Artículo

Endocannabinoids in TNF-α and ethanol actions

Besuhli, Valeria Icon; Fernández Solari, José Javier Icon; Prestifilippo, Juan Pablo Icon; Mohn, Claudia Ester Icon; de Laurentiis, Andrea Icon; Bornstein, Stefan R. ; Ehrhart Bornstein, Monika ; Elverdín, Juan Carlos ; McCann Samuel M. Icon

Otros responsables

Fecha

12/2007

Editorial

Karger

Revista

Neuroimmunomodulation

Título del libro

Nombre del evento

Fecha del evento

Institución organizadora

ISSN

1021-7401

eISSN

ISBN

Idioma

Inglés

Tipo del evento

Clasificación temática

Resumen

During marijuana and alcohol consumption as well as during inflammation the reproductive axis is inhibited, mainly through the inhibition of luteinizing hormone-releasing hormone release. In male rats, this inhibitory effect is mediated, at least in part, by the activation of hypothalamic cannabinoid type 1 receptors (CB1). During inflammation, this activation of the endocannabinoid system seems to be mediated by an increase in TNF-α production followed by anandamide augmentations, similarly the effect of intragastric administration of ethanol (3 g/kg) seems to be due to an increase in anandamide. On the other hand, a number of different actions mediated by the endocannabinoid system in various organs and tissues have been described. Both cannabinoid receptors, CB1 and CB2, are localized in the submandibular gland where they mediate the inhibitory effect of intrasubmandibular injections of the endocannabinoid anandamide (6 × 10–5M) on salivary secretion. Lipopolysaccharide (5 mg/kg/3 h) injected intraperitoneally and ethanol (3 g/kg/1 h) injected intragastrically inhibited the salivary secretion induced by the sialogogue metacholine; this inhibitory effect was blocked by CB1 and/or CB2 receptor antagonists. Similar to the hypothalamus, these effects seem to be mediated by increased anandamide. In summary, similar mechanisms mediate the inhibitory actions of endocannabinoids and cannabinoids in both hypothalamus and submandibular gland during drug consumption and inflammation.

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