Meal-feeding promotes skeletal growth by ghrelin-dependent enhancement of growth hormone rhythmicity

Amanda Hornsby, Richard C. Brown, Thomas W. Tilston, Harry A. Smith, Alfonso Moreno-Cabañas, Bradley Arms-Williams, Anna L. Hopkins, Katie D. Taylor, Simran K. R. Rogaly, Lois H. M. Wells, Jamie J. Walker, Jeffrey S. Davies, Yuxiang Sun, Jeffrey M. Zigman, James A. Betts, Timothy Wells

Research output: Contribution to journalArticlepeer-review

2 Citations (SciVal)

Abstract

The physiological effect of ultradian temporal feeding patterns remains a major unanswered question in nutritional science. We have used automated and nasogastric feeding to address this question in male rodents and human volunteers. While grazing and meal-feeding reduced food intake in parallel (compared with ad libitum–fed rodents), body length and tibial epiphysial plate width were maintained in meal-fed rodents via the action of ghrelin and its receptor, GHS-R. Grazing and meal-feeding initially suppressed elevated preprandial ghrelin levels in rats, followed by either a sustained elevation in ghrelin in grazing rats or preprandial ghrelin surges in meal-fed rats. Episodic growth hormone (GH) secretion was largely unaffected in grazing rats, but meal-feeding tripled GH secretion, with burst height augmented and 2 additional bursts of GH per day. Continuous nasogastric infusion of enteral feed in humans failed to suppress circulating ghrelin, producing continuously elevated circulating GH levels with minimal rhythmicity. In contrast, bolus enteral infusion elicited postprandial ghrelin troughs accompanied by reduced circulating GH, with enhanced ultradian rhythmicity. Taken together, our data imply that the contemporary shift from regular meals to snacking behavior may be detrimental to optimal skeletal growth outcomes by sustaining circulating ghrelin at levels associated with undernourishment and diminishing GH pulsatility.

Original languageEnglish
Article numbere189202
JournalJournal of Clinical Investigation
Volume135
Issue number12
Early online date1 Apr 2025
DOIs
Publication statusPublished - 16 Jun 2025

Bibliographical note

Publisher Copyright:
© 2025, Hornsby et al.

Data Availability Statement

Underlying data for this publication are accessible in the Supporting
Data Values file.

Funding

The authors gratefully acknowledge the financial support of the Bill & Melinda Gates Foundation (OPP1061040); the Rosetrees Trust (A2248); the Waterloo Foundation (1403/3689, 1403/3758, 1403/4120); and Cardiff University’s School of Biosciences Equipment Fund, Research Contingency Fund, and the Neuroscience and Mental Health Research Institute Seedcorn Fund and Future Minds Programme. JAB is an investigator on research funded by Biotechnology and Biological Sciences Research Council, Medical Research Council, and National Institute for Health and Care Research. Enteral formula for the human feeding study was supplied by Nestlé Health Sciences. JJW acknowledges financial support from the Medical Research Council (MR/N008936/1 and MR/T032480/1).

FundersFunder number
Neuroscience and Mental Health Research Institute Seedcorn Fund and Future Minds Programme
Medical Research Council
Cardiff University
Biotechnology and Biological Sciences Research Council
Rosetrees TrustA2248
National Institute for Health and Care ResearchMR/T032480/1, MR/N008936/1
Waterloo Foundation1403/4120, 1403/3758, 1403/3689
Bill and Melinda Gates FoundationOPP1061040

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 2 - Zero Hunger
    SDG 2 Zero Hunger

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