You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/70535
Full metadata record
DC FieldValueLanguage
dc.contributor.authorClaro, Sandra-
dc.contributor.authorOshiro, Maria Etsuko Miyamoto-
dc.contributor.authorFreymuller, Edna-
dc.contributor.authorKatchburian, Eduardo-
dc.contributor.authorKallas, Esper George-
dc.contributor.authorCerri, Paulo Sérgio-
dc.contributor.authorFerreira, Alice Teixeira-
dc.date.accessioned2014-05-27T11:23:38Z-
dc.date.accessioned2016-10-25T18:25:53Z-
dc.date.available2014-05-27T11:23:38Z-
dc.date.available2016-10-25T18:25:53Z-
dc.date.issued2008-08-20-
dc.identifierhttp://dx.doi.org/10.1016/j.ejphar.2008.05.038-
dc.identifier.citationEuropean Journal of Pharmacology, v. 590, n. 1-3, p. 20-28, 2008.-
dc.identifier.issn0014-2999-
dc.identifier.urihttp://hdl.handle.net/11449/70535-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/70535-
dc.description.abstractWe investigated the effects of γ-radiation on cells isolated from the longitudinal smooth muscle layer of the guinea pig ileum, a relatively radioresistant tissue. Single doses (up to 50 Gy) reduced the amount of sarcoplasmatic reticulum and condensed the myofibrils, as shown by electron microscopy 3 days post-irradiation. After that, contractility of smooth muscle strips was reduced. Ca2+ handling was altered after irradiation, as shown in fura-2 loaded cells, with elevated basal intracellular Ca2+, reduced amount of intrareticular Ca2+, and reduced capacitive Ca2+ entry. Radiation also induced apoptosis, judged from flow cytometry of cells loaded with proprium iodide. Electron microscopy showed that radiation caused condensation of chromatin in dense masses around the nuclear envelope, the presence of apoptotic bodies, fragmentation of the nucleus, detachment of cells from their neighbors, and reductions in cell volume. Radiation also caused activation of caspase 12. Apoptosis was reduced by the administration of the caspase inhibitor Z-Val-Ala-Asp-fluoromethyl-ketone methyl ester (Z-VAD-FMK) during the 3 day period after irradiation, and by the chelator of intracellular Ca2+, 1,2-bis(o-aminophenoxy)-ethane-N,N,N′,N′-tetraacetic acid (BAPTA), from 1 h before until 2 h after irradiation. BAPTA also reduced the effects of radiation on contractility, basal intracellular Ca2+, amount of intrareticular Ca2+, capacitative Ca2+ entry, and apoptosis. In conclusion, the effects of gamma radiation on contractility, Ca2+ handling, and apoptosis appear due to a toxic action of intracellular Ca2+. Ca2+-induced damage to the sarcoplasmatic reticulum seems a key event in impaired Ca2+ handling and apoptosis induced by γ-radiation. © 2008 Elsevier B.V. All rights reserved.en
dc.format.extent20-28-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectγ-Radiation-
dc.subjectApoptosis-
dc.subjectCalcium-
dc.subjectCaspase 12-
dc.subjectIleum-
dc.subjectSarco/endoplasmic reticulum-
dc.subjectbenzyloxycarbonylvalylalanylaspartyl fluoromethyl ketone-
dc.subjectcalcium-
dc.subjectcaspase 12-
dc.subjectethylene glycol 1,2 bis(2 aminophenyl) ether n,n,n',n' tetraacetic acid-
dc.subjectfura 2-
dc.subjectpropidium iodide-
dc.subjectanimal tissue-
dc.subjectapoptosis-
dc.subjectcalcium cell level-
dc.subjectcell nucleus membrane-
dc.subjectcell volume-
dc.subjectchromatin condensation-
dc.subjectelectron microscopy-
dc.subjectenzyme activation-
dc.subjectflow cytometry-
dc.subjectgamma radiation-
dc.subjectguinea pig-
dc.subjectileum-
dc.subjectintestine muscle-
dc.subjectmuscle fibril-
dc.subjectnonhuman-
dc.subjectpriority journal-
dc.subjectradiosensitivity-
dc.subjectsarcoplasmic reticulum-
dc.subjectsmooth muscle contractility-
dc.subjectAnimals-
dc.subjectCaspases-
dc.subjectCells, Cultured-
dc.subjectEgtazic Acid-
dc.subjectGamma Rays-
dc.subjectGuinea Pigs-
dc.subjectMuscle Contraction-
dc.subjectMyocytes, Smooth Muscle-
dc.subjectSarcoplasmic Reticulum-
dc.titleγ-Radiation induces apoptosis via sarcoplasmatic reticulum in guinea pig ileum smooth muscle cellsen
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Biophysics Federal University of São Paulo (UNIFESP-EPM), São Paulo, SP-
dc.description.affiliationCentre of Electron Microscopy Federal University of São Paulo (UNIFESP-EPM), São Paulo, SP-
dc.description.affiliationDepartment of Morphology Federal University of São Paulo (UNIFESP-EPM), São Paulo, SP-
dc.description.affiliationDepartment of Gene Therapy Federal University of São Paulo (UNIFESP-EPM), São Paulo, SP-
dc.description.affiliationDepartment of Morphology School of Dentistry São Paulo State University (UNESP), Araraquara, SP-
dc.description.affiliationUnespDepartment of Morphology School of Dentistry São Paulo State University (UNESP), Araraquara, SP-
dc.identifier.doi10.1016/j.ejphar.2008.05.038-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofEuropean Journal of Pharmacology-
dc.identifier.scopus2-s2.0-48149091755-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.