5-HT(2C) Receptor Desensitization Moderates Anxiety in 5-HTT Deficient Mice: From Behavioral to Cellular Evidence

BACKGROUND: Desensitization and blockade of 5-HT(2C) receptors (5-HT(2C)R) have long been thought to be central in the therapeutic action of antidepressant drugs. However, besides behavioral pharmacology studies, there is little in vivo data documenting antidepressant-induced 5-HT(2C)R desensitizati...

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Detalles Bibliográficos
Autores principales: Martin, Cédric BP, Martin, Vincent S., Trigo, José M., Chevarin, Caroline, Maldonado, Rafael, Fink, Latham H., Cunningham, Kathryn A., Hamon, Michel, Lanfumey, Laurence, Mongeau, Raymond
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4360241/
https://www.ncbi.nlm.nih.gov/pubmed/25522398
http://dx.doi.org/10.1093/ijnp/pyu056
Descripción
Sumario:BACKGROUND: Desensitization and blockade of 5-HT(2C) receptors (5-HT(2C)R) have long been thought to be central in the therapeutic action of antidepressant drugs. However, besides behavioral pharmacology studies, there is little in vivo data documenting antidepressant-induced 5-HT(2C)R desensitization in specific brain areas. METHODS: Mice lacking the 5-HT reuptake carrier (5-HTT(-/-)) were used to model the consequences of chronic 5-HT reuptake inhibition with antidepressant drugs. The effect of this mutation on 5-HT(2C)R was evaluated at the behavioral (social interaction, novelty-suppressed feeding, and 5-HT(2C)R–induced hypolocomotion tests), the neurochemical, and the cellular (RT-qPCR, mRNA editing, and c-fos–induced expression) levels. RESULTS: Although 5-HTT(-/-) mice had an anxiogenic profile in the novelty-suppressed feeding test, they displayed less 5-HT(2C)R–mediated anxiety in response to the agonist m-chlorophenylpiperazine in the social interaction test. In addition, 5-HT2CR–mediated inhibition of a stress-induced increase in 5-HT turnover, measured in various brain areas, was markedly reduced in 5-HTT(-/-) mutants. These indices of tolerance to 5-HT(2C)R stimulation were associated neither with altered levels of 5-HT(2C)R protein and mRNA nor with changes in pre-mRNA editing in the frontal cortex. However, basal c-fos mRNA production in cells expressing 5-HT(2C)R was higher in 5-HTT(-/-) mutants, suggesting an altered basal activity of these cells following sustained 5-HT reuptake carrier inactivation. Furthermore, the increased c-fos mRNA expression in 5-HT(2C)R–like immune-positive cortical cells observed in wild-type mice treated acutely with the 5-HT(2C)R agonist RO-60,0175 was absent in 5-HTT(-/-) mutants. CONCLUSIONS: Such blunted responsiveness of the 5-HT(2C)R system, observed at the cell signaling level, probably contributes to the moderation of the anxiety phenotype in 5-HTT(-/-) mice.

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