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Vertebrate reproductive science and technology
RESEARCH ARTICLE

Endocrine changes induced by GnRH immunisation and subsequent early re-stimulation of testicular function with a GnRH agonist in stallions

Camille Gautier https://orcid.org/0000-0002-3604-4836 A * , Jörg Aurich B , Maria Melchert B , Lisa-Hélène Wagner A , Martim Kaps A , Carolina T. C. Okada A , Reinhard Ertl https://orcid.org/0000-0001-7485-3661 C , Ingrid Walter C D and Christine Aurich https://orcid.org/0000-0001-6077-7362 A
+ Author Affiliations
- Author Affiliations

A Artificial Insemination and Embryo Transfer, Department for Small Animals and Horses, Vetmeduni Vienna, Veterinärplatz 1, Vienna 1210, Austria.

B Obstetrics, Gynecology and Andrology, Department for Small Animals and Horses, Vetmeduni Vienna, Veterinärplatz 1, Vienna 1210, Austria.

C VetCore Facility for Research, Vetmeduni Vienna, Veterinärplatz 1, Vienna 1210, Austria.

D Institute of Morphology, Department of Pathobiology, Vetmeduni Vienna, Veterinärplatz 1, Vienna 1210, Austria.


Handling Editor: Marc Yeste

Reproduction, Fertility and Development 36, RD23185 https://doi.org/10.1071/RD23185
Submitted: 10 October 2023  Accepted: 23 December 2023  Published online: 19 January 2024

© 2024 The Author(s) (or their employer(s)). Published by CSIRO Publishing

Abstract

Context

Resumption of testicular function after gonadotrophin-releasing hormone (GnRH) immunisation varies among individual animals and some stallions regain fertility only after a prolonged time.

Aims

This study evaluated endocrine effects of GnRH immunisation and early subsequent re-stimulation with a GnRH agonist. We hypothesised that GnRH agonist treatment advances resumption of normal endocrine function in GnRH-vaccinated stallions.

Methods

Shetland stallions were assigned to an experimental and a control group (n = 6 each). Experimental stallions were GnRH-immunised twice, 4 weeks apart. Each experimental stallion was hemicastrated together with an age-matched control animal when testosterone concentration decreased below 0.3 ng/mL. Three weeks later, daily treatment with the GnRH agonist buserelin was initiated (4 μg/day for 4 weeks followed by 8 μg/day). The remaining testicle was removed when testosterone concentration exceeded 0.5 ng/mL in vaccinated stallions. Blood was collected for LH, FSH, oestradiol and anti-müllerian hormone (AMH) analyses, and testicular and epididymal tissue were conserved for real-time qPCR and histology.

Key results

GnRH vaccination reduced blood concentrations of LH and FSH, with a structural deterioration of testicular tissue and disruption of spermatogenesis. Daily buserelin treatment for approximately 60 days partially restored gonadotropin secretion and induced a recovery of the functional organisation of the testicular tissue with effective spermatogenesis.

Conclusions

Endocrine testicular function can be restored in GnRH-vaccinated stallions by daily low-dose buserelin treatment. The buserelin treatment protocol may potentially be improved regarding the dose, interval and duration.

Implications

Daily buserelin treatment can be recommended for treatment of GnRH-vaccinated stallions with prolonged inhibition of testicular function.

Keywords: buserelin, CYP19A1, FSH, GnRH vaccination, horse, LH, reproduction, testis.

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