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J Biochem Mol Toxicol. 2019 Apr 1:e22320. doi: 10.1002/jbt.22320. [Epub ahead of print]

Protective effects of curcumin on biochemical and molecular changes in sodium arsenite-induced oxidative damage in embryonic fibroblast cells.

Author information

1
Department of Biology, Institute of Graduate Studies in Sciences, Istanbul University, Istanbul, Turkey.
2
Department of Biology, Faculty of Sciences, Istanbul University, Istanbul, Turkey.

Abstract

The present study was aimed at determining the oxidative damage caused by sodium arsenite in 3T3 fibroblast cells and the possible protective role of curcumin (Cur) against sodium arsenite toxicity. Embryonic fibroblast cells were exposed to sodium arsenite (0.01, 0.1, 1, and 10 μM) in the presence and absence of Cur (2.5 μM) for 24 hours. Cell viability, cytotoxicity, lipid peroxidation, hydroxyl radical, hydrogen peroxide, antioxidant enzymes (superoxide dismutase, catalase, glutathione peroxidase, and glutathione-S-transferase) and expression levels of antioxidant genes (superoxide dismutase, catalase, and glutathione peroxidase) were measured in embryonic fibroblast cells. Results demonstrated that sodium arsenite directly affects antioxidant enzymes and genes in 3T3 embryonic fibroblast cells and induces oxidative damage by increasing the amount of hydrogen peroxide, hydroxyl radical, and lipid peroxidation in the cell. Furthermore, the study indicated that Cur might be a potential ameliorative antioxidant to protect the fibroblast cell toxicity induced by sodium arsenite.

KEYWORDS:

curcumin; embryonic fibroblast; oxidative damage; sodium arsenite

PMID:
30934151
DOI:
10.1002/jbt.22320

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