Cited by 249Nitric Oxide and Endothelin EffectsNeutrophil, Myeloperoxidase and Oxidative MechanismsAtherosclerosis and Cardiovascular Diseases

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Postprandial recruitment of neutrophils may contribute to endothelial dysfunction

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van Oostrom, A.J.H.H.M., Sijmonsma, T.P., Verseyden, C., Jansen, E.H.J.M., de Koning, E.J.P., Rabelink, T.J., Castro Cabezas, M.·2003·Journal of Lipid Research

DOI 10.1194/jlr.m200419-jlr200

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Abstract

Atherosclerosis is a low-grade inflammatory disease involving leukocytes, lipids, and glucose leading to endothelial dysfunction. Since activation of neutrophils by triglycerides and glucose has been described in vitro, we hypothesized that the postprandial phase is an inflammatory state affecting leukocytes, possibly contributing to endothelial dysfunction. We measured postprandial blood leukocyte counts, cytokines, hydroperoxides (HPOs), and flow-mediated vasodilation (FMD) in eight healthy males (age 23 +/- 2 years) after a FAT (50 g/m2) and GLUCOSE challenge (37.5 g/m2), a combination of both (MIXED test), and after WATER. All tests, except WATER, resulted in significantly impaired FMD (10% reduction) between t = 1 h and t = 3 h, accompanied by a significant increase of neutrophils (59% after FAT and 28% after GLUCOSE and MIXED), total plasma HPOs (15 to 31% increase), and plasma interleukin-8 (IL-8) (50-130% increase). WATER did not affect FMD, neutrophils, HPOs, or IL-8. Lymphocytes increased gradually in all tests (40-70% increase at t = 10 h compared with t = 0; P < 0.005), paralleling a gradual 3- to 5-fold interleukin-6 increase. Monocyte and erythrocyte counts did not change in any test. In conclusion, the neutrophil increment during postprandial lipemia and glycemia with concomitant IL-8 and HPO increases may contribute to endothelial dysfunction. Lymphocyte increment is a nonspecific diurnal process. Postprandial intravascular inflammatory changes may be relevant for the pathogenesis of atherosclerosis.

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Authors: van Oostrom, A. J. H. H. M., Sijmonsma, T. P., Verseyden, C., Jansen, E. H. J. M., de Koning, E. J. P., Rabelink, T. J., & Castro Cabezas, M.
Affiliations: University Medical Center Utrecht (NL)
National Institute for Public Health and the Environment (NL)
ORCID: Sijmonsma, T.P.
Jansen, E.H.J.M.
Rabelink, T.J.
Venue: Journal of Lipid Research
Publisher: Elsevier BV
Published: 2003-03
Volume: 44
Issue: 3
Pages: 576-583
ISSN: 0022-2275 (ISSN-L)
DOI: 10.1194/jlr.m200419-jlr200
OpenAlex: W2131142277
Cited by: 249
References: 54
Citations by year: 2026: 2 · 2025: 2 · 2024: 2 · 2023: 5 · 2022: 7 · 2021: 4 · 2020: 12 · 2019: 7 · 2018: 7 · 2017: 13 · 2016: 13 · 2015: 14 · 2014: 23 · 2013: 16 · 2012: 9
FWCI: 7.28
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: cc-by
www.elsevier.com/tdm/userlicense/1.0/ (tdm)
creativecommons.org/licenses/by/4.0/ (vor, 6382 d)
Locations: Journal of Lipid Research (publishedVersion, cc-by)
PubMed (publishedVersion)
DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Rivm Repository (Netherlands National Institute for Public Health and the Environment) (submittedVersion)
Topics: Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
Life Sciences › Immunology and Microbiology › Immunology › Atherosclerosis and Cardiovascular Diseases
Keywords: postprandial lipemia, postprandial blood glucose, neutrophil recruitment, endothelial dysfunction, atherosclerosis, interleukin-8, interleukin-6, hydroperoxides, flow-mediated dilation, lymphocyte count, glucose challenge test, low-grade inflammation
MeSH terms: Adult, Arteriosclerosis, Blood Glucose, Dietary Fats, Endothelium, Vascular, Fasting, Fatty Acids, Nonesterified, Glucose, Humans, Hydrogen Peroxide, Inflammation, Insulin, Leukocyte Count, Male, Models, Biological, Neutrophils, Time Factors, Triglycerides, Interleukin-6, Interleukin-8, Postprandial Period

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Postprandial recruitment of neutrophils may contribute to endothelial dysfunction

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