Publicação:
Melatonin Protective Role in Mouse Cauda Epipidymal Spermatozoa Damage Induced by Sodium Arsenite

dc.contributor.authorBustos-Obregon, Eduardo
dc.contributor.authorPoblete, Daniel
dc.contributor.authorCatriao, Roberto
dc.contributor.authordel Sol, Mariano
dc.contributor.authorHenrique Fernandes, Fabio [UNESP]
dc.contributor.institutionUniv La Frontera
dc.contributor.institutionUniv Chile
dc.contributor.institutionUniv Santo Tomas
dc.contributor.institutionUniv Autonoma Chile
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-12-03T13:08:42Z
dc.date.available2014-12-03T13:08:42Z
dc.date.issued2013-12-01
dc.description.abstractWe evaluated the sperm parameters such as cauda epididymis weight, sperm count, sperm morphology and sperm DNA stability of adult CF-1 male mice treated daily (oral exposure) with the toxic sodium arsenite (As, 7.0 mg/kg/body weight); Melatonin (Me, 10.0 mg/kg/bw), Me (10.0 mg/kg/bw) plus As (7.0 mg/kg/bw) and Negative Control (NaCl 0.9%) to assess acute (8.3 days), chronic (33.2 days) and recovery of testicular damage (66.4 days). Arsenic decreases the number of sperm from chronic treatment (33.2 days) and this effect continued until 66.4 days of treatment. The toxic effect of As also altered the morphology of spermatozoa in all treatment periods when compared to the negative control group. However, Metalonin induced protective effects in periods of 33.2 and 66.4 days of treatment. Additionally, the stability of DNA was significantly affected by arsenic in all periods, but the chronic treatment (33.2 days) in the AsMe revealed increased stability compared to the group treated with arsenic only. Melatonin partially protects sperm toxicity caused by Arsenic, especially during periods of 33.2 and 66.4 days.en
dc.description.affiliationUniv La Frontera, Temuco, Chile
dc.description.affiliationUniv Chile, Sch Med, Santiago, Chile
dc.description.affiliationUniv Santo Tomas, Sch Vet, Santiago, Chile
dc.description.affiliationUniv Autonoma Chile, Ctr Invest Ciencias Biomed, Temuco, Chile
dc.description.affiliationSao Paulo State Univ, Botucatu, SP, Brazil
dc.description.affiliationUnespSao Paulo State Univ, Botucatu, SP, Brazil
dc.format.extent1251-1256
dc.identifierhttp://dx.doi.org/10.4067/S0717-95022013000400017
dc.identifier.citationInternational Journal of Morphology. Temuco: Soc Chilena Anatomia, v. 31, n. 4, p. 1251-1256, 2013.
dc.identifier.fileS0717-95022013000400017.pdf
dc.identifier.issn0717-9502
dc.identifier.scieloS0717-95022013000400017
dc.identifier.urihttp://hdl.handle.net/11449/111488
dc.identifier.wosWOS:000332286400017
dc.language.isoeng
dc.publisherSoc Chilena Anatomia
dc.relation.ispartofInternational Journal of Morphology
dc.relation.ispartofjcr0.336
dc.relation.ispartofsjr0,207
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.subjectMouseen
dc.subjectMelatoninen
dc.subjectArsenicen
dc.subjectSpermen
dc.subjectDNA stabilityen
dc.titleMelatonin Protective Role in Mouse Cauda Epipidymal Spermatozoa Damage Induced by Sodium Arseniteen
dc.typeArtigo
dcterms.rightsHolderSoc Chilena Anatomia
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.departmentGenética - IBBpt

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