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Tannic acid protects neuroblastoma cells against hydrogen peroxide - triggered oxidative stress by suppressing oxidative stress and apoptosis.

Authors :
Yulak F
Ergul M
Source :
Brain research [Brain Res] 2024 Dec 01; Vol. 1844, pp. 149175. Date of Electronic Publication: 2024 Aug 19.
Publication Year :
2024

Abstract

Recent investigations indicate that tannic acid is associated with a decrease in oxidative damage. Growing evidence supports the protective effects of tannic acid on the central nervous system (CNS). However, uncertainties persist regarding its influence on hydrogen peroxide (H <subscript>2</subscript> O <subscript>2</subscript> )-triggered oxidative impairment in nerve cells and its interaction with apoptosis. Hence, the objective of this work was to examine the neuroprotective impact of tannic acid on SH-SY5Y cell impairment following H <subscript>2</subscript> O <subscript>2</subscript> -induced oxidative stress, particularly concerning apoptotic pathways. The control group received no treatment, while the H <subscript>2</subscript> O <subscript>2</subscript> group underwent treatment with 0.5 mM H <subscript>2</subscript> O <subscript>2</subscript> for a duration of 24 h. The tannic acid group received treatment with different concentrations of tannic acid for a duration of 24 h. Meanwhile, the tannic acid + H <subscript>2</subscript> O <subscript>2</subscript> group underwent pre-treatment with tannic acid for one hour and was subsequently subjected to 0.5 mM H <subscript>2</subscript> O <subscript>2</subscript> for one day. Within the tannic acid + H <subscript>2</subscript> O <subscript>2</subscript> group, the cell viability in SH-SY5Y cells was notably enhanced by tannic acid at concentrations of 2.5, 5, and 10 μM. It also resulted in a considerable rise in TAS (Total Antioxidant Status) levels and a concurrent decline in TOS (Total Oxidant Status) levels, serving as indicators of reduced oxidative stress. Additionally, tannic acid treatment resulted in decreased levels of apoptotic markers (Bax, cleaved PARP, and cleaved caspase 3) and oxidative DNA damage marker (8-oxo-dG), while increasing the anti-apoptotic marker Bcl-2. The findings from flow cytometry also revealed a significant reduction in the apoptosis rate following pretreatment with tannic acid. In summary, tannic acid demonstrates protective effects on SH-SY5Y cells in the face of H <subscript>2</subscript> O <subscript>2</subscript> -triggered oxidative damage by suppressing both oxidative stress and apoptosis. Nevertheless, additional research is warranted to assess the neuroprotective potential of tannic acid.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1872-6240
Volume :
1844
Database :
MEDLINE
Journal :
Brain research
Publication Type :
Academic Journal
Accession number :
39168266
Full Text :
https://doi.org/10.1016/j.brainres.2024.149175