Equol is a novel anti-androgen that inhibits prostate growth and hormone feedback

被引:187
作者
Lund, TD
Munson, DJ
Haldy, ME
Setchell, KDR
Lephart, ED
Handa, RJ
机构
[1] Colorado State Univ, Dept Biomed Sci, Ft Collins, CO 80523 USA
[2] Childrens Hosp, Med Ctr, Clin Mass Spectrometry, Cincinnati, OH 45229 USA
[3] Brigham Young Univ, Ctr Neurosci, Provo, UT 84602 USA
[4] Brigham Young Univ, Dept Physiol & Dev Biol, Provo, UT 84602 USA
关键词
androgen receptor; epididymis; prostate; steroid hormones; testosterone;
D O I
10.1095/biolreprod.103.023713
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Equol (7-hydroxy-3[4'hydroxyphenyl]-chroman) is the major metabolite of the phytoestrogen daidzein, one of the main isoflavones found abundantly in soybeans and soy foods. Equol may be an important biologically active molecule based on recent studies demonstrating that equol can modulate reproductive function. In this study, we examined the effects of equol on prostate growth and LH secretion and determined some of the mechanisms by which it might act. Administration of equol to intact male rats for 4-7 days reduced ventral prostate and epididymal weight and increased circulating LH levels. Using binding assays, we determined that equol specifically binds 5alpha-dihydrotestosterone (DHT), but not testosterone, dehydroepiandrosterone, or estrogen with high affinity. Equol does not bind the prostatic androgen receptor, and has a modest affinity for recombinant estrogen receptor (ER) beta, and no affinity for ERalpha. In castrated male rats treated with DHT, concomitant treatment with equol blocked DHT's trophic effects on the ventral prostate gland growth and inhibitory feedback effects on plasma LH levels without changes in circulating DHT. Therefore, equol can bind circulating DHT and sequester it from the androgen receptor, thus altering growth and physiological hormone responses that are regulated by androgens. These data suggest a novel model to explain equols biological properties. The significance of equol's ability to specifically bind and sequester DHT from the androgen receptor have important ramifications in health and disease and may indicate a broad and important usage for equol in the treatment of androgen-mediated pathologies.
引用
收藏
页码:1188 / 1195
页数:8
相关论文
共 47 条
[11]   PHYTOESTROGENS - NEW LIGANDS FOR RAT AND HUMAN ALPHA-FETOPROTEIN [J].
GARREAU, B ;
VALLETTE, G ;
ADLERCREUTZ, H ;
WAHALA, K ;
MAKELA, T ;
BENASSAYAG, C ;
NUNEZ, EA .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1094 (03) :339-345
[12]  
Griffiths K, 1997, EUR UROL, V32, P24
[13]  
Halbreich U, 2000, Expert Opin Pharmacother, V1, P1385, DOI 10.1517/14656566.1.7.1385
[14]   THE QUANTITATIVE DISTRIBUTION OF CYTOSOLIC ANDROGEN RECEPTORS IN MICRODISSECTED AREAS OF THE MALE-RAT BRAIN - EFFECTS OF ESTROGEN-TREATMENT [J].
HANDA, RJ ;
ROSELLI, CE ;
HORTON, L ;
RESKO, JA .
ENDOCRINOLOGY, 1987, 121 (01) :233-240
[15]   ANDROGEN RECEPTORS IN BRAIN AND PITUITARY OF FEMALE RATS - CYCLIC CHANGES AND COMPARISONS WITH THE MALE [J].
HANDA, RJ ;
REID, DL ;
RESKO, JA .
BIOLOGY OF REPRODUCTION, 1986, 34 (02) :293-303
[16]   Soy isoflavonoid equol modulates the growth of benign and malignant prostatic epithelial cells in vitro [J].
Hedlund, TE ;
Johannes, WU ;
Miller, GJ .
PROSTATE, 2003, 54 (01) :68-78
[17]   Isoflavonoids do not inhibit in vivo lipid peroxidation in subjects with high-normal blood pressure [J].
Hodgson, JM ;
Puddey, IB ;
Croft, KD ;
Mori, TA ;
Rivera, J ;
Beilin, LJ .
ATHEROSCLEROSIS, 1999, 145 (01) :167-172
[18]   Selective estrogen receptor modulators and postmenopausal women's health [J].
Hol, T ;
Cox, MB ;
Bryant, HU ;
Draper, MW .
JOURNAL OF WOMENS HEALTH, 1997, 6 (05) :523-531
[19]   Interaction of estrogenic chemicals and phytoestrogens with estrogen receptor β [J].
Kuiper, GGJM ;
Lemmen, JG ;
Carlsson, B ;
Corton, JC ;
Safe, SH ;
van der Saag, PT ;
van der Burg, P ;
Gustafsson, JÄ .
ENDOCRINOLOGY, 1998, 139 (10) :4252-4263
[20]   Comparison of the ligand binding specificity and transcript tissue distribution of estrogen receptors alpha and beta [J].
Kuiper, GGJM ;
Carlsson, B ;
Grandien, K ;
Enmark, E ;
Haggblad, J ;
Nilsson, S ;
Gustafsson, JA .
ENDOCRINOLOGY, 1997, 138 (03) :863-870