Reduced glucocorticoid receptor α expression in mood disorder patients and first-degree relatives

被引:78
作者
Matsubara, T [1 ]
Funato, H [1 ]
Kobayashi, A [1 ]
Nobumoto, M [1 ]
Watanabe, Y [1 ]
机构
[1] Yamaguchi Univ, Sch Med, Dept Neurosci, Div Neuropsychiat, Ube, Yamaguchi 7558505, Japan
关键词
glucocorticoid receptor isoforms alpha; beta; mood disorder; first-degree relatives of mood disorders; HPA axis; trait-marker; DEX/CRH test;
D O I
10.1016/j.biopsych.2005.09.026
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Individuals with mood disorders exhibit altered function of the hypothalamic-pituitiary-adrenal (HPA) axis in response to stress. The glucocorticoid receptor (GR) plays an important role in the negative feedback regulation of The HPA axis. There are two protein isoforms of GR GR alpha and GR beta which have distinct biological activity, It has not been examined whether GR alpha messenger RNA (mMNA) and GR beta mRNA expressions are altered in peripheral blood cells of mood disorder patients. Methods: Using quantitative reverse transcription polymerase chain. reaction (RT-PCR), GR alpha mRNA and GRP mRNA were measured in peripheral blood cells of major depressive disorder patients (depressive n = 18; remissive n = 38), bipolar disorder patients (depressive n = 13, remissive n = 35), normal control subjects (n = 31), and first-degree relatives bipolar depressive (n = 17) and bipolar (n = 15) disorder patients. Results: Reduced expression of GR alpha mRNA was shown in both bipolar and major depressive disorderpatients in a current depressive state as well as in remission. First-degree relatives of bipolar disorderpatients also showed GR alpha mRNA reduction, Altered GR beta mRNA expression was not found in mood disorder patients. Conclusions: Our results suggest that reduced GR alpha mRNA expression might be trait-dependent and associated with the pathophysiology of mood disorders.
引用
收藏
页码:689 / 695
页数:7
相关论文
共 61 条
[41]   Mice with genetically altered glucocorticoid receptor expression show altered sensitivity for stress-induced depressive reactions [J].
Ridder, S ;
Chourbaji, S ;
Hellweg, R ;
Urani, A ;
Zacher, C ;
Schmid, W ;
Zink, M ;
Hörtnagl, H ;
Flor, H ;
Henn, FA ;
Schütz, G ;
Gass, P .
JOURNAL OF NEUROSCIENCE, 2005, 25 (26) :6243-6250
[42]   LYMPHOCYTE GLUCOCORTICOID RECEPTOR-BINDING DURING DEPRESSION AND AFTER CLINICAL RECOVERY [J].
RUPPRECHT, R ;
KORNHUBER, J ;
WODARZ, N ;
LUGAUER, J ;
GOBEL, C ;
RIEDERER, P ;
BECKMANN, H .
JOURNAL OF AFFECTIVE DISORDERS, 1991, 22 (1-2) :31-35
[43]   How do glucocorticoids influence stress responses? Integrating permissive, suppressive, stimulatory, and preparative actions [J].
Sapolsky, RM ;
Romero, LM ;
Munck, AU .
ENDOCRINE REVIEWS, 2000, 21 (01) :55-89
[44]   ANTIDEPRESSANTS INCREASE GLUCOCORTICOID AND MINERALOCORTICOID RECEPTOR MESSENGER-RNA EXPRESSION IN RAT HIPPOCAMPUS INVIVO [J].
SECKL, JR ;
FINK, G .
NEUROENDOCRINOLOGY, 1992, 55 (06) :621-626
[45]   Glucocorticoid resistance in asthma is associated with elevated in vivo expression of the glucocorticoid receptor β-isoform [J].
Sousa, AR ;
Lane, SJ ;
Cidlowski, JA ;
Staynov, DZ ;
Lee, TH .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2000, 105 (05) :943-950
[46]   High constitutive glucocorticoid receptor β in human neutrophils enables them to reduce their spontaneous rate of cell death in response to corticosteroids [J].
Strickland, I ;
Kisich, K ;
Hauk, PJ ;
Vottero, A ;
Chrousos, GP ;
Klemm, DJ ;
Leung, DYM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 193 (05) :585-593
[47]   Glucocorticoid receptor isoforms α and β in in vitro cytokine-induced glucocorticoid insensitivity [J].
Torrego, A ;
Pujols, L ;
Roca-Ferrer, J ;
Mullol, J ;
Xaubet, A ;
Picado, C .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2004, 170 (04) :420-425
[48]   Regulation of glucocorticoidreceptor-mRNA in human blood cells by amitriptyline and dexamethasone [J].
Vedder, H ;
Bening-Abu-Shach, U ;
Lanquillon, S ;
Krieg, JC .
JOURNAL OF PSYCHIATRIC RESEARCH, 1999, 33 (04) :303-308
[49]   Glucocorticoid receptor β:: View I [J].
Vottero, A ;
Chrousos, GP .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 1999, 10 (08) :333-338
[50]   Hippocampal volume, memory, and cortisol status in major depressive disorder: Effects of treatment [J].
Vythilingam, M ;
Vermetten, E ;
Anderson, GM ;
Luckenbaugh, D ;
Anderson, ER ;
Snow, J ;
Staib, LH ;
Charney, DS ;
Bremner, JD .
BIOLOGICAL PSYCHIATRY, 2004, 56 (02) :101-112