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Effects of postnatal growth restriction and subsequent catch-up growth on neurodevelopment and glucose homeostasis in rats
BACKGROUND: There is increasing evidence that poor growth of preterm infants is a risk factor for poor long-term development, while the effects of early postnatal growth restriction are not well known. We utilized a rat model to examine the consequences of different patterns of postnatal growth and...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4455975/ https://www.ncbi.nlm.nih.gov/pubmed/26040642 http://dx.doi.org/10.1186/s12899-015-0017-5 |
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author | Alexeev, Erica E. Lönnerdal, Bo Griffin, Ian J. |
author_facet | Alexeev, Erica E. Lönnerdal, Bo Griffin, Ian J. |
author_sort | Alexeev, Erica E. |
collection | PubMed |
description | BACKGROUND: There is increasing evidence that poor growth of preterm infants is a risk factor for poor long-term development, while the effects of early postnatal growth restriction are not well known. We utilized a rat model to examine the consequences of different patterns of postnatal growth and hypothesized that early growth failure leads to impaired development and insulin resistance. Rat pups were separated at birth into normal (N, n = 10) or restricted intake (R, n = 16) litters. At d11, R pups were re-randomized into litters of 6 (R-6), 10 (R-10) or 16 (R-16) pups/dam. N pups remained in litters of 10 pups/dam (N-10). Memory and learning were examined through T-maze test. Insulin sensitivity was measured by i.p. insulin tolerance test and glucose tolerance test. RESULTS: By d10, N pups weighed 20 % more than R pups (p < 0.001). By d15, the R-6 group caught up to the N-10 group in weight, the R-10 group showed partial catch-up growth and the R-16 group showed no catch-up growth. All R groups showed poorer scores in developmental testing when compared with the N-10 group during T-Maze test (p < 0.05). Although R-16 were more insulin sensitive than R-6 and R-10, all R groups were more glucose tolerant than N-10. CONCLUSION: In rats, differences in postnatal growth restriction leads to changes in development and in insulin sensitivity. These results may contribute to better elucidating the causes of poor developmental outcomes in human preterm infants. |
format | Online Article Text |
id | pubmed-4455975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44559752015-06-05 Effects of postnatal growth restriction and subsequent catch-up growth on neurodevelopment and glucose homeostasis in rats Alexeev, Erica E. Lönnerdal, Bo Griffin, Ian J. BMC Physiol Research Article BACKGROUND: There is increasing evidence that poor growth of preterm infants is a risk factor for poor long-term development, while the effects of early postnatal growth restriction are not well known. We utilized a rat model to examine the consequences of different patterns of postnatal growth and hypothesized that early growth failure leads to impaired development and insulin resistance. Rat pups were separated at birth into normal (N, n = 10) or restricted intake (R, n = 16) litters. At d11, R pups were re-randomized into litters of 6 (R-6), 10 (R-10) or 16 (R-16) pups/dam. N pups remained in litters of 10 pups/dam (N-10). Memory and learning were examined through T-maze test. Insulin sensitivity was measured by i.p. insulin tolerance test and glucose tolerance test. RESULTS: By d10, N pups weighed 20 % more than R pups (p < 0.001). By d15, the R-6 group caught up to the N-10 group in weight, the R-10 group showed partial catch-up growth and the R-16 group showed no catch-up growth. All R groups showed poorer scores in developmental testing when compared with the N-10 group during T-Maze test (p < 0.05). Although R-16 were more insulin sensitive than R-6 and R-10, all R groups were more glucose tolerant than N-10. CONCLUSION: In rats, differences in postnatal growth restriction leads to changes in development and in insulin sensitivity. These results may contribute to better elucidating the causes of poor developmental outcomes in human preterm infants. BioMed Central 2015-06-05 /pmc/articles/PMC4455975/ /pubmed/26040642 http://dx.doi.org/10.1186/s12899-015-0017-5 Text en © Alexeev et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Alexeev, Erica E. Lönnerdal, Bo Griffin, Ian J. Effects of postnatal growth restriction and subsequent catch-up growth on neurodevelopment and glucose homeostasis in rats |
title | Effects of postnatal growth restriction and subsequent catch-up growth on neurodevelopment and glucose homeostasis in rats |
title_full | Effects of postnatal growth restriction and subsequent catch-up growth on neurodevelopment and glucose homeostasis in rats |
title_fullStr | Effects of postnatal growth restriction and subsequent catch-up growth on neurodevelopment and glucose homeostasis in rats |
title_full_unstemmed | Effects of postnatal growth restriction and subsequent catch-up growth on neurodevelopment and glucose homeostasis in rats |
title_short | Effects of postnatal growth restriction and subsequent catch-up growth on neurodevelopment and glucose homeostasis in rats |
title_sort | effects of postnatal growth restriction and subsequent catch-up growth on neurodevelopment and glucose homeostasis in rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4455975/ https://www.ncbi.nlm.nih.gov/pubmed/26040642 http://dx.doi.org/10.1186/s12899-015-0017-5 |
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