DeLeo J A, Floyd R A, Carney J M
Neurosci Lett. 1986 Jun 6;67(1):63-7. doi: 10.1016/0304-3940(86)90209-0.
The in vitro thiobarbituric acid test was used as a measure of lipid peroxidation in the gerbil and rat. Synaptosomal preparations were isolated from the cerebral cortex of each species and incubated with a free radical generating system. Varying concentrations of ADP-Fe3+, with ascorbate and oxygenated incubation medium were used to generate hydroxy-radicals. Peroxidation of the synaptosomal membrane lipids was determined using malondialdehyde (MDA) accumulation. Both the gerbil and rat demonstrated significant increases in MDA in the presence of the generating system, while the gerbil P2 fraction consistently showed an increased level of MDA accumulation as compared with rat at each of the concentrations of ADP-Fe3+. Across a range of concentrations, there was a 2-2.6-fold greater increase in MDA accumulation in gerbil as compared with rat. Free radical generation is currently thought to be involved in the associated damage following cerebral ischemia. An in vitro model capable of producing biochemically similar damage to membrane systems by means of a controlled free-radical generating system may prove useful in studying possible mechanisms of ischemic damage.
体外硫代巴比妥酸试验被用作衡量沙鼠和大鼠脂质过氧化的指标。从每个物种的大脑皮层分离出突触体制剂,并与自由基生成系统一起孵育。使用不同浓度的ADP-Fe3+、抗坏血酸和充氧的孵育培养基来产生羟基自由基。使用丙二醛(MDA)积累来测定突触体膜脂质的过氧化。在存在生成系统的情况下,沙鼠和大鼠的MDA均显著增加,而在每个ADP-Fe3+浓度下,沙鼠P2组分的MDA积累水平始终高于大鼠。在一系列浓度范围内,沙鼠的MDA积累增加幅度比大鼠高2至2.6倍。目前认为自由基生成与脑缺血后的相关损伤有关。一个能够通过可控的自由基生成系统对膜系统产生生物化学上类似损伤的体外模型,可能对研究缺血损伤的可能机制有用。