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Neurotoxic effects of ochratoxin A on the subventricular zone of adult mouse brain.
Paradells, Sara; Rocamonde, Brenda; Llinares, Cristina; Herranz-Pérez, Vicente; Jimenez, Misericordia; Garcia-Verdugo, Jose Manuel; Zipancic, Ivan; Soria, Jose Miguel; Garcia-Esparza, Ma Angeles.
Afiliación
  • Paradells S; Facultad Ciencias de la Salud, Universidad CEU Cardenal Herrera, Avda Seminario, 46113, Moncada, Valencia, Spain.
  • Rocamonde B; Facultad Ciencias de la Salud, Universidad CEU Cardenal Herrera, Avda Seminario, 46113, Moncada, Valencia, Spain.
  • Llinares C; Facultad Ciencias de la Salud, Universidad CEU Cardenal Herrera, Avda Seminario, 46113, Moncada, Valencia, Spain.
  • Herranz-Pérez V; Laboratorio de Neurobiología Comparada, Instituto Cavanilles de Biodiversidad y Biología Evolutiva, Universitat de València, 46980, Paterna, Valencia, CIBERNED, Spain.
  • Jimenez M; Unidad mixta de Esclerosis múltiple y neurorregeneración, IIS Hospital La Fe-UVEG, 46013, Valencia, Spain.
  • Garcia-Verdugo JM; Departamento de Microbiología y Ecología, Universitat de València, Burjassot, Spain.
  • Zipancic I; Laboratorio de Neurobiología Comparada, Instituto Cavanilles de Biodiversidad y Biología Evolutiva, Universitat de València, 46980, Paterna, Valencia, CIBERNED, Spain.
  • Soria JM; Unidad mixta de Esclerosis múltiple y neurorregeneración, IIS Hospital La Fe-UVEG, 46013, Valencia, Spain.
  • Garcia-Esparza MA; Facultad Ciencias de la Salud, Universidad CEU Cardenal Herrera, Avda Seminario, 46113, Moncada, Valencia, Spain.
J Appl Toxicol ; 35(7): 737-51, 2015 Jul.
Article en En | MEDLINE | ID: mdl-25256750
ABSTRACT
Ochratoxin A (OTA), a mycotoxin that was discovered as a secondary metabolite of the fungal species Aspergillus and Penicillium, is a common contaminant in food and animal feed. This mycotoxin has been described as teratogenic, carcinogenic, genotoxic, immunotoxic and has been proven a potent neurotoxin. Other authors have previously reported the effects of OTA in different structures of the central nervous system as well as in some neurogenic regions. However, the impact of OTA exposure in the subventricular zone (SVZ) has not been assessed yet. To elucidate whether OTA affects neural precursors of the mouse SVZ we investigated, in vitro and in vivo, the effects of OTA exposure on the SVZ and on the neural precursors obtained from this neurogenic niche. In this work, we prove the cumulative effect of OTA exposure on proliferation, differentiation and depletion of neural stem cells cultured from the SVZ. In addition, we corroborated these results in vivo by immunohistochemistry and electron microscopy. As a result, we found a significant alteration in the proliferation process, which was evidenced by a decrease in the number of 5-bromo-2-deoxyuridine-positive cells and glial cells, as well as, a significant decrease in the number of neuroblasts in the SVZ. To summarize, in this study we demonstrate how OTA could be a threat to the developing and the adult SVZ through its impact in cell viability, proliferation and differentiation in a dose-dependent manner.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Ventrículos Laterales / Micotoxinas / Ocratoxinas Límite: Animals Idioma: En Revista: J Appl Toxicol Año: 2015 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Ventrículos Laterales / Micotoxinas / Ocratoxinas Límite: Animals Idioma: En Revista: J Appl Toxicol Año: 2015 Tipo del documento: Article País de afiliación: España