SwePub
Sök i LIBRIS databas

  Extended search

onr:"swepub:oai:gup.ub.gu.se/223597"
 

Search: onr:"swepub:oai:gup.ub.gu.se/223597" > Model-Based Quantif...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Model-Based Quantification of the Systemic Interplay between Glucose and Fatty Acids in the Postprandial State

Sips, F. L. P. (author)
Eindhoven University of Technology, Netherlands
Nyman, Elin (author)
Linköpings universitet,Institutionen för medicinsk teknik,Tekniska fakulteten,CVMD iMED DMPK AstraZeneca RandD, Sweden
Adiels, Martin, 1976 (author)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för molekylär och klinisk medicin,Institute of Medicine, Department of Molecular and Clinical Medicine,University of Gothenburg,University of Gothenburg, Sweden
show more...
Hilbers, P. A. J. (author)
Eindhoven University of Technology, Netherlands
Strålfors, Peter (author)
Linköpings universitet,Avdelningen för cellbiologi,Medicinska fakulteten
van Riel, N. A. W. (author)
Eindhoven University of Technology, Netherlands
Cedersund, Gunnar, 1978 (author)
Linköpings universitet,Institutionen för medicinsk teknik,Tekniska fakulteten,Avdelningen för cellbiologi,Medicinska fakulteten
show less...
 (creator_code:org_t)
2015-09-10
2015
English.
In: Plos One. - : Public Library of Science (PLoS). - 1932-6203. ; 10:9
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • In metabolic diseases such as Type 2 Diabetes and Non-Alcoholic Fatty Liver Disease, the systemic regulation of postprandial metabolite concentrations is disturbed. To understand this dysregulation, a quantitative and temporal understanding of systemic postprandial metabolite handling is needed. Of particular interest is the intertwined regulation of glucose and non-esterified fatty acids (NEFA), due to the association between disturbed NEFA metabolism and insulin resistance. However, postprandial glucose metabolism is characterized by a dynamic interplay of simultaneously responding regulatory mechanisms, which have proven difficult to measure directly. Therefore, we propose a mathematical modelling approach to untangle the systemic interplay between glucose and NEFA in the postprandial period. The developed model integrates data of both the perturbation of glucose metabolism by NEFA as measured under clamp conditions, and postprandial time-series of glucose, insulin, and NEFA. The model can describe independent data not used for fitting, and perturbations of NEFA metabolism result in an increased insulin, but not glucose, response, demonstrating that glucose homeostasis is maintained. Finally, the model is used to show that NEFA may mediate up to 30-45% of the postprandial increase in insulin-dependent glucose uptake at two hours after a glucose meal. In conclusion, the presented model can quantify the systemic interactions of glucose and NEFA in the postprandial state, and may therefore provide a new method to evaluate the disturbance of this interplay in metabolic disease.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine (hsv//eng)

Keyword

HEPATIC INSULIN-RESISTANCE
NUCLEAR-MAGNETIC-RESONANCE
DIACYLGLYCEROL
ACTIVATION
CARDIOVASCULAR-DISEASE
LIPOPROTEIN METABOLISM
DIABETES-MELLITUS
OBESE-PATIENTS
MINIMAL MODEL
HUMANS
LIVER
Multidisciplinary Sciences
HUMANS

Publication and Content Type

ref (subject category)
art (subject category)

Find in a library

  • Plos One (Search for host publication in LIBRIS)

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view