Department of Physiology and Pharmacology, Tel Aviv University, Sackler Medical School, Ramat Aviv, Tel Aviv 69978, Israel.
Department of Physiology and Pharmacology, Tel Aviv University, Sackler Medical School, Ramat Aviv, Tel Aviv 69978, Israel.
Chem Phys Lipids. 2014 Feb;178:63-76. doi: 10.1016/j.chemphyslip.2013.12.001. Epub 2013 Dec 11.
Measuring peroxidation of aggregated lipids in model systems (liposomes, micelles, emulsions or microemulsions) as well as in samples of biological origin ex vivo (isolated lipoproteins, blood sera or plasma) is widely used in medical and biological investigations, to evaluate the oxidative stress, antioxidants' efficiency and lipid oxidizability in different pathophysiological states. To avoid possible artifacts, such investigations must be based on the time course of peroxidation (i.e. on kinetic studies). To be able to compare complex kinetic profiles, it is important to characterize them in terms of mechanistically meaningful and experimentally unequivocal parameters. In this review, we characterize the typically observed continuous kinetic profiles in terms of a limited number of characteristic time-points (both commonly used and additional time-points and their combinations) that can be derived from experimental time-dependencies. The meaning of each of the experimentally observed characteristic parameters is presented in terms of rate constants and concentrations, derived on the basis of mechanistic considerations. Theoretical expressions for these characteristic parameters are based on a model that includes both the inhibited peroxidation and the uninhibited peroxidation occurring after consumption of the antioxidant(s). Comparison between theoretically predicted dependencies and experimental data support our treatment considered with special emphasis on transition metals-induced peroxidation of lipoproteins.
在医学和生物学研究中,广泛采用测量模型体系(脂质体、胶束、乳液或微乳液)以及体外生物样本(分离的脂蛋白、血清或血浆)中聚集脂质过氧化的方法,以评估不同病理生理状态下的氧化应激、抗氧化剂的效率和脂质的氧化性。为了避免可能的假象,此类研究必须基于过氧化的时程(即动力学研究)。为了能够比较复杂的动力学曲线,重要的是用具有机制意义和实验上明确的参数来对其进行特征描述。在这篇综述中,我们用有限数量的特征时间点(包括常用的和额外的时间点及其组合)来对典型的连续动力学曲线进行特征描述,这些时间点可以从实验的时程依赖性中推导出来。根据机制考虑,我们用速率常数和浓度来表示每个实验观察到的特征参数的意义。这些特征参数的理论表达式基于一个模型,该模型同时包含了抗氧化剂消耗后发生的抑制性过氧化和非抑制性过氧化。理论预测依赖性和实验数据之间的比较支持了我们的处理方法,特别强调了过渡金属诱导的脂蛋白过氧化。