RESUMEN
In a rat model of acute neuroinflammation, produced by a 6-day intracerebral ventricular infusion of bacterial lipopolysaccharide (LPS), we measured brain activities and protein levels of three phospholipases A2 (PLA2) and of cyclo-oxygenase-1 and -2, and quantified other aspects of brain phospholipid and fatty acid metabolism. The 6-day intracerebral ventricular infusion increased lectin-reactive microglia in the cerebral ventricles, pia mater, and the glial membrane of the cortex and resulted in morphological changes of glial fibrillary acidic protein (GFAP)-positive astrocytes in the cortical mantel and areas surrounding the cerebral ventricles. LPS infusion increased brain cytosolic and secretory PLA2 activities by 71% and 47%, respectively, as well as the brain concentrations of non-esterified linoleic and arachidonic acids, and of prostaglandins E2 and D2. LPS infusion also increased rates of incorporation and turnover of arachidonic acid in phosphatidylethanolamine, plasmenylethanolamine, phosphatidylcholine, and plasmenylcholine by 1.5- to 2.8-fold, without changing these rates in phosphatidylserine or phosphatidylinositol. These observations suggest that selective alterations in brain arachidonic acid metabolism involving cytosolic and secretory PLA2 contribute to early pathology in neuroinflammation.
Asunto(s)
Ácido Araquidónico/metabolismo , Encéfalo/metabolismo , Encefalitis/metabolismo , Lipopolisacáridos , Animales , Encéfalo/patología , Química Encefálica , Ciclooxigenasa 1 , Ciclooxigenasa 2 , Modelos Animales de Enfermedad , Eicosanoides/metabolismo , Encefalitis/inducido químicamente , Encefalitis/patología , Inmunohistoquímica , Infusiones Parenterales , Inyecciones Intraventriculares , Isoenzimas/metabolismo , Metabolismo de los Lípidos , Lipopolisacáridos/administración & dosificación , Proteínas de la Membrana , Microglía/efectos de los fármacos , Microglía/metabolismo , Microglía/patología , Fosfolipasas A/metabolismo , Fosfolipasas A2 , Fosfolípidos/metabolismo , Prostaglandina-Endoperóxido Sintasas/metabolismo , Ratas , Factores de TiempoRESUMEN
The peroxisomal proliferator-activated receptor beta (delta) (PPARbeta) is a nuclear hormone receptor that is ubiquitously expressed and that regulates the transcription of genes involved in lipid metabolism. A homozygous PPARbeta-null mouse has been developed in which the ligand-binding domain of the PPARbeta receptor is disrupted. Analysis of brains from these animals shows that female null mice have 24 and 17% increases in plasmenylethanolamine and phosphatidylserine and a 9% decrease in the level of phosphatidylinositol when compared to controls. The phospholipid changes found in female null mice were associated with increased levels of esterified 18:1n-9, 20:1n-9, 20:4n-6, and 22:5n-3 FA in plasmenylethanolamine, 20:1n-9 in phosphaticlylinositol, and 18:0, 18:1n-9, 18:3n-6, 20:1 n-9, and 20:4n-6 in phosphatidylserine. Increased levels of esterified 18:1n-9, 18:2n-6, 18:3n-6, and 20:1n-9 were also found in the phosphatidylethanolamine fraction despite its cellular content remaining unchanged. Brain phospholipid content in male PPARbeta-null mice did not differ from controls, but increased levels of 20:1n-9 in the phosphatidylinositol and 18:1n-9 in the phosphatidylserine fractions were observed. No changes were found in the content of brain cholesterol, TAG, and FFA in either female or male PPARbeta-null mice. These data suggest that PPARbeta is involved in maintaining FA and phospholipid levels in adult female mouse brain and provide strong evidence that suggests a role for PPARbeta in brain peroxisomal acyl-CoA utilization.