Carcinogen sodium arsenite disrupts antioxidant and redox homeostasis in Drosophila melanogaster

Author:

Oyibo Aghogho1,Abolaji Amos O.2,Odunola Oyeronke A.1

Affiliation:

1. Cancer Research and Molecular Biology Laboratories, Department of Biochemistry, Faculty of Basic Medical Sciences, College of Medicine , University of Ibadan , Ibadan , Nigeria

2. Drosophila Laboratory, Department of Biochemistry, Molecular Drug Metabolism and Toxicology Unit, Faculty of Basic Medical Sciences, College of Medicine , University of Ibadan , Ibadan , Nigeria

Abstract

Abstract Objectives The inadvertent exposure to environmental contaminants has been reported to induce cancer in different animal models. Here, we investigated the toxicity of Sodium Arsenite (SA), a Class I Carcinogen in Drosophila melanogaster. Methods Harwich fly strain (1–3 days old) of both sexes were orally exposed to SA (0, 0.0312, 0.0625 and 0.125 mM) for 14 days for survival study. Thereafter, 5 days exposure period was selected to assess the toxic effects of SA on oxidative stress and antioxidant markers. Results The results indicated that SA induced significant reduction in survival and emergence rate of flies. Furthermore, SA significantly increased Nitric Oxide (NO, nitrite and nitrate) and Hydrogen Peroxide (H2O2) levels in flies compared with control (p<0.05). In addition, SA inhibited catalase and glutathione-S-transferase (GST) activities, and depleted total thiol and glutathione (GSH) contents. Moreover, acetylcholinesterase activity significantly increased in flies treated with SA when compared with control. Conclusions Sodium arsenite-induced reduction in survival and emergence rates of flies occurred via the disruption of oxidative stress-antioxidant homeostasis in D. melanogaster.

Publisher

Walter de Gruyter GmbH

Subject

Drug Discovery,Pharmacology,General Medicine,Physiology

Reference37 articles.

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3. Dilda, PJ, Hogg, PJ. Arsenical-based cancer drugs. Canc Treat Rev 2008;33:542–64. https://doi.org/10.1016/j.ctrv.2007.05.001.

4. Abolaji, AO, Kamdem, JP, Farombi, EO, Rocha, JBT. Drosophila melanogaster as a promising model organism in toxicological studies. Arch Bas App Med 2013;1:33–8.

5. Adedara, IA, Rosemberg, DB, Souza, DO, Kamdem, JP, Farombi, EO, Aschner, M, et al.. Biochemical and behavioral deficits in the lobster cockroach Nauphoeta cinerea model of methylmercury exposure. Toxicol Res 2015;4:442–51. https://doi.org/10.1039/c4tx00231h.

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