Please use this identifier to cite or link to this item: 10.1038/s41598-017-17797-x
Title: Plasma acylcarnitine concentrations reflect the acylcarnitine profile in cardiac tissues
Authors: Makrecka-Kuka, Marina
Sevostjanovs, Eduards
Vilks, Karlis
Volska, Kristine
Antone, Unigunde
Kuka, Janis
Makarova, Elina
Pugovics, Osvalds
Dambrova, Maija
Liepinsh, Edgars
Faculty of Pharmacy
Keywords: 3.1 Basic medicine;1.1. Scientific article indexed in Web of Science and/or Scopus database;General
Issue Date: 1-Dec-2017
Citation: Makrecka-Kuka , M , Sevostjanovs , E , Vilks , K , Volska , K , Antone , U , Kuka , J , Makarova , E , Pugovics , O , Dambrova , M & Liepinsh , E 2017 , ' Plasma acylcarnitine concentrations reflect the acylcarnitine profile in cardiac tissues ' , Scientific Reports , vol. 7 , no. 1 , 17528 . https://doi.org/10.1038/s41598-017-17797-x
Abstract: 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.
Description: Funding Information: This study was supported by the Latvian National Research Program BIOMEDICINE. E. Liepinsh was supported by the FP7 project InnovaBalt [grant Nr. 316149]. We would like to thank Dr. Reinis Vilskersts and Gita Dambrova for help with the isolated skeletal muscle experiments. Publisher Copyright: © 2017 The Author(s).
DOI: 10.1038/s41598-017-17797-x
ISSN: 2045-2322
Appears in Collections:Research outputs from Pure / Zinātniskās darbības rezultāti no ZDIS Pure

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