AI Article Synopsis

  • Oxytocin plays a key role in childbirth by stimulating uterine contractions, enabling lactation, and promoting maternal bonding behaviors, with mice lacking oxytocin or its receptor showing failure to nurture.
  • This maternal behavior can be restored in some cases with oxytocin replacement, indicating that the hormone can enter the brain and influence behavior despite general restrictions on polypeptides crossing the blood-brain barrier.
  • Research highlights that receptor for advanced glycation end-products (RAGE) on brain capillary cells is crucial for transporting oxytocin into the brain, and without RAGE, male mice exhibit issues with maternal bonding and increased hyperactivity, underscoring RAGE’s importance in oxytocin's parenting and social bonding effects.

Article Abstract

Oxytocin sets the stage for childbirth by initiating uterine contractions, lactation and maternal bonding behaviours. Mice lacking secreted oxcytocin ( , ) or its receptor ( ) fail to nurture. Normal maternal behaviour is restored by peripheral oxcytocin replacement in and , but not mice, implying that circulating oxcytocin crosses the blood-brain barrier. Exogenous oxcytocin also has behavioural effects in humans. However, circulating polypeptides are typically excluded from the brain. We show that oxcytocin is transported into the brain by receptor for advanced glycation end-products (RAGE) on brain capillary endothelial cells. The increases in oxcytocin in the brain which follow exogenous administration are lost in male mice lacking RAGE, and behaviours characteristic to abnormalities in oxcytocin signalling are recapitulated in mice, including deficits in maternal bonding and hyperactivity. Our findings show that RAGE-mediated transport is critical to the behavioural actions of oxcytocin associated with parenting and social bonding.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389896PMC
http://dx.doi.org/10.1038/s42003-019-0325-6DOI Listing

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