Effect of the glucocorticoid receptor antagonist Org 34850 on basal and stress-induced corticosterone secretion

被引:43
作者
Spiga, F.
Harrison, L. R.
Wood, S. A.
Atkinson, H. C.
MacSweeney, C. P.
Thomson, F.
Craighead, M.
Grassie, M.
Lightman, S. L.
机构
[1] Univ Bristol, Henry Wellcome Labs Integrat Neurosci & Endocrino, Bristol BS1 3NY, Avon, England
[2] Oraganon Labs Ltd, Dept Pharmacol, Newhouse, Lanark, Scotland
[3] Oraganon Labs Ltd, Dept Mol Pharmacol, Newhouse, Lanark, Scotland
关键词
glucocorticoids; corticosterone; glucocorticoid receptor antagonist; depression; stress;
D O I
10.1111/j.1365-2826.2007.01605.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The activity of the hypothalamic-pituitary-adrenal (HPA) axis is characterised both by an ultradian pulsatile pattern of glucocorticoid secretion and an endogenous diurnal rhythm. Glucocorticoid feedback plays a major role in regulating HPA axis activity and this mechanism occurs via two different receptors: mineralocorticoid (MR) and glucocorticoid receptors (GR). In the present study, the effects of both acute and subchronic treatment with the GR antagonist Org 34850 on basal and stress-induced HPA axis activity in male rats were evaluated. To investigate the effect of Org 34850 on basal diurnal corticosterone rhythm over the 24-h cycle, an automated blood sampling system collected samples every 10 min. Acute injection of Org 34850 (10 mg/kg, s.c.) did not affect basal or stress-induced corticosterone secretion, but was able to antagonise the inhibitory effect of the glucocorticoid agonist methylprednisolone on stress-induced corticosterone secretion. However, 5 days of treatment with Org 34850 (10 mg/kg, s.c., two times a day), compared to rats treated with vehicle (5% mulgofen in 0.9% saline, 1 ml/kg, s.c.), increased corticosterone secretion over the 24-h cycle and resulted in changes in the pulsatile pattern of hormone release, but had no significant effect on adrenocorticotrophic hormone secretion or on stress-induced corticosterone secretion. Subchronic treatment with Org 34850 did not alter GR mRNA expression in the hippocampus, paraventricular nucleus of the hypothalamus or anterior-pituitary, or MR mRNA expression in the hippocampus. Our data suggest that a prolonged blockade of GRs is required to increase basal HPA axis activity. The changes observed here with ORG 34850 are consistent with inhibition of GR-mediated negative feedback of the HPA axis. In light of the evidence showing an involvement of dysfunctional HPA axis in the pathophysiology of depression, Org 34850 could be a potential treatment for mood disorders.
引用
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页码:891 / 900
页数:10
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