Satiety Hormone Dynamics is the study of the complex temporal release patterns, half-lives, and receptor interactions of the gut and adipose-derived hormones that signal fullness and inhibit food intake. These hormones, including leptin, Peptide YY (PYY), and cholecystokinin (CCK), are crucial regulators of short-term and long-term energy homeostasis. Dysregulation in these dynamics is a central component of pathological overeating and weight gain.
Origin
This field is a modern specialization within endocrinology and metabolism, significantly advanced by the discovery of leptin in the 1990s, which established a hormonal link between fat mass and brain appetite centers. The term emphasizes the dynamic, meal-responsive nature of these signals, contrasting with earlier, static models of appetite control. Its clinical relevance is paramount in developing anti-obesity therapeutics.
Mechanism
The dynamics involve the rapid post-prandial release of anorexigenic peptides from the gut in response to nutrient presence, which then act on receptors in the hindbrain and hypothalamus to terminate the meal. Long-term regulation is mediated by leptin, whose circulating levels reflect adipose tissue mass and modulate the sensitivity of central appetite circuits. The mechanism seeks to optimize the magnitude and duration of these satiety signals to naturally reduce caloric consumption.
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