Source:http://linkedlifedata.com/resource/pubmed/id/12371478
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2002-10-9
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pubmed:abstractText |
Seven reaction products (2-chloro-4-nonylphenol [NP], 2,6-dichloro-4-NP, trichlorophenol, 4-propyl-2'-hydroxyphenol, 4-isobutyl-2'-hydroxyphenol, 4-isoamyl-2'-hydroxyphenol, and 4-isopentyl-2'-hydroxyphenol) were identified by gas chromatography/mass spectrometry (GC/MS) in order to assess the estrogenic activity originated from 4-nonylphenol (4-NP) in drinking water. The estrogenic activities of the aqueous chlorinated 4-NP solution at 10, 60, and 120 min chlorination time were assessed by a yeast two-hybrid system based on the ligand-dependent interaction of two proteins, a human estrogen receptor (ER), and a coactivator. It was found that all three solutions inhibited transcriptional activation induction by 4-NP. Further experiments showed that these solutions also inhibited beta-galactosidase induction by 17beta-estradiol. For the solution at 10 min, the inhibition was found to be due to its toxicity, with an inhibition concentration (IC50) of about 10-fold of concentration of chlorinated 4-NP solution, suggesting the existence of some products with higher yeast toxicity than that of the parent 4-NP. Similar inhibition trends were also found in the dose response of the two solutions at 60 and 120 min, with an IC50 of 10-fold concentration. In these cases, the effects were considered to result from their antagonist action because the two solutions show lower yeast toxicity of which IC50 is 45-fold concentration. This suggests that some products in the chlorinated 4-NP solution elicit the antiestrogenic activities.
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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/4-nonylphenol,
http://linkedlifedata.com/resource/pubmed/chemical/Chlorophenols,
http://linkedlifedata.com/resource/pubmed/chemical/Estrogens, Non-Steroidal,
http://linkedlifedata.com/resource/pubmed/chemical/Phenols,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Estrogen,
http://linkedlifedata.com/resource/pubmed/chemical/Water Pollutants, Chemical,
http://linkedlifedata.com/resource/pubmed/chemical/beta-Galactosidase
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0730-7268
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
21
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2034-9
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12371478-Chlorophenols,
pubmed-meshheading:12371478-Dose-Response Relationship, Drug,
pubmed-meshheading:12371478-Estrogens, Non-Steroidal,
pubmed-meshheading:12371478-Humans,
pubmed-meshheading:12371478-Phenols,
pubmed-meshheading:12371478-Receptors, Estrogen,
pubmed-meshheading:12371478-Saccharomyces cerevisiae,
pubmed-meshheading:12371478-Time Factors,
pubmed-meshheading:12371478-Water Pollutants, Chemical,
pubmed-meshheading:12371478-Water Purification,
pubmed-meshheading:12371478-Water Supply,
pubmed-meshheading:12371478-beta-Galactosidase
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pubmed:year |
2002
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pubmed:articleTitle |
Products of aqueous chlorination of 4-nonylphenol and their estrogenic activity.
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pubmed:affiliation |
Department of Urban and Environmental Science, Peking University, Beijing, China. hujy@urban.pku.edu.cn
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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