Title of article :
Equol Is a Novel Anti-Androgen that Inhibits Prostate Growth and Hormone Feedback
Author/Authors :
Handa، Robert J. نويسنده , , Lund، Trent D. نويسنده , , Munson، Daniel J. نويسنده , , Haldy، Megan E. نويسنده , , Setchell، Kenneth D.R. نويسنده , , Lephart، Edwin D. نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2004
Pages :
-1187
From page :
1188
To page :
0
Abstract :
Equol (7-hydroxy-3[4ʹhydroxyphenyl]-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 5(alpha)-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) ?, and no affinity for ER(alpha)In castrated male rats treated with DHT, concomitant treatment with equol blocked DHTʹs 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 equolʹs biological properties. The significance of equolʹs 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.
Keywords :
motion segmentation , structure from motion , computer vision , dynamic scene reconstruction
Journal title :
Biology of Reproduction
Serial Year :
2004
Journal title :
Biology of Reproduction
Record number :
88515
Link To Document :
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