Continuous un-gated operational inputs cause persistent neuroendocrine activation, downregulating cellular receptors and forcing biological throttling.
Biological throttling down-regulates executive capacity to shield metabolic reserves under continuous load, unlike depression which impairs affect globally.
Flattened diurnal cortisol curves reflect chronic endocrine adaptation that degrades prefrontal cortex working memory headroom and executive control.
System throttling is an adaptive physiological down-regulation caused by allostatic overload, distinct from clinical depression's neurochemical failure.
Operational transfer protocols automate the migration of critical executive authority to secondary roles when physical strain breaches defined baseline thresholds.
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