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dc.contributor.authorTonon, M.C.fr_FR
dc.contributor.authorSmih-Rouet, F.fr_FR
dc.contributor.authorLamacz, M.fr_FR
dc.contributor.authorLouiset, E.fr_FR
dc.contributor.authorPelletier, G.fr_FR
dc.contributor.authorVaudry, H.fr_FR
dc.date.accessioned2013-02-15T12:00:00Z
dc.date.available2013-02-15T12:00:00Z
dc.date.issued1994fr_FR
dc.identifier.citationTonon, M.C. ; Smih-Rouet, F. ; Lamacz, M. ; Louiset, E. ; Pelletier, G. ; Vaudry, H., Les endozépines, ligands endogènes des récepteurs des benzodiazépines, Med Sci (Paris), 1994, Vol. 10, N° 4; p.433-443fr_FR
dc.identifier.issn1958-5381fr_FR
dc.identifier.urihttp://hdl.handle.net/10608/2633
dc.description.abstractBecause of their anxiolytic, sedative and myo-relaxant properties, benzodiazepines are among the most commonly used drugs in clinical practice. The actions of benzodiazepines are mediated by two classes of receptors i.e. receptors associated with the GABA(A-) chloride channel complex also named central-type benzodiazepine receptors and receptors localized in the mitochondrial membrane called peripheral-type benzodiazepine receptors. The existence of binding sites for benzodiazepines has suggested the existence of endogenous ligands capable of interacting with either central or peripheral type benzodiazepine receptors. This hypothesis has led to the dicovery of a family of regulatory peptides named endozepines which displace diazepam from its neuronal binding sites and exert a wide range of biological activities.fr
dc.language.isofrfr_FR
dc.publisherJohn Libbey Eurotext, Montrougefr_FR
dc.rightsArticle en libre accèsfr
dc.rightsMédecine/Sciences - Inserm - SRMSfr
dc.sourceM/S. Médecine sciences [revue papier, ISSN : 0767-0974], 1994, Vol. 10, N° 4; p.433-443fr_FR
dc.titleLes endozépines, ligands endogènes des récepteurs des benzodiazépinesfr
dc.typeArticlefr_FR
dc.identifier.doi10.4267/10608/2633


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