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http://hdl.handle.net/10261/11328
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dc.contributor.author | Babín, M. del Mar | - |
dc.contributor.author | Casado, Susana | - |
dc.contributor.author | Chana López, Antonio | - |
dc.contributor.author | Herradón García, Bernardo | - |
dc.contributor.author | Segner, Helmut | - |
dc.contributor.author | Tarazona, José V. | - |
dc.contributor.author | Navas, José M. | - |
dc.date.accessioned | 2009-03-06T12:50:37Z | - |
dc.date.available | 2009-03-06T12:50:37Z | - |
dc.date.issued | 2005-08-10 | - |
dc.identifier.citation | Toxicology in Vitro 19(7): 899-902 (2005) | en_US |
dc.identifier.issn | 0887-2333 | - |
dc.identifier.uri | http://hdl.handle.net/10261/11328 | - |
dc.description | 4 pages, 2 figures.-- PMID: 16095870 [PubMed].-- Printed version published Oct 2005.-- Issue title: Thirteenth International Workshop on In Vitro Toxicology (Zegrze, Poland, Sep 4-11, 2004). | en_US |
dc.description.abstract | A variety of aquatic pollutants are able to induce cytochrome P4501A (CYP1A) in fish by ligand binding to the aryl hydrocarbon receptor (AhR). High-affinity AhR ligands are planar aromatic polycyclic molecules such as the prototypical ligand, 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). The present work investigates the ability of the imidazole derivative, Prochloraz (PRO), to induce CYP1A. Computational studies on the molecular structure of PRO indicated that it is highly unlikely for PRO to have both aromatic rings of the molecule, i.e. the imidazole and the benzene ring, in the same plane. Thus, the possible conformers do not take planar structures, in contrast to the typically planar AhR ligands. Experimentally, the capability of PRO to induce CYP1A was assessed using the rainbow trout liver cell line, RTL-W1, as in vitro model. PRO increased in a concentration-dependent way the catalytic activity of CYP1A (determined as 7-ethoxyresorufin-O-deethylase, EROD, activity) in RTL-W1 cells. The potency of PRO was lower than that of a reference AhR-ligand, β-naphthoflavone (βNF). In addition to the catalytic level, PRO activated CYP1A also at the transcriptional level as determined by RT-PCR analysis of CYP1A mRNA. These results indicate that PRO, although its structure is not corresponding to the typical features of CYP1A-inducing AhR ligands, still is able to activate CYP1A expression. | en_US |
dc.description.sponsorship | J.M. Navas holds a Ramón y Cajal Contract from the Spanish Ministry of Education and Science (MEC). This work was financially supported by projects REN2002-00639/GLO (MEC) and 07/0032/2002 (Autonomic Community of Madrid). | en_US |
dc.format.extent | 918459 bytes | - |
dc.format.mimetype | application/pdf | - |
dc.language.iso | eng | en_US |
dc.publisher | Elsevier | en_US |
dc.rights | closedAccess | en_US |
dc.subject | Cytochrome P4501A | en_US |
dc.subject | Prochloraz | en_US |
dc.subject | Aryl hydrocarbon receptor | en_US |
dc.subject | RTL-W1 | en_US |
dc.subject | Hepatocyte | en_US |
dc.title | Cytochrome P4501A induction caused by the imidazole derivative Prochloraz in a rainbow trout cell line | en_US |
dc.type | artículo | en_US |
dc.identifier.doi | 10.1016/j.tiv.2005.06.037 | - |
dc.description.peerreviewed | Peer reviewed | en_US |
dc.relation.publisherversion | http://dx.doi.org/10.1016/j.tiv.2005.06.037 | en_US |
dc.type.coar | http://purl.org/coar/resource_type/c_6501 | es_ES |
item.fulltext | No Fulltext | - |
item.languageiso639-1 | en | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.openairetype | artículo | - |
item.cerifentitytype | Publications | - |
item.grantfulltext | none | - |
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