Equine 5α-reductase activity and expression in epididymis

C. J. Corbin, E. L. Legacki, B. A. Ball, K. E. Scoggin, Scott D Stanley, Alan J Conley

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

The 5α-reductase enzymes play an important role during male sexual differentiation, and in pregnant females, especially equine species where maintenance relies on 5α-reduced progesterone, 5α-dihydroprogesterone (DHP). Epididymis expresses 5α-reductases but was not studied elaborately in horses. Epididymis from younger and older postpubertal stallions was divided into caput, corpus and cauda and examined for 5α-reductase activity and expression of type 1 and 2 isoforms by quantitative realtime polymerase chain reaction (qPCR). Metabolism of progesterone and testosterone to DHP and dihydrotestosterone (DHT), respectively, by epididymal microsomal protein was examined by thin-layer chromatography and verified by liquid chromatography tandem mass spectrometry (LC-MS/MS). Relative inhibitory potencies of finasteride and dutasteride toward equine 5α-reductase activity were investigated. Pregnenolone was investigated as an additional potential substrate for 5α-reductase, suggested previously from in vivo studies in mares but never directly examined. No regional gradient of 5α-reductase expression was observed by either enzyme activity or transcript analysis. Results of PCR experiments suggested that type 1 isoform predominates in equine epididymis. Primers for the type 2 isoform were unable to amplify product from any samples examined. Progesterone and testosterone were readily reduced to DHP and DHT, and activity was effectively inhibited by both inhibitors. Using epididymis as an enzyme source, no experimental evidence was obtained supporting the notion that pregnenolone could be directly metabolized by equine 5α-reductases as has been suggested by previous investigators speculating on alternative metabolic pathways leading to DHP synthesis in placenta during equine pregnancies.

Original languageEnglish (US)
Pages (from-to)23-33
Number of pages11
JournalJournal of Endocrinology
Volume231
Issue number1
DOIs
StatePublished - 2016

Fingerprint

Epididymis
Horses
20-alpha-Dihydroprogesterone
Oxidoreductases
Progesterone
Pregnenolone
Protein Isoforms
Dihydrotestosterone
Testosterone
Enzymes
Finasteride
Polymerase Chain Reaction
Sex Differentiation
Thin Layer Chromatography
Tandem Mass Spectrometry
Metabolic Networks and Pathways
Liquid Chromatography
Placenta
Maintenance
Research Personnel

Keywords

  • Epididymis
  • Equine
  • Pregnancy
  • Progesterone
  • Reductase
  • Steroidogenesis
  • Testosterone

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Endocrinology

Cite this

Equine 5α-reductase activity and expression in epididymis. / Corbin, C. J.; Legacki, E. L.; Ball, B. A.; Scoggin, K. E.; Stanley, Scott D; Conley, Alan J.

In: Journal of Endocrinology, Vol. 231, No. 1, 2016, p. 23-33.

Research output: Contribution to journalArticle

Corbin, C. J. ; Legacki, E. L. ; Ball, B. A. ; Scoggin, K. E. ; Stanley, Scott D ; Conley, Alan J. / Equine 5α-reductase activity and expression in epididymis. In: Journal of Endocrinology. 2016 ; Vol. 231, No. 1. pp. 23-33.
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