Musiek Erik S, Morrow Jason D
Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
Curr Protoc Toxicol. 2005 Jun;Chapter 17:Unit 17.6. doi: 10.1002/0471140856.tx1706s24.
Oxidative stress has been implicated in a wide variety of disease processes. One method to quantify oxidative injury is to measure lipid peroxidation. Most methods to do this are fraught with problems particularly when utilized to assess oxidative stress in vivo. On the other hand, quantification of a group of prostaglandin F(2)-like compounds, termed the F(2)-isoprostanes (F(2)-IsoPs) provides an accurate assessment of oxidative stress both in vitro and in vivo and has come to be regarded as the gold standard to quantify lipid peroxidation. This unit describes methods to assess lipid peroxidation associated with oxidant injury in vivo by quantifying concentrations of either esterified or free F(2)-IsoPs in biological fluids and tissues. The techniques employed for the analysis of these compounds from biological sources that are detailed herein utilize mass spectrometric approaches. Measurement of F(2)-IsoPs represents an important advance in the ability to assess the role of oxidative stress in human disease.
氧化应激与多种疾病过程有关。量化氧化损伤的一种方法是测量脂质过氧化。大多数用于此的方法都存在问题,尤其是在用于评估体内氧化应激时。另一方面,一组称为F(2)-异前列腺素(F(2)-IsoPs)的前列腺素F(2)样化合物的定量提供了体外和体内氧化应激的准确评估,并已被视为量化脂质过氧化的金标准。本单元描述了通过量化生物流体和组织中酯化或游离F(2)-IsoPs的浓度来评估体内与氧化损伤相关的脂质过氧化的方法。本文详细介绍的用于分析来自生物来源的这些化合物的技术采用了质谱方法。F(2)-IsoPs的测量代表了评估氧化应激在人类疾病中作用能力的一项重要进展。