First Author | Rosenberger TA | Year | 2003 |
Journal | J Lipid Res | Volume | 44 |
Issue | 1 | Pages | 109-17 |
PubMed ID | 12518029 | Mgi Jnum | J:81294 |
Mgi Id | MGI:2448799 | Doi | 10.1194/jlr.m200298-jlr200 |
Citation | Rosenberger TA, et al. (2003) Brain lipid metabolism in the cPLA(2) knockout mouse. J Lipid Res 44(1):109-17 |
abstractText | We examined brain phospholipid metabolism in mice in which the cytosolic phospholipase A(2) (cPLA(2,) Type IV, 85 kDa) was knocked out (cPLA(2)(-/-) mice). Compared with controls, these mice demonstrated altered brain concentrations of several phospholipids, reduced esterified linoleate, arachidonate, and docosahexaenoate in choline glycerophospholipid, and reduced esterified arachidonate in phosphatidylinositol. Unanesthetized cPLA(2)(-/-) mice had reduced rates of incorporation of unlabeled arachidonate from plasma and from the brain arachidonoyl-CoA pool into ethanolamine glycerophospholipid and choline glycerophospholipid, but elevated rates into phosphatidylinositol. These differences corresponded to altered turnover and metabolic loss of esterified brain arachidonate. These results suggests that cPLA(2) is necessary to maintain normal brain concentrations of phospholipids and of their esterified polyunsaturated fatty acids. Reduced esterified arachidonate and docosahexaenoate may account for the resistance of the cPLA(2)(-/-) mouse to middle cerebral artery occlusion, and should influence membrane fluidity, neuroinflammation, signal transduction, and other brain processes. |