Strain-dependent antidepressant-like effects of citalopram in the mouse tail suspension test

被引:129
作者
Crowley, JJ
Blendy, JA
Lucki, I
机构
[1] Univ Penn, Dept Psychiat, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Pharmacol, Philadelphia, PA 19104 USA
关键词
tail suspension test; depression; citalopram; genetics; pharmacogenetics; mouse;
D O I
10.1007/s00213-005-0166-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rationale: Variations in the effects of antidepressant drugs between different mouse strains are important for drug discovery and could lead to the identification of genes that predict differences in drug efficacy. Objectives: This study compared behavioral baselines and dose-dependent responses to the selective serotonin re-uptake inhibitor (SSRI) citalopram in eight inbred mouse strains (C57BL/6J, DBA/2J, C3H/HeJ, BALB/cJ, A/J, 129/SvEmsJ, 129/SvImJ, and BTBR) using the tail suspension test (TST). Results: The DBA/2J, BALB/cJ, and BTBR strains were the most responsive to the effects of citalopram. Citalopram was least effective in the C57BL/6J and A/J strains. The antidepressant-like effects of citalopram in the TST were not correlated with changes in locomotor activity or deprivation-induced feeding behavior across the individual mouse strains, suggesting that patterns of sensitivity to citalopram are behaviorally specific and unlikely to result from pharmacokinetic variables. As an initial search for genetic polymorphisms causing differences in citalopram sensitivity, polymorphic forms of the tryptophan hydroxylase 2 (tph2) gene were genotyped and found to be not correlated with citalopram responsive (DBA/2J and BALB/cJ) and nonresponsive (A/J and C57BL/6J) strains. Conclusions: The TST strain survey described here: (1) suggested the most appropriate strains for screening potential antidepressants, (2) identified parental strains appropriate for quantitative trait loci mapping of genomic loci regulating SSRI sensitivity, and (3) indicated appropriate background strains for measuring an antidepressant-like response to the SSRI citalopram. The pattern of response agrees with a previous mouse strain survey that examined sensitivity to fluoxetine in the forced swim test.
引用
收藏
页码:257 / 264
页数:8
相关论文
共 32 条
[1]  
ARIAS B, 2001, WORLD J BIOL PSYCHIA, V2, pS9
[2]   Induction of hyperlocomotion in mice exposed to a novel environment by inhibition of serotonin reuptake - A pharmacological characterization of diverse classes of antidepressant agents [J].
Brocco, M ;
Dekeyne, A ;
Veiga, S ;
Girardon, S ;
Millan, MJ .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2002, 71 (04) :667-680
[3]   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
[4]   Opportunities to discover genes regulating depression and antidepressant response from rodent behavioral genetics [J].
Crowley, JJ ;
Lucki, I .
CURRENT PHARMACEUTICAL DESIGN, 2005, 11 (02) :157-169
[5]   Automated tests for measuring the effects of antidepressants in mice [J].
Crowley, JJ ;
Jones, MD ;
O'Leary, OF ;
Lucki, I .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2004, 78 (02) :269-274
[6]  
CRYAN JF, 2005, IN PRESS NEUROSCI BI
[7]   Antidepressant-like effects in various mice strains in the forced swimming test [J].
David, DJP ;
Renard, CE ;
Jolliet, P ;
Hascoët, M ;
Bourin, M .
PSYCHOPHARMACOLOGY, 2003, 166 (04) :373-382
[8]   The serotonin transporter polymorphism, 5HTTLPR, is associated with a faster response time to sertraline in an elderly population with major depressive disorder [J].
Durham, LK ;
Webb, SM ;
Milos, PM ;
Clary, CM ;
Seymour, AB .
PSYCHOPHARMACOLOGY, 2004, 174 (04) :525-529
[9]  
Edenberg HJ, 1997, AM J MED GENET, V74, P238, DOI 10.1002/(SICI)1096-8628(19970531)74:3<238::AID-AJMG2>3.0.CO
[10]  
2-M