Department of Pharmaceutical Sciences (DISFARM), Università Degli Studi di Milano, Via Mangiagalli 25, 20133, Milan, Italy.
Centro Cardiologico Monzino, IRCCS, Via Parea 4, 20138, Milan, Italy.
Redox Biol. 2021 Jun;42:101899. doi: 10.1016/j.redox.2021.101899. Epub 2021 Feb 17.
Reactive carbonyl species (RCS) formed by lipidperoxidation as free forms or as enzymatic and non-enzymatic conjugates are widely used as an index of oxidative stress. Besides general measurements based on derivatizing reactions, more selective and sensitive MS based analyses have been proposed in the last decade. Untargeted and targeted methods for the measurement of free RCS and adducts have been described and their applications to in vitro and ex vivo samples have permitted the identification of many biological targets, reaction mechanisms and adducted moieties with a particular relevance to RCS protein adducts. The growing interest in protein carbonylation can be explained by considering that protein adducts are now recognized as being involved in the damaging action of oxidative stress so that their measurement is performed not only to obtain an index of lipid peroxidation but also to gain a deeper insight into the molecular mechanisms of oxidative stress. The aim of the review is to discuss the most novel analytical approaches and their application for profiling reactive carbonyl species and their enzymatic and non-enzymatic metabolites as an index of lipid-oxidation and oxidative stress. Limits and perspectives will be discussed.
活性羰基化合物(RCS)由脂质过氧化形成游离形式或酶和非酶结合物,被广泛用作氧化应激的指标。除了基于衍生反应的一般测量方法外,过去十年中还提出了更具选择性和灵敏度的基于 MS 的分析方法。已经描述了用于测量游离 RCS 和加合物的非靶向和靶向方法,它们在体外和体内样本中的应用允许鉴定许多具有与 RCS 蛋白加合物特别相关的生物学靶标、反应机制和加合部分。人们对蛋白质羰基化的兴趣日益增加,可以通过考虑到蛋白质加合物现在被认为参与氧化应激的损伤作用来解释,因此不仅要测量它们以获得脂质过氧化的指标,还要更深入地了解氧化应激的分子机制。本综述的目的是讨论最新型的分析方法及其在作为脂质氧化和氧化应激指标的活性羰基化合物及其酶和非酶代谢物的分析中的应用。将讨论其局限性和前景。