Kingsley Philip J, Marnett Lawrence J
Department of Biochemistry, Vanderbilt Institute of Chemical Biology, Center in Molecular Toxicology, Vanderbilt-Ingram Cancer Center, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
Methods Enzymol. 2007;433:91-112. doi: 10.1016/S0076-6879(07)33005-X.
The neutral arachidonic acid derivatives N-arachidonoyl ethanolamine (anandamide or AEA), and 2-arachidonoylglycerol (2-AG) have been identified as endogenous ligands for the cannabinoid receptors. Additionally, these compounds have been identified as substrates of the second isoform of the cyclooxygenase enzyme (COX-2). Through the action of COX-2 and downstream prostaglandin synthases, a diverse family of prostaglandin glycerol esters (PG-Gs) and prostaglandin ethanolamides (PG-EAs) have been identified. Sensitive and reliable analytical methodology is crucial for the continued research on the biological roles of this family of lipids. In this chapter, we discuss methods for analyzing both the precursor endocannabinoids and their PG-like products by LC-MS-MS. Cation coordination provides the ionization, and selected reaction monitoring is successfully employed to provide a method of analysis that is both sensitive and specific.
中性花生四烯酸衍生物N-花生四烯酰乙醇胺(花生四烯乙醇胺或AEA)和2-花生四烯酰甘油(2-AG)已被鉴定为大麻素受体的内源性配体。此外,这些化合物已被鉴定为环氧化酶(COX-2)第二种同工型的底物。通过COX-2和下游前列腺素合成酶的作用,已鉴定出多种前列腺素甘油酯(PG-Gs)和前列腺素乙醇酰胺(PG-EAs)。灵敏可靠的分析方法对于持续研究这类脂质的生物学作用至关重要。在本章中,我们将讨论通过液相色谱-串联质谱法分析前体内源性大麻素及其类PG产物的方法。阳离子配位提供电离,成功采用选择反应监测来提供一种灵敏且特异的分析方法。