DT-diaphorase protects astrocytes from aminochrome-induced toxicity
Author
dc.contributor.author
Huenchuguala, Sandro
Author
dc.contributor.author
Muñoz, Patricia
Author
dc.contributor.author
Graumann, Rebecca
Author
dc.contributor.author
Paris Pizarro, Irmgard
Author
dc.contributor.author
Segura Aguilar, Juan
Admission date
dc.date.accessioned
2016-12-19T20:31:38Z
Available date
dc.date.available
2016-12-19T20:31:38Z
Publication date
dc.date.issued
2016
Cita de ítem
dc.identifier.citation
NeuroToxicology 55 (2016) 10–12
es_ES
Identifier
dc.identifier.other
10.1016/j.neuro.2016.04.014
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/141984
Abstract
dc.description.abstract
Astrocytes are exposed to aminochrome via the oxidation of dopamine that is taken up from the synaptic cleft after its release from dopaminergic neurons. Glutathione transferase M2-2 (GSTM2) has been shown to protect astrocytes from aminochrome-induced toxicity, but astrocytes also express DT-diaphorase, which has been shown to prevent aminochrome-induced neurotoxicity in dopaminergic neurons. Therefore, the question is whether DT-diaphorase also protects astrocytes from aminochrome-induced toxicity. DT-diaphorase is constitutively expressed in U373MG cells, and its inhibition by dicoumarol induced a significant increase of aminochrome-induced cell death. However, the inhibition of DT-diaphorase in U373MGsiGST6 cells, which have 74% of GSTM2 gene expression silenced, resulted in a more than 2-fold increase in cell death, suggesting that DT-diaphorase plays an important role in preventing aminochrome-induced toxicity in astrocytes.