van Zadelhoff_2016_Methods.Mol.Biol_1412_217

Reference

Title : Oxygenation of Anandamide by Lipoxygenases - van Zadelhoff_2016_Methods.Mol.Biol_1412_217
Author(s) : van Zadelhoff G , van der Stelt M
Ref : Methods Mol Biol , 1412 :217 , 2016
Abstract :

The endocannabinoids anandamide and 2-arachidonoylglycerol are not only metabolized by serine hydrolases, such as fatty acid amide hydrolase, monoacylglycerol lipase, and alpha,beta-hydrolases 6 and 12, but they also serve as substrates for cyclooxygenases and lipoxygenases. These enzymes oxygenate the 1Z,4Z-pentadiene system of the arachidonic acid backbone of endocannabinoids, thereby giving rise to an entirely new array of bioactive lipids. Hereby, a protocol is provided for the enzymatic synthesis, purification, and characterization of various oxygenated metabolites of anandamide generated by lipoxygenases, which enables the biological study and detection of these metabolites.

PubMedSearch : van Zadelhoff_2016_Methods.Mol.Biol_1412_217
PubMedID: 27245907

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Citations formats

van Zadelhoff G, van der Stelt M (2016)
Oxygenation of Anandamide by Lipoxygenases
Methods Mol Biol 1412 :217

van Zadelhoff G, van der Stelt M (2016)
Methods Mol Biol 1412 :217