Adverse effects of textile dyes on antioxidant enzymes and cholinesterase activities in Drosophila melanogaster (Oregon R⁺)

References

• Akar, S.T., et al., 2009. Biosorption of Reactive Blue 49 dye under batch and continuous mode using a mixed biosorbent of macro-fungus Agaricus bisporus and Thuja orientalis cones. Chemical Engineering Journal, 148 (1), 26–34.
   Web of Science ®Google Scholar
• Al-Sabti, K., Akar, S.T., Özcan, A.S., et al., 2009. Biosorption of a reactive textile dye from aqueous solutions utilizing an agro-waste. Desalination, 249 (2), 757–761.
   Web of Science ®Google Scholar
• Beyer, W.F., Jr., and Fridovich, I., 1987. Assaying for SOD activity: some large consequences of minor changes in conditions. Analytical Biochemistry, 161 (2), 559–566.
   PubMed Web of Science ®Google Scholar
• Buonocore, G., Perrone, S., and Tataranno, M.L., 2010. Oxygen toxicity: chemistry and biology of reactive oxygen species. Seminars in Fetal & Neonatal Medicine, 15 (4), 186–190.
   PubMed Web of Science ®Google Scholar
• Caliskaner, Z., et al., 2012. A case of textile dermatitis due to disperse blue on the surgical wound. Human & Experimental Toxicology, 31 (1), 101–103.
   PubMed Web of Science ®Google Scholar
• Carneiro, P.A., et al., 2010. Assessment of water contamination caused by a mutagenic textile effluent/dyehouse effluent bearing disperse dyes. Journal of Hazardous Materials, 174 (1–3), 694–699.
   PubMed Web of Science ®Google Scholar
• Chance, B., and Maehly, A.C., 1995. Assay of CATs and peroxidases. Methods in Enzymology., 136, 764–775.
   Google Scholar
• Chequer, F.M., et al., 2011. Analyses of the genotoxic and mutagenic potential of the products formed after the biotransformation of the azo dye Disperse Red 1. Toxicology In Vitro: An International Journal Published in Association with Bibra, 25 (8), 2054–2063.
   PubMed Web of Science ®Google Scholar
• Craig, L.A., Hong, N.S., and McDonald, R.J., 2011. Revisiting the cholinergic hypothesis in the development of Alzheimer’s disease. Neuroscience and Biobehavioral Reviews, 35 (6), 1397–1409.
   PubMed Web of Science ®Google Scholar
• Ellman, G.L., et al., 1961. A new and rapid colorimetric determination of acetylcholinesterase activity. Biochemical Pharmacology, 7 (2), 88–95.
   PubMed Web of Science ®Google Scholar
• Fedorova, T., et al., 2015. Salivary acetylcholinesterase activity is increased in Parkinson’s disease: a potential marker of parasympathetic dysfunction. Parkinson’s Disease, 2015, 156479.
   PubMed Web of Science ®Google Scholar
• Fernandes, F.H., et al., 2018. In vivo genotoxicity of a commercial CI Disperse Red 1 dye. Environmental and Molecular Mutagenesis, 59 (9), 822–828.
   PubMed Web of Science ®Google Scholar
• Franco, J.H., et al., 2018. Influence of auxochrome group in disperse dyes bearing azo groups as chromophore center in the biotransformation and molecular docking prediction by reductase enzyme: Implications and assessment for environmental toxicity of xenobiotics. Ecotoxicology and Environmental Safety, 160, 114–126.
   PubMed Web of Science ®Google Scholar
• Glorieux, C., and Calderon, P.B., 2017. Catalase, a remarkable enzyme: targeting the oldest antioxidant enzyme to find a new cancer treatment approach. Biological Chemistry, 398 (10), 1095–1108.
   PubMed Web of Science ®Google Scholar
• Hai, A., et al., 2013. Porphyrin derivatives as inhibitors for acetylcholinesterase from Drosophila melanogaster. Bioinformation, 9 (12), 645–649.
   PubMedGoogle Scholar
• Iqbal, M., et al., 1996. Glutathione metabolizing enzymes and oxidative stress in ferric nitrilotriacetate mediated hepatic injury. Redox Report: Communications in Free Radical Research, 2 (6), 385–391.
   PubMed Web of Science ®Google Scholar
• Jäger, I., Hafner, C., and Schneider, K., 2004. Mutagenicity of different textile dye products in Salmonella typhimurium and mouse lymphoma cells. Mutation Research, 561 (1–2), 35–44.
   PubMed Web of Science ®Google Scholar
• Jha, P., et al., 2015. Differential expression of antioxidant enzymes during degradation of azo dye reactive black 8 in hairy roots of Physalis minima L. International Journal of Phytoremediation, 17 (1-6), 305–312.
   PubMed Web of Science ®Google Scholar
• Karami, A., et al., 2015. Changes in CSF cholinergic biomarkers in response to cell therapy with NGF in patients with Alzheimer’s disease. Alzheimer’s. Alzheimer’s & Dementia: The Journal of the Alzheimer’s Association, 11 (11), 1316–1328.
   PubMed Web of Science ®Google Scholar
• Koprivanac, N., et al., 1993. Treatment of wastewaters from dye industry. Environmental Technology, 14 (4), 385–390.
   Web of Science ®Google Scholar
• Kuçukkilinç, T.T., and Ozer, I., 2008. Inhibition of electric eel acetylcholinesterase by triarylmethane dyes. Chemico-Biological Interactions, 175 (1–3), 309–311.
   PubMed Web of Science ®Google Scholar
• Lademann, J., et al., 2009. Analysis of in vivo penetration of textile dyes causing allergic reactions. Laser Physics Letters, 6 (10), 759–763.
   Web of Science ®Google Scholar
• Landmesser, U., et al., 2002. Vascular oxidative stress and endothelial dysfunction in patients with chronic heart failure: role of xanthine-oxidase and extracellular SOD. Circulation, 106 (24), 3073–3078.
   PubMed Web of Science ®Google Scholar
• Leme, D.M., et al., 2018. In vitro characterization of cutaneous immunotoxicity of immortalized human keratinocytes (HaCaT) exposed to reactive and disperse textile dyes. Journal of Toxicology and Environmental Health. Part A, 81 (13), 589–603.
   PubMed Web of Science ®Google Scholar
• Lowry, O.H., et al., 1951. Protein measurement with the Folin phenol reagent. The Journal of Biological Chemistry, 193 (1), 265–275.
   PubMed Web of Science ®Google Scholar
• Mahmoudabadi, T.Z., Talebi, P., and Jalili, M., 2019. Removing Disperse red 60 and Reactive blue 19 dyes removal by using Alcea rosea root mucilage as a natural coagulant. AMB Express, 9 (1), 1–8.
   PubMed Web of Science ®Google Scholar
• Meireles, G., et al., 2018. Red disperse dyes (DR 60, DR 73 and DR 78) at environmentally realistic concentrations impact biochemical profile of early life stages of zebrafish (Danio rerio). Chemico-Biological Interactions, 292, 94–100.
   PubMed Web of Science ®Google Scholar
• Milani, D., et al., 2018. Comparative toxicity of azo dyes to two infaunal organisms (Hexagenia spp. and Tubifex tubifex) in spiked-sediment exposures. Environmental Science and Pollution Research International, 25 (7), 6937–6950.
   PubMed Web of Science ®Google Scholar
• Mockett, R.J., et al., 2003. Ectopic expression of CAT in Drosophila mitochondria increases stress resistance but not longevity. Free Radical Biology and Medicine, 34 (2), 207–217.
   PubMed Web of Science ®Google Scholar
• Msagati, T.A. 2013. The chemistry of food additives and preservatives. Wiley-Blackwell.
   Google Scholar
• Nojavan, S., et al., 2013. Electrically enhanced liquid-phase microextraction of three textile azo dyes from wastewater and plant samples. Journal of Separation Science, 36 (19), 3256–3263.
   PubMed Web of Science ®Google Scholar
• Pacher, P.A., Nivorozhkin, A., and Szabó, C., 2006. Therapeutic effects of xanthine oxidase inhibitors: renaissance half a century after the discovery of allopurinol. Pharmacological Reviews, 58 (1), 87–114.
   PubMed Web of Science ®Google Scholar
• Pagano, G., 2002. Redox-modulated xenobiotic action and ROS formation: a mirror or a window? Human & Experimental Toxicology, 21 (2), 77–81.
   PubMed Web of Science ®Google Scholar
• Pragasam, V., et al., 2006. Immunological detection of nitrosative stress-mediated modified Tamm–Horsfall glycoprotein (THP) in calcium oxalate stone formers. Biomarkers, 11 (2), 153–163.
   PubMed Web of Science ®Google Scholar
• Romagnoli, M., Gomez-Cabrera, M.C., et al., 2010. Xanthine oxidase-induced oxidative stress causes activation of NF-kappaB and inflammation in the liver of type I diabetic rats. Free Radical Biology & Medicine, 49 (2), 171–177.
   PubMed Web of Science ®Google Scholar
• Sies, H., Berndt, C., and Jones, D.P., 2017. Oxidative stress. Annual Review of Biochemistry, 86, 715–748.
   PubMed Web of Science ®Google Scholar
• Singh, M.P., et al., 2010. Effects of co-exposure of benzene, toluene and xylene to Drosophila melanogaster: alteration in hsp70, hsp60, hsp83, hsp26, ROS generation and oxidative stress markers. Chemosphere, 79 (5), 577–587.
   PubMed Web of Science ®Google Scholar
• Singh, M.P., et al., 2009. Induction of hsp70, hsp60, hsp83, hsp26 and oxidative stress markers in benzene, toluene and xyleneexposed Drosophila melanogaster: role of ROS generation. Toxicology and Applied Pharmacology, 235 (2), 226–243.
   PubMed Web of Science ®Google Scholar
• Stahlmann, R., et al., 2006. Sensitising potential of four textile dyes and some of their metabolites in a modified local lymph node assay. Toxicology, 219 (1–3), 113–123.
   PubMed Web of Science ®Google Scholar
• Trott, O., and Olson, A.J., 2010. AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading. Journal of Computational Chemistry, 31 (2), 455–461.
   PubMed Web of Science ®Google Scholar
• Tsuboy, M.S., et al., 2007. Genotoxic, mutagenic and cytotoxic effects of the commercial dye CI Disperse Blue 291 in the human hepatic cell line HepG2. Toxicology in vitro: An International Journal Published in Association with Bibra, 21 (8), 1650–1655.
   PubMed Web of Science ®Google Scholar
• Vacchi, F.I., et al., 2017. Quantifying the contribution of dyes to the mutagenicity of waters under the influence of textile activities. The Science of the Total Environment, 601-602, 230–236.
   PubMed Web of Science ®Google Scholar
• Velan, B., et al., 1993. N-glycosylation of human acetylcholinesterase: effects on activity, stability and biosynthesis. Biochemical Journal, 296 (3), 649–656.
   PubMed Web of Science ®Google Scholar
• Wang, X., et al., 2007. Carbon monoxide protects against hyperoxia-induced endothelial cell apoptosis by inhibiting reactive oxygen species formation. The Journal of Biological Chemistry, 282 (3), 1718–1726.
   PubMed Web of Science ®Google Scholar
• Wernick, T., Lanman, B.M., and Fraux, J.L., 1975. Chronic toxicity, teratologic, and reproduction studies with hair dyes. Toxicology and Applied Pharmacology, 32 (3), 450–460.
   PubMed Web of Science ®Google Scholar
• Westerfeld, W.W., Richert, D.A., and Hilfinger, M.F., 1950. Studies on xanthine oxidase during carcinogenesis by p-dimethylaminoazobenzene. Cancer Research, 10 (8), 486–494.
   PubMed Web of Science ®Google Scholar
• Yildirim, N.C., et al., 2018. Biochemical responses of Gammarus pulex to malachite green solutions decolorized by Coriolus versicolor as a biosorbent under batch adsorption conditions optimized with response surface methodology. Ecotoxicology and Environmental Safety, 156, 41–47.
   PubMed Web of Science ®Google Scholar
• Yildirim, N.C., and Yaman, M., 2019. The usability of oxidative stress and detoxification biomarkers in Gammarus pulex for ecological risk assessment of textile dye methyl orange. Chemistry and Ecology, 35 (4), 319–329.
   Web of Science ®Google Scholar
• Yousefi Babadi, V., et al., 2014. The toxic effect of manganese on the acetylcholinesterase activity in rat brains. Journal of Toxicology, 2014, 946372.
   PubMedGoogle Scholar
• Zhang, X., et al., 2013. Catalpol improves cholinergic function and reduces inflammatory cytokines in the senescent mice induced by D-galactose. Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research Association, 58, 50–55.
   PubMed Web of Science ®Google Scholar
• Zocolo, G.J., et al., 2015. Using SPE-LC-ESI-MS/MS analysis to assess disperse dyes in environmental water samples. Journal of Chromatographic Science, 53 (8), 1257–1264.
   PubMed Web of Science ®Google Scholar