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Reproduction, Fertility and Development Reproduction, Fertility and Development Society
Vertebrate reproductive science and technology
RESEARCH ARTICLE

Inherent capacity of the pituitary gland to produce gonadotropins is not influenced by the number of ovarian follicles ≥3 mm in diameter in cattle

F. Mossa A , F. Jimenez-Krassel B , S. Walsh A , D. P. Berry C , S. T. Butler C , J. Folger B , G. W. Smith B , J. L. H. Ireland B , P. Lonergan A , J. J. Ireland B and A. C. O. Evans A D
+ Author Affiliations
- Author Affiliations

A School of Agriculture, Food Science, and Veterinary Medicine, and Conway Institute, College of Life Sciences, University College Dublin, Belfield, Dublin 4, Ireland.

B Department of Animal Science, Michigan State University, East Lansing, MI 48824, USA.

C Teagasc, Moorepark Dairy Research Centre, Fermoy, Cork, Ireland.

D Corresponding author. Email: alex.evans@ucd.ie

Reproduction, Fertility and Development 22(3) 550-557 https://doi.org/10.1071/RD09100
Submitted: 22 April 2009  Accepted: 23 September 2009   Published: 15 February 2010

Abstract

We hypothesised that higher serum FSH concentrations in cattle with low v. high follicle numbers during follicular waves are caused by a different capacity of the pituitary gland to produce gonadotropins. Dairy cows with high (≥30; n = 5) and low (≤15; n = 5) follicle numbers were selected and serum concentrations of oestradiol and FSH during an oestrous cycle were measured. Cows were ovariectomised at oestrus and bled frequently up to 8 days after ovariectomy. After 33 days, cows were injected with gonadotropin-releasing hormone (GnRH) and bled intensively up to 8 h after GnRH injection. One day later, animals were injected with follicular fluid (FF) from bovine follicles and were bled intensively up to 2 days after the first injection. Serum concentrations of FSH and LH were measured. After 2 days, cows were killed and their pituitary glands collected. Prior to ovariectomy, serum oestradiol concentrations were similar between groups, whereas FSH concentrations were higher in cattle with low v. high numbers of follicles. No differences were detected in serum gonadotropin concentrations after ovariectomy, GnRH injection or FF challenge between groups. The results indicate that the inherent capacity of the pituitary gland to secrete gonadotropins does not differ between cattle with high v. low numbers of follicles during follicular waves.

Additional keywords: FSH, LH.


Acknowledgements

The authors thank P. Furney, P. Duffy and F. Carter for their technical support and helpful comments and S. Lott for his help with the management and care of the animals. This work was funded by the Irish Department of Agriculture, Fisheries and Food Research Stimulus Fund program 2006 (RSF 06–328).


References

Adams, G. P. , Matteri, R. I. , Kastelic, J. P. , Ko, J. C. H. , and Ginther, O. J. (1992). Association between surges of follicle-stimulating hormone and the emergence of follicular waves in heifers. J. Reprod. Fertil. 94, 177–188.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Beard, A. J. , Savva, D. , Glencross, R. G. , McLeod, B. J. , and Knight, P. G. (1989). Treatment of ovariectomized heifers with bovine follicular fluid specifically suppresses pituitary levels of FSH-beta mRNA. J. Mol. Endocrinol. 3, 85–91.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Beard, A. J. , Castillo, R. J. , McLeod, B. J. , Glencross, R. G. , and Knight, P. G. (1990). Comparison of the effects of crude and highly purified bovine inhibin (Mr 32,000) on plasma concentrations of FSH and LH in chronically ovariectomized prepubertal heifers. J. Endocrinol. 125, 21–30.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Bleach, E. C. , Glencross, R. G. , Feist, S. A. , Groome, N. P. , and Knight, P. G. (2001). Plasma inhibin A in heifers: relationship with follicle dynamics, gonadotropins, and steroids during the estrous cycle and after treatment with bovine follicular fluid. Biol. Reprod. 64, 743–752.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Burns, D. S. , Jimenez-Krassel, F. , Ireland, J. L. , Knight, P. G. , and Ireland, J. J. (2005). Numbers of antral follicles during follicular waves in cattle: evidence for high variation among animals, very high repeatability in individuals, and an inverse association with serum follicle-stimulating hormone concentrations. Biol. Reprod. 73, 54–62.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Cooke, D. J. , Crowe, M. A. , and Roche, J. F. (1997). Circulating FSH isoform patterns during recurrent increases in FSH throughout the oestrous cycle of heifers. J. Reprod. Fertil. 110, 339–345.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Crowe, M. A. , Padmanabhan, V. , Hynes, N. , Sunderland, S. J. , Enright, W. J. , Beitins, I. Z. , and Roche, J. F. (1997). Validation of a sensitive radioimmunoassay to measure serum follicle-stimulating hormone in cattle: correlation with biological activity. Anim. Reprod. Sci. 48, 123–136.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Dissen, G. A. , Mollett, T. A. , Youngquist, R. S. , and Garverick, H. A. (1988). Dynamics of gonadotropin release following ovariectomy and injection of gonadotropin-releasing hormone in early postpartum dairy cows. J. Dairy Sci. 71, 3489–3496.
PubMed |  CAS |

Drost, M. , Savio, J. D. , Barros, C. M. , Badinga, L. , and Thatcher, W. W. (1992). Ovariectomy by colpotomy in cows. J. Am. Vet. Med. Assoc. 200, 337–339.
PubMed |  CAS |

Duello, T. M. , and Nett, T. M. (1980). Uptake, localization, and retention of gonadotropin-releasing hormone and gonadotropin-releasing hormone analogs in rat gonadotrophs. Mol. Cell. Endocrinol. 19, 101–112.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Eppig, J. J. , O’Brien, M. J. , Pendola, F. L. , and Watanabe, S. (1998). Factors affecting the developmental competence of mouse oocytes grown in vitro: follicle-stimulating hormone and insulin. Biol. Reprod. 59, 1445–1453.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Gibbons, J. R. , Wiltbank, M. C. , and Ginther, O. J. (1997). Functional interrelationships between follicles greater than 4 mm and the follicle-stimulating hormone surge in heifers. Biol. Reprod. 57, 1066–1073.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Good, T. E. M. , Weber, P. S. D. , Ireland, J. L. , Pulaski, J. , Padmanabhan, V. , Schneyer, A. L. , Lambert-Messerlian, G. , Ghosh, B. R. , Miller, W. L. , and Groome, N. (1995). Isolation of nine different biologically and immunologically active molecular variants of bovine follicular inhibin. Biol. Reprod. 53, 1478–1488.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Groome, N. P. , Tsigou, A. , Cranfield, M. , Knight, P. G. , and Robertson, D. M. (2001). Enzyme immunoassays for inhibins, activins and follistatins. Mol. Cell. Endocrinol. 180, 73–77.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Haughian, J. M. , Ginther, O. J. , Kot, K. , and Wiltbank, M. C. (2004). Relationship between FSH patterns and follicular dynamics and the temporal associations among hormones in natural and GnRH-induced gonadotropin surges in heifers. Reproduction 127, 23–33.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Ireland, J. J. , and Roche, J. F. (1983). Growth and differentiation of large antral follicles after spontaneous luteolysis in heifers: changes in concentration of hormones in follicular fluid and specific binding of gonadotropins to follicles. J. Anim. Sci. 57, 157–167.
PubMed |  CAS |

Ireland, J. J. , Ward, F. , Jimenez-Krassel, F. , Ireland, J. L. , Smith, G. W. , Lonergan, P. , and Evans, A. C. (2007). Follicle numbers are highly repeatable within individual animals but are inversely correlated with FSH concentrations and the proportion of good-quality embryos after ovarian stimulation in cattle. Hum. Reprod. 22, 1687–1695.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Ireland, J. J. , Zielak-Steciwko, A. E. , Jimenez-Krassel, F. , Folger, J. , and Bettegowda, A. , et al. (2009). Variation in the ovarian reserve is linked to alterations in intrafollicular estradiol production and ovarian biomarkers of follicular differentiation and oocyte quality in cattle. Biol. Reprod. 80, 954–964.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Jimenez-Krassel, F. , Folger, J. K. , Mondal, M. , Scheetz, D. M. , Ireland, J. L. H. , Smith, G. W. , Mossa, F. , Lonergan, P. , Evans, A. C. O. , and Ireland, J. J. (2009). Evidence that the inherently high variation in ovarian reserves is positively associated with androgen and estradiol production in cattle. Biol. Reprod. 81, 541.


Knight, P. G. (1996). Roles of inhibins, activins, and follistatin in the female reproductive system. Front. Neuroendocrinol. 17, 476–509.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Kumar, T. R. , Wang, Y. , Lu, N. , and Matzuk, M. M. (1997). Follicle stimulating hormone is required for ovarian follicle maturation but not male fertility. Nat. Genet. 15, 201–204.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Malhi, P. S. , Adams, G. P. , and Singh, J. (2005). Bovine model for the study of reproductive aging in women: follicular, luteal, and endocrine characteristics. Biol. Reprod. 73, 45–53.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Mihm, M. , and Evans, A. C. (2008). Mechanisms for dominant follicle selection in monovulatory species: a comparison of morphological, endocrine and intraovarian events in cows, mares and women. Reprod. Domest. Anim. 43(Suppl. 2), 48–56.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Nett, T. M. , Turzillo, A. M. , Baratta, M. , and Rispoli, L. A. (2002). Pituitary effects of steroid hormones on secretion of follicle-stimulating hormone and luteinizing hormone. Domest. Anim. Endocrinol. 23, 33–42.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

O’Rourke, M. , Diskin, M. G. , Sreenan, J. M. , and Roche, J. F. (2000). The effect of dose and route of oestradiol benzoate administration on plasma concentrations of oestradiol and FSH in long-term ovariectomised heifers. Anim. Reprod. Sci. 59, 1–12.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Prendiville, D. J. , Enright, W. J. , Crowe, M. A. , Vaughan, L. , and Roche, J. F. (1995). Immunization of prepubertal beef heifers against gonadotropin-releasing hormone: immune, estrus, ovarian, and growth responses. J. Anim. Sci. 73, 3030–3037.
PubMed |  CAS |

Quirk, S. M. , and Fortune, J. E. (1986). Plasma concentrations of gonadotrophins, preovulatory follicular development and luteal function associated with bovine follicular fluid-induced delay of oestrus in heifers. J. Reprod. Fertil. 76, 609–621.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Schallenberger, E. , and Peterson, A. J. (1982). Effect of ovariectomy on tonic gonadotrophin secretion in cyclic and post-partum dairy cows. J. Reprod. Fertil. 64, 47–52.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Schoenemann, H. M. , Humphrey, W. D. , Crowder, M. E. , Nett, T. M. , and Reeves, J. J. (1985). Pituitary luteinizing hormone-releasing hormone receptors in ovariectomized cows after challenge with ovarian steroids. Biol. Reprod. 32, 574–583.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Singh, J. , Dominguez, M. , Jaiswal, R. , and Adams, G. P. (2004). A simple ultrasound test to predict the superstimulatory response in cattle. Theriogenology 62, 227–243.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Sunderland, S. J. , Crowe, M. A. , Boland, M. P. , Roche, J. F. , and Ireland, J. J. (1994). Selection, dominance and atresia of follicles during the oestrous cycle of heifers. J. Reprod. Fertil. 101, 547–555.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

te Velde, E. R. , Scheffer, G. J. , Dorland, M. , Broekmans, F. J. , and Fauser, B. C. J. M. (1998). Developmental and endocrine aspects of normal ovarian aging. Mol. Cell. Endocrinol. 145, 67–73.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Turzillo, A. M. , and Fortune, J. E. (1990). Suppression of the secondary FSH surge with bovine follicular fluid is associated with delayed ovarian follicular development in heifers. J. Reprod. Fertil. 89, 643–653.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Turzillo, A. M. , and Fortune, J. E. (1993). Effects of suppressing plasma FSH on ovarian follicular dominance in cattle. J. Reprod. Fertil. 98, 113–119.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Turzillo, A. M. , and Nett, T. M. (1999). Regulation of GnRH receptor gene expression in sheep and cattle. J. Reprod. Fertil. Suppl. 54, 75–86.
PubMed |  CAS |

Wise, P. M. , Smith, M. J. , Dubal, D. B. , Wilson, M. E. , Krajnak, K. M. , and Rosewell, K. L. (1999). Neuroendocrine influences and repercussions of the menopause. Endocr. Rev. 20, 243–248.
Crossref | GoogleScholarGoogle Scholar | PubMed | CAS |

Wolfe, M. W. , Roberson, M. S. , Stumpf, T. T. , Kittok, R. J. , and Kinder, J. E. (1992). Circulating concentrations and pattern of luteinizing hormone and follicle-stimulating hormone in circulation are changed by the circulating concentration of 17 beta-estradiol in the bovine male and female. J. Anim. Sci. 70, 248–253.
PubMed |  CAS |