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Alpha lipoic acid attenuates hypoxia-induced apoptosis, inflammation and mitochondrial oxidative stress via inhibition of TRPA1 channel in human glioblastoma cell line

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dc.creator DEVECİ, HACİ AHMET
dc.creator NUR, GÖKHAN
dc.creator Akyuva, Yener
dc.creator NAZIROĞLU, Mustafa
dc.date 2019-02-28T21:00:00Z
dc.date.accessioned 2020-10-06T09:32:39Z
dc.date.available 2020-10-06T09:32:39Z
dc.identifier 2493064c-2d28-4182-a59e-836528eaa45a
dc.identifier 10.1016/j.biopha.2018.12.077
dc.identifier https://avesis.sdu.edu.tr/publication/details/2493064c-2d28-4182-a59e-836528eaa45a/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/55531
dc.description Apoptosis, overload Ca2+ entry and oxidative stress are induced in neurons by hypoxia. Drug-resistant cancer cells are killed by hypoxic conditions. a-Lipoic acid (ALA) has antioxidant and pro-oxidant functions. The TRPA1 channel is activated by oxidative stress and pro-oxidant ALA may have a regulator role in the TRPA1 activity in the human glioblastoma (DBTRG) cells. The aim of this study was to evaluate if a combination therapy of ALA with a hypoxia can alter the effect of this hypoxia through TRPA1 activation in the DBTRG cells.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Alpha lipoic acid attenuates hypoxia-induced apoptosis, inflammation and mitochondrial oxidative stress via inhibition of TRPA1 channel in human glioblastoma cell line
dc.type info:eu-repo/semantics/article


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