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Immunization against recombinant GnRH-I alters ultrastructure of gonadotropin cell in an experimental boar model
BACKGROUND: Gonadotropin cell is the main responsible for the secretion of follicle stimulating hormone (FSH) and luteinizing hormone (LH), and immunocastration reduces the concentrations of serum FSH and LH. A few studies have reported the histological structure of gonadotropin cells obtained from...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3720181/ https://www.ncbi.nlm.nih.gov/pubmed/23855561 http://dx.doi.org/10.1186/1477-7827-11-63 |
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author | Fang, Fugui Su, Shiping Liu, Ya Zhang, Yunhai Pu, Yong Zhao, Xijie Li, Yunsheng Cao, Hongguo Wang, Juhua Zhou, Jie Zhang, Xiaorong |
author_facet | Fang, Fugui Su, Shiping Liu, Ya Zhang, Yunhai Pu, Yong Zhao, Xijie Li, Yunsheng Cao, Hongguo Wang, Juhua Zhou, Jie Zhang, Xiaorong |
author_sort | Fang, Fugui |
collection | PubMed |
description | BACKGROUND: Gonadotropin cell is the main responsible for the secretion of follicle stimulating hormone (FSH) and luteinizing hormone (LH), and immunocastration reduces the concentrations of serum FSH and LH. A few studies have reported the histological structure of gonadotropin cells obtained from immunocastration animals at the light microscopy level. However, the ultrastructure of gonadotropin cells remains largely unexplored. The aim of this study was to evaluate and to compare ultrastructure of gonadotropin cell in gonadally intact boars and immunologically castrated male animals. FINDINGS: In this study, serum and adenohypophysis tissue were collected from nine gonadally intact boars and nine male pigs treated with recombinant gonadotropin releasing hormone I (GnRH-I). Anti-GnRH-I antibodies in serum and the ultrastructure of gonadotropin cell in adenohypophysis were determined by enzymelinked immunosorbent assay and electron microscopy, respectively. The results demonstrated that active immunization against recombinant GnRH-I increased serum GnRH-I antibody levels (P<0.05). Ultramicroscopic analysis of gonadotropin cell revealed a decrease (P<0.05) in the number and size of the large granules and small granules in the recombinant GnRH-I immunized animals. CONCLUSIONS: We conclude that immunization against recombinant GnRH-I induces severe atrophy of granules in gonadotropin cell of boars, possibly reflecting GnRH-I regulation of gonadotropin cell. |
format | Online Article Text |
id | pubmed-3720181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37201812013-07-24 Immunization against recombinant GnRH-I alters ultrastructure of gonadotropin cell in an experimental boar model Fang, Fugui Su, Shiping Liu, Ya Zhang, Yunhai Pu, Yong Zhao, Xijie Li, Yunsheng Cao, Hongguo Wang, Juhua Zhou, Jie Zhang, Xiaorong Reprod Biol Endocrinol Short Communication BACKGROUND: Gonadotropin cell is the main responsible for the secretion of follicle stimulating hormone (FSH) and luteinizing hormone (LH), and immunocastration reduces the concentrations of serum FSH and LH. A few studies have reported the histological structure of gonadotropin cells obtained from immunocastration animals at the light microscopy level. However, the ultrastructure of gonadotropin cells remains largely unexplored. The aim of this study was to evaluate and to compare ultrastructure of gonadotropin cell in gonadally intact boars and immunologically castrated male animals. FINDINGS: In this study, serum and adenohypophysis tissue were collected from nine gonadally intact boars and nine male pigs treated with recombinant gonadotropin releasing hormone I (GnRH-I). Anti-GnRH-I antibodies in serum and the ultrastructure of gonadotropin cell in adenohypophysis were determined by enzymelinked immunosorbent assay and electron microscopy, respectively. The results demonstrated that active immunization against recombinant GnRH-I increased serum GnRH-I antibody levels (P<0.05). Ultramicroscopic analysis of gonadotropin cell revealed a decrease (P<0.05) in the number and size of the large granules and small granules in the recombinant GnRH-I immunized animals. CONCLUSIONS: We conclude that immunization against recombinant GnRH-I induces severe atrophy of granules in gonadotropin cell of boars, possibly reflecting GnRH-I regulation of gonadotropin cell. BioMed Central 2013-07-15 /pmc/articles/PMC3720181/ /pubmed/23855561 http://dx.doi.org/10.1186/1477-7827-11-63 Text en Copyright © 2013 Fang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication Fang, Fugui Su, Shiping Liu, Ya Zhang, Yunhai Pu, Yong Zhao, Xijie Li, Yunsheng Cao, Hongguo Wang, Juhua Zhou, Jie Zhang, Xiaorong Immunization against recombinant GnRH-I alters ultrastructure of gonadotropin cell in an experimental boar model |
title | Immunization against recombinant GnRH-I alters ultrastructure of gonadotropin cell in an experimental boar model |
title_full | Immunization against recombinant GnRH-I alters ultrastructure of gonadotropin cell in an experimental boar model |
title_fullStr | Immunization against recombinant GnRH-I alters ultrastructure of gonadotropin cell in an experimental boar model |
title_full_unstemmed | Immunization against recombinant GnRH-I alters ultrastructure of gonadotropin cell in an experimental boar model |
title_short | Immunization against recombinant GnRH-I alters ultrastructure of gonadotropin cell in an experimental boar model |
title_sort | immunization against recombinant gnrh-i alters ultrastructure of gonadotropin cell in an experimental boar model |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3720181/ https://www.ncbi.nlm.nih.gov/pubmed/23855561 http://dx.doi.org/10.1186/1477-7827-11-63 |
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