Neutralization of iron oxide magnetic nanoparticle aquatoxicity on Oncorhynchus mykiss via supplementation with ulexite

References

• Abdel-Latif, H.M., et al., 2021. Copper oxide nanoparticles alter serum biochemical indices, induce histopathological alterations, and modulate transcription of cytokines, HSP70, and oxidative stress genes in Oreochromis niloticus. Animals, 11 (3), 652.
   Web of Science ®Google Scholar
• Aebi, H., 1984. Catalase in vitro. Methods in Enzymology, 105, 121–126.
   PubMed Web of Science ®Google Scholar
• Afifi, M., Saddick, S., and Abu Zinada, O.A., 2016. Toxicity of silver nanoparticles on the brain of Oreochromis niloticus and Tilapia zillii. Saudi Journal of Biological Sciences, 23 (6), 754–760.
   PubMed Web of Science ®Google Scholar
• Agayeva, N.J., et al., 2020. Exposure of rainbow trout (Oncorhynchus mykiss) to magnetite (Fe3O4) nanoparticles in simplified food chain: study on ultrastructural characterization. Saudi Journal of Biological Sciences, 27 (12), 3258–3266.
   PubMed Web of Science ®Google Scholar
• Ahmed, I., Reshi, Q.M., and Fazio, F., 2020. The influence of the endogenous and exogenous factors on hematological parameters in different fish species: a review. Aquaculture International, 28, 869–899.
   Web of Science ®Google Scholar
• Alak, G., et al., 2019b. Neurophysiological responses in the brain tissues of rainbow trout (Oncorhynchus mykiss) treated with bio-pesticide. Drug and Chemical Toxicology, 42 (2), 203–209.
   PubMed Web of Science ®Google Scholar
• Alak, G., et al., 2018. Neuroprotective effects of dietary borax in the brain tissue of rainbow trout (Oncorhynchus mykiss) exposed to copper-induced toxicity. Fish Physiology and Biochemistry, 44 (5), 1409–1420.
   PubMed Web of Science ®Google Scholar
• Alak, G., et al., 2019a. Therapeutic effect of N-acetyl cysteine as an antioxidant on rainbow trout’s brain in cypermethrin toxicity. Chemosphere, 221, 30–36.
   PubMed Web of Science ®Google Scholar
• Bacchetta, C., et al., 2017. Genotoxicity and oxidative stress in fish after a short-term exposure to silver nanoparticles. Ecological Indicators., 76, 230–239.
   Web of Science ®Google Scholar
• Beutler, E., 1984. Glutathione peroxidase (GSH-Px). Red cell metabolism: A manual of biochemical methods. United States: Grune & Stratton.
   Google Scholar
• Beutler, E., and Kelly, B.M., 1963. The effect of sodium nitrite on red cell GSH. Experientia, 19 (2), 96–97.
   PubMedGoogle Scholar
• Bolognesi, C., et al., 2006. Assessment of micronuclei induction in peripheral erythrocytes of fish exposed to xenobiotics under controlled conditions. Aquatic Toxicology., 78, S93–S98.
   PubMed Web of Science ®Google Scholar
• Bradley, P.P., et al., 1982. Measurement of cutaneous inflammation: estimation of neutrophil content with an enzyme marker. Journal of Investigative Dermatology, 78 (3), 206–209.
   PubMed Web of Science ®Google Scholar
• Brown, D., et al., 2004. Calcium and ROS-mediated activation of transcription factors and TNF-alpha cytokine gene expression in macrophages exposed to ultrafine particles. American Journal of Physiology. Lung Cellular and Molecular Physiology, 286 (2), L344–53.
   PubMed Web of Science ®Google Scholar
• Buchmann, K., 2014. Evolution of innate immunity: clues from invertebrates via fish to mammals. Frontiers in Immunology, 5, 459.
   PubMed Web of Science ®Google Scholar
• Čaloudová, H., Čaloudová, J., and Svobodová, Z., 2021. A review of the effects of metallic nanoparticles on fish. Acta Veterinaria Brno, 90 (3), 331–347.
   Web of Science ®Google Scholar
• Canli, E.G., and Canli, M., 2017. Effects of aluminum, copper, and titanium nanoparticles on some blood parameters in Wistar rats. Turkısh Journal of Zoology, 41 (2), 259–266.
   Web of Science ®Google Scholar
• Canli, E.G., Dogan, A., and Canli, M., 2018. Serum biomarker levels alter following nanoparticle (Al2O3, CuO, TiO2) exposures in freshwater fish (Oreochromis niloticus). Environmental Toxicology and Pharmacology, 62, 181–187.
   PubMed Web of Science ®Google Scholar
• Carmo, T.L., et al., 2019. Overview of the toxic effects of titanium dioxide nanoparticles in blood, liver, muscles, and brain of a neotropical detritivorous fish. Environmental Toxicology, 34 (4), 457–468.
   PubMed Web of Science ®Google Scholar
• Culcasi, M., et al., 2012. EPR spin trapping evaluation of ROS production in human fibroblasts exposed to cerium oxide nanoparticles: evidence for NADPH oxidase and mitochondrial stimulation. Chemico-Biological İnteractions, 199 (3), 161–176.
   PubMed Web of Science ®Google Scholar
• Das, P., et al., 2004. Nitrite toxicity in Cirrhinus mrigala (Ham.): acute toxicity and sublethal effect on selected hematological parameters. Aquaculture, 235 (1–4), 633–644.
   Web of Science ®Google Scholar
• de Oliveira, L.F., et al., 2018. Triple‐mixture of Zn, Mn, and Fe increases bioaccumulation and causes oxidative stress in freshwater neotropical fish. Environmental Toxicology and Chemistry, 37 (6), 1749–1756.
   PubMed Web of Science ®Google Scholar
• Delmond, K.A., et al., 2019. Antioxidant imbalance and genotoxicity detected in fish induced by titanium dioxide nanoparticles (NpTiO2) and inorganic lead (PbII). Environmental Toxicology and Pharmacology, 67, 42–52.
   PubMed Web of Science ®Google Scholar
• Eom, H.J., and Choi, J., 2010. p38 MAPK activation, DNA damage, cell cycle arrest and apoptosis as mechanisms of toxicity of silver nanoparticles in Jurkat T cells. Environmental Science & Technology, 44 (21), 8337–8342.
   PubMed Web of Science ®Google Scholar
• Fazio, F., 2019. Fish hematology analysis as an important tool of aquaculture: a review. Aquaculture, 500, 237–242.
   Web of Science ®Google Scholar
• García-Medina, S., et al., 2022. Bioaccumulation and oxidative stress caused by aluminium nanoparticles and the integrated biomarker responses in the common carp (Cyprinus carpio). Chemosphere, 288 (Pt 2), 132462.
   PubMed Web of Science ®Google Scholar
• Habib, G.M., Shi, Z.Z., and Lieberman, M.W., 2007. Glutathione protects cells against arsenite-induced toxicity. Free Radical Biology & Medicine, 42 (2), 191–201.
   PubMed Web of Science ®Google Scholar
• Handy, R.D., et al., 2008. Manufactured nanoparticles: their uptake and effects on fish—a mechanistic analysis. Ecotoxicology (London, England), 17 (5), 396–409.
   PubMed Web of Science ®Google Scholar
• Harabawy, A.S., and Ibrahim, A.T.A., 2014. Sublethal toxicity of carbofuran pesticide on the African catfish Clarias gariepinus (Burchell, 1822): hematological, biochemical and cytogenetic response. Ecotoxicology and Environmental Safety, 103, 61–67.
   PubMed Web of Science ®Google Scholar
• Hoseini, S.M., et al., 2016. Toxic effects of copper sulfate and copper nanoparticles on minerals, enzymes, thyroid hormones and protein fractions of plasma and histopathology in common carp Cyprinus carpio. Experimental and Toxicologic Pathology : Official Journal of the Gesellschaft Fur Toxikologische Pathologie, 68 (9), 493–503.
   PubMedGoogle Scholar
• Huang, T.C., et al., 2011. Resveratrol protects rats from Aβ-induced neurotoxicity by the reduction of iNOS expression and lipid peroxidation. PloS One, 6 (12), e29102.
   PubMed Web of Science ®Google Scholar
• Huang, W., Tang, Y., and Li, L., 2010. HMGB1, a potent proinflammatory cytokine in sepsis. Cytokine, 51 (2), 119–126.
   PubMed Web of Science ®Google Scholar
• Ibrahim, A.T.A., 2020. Toxicological impact of green synthesized silver nanoparticles and protective role of different selenium type on Oreochromis niloticus: hematological and biochemical response. Journal of Trace Elements in Medicine and Biology : organ of the Society for Minerals and Trace Elements (GMS), 61, 126507.
   PubMed Web of Science ®Google Scholar
• Kaewamatawong, T., et al., 2006. Acute and subacute pulmonary toxicity of low dose of ultrafine colloidal silica particles in mice after intratracheal instillation. Toxicologic Pathology, 34 (7), 958–965.
   PubMed Web of Science ®Google Scholar
• Kaloyianni, M., et al., 2020. Magnetite nanoparticles effects on adverse responses of aquatic and terrestrial animal models. Journal of Hazardous Materials, 383, 121204.
   PubMed Web of Science ®Google Scholar
• Kaviyarasu, K., et al., 2020. High performance of pyrochlore like Sm2Ti2O7 heterojunction photocatalyst for efficient degradation of rhodamine-B dye with waste water under visible light irradiation. Journal of King Saud University, Science, 32 (2), 1516–1522.
   Web of Science ®Google Scholar
• Kazemian, M., and Bakhshi, M., 2019. Performance of different levels of ZnO nanoparticles on the amount of antioxidant enzymes in the liver of Koi fish (Cyprinus carpio). J. Anim. Environ. Sci, 11 (4), 243–248.
   Google Scholar
• Kim, J.E., Shin, J.Y., and Cho, M.H., 2012. Magnetic nanoparticles: an update of application for drug delivery and possible toxic effects. Archives of Toxicology, 86 (5), 685–700.
   PubMed Web of Science ®Google Scholar
• Kumar, R., and Banerjee, T.K., 2016. Arsenic induced hematological and biochemical responses in nutritionally important catfish Clarias batrachus (L.). Toxicology Reports, 3, 148–152.
   PubMed Web of Science ®Google Scholar
• Kurian, A., and Elumalai, P., 2021. Study on the impacts of chemical and green synthesized (Leucas aspera and oxy-cyclodextrin complex) dietary zinc oxide nanoparticles in Nile tilapia (Oreochromis niloticus). Environmental Science and Pollution Research, 28 (16), 20344–20361.
   PubMed Web of Science ®Google Scholar
• Li, Y., et al., 2013. Surface-coating-dependent dissolution, aggregation, and reactive oxygen species (ROS) generation of silver nanoparticles under different irradiation conditions. Environmental Science & Technology, 47 (18), 10293–10301.
   PubMed Web of Science ®Google Scholar
• Li, N., et al., 2010. Berberine attenuates pro-inflammatory cytokine-induced tight junction disruption in an in vitro model of intestinal epithelial cells. European Journal of Pharmaceutical Sciences., 40 (1), 1–8.
   PubMed Web of Science ®Google Scholar
• Li, N., Xia, T., and Nel, A.E., 2008. The role of oxidative stress in ambient particulate matter-induced lung diseases and its implications in the toxicity of engineered nanoparticles. Free Radical Biology & Medicine, 44 (9), 1689–1699.
   PubMed Web of Science ®Google Scholar
• Liu, X., et al., 2004. Preparation and characterization of amino–silane modified superparamagnetic silica nanospheres. Journal of Magnetism and Magnetic Materials., 270 (1-2), 1–6. 1–6.
   Web of Science ®Google Scholar
• Liu, J., et al., 2020. World record 32.35 tesla direct-current magnetic field generated with an all-superconducting magnet. Superconductor Science and Technology, 33 (3), 03LT01.
   Web of Science ®Google Scholar
• Liu, L., et al., 2019. Peptide-functionalized upconversion nanoparticles-based FRET sensing platform for Caspase-9 activity detection in vitro and in vivo. Biosensors & Bioelectronics, 141, 111403.
   PubMed Web of Science ®Google Scholar
• Luo, Y., et al., 2006. 2-chlorophenol induced ROS generation in fish Carassius auratus based on the EPR method. Chemosphere, 65 (6), 1064–1073.
   PubMed Web of Science ®Google Scholar
• Mahmoud, A.M., et al., 2021. The role of natural and synthetic antioxidants in modulating oxidative stress in drug-induced injury and metabolic disorders. Oxidative Medicine and Cellular Longevity, 2021, 1–3. 2021.
   Web of Science ®Google Scholar
• Malhotra, N., et al., 2020. Potential toxicity of iron oxide magnetic nanoparticles: a review. Molecules, 25 (14), 3159.
   Web of Science ®Google Scholar
• Marano, F., et al., 2011. Nanoparticles: molecular targets and cell signalling. Archives of Toxicology, 85 (7), 733–741.
   PubMed Web of Science ®Google Scholar
• Naeemi, A.S., et al., 2020. Copper oxide nanoparticles induce oxidative stress mediated apoptosis in carp (Cyprinus carpio) larva. Gene Reports, 19, 100676.
   Web of Science ®Google Scholar
• Neumann, N.F., Stafford, J.L., and Belosevic, M., 2000. Biochemical and functional characterisation of macrophage stimulating factors secreted by mitogen-induced goldfish kidney leucocytes. Fish & Shellfish Immunology, 10 (2), 167–186.
   Web of Science ®Google Scholar
• Oliveira, M., et al., 2010. Evaluation of oxidative DNA lesions in plasma and nuclear abnormalities in erythrocytes of wild fish (Liza aurata) as an integrated approach to genotoxicity assessment. Mutation Research/Genetic Toxicology and Environmental Mutagenesis, 703 (2), 83–89.
   PubMed Web of Science ®Google Scholar
• Öz, M., Tatil, T., and Dikel, S., 2021. Effects of boric acid on the growth performance and nutritional content of rainbow trout (Oncorhynchus mykiss). Chemosphere, 272, 129895.
   PubMed Web of Science ®Google Scholar
• Parveen, N., and Shadab, G.G.H.A., 2012. Cytogenetic evaluation of cadmium chloride on Channa punctatus. Journal of Environmental Biology, 33 (3), 663–666.
   PubMed Web of Science ®Google Scholar
• Perrier, F., et al., 2018. Gold nanoparticle trophic transfer from natural biofilm to grazer fish. Gold Bulletin, 51 (4), 163–173.
   Web of Science ®Google Scholar
• Radwan, M.A., El-Gendy, K.S., and Gad, A.F., 2020. Biomarker responses in terrestrial gastropods exposed to pollutants: a comprehensive review. Chemosphere, 257, 127218.
   PubMed Web of Science ®Google Scholar
• Rahman, I., et al., 2005. Glutathione, stress responses, and redox signaling in lung inflammation. Antioxidants & Redox Signaling, 7 (1–2), 42–59.
   PubMed Web of Science ®Google Scholar
• Sawhney, A.K., and Johal, M.S., 2000. Effect of an organophosphorus insecticide, malathion on pavement cells of the gill epithelia of Channa punctatus (Bloch) Pollut. Arch. Hydrobiol, 47, 195–203.
   Google Scholar
• Shen, Y., et al., 2018. Fish red blood cells express immune genes and responses. Aquaculture and Fisheries, 3 (1), 14–21.
   Google Scholar
• Singh, M., et al., 2019. Iron mediated hematological, oxidative and histological alterations in freshwater fish Labeo rohita. Ecotoxicology and Environmental Safety, 170, 87–97.
   PubMed Web of Science ®Google Scholar
• Singh, N., et al., 2010. Potential toxicity of superparamagnetic iron oxide nanoparticles (SPION). Nano Reviews, 1 (1), 5358.
   PubMedGoogle Scholar
• Souza, I.D.C., et al., 2019. Nanoparticle transport and sequestration: intracellular titanium dioxide nanoparticles in a neotropical fish. Science of the Total Environment., 658, 798–808.
   PubMed Web of Science ®Google Scholar
• Sönmez, E., et al., 2016. Cytotoxicity and genotoxicity of iron oxide nanoparticles: an in vitro biosafety study. Archives of Biological Sciences, 68 (1), 41–50.
   Web of Science ®Google Scholar
• Sun, L., et al., 2020. Innate-adaptive immunity interplay and redox regulation in immune response. Redox Biology, 37, 101759.
   PubMed Web of Science ®Google Scholar
• Sun, Y., Oberley, L.W., and Li, Y., 1988. A simple method for clinical assay of superoxide dismutase. Clinical Chemistry, 34 (3), 497–500.
   PubMed Web of Science ®Google Scholar
• Tamilmathi, D., and Rajan, M.R., 2021. Genotoxic effect of iron oxide nanoparticles treated tannery effluent on Zebrafish Danio rerio. Nature Environment and Pollution Technology, 20 (1), 211–219.
   Google Scholar
• Tavares-Dias, M., Schalch, S. E. C., and Moraes, F. R., 2003. Hematological characteristics of Brazilian teleosts. VII. Parameters of seven species collected in Guariba, São Paulo State, Brazil. Boletim do Instituo de Pesca, São Paulo, 29, 109–115.
   Google Scholar
• Terzi, E., et al., 2017. Biological performance of particleboard incorporated with boron minerals. Journal of Forestry Research, 28 (1), 195–203.
   Web of Science ®Google Scholar
• TÜİK 2019. http://tuik.gov.tr/UstMenu.do?metod=temelist.01.10(2019)
   Google Scholar
• Uçar, A., et al., 2021. Assesment of hematotoxic, oxidative and genotoxic damage potentials of fipronil in rainbow trout Oncorhynchus mykiss. Toxicology Mechanisms and Methods, 31 (1), 73–80.
   PubMed Web of Science ®Google Scholar
• Watanabe, M., et al., 2013. Effects of Fe3O4 magnetic nanoparticles on A549 cells. International Journal of Molecular Sciences, 14 (8), 15546–15560.
   PubMed Web of Science ®Google Scholar
• Zemheri-Navruz, F., Acar, Ü., and Yılmaz, S., 2019. Dietary supplementation of olive leaf extract increases haematological, serum biochemical parameters and immune related genes expression level in common carp (Cyprinus carpio) juveniles. Fish & Shellfish İmmunology, 89, 672–676.
   PubMed Web of Science ®Google Scholar