Intermittent Bolus Feeding Enhances Organ Growth More Than Continuous Feeding in a Neonatal Piglet Model
Autor: | Scot R. Kimball, Agus Suryawan, Samer W. El-Kadi, Claire Boutry-Regard, Teresa A. Davis, Marta L. Fiorotto, Hanh V. Nguyen |
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Přispěvatelé: | Animal and Poultry Sciences |
Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
medicine.medical_specialty protein synthesis Medicine (miscellaneous) Ileum liver translation initiation Jejunum AcademicSubjects/MED00060 03 medical and health sciences 0302 clinical medicine Suidae 030225 pediatrics Internal medicine medicine pig model Nutrition Kidney Meal Nutrition and Dietetics biology business.industry digestive oral and skin physiology Eukaryotic initiation factor 4E binding ORIGINAL RESEARCH biology.organism_classification nutrition 030104 developmental biology medicine.anatomical_structure Endocrinology Maternal and Pediatric Nutrition Ribosomal protein s6 medicine.symptom neonate business Weight gain Food Science |
Zdroj: | Current Developments in Nutrition |
Popis: | Background: Orogastric tube feeding is frequently prescribed for neonates who cannot ingest food normally. In a piglet model of the neonate, greater skeletal muscle growth is sustained by upregulation of translation initiation signaling when nutrition is delivered by intermittent bolus meals, rather than continuously. Objectives: The objective of this study was to determine the long-term effects of feeding frequency on organ growth and the mechanism by which feeding frequency modulates protein anabolism in these organs. Methods: Eighteen neonatal pigs were fed by gastrostomy tube the same amount of a sow milk replacer either by continuous infusion (CON) or on an intermittent bolus schedule (INT). After 21 d of feeding, the pigs were killed without interruption of feeding (CON; n = 6) or immediately before (INT-0; n = 6) or 60 min after (INT-60; n = 6) a meal, and fractional protein synthesis rates and activation indexes of signaling pathways that regulate translation initiation were measured in the heart, jejunum, ileum, kidneys, and liver. Results: Compared with continuous feeding, intermittent feeding stimulated the growth of the liver (+64%), jejunum (+48%), ileum (+40%), heart (+64%), and kidney (+56%). The increases in heart, kidney, jejunum, and ileum masses were proportional to whole body lean weight gain, but liver weight gain was greater in the INT-60 than the CON, and intermediate for the INT-0 group. For the liver and ileum, but not the heart, kidney, and jejunum, INT-60 compared with CON pigs had greater fractional protein synthesis rates (22% and 48%, respectively) and was accompanied by an increase in ribosomal protein S6 kinase 1 and eukaryotic initiation factor 4E binding protein 1 phosphorylation. Conclusions: These results suggest that intermittent bolus compared with continuous orogastric feeding enhances organ growth and that in the ileum and liver, intermittent feeding enhances protein synthesis by stimulating translation initiation. National Institute of Arthritis and Musculoskeletal and Skin DiseasesUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Institute of Arthritis & Musculoskeletal & Skin Diseases (NIAMS) [AR044474, AR46308]; National Institute of Child Health and Human DevelopmentUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD) [HD072891, HD085573, HD099080]; National Institute of Diabetes and Digestive and Kidney DiseasesUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Institute of Diabetes & Digestive & Kidney Diseases (NIDDK) [DK15658]; United States Department of Agriculture National Institute of Agriculture [2013-67015-20438]; USDA/ARSUnited States Department of Agriculture (USDA)USDA Agricultural Research Service [3092-51000-060] Supported by National Institute of Arthritis and Musculoskeletal and Skin Diseases Grants AR044474 (TAD) and AR46308 (MLF), National Institute of Child Health and Human Development HD072891 (TAD), HD085573 (TAD), and HD099080 (TAD and MLF), National Institute of Diabetes and Digestive and Kidney Diseases DK15658 (SRK), United States Department of Agriculture National Institute of Agriculture grant 2013-67015-20438 (TAD), and by the USDA/ARS under Cooperative Agreement no. 3092-51000-060 (TAD). Public domain – authored by a U.S. government employee |
Databáze: | OpenAIRE |
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