A functional Tph2 C1473G polymorphism causes an anxiety phenotype via compensatory changes in the serotonergic system

• Verfasst von: Berger, Stefan [VerfasserIn]
• Verfasst von: Maser-Gluth, Christiane [VerfasserIn]
• Verfasst von: Gass, Peter [VerfasserIn]
• Verfasst von: Spanagel, Rainer [VerfasserIn]
• Verfasst von: Bartsch, Dusan [VerfasserIn]
• Titel: A functional Tph2 C1473G polymorphism causes an anxiety phenotype via compensatory changes in the serotonergic system
• Verf.angabe: Stefan M. Berger, Tillmann Weber, Stephanie Perreau-Lenz, Miriam A. Vogt, Sarah E. Gartside, Christiane Maser-Gluth, Laurence Lanfumey, Peter Gass, Rainer Spanagel and Dusan Bartsch
• Jahr: 2012
• Umfang: 13 S.
• Fussnoten: Published 11 April 2012 ; Gesehen am 28.06.2018
• Titel Quelle: Enthalten in: Neuropsychopharmacology
• Ort Quelle: London : Springer Nature, 1993
• Jahr Quelle: 2012
• Band/Heft Quelle: 37(2012), 9, Seite 1986-1998
• ISSN Quelle: 1740-634X
• DOI: doi:10.1038/npp.2012.46
• Datenträger: Online-Ressource
• Sprache: eng
• K10plus-PPN: 1577017838

Abstract

The association of single-nucleotide polymorphisms (SNPs) in the human tryptophan hydroxylase 2 (TPH2) gene with anxiety traits and depression has been inconclusive. Observed inconsistencies might result from the fact that TPH2 polymorphisms have been studied in a genetically heterogeneous human population. A defined genetic background, control over environmental factors, and the ability to analyze the molecular and neurochemical consequences of introduced genetic alterations constitute major advantages of investigating SNPs in inbred laboratory mouse strains. To investigate the behavioral and neurochemical consequences of a functional C1473G SNP in the mouse Tph2 gene, we generated congenic C57BL/6N mice homozygous for the Tph2 1473G allele. The Arg447 substitution in the TPH2 enzyme resulted in a significant reduction of the brain serotonin (5-HT) in vivo synthesis rate. Despite decreased 5-HT synthesis, we could detect neither a reduction of brain region-specific 5-HT concentrations nor changes in baseline and stress-induced 5-HT release using a microdialysis approach. However, using a [35S]GTP-γ-S binding assay and 5-HT1A receptor autoradiography, a functional desensitization of 5-HT1A autoreceptors could be identified. Furthermore, behavioral analysis revealed a distinct anxiety phenotype in homozygous Tph2 1473G mice, which could be reversed with chronic escitalopram treatment. Alterations in depressive-like behavior could not be detected under baseline conditions or after chronic mild stress. These findings provide evidence for an involvement of functional Tph2 polymorphisms in anxiety-related behaviors, which are likely not caused directly by alterations in 5-HT content or release but are rather due to compensatory changes during development involving functional desensitization of 5-HT1A autoreceptors.