The characteristic, highly rhythmic secretion pattern of Growth Hormone (GH) that occurs predominantly during the hours of sleep, specifically peaking during the deepest stages of Non-REM sleep. This pulsatility is the single largest secretory event of GH in a 24-hour cycle and is critical for driving systemic repair, cellular regeneration, and metabolic regulation. Diminished pulsatility is a clinical feature of somatopause, or age-related GH decline.
Origin
This term is a core concept in neuroendocrinology, established through early 20th-century studies that utilized frequent blood sampling across the sleep-wake cycle. The discovery of the strong correlation between GH release and Slow-Wave Sleep provided a functional link between sleep architecture and the anabolic drive. It belongs to the study of the hypothalamic-pituitary-somatotropic axis.
Mechanism
The pulsatile release is controlled by the hypothalamic interplay between Growth Hormone-Releasing Hormone (GHRH), which stimulates release, and somatostatin, which inhibits it. During deep sleep, the central nervous system reduces somatostatin tone and increases GHRH secretion, resulting in a large, high-amplitude pulse of GH. This nocturnal surge then triggers the downstream production of Insulin-like Growth Factor 1 (IGF-1) in the liver, initiating widespread anabolic and regenerative effects throughout the body.
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