Effects of pre- and postnatal protein restriction on maternal and offspring metabolism in the nonhuman primate

Author:

Kirigiti Melissa A.1,Frazee Tim1,Bennett Baylin1,Arik Anam1,Blundell Peter1,Bader Lindsay1,Bagley Jennifer2,Frias Antonio E.34,Sullivan Elinor L.25,Roberts Charles T.13,Kievit Paul1ORCID

Affiliation:

1. Division of Cardiometabolic Health, Oregon National Primate Research Center, Beaverton, Oregon

2. Division of Neuroscience, Oregon National Primate Research Center, Beaverton, Oregon

3. Division of Reproductive and Developmental Sciences, Oregon National Primate Research Center, Beaverton, Oregon

4. Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Oregon Health & Science University, Portland, Oregon

5. Department of Human Physiology, University of Oregon, Eugene, Oregon

Abstract

Women in low- and middle-income countries frequently consume a protein-deficient diet during pregnancy and breastfeeding. The effects of gestational malnutrition on fetal and early postnatal development can have lasting adverse effects on offspring metabolism. Expanding on previous studies in rodent models, we utilized a nonhuman primate model of gestational and early-life protein restriction (PR) to evaluate effects on the organ development and glucose metabolism of juvenile offspring. Offspring were born to dams that had consumed a control diet containing 26% protein or a PR diet containing 13% protein. Offspring were maintained on the PR diet and studied [body and serum measurements, intravenous glucose tolerance tests (ivGTTs), and dual-energy X-ray absorptiometry scans] up to 7 mo of age, at which time tissues were collected for analysis. PR offspring had age-appropriate body weight and were euglycemic but exhibited elevated fasting insulin and reduced initial, but increased total, insulin secretion during an ivGTT at 6 mo of age. No changes were detected in pancreatic islets of PR juveniles; however, PR did induce changes, including reduced kidney size, and changes in liver, adipose tissue, and muscle gene expression in other peripheral organs. Serum osteocalcin was elevated and bone mineral content and density were reduced in PR juveniles, indicating a significant impact of PR on early postnatal bone development.

Funder

HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases

HHS | NIH | NIH Office of the Director

Bill and Melinda Gates Foundation

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology

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