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.

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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
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article

Tph2 deficiency leads to alterations in social adjustment and socio-affective communication in neonatal rats: No rescue effect of communal nesting

Sharon M. Kolk, Michael Bäder, Tianhua Wang, Jinye Dai et al.
Progress in Neuro-Psychopharmacology and Biological Psychiatry
Neuroendocrine regulation and behavior
article

Tph2 deficiency leads to alterations in social adjustment and socio-affective communication in neonatal rats: No rescue effect of communal nesting

Sharon M. Kolk, Michael Bäder, Tianhua Wang, Jinye Dai, Markus Wöhr, Natalia V. Alenina, Rogério C. R. Castro, Judith Regina Homberg, Marta C. F. Samina, Aaron L Gnade
article en

Abstract

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.

Progress in Neuro-Psychopharmacology and Biological PsychiatryVol. 141
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)
European Commission, Deutsche Forschungsgemeinschaft, Fonds Wetenschappelijk Onderzoek, Vlaamse regering
Openalex Percentile: Top 76%
Neuroendocrine regulation and behavior
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