El-Sayed, Y. S., Saad, T. T. & El-Bahr, S. M. Acute intoxication of deltamethrin in monosex Nile tilapia, Oreochromis niloticus with special reference to the clinical, biochemical and haematological effects. Environ. Toxicol. Pharmacol. 24, 212–217 (2007).
Google Scholar
Suman, B., Nilanjan, C. H., Lopamudra, G., Sayan, M. & Ganguly, P. M. K. Modulation of blood profile of juvenile Cyprinus carpio exposed to imidacloprid. Int. J. Life Sci. 5, 627–630 (2017).
Santos, E. L., WINTERLE, Waleska de Melo Costa, Ludke, Maria do Carmo M. M.; Barbosa, J. M. Digestibilidade de ingredientes alternativos para tilápia-do-nilo (Oreochromis niloticus): Revisão. Rev. Bras. Eng. Pesca 3, 135–149 (2008).
Américo-Pinheiro, J.H.P., da Cruz, C., Aguiar, M.M. et al. Sublethal effects of imidacloprid in hematological parameters of tilapia (Oreochromis niloticus). Water. Air. Soil Pollut. 230 (2019).
Omar, R. H., Hagras, A. A., El-naggar, A. M. & Mashaly, M. I. Ecological, hematological and parasitological studies on Oreochromis niloticus Linnaeus 1757 in the Nile Delta Region, Egypt. . Egypt. J. Aquat. Biol. Fish. 25, 795–819 (2021).
Google Scholar
Tomlin. the pesticide manual 12 edition. Farnham, Surrey, UK: British Crop Protection Council (2000).
Vieira, C. E. D., Pérez, M. R., Acayaba, R. D. A., Raimundo, C. C. M. & dos Reis Martinez, C. B. DNA damage and oxidative stress induced by imidacloprid exposure in different tissues of the Neotropical fish Prochilodus lineatus. Chemosphere https://doi.org/10.1016/j.chemosphere.2017.12.077 (2018).
Google Scholar
Mason, R. Immune suppression by neonicotinoid insecticides at the root of global wildlife declines. J. Enviromental Immunol. Toxicol. 1, 3 (2013).
Google Scholar
Berheim, E. H. et al. Effects of neonicotinoid insecticides on physiology and reproductive characteristics of captive female and fawn white-tailed deer. Sci. Rep. 9, 1–10 (2019).
Google Scholar
Jeschke, P., Nauen, R., Schindler, M. & Elbert, A. Overview of the status and global strategy for neonicotinoids. J. Agric. Food Chem. https://doi.org/10.1021/jf101303g (2011).
Google Scholar
Goulson, D. An overview of the environmental risks posed by neonicotinoid insecticides. J. Appl. Ecol. 50, 977–987 (2013).
Google Scholar
Valavanidis, A., Vlahogianni, T., Dassenakis, M. & Scoullos, M. Molecular biomarkers of oxidative stress in aquatic organisms in relation to toxic environmental pollutants. Ecotoxicol. Environ. Saf. 64, 178–189 (2006).
Google Scholar
Özkan, F., Gündüz, S. G., Berköz, M., Hunt, A. Ö. & Yalın, S. The protective role of ascorbic acid (vitamin C) against chlorpyrifos-induced oxidative stress in Oreochromis niloticus. Fish Physiol. Biochem. 38, 635–643 (2012).
Google Scholar
Saeed, M., Amen, A., Fahmi, A., Garawani, I. E. & Sayed, S. The possible protective effect of Coriandrum sativum seeds methanolic extract on hepato-renal toxicity induced by sodium arsenite in albino rats. J. Appl. Pharm. Sci. 4, 044–051 (2014).
Google Scholar
Gibbons, D., Morrissey, C. & Mineau, P. A review of the direct and indirect effects of neonicotinoids and fipronil on vertebrate wildlife. Environ. Sci. Pollut. Res. 22, 103–118 (2015).
Google Scholar
Özdemir, S., Altun, S. & Arslan, H. Imidacloprid exposure cause the histopathological changes, activation of TNF-α iNOS, 8-OHdG biomarkers, and alteration of caspase 3, iNOS, CYP1A, MT1 gene expression levels in common carp (Cyprinus carpio L.). Toxicol. Rep. 5, 125–133 (2018).
Google Scholar
Iturburu, F. G., Simoniello, M. F., Medici, S., Panzeri, A. M. & Menone, M. L. Imidacloprid causes DNA damage in fish: Clastogenesis as a mechanism of genotoxicity. Bull. Environ. Contam. Toxicol. 100, 760–764 (2018).
Google Scholar
Shan, Y., Yan, S., Hong, X., Zha, J. & Qin, J. Effect of imidacloprid on the behavior, antioxidant system, multixenobiotic resistance, and histopathology of Asian freshwater clams (Corbicula fluminea). Aquat. Toxicol. 218, 105333 (2020).
Google Scholar
Anderson, S. et al. Genetic and molecular ecotoxicology: A research framework. Environ. Health Perspect. 102, 3–8 (1994).
Google Scholar
Bolognesi, C., Perrone, E., Roggieri, P., Pampanin, D. M. & Sciutto, A. Assessment of micronuclei induction in peripheral erythrocytes of fish exposed to xenobiotics under controlled conditions. Aquat. Toxicol. 78, S93–S98 (2006).
Google Scholar
Guilherme, S., Santos, M. A., Barroso, C., Gaivão, I. & Pacheco, M. Differential genotoxicity of Roundup® formulation and its constituents in blood cells of fish (Anguilla anguilla): Considerations on chemical interactions and DNA damaging mechanisms. Ecotoxicology 21, 1381–1390 (2012).
Google Scholar
Hoshina, M. M. & Marin-Morales, M. A. Evaluation of the genotoxicity of petroleum refinery effluents using the comet assay in Oreochromis niloticus (Nile tilapia). J. Brazilian Soc. Ecotoxicol. 5, 75–79 (2010).
Google Scholar
Poletta, G. L. et al. Comet assay in gill cells of Prochilodus lineatus exposed in vivo to cypermethrin. Pestic. Biochem. Physiol. 107, 385–390 (2013).
Google Scholar
Cheng, C. H. et al. Effect of nitrite exposure on oxidative stress, DNA damage and apoptosis in mud crab (Scylla paramamosain). Chemosphere 239, 124668 (2020).
Google Scholar
Alvim, T. T. & dos Martinez, C. B. R. Genotoxic and oxidative damage in the freshwater teleost Prochilodus lineatus exposed to the insecticides lambda-cyhalothrin and imidacloprid alone and in combination. Mutat. Res. Genet. Toxicol. Environ. Mutagen. 842, 85–93 (2019).
Google Scholar
El-Garawani, I. M., El-Nabi, S. H., El-Shafey, S., Elfiky, M. & Nafie, E. Coffea arabica bean extracts and vitamin C: A novel combination unleashes MCF-7 cell death. Curr. Pharm. Biotechnol. https://doi.org/10.2174/1389201020666190822161337 (2019).
Google Scholar
Garg, M. C. & Bansal, D. D. Protective antioxidant effect of vitamins C and E in streptozotocin induced diabetic rats. Indian J. Exp. Biol. 38, 101–104 (2000).
Google Scholar
Al-Anazi, M. S., Virk, P., Elobeid, M. & Siddiqui, M. I. Ameliorative effects of Rosmarry on cadmium. J. Environ. Biol. 36, 1401–1408 (2015).
Google Scholar
Erdman, J. W., MacDonald, I. A. & Zeisel, S. H. Present Knowledge in Nutrition: Tenth Edition. (2012). https://doi.org/10.1002/9781119946045
Bruno, R. S. et al. Faster plasma vitamin E disappearance in smokers is normalized by vitamin C supplementation. Free Radic. Biol. Med. 40, 689–697 (2006).
Google Scholar
Bebe, F. N. & Panemangalore, M. Exposure to low doses of endosulfan and chlorpyrifos modifies endogenous antioxidants in tissues of rats. J. Environ. Sci. Heal. Part B Pestic Food Contam. Agric. Wastes 38, 349–363 (2003).
Google Scholar
Yen, G. C., Duh, P. D. & Tsai, H. L. Antioxidant and pro-oxidant properties of ascorbic acid and gallic acid. Food Chem. 79, 307–313 (2002).
Google Scholar
Fathima, P. S., Priyatha, C. V & Chitra, K. C. Ameliorating effect of vitamin c on acid orange 7 induced oxidative stress in the gill of the fish, Anabas testudineus (Bloch, 1792). Res. Rev.: J. Toxicol 8, 15–27 (2018).
Ghazanfar, M., Shahid, S. & Qureshi, I. Z. Vitamin C attenuates biochemical and genotoxic damage in common carp (Cyprinus carpio) upon joint exposure to combined toxic doses of fipronil and buprofezin insecticides. Aquat. Toxicol 196, 43-52 (2018).
Verlhac, V., Obach, A., Gabaudan, J., Schüep, W. & Hole, R. Immunomodulation by dietary vitamin C and glucan in rainbow trout (Oncorhynchus mykiss). Fish Shellfish Immunol. 8, 409–424 (1998).
Google Scholar
Ge, W. et al. Oxidative stress and DNA damage induced by imidacloprid in zebrafish (Danio rerio). J. Agric. Food Chem. https://doi.org/10.1021/jf504895h (2015).
Google Scholar
Zhang, T. et al. Effects of acute ammonia toxicity on oxidative stress, DNA damage and apoptosis in digestive gland and gill of Asian clam (Corbicula fluminea). Fish Shellfish Immunol. 99, 514–525 (2020).
Google Scholar
Burk, R., Hill, K. & Nutrition, A.M.-T.J. Selenoprotein metabolism and function: Evidence for more than one function for selenoprotein P. J. Nutr. 133(5 Suppl 1), 1517S–20S (2003).
Google Scholar
Atencio, L. et al. Effects of dietary selenium on the oxidative stress and pathological changes in tilapia (Oreochromis niloticus) exposed to a microcystin-producing cyanobacterial water bloom. Toxicon https://doi.org/10.1016/j.toxicon.2008.11.011 (2009).
Google Scholar
Pacini, N., Abete, M. C., Dörr, A. J. M., Prearo, M., Natali, M., & Elia, A. C. Detoxifying response in juvenile tench fed by selenium diet. Environ. Toxicol. Pharmacol. 33(1), 46-52 (2011).
Neamat-Allah, A. N. F., Mahmoud, E. A. & Abd El Hakim, Y. Efficacy of dietary Nano-selenium on growth, immune response, antioxidant, transcriptomic profile and resistance of Nile tilapia, Oreochromis niloticus against Streptococcus iniae infection. Fish Shellfish Immunol. 94, 280–287 (2019).
Google Scholar
Saddick, S., Afifi, M. & Abu Zinada, O. A. Effect of Zinc nanoparticles on oxidative stress-related genes and antioxidant enzymes activity in the brain of Oreochromis niloticus and Tilapia zillii. Saudi J. Biol. Sci. 24, 1672–1678 (2017).
Google Scholar
Gatta, P. P., Pirini, M., Testi, S., Vignola, G. & Monetti, P. G. The influence of different levels of dietary vitamin E on sea bass Dicentrarchus labrax flesh quality. Aquac. Nutr. 6, 47–52 (2000).
Google Scholar
Neamat-Allah, A. N. F., Mahmoud, E. A., Abd, Y. & Hakim, E. Efficacy of dietary Nano-selenium on growth, immune response, antioxidant, transcriptomic profile and resistance of Nile tilapia, Oreochromis niloticus against Streptococcus iniae infection. Fish Shellfish Immunol. 94, 280–287 (2019).
Google Scholar
Nikinmaa, M. & Rytkönen, K. T. Functional genomics in aquatic toxicology-Do not forget the function. Aquat. Toxicol. 105, 16–24 (2011).
Google Scholar
El-Garawani, I. M. et al. A newly isolated strain of Halomonas sp. (HA1) exerts anticancer potential via induction of apoptosis and G2/M arrest in hepatocellular carcinoma (HepG2) cell line. Sci. Rep. https://doi.org/10.1038/s41598-020-70945-8 (2020).
Google Scholar
Iturburu, F. G. et al. Uptake, distribution in different tissues, and genotoxicity of imidacloprid in the freshwater fish australoheros facetus. Wiley Online Libr. 36, 699–708 (2017).
Google Scholar
Paravani, E., Simoniello, M. F., Poletta, G. L. & Casco, V. H. Cypermethrin induction of DNA damage and oxidative stress in zebrafish gill cells. Ecotoxicol. Environ. Saf. 30, 1–7 (2019).
Google Scholar
Saxena, K. B., Kumar, R. V., Srivastava, N. & Shiying, B. A cytoplasmic-nuclear male-sterility system derived from a cross between Cajanus cajanifolius and Cajanus cajan. Euphytica 145, 289–294 (2005).
Google Scholar
Bolognesi, C. & Cirillo, S. Genotoxicity biomarkers in aquatic bioindicators. Curr. Zool. 60, 273–284 (2014).
Google Scholar
Grummt, T., Grummt, H. J. & Schott, G. Chromosomal aberrations in peripheral lymphocytes of nurses and physicians handling antineoplastic drugs. Mutat. Res. Lett. 302, 19–24 (1993).
Google Scholar
Alimba, C. G., Ajiboye, R. D. & Fagbenro, O. S. Dietary ascorbic acid reduced micronucleus and nuclear abnormalities in Clarias gariepinus (Burchell 1822) exposed to hospital effluent. Fish Physiol. Biochem. 43, 1325–1335 (2017).
Google Scholar
Moore, P. D., Patlolla, A. K. & Tchounwou, P. B. Cytogenetic evaluation of malathion-induced toxicity in Sprague–Dawley rats. Mutat. Res. Genet. Toxicol. Environ. Mutagen. 725, 78–82 (2011).
Google Scholar
Mužinić, V., Ramić, S. & Želježić, D. Chromosome missegregation and aneuploidy induction in human peripheral blood lymphocytes in vitro by low concentrations of chlorpyrifos, imidacloprid and α-cypermethrin. . Environ. Mol. Mutagen. https://doi.org/10.1002/em.22235 (2019).
Google Scholar
Ali, D. et al. Assessment of genotoxic and mutagenic effects of chlorpyrifos in freshwater fish Channa punctatus (Bloch) using micronucleus assay and alkaline single-cell gel electrophoresis. Food Chem. Toxicol. https://doi.org/10.1016/j.fct.2008.12.021 (2009).
Google Scholar
El-Garawani, I., Hassab, S., Nabi, E. & El-Ghandour, E. The protective effect of (Foeniculum vulgare) oil on etoposide-induced genotoxicity on male albino rats. Eur. J. Pharm. Med. Res. 4, 180–194 (2017).
El-Garawani, I. et al. In vitro antigenotoxic, antihelminthic and antioxidant potentials based on the extracted metabolites from lichen, candelariella vitellina. Pharmaceutics https://doi.org/10.3390/pharmaceutics12050477 (2020).
Google Scholar
Ojha, A. & Srivastava, N. In vitro studies on organophosphate pesticides induced oxidative DNA damage in rat lymphocytes. Mutat. Res. Genet. Toxicol. Environ. Mutagen. https://doi.org/10.1016/j.mrgentox.2014.01.007 (2010).
Google Scholar
Wang, J. et al. The enzyme toxicity and genotoxicity of chlorpyrifos and its toxic metabolite TCP to zebrafish Danio rerio. Ecotoxicology https://doi.org/10.1007/s10646-014-1321-8 (2014).
Google Scholar
Rosenfeld, L. Vitamine—vitamin. The early years of discovery. Clin. Chem. 680–685 (1997).
Bigard, A. X. Lésions musculaires induites par l’exercice et surentraînement. Sci. Sports https://doi.org/10.1016/S0765-1597(00)00037-X (2001).
Google Scholar
Padayatty, S. J. et al. Vitamin C as an antioxidant: Evaluation of its role in disease prevention. J. Am. Coll. Nutr. 22, 18–35 (2003).
Google Scholar
Sarma, K. et al. Dietary high protein and vitamin C mitigates endosulfan toxicity in the spotted murrel, Channa punctatus (Bloch, 1793). Sci. Total Environ. 407(12), 3668–3673 (2009).
Google Scholar
Mirvaghefi, A., Mohsen, A. & Hadi Poorbagher, A. Effects of vitamin C on oxidative stress parameters in rainbow trout exposed to diazinon. Ege J. Fish. Aquat. Sci. 33, 113–120 (2016).
Narra, M. R., Rajender, K., Rudra Reddy, R., Rao, J. V., & Begum, G. The role of vitamin C as antioxidant in protection of biochemical and haematological stress induced by chlorpyrifos in freshwater fish Clarias batrachus. Chemosphere 132, 172-178 (2015).
Zhou, Q. et al. Effect of dietary vitamin C on the growth performance and innate immunity of juvenile cobia (Rachycentron canadum). Fish Shellfish Immunol. 32(6), 969–975 (2012).
Google Scholar
Kc, S., Càrcamo, J. M. & Golde, D. W. Vitamin C enters mitochondria via facilitative glucose transporter 1 (Gluti) and confers mitochondrial protection against oxidative injury. FASEB J. 19, 1657–1667 (2005).
Google Scholar
Lee, Y. C., Huang, H. Y., Chang, C. J., Cheng, C. H. & Chen, Y. T. Mitochondrial GLUT10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: Mechanistic insight into arterial tortuosity syndrome. Hum. Mol. Genet. 19, 3721–3733 (2010).
Google Scholar
Banerjee, T. K. Estimation of acute toxicity of ammonium sulphate to the fresh water catfish, Heteropneustes fossilis I. Analysis of LC50 values determined by various methods. Biomed. Environ. Sci. 6, 31–36 (1993).
Google Scholar
Hamilton, M. A., Russo, R. C. & Thurston, R. V. Trimmed Spearman–Karber method for estimating median lethal concentrations in toxicity bioassays. Environ. Sci. Technol. 11, 714–719 (1977).
Google Scholar
Redlich, D., Shahin, N., Ekici, P., Friess, A. & Parlar, H. Kinetical study of the photoinduced degradation of imidacloprid in aquatic media. CLEAN Soil Air Water 35, 452–458 (2007).
Google Scholar
Çakmakçi, S. & Turgut, T. Influence of different light sources, illumination intensities and storage times on the vitamin C content in pasteurized milk. Turkish J. Vet. Anim. Sci. 29, 1097–1100 (2005).
Bradford, M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72,248-254 (1976).
Ohkawa, H., Ohishi, N. & Yagi, K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal. Biochem. 95(2), 351-358 (1979).
Nishikimi, M., Appaji Rao, N., & Yagi, K. The occurrence of superoxide anion in the reaction of reduced phenazine methosulfate and molecular oxygen. Biochem. Biophys. Res. Commun. 46(2), 849–54 (1972).
Aebi, H. Catalase in vitro. Methods Enzymol. 105, 121–126 (1984).
Google Scholar
Aglia, D. & Valentine, W. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J. Lab. Clin. Med. 70(1), 158–69 (1967).
Abdelazim, A. M., Saadeldin, I. M., Swelum, A. A.-A., Afifi, M. M., & Alkaladi, A Oxidative stress in the muscles of the fish Nile tilapia caused by zinc oxide nanoparticles and its modulation by vitamins C and E. Oxid. Med. Cell. Longev. 6926712 (2018).
Singh, N. P., McCoy, M. T., Tice, R. R. & Schneider, E. L. A simple technique for quantitation of low levels of DNA damage in individual cells. Exp. Cell Res. 175, 184–191 (1988).
Google Scholar
Chen, T. & Ebeling, A. Karyological evidence of female heterogamety in the mosquitofish, Gambusia affinis. Copeia 1, 70–75 (1968).
Google Scholar
Nanda, I. et al. Chromosomal evidence for laboratory synthesis of a triploid hybrid between the gynogenetic teleost Poecilia formosa and its host species. J. Fish Biol. 47, 619–623 (1995).
Source: Ecology - nature.com
