Document Detail


Fluorotelomer alcohols induce hepatic vitellogenin through activation of the estrogen receptor in male medaka (Oryzias latipes).
MedLine Citation:
PMID:  18334264     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Here we report on the in vivo estrogenic effects of two fluorotelomer alcohols, such as 1H,1H,2H,2H-perfluorooctan-1-ol (6:2 FTOH) and 1H,1H,2H,2H-perfluorodecan-1-ol (8:2 FTOH), in male medaka (Oryzias latipes). An in vitro yeast two-hybrid assay indicated a significant, dose-dependent interaction between medaka estrogen receptor alpha (ERalpha) and coactivator TIF2 upon treatment with 6:2 FTOH, 8:2 FTOH or 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-nonadecafluoro-1-decanol (NFDH). The relative ranks of tested chemicals on the estrogenic effects for medaka ERalpha descended in the order of estradiol-17beta (100)>>6:2 FTOH (0.16)>NFDH (0.016)>8:2 FTOH (0.0044). In contrast, no interaction with the ERalpha was observed upon treatment with perfluorooctane sulfonate (PFOS), perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), perfluorododecanoic acid (PFDA) or perfluoroundecanoic acid (PFUnDA). Expression analysis of hepatic vitellogenin (VTG) protein showed estrogenic potentials with, 6:2 FTOH and 8:2 FTOH, indicative of the induction of VTG synthesis in the livers of male medaka. We also investigated mRNA expression levels of two ER subtypes (ERalpha and beta) and two VTGs (VTG I and VTG II) in the livers of male medaka following exposure to FTOHs. Quantitative real-time polymerase chain reaction analyses revealed that hepatic ERalpha, VTG I, and VTG II mRNA responded rapidly to FTOHs such as 6:2 FTOH and 8:2 FTOH after 8-h exposure, whereas no effects of these compounds on ERbeta mRNA transcription were observed. These results from both in vitro and in vivo assays strongly suggest that certain FTOHs, such as 6:2 FTOH and 8:2 FTOH, induce hepatic VTG through activation of ERalpha in male medaka.
Authors:
Hiroshi Ishibashi; Ryoko Yamauchi; Munekazu Matsuoka; Joon-Woo Kim; Masashi Hirano; Akemi Yamaguchi; Nobuaki Tominaga; Koji Arizono
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Publication Detail:
Type:  Journal Article     Date:  2008-03-10
Journal Detail:
Title:  Chemosphere     Volume:  71     ISSN:  0045-6535     ISO Abbreviation:  Chemosphere     Publication Date:  2008 May 
Date Detail:
Created Date:  2008-04-21     Completed Date:  2008-09-09     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0320657     Medline TA:  Chemosphere     Country:  England    
Other Details:
Languages:  eng     Pagination:  1853-9     Citation Subset:  IM    
Affiliation:
Faculty of Environmental and Symbiotic Sciences, Prefectural University of Kumamoto, 3-1-100 Tsukide, Kumamoto 862-8502, Japan.
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MeSH Terms
Descriptor/Qualifier:
Alcohols / toxicity*
Animals
Estrogen Receptor beta / genetics
Estrogens, Non-Steroidal / toxicity*
Fluorocarbons / toxicity*
Liver / drug effects,  metabolism
Male
Oryzias / metabolism*
RNA, Messenger / metabolism
Receptors, Estrogen / genetics*
Saccharomyces cerevisiae / genetics
Vitellogenins / genetics*
Water Pollutants, Chemical / toxicity*
Chemical
Reg. No./Substance:
0/Alcohols; 0/Estrogen Receptor beta; 0/Estrogens, Non-Steroidal; 0/Fluorocarbons; 0/RNA, Messenger; 0/Receptors, Estrogen; 0/Vitellogenins; 0/Water Pollutants, Chemical; 0/estrogen receptor alpha, medaka

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