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Immunocastration in adult boars as a model for late‐onset hypogonadism

BACKGROUND: While immunocastration has been studied in male pre‐pubertal pigs, data on older, sexually mature animals are limited. To understand the physiological effects of androgen deprivation in the late sexual development phase, we compared mature immunocastrated boars (n = 19; average age = 480...

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Autores principales: Batorek‐Lukač, Nina, Kress, Kevin, Čandek‐Potokar, Marjeta, Fazarinc, Gregor, Škrlep, Martin, Poklukar, Klavdija, Wesoly, Raffael, Stefanski, Volker, Vrecl, Milka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545940/
https://www.ncbi.nlm.nih.gov/pubmed/35752946
http://dx.doi.org/10.1111/andr.13219
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author Batorek‐Lukač, Nina
Kress, Kevin
Čandek‐Potokar, Marjeta
Fazarinc, Gregor
Škrlep, Martin
Poklukar, Klavdija
Wesoly, Raffael
Stefanski, Volker
Vrecl, Milka
author_facet Batorek‐Lukač, Nina
Kress, Kevin
Čandek‐Potokar, Marjeta
Fazarinc, Gregor
Škrlep, Martin
Poklukar, Klavdija
Wesoly, Raffael
Stefanski, Volker
Vrecl, Milka
author_sort Batorek‐Lukač, Nina
collection PubMed
description BACKGROUND: While immunocastration has been studied in male pre‐pubertal pigs, data on older, sexually mature animals are limited. To understand the physiological effects of androgen deprivation in the late sexual development phase, we compared mature immunocastrated boars (n = 19; average age = 480 days) to young male immunocastrated pigs (n = 6; average age = 183 days) and young entire males (n = 6; average age = 186 days) as positive and negative controls, respectively. OBJECTIVES: We hypothesized that the timing of gonadotropin‐releasing hormone suppression (early or late sexual development phases) influences the extent of reproductive function inhibition, histological structure of testicular tissue, and expression levels of selected genes related to steroid metabolism. MATERIALS AND METHODS: Antibody titer, hormonal status, and histomorphometric analysis of testicular tissue were subjected to principal component analysis followed by hierarchical clustering to evaluate the immunocastration effectiveness in mature boars. RESULTS: Hierarchical clustering differentiated mature immunocastrated boars clustered with young immunocastrated pigs from those clustered with entire males. Although all mature immunocastrated boars responded to vaccination, as evidenced by the increased gonadotropin‐releasing hormone antibody titers (p < 0.001), decreased serum luteinizing hormone concentrations (p = 0.002), and changes in testicular tissue vascularization (lighter and less red testicular parenchyma; p ≤ 0.001), the responses were variable. Sharp decreases in testes index (p < 0.001), Leydig cell volume density (p < 0.001), Leydig cell nucleus‐to‐cytoplasm ratio (p < 0.001), and testosterone concentration (p < 0.001) were observed in mature immunocastrated boars clustered with young immunocastrated pigs compared with those that clustered with entire males. Additionally, mature immunocastrated boars clustered with young immunocastrated pigs showed lower hydroxysteroid 17‐beta dehydrogenase 7 expression than entire males (p < 0.05). The young immunocastrated pigs group showed higher follicle‐stimulating hormone receptors than the entire males and mature immunocastrated boars, lower steroidogenic acute regulatory protein expression levels compared with entire males, and mature immunocastrated boars clustered with entire males (p < 0.01). CONCLUSION: The two‐dose vaccination regime resulted in progressive but variable regression of testicular function in adult (post‐pubertal) pigs; however, it was insufficient to induce a complete immunocastration response in all animals.
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spelling pubmed-95459402022-10-14 Immunocastration in adult boars as a model for late‐onset hypogonadism Batorek‐Lukač, Nina Kress, Kevin Čandek‐Potokar, Marjeta Fazarinc, Gregor Škrlep, Martin Poklukar, Klavdija Wesoly, Raffael Stefanski, Volker Vrecl, Milka Andrology Original Articles BACKGROUND: While immunocastration has been studied in male pre‐pubertal pigs, data on older, sexually mature animals are limited. To understand the physiological effects of androgen deprivation in the late sexual development phase, we compared mature immunocastrated boars (n = 19; average age = 480 days) to young male immunocastrated pigs (n = 6; average age = 183 days) and young entire males (n = 6; average age = 186 days) as positive and negative controls, respectively. OBJECTIVES: We hypothesized that the timing of gonadotropin‐releasing hormone suppression (early or late sexual development phases) influences the extent of reproductive function inhibition, histological structure of testicular tissue, and expression levels of selected genes related to steroid metabolism. MATERIALS AND METHODS: Antibody titer, hormonal status, and histomorphometric analysis of testicular tissue were subjected to principal component analysis followed by hierarchical clustering to evaluate the immunocastration effectiveness in mature boars. RESULTS: Hierarchical clustering differentiated mature immunocastrated boars clustered with young immunocastrated pigs from those clustered with entire males. Although all mature immunocastrated boars responded to vaccination, as evidenced by the increased gonadotropin‐releasing hormone antibody titers (p < 0.001), decreased serum luteinizing hormone concentrations (p = 0.002), and changes in testicular tissue vascularization (lighter and less red testicular parenchyma; p ≤ 0.001), the responses were variable. Sharp decreases in testes index (p < 0.001), Leydig cell volume density (p < 0.001), Leydig cell nucleus‐to‐cytoplasm ratio (p < 0.001), and testosterone concentration (p < 0.001) were observed in mature immunocastrated boars clustered with young immunocastrated pigs compared with those that clustered with entire males. Additionally, mature immunocastrated boars clustered with young immunocastrated pigs showed lower hydroxysteroid 17‐beta dehydrogenase 7 expression than entire males (p < 0.05). The young immunocastrated pigs group showed higher follicle‐stimulating hormone receptors than the entire males and mature immunocastrated boars, lower steroidogenic acute regulatory protein expression levels compared with entire males, and mature immunocastrated boars clustered with entire males (p < 0.01). CONCLUSION: The two‐dose vaccination regime resulted in progressive but variable regression of testicular function in adult (post‐pubertal) pigs; however, it was insufficient to induce a complete immunocastration response in all animals. John Wiley and Sons Inc. 2022-07-08 2022-09 /pmc/articles/PMC9545940/ /pubmed/35752946 http://dx.doi.org/10.1111/andr.13219 Text en © 2022 The Authors. Andrology published by Wiley Periodicals LLC on behalf of American Society of Andrology and European Academy of Andrology. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Batorek‐Lukač, Nina
Kress, Kevin
Čandek‐Potokar, Marjeta
Fazarinc, Gregor
Škrlep, Martin
Poklukar, Klavdija
Wesoly, Raffael
Stefanski, Volker
Vrecl, Milka
Immunocastration in adult boars as a model for late‐onset hypogonadism
title Immunocastration in adult boars as a model for late‐onset hypogonadism
title_full Immunocastration in adult boars as a model for late‐onset hypogonadism
title_fullStr Immunocastration in adult boars as a model for late‐onset hypogonadism
title_full_unstemmed Immunocastration in adult boars as a model for late‐onset hypogonadism
title_short Immunocastration in adult boars as a model for late‐onset hypogonadism
title_sort immunocastration in adult boars as a model for late‐onset hypogonadism
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545940/
https://www.ncbi.nlm.nih.gov/pubmed/35752946
http://dx.doi.org/10.1111/andr.13219
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