Stress models of depression

被引:84
作者
Vollmayr, B [1 ]
Henn, FA [1 ]
机构
[1] Cent Inst Mental Hlth, D-68159 Mannheim, Germany
关键词
animal model; major depression; learned helplessness; chronic mild stress; anhedonia; rats; mice;
D O I
10.1016/S1566-2772(03)00086-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In order to understand the molecular changes underlying major depression animal models are needed. The best animal model of depression simulates the etiology and replicates symptoms, course and treatment of human depression. This article reviews the two most valid and best established animal models of depression, learned helplessness and chronic mild stress. Both models use uncontrollable stress to induce depressive like behavior, both have excellent face validity and replicate anhedonia and anergia in analogy to loss of interest and pleasure, one of two essential features of depression. In addition, both models demonstrate a variety of less specific symptoms like changes in locomotion, impaired learning ability, sleep alterations, loss of weight and decrease of sexual behavior. Endocrine disturbances of major depression as hypercortisolemia and dexamethasone non-suppression are also simulated in the two animal models. Neurobiological changes accompanying the depressive like behavior include dynamic changes of the monoamine systems and several peptide systems including the opioid system. Behavioral and neurobiological changes can be renormalized in both models by antidepressant treatment, which adds predictive validity to these models. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:245 / 251
页数:7
相关论文
共 75 条
[1]   CROSS-STRESSOR IMMUNIZATION AGAINST THE BEHAVIORAL DEFICITS INTRODUCED BY UNCONTROLLABLE SHOCK [J].
ANISMAN, H ;
IRWIN, J ;
BEAUCHAMP, C ;
ZACHARKO, R .
BEHAVIORAL NEUROSCIENCE, 1983, 97 (03) :452-461
[2]   DEPRESSION AS A CONSEQUENCE OF INADEQUATE NEUROCHEMICAL ADAPTATION IN RESPONSE TO STRESSORS [J].
ANISMAN, H ;
ZACHARKO, RM .
BRITISH JOURNAL OF PSYCHIATRY, 1992, 160 :36-43
[3]   EFFECTS OF CHRONIC MILD STRESS ON SERUM COMPLEMENT ACTIVITY, SACCHARIN PREFERENCE, AND CORTICOSTERONE LEVELS IN FLINDERS LINES OF RATS [J].
AYENSU, WK ;
PUCILOWSKI, O ;
MASON, GA ;
OVERSTREET, DH ;
REZVANI, AH ;
JANOWSKY, DS .
PHYSIOLOGY & BEHAVIOR, 1995, 57 (01) :165-169
[4]  
Bertrand E, 1997, NEUROSCIENCE, V80, P17
[5]   A second look at comorbidity in victims of trauma: The posttraumatic stress disorder-major depression connection [J].
Breslau, N ;
Davis, GC ;
Peterson, EL ;
Schultz, LR .
BIOLOGICAL PSYCHIATRY, 2000, 48 (09) :902-909
[6]   EVIDENCE FOR A SEROTONERGIC MECHANISM OF THE LEARNED HELPLESSNESS PHENOMENON [J].
BROWN, L ;
ROSELLINI, RA ;
SAMUELS, OB ;
RILEY, EP .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1982, 17 (05) :877-883
[7]   Finding the intracellular signaling pathways affected by mood disorder treatments [J].
Coyle, JT ;
Duman, RS .
NEURON, 2003, 38 (02) :157-160
[8]   Diurnal variation in the effect of chronic mild stress on sucrose intake and preference [J].
DAquila, PS ;
Newton, J ;
Willner, P .
PHYSIOLOGY & BEHAVIOR, 1997, 62 (02) :421-426
[9]   EFFECTS OF CHRONIC MILD STRESS ON PERFORMANCE IN BEHAVIORAL-TESTS RELEVANT TO ANXIETY AND DEPRESSION [J].
DAQUILA, PS ;
BRAIN, P ;
WILLNER, P .
PHYSIOLOGY & BEHAVIOR, 1994, 56 (05) :861-867
[10]   Neuronal plasticity and survival in mood disorders [J].
Duman, RS ;
Malberg, J ;
Nakagawa, S ;
D'Sa, C .
BIOLOGICAL PSYCHIATRY, 2000, 48 (08) :732-739