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Negative endocrine control system for inflammation in rats
Authors:Dr. V. I. Stenberg  M. G. Bouley  B. M. Katz  K. J. Lee  S. S. Parmar
Affiliation:(1) Department of Chemistry, The University of North Dakota, Box 7185, 58202 Grand Forks, ND, USA
Abstract:Inflammatory processes may be suppressed by endogenous mechanisms such as release of adrenocorticosteroid hormones through stimulation of the hypothalamus-pituitary-adrenal axis. In the present study, the relationship between the temporal development of carrageenan-induced edema in the hindlimb of the rat and release in plasma of the principal endogenous adrenocorticosteroid of the rat corticosterone was investigated. Suplantar injection of carrageenan produced a biphasic increase in basal plasma corticosterone levels that was not attributed to diurnal variation. The plasma level of corticosterone increased rapidly after injection of carrageenan and peaked 12-fold at 20 min. This first phase increase was attributed to the stress of the injection since it was mimicked by subplantar injection of saline. The second phase of corticosterone relase was gradual and peaked 12-fold 7hr after injection of carrageenan. The second phase was not elicited by subplantar injection of saline. When the hypothalamus-pituitary-adrenal axis is impaired via hypophysectomy, carrageenan-induced edema is more intense and lasts longer than in control rats. The results demonstrate that adrenocorticosteroid hormones are released as a result of the stress of injection and by the inflammatory response. Release of adrenocorticosteroids acts as a feedback mechanism to suppress the inflammatory response.The reader is directed to two excellent, complimentary, pertinent journal articles which have appeared since this article was submitted for publication: E. M. Sternberg, J. M. Hill, G. P. Chrousos, T. Kamilaris, S. J. Listwak, P. W. Gold and R. L. Wilder,Inflammatory Mediator-induced hypothalamic-pituitary-adrenal axis activation is defective in streptococcal cell wall arthritis-susceptible Lewis rats. Proc. Natl. Acad. Sci.86, 2374–2378 (1989) and E. M. Sternberg, W. S. Young, R. Bernardini, A. E. Calogers, G. P. Chrousos, P. W. Gold and R. L. Wilder, A central nervous system defect in biosynthesis of corticotropin-releasing hormone is associated with susceptibility to streptococcal cell wall-induced arthritis in Lewis rats. Proc. Natl. Acad. Sci.86, 4771–4775 (1989).
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