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  3. Compositional marker in vivo reveals intramyocellular lipid turnover during fasting-induced lipolysis.
 

Compositional marker in vivo reveals intramyocellular lipid turnover during fasting-induced lipolysis.

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BORIS DOI
10.7892/boris.111818
Publisher DOI
10.1038/s41598-018-21170-x
PubMed ID
29426847
Description
Intramyocellular lipid (IMCL) is of particular metabolic interest, but despite many proton magnetic resonance spectroscopy (H MRS) studies reporting IMCL content measured by the methylene (CH) resonance signal, little is known about its composition. Here we validated IMCL CH:CHratio as a compositional marker usingH MRS at short echo time, and investigated IMCL content and composition during a 28-hour fast in 24 healthy males. Increases in IMCL CHrelative to the creatine and phosphocreatine resonance (Cr) at 3.0 ppm (an internal standard) correlated with circulating free fatty acid (FA) concentrations, supporting the concept of increased FA influx into IMCL. Significant decreases in IMCL CH:CHratio indicated a less unsaturated IMCL pool after fasting, and this compositional change related inversely to IMCL baseline composition, suggesting a selective efflux of unsaturated shorter-chain FA from the IMCL pool. This novel in vivo evidence reveals IMCL turnover during extended fasting, consistent with the concept of a flexible, responsive myocellular lipid store. There were also differences between soleus and tibialis anterior in basal IMCL composition and in response to fasting. We discuss the potential of this marker for providing insights into normal physiology and mechanisms of disease.
Date of Publication
2018-02-09
Publication Type
Article
Language(s)
en
Contributor(s)
Thankamony, Ajay
Kemp, Graham J
Koulman, Albert
Bokii, Vlada
Savage, David B
Boesch, Christoph Hansorcid-logo
Lehrkörper, Medizinische Fakultät
DIPR, Magnetresonanz-Spektroskopie und Methodologie (AMSM)
Department for BioMedical Research, Abt. Magnetresonanz-Spektroskopie und Methodologie, AMSM
Hodson, Leanne
Dunger, David B
Sleigh, Alison
Additional Credits
Lehrkörper, Medizinische Fakultät
Series
Scientific Reports
Publisher
Nature Publishing Group
ISSN
2045-2322
Access(Rights)
open.access
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