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 Ϯ 0.4 leptin pulses/12 h. Leptin secretion correlated highly with total body fat (r ϭ 0.78, P Ͻ 0.001) and regional fat depots. In contrast, leptin pulsatility did not correlate with total fat (r ϭ 0.07, P ϭ 0.785) or other measures of fat. There was synchronicity between GH and leptin (lag Ϫ39 minutes), cortisol and leptin (lag Ϫ211 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 Ϯ 0.030), cortisol (0.891 Ϯ 0.023), and insulin (0.868 Ϯ 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 LEPTIN, AN ADIPOCYTE-DERIVED HORMONE, has been implicated in the regulation of food intake, metabolism, and neuroendocrine function (2, 39). Circulating leptin concentrations are highly correlated to weight and body fat in animals and humans (39), suggesting that leptin is an important component of a complex neuroendocrine signaling system to sense and effect changes in overall nutritional status (2). For example, leptin deficiency (undernutrition) results in hyperphagia and reduced energy metabolism, whereas leptin excess (overnutrition) results in hypophagia and increased energy metabolism (14). Moreover, nutritionally mediated changes in leptin significantly affect neuroendocrine function. Leptin administration blunts food deprivation-induced hypercortisolemia, hypothyroidism, and hypogonadism in animals (2). Plasma leptin levels are inversely related to those of ACTH in young men (20) and display pattern synchrony with those of luteinizing hormone and estradiol in young women (21). In addition, leptin is related to growth hormone (GH), and GH replacement may increase leptin pulsatility (3, 31). Furthermore, insulin has been implicated in the physiological regulation of leptin independently of changes in body compositio...