Non-classical actions of testosterone: an update

被引:139
作者
Rahman, Faisal [1 ]
Christian, Helen C. [1 ]
机构
[1] Univ Oxford, Dept Physiol Anat & Genet, Oxford OX1 3QX, England
基金
英国惠康基金;
关键词
D O I
10.1016/j.tem.2007.09.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Androgens are known to exert their effects via genomic signalling, which involves intracellular androgen receptors that modulate gene expression on steroid binding. Whereas non-classical estrogen effects are well established, it is only recently that non-classical, rapid, membrane-initiated testosterone actions have received attention. Non-classical effects of testosterone have now been demonstrated convincingly in several tissues, in particular in the reproductive, cardiovascular, immune and musculoskeletal systems. There is evidence for the participation of the classical intracellular androgen receptor and for involvement of novel, membrane-associated androgen receptors in the non-classical actions of testosterone. Here we discuss evidence for rapid testosterone actions, which have clinical implications in fertility, cardiovascular disease and the treatment of prostate cancer.
引用
收藏
页码:371 / 378
页数:8
相关论文
共 87 条
[61]   BIOLOGICAL ACTIONS OF ANDROGENS [J].
MOORADIAN, AD ;
MORLEY, JE ;
KORENMAN, SG .
ENDOCRINE REVIEWS, 1987, 8 (01) :1-28
[62]   Estradiol activates the prostate androgen receptor and prostate-specific antigen secretion through the intermediacy of sex hormone-binding globulin [J].
Nakhla, AM ;
Romas, NA ;
Rosner, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (11) :6838-6841
[63]   Sex hormone-binding globulin receptor signal transduction proceeds via a G protein [J].
Nakhla, AM ;
Leonard, J ;
Hryb, DJ ;
Rosner, W .
STEROIDS, 1999, 64 (03) :213-216
[64]   BIOLOGICALLY-ACTIVE STEROIDS ACTIVATE RECEPTOR-BOUND HUMAN SEX HORMONE-BINDING GLOBULIN TO CAUSE LNCAP CELLS TO ACCUMULATE ADENOSINE-3',5'-MONOPHOSPHATE [J].
NAKHLA, AM ;
KHAN, MS ;
ROSNER, W .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1990, 71 (02) :398-404
[65]   A conserved mechanism for steroid receptor translocation to the plasma membrane [J].
Pedram, Ali ;
Razandi, Mahnaz ;
Sainson, Richard C. A. ;
Kim, Jin K. ;
Hughes, Christopher C. ;
Levin, Ellis R. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (31) :22278-22288
[66]   Acute anti-ischemic effect of testosterone in men with coronary artery disease [J].
Rosano, GMC ;
Leonardo, F ;
Pagnotta, P ;
Pelliccia, F ;
Panina, G ;
Cerquetani, E ;
della Monica, PL ;
Bonfigli, B ;
Volpe, M ;
Chierchia, SL .
CIRCULATION, 1999, 99 (13) :1666-1670
[67]   EFFECTS OF GENDER AND SEX STEROIDS ON THE IMMUNE-RESPONSE [J].
SCHUURS, AHWM ;
VERHEUL, HAM .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1990, 35 (02) :157-172
[68]   Delivery of a cyclic adenosine 3′,5′-monophosphate response element-binding protein (CREB) mutant to seminiferous tubules results in impaired spermatogenesis [J].
Scobey, MJ ;
Bertera, S ;
Somers, JP ;
Watkins, SC ;
Zeleznik, AJ ;
Walker, WH .
ENDOCRINOLOGY, 2001, 142 (02) :948-954
[69]   Testosterone is a potent inhibitor of L-type Ca2+ channels [J].
Scragg, JL ;
Jones, RD ;
Jones, TH ;
Peers, C .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 318 (02) :503-506
[70]  
SIMENTAL JA, 1991, J BIOL CHEM, V266, P510