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Nonmonotonic Effects of Chronic Low-Dose Di(2-ethylhexyl) Phthalate on Gonadal Weight and Reproductive

Endocrine disruptors have been concerned in toxicology but now challenged as physiological point especially concerned with exposing dose and period. In this study the low-dose chronic administration of di(2-ethylhexyl) phthaltae (DEHP) during reproductive period was examined to evaluate the possible...

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Autores principales: Cha, Sunyeong, Jung, Kayeon, Lee, Min Young, Hwang, Yeon Jeong, Yang, Eunhyeok, Lee, Sung-Ho, Jung, Hyo-il, Cheon, Yong-Pil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Developmental Biology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915770/
https://www.ncbi.nlm.nih.gov/pubmed/29707687
http://dx.doi.org/10.12717/DR.2018.22.1.085
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author Cha, Sunyeong
Jung, Kayeon
Lee, Min Young
Hwang, Yeon Jeong
Yang, Eunhyeok
Lee, Sung-Ho
Jung, Hyo-il
Cheon, Yong-Pil
author_facet Cha, Sunyeong
Jung, Kayeon
Lee, Min Young
Hwang, Yeon Jeong
Yang, Eunhyeok
Lee, Sung-Ho
Jung, Hyo-il
Cheon, Yong-Pil
author_sort Cha, Sunyeong
collection PubMed
description Endocrine disruptors have been concerned in toxicology but now challenged as physiological point especially concerned with exposing dose and period. In this study the low-dose chronic administration of di(2-ethylhexyl) phthaltae (DEHP) during reproductive period was examined to evaluate the possible roles. Adult male and female CD-1 mice were exposed to DEHP with drinking water containing 133 1g/L and 1,330 /g/L DEHP in water according to OECD 433 guide line and sacrificed just after weaning. The weights of uterus and ovary were decreased by drinking of 1,330 /g/L DEHP water. There was not adverse effects on either accumulated mating rate and mating rate depend on estrus stage, pregnancy duration, and sex ration at birth. However, the accumulated rate of successful delivery and litter size were significantly high at 1,330 dg/L DEHP water. The number of epididymal sperm was significantly increased by drinking of 1,330 g/L DEHP water. In addition, the number of follicles (primary, secondary, tertiary) were more many than control at 1,330 /g/L DEHP water drunk mother. Though further studies are needed to identify what are the mechanism of DEHP in folliculogenesis and spermatogenesis. From this study we firstly report the effect of low-dose chronic administration of DEHP with drinking could change the ovarian follicle population size and spermatogenesis rate. Put together, those finding is different from previous high-dose effects and suggest the physiological role of DEHP in gonads and uterus.
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spelling pubmed-59157702018-04-27 Nonmonotonic Effects of Chronic Low-Dose Di(2-ethylhexyl) Phthalate on Gonadal Weight and Reproductive Cha, Sunyeong Jung, Kayeon Lee, Min Young Hwang, Yeon Jeong Yang, Eunhyeok Lee, Sung-Ho Jung, Hyo-il Cheon, Yong-Pil Dev Reprod Original Research Paper Endocrine disruptors have been concerned in toxicology but now challenged as physiological point especially concerned with exposing dose and period. In this study the low-dose chronic administration of di(2-ethylhexyl) phthaltae (DEHP) during reproductive period was examined to evaluate the possible roles. Adult male and female CD-1 mice were exposed to DEHP with drinking water containing 133 1g/L and 1,330 /g/L DEHP in water according to OECD 433 guide line and sacrificed just after weaning. The weights of uterus and ovary were decreased by drinking of 1,330 /g/L DEHP water. There was not adverse effects on either accumulated mating rate and mating rate depend on estrus stage, pregnancy duration, and sex ration at birth. However, the accumulated rate of successful delivery and litter size were significantly high at 1,330 dg/L DEHP water. The number of epididymal sperm was significantly increased by drinking of 1,330 g/L DEHP water. In addition, the number of follicles (primary, secondary, tertiary) were more many than control at 1,330 /g/L DEHP water drunk mother. Though further studies are needed to identify what are the mechanism of DEHP in folliculogenesis and spermatogenesis. From this study we firstly report the effect of low-dose chronic administration of DEHP with drinking could change the ovarian follicle population size and spermatogenesis rate. Put together, those finding is different from previous high-dose effects and suggest the physiological role of DEHP in gonads and uterus. The Korean Society of Developmental Biology 2018-03 2018-03-31 /pmc/articles/PMC5915770/ /pubmed/29707687 http://dx.doi.org/10.12717/DR.2018.22.1.085 Text en © Copyright 2018 The Korean Society of Developmental Biology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Paper
Cha, Sunyeong
Jung, Kayeon
Lee, Min Young
Hwang, Yeon Jeong
Yang, Eunhyeok
Lee, Sung-Ho
Jung, Hyo-il
Cheon, Yong-Pil
Nonmonotonic Effects of Chronic Low-Dose Di(2-ethylhexyl) Phthalate on Gonadal Weight and Reproductive
title Nonmonotonic Effects of Chronic Low-Dose Di(2-ethylhexyl) Phthalate on Gonadal Weight and Reproductive
title_full Nonmonotonic Effects of Chronic Low-Dose Di(2-ethylhexyl) Phthalate on Gonadal Weight and Reproductive
title_fullStr Nonmonotonic Effects of Chronic Low-Dose Di(2-ethylhexyl) Phthalate on Gonadal Weight and Reproductive
title_full_unstemmed Nonmonotonic Effects of Chronic Low-Dose Di(2-ethylhexyl) Phthalate on Gonadal Weight and Reproductive
title_short Nonmonotonic Effects of Chronic Low-Dose Di(2-ethylhexyl) Phthalate on Gonadal Weight and Reproductive
title_sort nonmonotonic effects of chronic low-dose di(2-ethylhexyl) phthalate on gonadal weight and reproductive
topic Original Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915770/
https://www.ncbi.nlm.nih.gov/pubmed/29707687
http://dx.doi.org/10.12717/DR.2018.22.1.085
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