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Evidence for liver energy metabolism programming in offspring subjected to intrauterine undernutrition during midgestation
BACKGROUND: Maternal undernutrition programs fetal energy homeostasis and increases the risk of metabolic disorders later in life. This study aimed to identify the signs of hepatic metabolic programming in utero and during the juvenile phase after intrauterine undernutrition during midgestation. MET...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423887/ https://www.ncbi.nlm.nih.gov/pubmed/30923555 http://dx.doi.org/10.1186/s12986-019-0346-7 |
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author | Zhou, Xiaoling Yang, Hong Yan, Qiongxian Ren, Ao Kong, Zhiwei Tang, Shaoxun Han, Xuefeng Tan, Zhiliang Salem, Abdelfattah Z. M. |
author_facet | Zhou, Xiaoling Yang, Hong Yan, Qiongxian Ren, Ao Kong, Zhiwei Tang, Shaoxun Han, Xuefeng Tan, Zhiliang Salem, Abdelfattah Z. M. |
author_sort | Zhou, Xiaoling |
collection | PubMed |
description | BACKGROUND: Maternal undernutrition programs fetal energy homeostasis and increases the risk of metabolic disorders later in life. This study aimed to identify the signs of hepatic metabolic programming in utero and during the juvenile phase after intrauterine undernutrition during midgestation. METHODS: Fifty-three pregnant goats were assigned to the control (100% of the maintenance requirement) or restricted (60% of the maintenance requirement from day 45 to day 100 of midgestation and realimentation thereafter) group to compare hepatic energy metabolism in the fetuses (day 100 of gestation) and kids (postnatal day 90). RESULTS: Undernutrition increased the glucagon concentration and hepatic hexokinase activity, decreased the body weight, liver weight and hepatic expression of G6PC, G6PD, and PGC1α mRNAs, and tended to decrease the hepatic glycogen content and ACOX1 mRNA level in the dams. Maternal undernutrition decreased the growth hormone (GH) and triglyceride concentrations, tended to decrease the body weight and hepatic hexokinase activity, increased the hepatic PCK1, PCK2 and PRKAA2 mRNAs levels and glucose-6-phosphatase activity, and tended to increase the hepatic PRKAB1 and CPT1α mRNAs levels in the male fetuses. In the restricted female fetuses, the hepatic hexokinase activity and G6PC mRNA level tended to be increased, but PKB1 mRNA expression was decreased and the ACACA, CPT1α, NR1H3 and STK11 mRNA levels tended to be decreased. Maternal undernutrition changed the hepatic metabolic profile and affected the metabolic pathway involved in amino acid, glycerophospholipid, bile acid, purine, and saccharide metabolism in the fetuses, but not the kids. Additionally, maternal undernutrition increased the concentrations of GH and cortisol, elevated the hepatic glucose-6-phosphate dehydrogenase activity, and tended to decrease the hepatic glycogen content in the male kids. No alterations in these variables were observed in the female kids. CONCLUSIONS: Maternal undernutrition affects the metabolic status in a sex- and stage-specific manner by changing the metabolic profile, expression of genes involved in glucose homeostasis and enzyme activities in the liver of the fetuses. The changes in the hormone levels in the male fetuses and kids, but not the female offspring, represent a potential sign of metabolic programming. |
format | Online Article Text |
id | pubmed-6423887 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64238872019-03-28 Evidence for liver energy metabolism programming in offspring subjected to intrauterine undernutrition during midgestation Zhou, Xiaoling Yang, Hong Yan, Qiongxian Ren, Ao Kong, Zhiwei Tang, Shaoxun Han, Xuefeng Tan, Zhiliang Salem, Abdelfattah Z. M. Nutr Metab (Lond) Research BACKGROUND: Maternal undernutrition programs fetal energy homeostasis and increases the risk of metabolic disorders later in life. This study aimed to identify the signs of hepatic metabolic programming in utero and during the juvenile phase after intrauterine undernutrition during midgestation. METHODS: Fifty-three pregnant goats were assigned to the control (100% of the maintenance requirement) or restricted (60% of the maintenance requirement from day 45 to day 100 of midgestation and realimentation thereafter) group to compare hepatic energy metabolism in the fetuses (day 100 of gestation) and kids (postnatal day 90). RESULTS: Undernutrition increased the glucagon concentration and hepatic hexokinase activity, decreased the body weight, liver weight and hepatic expression of G6PC, G6PD, and PGC1α mRNAs, and tended to decrease the hepatic glycogen content and ACOX1 mRNA level in the dams. Maternal undernutrition decreased the growth hormone (GH) and triglyceride concentrations, tended to decrease the body weight and hepatic hexokinase activity, increased the hepatic PCK1, PCK2 and PRKAA2 mRNAs levels and glucose-6-phosphatase activity, and tended to increase the hepatic PRKAB1 and CPT1α mRNAs levels in the male fetuses. In the restricted female fetuses, the hepatic hexokinase activity and G6PC mRNA level tended to be increased, but PKB1 mRNA expression was decreased and the ACACA, CPT1α, NR1H3 and STK11 mRNA levels tended to be decreased. Maternal undernutrition changed the hepatic metabolic profile and affected the metabolic pathway involved in amino acid, glycerophospholipid, bile acid, purine, and saccharide metabolism in the fetuses, but not the kids. Additionally, maternal undernutrition increased the concentrations of GH and cortisol, elevated the hepatic glucose-6-phosphate dehydrogenase activity, and tended to decrease the hepatic glycogen content in the male kids. No alterations in these variables were observed in the female kids. CONCLUSIONS: Maternal undernutrition affects the metabolic status in a sex- and stage-specific manner by changing the metabolic profile, expression of genes involved in glucose homeostasis and enzyme activities in the liver of the fetuses. The changes in the hormone levels in the male fetuses and kids, but not the female offspring, represent a potential sign of metabolic programming. BioMed Central 2019-03-18 /pmc/articles/PMC6423887/ /pubmed/30923555 http://dx.doi.org/10.1186/s12986-019-0346-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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 Zhou, Xiaoling Yang, Hong Yan, Qiongxian Ren, Ao Kong, Zhiwei Tang, Shaoxun Han, Xuefeng Tan, Zhiliang Salem, Abdelfattah Z. M. Evidence for liver energy metabolism programming in offspring subjected to intrauterine undernutrition during midgestation |
title | Evidence for liver energy metabolism programming in offspring subjected to intrauterine undernutrition during midgestation |
title_full | Evidence for liver energy metabolism programming in offspring subjected to intrauterine undernutrition during midgestation |
title_fullStr | Evidence for liver energy metabolism programming in offspring subjected to intrauterine undernutrition during midgestation |
title_full_unstemmed | Evidence for liver energy metabolism programming in offspring subjected to intrauterine undernutrition during midgestation |
title_short | Evidence for liver energy metabolism programming in offspring subjected to intrauterine undernutrition during midgestation |
title_sort | evidence for liver energy metabolism programming in offspring subjected to intrauterine undernutrition during midgestation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423887/ https://www.ncbi.nlm.nih.gov/pubmed/30923555 http://dx.doi.org/10.1186/s12986-019-0346-7 |
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