Subtle modifications to oxytocin produce ligands that retain potency and improved selectivity across species.


Muttenthaler, Markus, Andersson, Åsa, Vetter, Irina, Menon, Rohit, Busnelli, Marta, Ragnarsson, Lotten, Bergmayr, Christian, Arrowsmith, Sarah, Deuis, Jennifer R, Chiu, Han Sheng et al (show 8 more authors) (2017) Subtle modifications to oxytocin produce ligands that retain potency and improved selectivity across species. Science signaling, 10 (508). eaan3398-.

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Abstract

Oxytocin and vasopressin mediate various physiological functions that are important for osmoregulation, reproduction, cardiovascular function, social behavior, memory, and learning through four G protein-coupled receptors that are also implicated in high-profile disorders. Targeting these receptors is challenging because of the difficulty in obtaining ligands that retain selectivity across rodents and humans for translational studies. We identified a selective and more stable oxytocin receptor (OTR) agonist by subtly modifying the pharmacophore framework of human oxytocin and vasopressin. [Se-Se]-oxytocin-OH displayed similar potency to oxytocin but improved selectivity for OTR, an effect that was retained in mice. Centrally infused [Se-Se]-oxytocin-OH potently reversed social fear in mice, confirming that this action was mediated by OTR and not by V1a or V1b vasopressin receptors. In addition, [Se-Se]-oxytocin-OH produced a more regular contraction pattern than did oxytocin in a preclinical labor induction and augmentation model using myometrial strips from cesarean sections. [Se-Se]-oxytocin-OH had no activity in human cardiomyocytes, indicating a potentially improved safety profile and therapeutic window compared to those of clinically used oxytocin. In conclusion, [Se-Se]-oxytocin-OH is a novel probe for validating OTR as a therapeutic target in various biological systems and is a promising new lead for therapeutic development. Our medicinal chemistry approach may also be applicable to other peptidergic signaling systems with similar selectivity issues.

Item Type: Article
Uncontrolled Keywords: COS Cells, Animals, Humans, Mice, Rats, Receptors, Oxytocin, Ligands, Anxiety, Chemistry, Pharmaceutical, Female, Male, HEK293 Cells, Infusions, Intraventricular, Chlorocebus aethiops, Conditioning, Psychological
Depositing User: Symplectic Admin
Date Deposited: 09 Jan 2018 09:27
Last Modified: 19 Jan 2023 06:46
DOI: 10.1126/scisignal.aan3398
Related URLs:
URI: https://livrepository.liverpool.ac.uk/id/eprint/3014883
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