Source:http://linkedlifedata.com/resource/pubmed/id/19095286
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2009-2-23
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pubmed:abstractText |
Enantioselectivity in the separation, toxicology, biodegradation and estrogenic activity of chiral pesticides has become a groundbreaking topic recently. In this study, real-time, quantitative polymerase chain reaction was adapted to investigate the induction of estrogen-responsive gene expression in embryo-larval zebrafish after 7 d of exposure to permethrin (PM) enantiomers. The PM enantiomers were completely separated by a chiral HPLC column. The in vivo study found that a 7 d exposure to 250 ng L(-1) PM racemate and its enantiomers was sufficient to stimulate vtg1, esralpha and cyp19b expression, while 1000 ng L(-1) exposure significantly induced gene expression in a pattern similar to that of the control (50 ng L(-1) E2), except for vtg2. Significant differences were detected between the enantiomers in the induction of estrogen-responsive gene expression. At the exposure level of 1000 ng L(-1), the vtg1, esralpha and cyp19b responses to the (-)-trans enantiomer were about 3.2-, 1.8- and 1.5-fold higher, respectively, than those in the group treated with (+)-trans enantiomer (p < 0.05). In the two cis-enantiomer treatment groups, (+)-cis increased the mRNA level of the cyp19b gene about 1.5-fold higher than the (-)-cis-enantiomer did. Of the four enantiomers, the (-)-trans enantiomer showed the greatest estrogenic activity. The results strongly indicate the occurrence of significant enantioselectivity in estrogenic activity of PM enantiomers exposed to embryo-larval zebrafish. These findings add to a growing body of evidence concerning enantioselectivity in the toxicity, endocrine-disrupting activity, and environmental biodegradation of chiral pesticides.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Aromatase,
http://linkedlifedata.com/resource/pubmed/chemical/CYP19a protein, zebrafish,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers,
http://linkedlifedata.com/resource/pubmed/chemical/Estrogens,
http://linkedlifedata.com/resource/pubmed/chemical/Insecticides,
http://linkedlifedata.com/resource/pubmed/chemical/Permethrin,
http://linkedlifedata.com/resource/pubmed/chemical/Zebrafish Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1879-1298
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
74
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1238-44
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pubmed:meshHeading |
pubmed-meshheading:19095286-Animals,
pubmed-meshheading:19095286-Aromatase,
pubmed-meshheading:19095286-Chromatography, High Pressure Liquid,
pubmed-meshheading:19095286-DNA Primers,
pubmed-meshheading:19095286-Dose-Response Relationship, Drug,
pubmed-meshheading:19095286-Estrogens,
pubmed-meshheading:19095286-Gene Expression Regulation,
pubmed-meshheading:19095286-Insecticides,
pubmed-meshheading:19095286-Permethrin,
pubmed-meshheading:19095286-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:19095286-Stereoisomerism,
pubmed-meshheading:19095286-Zebrafish,
pubmed-meshheading:19095286-Zebrafish Proteins
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pubmed:year |
2009
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pubmed:articleTitle |
Enantioselective induction of estrogen-responsive gene expression by permethrin enantiomers in embryo-larval zebrafish.
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pubmed:affiliation |
College of Biological and Environmental Engineering, Zhejiang University of Technology, Hangzhou 310032, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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