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Oxytocin, Epigenetic Aging, and the Social Regulation of Health: A Lifecourse Perspective on the Maejima et al. Findings

  • Kerstin Uvnäs-Moberg
  • , Mechthild M. Gross
  • , Jean Calleja-Agius
  • , Jonathan D. Turner*
  • *Corresponding author for this work

Research output: Contribution to journalComment/debate

Abstract

The elegant work by Maejima et al. recently published in Aging Cell reveals a previously unrecognized mechanism linking age-related oxytocin (OXT) decline to epigenetic remodeling, mitochondrial dysfunction, and systemic inflammation (Maejima et al. 2025). Beyond documenting this relationship, the authors demonstrate its remarkable reversibility through nasal OXT administration. These findings provide the first molecular evidence supporting what has long been proposed: that the OXT system functions as a fundamental long-term regulator of health across the entire lifespan, from early development through aging (Moberg 2024, 2003; Uvnas-Moberg 1998). The current work now gives a tantalizing glimpse into the epigenetic mechanism behind this life course regulation.

Original languageEnglish
Article numbere70363
Number of pages5
JournalAging Cell
Volume25
Issue number2
DOIs
Publication statusPublished - Feb 2026

Keywords

  • DNA methylation
  • HPA axis
  • TET enzymes
  • early life programming
  • epigenetic aging
  • lifecourse epidemiology
  • noradrenergic/sympathetic nervous system
  • oxytocin
  • personalized epigenetic medicine
  • social connection
  • Aging/genetics
  • Humans
  • Epigenesis, Genetic
  • Animals
  • Oxytocin/metabolism

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