The role of the dopamine D1 receptor in social cognition: studies using a novel genetic rat model­

Disease Models & Mechanisms

Gert Vriend¹  Jocelien D. A. Olivier²  Sharon Ooms³  Mareike Muller³  Ling Shan³  Alexander R. Cools³  Monique Balemans³  Jacqueline Langedijk³  Peter Karel³  Judith R. Homberg³  Ruben van Boxtel⁴  Edwin Cuppen⁴  Bart A. Ellenbroek⁵  Jiun Youn⁵  Arabella K. Ellenbroek⁵  Marie VandenBroeke⁵ 

[1] CMBI, Radboud University Nijmegen Medical Centre, Geert Grooteplein 26–28, Nijmegen 6525 GA, The Netherlands;Department of Neurobiology, Unit Behavioural Neuroscience, Groningen Institute for Evolutionary Life Sciences, University of Groningen, Groningen 9700 CC, The Netherlands;Donders Institute for Brain, Cognition and Behaviour, Department of Cognitive Neuroscience, Radboud University Medical Centre, Nijmegen 6525 EZ, The Netherlands;Hubrecht Institute, KNAW and University Medical Centre Utrecht, Utrecht 3584 CT, The Netherlands;Victoria University of Wellington, School of Psychology, PO Box 600, Wellington 6040, New Zealand;

关键词: Dopamine D1 receptor;    Mutant rat;    Social cognition;    Characterization;    Schizophrenia;   

DOI  :  10.1242/dmm.024752

来源: DOAJ

【 摘 要 】

Social cognition is an endophenotype that is impaired in schizophrenia and several other (comorbid) psychiatric disorders. One of the modulators of social cognition is dopamine, but its role is not clear. The effects of dopamine are mediated through dopamine receptors, including the dopamine D1 receptor (Drd1). Because current Drd1 receptor agonists are not Drd1 selective, pharmacological tools are not sufficient to delineate the role of the Drd1. Here, we describe a novel rat model with a genetic mutation in Drd1 in which we measured basic behavioural phenotypes and social cognition. The I116S mutation was predicted to render the receptor less stable. In line with this computational prediction, this Drd1 mutation led to a decreased transmembrane insertion of Drd1, whereas Drd1 expression, as measured by Drd1 mRNA levels, remained unaffected. Owing to decreased transmembrane Drd1 insertion, the mutant rats displayed normal basic motoric and neurological parameters, as well as locomotor activity and anxiety-like behaviour. However, measures of social cognition like social interaction, scent marking, pup ultrasonic vocalizations and sociability, were strongly reduced in the mutant rats. This profile of the Drd1 mutant rat offers the field of neuroscience a novel genetic rat model to study a series of psychiatric disorders including schizophrenia, autism, depression, bipolar disorder and drug addiction.

【 授权许可】

Unknown