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Published on: June 15, 2019
Hypothalamic-pituitary-adrenal axis in lethal canine Staphylococcus aureus pneumonia
Irene Cortés-Puch1, Caitlin W Hicks2, Junfeng Sun3
1Critical Care Medicine Department, Clinical Center, National Institutes of Health, Bethesda, Maryland; irene.cortespuch@nih.gov.
Critical illness-related corticosteroid insufficiency is debated. In canine pneumonia, dexamethasone improved outcomes by modulating the hypothalamic-pituitary-adrenal (HPA) axis, while high aldosterone indicated poor prognosis.
Area of Science:
- Endocrinology
- Critical Care Medicine
- Veterinary Pathology
Background:
- The existence and clinical relevance of critical illness-related corticosteroid insufficiency remain controversial.
- Severe Staphylococcus aureus pneumonia in canines serves as a model to investigate hypothalamic-pituitary-adrenal (HPA) axis function during critical illness.
Purpose of the Study:
- To characterize HPA axis function in severe canine pneumonia.
- To evaluate the impact of dexamethasone and desoxycorticosterone on outcomes.
- To identify HPA axis markers predictive of prognosis in septic shock.
Main Methods:
- Animals received antibiotics and supportive care.
- Serial measurements of cortisol, ACTH, and aldosterone were performed.
- ACTH stimulation tests were conducted.
- Dexamethasone treatment was administered and its effects analyzed.
Main Results:
- Dexamethasone, but not desoxycorticosterone, improved outcomes.
- Early HPA axis stress response (cortisol) was not predictive of outcome.
- Aldosterone levels were elevated longer and associated with survival.
- Dexamethasone suppressed cortisol/ACTH and restored responsiveness in survivors.
- Nonsurvivors exhibited hypercortisolemia, high ACTH, and hyporesponsiveness, unaffected by dexamethasone.
Conclusions:
- HPA axis unresponsiveness and elevated aldosterone identify a septic shock subpopulation with poor prognosis.
- Serial HPA axis measurements and provocative testing are crucial for assessing prognosis.
- This subpopulation may benefit from novel therapeutic strategies.
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