A mild impairment in reversal learning in a bowl‐digging substrate deterministic task but not other cognitive tests in the Dlg2+/− rat model of genetic risk for psychiatric disorder

Simonas Griesius, Sophie Waldron, Katie A Kamenish, Nick Cherbanich, Lawrence S Wilkinson, Kerrie L. Thomas, Jeremy Hall, Jack R Mellor, Dominic M Dwyer, Emma S J Robinson*

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

2 Citations (Scopus)

Abstract

Variations in the Dlg2 gene have been linked to increased risk for psychiatric disorders, including schizophrenia, autism spectrum disorders, intellectual disability, bipolar disorder, attention deficit hyperactivity disorder, and pubertal disorders. Recent studies have reported disrupted brain circuit function and behaviour in models of Dlg2 knockout and haploinsufficiency. Specifically, deficits in hippocampal synaptic plasticity were found in heterozygous Dlg2+/− rats suggesting impacts on hippocampal dependent learning and cognitive flexibility. Here, we tested these predicted effects with a behavioural characterisation of the heterozygous Dlg2+/− rat model. Dlg2+/− rats exhibited a specific, mild impairment in reversal learning in a substrate deterministic bowl-digging reversal learning task. The performance of Dlg2+/− rats in other bowl digging task, visual discrimination and reversal, novel object preference, novel location preference, spontaneous alternation, modified progressive ratio, and novelty-suppressed feeding test were not impaired. These findings suggest that despite altered brain circuit function, behaviour across different domains is relatively intact in Dlg2+/− rats, with the deficits being specific to only one test of cognitive flexibility. The specific behavioural phenotype seen in this Dlg2+/− model may capture features of the clinical presentation associated with variation in the Dlg2 gene.
Original languageEnglish
Article numbere12865
JournalGenes, Brain and Behavior
Volume22
Issue number6
Early online date10 Sept 2023
DOIs
Publication statusE-pub ahead of print - 10 Sept 2023

Bibliographical note

Funding Information:
Funding was provided by grants from Medical Research Council (UK) (GW4 BIOMED PhD studentship to SG), Biotechnology and Biological Science Research Council (UK) (JRM) and Wellcome Trust (UK) (JRM, PhD studentship to SW).

Funding Information:
The authors gratefully acknowledge funding from Medical Research Council (UK) (GW4 BIOMED PhD studentship to SG), Biotechnology and Biological Science Research Council (UK) (JRM), Wellcome Trust (UK) (JRM, PhD studentship to SW). The Dlg2+/− rats were generated as part of a Wellcome Trust Strategic Award ‘DEFINE’ (JH and LSW) and the Wellcome Trust Strategic Award and the Neuroscience and Mental Health Research Institute, Cardiff University, UK provided core support.

Publisher Copyright:
© 2023 The Authors. Genes, Brain and Behavior published by International Behavioural and Neural Genetics Society and John Wiley & Sons Ltd.

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