Cited by 178

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Caloric Restriction and Exercise Increase Plasma ANGPTL4 Levels in Humans via Elevated Free Fatty Acids

Kersten, Sander, Lichtenstein, Laeticia, Steenbergen, Emma, Mudde, Karin, Hendriks, Henk F.J., Hesselink, Matthijs K., Schrauwen, Patrick, Müller, Michael·2009·Arteriosclerosis, Thrombosis, and Vascular Biology

Abstract

Objective— Plasma lipoprotein levels are determined by the balance between lipoprotein production and clearance. Recently, angiopoietin-like protein 4 (ANGPTL4) was uncovered as a novel endocrine factor that potently raises plasma triglyceride levels by inhibiting triglyceride clearance. However, very little is known about ANGPTL4 in human. Here we set out to identify physiological determinants of plasma ANGPTL4 levels in humans, focusing on the effect of energy restriction and plasma FFAs. Methods and Results— We developed an ELISA for quantitative measurement of ANGPTL4 in human plasma. Using this assay we found major variations in baseline plasma ANGPTL4 levels between individuals. Within an individual, plasma ANGPTL4 levels remain stable throughout the day but increase significantly in response to long-term fasting, chronic caloric restriction, and endurance exercise. Intralipid injection as well as treatment with a β-adrenergic agonist, both of which lead to elevated plasma FFA levels, increased plasma ANGPTL4 levels compared to control treatment. Fatty acids markedly induced ANGPTL4 gene expression in rat hepatoma FAO cells, human primary myocytes, and mouse intestinal MSIE cells. Conclusion— In conclusion, our results show that plasma ANGPTL4 levels are increased by fasting, caloric restriction, and exercise, which is likely mediated by elevated plasma FFAs.

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Crossref · 10.1161/atvbaha.108.182147

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  • ANGPTL4 is robustly expressed in the liver in mice, and in humans liver is the tissue with greatest ANGPTL4 expression.

    “ANGPTL4 is robustly expressed in the liver in mice, and in humans liver is the tissue with greatest ANGPTL4 expression (86, 87).”

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Research works printed but not linked: 33

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Metadata

Authors
Kersten, S., Lichtenstein, L., Steenbergen, E., Mudde, K., Hendriks, H. F. J., Hesselink, M. K., Schrauwen, P., & Müller, M.
Affiliations
From the Nutrigenomics Consortium (S.K., L.L., P.S., M.M.), TI Food and Nutrition, Wageningen, The Netherlands; Nutrition, Metabolism, and Genomics Group, Division of Human Nutrition (S.K., L.L., E.S., K.M., M.M.), Wageningen University, The Netherlands; Business Unit Biosciences (H.F.J.H.), TNO Quality of Life, Zeist, The Netherlands; and the Department of Human Movement Sciences (M.K.H.) and the Department of Human Biology (P.S.), Maastricht University, The Netherlands.
Venue
Arteriosclerosis, Thrombosis, and Vascular Biology
Published
2009-06
Volume
29
Issue
6
Pages
969-974
ISSN
  • 1079-5642
  • 1524-4636
Cited by
178
References
2
Language
en

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