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首页> 外文期刊>Experimental Brain Research >Generation of lipid radicals in the hippocampus of neonatal rats after acute hypoxic-ischemic brain damage.
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Generation of lipid radicals in the hippocampus of neonatal rats after acute hypoxic-ischemic brain damage.

机译:急性缺氧缺血性脑损伤后新生大鼠海马脂质自由基的产生。

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摘要

Free radical-mediated lipid peroxidation has been strongly suggested to be the main cause of neuronal toxicity in the rat brain, including neonatal brain damage. The primary objective of this experiment was to see if the generation of free radicals occurred in the acute phase of ischemic-hypoxic insult in neonatal rats, by electron paramagnetic resonance (EPR) spectroscopy and in vivo brain microdialysis. A spin trap agent, alpha-(4-pyridyl-N-oxide)-N-tert-butylnitrone was perfused through a probe in the hippocampus before and after hypoxia and then an analysis was performed by EPR. From the EPR analysis of spin adduct in the dialysates, we obtained the EPR spectrum of six line spectra for which the hyperfine coupling constants corresponded to those of the EPR signal from the lipoxygenase/linoleic acid (LPX/LA), a lipid radical generating system, increased transiently just after hypoxia. The results of our in vivo study show the lipid peroxidation of the neuronal membrane to progress during neonatal ischemic-hypoxic insult. We hypothesize that an increased formation of lipid radicals may participate in the cascade of reactions leading to neuronal damage in the hippocampus following ischemic-hypoxic insult in neonatal rats.
机译:强烈建议自由基介导的脂质过氧化作用是大鼠大脑神经元毒性(包括新生儿脑损伤)的主要原因。该实验的主要目的是通过电子顺磁共振(EPR)光谱和体内脑微透析,观察新生大鼠缺血缺氧性损伤急性期是否发生自由基的产生。在缺氧前后,通过海马中的探针向自旋捕集剂α-(4-吡啶基-N-氧化物)-N-叔丁基硝酮灌流,然后通过EPR进行分析。从透析液中自旋加合物的EPR分析中,我们获得了六个线谱的EPR谱,其中超细偶合常数对应于脂氧合酶/亚油酸(LPX / LA)(脂质自由基生成系统)的EPR信号,在缺氧后短暂增加。我们的体内研究结果表明,在新生儿缺血缺氧性损伤期间,神经元膜的脂质过氧化作用得以发展。我们假设在新生大鼠缺血缺氧后,脂质自由基形成的增加可能参与导致海马神经元损伤的反应级联反应。

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