Multifaceted strain-specific effects in a mouse model of depression and of antidepressant reversal

被引:98
作者
Ibarguen-Vargas, Yadira [1 ,2 ]
Surget, Alexandre [1 ,2 ]
Touma, Chadi [3 ]
Palme, Rupert [4 ]
Belzung, Catherine [1 ,2 ]
机构
[1] Univ Tours, Fac Sci & Tech, F-37200 Tours, France
[2] INSERM, CNRS, U930, FRE 2448, Tours, France
[3] Max Planck Inst Psychiat, Dept Behav Neuroendocrinol, D-80804 Munich, Germany
[4] Univ Vet Med, Dept Nat Sci, Inst Biochem, Vienna, Austria
关键词
Inbred mouse strains; Unpredictable chronic mild stress; Imipramine; Corticosterone; HPA axis; Novelty-suppressed feeding;
D O I
10.1016/j.psyneuen.2008.07.010
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Etiopathogenesis of depression and the cause of insensitivity to treatment remain poorly understood, although genetic makeup has been established as a contributing factor. The isogenicity of inbred mouse strains provides a useful toot for investigating the link between genes and behavior or drug response. Hence, our aim was to identify inbred mouse strains (among A/J, BALB/c, C3H, C57BL/6, CBA, DBA and FVB) sensitive to a 9-week period of unpredictable chronic mild stress (UCMS) and, from the fifth week onward, to the reversal effect of an antidepressant (AD) (imipramine, 20 mg/kg/day i.p.) on various depression-related changes: physical, behavioral and neuroendocrine states. UCMS induced a significant deterioration of the coat state (in all the strains), blunted emotional reactivity in the novelty-suppressed feeding (NSF) test (A/J, BALB/c, C57BL/6), and changes in the level of fecal corticosterone metabolites (BALB/c, C57BL/6, DBA, FVB). Imipramine treatment reversed the UCMS-induced alterations of the coat state (BALB/c, DBA), in the NSF test (A/J, BALB/c, C57BL/6) and in fecal corticosterone metabolites (BALB/c, C57BL/6). C3H, CBA and FVB mice were irresponsive to imipramine treatment. It is noteworthy that UCMS-induced physical or behavioral changes occurred without hypothalamo-pituitary-adrenal (HPA) axis alterations in some strains (A/J, C3H, CBA), although the AD-induced reversal of these changes in BALB/c and C57BL/6 was associated with HPA axis normalization. Finally, UCMS is shown to discriminate various alterations and to replicate in a strain-dependent manner diverse profiles reminiscent of human disease subtypes. UCMS may thus enable the selection of strains suitable for investigating specific depression-related features and could be an appropriate model for identifying genetic factors associated with increased vulnerability, specific symptoms of affective disorders, and AD resistance. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1357 / 1368
页数:12
相关论文
共 47 条
[1]
Blockade of CRF1 or V1b receptors reverses stress-induced suppression of neurogenesis in a mouse model of depression [J].
Alonso, R ;
Griebel, G ;
Pavone, G ;
Stemmelin, J ;
Le Fur, G ;
Soubrié, P .
MOLECULAR PSYCHIATRY, 2004, 9 (03) :278-286
[2]
Depressive disorders - is it time to endorse different pathophysiologies? [J].
Antonijevic, IA .
PSYCHONEUROENDOCRINOLOGY, 2006, 31 (01) :1-15
[3]
The role of corticotropin-releasing factor in depression and anxiety disorders [J].
Arborelius, L ;
Owens, MJ ;
Plotsky, PM ;
Nemeroff, CB .
JOURNAL OF ENDOCRINOLOGY, 1999, 160 (01) :1-12
[4]
STRESS HORMONES - THEIR INTERACTION AND REGULATION [J].
AXELROD, J ;
REISINE, TD .
SCIENCE, 1984, 224 (4648) :452-459
[5]
Intra- and interstrain differences in models of "behavioral despair" [J].
Bai, F ;
Li, X ;
Clay, M ;
Lindstrom, T ;
Skolnick, P .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2001, 70 (2-3) :187-192
[6]
Barden N, 2004, J PSYCHIATR NEUROSCI, V29, P185
[7]
BELZUNG C, 2008, EXPT MODELS NEUROBEH
[8]
Emotional reactivity in mice may not be inherited but influenced by parents [J].
Calatayud, F ;
Coubard, S ;
Belzung, C .
PHYSIOLOGY & BEHAVIOR, 2004, 80 (04) :465-474
[9]
Influence of life stress on depression: Moderation by a polymorphism in the 5-HTT gene [J].
Caspi, A ;
Sugden, K ;
Moffitt, TE ;
Taylor, A ;
Craig, IW ;
Harrington, H ;
McClay, J ;
Mill, J ;
Martin, J ;
Braithwaite, A ;
Poulton, R .
SCIENCE, 2003, 301 (5631) :386-389
[10]
Genetics of affective (mood) disorders [J].
Craddock, Nick ;
Forty, Liz .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2006, 14 (06) :660-668