Involvement of the agmatinergic system in the depressive-like phenotype of the Crtc1 knockout mouse model of depression.
journal contributionposted on 25.04.2018, 14:45 by E. M. Meylan, L. Breuillaud, T. Seredenina, P. J. Magistretti, O. Halfon, Ruth Luthi-Carter, J-R. Cardinaux
Recent studies implicate the arginine-decarboxylation product agmatine in mood regulation. Agmatine has antidepressant properties in rodent models of depression, and agmatinase (Agmat), the agmatine-degrading enzyme, is upregulated in the brains of mood disorder patients. We have previously shown that mice lacking CREB-regulated transcription coactivator 1 (CRTC1) associate behavioral and molecular depressive-like endophenotypes, as well as blunted responses to classical antidepressants. Here, the molecular basis of the behavioral phenotype of Crtc1(-/-) mice was further examined using microarray gene expression profiling that revealed an upregulation of Agmat in the cortex of Crtc1(-/-) mice. Quantitative polymerase chain reaction and western blot analyses confirmed Agmat upregulation in the Crtc1(-/-) prefrontal cortex (PFC) and hippocampus, which were further demonstrated by confocal immunofluorescence microscopy to comprise an increased number of Agmat-expressing cells, notably parvalbumin- and somatostatin-positive interneurons. Acute agmatine and ketamine treatments comparably improved the depressive-like behavior of male and female Crtc1(-/-) mice in the forced swim test, suggesting that exogenous agmatine has a rapid antidepressant effect through the compensation of agmatine deficit because of upregulated Agmat. Agmatine rapidly increased brain-derived neurotrophic factor (BDNF) levels only in the PFC of wild-type (WT) females, and decreased eukaryotic elongation factor 2 (eEF2) phosphorylation in the PFC of male and female WT mice, indicating that agmatine might be a fast-acting antidepressant with N-methyl-D-aspartate (NMDA) receptor antagonist properties. Collectively, these findings implicate Agmat in the depressive-like phenotype of Crtc1(-/-) mice, refine current understanding of the agmatinergic system in the brain and highlight its putative role in major depression.
CitationTranslational Psychiatry, 2016, 6, e852
Author affiliation/Organisation/COLLEGE OF LIFE SCIENCES/Biological Sciences/Neuroscience, Psychology and Behaviour
VersionVoR (Version of Record)
Published inTranslational Psychiatry
PublisherNature Publishing Group
AgmatineAnimalsBehavior, AnimalBlotting, WesternBrainBrain-Derived Neurotrophic FactorCerebral CortexDepressive DisorderEukaryotic Initiation Factor-2Excitatory Amino Acid AntagonistsFemaleGene Expression ProfilingHippocampusInterneuronsKetamineMaleMiceMice, KnockoutMicroarray AnalysisPhenotypePhosphorylationPolymerase Chain ReactionPrefrontal CortexTranscription FactorsUreohydrolases