The comprehensive study of how the entire organism responds to and integrates various forms of physiological and psychological stress, viewing the response as a complex, interconnected network rather than a linear cascade. This approach uses high-throughput data and computational models to map the interactions between the neuroendocrine, immune, and metabolic systems during periods of acute and chronic stress. Understanding this biology is crucial for developing personalized strategies to maintain allostasis, the process of achieving stability through physiological change.
Origin
The term is a fusion of “systems biology,” a discipline that models biological processes as complex networks, and the classic physiological concept of “stress,” introduced by Hans Selye in the 1930s. The modern clinical application of this framework recognizes that chronic stress leads to allostatic overload, driving a wide range of chronic diseases. This holistic view provides a deeper understanding of the body’s resilience and vulnerability.
Mechanism
The core mechanism involves the rapid activation of the Hypothalamic-Pituitary-Adrenal (HPA) axis and the sympathetic nervous system. The systems biology approach models how these primary signals interact with and modulate the immune system via glucocorticoid receptors and catecholamine signaling. Chronic activation leads to network changes, such as HPA axis dysregulation, insulin resistance, and a shift toward a pro-inflammatory immune phenotype, demonstrating the profound, interconnected effects of sustained allostatic load on systemic health.
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