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CYPROTERONE ACETATE This is not a medical report. Its information is presented by non medical personnel. Any drug program should be discussed with your physician or endocronologist!
Cyproterone acetate
blocks the binding of DHT dihydrotestosterone to its receptors. In a
study conducted by Peereboom-Wynia JD; van der Willigen AH; van Joost T;
Stolz E (Acta Derm Venereol 1989; 69 (5): 395-8) showed that female test
subjects who were treated with cyproterone acetate exhibited a
statistically significant increase in anagen hairs as well as a
statistically significant decrease in telogen hairs as compared to the
control group. In men, cyproterone acetate competitively inhibits the effect of androgens from both the testis and the adrenal cortex. The sex drive and virility are also reduced and the function of the testis inhibited. These changes are reversible after discontinuation of the therapy. This drug can have some serious effects on male's sex drive and is sometimes prescribed for people undergoing male-female sex change. Recently,
a study by Gruber DM, Sator MO, Joura EA, Kokoschka EM, Heinze G, Huber
JC. (Arch Dermatol. 1998 Apr;134(4):459-63. Related Articles, Links)
concluded that topically applied cyproterone acetate in combination with
liposomes are as effective as oral antiandrogen medication in acne
treatment while reducing the risk of adverse effects and avoiding high
serum cyproterone acetate concentrations. This suggests that topical
cyproterone may be effective in treating hairloss in some patients by
working as an androgen receptors blocker. More
info
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