Publicação:
Cadmium exposure inhibits MMP2 and MMP9 activities in the prostate and testis

dc.contributor.authorLacorte, Livia Maria [UNESP]
dc.contributor.authorRinaldi, Jaqueline de Carvalho [UNESP]
dc.contributor.authorJustulin Junior, Luis Antônio [UNESP]
dc.contributor.authorDelella, Flavia Karina [UNESP]
dc.contributor.authorMoroz, Andrei [UNESP]
dc.contributor.authorFelisbino, Sérgio Luis [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2015-10-21T13:11:50Z
dc.date.available2015-10-21T13:11:50Z
dc.date.issued2015-02-20
dc.description.abstractMatrix metalloproteinases (MMPs) are zinc (Zn2+) and calcium (Ca2+) dependant endopeptidases, capable of degradation of numerous components of the extracellular matrix. Cadmium (Cd2+) is a well known environmental contaminant which could impair the activity of MMPs. In this sense, this study was conducted to evaluate if Cd2+ intake inhibits these endopeptidases activities at the rat prostate and testicles and if it directly inhibits the activity of MMP2 and MMP9 at gelatinolytic assays when present in the incubation buffer. To investigate this hypothesis, Wistar rats (5 weeks old), were given tap water (untreated, n = 9), or 15 ppm CdCl2 diluted in drinking water, during 10 weeks (n = 9) and 20 weeks (n = 9). The animals were euthanized and their ventral prostate, dorsal prostate, and testicles were removed. These tissue samples were processed for protein extraction and subjected to gelatin zymography evaluation. Additionally, we performed an experiment of gelatin zymography in which 5 mu M or 2 mM cadmium chloride (CdCl2) was directly dissolved at the incubation buffer, using the prostatic tissue samples from untreated animals that exhibited the highest MMP2 and MMP9 activities in the previous experiment. We have found that CdCl2 intake in the drinking water led to the inhibition of 35% and 30% of MMP2 and MMP9 (p < 0.05) at the ventral prostate and testis, respectively, in Cd2+ treated animals when compared to controls. Moreover, the activities of the referred enzymes were 80% and 100% inhibited by 5 mu M and 2 mM of CdCl2, respectively, even in the presence of 10 mM of CaCl2 within the incubation buffer solution. These important findings demonstrate that environmental cadmium contamination may deregulate the natural balance in the extracellular matrix turnover, through MMPs downregulation, which could contribute to the toxic effects observed in prostatic and testicular tissue after its exposure.en
dc.description.affiliationUnespUniversidade Estadual Paulista, Departamento de Morfologia, Instituto de Biociências de Botucatu
dc.description.affiliationUnespUniversidade Estadual Paulista, Departamento de Bioprocessos e Biotecnologia, Faculdade de Ciências Farmacêuticas de Araraquara
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 09/52747-7
dc.description.sponsorshipIdFAPESP: 09/50850-5
dc.format.extent538-541
dc.identifierhttp://www.sciencedirect.com/science/article/pii/S0006291X15000418
dc.identifier.citationBiochemical And Biophysical Research Communications. San Diego: Academic Press Inc Elsevier Science, v. 457, n. 4, p. 538-541, 2015.
dc.identifier.doi10.1016/j.bbrc.2015.01.019
dc.identifier.issn0006-291X
dc.identifier.lattes7263490918934874
dc.identifier.lattes8152477449159336
dc.identifier.orcid0000-0002-7358-3302
dc.identifier.urihttp://hdl.handle.net/11449/128645
dc.identifier.wosWOS:000350838800008
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofBiochemical And Biophysical Research Communications
dc.relation.ispartofjcr2.559
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectProstateen
dc.subjectCadmiumen
dc.subjectMatrix metalloproteinasesen
dc.subjectMMP2en
dc.subjectMMP9en
dc.subjectZymographyen
dc.titleCadmium exposure inhibits MMP2 and MMP9 activities in the prostate and testisen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
unesp.author.lattes7263490918934874
unesp.author.lattes8152477449159336
unesp.author.lattes6926124203948011[5]
unesp.author.orcid0000-0001-6362-5882[4]
unesp.author.orcid0000-0002-4498-9784[5]
unesp.author.orcid0000-0001-6142-3515[3]
unesp.author.orcid0000-0002-7358-3302
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentMorfologia - IBBpt
unesp.departmentBioquímica e Tecnologia - IQpt

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