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PMID: 2142692 Published · ppublish English Journal Article

Restraint stress-induced elevations in plasma corticosterone and beta-endorphin are not accompanied by alterations in immune function.

Journal of neuroimmunology ·Vol. 28 ·No. 3 ·1990-08-00 ·Pages 219-25

Flores CM, Hernandez MC, Hargreaves KM, Bayer BM

Abstract

A variety of stressors activate the hypothalamic-pituitary-adrenal (HPA) axis, thereby resulting in elevated levels of circulating ACTH, beta-endorphin and corticosterone. Since these hormones have been shown previously to alter measures of immune function, we determined whether presentation of a stressor which activates the HPA axis produces a concomitant alteration in immune function. Restraint stress resulted in significantly elevated levels of corticosterone and beta-endorphin without affecting either proliferative or cytolytic activities of lymphocytes. At concentrations similar to those achieved during stress, in vivo, corticosterone exhibited a dose- and time-dependent reduction in both lymphocyte proliferation as well as natural killer cytotoxicity, in vitro. beta-Endorphin, on the other hand, was without direct or modulatory effects. These results indicate that restraint stress-induced activation of the HPA axis occurs without accompanying alterations in immune function.

MeSH Terms
Animals Corticosterone/blood,pharmacology Hypothalamo-Hypophyseal System Killer Cells, Natural/immunology Lymphocyte Activation/drug effects Male Pituitary-Adrenal System Rats Rats, Inbred Strains Restraint, Physical Stress, Physiological/blood,immunology beta-Endorphin/blood,pharmacology
Chemicals
beta-Endorphin Corticosterone
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Flores C M
Department of Pharmacology, Georgetown University Medical Center, Washington, DC 20007.
Hernandez M C
Hargreaves K M
Bayer B M
Article Info
Journal
Journal of neuroimmunology
Abbr.
J Neuroimmunol
ISSN
0165-5728
Published
1990-08-00
Pages
219-25
Language
English
Region
Netherlands
NLM ID
8109498
Subset
IM
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