The role of oxidative stress in the protective effect of boric acid against glutamate excitotoxicity in C6 glioma cells

This study designed to investigate the biochemical changes in glial cells' oxidant/antioxidant systems in response to glutamate-induced excitotoxicity of boric acid (BA). The present study employed C6 glial cells. For the study, cells were separated into 4 groups as control, glutamate (10mM), glutamate+BA (0,23; 0,46; 0,93; 1,87 and 3,75 μg/mL), and BA (0,23; 0,46; 0,93; 1,87 and 3,75 μg/mL). The control group was not treated. The cells in the glutamate group were treated with 10 mM glutamate for 24 hours. BA was administered one hour prior to the addition of glutamate and incubated for 24 hours. The viability of the cells was evaluated using an XTT assay. Commercial kits were used for biochemical analyses. Significance was set at less than 0.05. The biochemical analysis revealed that the levels of malondialdehyde (MDA), nitric oxide (NO), inducible nitric oxide snythase (iNOS), neuronal nitric oxide synthase (nNOS), and total oxidant status (TOS) were elevated in the glutamate group compared to the control group (p

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Journal
Journal of Boron
Published
2025-04-01
DOI
https://doi.org/10.30728/boron.1519354
Primary Topic
Neuroscience and Neuropharmacology Research
Type
article
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article

The role of oxidative stress in the protective effect of boric acid against glutamate excitotoxicity in C6 glioma cells

Ahmet Şevki Taşkıran, Ayşegül Öztürk, Emin Gündoğdu
Journal of Boron
Neuroscience and Neuropharmacology Research
article

The role of oxidative stress in the protective effect of boric acid against glutamate excitotoxicity in C6 glioma cells

Ahmet Şevki Taşkıran, Ayşegül Öztürk, Emin Gündoğdu
article en

Abstract

This study designed to investigate the biochemical changes in glial cells' oxidant/antioxidant systems in response to glutamate-induced excitotoxicity of boric acid (BA). The present study employed C6 glial cells. For the study, cells were separated into 4 groups as control, glutamate (10mM), glutamate+BA (0,23; 0,46; 0,93; 1,87 and 3,75 μg/mL), and BA (0,23; 0,46; 0,93; 1,87 and 3,75 μg/mL). The control group was not treated. The cells in the glutamate group were treated with 10 mM glutamate for 24 hours. BA was administered one hour prior to the addition of glutamate and incubated for 24 hours. The viability of the cells was evaluated using an XTT assay. Commercial kits were used for biochemical analyses. Significance was set at less than 0.05. The biochemical analysis revealed that the levels of malondialdehyde (MDA), nitric oxide (NO), inducible nitric oxide snythase (iNOS), neuronal nitric oxide synthase (nNOS), and total oxidant status (TOS) were elevated in the glutamate group compared to the control group (p

Journal of BoronVol. 10(1)
Sivas Cumhuriyet Üniversitesi (TR)
Openalex Percentile: Top 91%
Neuroscience and Neuropharmacology Research
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The role of oxidative stress in the protective effect of boric acid against glutamate excitotoxicity in C6 glioma cells — Ahmet Şevki Taşkıran, Ayşegül Öztürk, et al. · Journal of Boron (2025) | TGRS Research Map | TGRS