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Plasma acylcarnitine concentrations reflect the acylcarnitine profile in cardiac tissues
Increased plasma concentrations of acylcarnitines (ACs) are suggested as a marker of metabolism disorders. The aim of the present study was to clarify which tissues are responsible for changes in the AC pool in plasma. The concentrations of medium- and long-chain ACs were changing during the fed-fas...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727517/ https://www.ncbi.nlm.nih.gov/pubmed/29235526 http://dx.doi.org/10.1038/s41598-017-17797-x |
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author | Makrecka-Kuka, Marina Sevostjanovs, Eduards Vilks, Karlis Volska, Kristine Antone, Unigunde Kuka, Janis Makarova, Elina Pugovics, Osvalds Dambrova, Maija Liepinsh, Edgars |
author_facet | Makrecka-Kuka, Marina Sevostjanovs, Eduards Vilks, Karlis Volska, Kristine Antone, Unigunde Kuka, Janis Makarova, Elina Pugovics, Osvalds Dambrova, Maija Liepinsh, Edgars |
author_sort | Makrecka-Kuka, Marina |
collection | PubMed |
description | Increased plasma concentrations of acylcarnitines (ACs) are suggested as a marker of metabolism disorders. The aim of the present study was to clarify which tissues are responsible for changes in the AC pool in plasma. The concentrations of medium- and long-chain ACs were changing during the fed-fast cycle in rat heart, muscles and liver. After 60 min running exercise, AC content was increased in fasted mice muscles, but not in plasma or heart. After glucose bolus administration in fasted rats, the AC concentrations in plasma decreased after 30 min but then began to increase, while in the muscles and liver, the contents of medium- and long-chain ACs were unchanged or even increased. Only the heart showed a decrease in medium- and long-chain AC contents that was similar to that observed in plasma. In isolated rat heart, but not isolated-contracting mice muscles, the significant efflux of medium- and long-chain ACs was observed. The efflux was reduced by 40% after the addition of glucose and insulin to the perfusion solution. Overall, these results indicate that during fed-fast cycle shifting the heart determines the medium- and long-chain AC profile in plasma, due to a rapid response to the availability of circulating energy substrates. |
format | Online Article Text |
id | pubmed-5727517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57275172017-12-18 Plasma acylcarnitine concentrations reflect the acylcarnitine profile in cardiac tissues Makrecka-Kuka, Marina Sevostjanovs, Eduards Vilks, Karlis Volska, Kristine Antone, Unigunde Kuka, Janis Makarova, Elina Pugovics, Osvalds Dambrova, Maija Liepinsh, Edgars Sci Rep Article Increased plasma concentrations of acylcarnitines (ACs) are suggested as a marker of metabolism disorders. The aim of the present study was to clarify which tissues are responsible for changes in the AC pool in plasma. The concentrations of medium- and long-chain ACs were changing during the fed-fast cycle in rat heart, muscles and liver. After 60 min running exercise, AC content was increased in fasted mice muscles, but not in plasma or heart. After glucose bolus administration in fasted rats, the AC concentrations in plasma decreased after 30 min but then began to increase, while in the muscles and liver, the contents of medium- and long-chain ACs were unchanged or even increased. Only the heart showed a decrease in medium- and long-chain AC contents that was similar to that observed in plasma. In isolated rat heart, but not isolated-contracting mice muscles, the significant efflux of medium- and long-chain ACs was observed. The efflux was reduced by 40% after the addition of glucose and insulin to the perfusion solution. Overall, these results indicate that during fed-fast cycle shifting the heart determines the medium- and long-chain AC profile in plasma, due to a rapid response to the availability of circulating energy substrates. Nature Publishing Group UK 2017-12-13 /pmc/articles/PMC5727517/ /pubmed/29235526 http://dx.doi.org/10.1038/s41598-017-17797-x 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 Makrecka-Kuka, Marina Sevostjanovs, Eduards Vilks, Karlis Volska, Kristine Antone, Unigunde Kuka, Janis Makarova, Elina Pugovics, Osvalds Dambrova, Maija Liepinsh, Edgars Plasma acylcarnitine concentrations reflect the acylcarnitine profile in cardiac tissues |
title | Plasma acylcarnitine concentrations reflect the acylcarnitine profile in cardiac tissues |
title_full | Plasma acylcarnitine concentrations reflect the acylcarnitine profile in cardiac tissues |
title_fullStr | Plasma acylcarnitine concentrations reflect the acylcarnitine profile in cardiac tissues |
title_full_unstemmed | Plasma acylcarnitine concentrations reflect the acylcarnitine profile in cardiac tissues |
title_short | Plasma acylcarnitine concentrations reflect the acylcarnitine profile in cardiac tissues |
title_sort | plasma acylcarnitine concentrations reflect the acylcarnitine profile in cardiac tissues |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727517/ https://www.ncbi.nlm.nih.gov/pubmed/29235526 http://dx.doi.org/10.1038/s41598-017-17797-x |
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