4.3 Article

Impairment of interstrain social recognition during territorial aggressive behavior in oxytocin receptor-null mice

Journal

NEUROSCIENCE RESEARCH
Volume 90, Issue -, Pages 90-94

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.neures.2014.05.003

Keywords

Oxytocin; Oxytocin receptor; Interstrain recognition; Aggressive behavior

Categories

Funding

  1. JSPS KAKENHI [23248049, 25660252, 25118007, 26292167]
  2. Azabu University
  3. Japan Society for the Promotion of Science for Young Scientists
  4. Grants-in-Aid for Scientific Research [25660252, 26450433, 26292167] Funding Source: KAKEN

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In humans, oxytocin has been shown to be involved in in-group cooperative behaviors and out-group aggression. Studies have also demonstrated that oxytocin plays a pivotal role in social recognition. However, no empirical research has investigated the effect of oxytocin on in-group and out-group aggressiveness. We employed a resident-intruder paradigm to assess the ability of resident male mice to discriminate intruder male strain differences. We found that resident male mice exhibited higher frequencies of attack bites against intruders of different strains than against intruders of their own strain. Subsequently, we examined whether the interstrain recognition was regulated by the oxytocin system using oxytocin receptor (OTR)-null mice. OTR wild-type or heterozygous residents displayed higher aggression toward intruders of a strain different from their own (C57BL/6J). On the other hand, OTR-null residents exhibited greater aggression toward intruders of the same strain compared to OTR wild-type or heterozygous residents, and aggression levels were not different compared to those exhibited toward other strains. Our findings demonstrated that the oxytocin system contributes to interstrain social recognition in territorial aggression in male mice, implying that one function of oxytocin is to promote an in-group tend-and-defend response, such as in-group favoritism, which could be evolutionarily conserved in mammals. (C) 2014 Elsevier Ireland Ltd and the Japan Neuroscience Society. All rights reserved.

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