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Am J Physiol Endocrinol Metab 285: E372-E379, 2003. First published April 29, 2003; doi:10.1152/ajpendo.00097.2003
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Characterization of leptin pulse dynamics and relationship to fat mass, growth hormone, cortisol, and insulin

Polyxeni Koutkia,1 Bridget Canavan,1 Michael L. Johnson,2 Alex DePaoli,3 and Steven Grinspoon1

1Program in Nutritional Metabolism and Neuroendocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114; 2Pharmacology Department, University of Virginia Health Sciences Center, Charlottesville, Virginia 22908; and 3Amgen, Inc., Thousand Oaks, California 91320

Submitted 5 March 2003 ; accepted in final form 23 April 2003

To investigate the regulation of leptin secretion and pulsatility by fat mass, we performed overnight leptin sampling every 20 min for 12 h and compared leptin dynamics with total body and regional fat measurements in 20 healthy male subjects. Simultaneous growth hormone (GH), cortisol, and insulin levels were assessed to determine relatedness and synchronicity during overnight fasting. Deconvolution analyses were performed to determine simultaneous hormonal dynamics, synchronicity, and interrelatedness using cross-correlation and cross-approximate entropy (X-ApEn) analyses. Subjects demonstrated 4.7 ± 0.4 leptin pulses/12 h. Leptin secretion correlated highly with total body fat (r = 0.78, P < 0.001) and regional fat depots. In contrast, leptin pulsatility did not correlate with total fat (r = 0.07, P = 0.785) or other measures of fat. There was synchronicity between GH and leptin (lag -39 minutes), cortisol and leptin (lag -211 min), and leptin and insulin, with leptin following insulin by 275 min. The mean random X-ApEn was significant between leptin and GH (0.854 ± 0.030), cortisol (0.891 ± 0.023), and insulin (0.868 ± 0.034), demonstrating a high degree of regularity and pattern frequency. These data demonstrate differential regulation of leptin secretion and pulsatility in adipocytes and suggest that the leptin pulse generator is extrinsic to fat, whereas fat mass acts as an amplifier to modulate secretion and amplitude for a given pulsatility. We demonstrate synchronicity between leptin and GH, cortisol, and insulin. The directionality of the cross correlation suggests a temporal construct in which changes in leptin follow those of insulin but precede those of GH and cortisol during overnight fasting.

subcutaneous fat; abdominal fat; synchronicity; pulsatility; cross-approximate entropy



Address for reprint requests and other correspondence: S. Grinspoon, Program in Nutritional Metabolism, Massachusetts General Hospital, Lon 207, 55 Fruit St., Boston, MA 02114 (E-mail: sgrinspoon{at}partners.org).




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