Analyze Diet
Animals : an open access journal from MDPI2021; 11(8); 2322; doi: 10.3390/ani11082322

Steroidogenic Enzyme and Steroid Receptor Expression in the Equine Accessory Sex Glands.

Abstract: The expression pattern and distribution of sex steroid receptors and steroidogenic enzymes during development of the equine accessory sex glands has not previously been described. We hypothesized that equine steroidogenic enzyme and sex steroid receptor expression is dependent on reproductive status. Accessory sex glands were harvested from mature stallions, pre-pubertal colts, geldings, and fetuses. Expression of mRNA for estrogen receptor 1 (ESR1), estrogen receptor 2 (ESR2), androgen receptor (AR), 3β-Hydroxysteroid dehydrogenase/Δ5-4 isomerase (3βHSD), P450,17α hydroxylase, 17-20 lyase (CYP17), and aromatase (CYP19) were quantified by RT-PCR, and protein localization of AR, ER-α, ER-β, and 3βHSD were investigated by immunohistochemistry. Expression of AR, ESR2, CYP17, or CYP19 in the ampulla was not different across reproductive statuses ( > 0.1), while expression of ESR1 was higher in the ampulla of geldings and fetuses than those of stallions or colts ( < 0.05). AR, ESR1 and ESR2 expression were decreased in stallion vesicular glands compared to the fetus or gelding, while AR, ESR1, and CYP17 expression were decreased in the bulbourethral glands compared to other glands. ESR1 expression was increased in the prostate compared to the bulbourethral glands, and no differences were seen with CYP19 or 3β-HSD. In conclusion, sex steroid receptors are expressed in all equine male accessory sex glands in all stages of life, while the steroidogenic enzymes were weakly and variably expressed.
Publication Date: 2021-08-06 PubMed ID: 34438779PubMed Central: PMC8388441DOI: 10.3390/ani11082322Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research study focuses on identifying sex steroid receptors and steroidogenic enzymes in the accessory sex glands of horses to determine if their expression is influenced by reproductive status. The work shows these receptors are present across all male accessory sex glands and stages of life, but the steroidogenic enzymes display inconsistent and weak expressions, suggesting sensitivity to reproductive stage variations.

Research Design and Methods

  • Accessory sex glands of several male horses were collected. These horses were of varied reproductive states, including mature stallions, pre-pubertal colts, geldings (neutered males), and fetuses.
  • The mRNA expression of several sex steroid receptors and steroidogenic enzymes were identified and quantified by reverse transcription-polymerase chain reaction (RT-PCR), a laboratory technique often used to detect a specific DNA sequence in a DNA sample.
  • These specific steroid receptors and enzymes included estrogen receptor 1 (ESR1), estrogen receptor 2 (ESR2), androgen receptor (AR), 3β-Hydroxysteroid dehydrogenase/Δ5-4 isomerase (3βHSD), P450, 17α hydroxylase, 17-20 lyase (CYP17), and aromatase (CYP19).
  • Immunohistochemistry, a technique used to visually detect specific proteins in cells or tissue, was used to study protein localization of select sex steroid receptors in the equine accessory sex glands.

Findings

  • The levels of AR, ESR2, CYP17, or CYP19 in the ampulla, a particular part of the male reproductive system, were not significantly influenced by the horses’ reproductive statuses.
  • In contrast, the expression of ESR1 was found to be higher in geldings and fetuses than in stallions or colts.
  • When comparing different accessory sex glands, researchers found decreased expressions of AR, ESR1, and ESR2 in stallion vesicular glands compared to geldings or fetuses.
  • A similar decrease in the expression of AR, ESR1, and CYP17 was observed in bulbourethral glands compared to other glands.
  • The prostate showed increased ESR1 expressions compared to the bulbourethral glands, whereas no differences were observed regarding CYP19 or 3β-HSD expressions.

Conclusion

  • The study concluded that sex steroid receptors are present in all male accessory sex glands at all stages of life
  • However, the expression of steroidogenic enzymes was weak and variable, suggesting an influence of reproductive status.

Cite This Article

APA
Ellerbrock RE, Podico G, Scoggin KE, Ball BA, Carossino M, Canisso IF. (2021). Steroidogenic Enzyme and Steroid Receptor Expression in the Equine Accessory Sex Glands. Animals (Basel), 11(8), 2322. https://doi.org/10.3390/ani11082322

Publication

ISSN: 2076-2615
NlmUniqueID: 101635614
Country: Switzerland
Language: English
Volume: 11
Issue: 8
PII: 2322

Researcher Affiliations

Ellerbrock, Robyn E
  • Department of Veterinary Clinical Medicine, College of Veterinary Medicine, University of Illinois Urbana-Champaign, 1008 W Hazelwood Drive, Urbana, IL 61802, USA.
Podico, Giorgia
  • Department of Veterinary Clinical Medicine, College of Veterinary Medicine, University of Illinois Urbana-Champaign, 1008 W Hazelwood Drive, Urbana, IL 61802, USA.
Scoggin, Kirsten E
  • Maxwell H. Gluck Equine Research Center, University of Kentucky, 1400 Nicholasville Rd, Lexington, KY 40546, USA.
Ball, Barry A
  • Maxwell H. Gluck Equine Research Center, University of Kentucky, 1400 Nicholasville Rd, Lexington, KY 40546, USA.
Carossino, Mariano
  • Maxwell H. Gluck Equine Research Center, University of Kentucky, 1400 Nicholasville Rd, Lexington, KY 40546, USA.
Canisso, Igor F
  • Department of Veterinary Clinical Medicine, College of Veterinary Medicine, University of Illinois Urbana-Champaign, 1008 W Hazelwood Drive, Urbana, IL 61802, USA.

Conflict of Interest Statement

The authors declare no conflict of interest.

References

This article includes 35 references
  1. Chernier TS. Anatomy and Physical Examination of the stallion. In: Samper J.C., editor. Equine Breeding Management and Artificial Insemination. W.B. Saunders; Philadelphia, PA, USA: 2009. pp. 2–15.
  2. Pozor MA, McDonnell SM. Ultrasonographic measurements of accessory sex glands, ampullae, and urethra of normal stallions of various size types.. Theriogenology 2002 Oct 15;58(7):1425-33.
    doi: 10.1016/S0093-691X(02)01034-8pubmed: 12387354google scholar: lookup
  3. Almeida J, Conley AJ, Mathewson L, Ball BA. Expression of steroidogenic enzymes during equine testicular development.. Reproduction 2011 Jun;141(6):841-8.
    doi: 10.1530/REP-10-0499pubmed: 21300693google scholar: lookup
  4. Ellem SJ, Risbridger GP. Aromatase and regulating the estrogen:androgen ratio in the prostate gland.. J Steroid Biochem Mol Biol 2010 Feb 28;118(4-5):246-51.
    doi: 10.1016/j.jsbmb.2009.10.015pubmed: 19896534google scholar: lookup
  5. Gallardo F, Mogas T, Baró T, Rabanal R, Morote J, Abal M, Reventós J, Lloreta J. Expression of androgen, oestrogen alpha and beta, and progesterone receptors in the canine prostate: differences between normal, inflamed, hyperplastic and neoplastic glands.. J Comp Pathol 2007 Jan;136(1):1-8.
    doi: 10.1016/j.jcpa.2006.08.007pubmed: 17078963google scholar: lookup
  6. Knobbe M, Levine D, Habecker P, Getman L, Beech J, Turner R. Prostatic Masses in Geldings: Two Cases. J. Equine Vet. Sci. 2012;32:628–633.
  7. Hess R, Carnes K. The role of estrogen in testis and the male reproductive tract: A review and species comparison. Anim. Reprod. 2004;1:5–30.
  8. Teng CT, Gladwell W, Beard C, Walmer D, Teng CS, Brenner R. Lactoferrin gene expression is estrogen responsive in human and rhesus monkey endometrium.. Mol Hum Reprod 2002 Jan;8(1):58-67.
    doi: 10.1093/molehr/8.1.58pubmed: 11756570google scholar: lookup
  9. Pearl CA, Roser JF. Lactoferrin expression and secretion in the stallion epididymis.. Reprod Biol 2014 Apr;14(2):148-54.
    doi: 10.1016/j.repbio.2013.10.005pubmed: 24856474google scholar: lookup
  10. Parlevliet JM, Pearl CA, Hess MF, Famula TR, Roser JF. Immunolocalization of estrogen and androgen receptors and steroid concentrations in the stallion epididymis.. Theriogenology 2006 Sep 1;66(4):755-65.
  11. Almeida J, Conley AJ, Ball BA. Expression of anti-Müllerian hormone, CDKN1B, connexin 43, androgen receptor and steroidogenic enzymes in the equine cryptorchid testis.. Equine Vet J 2013 Sep;45(5):538-45.
    doi: 10.1111/evj.12013pubmed: 23294085google scholar: lookup
  12. Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method.. Methods 2001 Dec;25(4):402-8.
    doi: 10.1006/meth.2001.1262pubmed: 11846609google scholar: lookup
  13. Pearl CA, Mason H, Roser JF. Immunolocalization of estrogen receptor alpha, estrogen receptor beta and androgen receptor in the pre-, peri- and post-pubertal stallion testis.. Anim Reprod Sci 2011 May;125(1-4):103-11.
  14. Shu J, Dolman GE, Duan J, Qiu G, Ilyas M. Statistical colour models: an automated digital image analysis method for quantification of histological biomarkers.. Biomed Eng Online 2016 Apr 27;15:46.
    doi: 10.1186/s12938-016-0161-6pmc: PMC4848853pubmed: 27121383google scholar: lookup
  15. R Core Team. R: A Language and Environment for Statistical Computing. R Core Team; Vienna, Austria: 2020.
  16. Silva ES, Scoggin KE, Canisso IF, Troedsson MH, Squires EL, Ball BA. Expression of receptors for ovarian steroids and prostaglandin E2 in the endometrium and myometrium of mares during estrus, diestrus and early pregnancy.. Anim Reprod Sci 2014 Dec 30;151(3-4):169-81.
  17. Zhu LJ, Hardy MP, Inigo IV, Huhtaniemi I, Bardin CW, Moo-Young AJ. Effects of androgen on androgen receptor expression in rat testicular and epididymal cells: a quantitative immunohistochemical study.. Biol Reprod 2000 Aug;63(2):368-76.
    doi: 10.1095/biolreprod63.2.368pubmed: 10906039google scholar: lookup
  18. Goyal HO, Bartol FF, Wiley AA, Khalil MK, Williams CS, Vig MM. Regulation of androgen and estrogen receptors in male excurrent ducts of the goat: an immunohistochemical study.. Anat Rec 1998 Feb;250(2):164-71.
  19. Ezer N, Robaire B. Androgenic regulation of the structure and function of the epididymis. In: Robaire B., Hinton H., editors. The Epididymis: From Molecules to Clinical Practice. Kluwer Academic/Plenum Publishers; New York, NY, USA: 2002. pp. 297–316.
  20. Gallardo F, Lloreta J, García F, Moll X, Baró T, González LA, Morote J, Reventos J, Mogas T. Immunolocalization of androgen receptors, estrogen alpha receptors, and estrogen beta receptors in experimentally induced canine prostatic hyperplasia.. J Androl 2009 May-Jun;30(3):240-7.
    doi: 10.2164/jandrol.108.006775pubmed: 19136389google scholar: lookup
  21. Forti G, Salerno R, Moneti G, Zoppi S, Fiorelli G, Marinoni T, Natali A, Costantini A, Serio M, Martini L. Three-month treatment with a long-acting gonadotropin-releasing hormone agonist of patients with benign prostatic hyperplasia: effects on tissue androgen concentration, 5 alpha-reductase activity and androgen receptor content.. J Clin Endocrinol Metab 1989 Feb;68(2):461-8.
    doi: 10.1210/jcem-68-2-461pubmed: 2465302google scholar: lookup
  22. Huang JK, Bartsch W, Voigt KD. Interactions of an anti-androgen (cyproterone acetate) with the androgen receptor system and its biological action in the rat ventral prostate.. Acta Endocrinol (Copenh) 1985 Aug;109(4):569-76.
    doi: 10.1530/acta.0.1090569pubmed: 2930988google scholar: lookup
  23. Murakoshi M, Tagawa M, Ikeda R, Nakayama T, Ishimura K. Histopathological and immunohistochemical studies of the effect of antiandrogen, chlormadinone acetate (CMA), on canine spontaneous benign prostatic hyperplasia (BPH). J. Toxicol. Pathol. 2000;13:29–35.
    doi: 10.1293/tox.13.29google scholar: lookup
  24. Sar M, Welsch F. Oestrogen receptor alpha and beta in rat prostate and epididymis.. Andrologia 2000 Sep;32(4-5):295-301.
  25. Savolainen S, Pakarainen T, Huhtaniemi I, Poutanen M, Mäkelä S. Delay of postnatal maturation sensitizes the mouse prostate to testosterone-induced pronounced hyperplasia: protective role of estrogen receptor-beta.. Am J Pathol 2007 Sep;171(3):1013-22.
    doi: 10.2353/ajpath.2007.060979pmc: PMC1959505pubmed: 17640960google scholar: lookup
  26. Lemazurier E, Sourdaine P, Nativelle C, Plainfossé B, Séralini G. Aromatase gene expression in the stallion.. Mol Cell Endocrinol 2001 Jun 10;178(1-2):133-9.
    doi: 10.1016/S0303-7207(01)00435-Xpubmed: 11403902google scholar: lookup
  27. Hess MF, Roser JF. Immunocytochemical localization of cytochrome P450 aromatase in the testis of prepubertal, pubertal, and postpubertal horses.. Theriogenology 2004 Jan 15;61(2-3):293-9.
    doi: 10.1016/S0093-691X(03)00237-1pubmed: 14662129google scholar: lookup
  28. Brodie AM, Son C, King DA, Meyer KM, Inkster SE. Lack of evidence for aromatase in human prostatic tissues: effects of 4-hydroxyandrostenedione and other inhibitors on androgen metabolism.. Cancer Res 1989 Dec 1;49(23):6551-5.
    pubmed: 2479464
  29. Negri-Cesi P, Poletti A, Colciago A, Magni P, Martini P, Motta M. Presence of 5alpha-reductase isozymes and aromatase in human prostate cancer cells and in benign prostate hyperplastic tissue.. Prostate 1998 Mar 1;34(4):283-91.
  30. Stone NN, Laudone VP, Fair WR, Fishman J. Aromatization of androstenedione to estrogen by benign prostatic hyperplasia, prostate cancer and expressed prostatic secretions.. Urol Res 1987;15(3):165-7.
    doi: 10.1007/BF00254430pubmed: 3629751google scholar: lookup
  31. Hiramatsu M, Maehara I, Ozaki M, Harada N, Orikasa S, Sasano H. Aromatase in hyperplasia and carcinoma of the human prostate.. Prostate 1997 May 1;31(2):118-24.
  32. Tsugaya M, Harada N, Tozawa K, Yamada Y, Hayashi Y, Tanaka S, Maruyama K, Kohri K. Aromatase mRNA levels in benign prostatic hyperplasia and prostate cancer.. Int J Urol 1996 Jul;3(4):292-6.
  33. Matzkin H, Soloway MS. Immunohistochemical evidence of the existence and localization of aromatase in human prostatic tissues.. Prostate 1992;21(4):309-14.
    doi: 10.1002/pros.2990210407pubmed: 1281323google scholar: lookup
  34. Ellem SJ, Schmitt JF, Pedersen JS, Frydenberg M, Risbridger GP. Local aromatase expression in human prostate is altered in malignancy.. J Clin Endocrinol Metab 2004 May;89(5):2434-41.
    doi: 10.1210/jc.2003-030933pubmed: 15126575google scholar: lookup
  35. Hwang K, Choi J, Bian S, Ayala G, Khera M, Lipschultz L, Lamb L, Delores J. Steroidogenic potential of adult mouse and humanprostate and penis. J. Urol. 2011;185:e364.

Citations

This article has been cited 0 times.