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Effect of Graphene Oxide and Ammonia-modified Graphene Oxide Particles on ATPase Activity of Rat Liver Mitochondria

Authors :
Natalia Krasteva
Milena Shkodrova
Milena Keremidarska-Markova
Dilyana Doncheva-Stoimenova
Kamelia Hristova-Panusheva
Milena Mishonova
Mariela Chichova
Source :
International Journal Bioautomation, Vol 28, Iss 1, Pp 45-58 (2024)
Publication Year :
2024
Publisher :
Bulgarian Academy of Sciences, 2024.

Abstract

Graphene and its derivatives have become promising materials for biomedical applications in the last decade. Before their widespread application, however, evaluating their toxicity and mechanisms underlying interactions with cellular components is imperative. Aims: Assessment of the effect of two graphene derivatives, pristine graphene oxide (GO) and ammonia-modified GO (GO-NH2) particles, on the ATPase activity of rat liver mitochondria and ROS production. Methods: Liver mitochondria were isolated from male albino rats and treated with different concentrations of GO and GO-NH2 particles (4, 10, 25, and 50 μg/ml). ATPase activity of both, intact and uncoupled by freezing/thawing mitochondria was determined by the measurement of inorganic phosphate (Pi) released from ATP. The generation of hydrogen peroxide (H2O2) after exposure of mitochondria to GO and GO-NH2 particles was determined by a DCFH-D assay. Results: GO and GO-NH2 particles applied at concentrations of 4 and 50 μg/ml did not affect the ATPase activity of intact mitochondria. In contrast, in uncoupled mitochondria, they demonstrated a stimulating effect on ATPase activity. The impact of GO-NH2 was more substantial and concentration-dependent. ROS production was also higher in GO-NH2-treated mitochondria. Conclusion: The present study demonstrated that GO and GO-NH2 particles can exert a cytotoxic effect on mitochondria even after a short-time of exposure to both types of particles.;

Details

Language :
English
ISSN :
13141902 and 13142321
Volume :
28
Issue :
1
Database :
Directory of Open Access Journals
Journal :
International Journal Bioautomation
Publication Type :
Academic Journal
Accession number :
edsdoj.08cbe178365a4eba851224367355ef06
Document Type :
article
Full Text :
https://doi.org/10.7546/ijba.2024.28.1.000957