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,
S. SMITZ and
R.VON FRENCKELL
Psychoneuroendocrinology Sectio Section, CHU, Local 4/12
Clinique Psychiatre, University of Leige B-4000 Liege, Belgium
Universita di Parma, Istituto di Clinica Medica Generale e Terapia Medica 43100 Parma, Italy
Address all correspondence and requests for reprints to: J. J. Legros, M.D., Psychoneuroendocrinology Section, CHU, local 4/12, University of Liege, SartTilman,B-4000 Liege, Belgium.
We previously demonstrated that acute injection of a pharmalogical dose of oxytocin (2 IU) in humans decreased the concentrations of ACTH and cortisol, a neuroendocrine action opposite that of vasopressin. In the present work the effect of continuous infusion of lower doses of oxytocin was tested. Plasma oxytocin was also measured using an oxytoxcin RIA to study the dose–response relation. Infusion of oxytocin (8 mlU/min for 30 min) resulted in a plasma oxytocin level of 9.9 ± 1.4 (±SD) µIU/ml and induced a decrease in the plasma concentration of ACTH in three of four normal subjects. Infusion of oxytocin at the rate of 16 mlU/ml for 30 min resulted in plasma oxytocin level of 17.7 ± 1.6 /IU/ml and decreases in plasma ACTH and cortisol concentrations in all six subjects tested. Increasing the oxytocin dose from 32 to 64 and 128 mlU/ min for three additional 30-min periods induced more pronounced decreases in plasma ACTH and cortisol. In each subject, there was a highly significant inverse relationship between plasma oxytocin, and ACTH and cortisol (r = –0.85 to –0.99). During saline infusion, a significant inverse relationship with a 10-min lag period between plasma oxytocin and ACTH (r = –0.55) was found in only one of six subjects.
These data demonstrate that infusion of exogenous oxytocin leading to plasma levels approximately 10 times higher than normal induced consistant decreases in corticotrope function. Because the oxytocin concentration in portal blood is approximately 300 times higher than that in peripheral blood, it is likely that the inhibitory action of oxytocin on ACTH secretion is of physiological significance.
* This work was supported by grants from the Belgian FRSM and the Fondation Reine Elisabeth. Presented in part at the Meeting of the International Society of Psychoneuroendocrinology, New York, NY, June 14, 1983 (Neuroendocr Lett 5:190,1983).
Received July 27, 1983.
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