4.2 Article

Indispensable role of the oxytocin receptor for allogrooming toward socially distressed cage mates in female mice

Journal

JOURNAL OF NEUROENDOCRINOLOGY
Volume 33, Issue 6, Pages -

Publisher

WILEY
DOI: 10.1111/jne.12980

Keywords

affiliative behaviour; allogrooming; social defeat stress; oxytocin

Funding

  1. JSPS KAKENHI [17H04026, 17K19636, 20H03419, 17K08574, 20K07264, 17K08573, 20K07278, 16K08527, 19H05026, 19K06910]
  2. Takeda Science Foundation
  3. JMU Graduate Student Start-Up Grant for Young Investigators
  4. Japan Agency for Medical Research and Development [18dm0107076h0003]
  5. Grants-in-Aid for Scientific Research [17K08574, 17H04026, 17K19636, 16K08527, 17K08573, 19K06910, 19H05026, 20K07278, 20K07264, 20H03419] Funding Source: KAKEN

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The study found that mice exhibit allogrooming behavior towards distressed conspecifics in a social defeat model, and this behavior is correlated with the activation of oxytocin receptor-expressing neurons in areas such as the anterior olfactory nucleus, cingulate cortex, insular cortex, lateral septum, and medial amygdala, especially in female mice. This suggests that the oxytocin receptor plays a key role in facilitating allogrooming behavior towards socially distressed familiar conspecifics in female mice.
Social contact reduces stress responses in social animals. Mice have been shown to show allogrooming behaviour toward distressed conspecifics. However, the precise neuronal mechanisms underlying allogrooming behaviour remain unclear. In the present study, we examined whether mice show allogrooming behaviour towards distressed conspecifics in a social defeat model and we also determined whether oxytocin receptor-expressing neurons were activated during allogrooming by examining the expression of c-Fos protein, a marker of neurone activation. Mice showed allogrooming behaviour toward socially defeated conspecifics. After allogrooming behaviour, the percentages of oxytocin receptor-expressing neurones expressing c-Fos protein were significantly increased in the anterior olfactory nucleus, cingulate cortex, insular cortex, lateral septum and medial amygdala of female mice, suggesting that oxytocin receptor-expressing neurones in these areas were activated during allogrooming behaviour toward distressed conspecifics. The duration of allogrooming was correlated with the percentages of oxytocin receptor-expressing neurones expressing c-Fos protein in the anterior olfactory nucleus, insular cortex, lateral septum and medial amygdala. In oxytocin receptor-deficient mice, allogrooming behaviour toward socially defeated cage mates was markedly reduced in female mice but not in male mice, indicating the importance of the oxytocin receptor for allogrooming behaviour in female mice toward distressed conspecifics. The results suggest that the oxytocin receptor, possibly in the anterior olfactory nucleus, insular cortex, lateral septum and/or medial amygdala, facilitates allogrooming behaviour toward socially distressed familiar conspecifics in female mice.

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