Tph2 deficiency leads to alterations in social adjustment and socio-affective communication in neonatal rats: No rescue effect of communal nesting
Deficiency of tryptophan hydroxylase 2 (TPH2), the rate-limiting enzyme for serotonin (5-hydroxytryptamine, 5-HT) synthesis in the brain, was repeatedly reported to cause impairments in socio-affective communication and maternal affiliation across species, including mice, rats, and monkeys. We recently applied a rescue protocol in the Tph2 knockout rat model and demonstrated that communal nesting ameliorates maternal affiliation impairments. Interestingly, however, this rescue strategy did not lead to improvements in socio-affective communication and was associated with an aggravated growth retardation phenotype in Tph2-deficient offspring. In the present study, we aimed to gain deeper insight into the interplay between socio-affective communication, nesting condition, and test context. To this aim, we studied Tph2<sup>-/-</sup> knockout, Tph2<sup>+/-</sup> heterozygous, and Tph2<sup>+/+</sup> wildtype rat pups of both sexes, randomly assigned to standard versus communal nesting. We performed detailed spectrographic analyses and compared the emission of isolation-induced ultrasonic vocalizations under social test conditions, i.e., the maternal preference test and the homing test, to non-social test conditions, i.e., the isolation box test. Our results show that Tph2 deficiency causes prominent alterations in isolation-induced ultrasonic calling linked to reduced maternal responsiveness, including changes in acoustic features, e.g., increased call duration but reduced frequency modulation. Remarkably, irrespective of communal nesting, Tph2<sup>-/-</sup> pups typically displayed either no evidence for social adjustment or even changes opposite to Tph2<sup>+/+</sup> littermates, suggesting a reduction and/or delay in the capability and/or motivation to appropriately adjust to changes in the social environment. Such alterations in social adjustment likely contribute to growth retardation through reduced quality of mother-pup interactions.
Authors
- Sharon M. Kolk (ORCID: https://orcid.org/0000-0003-2116-5456)
- Michael Bäder (ORCID: https://orcid.org/0000-0003-4780-4164)
- Tianhua Wang (ORCID: https://orcid.org/0009-0008-3859-9406)
- Jinye Dai (ORCID: https://orcid.org/0000-0002-8497-3154)
- Markus Wöhr (ORCID: https://orcid.org/0000-0001-6986-5684)
- Natalia V. Alenina (ORCID: https://orcid.org/0000-0002-6071-5433)
- Rogério C. R. Castro (ORCID: https://orcid.org/0000-0003-0388-3040)
- Judith Regina Homberg (ORCID: https://orcid.org/0000-0002-7621-1010)
- Marta C. F. Samina (ORCID: https://orcid.org/0009-0002-9766-1333)
- Aaron L Gnade
Institutions
- Allen Institute for Brain Science (US)
- Radboud University Nijmegen (NL)
- Philipps University of Marburg (DE)
- Max Delbrück Center (DE)
- Radboud University Medical Center (NL)
- VIB-KU Leuven Center for Brain & Disease Research (BE)
- University of Lübeck (DE)
Publication Details
- Journal
- Progress in Neuro-Psychopharmacology and Biological Psychiatry
- Published
- 2025-08-01
- DOI
- https://doi.org/10.1016/j.pnpbp.2025.111469
- Primary Topic
- Neuroendocrine regulation and behavior
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- European Commission
- Deutsche Forschungsgemeinschaft
- Fonds Wetenschappelijk Onderzoek
- Vlaamse regering