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A possible critical dosing period of p-cumylphenol for development of cystic kidneys in rat neonates

In accordance with a previous report on cystic kidneys induced in rat neonates when dosed with p-cumylphenol (PCP) for 18 days from postnatal day (PND) 4, 3 rat neonates were dosed with PCP once a day for 14 days, either from PND 14, 21, 28, 35, or 42 as W2, W3, W4, W5, and W6 groups, respectively,...

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Autores principales: Nakazawa, Tomomi, Yamaguchi, Yuko, Fukunaga, Yachiyo, Tamura, Kazutoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society of Toxicologic Pathology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8828611/
https://www.ncbi.nlm.nih.gov/pubmed/35221506
http://dx.doi.org/10.1293/tox.2021-0010
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author Nakazawa, Tomomi
Yamaguchi, Yuko
Fukunaga, Yachiyo
Tamura, Kazutoshi
author_facet Nakazawa, Tomomi
Yamaguchi, Yuko
Fukunaga, Yachiyo
Tamura, Kazutoshi
author_sort Nakazawa, Tomomi
collection PubMed
description In accordance with a previous report on cystic kidneys induced in rat neonates when dosed with p-cumylphenol (PCP) for 18 days from postnatal day (PND) 4, 3 rat neonates were dosed with PCP once a day for 14 days, either from PND 14, 21, 28, 35, or 42 as W2, W3, W4, W5, and W6 groups, respectively, to investigate whether dosing periods in different PNDs influenced the development of cystic renal tubules. The lesion was striking in the W2 group and at a lesser magnitude in the W3 group, whereas either kidney was unaffected when dosing was initiated beyond PND 28. These findings, together with the results from the previous study, suggested that PND 14-28 is a critical dosing period for PCP to develop cystic kidneys in rat neonates. The lining epithelium of the cystic tubules was immunohistochemically positive for AQP2. This finding and the anatomical location indicated that the cystic tubules were of collecting duct origin. Either obstruction, fluid accumulation, or reparative hyperplasia of the lining epithelium was unlikely to be involved in the formation of cystic tubules lined with a monolayer of cuboidal or columnar epithelium with a high nuclear density. Thus, the follow-up investigation on PCP suggested a critical dosing period of PND 14-28 in rat neonates for the development of cystic dilation of renal collecting ducts. This study further supports that additive hyperplasia of the lining epithelium is a fundamental basis of this unique lesion.
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spelling pubmed-88286112022-02-25 A possible critical dosing period of p-cumylphenol for development of cystic kidneys in rat neonates Nakazawa, Tomomi Yamaguchi, Yuko Fukunaga, Yachiyo Tamura, Kazutoshi J Toxicol Pathol Short Communication In accordance with a previous report on cystic kidneys induced in rat neonates when dosed with p-cumylphenol (PCP) for 18 days from postnatal day (PND) 4, 3 rat neonates were dosed with PCP once a day for 14 days, either from PND 14, 21, 28, 35, or 42 as W2, W3, W4, W5, and W6 groups, respectively, to investigate whether dosing periods in different PNDs influenced the development of cystic renal tubules. The lesion was striking in the W2 group and at a lesser magnitude in the W3 group, whereas either kidney was unaffected when dosing was initiated beyond PND 28. These findings, together with the results from the previous study, suggested that PND 14-28 is a critical dosing period for PCP to develop cystic kidneys in rat neonates. The lining epithelium of the cystic tubules was immunohistochemically positive for AQP2. This finding and the anatomical location indicated that the cystic tubules were of collecting duct origin. Either obstruction, fluid accumulation, or reparative hyperplasia of the lining epithelium was unlikely to be involved in the formation of cystic tubules lined with a monolayer of cuboidal or columnar epithelium with a high nuclear density. Thus, the follow-up investigation on PCP suggested a critical dosing period of PND 14-28 in rat neonates for the development of cystic dilation of renal collecting ducts. This study further supports that additive hyperplasia of the lining epithelium is a fundamental basis of this unique lesion. Japanese Society of Toxicologic Pathology 2021-09-24 2022-01 /pmc/articles/PMC8828611/ /pubmed/35221506 http://dx.doi.org/10.1293/tox.2021-0010 Text en ©2022 The Japanese Society of Toxicologic Pathology https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Short Communication
Nakazawa, Tomomi
Yamaguchi, Yuko
Fukunaga, Yachiyo
Tamura, Kazutoshi
A possible critical dosing period of p-cumylphenol for development of cystic kidneys in rat neonates
title A possible critical dosing period of p-cumylphenol for development of cystic kidneys in rat neonates
title_full A possible critical dosing period of p-cumylphenol for development of cystic kidneys in rat neonates
title_fullStr A possible critical dosing period of p-cumylphenol for development of cystic kidneys in rat neonates
title_full_unstemmed A possible critical dosing period of p-cumylphenol for development of cystic kidneys in rat neonates
title_short A possible critical dosing period of p-cumylphenol for development of cystic kidneys in rat neonates
title_sort possible critical dosing period of p-cumylphenol for development of cystic kidneys in rat neonates
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8828611/
https://www.ncbi.nlm.nih.gov/pubmed/35221506
http://dx.doi.org/10.1293/tox.2021-0010
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