# Prolactin and oxytocin as modulators of intestinal contractility and glucose uptake

**Authors:** Perla Alejandra Figueroa-Carrasco, Aída Jimena Velarde-Salcedo, Carmen Gonzalez

PMC · DOI: 10.3389/fphys.2026.1703887 · Frontiers in Physiology · 2026-02-26

## TL;DR

Prolactin and oxytocin in maternal milk affect intestinal contractions and glucose absorption in infants, with combined effects varying by gut segment.

## Contribution

This study identifies how prolactin and oxytocin individually and jointly modulate intestinal motility and glucose uptake in different gut regions.

## Key findings

- Prolactin and oxytocin modulate intestinal contractility, with varying effects across gut segments.
- Oxytocin increases nitric oxide production more than prolactin at similar concentrations.
- Combined prolactin and oxytocin reduce glucose uptake, suggesting a regulatory mechanism for nutrient absorption.

## Abstract

Prolactin (PRL) and oxytocin (OT) are bioactive hormones naturally present in maternal milk that support neonatal development, contribute to immune regulation and gut maturation in infants, and promote growth and cell differentiation in the small intestine. However, the individual and combined roles of these hormones in intestinal function remain unclear. This study aims to elucidate the physiological effects of PRL and OT on intestinal motility, nitric oxide (NO) production, and glucose uptake to better understand their influence during early development.

Precontracted intestinal segments were placed in physiological solution, connected to isometric transducers, and exposed to various concentrations of PRL, OT, or PRL + OT, and changes in contractile responses were recorded. Glucose uptake was measured using everted sacs, and NO production was measured via the Griess method. PRL, OT, and PRL + OT modulated intestinal contractile activity, with effects varying by segment. OT induced higher NO levels than PRL at cumulative concentrations.

A single concentration of PRL or OT mostly preserved the contraction vs. % of the maximal contraction induced by KCl (100%), while PRL + OT reduced it and NO production in the duodenum and jejunum, but not in the ileum. Individually, PRL and OT increased glucose uptake, while their combination inhibited it, suggesting a modulatory mechanism regulating nutrient absorption. These findings support the role of PRL and OT as maternal milk-derived regulators of intestinal functions.

## Linked entities

- **Proteins:** PROLACTIN (PROLACTIN protein), OXT (oxytocin/neurophysin I prepropeptide)

## Full-text entities

- **Genes:** OXT (oxytocin/neurophysin I prepropeptide) [NCBI Gene 5020] {aka OT, OT-NPI, OXT-NPI}, PRL (prolactin) [NCBI Gene 5617] {aka GHA1, pPRL}
- **Chemicals:** Glucose (MESH:D005947), NO (MESH:D009569), KCl (MESH:D011189)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12979113/full.md

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12979113/full.md

## References

78 references — full list in the complete paper: https://tomesphere.com/paper/PMC12979113/full.md

---
Source: https://tomesphere.com/paper/PMC12979113