Mice with mutations in the HPA-system as models for symptoms of depression

被引:61
作者
Mueller, Marianne B. [1 ]
Holsboer, Florian [1 ]
机构
[1] Max Planck Inst Psychiat, D-80804 Munich, Germany
关键词
depression; mouse mutants; stress hormones; CRH; epigenetic programming;
D O I
10.1016/j.biopsych.2006.02.008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Genetically engineered mice hold promise to help us understand the effects of enhanced or reduced gene activity upon behavior and metabolism. Because many basic and clinical studies suggest that alterations of the hypothalamic pituitary adrenocortical (HPA) system are involved in the development and course of depression, mouse mutants with genetic modifications of genes regulating the HPA system were generated. This review summarizes these effects and concludes that advanced technologies allowing for regional overexpression or inactivation of genes or introduction of polymorphisms into the mouse genome are well suited to explain individual symptoms or symptom patterns prevalent among depressives. However, as depression is a complex disorder in which minor changes of many genes as well as environmental factors (including epigenetic programming) play a causal role and determine the phenotype, the use of mice with single gene mutations needs to be critically discussed when attempting to create a genetic animal model of depression.
引用
收藏
页码:1104 / 1115
页数:12
相关论文
共 133 条
[1]   Subtle shifts in the ratio between pro- and antiapoptotic molecules after activation of corticosteroid receptors decide neuronal fate [J].
Almeida, OFX ;
Condé, GL ;
Crochemore, C ;
Demeneix, BA ;
Fischer, D ;
Hassan, AHS ;
Meyer, M ;
Holsboer, F ;
Michaelidis, TM .
FASEB JOURNAL, 2000, 14 (05) :779-790
[2]   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
[3]   Developmental regulation of the 5-HT7 serotonin receptor and transcription factor NGFI-A in the fetal guinea-pig limbic system: influence of GCs [J].
Andrews, MH ;
Kostaki, A ;
Setiawan, E ;
McCabe, L ;
Owen, D ;
Banjanin, S ;
Matthews, SG .
JOURNAL OF PHYSIOLOGY-LONDON, 2004, 555 (03) :659-670
[4]   CRF and CRF receptors: Role in stress responsivity and other behaviors [J].
Bale, TL ;
Vale, WW .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2004, 44 :525-557
[5]  
Bale TL, 2003, J NEUROSCI, V23, P5295
[6]   Mice deficient for both corticotropin-releasing factor receptor 1 (CRFR1) and CRFR2 have an impaired stress response and display sexually dichotomous anxiety-like behavior [J].
Bale, TL ;
Picetti, R ;
Contarino, A ;
Koob, GF ;
Vale, WW ;
Lee, KF .
JOURNAL OF NEUROSCIENCE, 2002, 22 (01) :193-199
[7]   Mice deficient for corticotropin-releasing hormone receptor-2 display anxiety-like behaviour and are hypersensitive to stress [J].
Bale, TL ;
Contarino, AB ;
Smith, GW ;
Chan, R ;
Gold, LH ;
Sawchenko, PE ;
Koob, GF ;
Vale, WW ;
Lee, KF .
NATURE GENETICS, 2000, 24 (04) :410-414
[8]   Endocrine profile and neuroendocrine challenge tests in transgenic mice expressing antisense RNA against the glucocorticoid receptor [J].
Barden, N ;
Stec, ISM ;
Montkowski, A ;
Holsboer, F ;
Reul, JMHM .
NEUROENDOCRINOLOGY, 1997, 66 (03) :212-220
[9]   Corticotropin-releasing hormone-mediated induction of intracellular signaling pathways and brain-derived neurotrophic factor expression is inhibited by the activation of the endocannabinoid system [J].
Bayatti, N ;
Hermann, H ;
Lutz, B ;
Behl, C .
ENDOCRINOLOGY, 2005, 146 (03) :1205-1213
[10]   STEROID-HORMONE RECEPTORS - MANY ACTORS IN SEARCH OF A PLOT [J].
BEATO, M ;
HERRLICH, P ;
SCHUTZ, G .
CELL, 1995, 83 (06) :851-857