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Fetal Programming of the Neuroendocrine-Immune System and Metabolic Disease

Adverse uterine environments experienced during fetal development can alter the projected growth pattern of various organs and systems of the body, leaving the offspring at an increased risk of metabolic disease. The thrifty phenotype hypothesis has been demonstrated as an alteration to the growth t...

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Detalles Bibliográficos
Autores principales: Fisher, R. E., Steele, M., Karrow, N. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3431117/
https://www.ncbi.nlm.nih.gov/pubmed/22970372
http://dx.doi.org/10.1155/2012/792934
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author Fisher, R. E.
Steele, M.
Karrow, N. A.
author_facet Fisher, R. E.
Steele, M.
Karrow, N. A.
author_sort Fisher, R. E.
collection PubMed
description Adverse uterine environments experienced during fetal development can alter the projected growth pattern of various organs and systems of the body, leaving the offspring at an increased risk of metabolic disease. The thrifty phenotype hypothesis has been demonstrated as an alteration to the growth trajectory to improve the survival and reproductive fitness of the individual. However, when the intrauterine environment does not match the extrauterine environment problems can arise. With the increase in metabolic diseases in both Westernized and developing countries, it is becoming apparent that there is an environmental disconnect with the extrauterine environment. Therefore, the focus of this paper will be to explore the effects of maternal malnutrition on the offspring's susceptibility to metabolic disorders such as obesity, cardiovascular disease, and diabetes with emphasis on programming of the neuroendocrine-immune system.
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spelling pubmed-34311172012-09-11 Fetal Programming of the Neuroendocrine-Immune System and Metabolic Disease Fisher, R. E. Steele, M. Karrow, N. A. J Pregnancy Review Article Adverse uterine environments experienced during fetal development can alter the projected growth pattern of various organs and systems of the body, leaving the offspring at an increased risk of metabolic disease. The thrifty phenotype hypothesis has been demonstrated as an alteration to the growth trajectory to improve the survival and reproductive fitness of the individual. However, when the intrauterine environment does not match the extrauterine environment problems can arise. With the increase in metabolic diseases in both Westernized and developing countries, it is becoming apparent that there is an environmental disconnect with the extrauterine environment. Therefore, the focus of this paper will be to explore the effects of maternal malnutrition on the offspring's susceptibility to metabolic disorders such as obesity, cardiovascular disease, and diabetes with emphasis on programming of the neuroendocrine-immune system. Hindawi Publishing Corporation 2012 2012-08-16 /pmc/articles/PMC3431117/ /pubmed/22970372 http://dx.doi.org/10.1155/2012/792934 Text en Copyright © 2012 R. E. Fisher et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Fisher, R. E.
Steele, M.
Karrow, N. A.
Fetal Programming of the Neuroendocrine-Immune System and Metabolic Disease
title Fetal Programming of the Neuroendocrine-Immune System and Metabolic Disease
title_full Fetal Programming of the Neuroendocrine-Immune System and Metabolic Disease
title_fullStr Fetal Programming of the Neuroendocrine-Immune System and Metabolic Disease
title_full_unstemmed Fetal Programming of the Neuroendocrine-Immune System and Metabolic Disease
title_short Fetal Programming of the Neuroendocrine-Immune System and Metabolic Disease
title_sort fetal programming of the neuroendocrine-immune system and metabolic disease
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3431117/
https://www.ncbi.nlm.nih.gov/pubmed/22970372
http://dx.doi.org/10.1155/2012/792934
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