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Neonatal leptin treatment reverses the bone-suppressive effects of maternal undernutrition in adult rat offspring
Alterations in the early life environment, including maternal undernutrition (UN) during pregnancy, can lead to increased risk of metabolic and cardiovascular disorders in offspring. Leptin treatment of neonates born to UN rats reverses the programmed metabolic phenotype, but the possible benefits o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5550441/ https://www.ncbi.nlm.nih.gov/pubmed/28794412 http://dx.doi.org/10.1038/s41598-017-07500-5 |
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author | Firth, Elwyn C. Gamble, Greg D. Cornish, Jillian Vickers, Mark H. |
author_facet | Firth, Elwyn C. Gamble, Greg D. Cornish, Jillian Vickers, Mark H. |
author_sort | Firth, Elwyn C. |
collection | PubMed |
description | Alterations in the early life environment, including maternal undernutrition (UN) during pregnancy, can lead to increased risk of metabolic and cardiovascular disorders in offspring. Leptin treatment of neonates born to UN rats reverses the programmed metabolic phenotype, but the possible benefits of this treatment on bone tissue have not been defined. We describe for the first time the effects of neonatal leptin treatment on bone in adult offspring following maternal UN. Offspring from either UN or ad libitum-fed (AD) rats were treated with either saline or leptin (2.5 µg/ g.d on postnatal days (D)3–13) and were fed either a chow or high fat (HF) diet from weaning until study completion at D170. Analysis of micro-tomographic data of the left femur showed highly significant effects of UN on cortical and trabecular bone tissue indices, contributing to inferior microstructure and bone strength, almost all of which were reversed by early leptin life treatment. The HF fat diet negatively affected trabecular bone tissue, but the effects of only trabecular separation and number were reversed by leptin treatment. The negative effects of maternal UN on skeletal health in adult offspring might be prevented or attenuated by various interventions including leptin. Establishment of a minimal efficacious leptin dose warrants further study. |
format | Online Article Text |
id | pubmed-5550441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55504412017-08-11 Neonatal leptin treatment reverses the bone-suppressive effects of maternal undernutrition in adult rat offspring Firth, Elwyn C. Gamble, Greg D. Cornish, Jillian Vickers, Mark H. Sci Rep Article Alterations in the early life environment, including maternal undernutrition (UN) during pregnancy, can lead to increased risk of metabolic and cardiovascular disorders in offspring. Leptin treatment of neonates born to UN rats reverses the programmed metabolic phenotype, but the possible benefits of this treatment on bone tissue have not been defined. We describe for the first time the effects of neonatal leptin treatment on bone in adult offspring following maternal UN. Offspring from either UN or ad libitum-fed (AD) rats were treated with either saline or leptin (2.5 µg/ g.d on postnatal days (D)3–13) and were fed either a chow or high fat (HF) diet from weaning until study completion at D170. Analysis of micro-tomographic data of the left femur showed highly significant effects of UN on cortical and trabecular bone tissue indices, contributing to inferior microstructure and bone strength, almost all of which were reversed by early leptin life treatment. The HF fat diet negatively affected trabecular bone tissue, but the effects of only trabecular separation and number were reversed by leptin treatment. The negative effects of maternal UN on skeletal health in adult offspring might be prevented or attenuated by various interventions including leptin. Establishment of a minimal efficacious leptin dose warrants further study. Nature Publishing Group UK 2017-08-09 /pmc/articles/PMC5550441/ /pubmed/28794412 http://dx.doi.org/10.1038/s41598-017-07500-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Firth, Elwyn C. Gamble, Greg D. Cornish, Jillian Vickers, Mark H. Neonatal leptin treatment reverses the bone-suppressive effects of maternal undernutrition in adult rat offspring |
title | Neonatal leptin treatment reverses the bone-suppressive effects of maternal undernutrition in adult rat offspring |
title_full | Neonatal leptin treatment reverses the bone-suppressive effects of maternal undernutrition in adult rat offspring |
title_fullStr | Neonatal leptin treatment reverses the bone-suppressive effects of maternal undernutrition in adult rat offspring |
title_full_unstemmed | Neonatal leptin treatment reverses the bone-suppressive effects of maternal undernutrition in adult rat offspring |
title_short | Neonatal leptin treatment reverses the bone-suppressive effects of maternal undernutrition in adult rat offspring |
title_sort | neonatal leptin treatment reverses the bone-suppressive effects of maternal undernutrition in adult rat offspring |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5550441/ https://www.ncbi.nlm.nih.gov/pubmed/28794412 http://dx.doi.org/10.1038/s41598-017-07500-5 |
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