Literature DB >> 1558816

Identification of 5 alpha-androstane-3 beta,17 beta-diol and 3 beta-hydroxy-5 alpha-androstan-17-one sulfates as quantitatively significant secretory products of porcine Leydig cells and their presence in testicular venous blood.

J I Raeside1, R L Renaud, D E Marshall.   

Abstract

By means of high performance liquid chromatography and gas chromatography-mass spectrometry it has been found that 5 alpha-androstane-3 beta,17 beta-diol sulfate and 3 beta-hydroxy-5 alpha-androstan-17-one sulfate (epiandrosterone) are major secretory steroids of the mature boar testes. These same compounds were similarly identified in culture media when porcine Leydig cells were incubated with androstenedione as substrate. In addition, they were seen as the principal secretory products when [3H]androstenedione and [3H]testosterone were used as substrates; and their presence was greatly reduced by an inhibitor of 5 alpha-reductase (N,N-diethyl,4-methyl-3-oxo-4-aza-5 alpha-androstane-17 beta-carboxamide). Greater quantities of 5 alpha-androstanediol than epiandrosterone were noted in all instances. These findings provide further evidence of the versatile activity of the boar testes in steroidogenesis.

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Year:  1992        PMID: 1558816     DOI: 10.1016/0960-0760(92)90017-d

Source DB:  PubMed          Journal:  J Steroid Biochem Mol Biol        ISSN: 0960-0760            Impact factor:   4.292


  2 in total

1.  The intensity of male-male competition may affect chemical scent constituents in the dark ventral patch of male Iberian red deer.

Authors:  Eva de la Peña; José Martín; Juan Carranza
Journal:  PLoS One       Date:  2019-09-03       Impact factor: 3.240

2.  Morphological characterization of fullerene-androsterone conjugates.

Authors:  Alberto Ruiz; Margarita Suárez; Nazario Martin; Fernando Albericio; Hortensia Rodríguez
Journal:  Beilstein J Nanotechnol       Date:  2014-03-28       Impact factor: 3.649

  2 in total

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