Literature DB >> 7805711

Comparison of finasteride (Proscar) and Serenoa repens (Permixon) in the inhibition of 5-alpha reductase in healthy male volunteers.

G Strauch1, P Perles, G Vergult, M Gabriel, B Gibelin, S Cummings, W Malbecq, M P Malice.   

Abstract

A total of 32 healthy male volunteers (age range 20-30 years) were enrolled in a 1-week open, randomized, placebo-controlled study comparing finasteride (Proscar), a 5 alpha-reductase inhibitor, with Permixon, the plant extract of Serenoa repens. The objective of the study was to evaluate the effect of single and multiple doses of the drugs on the inhibition of 5 alpha-reductase as assessed by serum dihydrotestosterone level determination. Following baseline measurements on day 1, the subjects were randomized to finasteride 5 mg once a day (n = 10), Permixon 80 mg x 2 twice a day (n = 11), or to placebo once a day (n = 11) for 7 days. Serum testosterone and dihydrotestosterone levels, were determined on day 1 (baseline and 12 h) and on days 2 (24 h), 3 (48 h), 4 (72 h), 6 (120 h), and 8 (168 h). After 12 h, a single dose of finasteride 5 mg reduced the serum dihydrotestosterone level by 65% (p < or = 0.01). The decreases ranged from -52 to -60% with multiple doses of finasteride 5 mg once a day (p < or = 0.01). As in the placebo group, there was no effect of Permixon on the serum dihydrotestosterone level. No significant difference was detected between finasteride and Permixon or between finasteride and placebo with respect to serum testosterone, except on days 3 and 6, respectively (p < or = 0.05). However, the corresponding serum testosterone levels remained within the normal ranges. These data confirm the efficacy of finasteride as inhibitor of 5 alpha-reductase.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1994        PMID: 7805711     DOI: 10.1159/000475388

Source DB:  PubMed          Journal:  Eur Urol        ISSN: 0302-2838            Impact factor:   20.096


  14 in total

Review 1.  Serenoa repens (Permixon). A review of its pharmacology and therapeutic efficacy in benign prostatic hyperplasia.

Authors:  G L Plosker; R N Brogden
Journal:  Drugs Aging       Date:  1996-11       Impact factor: 3.923

Review 2.  Serenoa repens for benign prostatic hyperplasia.

Authors:  James Tacklind; Roderick Macdonald; Indy Rutks; Judith U Stanke; Timothy J Wilt
Journal:  Cochrane Database Syst Rev       Date:  2012-12-12

Review 3.  Use of saw palmetto (Serenoa repens) extract for benign prostatic hyperplasia.

Authors:  Youngjoo Kwon
Journal:  Food Sci Biotechnol       Date:  2019-04-17       Impact factor: 2.391

4.  Saw Palmetto Berry as a Treatment for BPH.

Authors:  E Fagelman; F C Lowe
Journal:  Rev Urol       Date:  2001

Review 5.  Medical treatment of benign prostatic hyperplasia.

Authors:  Stephen S Connolly; John M Fitzpatrick
Journal:  Postgrad Med J       Date:  2007-02       Impact factor: 2.401

Review 6.  Serenoa repens (saw palmetto): a systematic review of adverse events.

Authors:  Taofikat B Agbabiaka; Max H Pittler; Barbara Wider; Edzard Ernst
Journal:  Drug Saf       Date:  2009       Impact factor: 5.606

Review 7.  Serenoa repens for benign prostatic hyperplasia.

Authors:  James Tacklind; Roderick MacDonald; Indy Rutks; Timothy J Wilt
Journal:  Cochrane Database Syst Rev       Date:  2009-04-15

Review 8.  Phytotherapy for chronic prostatitis.

Authors:  F C Lowe; E Fagelman
Journal:  Curr Urol Rep       Date:  2000-08       Impact factor: 3.092

Review 9.  Saw palmetto and finasteride in the treatment of category-III prostatitis/chronic pelvic pain syndrome.

Authors:  Jennifer Yang; Alexis E Te
Journal:  Curr Urol Rep       Date:  2005-07       Impact factor: 2.862

10.  Fatty acid and phytosterol content of commercial saw palmetto supplements.

Authors:  Kavitha Penugonda; Brian L Lindshield
Journal:  Nutrients       Date:  2013-09-13       Impact factor: 5.717

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