Homeostatic Correction During Severe Physiologic Stress: A Phase-Specific Model for GC-GRα-Coordinated Organism-Wide Adaptation.
- 1Department of Medicine and Pharmaceutical Sciences, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
- 2Institut d'Investigacions Biomédiques August Pi i Sunyer (IDIBAPS), University of Barcelona, CIBERES, 08036 Barcelona, Spain.
- 3Centro de Investigación Biomédica en Red de Enfermedades Respiratorias (CIBERES), 28029 Madrid, Spain.
Abstract
Critical illness is increasingly recognized as a disorder of disrupted systemic homeostasis rather than simply a consequence of maladaptive systemic inflammation or isolated organ failure. Although researchers have extensively investigated adaptive biologic responses to severe physiologic stress, far less attention has been paid to the integrative mechanisms that coordinate these responses across multiple organ systems throughout the course of illness. This review synthesizes current evidence from systems biology, immunology, endocrinology, network physiology, and critical care to present a systems-level conceptual model of homeostatic correction that explains how coordinated adaptive biologic programs restore organismal homeostasis after severe physiologic stress. The model organizes these responses into three dynamic, partially overlapping phases: Priming, which establishes adaptive readiness and immediate survival responses; Modulatory, which limits excessive activation while preserving essential host-defense and physiologic functions; and Restorative, which promotes resolution, tissue repair, regenerative recovery, and the restoration of integrated organ-system function. In this model, glucocorticoid-glucocorticoid receptor alpha (GC-GRα) signaling serves as a central integrative regulator coordinating immune, neuroendocrine, metabolic, mitochondrial, vascular, epithelial, lymphatic, microbiome, and regenerative adaptive biologic programs through context-, tissue-, and phase-specific mechanisms. Rather than acting solely as an anti-inflammatory pathway, GC-GRα signaling functions as a dynamic, systems-level regulator coordinating adaptive capacity, inter-organ communication, disease tolerance, tissue protection, and recovery while preserving essential host-defense functions. The proposed model shifts the focus from isolated pathophysiologic abnormalities to understanding critical illness as a disorder of disrupted organism-wide adaptive coordination. It provides a biologically organized foundation for investigating adaptive capacity, identifying phase-specific biomarkers, and developing precision therapeutic strategies to restore homeostatic resilience across acute and chronic disease states.
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BibTeX
@article{meduri2026homeostatic,
title = {{Homeostatic Correction During Severe Physiologic Stress: A Phase-Specific Model for GC-GRα-Coordinated Organism-Wide Adaptation.}},
author = {Gianfranco Umberto Meduri and Antoni Torres},
journal = {Medical sciences (Basel, Switzerland)},
year = {2026},
month = oct,
doi = {10.3390/medsci14060638},
url = {https://europepmc.org/article/MED/42930557},
note = {CC BY},
}
RIS
TY - JOUR
TI - Homeostatic Correction During Severe Physiologic Stress: A Phase-Specific Model for GC-GRα-Coordinated Organism-Wide Adaptation.
AU - Gianfranco Umberto Meduri
AU - Antoni Torres
PY - 2026
DA - 2026/10/04
JO - Medical sciences (Basel, Switzerland)
DO - 10.3390/medsci14060638
UR - https://europepmc.org/article/MED/42930557
AB - Critical illness is increasingly recognized as a disorder of disrupted systemic homeostasis rather than simply a consequence of maladaptive systemic inflammation or isolated organ failure. Although researchers have extensively investigated adaptive biologic responses to severe physiologic stress, far less attention has been paid to the integrative mechanisms that coordinate these responses across multiple organ systems throughout the course of illness. This review synthesizes current evidence from systems biology, immunology, endocrinology, network physiology, and critical care to present a systems-level conceptual model of homeostatic correction that explains how coordinated adaptive biologic programs restore organismal homeostasis after severe physiologic stress. The model organizes these responses into three dynamic, partially overlapping phases: Priming, which establishes adaptive readiness and immediate survival responses; Modulatory, which limits excessive activation while preserving essential host-defense and physiologic functions; and Restorative, which promotes resolution, tissue repair, regenerative recovery, and the restoration of integrated organ-system function. In this model, glucocorticoid-glucocorticoid receptor alpha (GC-GRα) signaling serves as a central integrative regulator coordinating immune, neuroendocrine, metabolic, mitochondrial, vascular, epithelial, lymphatic, microbiome, and regenerative adaptive biologic programs through context-, tissue-, and phase-specific mechanisms. Rather than acting solely as an anti-inflammatory pathway, GC-GRα signaling functions as a dynamic, systems-level regulator coordinating adaptive capacity, inter-organ communication, disease tolerance, tissue protection, and recovery while preserving essential host-defense functions. The proposed model shifts the focus from isolated pathophysiologic abnormalities to understanding critical illness as a disorder of disrupted organism-wide adaptive coordination. It provides a biologically organized foundation for investigating adaptive capacity, identifying phase-specific biomarkers, and developing precision therapeutic strategies to restore homeostatic resilience across acute and chronic disease states.
SN - 2076-3271
ER -