Cortisol-dependent stress effects on cell distribution in healthy individuals and individuals suffering from chronic adrenal insufficiency

Research output: Contribution to journal › Research article › Contributed › peer-review

Contributors

  • Ashley M. Geiger - , Brandeis University (Author)
  • Kenneth P. Pitts - , Brandeis University (Author)
  • Joachim Feldkamp - , Central Hospital Bielefeld (Author)
  • Clemens Kirschbaum - , Chair of Biopsychology (Author)
  • Jutta M. Wolf - , Brandeis University (Author)

Abstract

Chronic adrenal insufficiency (CAI) is characterized by a lack of glucocorticoid and mineralocorticoid production due to destroyed adrenal cortex cells. However, elevated cortisol secretion is thought to be a central part in a well-orchestrated immune response to stress. This raises the question to what extent lack of cortisol in CAI affects stress-related changes in immune processes.To address this question, 28 CAI patients (20 females) and 18 healthy individuals (11 females) (age: 44.3 ± 8.4 years) were exposed to a psychosocial stress test (Trier Social Stress Test: TSST). Half the patients received a 0.03 mg/kg body weight injection of hydrocortisone (HC) post-TSST to mimic a healthy cortisol stress response. Catecholamines and immune cell composition were assessed in peripheral blood and free cortisol measured in saliva collected before and repeatedly after TSST.CAI patients showed norepinephrine (NE) stress responses similar to healthy participants, however, epinephrine (E) as well as cortisol levels were significantly lower. HC treatment post-TSST resulted in cortisol increases comparable to those observed in healthy participants (interaction effects - NE: F = 1.05, p = .41; E: F = 2.56, p = .045; cortisol: F = 13.28, p < .001). Healthy individuals showed the expected pattern of stress-related early lymphocyte increase with subsequent decrease below baseline. The opposite pattern was observed in granulocytes. While exhibiting a similar initial increase, lymphocytes kept increasing over the following 2 h in untreated patients. HC treatment buffered this effect (interaction effects - lymphocyte%: F = 7.31, p < .001; granulocyte%: F = 7.71, p < .001).Using CAI in humans as a model confirms cortisol's central involvement in post-stress lymphocyte migration from blood into immune-relevant body compartments. As such, future studies should investigate whether psychosocial stress exposure may put CAI patients at an increased health risk due to attenuated immune responses to pathogens.

Details

Original languageEnglish
Pages (from-to)241-248
Number of pages8
JournalBrain, behavior, and immunity
Volume50
Publication statusPublished - 1 Nov 2015
Peer-reviewedYes

External IDs

PubMed 26184081

Keywords

Keywords

  • Catecholamines, Cell trafficking, Chronic adrenal insufficiency, Cortisol, Psychosocial stress