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dc.contributor.authorNam, C.es
dc.contributor.authorWoo, G.H.es
dc.contributor.authorUetsuka, K.-
dc.contributor.authorNakayama, Hiroyuki-
dc.contributor.authorDoi, K.-
dc.date.accessioned2011-06-30T12:02:22Z-
dc.date.available2011-06-30T12:02:22Z-
dc.date.issued2006-
dc.identifier.issn0213-3911es
dc.identifier.urihttp://hdl.handle.net/10201/22626-
dc.description.abstractEtoposide (VP-16), a topoisomerase II inhibitor, is an anti-tumor agent which is also known to show embryotoxicity, and teratogenicity when administered to pregnant rodents. We examined VP-16- induced histopathological changes in the brain of mouse fetuses. Pregnant mice were intraperitoneally injected with VP-16 (4 mg/kg) on day 12 of gestation (GD 12), and fetuses were collected from 1 to 48 hours after treatment (HAT). Mitotic neuroepithelial cells in the telencephalic wall prominently decreased at 2 HAT, and were hardly observed at 4 HAT. The number of pyknotic neuroepithelial cells in the fetal brain began to increase at 4 HAT, and became prominent from 8 to 24 HAT. These pyknotic cells were also positively stained by TUNEL method, which can detect fragmented DNA, and showed ultrastructural characteristics of apoptosis. Additionally, these cells were also positive for cleaved caspase-3, an essential executioner of apoptosis. This indicated that excessive neuroepithelial cell apoptosis was induced in the brain of mouse fetuses following VP- 16 treatment on GD 12.es
dc.formatapplication/pdfes
dc.format.extent7es
dc.languageenges
dc.publisherMurcia : F. Hernándezes
dc.relation.ispartofHistology and histopathologyes
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.subjectApoptosises
dc.subjectEtoposidees
dc.subject.otherCDU::6 - Ciencias aplicadas::63 - Agricultura. Silvicultura. Zootecnia. Caza. Pesca::636 - Veterinaria. Explotación y cría de animales. Cría del ganado y de animales domésticoses
dc.titleHistopathological changes in the brain of mouse fetuses by etoposide-administrationes
dc.typeinfo:eu-repo/semantics/articlees
Aparece en las colecciones:Vol.21, nº 3 (2006)

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