A direct androgenic involvement in the expression of human corticotropin-releasing hormone

被引:88
作者
Bao, A. -M.
Fischer, D. F.
Wu, Y. -H.
Hol, E. M.
Balesar, R.
Unmehopa, U. A.
Zhou, J. -N.
Swaab, D. F. [1 ]
机构
[1] Netherlands Inst Brain Res, NL-1105 AZ Amsterdam, Netherlands
[2] Anhui Med Univ, Affiliated Hosp 1, Dept Endocrinol, Hefei, Anhui, Peoples R China
[3] Vrije Univ Amsterdam, Dept Funct Gen, Ctr Neurogen & Cognit Res, Amsterdam, Netherlands
[4] Vrije Univ Amsterdam Med Ctr, Amsterdam, Netherlands
[5] Univ Sci & Technol China, Dept Neurobiol, Sch Life Sci, Hefei 230026, Anhui, Peoples R China
关键词
hypothalamic-pituitary-adrenal axis; corticotropin-releasing hormone; androgen receptor; androgen-responsive element;
D O I
10.1038/sj.mp.4001800
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
We investigated the possibility of a direct action of androgens on the expression of the human corticotropin-releasing hormone (CRH), which plays a central role in the hypothalamic pituitary-adrenal (HPA)-axis. Colocalization of CRH and nuclear/cytoplasmic androgen receptor (AR) was found in neurons of the paraventricular nucleus (PVN) in the human hypothalamus. A potential androgen-responsive element (ARE) in the human CRH promoter was subsequently analyzed with bandshifts and cotransfections in neuroblastoma cells. In the presence of testosterone, recombinant human AR bound specifically to the CRH-ARE. Expression of AR in combination with testosterone repressed CRH promoter activity through the ARE. We conclude that androgens may directly affect CRH neurons in the human PVN via AR binding to the CRH-ARE, which may have consequences for sex-specific pathogenesis of mood disorders.
引用
收藏
页码:567 / 576
页数:10
相关论文
共 83 条
[1]
BIOTIN AMPLIFICATION OF BIOTIN AND HORSERADISH-PEROXIDASE SIGNALS IN HISTOCHEMICAL STAINS [J].
ADAMS, JC .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1992, 40 (10) :1457-1463
[2]
REGULATION OF GLUCOCORTICOID RECEPTOR IMMUNOREACTIVITY IN THE RAT HIPPOCAMPUS BY ANDROGENIC-ANABOLIC STEROIDS [J].
AHIMA, RS ;
HARLAN, RE .
BRAIN RESEARCH, 1992, 585 (1-2) :311-314
[3]
ALONSO G, 1986, EXP BRAIN RES, V61, P497
[4]
Colocalization of corticotropin-releasing hormone and oestrogen receptor-α in the paraventricular nucleus of the hypothalamus in mood disorders [J].
Bao, AM ;
Hestiantoro, A ;
Van Someren, EJW ;
Swaab, DF ;
Zhou, JN .
BRAIN, 2005, 128 :1301-1313
[5]
EVIDENCE THAT HYPOTHALAMUS IS RESPONSIBLE FOR ANDROGEN-INDUCED STERILITY IN FEMALE RAT [J].
BARRACLOUGH, C ;
GORSKI, RA .
ENDOCRINOLOGY, 1961, 68 (01) :68-&
[6]
Bioavailable testosterone and depressed mood in older men:: The Rancho Bernardo study [J].
Barrett-Connor, E ;
Von Mühlen, DG ;
Kritz-Silverstein, D .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (02) :573-577
[7]
ANDROGEN INHIBITS THE INCREASES IN HYPOTHALAMIC CORTICOTROPIN-RELEASING HORMONE (CRH) AND CRH-IMMUNOREACTIVITY FOLLOWING GONADECTOMY [J].
BINGAMAN, EW ;
MAGNUSON, DJ ;
GRAY, TS ;
HANDA, RJ .
NEUROENDOCRINOLOGY, 1994, 59 (03) :228-234
[8]
LOCALIZATION OF ANDROGEN RECEPTOR WITHIN PEPTIDERGIC NEURONS OF THE RAT FOREBRAIN [J].
BINGAMAN, EW ;
BAECKMAN, LM ;
YRACHETA, JM ;
HANDA, RJ ;
GRAY, TS .
BRAIN RESEARCH BULLETIN, 1994, 35 (04) :379-382
[9]
BISSETTE G, 1990, CORTICOTROPIN RELEAS, P21
[10]
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3