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Vertebrate reproductive science and technology
RESEARCH ARTICLE

Aromatase and 11β-hydroxysteroid dehydrogenase 2 localisation in the testes of pigs from birth to puberty linked to changes of hormone pattern and testicular morphology

A. Wagner A and R. Claus A B
+ Author Affiliations
- Author Affiliations

A Universität Hohenheim, Institut für Tierhaltung und Tierzüchtung, Fachgebiet Tierhaltung und Leistungsphysiologie (470A), Garbenstr. 17, 70599 Stuttgart, Germany.

B Corresponding author. Email: thsekret@uni-hohenheim.de

Reproduction, Fertility and Development 20(4) 505-512 https://doi.org/10.1071/RD07136
Submitted: 23 August 2007  Accepted: 20 January 2008   Published: 11 April 2008

Abstract

Oestrogens and glucocorticoids are important for spermatogenesis and are regulated via aromatase for oestradiol synthesis and 11β-hydroxysteroid dehydrogenase 2 (11β-HSD 2) as an inactivator of cortisol. In the present study postnatal changes of these two enzymes were monitored together with testicular development and hormone concentrations. Pigs were assigned to three periods: Weeks 0–5, Weeks 5–11 or Weeks 11–17. In Period 1, groups of four piglets were killed after each week. Blood plasma and testes were sampled immediately post mortem. For Periods 2 and 3, groups of six pigs were fitted with vein catheters for daily blood collection. Testes from all pigs were obtained after killing. Levels of testosterone, oestradiol, LH, FSH and cortisol were determined radioimmunologically. The 11β-HSD 2- and aromatase-expressing cells were stained immunocytochemically. All hormones were maximal 2 weeks after birth. A rise of LH, testosterone and oestradiol occurred again at Week 17. FSH and cortisol remained basal. Parallel to the first postnatal rise, the presence of aromatase and 11β-HSD 2 in Leydig cells increased, together with germ and Sertoli cell numbers. Expression was low from 3 to 5 weeks, was resumed after Week 5 and was maximal at Week 17. The amount of 11β-HSD 2 in germ cells was greatest at birth, decreased thereafter and was absent after Week 3.

Additional keywords: pig testis, postnatal development.


Acknowledgements

We thank H. Hägele and S. Knöllinger for their help in histological and steroid determinations. We also thank C. Fischinger, W. Dunne and M. Mecellem for care of the animals. This project was supported by the German Research Organisation (DFG).


References

Abercrombie, M. (1946). Estimation of nuclear population from microtome sections. Anat. Rec. 94, 239–246.
Crossref | GoogleScholarGoogle Scholar | Romeis B. (1989). Chapt. V. Einbetten der fixierten Präparate. In ‘Mikroskopische Technik’. 17th edn. (Ed. P. Böck.) pp. 113–133. (Urban und Schwarzenberg : München Wien Baltimore.)

Rommerts, F. F. G. , de Jong, F. H. , Brinkmann, A. O. , and van der Molen, H. J. (1982). Development and cellular localization of rat testicular aromatase activity. J. Reprod. Fertil. 65, 281–288.
PubMed |

Sanchez, I. , Goya, I. , Vallerga, A. K. , and Firestone, G. L. (1993). Glucocorticoids reversibly arrest rat hepatoma cell growth by inducing an early G1 block in cell cycle progression. Cell Growth Differ. 4, 215–225.
PubMed |

Schwarzenberger, F. , Toole, G. S. , Christie, H. L. , and Raeside, J. I. (1993). Plasma levels of several androgens and estrogens from birth to puberty in male domestic pigs. Acta Endocrinol. (Copenh.) 128, 173–177.
PubMed |

Swanlund, D. J. , N’Diaye, M. R. , Loseth, K. J. , Pryor, J. L. , and Crabo, B. G. (1995). Diverse testicular responses to exogenous growth hormone and follicle-stimulating hormone in prepubertal boars. Biol. Reprod. 53, 749–757.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Van Straaten, H. W. M. , and Wensing, C. J. G. (1978). Leydig cell development in the testis of the pig. Biol. Reprod. 18, 86–93.
Crossref | GoogleScholarGoogle Scholar | PubMed |

van Vorstenbosch, C. J. , Colenbrander, B. , and Wensing, C. J. G. (1982). Leydig cell development of pig testis in the early fetal period: an ultrastructural study. Am. J. Anat. 165, 305–318.
Crossref | GoogleScholarGoogle Scholar | PubMed |

van Vorstenbosch, C. J. , Spek, E. , Colenbrander, B. , and Wensing, C. J. B. (1987). The ultrastructure of normal fetal and neonatal pig testis germ cells and the influence of fetal decapitation on the germ cell development. Development 99, 553–563.
PubMed |

Van Weerden, E. J. , and Grandadam, J. A. (1976). The effect of an anabolic agent on N depostition, growth performance and nitrogen deposition of hybrid boars, gilts and castrated male pigs. Environmental Quality and Safety Suppl. 5, 115–122.


Vogl, S. E. , Worda, C. , Egarter, C. , Bieglmayer, C. , Szekeres, T. , Huber, J. , and Husslein, P. (2006). Mode of delivery is associated with maternal and fetal endocrine stress response. BJOG 113, 441–445.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Wagner, A. , and Claus, R. (2004). Involvement of glucocorticoids in testicular involution after active immunization of boars against GnRH. Reproduction 127, 275–283.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Wagner, A. , Messe, N. , Bergmann, M. , Lekhkota, O. , and Claus, R. (2006). Effects of estradiol infusion in GnRH-immunized boars on spermatogenesis. J. Androl. 27, 880–889.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Welsh, T. H. , Bambino, T. H. , and Hsueh, A. J. (1982). Mechanism of glucocorticoid-induced suppression of testicular androgen biosynthesis in vitro. Biol. Reprod. 27, 1138–1146.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Zhang, Z. , Laping, J. , Glasser, S. , Day, P. , and Mulholland, J. (1998). Mediators of estradiol-stimulated mitosis in the rat uterine luminal epithelium. Endocrinology 139, 961–966.
Crossref | GoogleScholarGoogle Scholar | PubMed |