Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 1979;1(4):285-92.
doi: 10.1016/0192-0561(79)90004-3.

Differential potencies of corticosterone and hydrocortisone in immune and immune-related processes in the mouse

Comparative Study

Differential potencies of corticosterone and hydrocortisone in immune and immune-related processes in the mouse

H Van Dijk et al. Int J Immunopharmacol. 1979.

Abstract

The effects of corticosterone and hydrocortisone on the thymus, the pituitary--adrenal axis, delayed hypersensitivity, the corticosterone plasma level and the numbers of circulating nucleated and monocytic cells were investigated in the mouse. Short-term effects within 48 h after one or two corticoid injections and late effects 7 days after a regimen of 4 corticoid injections were discerned. In short-term experiments hydrocortisone was more active than corticosterone upon the induction of leukopenia and monocytopenia and the inhibition of delayed hypersensitivity. However, regarding late effects and the short-term effect on adrenal weight, corticosterone far exceeded hydrocortisone in activity. Our results could be explained by assuming two feedback-inhibition systems for glycocorticoids. The first, likely to be responsible for the changes observed for the adrenal weight and the numbers of ciruclating white cells after a single glucocorticoid injection, was shown to be expressed in a soluble factor released in the blood stream tentatively designated "glucocorticoid inhibiting factor. The factor was more readily induced by hydrocortisone but displayed a greater specificity in inhibiting effects of corticosterone. The second feedback-inhibition system, responsible for increased numbers of circulating monocytes paralleled by an enhanced delayed hypersensitivity response, was expressed in a decreased corticosterone plasma level, most probably secondary to a diminished release of ACTH from the pituitary gland. With the glucocorticoid doses we used the second feedback-inhibition system was only triggered by the more physiological hormone, corticosterone.

PubMed Disclaimer

Similar articles

Cited by

Publication types

LinkOut - more resources