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Changes in fetal mannose and other carbohydrates induced by a maternal insulin infusion in pregnant sheep

BACKGROUND: The importance of non-glucose carbohydrates, especially mannose and inositol, for normal development is increasingly recognized. Whether pregnancies complicated by abnormal glucose transfer to the fetus also affect the regulation of non-glucose carbohydrates is unknown. In pregnant sheep...

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Autores principales: Brown, Laura D, Thorn, Stephanie R, Cheung, Alex, Lavezzi, Jinny R, Battaglia, Frederick C, Rozance, Paul J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051387/
https://www.ncbi.nlm.nih.gov/pubmed/24917928
http://dx.doi.org/10.1186/2049-1891-5-28
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author Brown, Laura D
Thorn, Stephanie R
Cheung, Alex
Lavezzi, Jinny R
Battaglia, Frederick C
Rozance, Paul J
author_facet Brown, Laura D
Thorn, Stephanie R
Cheung, Alex
Lavezzi, Jinny R
Battaglia, Frederick C
Rozance, Paul J
author_sort Brown, Laura D
collection PubMed
description BACKGROUND: The importance of non-glucose carbohydrates, especially mannose and inositol, for normal development is increasingly recognized. Whether pregnancies complicated by abnormal glucose transfer to the fetus also affect the regulation of non-glucose carbohydrates is unknown. In pregnant sheep, maternal insulin infusions were used to reduce glucose supply to the fetus for both short (2-wk) and long (8-wk) durations to test the hypothesis that a maternal insulin infusion would suppress fetal mannose and inositol concentrations. We also used direct fetal insulin infusions (1-wk hyperinsulinemic-isoglycemic clamp) to determine the relative importance of fetal glucose and insulin for regulating non-glucose carbohydrates. RESULTS: A maternal insulin infusion resulted in lower maternal (50%, P < 0.01) and fetal (35-45%, P < 0.01) mannose concentrations, which were highly correlated (r(2) = 0.69, P < 0.01). A fetal insulin infusion resulted in a 50% reduction of fetal mannose (P < 0.05). Neither maternal nor fetal plasma inositol changed with exogenous insulin infusions. Additionally, maternal insulin infusion resulted in lower fetal sorbitol and fructose (P < 0.01). CONCLUSIONS: Chronically decreased glucose supply to the fetus as well as fetal hyperinsulinemia both reduce fetal non-glucose carbohydrates. Given the role of these carbohydrates in protein glycosylation and lipid production, more research on their metabolism in pregnancies complicated by abnormal glucose metabolism is clearly warranted.
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spelling pubmed-40513872014-06-11 Changes in fetal mannose and other carbohydrates induced by a maternal insulin infusion in pregnant sheep Brown, Laura D Thorn, Stephanie R Cheung, Alex Lavezzi, Jinny R Battaglia, Frederick C Rozance, Paul J J Anim Sci Biotechnol Research BACKGROUND: The importance of non-glucose carbohydrates, especially mannose and inositol, for normal development is increasingly recognized. Whether pregnancies complicated by abnormal glucose transfer to the fetus also affect the regulation of non-glucose carbohydrates is unknown. In pregnant sheep, maternal insulin infusions were used to reduce glucose supply to the fetus for both short (2-wk) and long (8-wk) durations to test the hypothesis that a maternal insulin infusion would suppress fetal mannose and inositol concentrations. We also used direct fetal insulin infusions (1-wk hyperinsulinemic-isoglycemic clamp) to determine the relative importance of fetal glucose and insulin for regulating non-glucose carbohydrates. RESULTS: A maternal insulin infusion resulted in lower maternal (50%, P < 0.01) and fetal (35-45%, P < 0.01) mannose concentrations, which were highly correlated (r(2) = 0.69, P < 0.01). A fetal insulin infusion resulted in a 50% reduction of fetal mannose (P < 0.05). Neither maternal nor fetal plasma inositol changed with exogenous insulin infusions. Additionally, maternal insulin infusion resulted in lower fetal sorbitol and fructose (P < 0.01). CONCLUSIONS: Chronically decreased glucose supply to the fetus as well as fetal hyperinsulinemia both reduce fetal non-glucose carbohydrates. Given the role of these carbohydrates in protein glycosylation and lipid production, more research on their metabolism in pregnancies complicated by abnormal glucose metabolism is clearly warranted. BioMed Central 2014-05-22 /pmc/articles/PMC4051387/ /pubmed/24917928 http://dx.doi.org/10.1186/2049-1891-5-28 Text en Copyright © 2014 Brown et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 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
Brown, Laura D
Thorn, Stephanie R
Cheung, Alex
Lavezzi, Jinny R
Battaglia, Frederick C
Rozance, Paul J
Changes in fetal mannose and other carbohydrates induced by a maternal insulin infusion in pregnant sheep
title Changes in fetal mannose and other carbohydrates induced by a maternal insulin infusion in pregnant sheep
title_full Changes in fetal mannose and other carbohydrates induced by a maternal insulin infusion in pregnant sheep
title_fullStr Changes in fetal mannose and other carbohydrates induced by a maternal insulin infusion in pregnant sheep
title_full_unstemmed Changes in fetal mannose and other carbohydrates induced by a maternal insulin infusion in pregnant sheep
title_short Changes in fetal mannose and other carbohydrates induced by a maternal insulin infusion in pregnant sheep
title_sort changes in fetal mannose and other carbohydrates induced by a maternal insulin infusion in pregnant sheep
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051387/
https://www.ncbi.nlm.nih.gov/pubmed/24917928
http://dx.doi.org/10.1186/2049-1891-5-28
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