缺血/再灌注糖尿病大鼠视网膜自由基的直接测定。

M E Szabo, M T Droy-Lefaix, M Doly
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引用次数: 0

摘要

采用电子顺磁共振(EPR)技术直接测定糖尿病大鼠缺血/再灌注视网膜自由基的生成。组织在缺血90 min、缺血90 min、再灌注1 min、3 min、5 min、24 h后分别于77℃冷冻。缺血90 min后再灌注1 min、3 min、5 min、24 h(每组10例),自由基信号强度由糖尿病非缺血控制值12 +/- 3任意单位增加到58 +/- 6 (P < 0.05)、62 +/- 7 (P < 0.05)、32 +/- 5 (P < 0.05)、14 +/- 4任意单位。在缺血90 min后再灌注3 min时观察自由基产生的峰值强度;因此,我们选择这个时间点来研究超氧化物歧化酶(聚乙二醇偶联,PEG-SOD)和EGb 761(银杏叶提取物)处理组视网膜自由基的产生。在7500、15000和30000 U/l的SOD和25、50和100 mg/kg的EGb 761中,分别检测到氧自由基产生的剂量依赖性减少,这可能是导致缺血和再灌注糖尿病视网膜异常的缺血后功能衰减的原因。
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Direct measurement of free radicals in ischemic/reperfused diabetic rat retina.

Electron paramagnetic resonance (EPR) spectroscopy was used to directly measure free radical generation in ischemic/reperfused diabetic rat retina. Tissue was frozen at 77 degrees K after 90 min ischemia, and 90 min ischemia followed by 1 min, 3 min, 5 min, and 24 hours reperfusion, respectively. After 90 min of ischemia followed by 1 min, 3 min, 5 min, and 24 hours of reperfusion (n = 10 in each group), free radical signal intensity was increased from its diabetic nonischemic control value of 12 +/- 3 arbitrary units to 58 +/- 6 (P < 0.05), 62 +/- 7 (P < 0.05), 32 +/- 5 (P < 0.05), and 14 +/- 4 arbitrary units, respectively. The peak intensity of free radical production was observed after 90 min ischemia followed by 3 min of reperfusion; therefore, this time point was selected to study the retinal free radical production in superoxide dismutase (conjugated with polyethylene glycol, PEG-SOD) and EGb 761 (Ginkgo biloba extract)-treated groups. With 7,500, 15,000, and 30,000 U/liter of SOD, and 25, 50, and 100 mg/kg of EGb 761, a dose-dependent reduction in oxygen free radical production was detected, respectively, which may be responsible for the attenuation of abnormal postischemic function in ischemic and reperfused diabetic retina.

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