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Updated: Jun 23, 2026

Assessment of Social Interaction Behaviors
Published on: February 25, 2011
Characterization of social behavior in young and middle-aged ChAT-IRES-Cre mouse
Cyril Lhopitallier1, Charlotte Perrault2, Frédéric Chauveau3
1Neurobiology of Decision Making, Paris-Saclay Institute of Neuroscience (NeuroPSI), CNRS, University Paris-Saclay, Gif-sur-Yvett, France.
ChAT-IRES-Cre mice show mild social deficits and anxiety, with cholinergic system alterations. Aging impacts social dominance, but not significantly amplified by these cholinergic changes.
Area of Science:
- Neuroscience
- Behavioral Science
Background:
- The cholinergic system modulates brain functions, including social behavior.
- Previous studies on cholinergic nicotinic receptors used mutant mice with confounding alterations.
- ChAT-IRES-Cre mice offer a specific tool to study cholinergic circuits, but their behavioral phenotype, especially social behavior and aging effects, is undercharacterized.
Purpose of the Study:
- To characterize the social behavior phenotype of ChAT-IRES-Cre mice at young and middle ages.
- To investigate the impact of aging on the cholinergic system and social behavior in these mice.
Main Methods:
- Behavioral phenotyping of ChAT-IRES-Cre mice at 2-3 months and 10-11 months.
- Assessment of gene expression for cholinergic markers (ChAT, CHT, VAChT) in the striatum.
- Evaluation of social behavior, dominance, and anxiety-like behaviors.
Main Results:
- ChAT-IRES-Cre mice exhibited decreased ChAT, CHT, and VAChT gene expression in the striatum.
- These molecular changes correlated with mild social disturbances and a tendency towards anxiety.
- Aging led to decreased social dominance, an effect not exacerbated by the observed cholinergic alterations.
Conclusions:
- ChAT-IRES-Cre mice present a valuable model for studying the cholinergic system's role in social behavior.
- The model is suitable for investigating cholinergic circuit modulation using techniques like optogenetics or DREADD.
- Aging affects social dominance independently of the specific cholinergic alterations identified in this study.
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