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Cited 13 time in webofscience Cited 14 time in scopus
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Assessment of human estrogen receptor agonistic/antagonistic effects of veterinary drugs used for livestock and farmed fish by OECD in vitro stably transfected transcriptional activation assays

Authors
Lee, Hee-SeokKim, Na-YeonSong, YoungSunOh, Gyeong-YongJung, Da-WoonJeong, Da-HyunKang, Hui-SeungOh, Hyun-SookPark, YooheonHong, Jeong SupKoo, Yong Eui
Issue Date
Aug-2019
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Veterinary drug; Human estrogen receptor; Agonist; Antagonist; OECD test guideline
Citation
TOXICOLOGY IN VITRO, v.58, pp 256 - 263
Pages
8
Indexed
SCI
SCIE
SCOPUS
Journal Title
TOXICOLOGY IN VITRO
Volume
58
Start Page
256
End Page
263
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/7865
DOI
10.1016/j.tiv.2019.02.003
ISSN
0887-2333
Abstract
The presence of veterinary drug residues in foods and the environment could potentially cause adverse effects on humans and wildlife. Several veterinary drugs were reported to exhibit endocrine disrupting effects via binding affinities to sexual hormone receptors such as estrogen and androgen receptors. Therefore, we confirmed the human estrogen receptor (ER) agonistic/antagonistic effects of 135 chemicals that were used as veterinary drugs in Korea by the official Organization for Economic Cooperation and Development (OECD) in vitro ER transcriptional activation (TA) assay using the VM7Luc4E2 cell line. In the case of ER agonist screening, 7 veterinary drugs (cefuroxime, cymiazole, trenbolone, zeranol, phoxim, altrenogest and nandrolone) were determined to be ER agonists. In addition, only zeranol was found to exhibit weak ER antagonistic activity. These 7 veterinary drugs, which were determined as ER agonists and/or antagonists by an OECD in vitro assay, were also found to have binding affinity to ERs. These results indicate that various veterinary drugs possess potential (anti-)estrogenic effects. However, further study is needed to determine the precise endocrine-disrupting effects of these compounds.
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