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1.
Glia ; 63(1): 163-76, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25130621

ABSTRACT

The endocannabinoids 2-araquidonoylglycerol (2-AG) and anandamide (AEA) are bioactive lipids crucially involved in the regulation of brain function in basal and pathological conditions. Blockade of endocannabinoid metabolism has emerged as a promising therapeutic strategy for inflammatory diseases of the central nervous system, including myelin disorders such as multiple sclerosis. Nevertheless, the biological actions of endocannabinoid degradation inhibitors in oligodendrocytes and white matter tracts are still ill defined. Here we show that the selective monoacylglycerol lipase (MAGL) inhibitor JZL184 suppressed cell death by mild activation of AMPA receptors in oligodendrocytes in vitro, an effect that was mimicked by MAGL substrate 2-AG and by the second major endocannabinoid AEA, in a concentration-dependent manner, whereas inhibition of the AEA metabolizing enzyme fatty acid amide hydrolase with URB597 was devoid of effect. Pharmacological experiments suggested that oligodendrocyte protection from excitotoxicity resulting from MAGL blockade involved the activation of cannabinoid CB1 receptors and the reduction of AMPA-induced cytosolic calcium overload, mitochondrial membrane depolarization, and production of reactive oxygen species. Administration of JZL184 under a therapeutic regimen decreased clinical severity, prevented demyelination, and reduced inflammation in chronic experimental autoimmune encephalomyelitis. Furthermore, MAGL inactivation robustly preserved myelin integrity and suppressed microglial activation in the cuprizone-induced model of T-cell-independent demyelination. These findings suggest that MAGL blockade may be a useful strategy for the treatment of immune-dependent and -independent damage to the white matter.


Subject(s)
Benzodioxoles/pharmacology , Demyelinating Diseases/prevention & control , Monoacylglycerol Lipases/antagonists & inhibitors , Oligodendroglia/metabolism , Piperidines/pharmacology , Receptor, Cannabinoid, CB1/metabolism , Amidohydrolases/metabolism , Animals , Benzamides , Cannabinoid Receptor Modulators/metabolism , Carbamates , Multiple Sclerosis/immunology , Multiple Sclerosis/metabolism , Rats, Sprague-Dawley
2.
La Paz; 1980. 83 p.
Thesis in Spanish | LIBOCS, LIBOSP | ID: biblio-1309678

ABSTRACT

Los metodos matriciales estan basados en el concepto de sustituir la estructura continua por un modelo equivalente, compuesto de lementos estructutarles discretos. Las estructuras reticulares de ingenieria pueden se visualizadas como el ensamble de elementos estructurales interconectadas en un numero discreto de puntos nodales. El presente trabajo utiliza el metodo de la rigidez orientado al problema especifico del calculo de parrillas.

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