PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
April 8, 2026European Journal of Inorganic Chemistry1 citations

Metal Modulation of Oxytocin Structure, Function, and Receptor Interactions

View Full Paper
JPJennifer ParkSahlgrenska University HospitalMHMarie C. HeffernUniversity of California, Davis

Key Points

  • The central aim is to understand how metal ions influence the structure and function of oxytocin.
  • Synthesis of existing literature on metal-oxytocin interactions
  • Analysis of how different metals modulate oxytocin's structure and receptor binding
  • Highlighting potential applications in biosensors and therapies
  • Divalent metal ions such as Cu2+, Zn2+, Mg2+, and Ca2+ significantly influence oxytocin's conformational changes.
  • Different metal ions interact with oxytocin through distinct coordination modes.
  • Advancements in understanding these interactions may lead to new therapeutic approaches for disorders related to oxytocin signaling.

Abstract

Oxytocin is a nine‐amino acid peptide hormone essential for reproduction, social bonding, and neuromodulation. Accumulating evidence demonstrates that divalent metal ions play critical roles in modulating oxytocin structure, receptor binding, and biological activity. Despite nearly five decades of research, a comprehensive molecular‐level understanding of metal–oxytocin interactions and their functional consequences remains incomplete. This review synthesizes current knowledge of how Cu 2+ , Zn 2+ , Mg 2+ , Ca 2+ , and other metals influence oxytocin's conformational landscape and receptor interactions through distinct coordination modes. We highlight emerging applications in biosensor development and therapeutic formulation that leverage these metal‐binding properties. Advancing our understanding of metal‐mediated modulation of oxytocin function will enhance our knowledge of peptide hormone regulation and provide new avenues for therapeutic intervention in conditions involving dysregulated oxytocin signaling.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Park et al. (2026) studied this question.

synapsesocial.com/papers/69d5f00974eaea4b11a79974https://doi.org/10.1002/ejic.202500462
Ask AI
Helpful
Bookmark
Share
View Full Paper