Human Glucocorticoid Feedback Inhibition Is Reduced in Older Individuals: Evening Study1
We have previously shown that when tested in the morning, older men and women, pretreated with metyrapone to block endogenous cortisol synthesis, exhibit delayed suppression of plasma ACTH in response to cortisol infusion. To confirm this finding and to determine whether aging-related changes in fee...
Gespeichert in:
Veröffentlicht in: | The journal of clinical endocrinology and metabolism 2001-02, Vol.86 (2), p.545-550 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | We have previously shown that when tested in the morning, older men and
women, pretreated with metyrapone to block endogenous cortisol
synthesis, exhibit delayed suppression of plasma ACTH in response to
cortisol infusion. To confirm this finding and to determine whether
aging-related changes in feedback responsiveness are exaggerated near
the time of the circadian nadir in adrenocortical secretion, we
performed a similar study in the evening. Healthy young (20–35 yr,
n = 22) and old (>65 yr, n = 21) men and women were
administered metyrapone orally (750 mg) at 1600 and 1900 h,
followed by a cortisol infusion of 0.06 mg/kg/h for 150 min. Blood
samples were taken at 15-min intervals for 4 h following infusion
onset for measurement of plasma ACTH, cortisol, 11-deoxycortisol, and
corticosteroid binding globulin. When corrections were made for
differences in circulating cortisol concentrations achieved
among age and gender subgroups, feedback inhibition of ACTH was found
to be significantly greater in young than in old subjects of both
genders. Our studies support the hypothesis that glucocorticoid
responses to stress in aging individuals are likely to be prolonged due
to blunted and delayed inhibition of ACTH secretion, thus increasing
the total exposure to glucocorticoids. |
---|---|
ISSN: | 0021-972X 1945-7197 |
DOI: | 10.1210/jcem.86.2.7232 |