Ng Sharon C W, Furman Ran, Axelsen Paul H, Shchepinov Mikhail S
Department of Pharmacology, 1009C Stellar Chance Laboratories, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6084, United States.
Retrotope Inc., Los Altos, California 94022, United States.
ACS Omega. 2022 Jul 14;7(29):25337-25345. doi: 10.1021/acsomega.2c02285. eCollection 2022 Jul 26.
Polyunsaturated fatty acyl chains (PUFAs) concentrate in the brain and give rise to numerous oxidative chemical degradation products. It is widely assumed that these products are the result of free radical chain reactions, and reactions of this type have been demonstrated in preparations where a single PUFA substrate species predominates. However, it is unclear whether such reactions can occur in the biologically complex milieu of lipid membranes where PUFA substrates are a minority species, and where diverse free radical scavengers or other quenching mechanisms are present. It is of particular interest to know whether they occur in brain, where PUFAs are concentrated and where PUFA oxidation products have been implicated in the pathogenesis of neurodegenerative disorders. To ascertain whether free radical chain reactions can occur in a complex brain lipid mixture, mouse brain lipids were extracted, formed into vesicles, and treated with a fixed number of hydroxyl radicals under conditions wherein the concentrations and types of PUFA-containing phospholipids were varied. Specific phospholipid species in the mixture were assayed by tandem mass spectrometry to quantify the oxidative losses of endogenous PUFA-containing phospholipids. Results reveal crosstalk between the oxidative degradation of ω3 and ω6 PUFAs that can only be explained by the occurrence of free radical chain reactions. These results demonstrate that PUFAs in a complex brain lipid mixture can participate in free radical chain reactions wherein the extent of oxidative degradation is not limited by the number of reactive oxygen species available to initiate such reactions. These reactions may help explain otherwise puzzling in vivo interactions between ω3 and ω6 PUFAs in mouse brain.
多不饱和脂肪酰链(PUFAs)在大脑中富集,并产生大量氧化化学降解产物。人们普遍认为这些产物是自由基链式反应的结果,并且在单一PUFA底物种类占主导的制剂中已证明了这种类型的反应。然而,尚不清楚此类反应是否能在脂质膜这种生物复杂环境中发生,在脂质膜中PUFA底物是少数种类,且存在多种自由基清除剂或其他淬灭机制。特别令人感兴趣的是,这些反应是否发生在大脑中,大脑中PUFAs富集,且PUFA氧化产物与神经退行性疾病的发病机制有关。为确定自由基链式反应是否能在复杂的脑脂质混合物中发生,提取小鼠脑脂质,形成囊泡,并在含PUFA的磷脂浓度和类型不同的条件下,用固定数量的羟基自由基进行处理。通过串联质谱分析混合物中的特定磷脂种类,以量化内源性含PUFA磷脂的氧化损失。结果揭示了ω3和ω6 PUFAs氧化降解之间的串扰,这只能通过自由基链式反应的发生来解释。这些结果表明,复杂脑脂质混合物中的PUFAs可参与自由基链式反应,其中氧化降解程度不受可引发此类反应的活性氧种类数量的限制。这些反应可能有助于解释小鼠脑中ω3和ω6PUFAs之间原本令人困惑的体内相互作用。