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.
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Acknowledgements
We thank Caroline Chevarin for her practical help in GTP-γ-S binding studies, Elke Herrmann for animal husbandry, and Cornelius Pawlak and Josef Frank for statistical support. This work has been supported by the following grants: EU HEALTH-F2-2007-201714 DEVANX (to DB and LL), DFG SFB 636 (to DB and PG), Bernstein Center for Computational Neuroscience Heidelberg/Mannheim 01GQ1003B to DB (TPA3) and RS (TPD1).
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Berger, S., Weber, T., Perreau-Lenz, S. et al. A Functional Tph2 C1473G Polymorphism Causes an Anxiety Phenotype via Compensatory Changes in the Serotonergic System. Neuropsychopharmacol 37, 1986–1998 (2012). https://doi.org/10.1038/npp.2012.46
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DOI: https://doi.org/10.1038/npp.2012.46
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