Properties of the omega-hydroxylation system of docosahexaenoic or arachidonic acid in brain or liver homogenate of rat

The homogenate of a brain or liver obtained from a 1-55-day-old rat was incubated with NADPH and docosahexaenoic or arachidonic acid as the substrate. omega-Hydroxydocosahexaenoic or omega-hydroxyeicosatetraenoic acid from an incubation mixture of the homogenate was detected on a selected-ion monitoring chromatogram of reversed phase-HPLC-thermospray-mass spectrometry, omega-Hydroxylation activity in the brain homogenate considerably increased with growth up to 55 days. Activity in the liver homogenate decreased much with growth up to 55 days. omega-Hydroxylation activity in homogenates of rat brain gray matter, white matter, medula oblongata and cerebellum was much the same. omega-Hydroxylation activity of docosahexaenoic acid in rat brain homogenate was maximal at pH 7.5-8.0 in 50 mM Tris-HCl buffer and was inhibited by CO gas, metyrapone, ADP-Fe3+, heat treatment at 100 degrees C for 5 min and without NADPH. Based on these results, it is suggested that omega-hydroxylation activity is associated with cytochrome P-450 without NADPH-ADP-Fe3+-dependent lipid peroxidation, and the omega-hydroxylation system may be a metabolic pathway of the fatty acids in adult rat brain or neonatal rat liver. Since omega-hydroxyeicosatetraenoic acid produces relaxation of artery, it is suggested that bloodflow changes in rat brain or liver with growth are caused by omega-hydroxylation activity changes in these organs with growth.