Orally administered oxytocin alters brain activation and behaviors of pre-weaning mice

Horm Behav. 2020 Feb:118:104613. doi: 10.1016/j.yhbeh.2019.104613. Epub 2019 Nov 14.

Abstract

Oxytocin (OXT) regulates adult social behavior and has been implicated in its development. Because mammalian milk contains OXT and we have recently identified OXT receptors (OXTR) in the face and oronasal cavity of pre-weaning mice, we hypothesize that orally applied OXT may impact brain activity and acute behavior in developing mice. Oral OXT may have effects in the absence of sensory stimulation or perhaps by modulating sensory input, such as whisker stimulation. The present study investigates the acute c-Fos response in the paraventricular nucleus of the hypothalamus (PVN) and along whisker sensory processing brain regions (trigeminothalamocortical circuit) to orally applied OXT, compared to saline, with and without whisker stimulation in postnatal day (P) 14 and P21 male and female mice. Acute behavioral responses were also quantified after oral OXT with whisker stimulation in a non-social context. Oral OXT with and without whisker stimulation increased c-Fos activity in the PVN of males and decreased c-Fos in the ventroposterior medial thalamus in both males and females compared to saline. Additionally, oral OXT with whisker stimulation decreased c-Fos activity across whisker sensory processing brain regions in males and females and decreased c-Fos activity in the trigeminal motor nucleus of females. Lastly, oral OXT with whisker stimulation increased males' locomotor behavior and decreased females' oromotor behavior compared to saline-treated controls. These data indicate that orally applied OXT has acute brain and behavioral effects on developing mice. OXT-modulated sensory signals may bias brain and behavior development toward the social world.

Keywords: Oromotor behavior; Oronasal cavity; Oxytocin; Oxytocin receptor; Pre-weaning; Trigeminal ganglion; Whisker stimulation; c-Fos; oxtr-egfp.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Animals
  • Animals, Suckling
  • Behavior, Animal / drug effects*
  • Brain / drug effects*
  • Brain / growth & development
  • Brain / metabolism
  • Female
  • Male
  • Mice
  • Mice, Transgenic
  • Oxytocin / administration & dosage*
  • Paraventricular Hypothalamic Nucleus / drug effects
  • Paraventricular Hypothalamic Nucleus / growth & development
  • Paraventricular Hypothalamic Nucleus / metabolism
  • Proto-Oncogene Proteins c-fos / metabolism
  • Receptors, Oxytocin / metabolism
  • Weaning

Substances

  • Proto-Oncogene Proteins c-fos
  • Receptors, Oxytocin
  • Oxytocin