Suppression of testicular function using two dose rates of a reversible water soluble gonadotrophin releasing hormone (GnRH) vaccine in colts.
Abstract: To investigate the effect of two dose rates (200 and 400 ng) of a gonadotrophin releasing hormone (GnRH) vaccine on testicular function. Methods: A vaccination dose rate experiment. Methods: Two injections were administered 4 weeks apart to six colts in each treatment group. To maintain immunosuppression until the end of the breeding season, a third injection was given if antibody titres fell below 1000. Results: Effective antibody titres were present for 12 to 27 weeks. Testosterone concentrations decreased from 2.22 to 0.31 nmol/L 6 weeks after primary vaccination. Androstenedione concentrations decreased from 1.78 to 0.28 nmol/L 5 weeks after vaccination. Testosterone and androstenedione concentrations above 0.69 and 0.87 nmol/L were attained 31 to 43 weeks after vaccination. Mean scrotal widths and lengths decreased over 29 weeks from 9.2 cm and 9.7 cm to 6.7 cm and 7.6 cm. At surgical castration these dimensions were 10.1 cm and 11.0 cm. Mean semen characteristics before vaccination and after recovery were: gel-free volume 16.5 and 13.5 mL, sperm concentration 295.5 x 10(6) and 315.6 x 10(6)/mL, total sperm per ejaculate 4041 x 10(6) and 4657 x 10(6) and live normal spermatozoa 32% and 60%. Histologically, the testes showed active spermatogenesis. The mean testicular parenchyma weights for the 200 and 400 mg groups were 129.0 g and 109.8 g. Daily sperm production per testis and per gram of testis for the 200 and 400 mg groups were 3.7 x 10(8) and 2.8 x 10(6), and 2.3 x 10(8) and 2.0 x 10(6). Conclusions: Both dose rates suppressed testicular function. Data showed that the vaccine effects were reversible. Individual immune response was less varied in the 200 mg group. Further work is necessary to achieve a less variable response in the immunosuppression of testicular function.
Publication Date: 1996-09-01 PubMed ID: 8894040DOI: 10.1111/j.1751-0813.1996.tb15410.xGoogle Scholar: Lookup
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Summary
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This research aimed to study how two different doses of a reversible gonadotrophin releasing hormone vaccine affected the testicular function in colts, with results suggesting they can suppress testicular function, and that these effects are reversible.
Methodology
- The researchers injected either a 200 ng or 400 ng dose of a gonadotrophin releasing hormone (GnRH) vaccine into colts. The injections were administered twice, spaced four weeks apart, with six colts in each dosage group.
- If the colt’s antibody levels dropped below 1000, a third injection was administered to maintain the suppression until the end of the breeding season.
Results
- The results showed that effective antibody titres were present for 12 to 27 weeks.
- Testosterone concentrations decreased from 2.22 to 0.31 nmol/L six weeks after the primary vaccination.
- Androstenedione concentrations decreased from 1.78 to 0.28 nmol/L five weeks after vaccination.
- Testosterone and androstenedione concentrations rose above 0.69 and 0.87 nmol/L respectively, 31 to 43 weeks after vaccination.
- Mean scrotal widths and lengths decreased over 29 weeks from 9.2 cm and 9.7 cm to 6.7 cm and 7.6 cm respectively. At the time of surgical castration, these dimensions were at 10.1 cm and 11.0 cm respectively.
- Semen characteristics were consistent before and after vaccination, with only minor decline in gel-free volume and slight increase in sperm concentration and total sperm per ejaculate, with significantly improved percentage of live normal spermatozoa after recovery.
- The study also found that the testes continued to produce sperm histologically, with no evidence of halting spermatogenesis.
- The mean testicular parenchyma weights for the 200 and 400 ng groups were 129.0 g and 109.8 g respectively.
- Daily sperm production per testis and per gram of testis showed a decrease in the 200 ng group compared to the 400 ng group.
Conclusions
- The study concluded that both dose rates were successful in suppressing testicular function in colts.
- The effects of the vaccine were found to be reversible, indicating that it could be a viable non-permanent contraceptive option for managing equine population.
- The hosts’ individual immune response was found to be less varied with the 200ng dosage compared to the 400ng one.
- Looking forward, the researchers indicated a need for additional study to decrease the variable response in the immunosuppression of testicular function to achieve more consistent results.
Cite This Article
APA
Dowsett KF, Knott LM, Tshewang U, Jackson AE, Bodero DA, Trigg TE.
(1996).
Suppression of testicular function using two dose rates of a reversible water soluble gonadotrophin releasing hormone (GnRH) vaccine in colts.
Aust Vet J, 74(3), 228-235.
https://doi.org/10.1111/j.1751-0813.1996.tb15410.x Publication
Researcher Affiliations
- Department of Farm Animal Medicine and Production, University of Queensland, New South Wales.
MeSH Terms
- Androstenedione / blood
- Animals
- Antibodies / analysis
- Antibodies / immunology
- Body Weight / physiology
- Dose-Response Relationship, Drug
- Gonadotropin-Releasing Hormone / immunology
- Gonadotropin-Releasing Hormone / pharmacology
- Horses / blood
- Horses / physiology
- Male
- Radioimmunoassay / veterinary
- Semen / physiology
- Spermatogenesis / physiology
- Testis / anatomy & histology
- Testis / drug effects
- Testis / physiology
- Testosterone / blood
- Vaccines / immunology
- Vaccines / pharmacology
Citations
This article has been cited 2 times.- Botha AE, Schulman ML, Birrell J, du Plessis L, Laver PN, Soley J, Colenbrander B, Bertschinger HJ. Effects of an anti-gonadoliberin releasing hormone vaccine on testicular, epididymal and spermatogenic development in the horse.. Reprod Domest Anim 2022 Aug;57(8):919-927.
- Lueders I, Young D, Maree L, van der Horst G, Luther I, Botha S, Tindall B, Fosgate G, Ganswindt A, Bertschinger HJ. Effects of GnRH vaccination in wild and captive African Elephant bulls (Loxodonta africana) on reproductive organs and semen quality.. PLoS One 2017;12(9):e0178270.
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