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A Histopathological Study of Multi-hormone Producing Proliferative Lesions in Estrogen-induced Rat Pituitary Prolactinoma
Rats with estrogen-induced prolactin-producing pituitary adenoma (E2-PRLoma) have been employed as an animal model of human PRL-producing pituitary adenoma in a large number of studies. Presently, we found that long-term administration of estrogen to SD rats resulted in the development of E2-PRLomas...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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JAPAN SOCIETY OF HISTOCHEMISTRY AND CYTOCHEMISTRY
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164703/ https://www.ncbi.nlm.nih.gov/pubmed/25392569 http://dx.doi.org/10.1267/ahc.14029 |
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author | Takekoshi, Susumu Yasui, Yuzo Inomoto, Chie Kitatani, Kanae Nakamura, Naoya Osamura, Robert Yoshiyuki |
author_facet | Takekoshi, Susumu Yasui, Yuzo Inomoto, Chie Kitatani, Kanae Nakamura, Naoya Osamura, Robert Yoshiyuki |
author_sort | Takekoshi, Susumu |
collection | PubMed |
description | Rats with estrogen-induced prolactin-producing pituitary adenoma (E2-PRLoma) have been employed as an animal model of human PRL-producing pituitary adenoma in a large number of studies. Presently, we found that long-term administration of estrogen to SD rats resulted in the development of E2-PRLomas, some of which included multi-hormone producing nodules. We herein report results of histopathological analyses of these lesions. PRLoma models were created in female SD rats by 22 weeks or longer administration of a controlled-release preparation of estradiol at a dose of 10 mg/kg/2 weeks. Ten of the 11 PRLoma model rats had proliferative nodular lesions composed of large eosinophilic cells like gonadotrophs inside the PRLoma. These lesions were positive for PRL, TSHβ, and α subunits and were negative for GH, LHβ, ACTH, and S-100. Double immunostaining revealed that these large eosinophilic cells showed coexpression of PRL and TSHβ, PRL and α subunits, and TSHβ and α subunits. Those results clarified that long-term estrogen administration to female SD rats induced multi-hormone producing neoplastic pituitary nodules that expressed PRL, TSHβ, and α subunits. We studied these neoplastic nodules obtained by laser microdissection to acquire findings similar to those of the immunohistochemical analysis. We consider that this animal model is useful for pathogenesis analyses and therapeutic agent development concerning human multi-hormone producing pituitary adenomas. |
format | Online Article Text |
id | pubmed-4164703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | JAPAN SOCIETY OF HISTOCHEMISTRY AND CYTOCHEMISTRY |
record_format | MEDLINE/PubMed |
spelling | pubmed-41647032014-11-12 A Histopathological Study of Multi-hormone Producing Proliferative Lesions in Estrogen-induced Rat Pituitary Prolactinoma Takekoshi, Susumu Yasui, Yuzo Inomoto, Chie Kitatani, Kanae Nakamura, Naoya Osamura, Robert Yoshiyuki Acta Histochem Cytochem Regular Article Rats with estrogen-induced prolactin-producing pituitary adenoma (E2-PRLoma) have been employed as an animal model of human PRL-producing pituitary adenoma in a large number of studies. Presently, we found that long-term administration of estrogen to SD rats resulted in the development of E2-PRLomas, some of which included multi-hormone producing nodules. We herein report results of histopathological analyses of these lesions. PRLoma models were created in female SD rats by 22 weeks or longer administration of a controlled-release preparation of estradiol at a dose of 10 mg/kg/2 weeks. Ten of the 11 PRLoma model rats had proliferative nodular lesions composed of large eosinophilic cells like gonadotrophs inside the PRLoma. These lesions were positive for PRL, TSHβ, and α subunits and were negative for GH, LHβ, ACTH, and S-100. Double immunostaining revealed that these large eosinophilic cells showed coexpression of PRL and TSHβ, PRL and α subunits, and TSHβ and α subunits. Those results clarified that long-term estrogen administration to female SD rats induced multi-hormone producing neoplastic pituitary nodules that expressed PRL, TSHβ, and α subunits. We studied these neoplastic nodules obtained by laser microdissection to acquire findings similar to those of the immunohistochemical analysis. We consider that this animal model is useful for pathogenesis analyses and therapeutic agent development concerning human multi-hormone producing pituitary adenomas. JAPAN SOCIETY OF HISTOCHEMISTRY AND CYTOCHEMISTRY 2014-08-29 2014-07-16 /pmc/articles/PMC4164703/ /pubmed/25392569 http://dx.doi.org/10.1267/ahc.14029 Text en 2014 The Japan Society of Histochemistry and Cytochemistry This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Regular Article Takekoshi, Susumu Yasui, Yuzo Inomoto, Chie Kitatani, Kanae Nakamura, Naoya Osamura, Robert Yoshiyuki A Histopathological Study of Multi-hormone Producing Proliferative Lesions in Estrogen-induced Rat Pituitary Prolactinoma |
title | A Histopathological Study of Multi-hormone Producing Proliferative Lesions in Estrogen-induced Rat Pituitary Prolactinoma |
title_full | A Histopathological Study of Multi-hormone Producing Proliferative Lesions in Estrogen-induced Rat Pituitary Prolactinoma |
title_fullStr | A Histopathological Study of Multi-hormone Producing Proliferative Lesions in Estrogen-induced Rat Pituitary Prolactinoma |
title_full_unstemmed | A Histopathological Study of Multi-hormone Producing Proliferative Lesions in Estrogen-induced Rat Pituitary Prolactinoma |
title_short | A Histopathological Study of Multi-hormone Producing Proliferative Lesions in Estrogen-induced Rat Pituitary Prolactinoma |
title_sort | histopathological study of multi-hormone producing proliferative lesions in estrogen-induced rat pituitary prolactinoma |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164703/ https://www.ncbi.nlm.nih.gov/pubmed/25392569 http://dx.doi.org/10.1267/ahc.14029 |
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