. We have used the electron paramagnetic resonance (EPR) spin-trapping technique to search for free radicals produced in vivo by ozone exposure. The spin trap alpha-(4-pyridyl-1-oxide)-N-tert-butylnitrone (4-POBN) was administered ip to male Sprague-Dawley rats. The rats were then exposed for 2 hr to either 0, 0.5, 1.0, 1.5, or 2.0 ppm ozone with 8% CO2 to increase their respiratory rate. A six-line 4-POBN/radical spin adduct signal (aN = 15.02 G and a beta H = 3.27 G) was detected by EPR spectroscopy in lipid extracts from lungs of rats treated with 4-POBN and then exposed to ozone. Only a weak signal was observed in the corresponding solution from rats exposed to 0 ppm ozone (air with CO2 only). The concentration of the radical adduct increased as a function of ozone concentration. After administration of 4-POBN, rats were exposed for either 0.5, 1.0, 2.0, or 4.0 hr to either 0 or 2.0 ppm ozone (with CO2). The radical adduct concentration of the ozone-exposed groups at exposure times of 2.0 and 4.0 hr was significantly different from that of the corresponding air control groups. A correlation was observed between the radical adduct concentration and the lung weight/body weight ratio. These results demonstrate that ozone induces the production of free radicals in rat lungs during inhalation exposure and that radical production may be involved in the induction of pulmonary toxicity by ozone. This is the first direct evidence for ozone-induced free radical production in vivo.

摘要

已知臭氧可诱导肺组织发生脂质过氧化,尽管尚未有自由基形成的直接证据报道。我们使用电子顺磁共振(EPR)自旋捕获技术来寻找臭氧暴露在体内产生的自由基。将自旋捕获剂α-(4-吡啶基-1-氧化物)-N-叔丁基硝酮(4-POBN)腹腔注射给雄性Sprague-Dawley大鼠。然后将大鼠暴露于含有8%二氧化碳的0、0.5、1.0、1.5或2.0 ppm臭氧中2小时,以提高它们的呼吸频率。通过EPR光谱在经4-POBN处理后再暴露于臭氧的大鼠肺脂质提取物中检测到一个六线4-POBN/自由基自旋加合物信号(aN = 15.02 G,aβH = 3.27 G)。在仅暴露于0 ppm臭氧(仅含二氧化碳的空气)的大鼠的相应溶液中仅观察到微弱信号。自由基加合物的浓度随臭氧浓度的增加而增加。给予4-POBN后,将大鼠暴露于0或2.0 ppm臭氧(含二氧化碳)中0.5、1.0、2.0或4.0小时。暴露2.0和4.0小时的臭氧暴露组的自由基加合物浓度与相应的空气对照组有显著差异。观察到自由基加合物浓度与肺重量/体重比之间存在相关性。这些结果表明,臭氧在吸入暴露期间诱导大鼠肺中自由基的产生,并且自由基的产生可能参与臭氧诱导的肺毒性。这是臭氧在体内诱导自由基产生的首个直接证据。

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