Opportunities to discover genes regulating depression and antidepressant response from rodent behavioral genetics

被引:30
作者
Crowley, JJ
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
genetics; depression; antidepressant; rat; mouse; behavior; QTL;
D O I
10.2174/1381612053382278
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Over the past several years, research has indicated that an individual's genetic makeup strongly influences not only their likelihood of developing depression, but also whether or not they will respond well to a particular antidepressant treatment. Identifying those genes regulating susceptibility to depression will increase our understanding of disease pathophysiology and direct the development of treatments that correct underlying neurobiological pathology related to stress-related psychiatric illnesses. Pharmacologically, the identification of genes regulating treatment response can lead to the design of novel pharmacological treatments and allow for more individualized, rational and successful drug treatments. Unfortunately, complex environmental and genetic mechanisms at play in depression and drug response make the discovery of susceptibility genes in humans quite difficult. Animal models may provide a more desirable system in which to discover susceptibility genes because environmental factors and tests can be regulated and more informative genetic methods can be used. Furthermore, a unique genetic opportunity exists with animal models of depression and antidepressant response because several rodent strains have been identified, or selectively bred, that display exaggerated depressive phenotypes on stress-related behavioral tests or divergent responses to antidepressant drugs. This paper reviews several of these rodent strains and illustrates the genetic strategies available to discover the long-sought susceptibility genes regulating these phenotypes.
引用
收藏
页码:157 / 169
页数:13
相关论文
共 142 条
[1]   Transcriptional regulation of the heme oxygenase-1 gene via the stress response element pathway [J].
Alam, J ;
Cook, JL .
CURRENT PHARMACEUTICAL DESIGN, 2003, 9 (30) :2499-2511
[2]   Serotonin 1A receptors, serotonin transporter binding and serotonin transporter mRNA expression in the brainstem of depressed suicide victims [J].
Arango, V ;
Underwood, MD ;
Boldrini, M ;
Tamir, H ;
Kassir, SA ;
Hsiung, SC ;
Chen, JJX ;
Mann, JJ .
NEUROPSYCHOPHARMACOLOGY, 2001, 25 (06) :892-903
[3]   5-HTTLPR polymorphism of the serotonin transporter gene predicts non-remission in major depression patients treated with citalopram in a 12-weeks follow up study [J].
Arias, B ;
Catalán, R ;
Gastó, C ;
Gutiérrez, B ;
Fañanás, L .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 2003, 23 (06) :563-567
[4]   Comparison of the behavioural and endocrine response to forced swimming stress in five inbred strains of rats [J].
Armario, A ;
Gavalda, A ;
Marti, J .
PSYCHONEUROENDOCRINOLOGY, 1995, 20 (08) :879-890
[5]   ATTENUATION OF HYPERCORTISOLEMIA IN FAWN-HOODED RATS BY ANTIDEPRESSANT DRUGS [J].
AULAKH, CS ;
HILL, JL ;
MURPHY, DL .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1993, 240 (01) :85-88
[6]  
BAUM AE, 2003, SOV NEUR ABSTR
[7]   CHROMOSOME MAPPING OF GENE LOCI AFFECTING MORPHINE AND AMPHETAMINE RESPONSES IN BXD RECOMBINANT INBRED MICE [J].
BELKNAP, JK ;
CRABBE, JC .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1992, 654 :311-323
[8]   Increased basal REM sleep but no difference in dark induction or light suppression of REM sleep in flinders rats with cholinergic supersensitivity [J].
Benca, RM ;
Overstreet, DE ;
Gilliland, MA ;
Russell, D ;
Bergmann, BM ;
Obermeyer, WH .
NEUROPSYCHOPHARMACOLOGY, 1996, 15 (01) :45-51
[9]  
BENCA RM, 1992, ARCH GEN PSYCHIAT, V49, P651
[10]   CONTRASTING LEVER-PRESS AVOIDANCE BEHAVIORS OF SPONTANEOUSLY HYPERTENSIVE AND NORMOTENSIVE RATS (RATTUS-NORVEGICUS) [J].
BERGER, DF ;
STARZEC, JJ .
JOURNAL OF COMPARATIVE PSYCHOLOGY, 1988, 102 (03) :279-286