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Targeting VEGF-B as a novel treatment for insulin resistance and type 2 diabetes

Carolina E. Hagberg, Annika Mehlem, Annelie Falkevall, Lars Muhl, Barbara C. Fam, Henrik Ortsäter, Pierre Scotney, Daniel Nyqvist, Erik Samén, Li Lu, Sharon Stone-Elander, Joseph Proietto, Sofianos Andrikopoulos, Åke Sjöholm, Andrew Nash and Ulf Eriksson ()
Additional contact information
Carolina E. Hagberg: Tissue Biology Group, Karolinska Institutet, SE-171 77 Stockholm, Sweden
Annika Mehlem: Tissue Biology Group, Karolinska Institutet, SE-171 77 Stockholm, Sweden
Annelie Falkevall: Tissue Biology Group, Karolinska Institutet, SE-171 77 Stockholm, Sweden
Lars Muhl: Tissue Biology Group, Karolinska Institutet, SE-171 77 Stockholm, Sweden
Barbara C. Fam: University of Melbourne
Henrik Ortsäter: Diabetes Research Unit, Södersjukhuset, Karolinska Institutet
Pierre Scotney: CSL Limited
Daniel Nyqvist: Tissue Biology Group, Karolinska Institutet, SE-171 77 Stockholm, Sweden
Erik Samén: Karolinska University Hospital
Li Lu: Karolinska University Hospital
Sharon Stone-Elander: Karolinska University Hospital
Joseph Proietto: University of Melbourne
Sofianos Andrikopoulos: University of Melbourne
Åke Sjöholm: Diabetes Research Unit, Södersjukhuset, Karolinska Institutet
Andrew Nash: CSL Limited
Ulf Eriksson: Tissue Biology Group, Karolinska Institutet, SE-171 77 Stockholm, Sweden

Nature, 2012, vol. 490, issue 7420, 426-430

Abstract: Inhibition of VEGF-B signalling is shown to limit ectopic fatty-acid accumulation, restore peripheral insulin sensitivity and muscle glucose uptake, and preserve pancreatic islet functionality.

Date: 2012
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DOI: 10.1038/nature11464

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