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Change in the Lipid Transport Capacity of the Liver and Blood during Reproduction in Rats

To support the high energetic demands of reproduction, female mammals display plasticity in many physiological processes, such as the lipid transport system. Lipids support the energy demands of females during reproduction, and energy and structural demands of the developing offspring via the placen...

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Autores principales: Zhang, Yufeng, Kallenberg, Christine, Hyatt, Hayden W., Kavazis, Andreas N., Hood, Wendy R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5527701/
https://www.ncbi.nlm.nih.gov/pubmed/28798692
http://dx.doi.org/10.3389/fphys.2017.00517
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author Zhang, Yufeng
Kallenberg, Christine
Hyatt, Hayden W.
Kavazis, Andreas N.
Hood, Wendy R.
author_facet Zhang, Yufeng
Kallenberg, Christine
Hyatt, Hayden W.
Kavazis, Andreas N.
Hood, Wendy R.
author_sort Zhang, Yufeng
collection PubMed
description To support the high energetic demands of reproduction, female mammals display plasticity in many physiological processes, such as the lipid transport system. Lipids support the energy demands of females during reproduction, and energy and structural demands of the developing offspring via the placenta in utero or milk during the suckling period. We hypothesized that key proteins supporting lipid transport in reproductive females will increase during pregnancy and lactation, but drop to non-reproductive levels shortly after reproduction has ended. We compared the relative protein levels of liver-type cytosolic fatty acid transporter (L-FABP(c)), plasma membrane fatty acid transporter (FABPpm), fatty acid translocase (FAT/CD36) in the liver, a key site of lipid storage and synthesis, and free fatty acid transporter albumin and triglyceride transporter [represented by apolipoprotein B (apoB)] levels in serum in reproductive Sprague-Dawley rats during late pregnancy, peak-lactation, and 1-week post-lactation as well as in non-reproductive rats. We found that all lipid transporter levels were greater in pregnant rats compared to non-reproductive rats. Lactating rats also showed higher levels of FAT/CD36 and FABPpm than non-reproductive rats. Moreover, all fat transporters also dropped back to non-reproductive levels during post-lactation except for FAT/CD36. These results indicate that fat uptake and transport capacities in liver cells are elevated during late gestation and lactation. Liver lipid secretion is up-regulated during gestation but not during lactation. These data supported the plasticity of lipid transport capacities in liver and blood during reproductive stages.
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spelling pubmed-55277012017-08-10 Change in the Lipid Transport Capacity of the Liver and Blood during Reproduction in Rats Zhang, Yufeng Kallenberg, Christine Hyatt, Hayden W. Kavazis, Andreas N. Hood, Wendy R. Front Physiol Physiology To support the high energetic demands of reproduction, female mammals display plasticity in many physiological processes, such as the lipid transport system. Lipids support the energy demands of females during reproduction, and energy and structural demands of the developing offspring via the placenta in utero or milk during the suckling period. We hypothesized that key proteins supporting lipid transport in reproductive females will increase during pregnancy and lactation, but drop to non-reproductive levels shortly after reproduction has ended. We compared the relative protein levels of liver-type cytosolic fatty acid transporter (L-FABP(c)), plasma membrane fatty acid transporter (FABPpm), fatty acid translocase (FAT/CD36) in the liver, a key site of lipid storage and synthesis, and free fatty acid transporter albumin and triglyceride transporter [represented by apolipoprotein B (apoB)] levels in serum in reproductive Sprague-Dawley rats during late pregnancy, peak-lactation, and 1-week post-lactation as well as in non-reproductive rats. We found that all lipid transporter levels were greater in pregnant rats compared to non-reproductive rats. Lactating rats also showed higher levels of FAT/CD36 and FABPpm than non-reproductive rats. Moreover, all fat transporters also dropped back to non-reproductive levels during post-lactation except for FAT/CD36. These results indicate that fat uptake and transport capacities in liver cells are elevated during late gestation and lactation. Liver lipid secretion is up-regulated during gestation but not during lactation. These data supported the plasticity of lipid transport capacities in liver and blood during reproductive stages. Frontiers Media S.A. 2017-07-26 /pmc/articles/PMC5527701/ /pubmed/28798692 http://dx.doi.org/10.3389/fphys.2017.00517 Text en Copyright © 2017 Zhang, Kallenberg, Hyatt, Kavazis and Hood. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Zhang, Yufeng
Kallenberg, Christine
Hyatt, Hayden W.
Kavazis, Andreas N.
Hood, Wendy R.
Change in the Lipid Transport Capacity of the Liver and Blood during Reproduction in Rats
title Change in the Lipid Transport Capacity of the Liver and Blood during Reproduction in Rats
title_full Change in the Lipid Transport Capacity of the Liver and Blood during Reproduction in Rats
title_fullStr Change in the Lipid Transport Capacity of the Liver and Blood during Reproduction in Rats
title_full_unstemmed Change in the Lipid Transport Capacity of the Liver and Blood during Reproduction in Rats
title_short Change in the Lipid Transport Capacity of the Liver and Blood during Reproduction in Rats
title_sort change in the lipid transport capacity of the liver and blood during reproduction in rats
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5527701/
https://www.ncbi.nlm.nih.gov/pubmed/28798692
http://dx.doi.org/10.3389/fphys.2017.00517
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