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Comparative in vitro study of the inhibition of human and hen esterases by methamidophos enantiomers

dc.contributor.authorEmerick, Guilherme Luz [UNESP]
dc.contributor.authorDeOliveira, Georgino H. [UNESP]
dc.contributor.authorOliveira, Regina V.
dc.contributor.authorEhrich, Marion
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)
dc.contributor.institutionVirginia Polytech Inst & State Univ
dc.date.accessioned2014-05-20T13:25:37Z
dc.date.available2014-05-20T13:25:37Z
dc.date.issued2012-02-26
dc.description.abstractThe current Organisation for Economic Co-operation and Development (OECD) guidelines for evaluating organophosphorus-induced delayed neuropathy (OPIDN) require the observation of dosed animals over several days and the sacrifice of 48 hens. Adhering to these protocols in tests with enantiomers is difficult because large quantities of the compound are needed and many animals must be utilized. Thus, developing an in vitro screening protocol to evaluate chiral organophosphorus pesticides (OPs) that can induce delayed neuropathy is important. This work aimed to evaluate, in blood and brain samples from hens, human blood, and human cell culture samples, the potential of the enantiomeric forms of methamidophos to induce acetylcholinesterase (AChE) inhibition and/or delayed neurotoxicity. Calpain activation was also evaluated in the hen brain and SH-SY5Y human neuroblastoma cells. The ratio between the inhibition of neuropathy target esterase (NTE) and AChE activities by the methamidophos enantiomers was evaluated as a possible indicator of the enantiomers' abilities to induce OPIDN. The (-)-methamidophos exhibited an IC50 value approximately 6 times greater than that of the (+)-methamidophos for the lymphocyte NTE (LNTE) of hens, and (+)-methamidophos exhibited an IC50 value approximately 7 times larger than that of the (-)-methamidophos for the hen brain AChE. The IC50 values were 7 times higher for the human erythrocyte AChE and 5 times higher for AChE in the SH-SY5Y human neuroblastoma cells. Considering the esterases inhibition and calpain results, (+)-methamidophos would be expected to have a greater ability to induce OPIDN than the (-)-methamidophos in humans and in hens. (C) 2011 Elsevier B.V. All rights reserved.en
dc.description.affiliationUniv Estadual Paulista UNESP, Sch Pharmaceut Sci, Dept Nat Act Principles & Toxicol, BR-14801902 Araraquara, SP, Brazil
dc.description.affiliationUniversidade Federal de São Carlos (UFSCar), Dept Chem, São Carlos, SP, Brazil
dc.description.affiliationVirginia Polytech Inst & State Univ, Virginia Maryland Reg Coll Vet Med, Dept Biomed Sci & Pathobiol, Blacksburg, VA 24061 USA
dc.description.affiliationUnespUniv Estadual Paulista UNESP, Sch Pharmaceut Sci, Dept Nat Act Principles & Toxicol, BR-14801902 Araraquara, SP, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipFundação para o Desenvolvimento da UNESP (FUNDUNESP)
dc.description.sponsorshipVirginia-Maryland Regional College of Veterinary Medicine
dc.description.sponsorshipIdFAPESP: 09/51048-8
dc.description.sponsorshipIdFUNDUNESP: 01318/10 DFP
dc.format.extent145-150
dc.identifierhttp://dx.doi.org/10.1016/j.tox.2011.12.004
dc.identifier.citationToxicology. Clare: Elsevier B.V., v. 292, n. 2-3, p. 145-150, 2012.
dc.identifier.doi10.1016/j.tox.2011.12.004
dc.identifier.fileWOS000300804700010.pdf
dc.identifier.issn0300-483X
dc.identifier.urihttp://hdl.handle.net/11449/8134
dc.identifier.wosWOS:000300804700010
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofToxicology
dc.relation.ispartofjcr3.265
dc.rights.accessRightsAcesso abertopt
dc.sourceWeb of Science
dc.subjectOrganophosphate pesticidesen
dc.subjectMethamidophosen
dc.subjectChiral pesticidesen
dc.subjectAcetylcholinesteraseen
dc.subjectNeuropathy target esteraseen
dc.subjectCalpainen
dc.titleComparative in vitro study of the inhibition of human and hen esterases by methamidophos enantiomersen
dc.typeArtigopt
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.orcid0000-0002-5061-5957[3]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentPrincípios Ativos Naturais e Toxicologia - FCFpt

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