Circadian activity of the hypothalamic-pituitary-adrenal axis is differentially affected in the rat chronic mild stress model of depression

被引:51
作者
Christiansen, S. [1 ]
Bouzinova, E. V. [1 ]
Palme, R. [2 ]
Wiborg, O. [1 ]
机构
[1] Aarhus Univ Hosp, Ctr Psychiat Res, DK-8000 Aarhus, Denmark
[2] Univ Vet Med, Dept Biomed Sci Biochem, Vienna, Austria
来源
STRESS-THE INTERNATIONAL JOURNAL ON THE BIOLOGY OF STRESS | 2012年 / 15卷 / 06期
关键词
Chronic mild stress; corticosterone; depression; dexamethasone; hypothalamic-pituitary-adrenal axis; stress resilience; CORTICOTROPIN-RELEASING HORMONE; MAJOR DEPRESSION; GLUCOCORTICOID-RECEPTORS; ANTIDEPRESSANT TREATMENT; ENDOGENOUS-DEPRESSION; GROWTH-HORMONE; HPA AXIS; MICE; DEXAMETHASONE; CORTISOL;
D O I
10.3109/10253890.2011.654370
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The altered activity of the hypothalamic-pituitary-adrenal (HPA) axis is often observed in stress-related disorders. According to the literature, about 60% of patients with major depressive disorder elicit high levels of cortisol. It is still unclear why high cortisol levels are not observed in all patients. In this study, we used the chronic mild stress (CMS) rat model of depression, which is based on continuous exposure to unpredictable stressors, to track longitudinal changes in HPA function using fecal corticosterone metabolites (FCM) as a read out. The dexamethasone suppression test was used to assess negative feedback inhibition of the HPA axis. Our results show (1) a disturbance in diurnal corticosterone rhythm measured as fluctuations of the diurnal FCM peak, (2) differences in corticosterone levels between stress-susceptible and stress-resilient animals, (3) recovery of diurnal corticosterone rhythm after 8 weeks of CMS, and (4) alterations in sensitivity to dexamethasone in negative feedback regulation of corticosterone secretion during the time course of CMS. Thus, a disruption of HPA axis circadian rhythmicity coincides with the initial state in the development of depression-like behavior. This chronobiological abnormality, as well as the hypersecretion of corticosterone, is state, rather than trait, dependent.
引用
收藏
页码:647 / 657
页数:11
相关论文
共 42 条
[1]  
[Anonymous], 1963, DISTRIBUTION FREE MU
[2]  
Antonijevic I A, 2000, Sleep Res Online, V3, P15
[3]   HPA axis and sleep: Identifying subtypes of major depression [J].
Antonijevic, Irina .
STRESS-THE INTERNATIONAL JOURNAL ON THE BIOLOGY OF STRESS, 2008, 11 (01) :15-27
[4]   ASSOCIATIONS AMONG DEXAMETHASONE NON-SUPPRESSION AND TRH-INDUCED HORMONAL RESPONSES - INCREASED SPECIFICITY FOR MELANCHOLIA [J].
BANKI, CM ;
ARATO, M ;
PAPP, Z ;
RIHMER, Z ;
KOVACS, Z .
PSYCHONEUROENDOCRINOLOGY, 1986, 11 (02) :205-211
[5]   COLD-RESTRAINT STRESS INCREASES RAT FECAL PELLET OUTPUT AND COLONIC TRANSIT [J].
BARONE, FC ;
DEEGAN, JF ;
PRICE, WJ ;
FOWLER, PJ ;
FONDACARO, JD ;
ORMSBEE, HS .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 258 (03) :G329-G337
[6]  
Barrett EJ, 2009, MED PHYSL, P1003
[7]   Characterization and functional significance of glucocorticoid receptors in patients with major depression: modulation by antidepressant treatment [J].
Calfa, G ;
Kademian, S ;
Ceschin, D ;
Vega, G ;
Rabinovich, GA ;
Volosin, M .
PSYCHONEUROENDOCRINOLOGY, 2003, 28 (05) :687-701
[8]   RESPONSE TO DEXAMETHASONE IN PSYCHOTIC DEPRESSION [J].
CAROFF, S ;
WINOKUR, A ;
RIEGER, W ;
SCHWEIZER, E ;
AMSTERDAM, J .
PSYCHIATRY RESEARCH, 1983, 8 (01) :59-64
[9]   CLINICAL-APPLICATIONS OF THE DEXAMETHASONE SUPPRESSION TEST FOR ENDOGENOUS-DEPRESSION [J].
CARROLL, BJ .
PHARMACOPSYCHIATRIA, 1982, 15 (01) :19-24
[10]  
Checkley S, 1996, BRIT MED BULL, V52, P597