Cited by 177Adipokines, Inflammation, and Metabolic DiseasesAdipose Tissue and MetabolismDiabetes, Cardiovascular Risks, and Lipoproteins

Impaired Postprandial Adipose Tissue Blood Flow Response Is Related to Aspects of Insulin Sensitivity

Karpe, Fredrik, Fielding, Barbara A., Ilic, Vera, Macdonald, Ian A., Summers, Lucinda K.M., Frayn, Keith N.·2002·Diabetes

Abstract

Obesity has been associated with dysfunctional postprandial adipose tissue blood flow (ATBF), but it has also been recognized that the interindividual response is highly variable. The present work aimed at characterizing this variability. Fifteen subjects were given 75 g oral glucose, and abdominal subcutaneous ATBF was monitored by the 133Xe washout method. Determinants of insulin sensitivity based on nonesterified fatty acid (NEFA) suppression after oral glucose administration [ISI(NEFA)] were higher in the top tertile ATBF response group (1.29 ± 0.09 vs. 0.90 ± 0.08 in the lower tertiles, P = 0.01). ISI(NEFA) was related to ATBF response (rs = 0.73, P < 0.002) as well as insulin sensitivity based on postprandial glycemia [ISI(gly), rs = 0.58, P < 0.05], whereas the homeostasis model assessment (HOMA) index (rs = −0.39, P = 0.16) was not. The relationship between increase in ATBF and ISI(NEFA) was independent of BMI (P = 0.015) in multivariate analysis. Subjects with a high ATBF response had significantly higher increase of plasma norepinephrine (P < 0.05), indicating a link between postprandial insulinemia, sympathetic activation, and ATBF response. There is a close relationship between insulin sensitivity and the regulation of postprandial ATBF, independent of adiposity. Impaired regulation of ATBF seems to be another facet of the insulin resistance syndrome.

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Crossref · 10.2337/diabetes.51.8.2467

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  • The postprandial increase in blood flow that is so frequently observed in lean individuals is dramatically reduced in obese individuals.

    “the postprandial increase in blood flow that is so frequently observed in lean individuals is dramatically reduced in obese individuals (95,96)”

    From Adipose tissue remodeling and obesity (2011) · cites this paper as [96]

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References 30 · Cited by 177

Authors
Karpe, F., Fielding, B. A., Ilic, V., Macdonald, I. A., Summers, L. K. M., & Frayn, K. N.
Affiliations
  • University of Oxford (GB)
  • University of Nottingham (GB)
Venue
Diabetes
Published
2002-08-01
Volume
51
Issue
8
Pages
2467-2473
ISSN
  • 0012-1797 (ISSN-L)
  • 1939-327X
OpenAlex
W2104540429
Cited by
177
References
30
Citations by year
2026: 2 · 2025: 5 · 2024: 1 · 2023: 3 · 2022: 4 · 2021: 9 · 2020: 4 · 2019: 6 · 2018: 7 · 2017: 11 · 2016: 3 · 2015: 15 · 2014: 7 · 2013: 12 · 2012: 19
FWCI
5.02
Type
journal article
Language
en
Open access
closed
Locations
  • Diabetes (publishedVersion)
  • PubMed (publishedVersion)
  • Open Research (University of Surrey) (submittedVersion)
  • Surrey Research Insight Open Access (The University of Surrey) (submittedVersion)
Funders
Wellcome Trust
Topics
  • Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
  • Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
Keywords
insulin sensitivity, metabolic syndrome, free fatty acids, oral glucose tolerance, norepinephrine, sympathetic activation, interindividual variability, subcutaneous adipose tissue, HOMA index, plasma insulin
MeSH terms
Adipose Tissue, Administration, Oral, Adult, Blood Flow Velocity, Blood Glucose, Fatty Acids, Nonesterified, Female, Glucose, Glucose Tolerance Test, Humans, Infusions, Intravenous, Insulin, Male, Middle Aged, Regional Blood Flow, Postprandial Period

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