Fatty acid profiles of mouse brain tissues were analyzed using gas chromatography as described previously79 (link). Briefly, tissues were homogenized by grinding in liquid nitrogen, and subjected to fatty acid methylation by mixing with 1 ml of hexane and 1 ml of 14% BF3/MeOH reagent at 100 °C for 1 h. Fatty acid methyl esters were extracted in the hexane phase, and then the fatty acid profiles were analyzed using a fully automated HP6890 gas chromatography system equipped with a flame-ionization detector (Agilent Technologies, Palo Alto, CA, USA). The fatty acid peaks were identified by comparing relative retention times with commercial mixed standards (Nu-Chek Prep, Elysian, MN, USA), and the area and its percentage for each peak were analyzed using GC Chemstation software. Data were analyzed using a two-tailed Student’s t-test.
Free full text: Click here