Literature DB >> 941190

The inhibition of the conversion of testosterone into 5alpha-dihydrotestosterone in the reproductive organs of the male rat.

S K Saksena, I F Lau, M C Chang.   

Abstract

The inhibition of testosterone 5alpha-reductase activity by 3-oxo-4-androstene-17beta-carboxylic acid in the male reproductive organs of the rat was demonstrated in vitro. The medium for incubation of caput epididymis showed the highest concentration of 5alpha-dihydrotestosterone (5alpha-DHT) whereas the highest concentration of testosterone (T) was recorded in medium for incubation of decapsulated testis after two hours of incubation. The 3-oxo-4-androstene-17beta-carboxylic acid (1.58 X 10(-5)M) inhibited the conversion of T to 5alpha-DHT in all the organs tested (testis, caput and cauda epididymis and ventral prostate) under identical incubation conditions.

Entities:  

Mesh:

Substances:

Year:  1976        PMID: 941190     DOI: 10.1016/0039-128x(76)90135-5

Source DB:  PubMed          Journal:  Steroids        ISSN: 0039-128X            Impact factor:   2.668


  3 in total

Review 1.  Adverse effects of 5α-reductase inhibitors: What do we know, don't know, and need to know?

Authors:  Abdulmaged M Traish; Roberto Cosimo Melcangi; Marco Bortolato; Luis M Garcia-Segura; Michael Zitzmann
Journal:  Rev Endocr Metab Disord       Date:  2015-09       Impact factor: 6.514

2.  Reduction of fertilizing capacity of epididymal spermatozoa by 5 alpha-steroid reductase inhibitors.

Authors:  J Cohen; M P Ooms; J T Vreeburg
Journal:  Experientia       Date:  1981

Review 3.  The dark side of 5α-reductase inhibitors' therapy: sexual dysfunction, high Gleason grade prostate cancer and depression.

Authors:  Abdulmaged M Traish; Ashwini Mulgaonkar; Nicholas Giordano
Journal:  Korean J Urol       Date:  2014-06-16
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.