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Atrial natriuretic peptide induces postprandial lipid oxidation in man

  1. Andreas L. Birkenfeld, M.D.1,2,
  2. Petra Budziarek1,
  3. Michael Boschmann, M.D.1,
  4. Cedric Moro, Ph.D.3,
  5. Frauke Adams, Ph.D.1,
  6. Gabriele Franke1,
  7. Michel Berlan, M.D.3,
  8. Marie A. Marques3,
  9. Fred C.G.J. Sweep, M.D.4,
  10. Friedrich C. Luft, M.D.1,
  11. Max Lafontan, Sc.D., Ph.D.3 and
  12. Jens Jordan, M.D. (jordan.jens{at}mh-hannover.de)5
  1. 1Experimental and Clinical Research Center, Medical Faculty of the Charité and HELIOS-Klinikum, Berlin, Germany
  2. 2Dept of Internal Medicine, Yale University School of Medicine, New Haven, CT, USA
  3. 3Inserm Unité 858, Institut de Médecine Moléculaire de Rangueil, & Université Paul Sabatier, Toulouse, France
  4. 4Department of Chemical Endocrinology, Radboud University Nijmegen Medical Centre, the Netherlands
  5. 5Institute of Clinical Pharmacology, Hannover Medical School,Hannover, Germany

    Abstract

    Objective. Atrial natriuretic peptide (ANP) regulates arterial blood pressure. In addition, ANP has recently been shown to promote human adipose tissue lipolysis through cGMP-mediated hormone sensitive lipase activation. We hypothesized that ANP increases postprandial free fatty acid availability and energy expenditure, while decreasing arterial blood pressure.

    Research Design and Methods. We infused human ANP (25 ng/kg/min) in 12 men (age 32±0.8 years, body mass index 23.3±0.4 kg/m2) before, during, and 2 h after ingestion of a standardized high-fat test meal in a randomized, double blind, cross-over fashion. Cardiovascular changes where monitored by continuous ECG and beat-by-beat blood pressure recordings. Metabolism was monitored through venous blood sampling, intramuscular and subcutaneous abdominal adipose tissue microdialysis, and indirect calorimetry.

    Results. ANP infusion decreased mean arterial blood pressure by 4 mmHg during the postprandial phase (p<0.01 vs placebo). At the same time, ANP induced lipolysis systemically (p<0.05 vs placebo) and locally in subcutaneous abdominal adipose tissue (p<0.0001 vs placebo), leading to a 50% increase in venous glycerol (p<0.01) and free fatty acid (FFA) (p<0.05) concentrations compared to placebo. The increase in FFA availability with ANP was paralleled by a 15% increase in lipid oxidation rates (p<0.05 vs placebo), driving a substantial increase in postprandial energy expenditure (p<0.05 vs placebo).

    Conclusions. Our data identifies the ANP system as a novel pathway regulating postprandial lipid oxidation, energy expenditure, and concomitantly arterial blood pressure. The findings could have therapeutic implications.

    Footnotes

      • Received May 15, 2008.
      • Accepted September 16, 2008.

    This Article

    1. Diabetes October 3, 2008
    1. » Abstract
    2. All Versions of this Article:
      1. db08-0649v1
      2. 57/12/3199 most recent

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