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DOI 10.1016/j.tiv.2018.04.004

Медицинская библиотека · Toxicology in vitro : an international journal published in association with BIBRA · 2018

3,4-Dihydroxybenzaldehyde quenches ROS and RNS and protects human blood cells from Cr(VI)-induced cytotoxicity and genotoxicity.

Husain Nazim, Mahmood Riaz

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Аннотация

Hexavalent chromium [Cr(VI)] is the most toxic and potent form of chromium and induces multiple organ damage in humans and experimental animals. Oxidative stress has been implicated in the toxicity of Cr(VI). We have examined the potential role of 3,4-dihydroxybenzaldehyde (DHB), a plant polyphenolic antioxidant, in protecting human erythrocytes and lymphocytes from Cr(VI)-induced cytotoxicity and genotoxicity. Erythrocytes were treated with potassium dichromate, a Cr(VI) compound, in presence and absence of DHB. Incubation of erythrocytes with Cr(VI) enhanced the generation of reactive oxygen and nitrogen species, increased lipid and protein oxidation, methemoglobin levels, and lowered antioxidant power of cells. However, prior treatment of erythrocytes with DHB, resulted in a significant DHB dose-dependent decrease in reactive oxygen and nitrogen species levels and restoration of oxidative stress parameters. DHB also improved the antioxidant power of erythrocytes and restored the activities of major antioxidant, metabolic and membrane bound enzymes. Electron microscopic studies images DHB prevented Cr(VI)-induced morphological changes in erythrocytes. The single cell gel electrophoresis assay showed that DHB mitigated Cr(VI)-induced DNA damage in lymphocytes. These results clearly show that DHB protects human blood cells from Cr(VI)-induced oxidative damage and can be potentially used in reducing the toxic effects of this metal ion.

Для цитирования: Husain Nazim, Mahmood Riaz. 3,4-Dihydroxybenzaldehyde quenches ROS and RNS and protects human blood cells from Cr(VI)-induced cytotoxicity and genotoxicity.. Toxicology in vitro : an international journal published in association with BIBRA. 2018. DOI: 10.1016/j.tiv.2018.04.004.

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