ROLE OF VITAMIN C AND E ON GENOTOXICITY, HEMATOLOGICAL AND BIOCHEMICAL INVESTIGATION IN CYPRINUS CARPIO L. FOLLOWING ZINC OXIDE NANOPARTICLES EXPOSURE
DOI:
https://doi.org/10.36103/ijas.v54i3.1752Keywords:
Common carp-Comet- DNA damage-Glutathione peroxidase- HematologyAbstract
This study was aimed to evaluate the role of vitamins C and E on genotoxicity, biochemical and hematological indices in common carp, Cyprinus carpio following zinc oxide nanoparticles exposure. Zinc oxide nanoparticles were synthesized (size was < 34nm) and characterized using Fourier Transform Infrared Spectra (FTIR) and X-Ray Diffraction (XRD) analysis. About 120 common carp (weight 20.0-32.0 g) were randomly divided into 12 tanks at rate of 10 fish/tank (two (replicates/treatment); fish were fed diet as follows: Control (C) were fed basal diet; T1 fish were fed basal diet mixed with vitamins C and E (400 mg/kg); T2 and T3 fish were fed basal diet mixed with 10%and 15% ZnONPs respectively; T4 and T5 fish were fed basal diet mixed with ZnONPs 10% and 15% plus vitamins C and E (400 mg/kg dw) respectively. Post 40 d feeding trail, variable changes were registered in blood indices (“Hb content, PCV%, WBCs and RBCs numbers”) in all treated groups compared to C and T1 groups. The highest DNA damage (% tail DNA using Comet assay) was seen in T2 and T3 which asserted highly significant increased (P≤0.01) compared to C and to treated groups. As well as, glutathione peroxidase (GPx) activity exhibited highly significant increase (P≤0.01) in T2 and T3 groups relative to C, T4, T1, T5 respectively. This investigation clearly proved that sub-lethal doses (10 and 15% in diet) of ZnONPs were able to induce an oxidative stress in carp fish as reflected by significantly increase of DNA damage to erythrocytes and “the combination of vitamins C and E was able to alleviate the oxidative stress generated due to exposure to ZnONPs.”
References
-Alkaladi, A., N. A. M. N. El-Deen, M. Afifi and O. A. A. Zinadah. 2015. Hematological and biochemical investigations on the effect of vitamin E and C on Oreochromis niloticus exposed to zinc oxide nanoparticles. Saudi J.Biolo. Sci. 22(5):556–563
- Al-Rudainy, A. J., S.A. Mustafa and M.A. Abulaziz. 2014. Toxic effects of mercuric chloride on DNA damage, hematological parameters an histopathological changes in common carp (Cyprinus carpio). Iraqi J. Vet. Med. 38(2):87-94
-Aschberger, K., C. Micheletti, B. Sokull-Klüttgen and F.M. Christensen. 2011. Analysis of currently available data for characterising the risk of engineered nanomaterials to the environment and human health—lessons learned from four case studies. Environ. Int. 37(6):1143–1156
-Belpaeme, K., K. Cooreman and M. Kirsch-Volders. 1998. Development and validation of the in vivo alkaline comet assay for detecting genomic damage in marine flatfish. Mutat Res Genet Toxicol Environ Mutagen. 415:167-184
-Celik, E.S., H. Kaya, S. Yilmaz, M. Akbulut and A. Tulgar. 2013. Effects of zinc exposure on the accumulation, haematology and immunology of Mozambique tilapia, Oreochromis mossambicus. Afr. J. Biotechnol., 12: 744‒753
-Chahardeh Baladehi, E. and S. Hedayati. 2017. The hematological improvement of rainbow trout (Oncorhynchus mykiss) during dietary supplementation with vitamin C after exposure to zinc nano-particles. Iranian J. Fisheries Sci., 17(1):162-169
-Divya, N.K. and P.P. Pradyumnan. 2017. Photoluminescence quenching and photocatalytic enhancement of Pr-doped ZnO nanocrystals. Bull Mater Sci. 40:1405–141
-Durmus, Z., B. Z. Kurt, and A. Durmus. 2019. Synthesis and characterization of graphene oxide/zinc oxide (GO/ZnO) nanocomposite and its utilization for photocatalytic degradation of basic fuchsin dye. Chemistry Select. 4: 271–8
-Fadhal, A.A. and S.A. Mustafa. 2020. Influence of phytase enzyme on growth performance and survival rate challenge with Saprolegnia spp. in common carp. Iraqi J. Agric. Sci. 51 (5): 158-1465. https://doi.org/10.36103/ijas.v51i5.1156
-Firat, O., 2007. Effects Of Metal (Zn, Cd) and Metal Mixtures (Zn + Cd) On Physiological and Biochemical Parameters in Blood Tissues of Oreochromis Niloticus. Ph. D Thesis, Çukurova University, Turkey
-Frenzilli, X., M. Nigro and B.P. Lyons. 2009. The Comet assay for the evaluation of genotoxic impact in aquatic environments, Muta. Res./Reviews in Muta. Res. 681(1):80-92
-Halliwell, B. and J. Gutteridge. 1999. Free radicals in biology and medicine. 3rd ed. Oxford: Oxford University Press; pp: 936
-Horie, M., K. Nishio, K. Fujita, S. Endoh, A. Miyauchi, Y. Saito, H. Iwahashi, K. Yamamoto, H. Murayama, and H. Nakano. 2009. Protein adsorption of ultrafine metal oxide and its influence on cytotoxicity toward cultured cells. Chem. Res. Toxicol., 22: 543–553
-Ji, J., Z.F. Long and D.H. Lin. 2011. Toxicity of oxide nanoparticles to the green algae Chlorella sp. Chem. Eng. J. 170: 525–530
-Kaya, H. and M. Akbulut. 2015. Effects of waterborne lead exposure in mozambique tilapia: oxidative stress, osmoregulatory responses, and tissue accumulation. J. Aquat. Anim. Health. 27(2):77–87
-Khan, M. F., A. H. Ansari, M. Hameedullah, E. Ahmad, F. M. Husain, Q. Zia, U. Baig, M. R. Zaheer, M. M. Alam, A. M. Khan, Z. A. AlOthman, I. Ahmad, G. M. Ashraf and G. Aliev. 2016. Sol-gel synthesis of thorn-like ZnO nanoparticles endorsing mechanical stirring effect and their antimicrobial activities: Potential role as nano-antibiotics. Scientific Reports. 6: 27689
-Kori-Siakpere, O., E.O. Ubogu and E. Oghoghene, 2008. Sublethal haematological effects of zinc on the fresh water fish, Heteroclarias spp. (Osteichthyes: Clariidae). Afr. J. Biotechnol. 7: 2068‒2073
-Kulkarni, S. S. and D. S. Mahendra. 2015. Optical and Structural Properties of Zinc Oxide Nanoparticles, International Journal of Advanced Research in Physical Science (IJARPS) Volume. 2(1):14-18
-Kumar, A. and A. Dhawan. 2013. Genotoxic and carcinogenic potential of engineered nanoparticles: an update. Arch Toxicol. 87(11):1883–1900
-Li, X., L. Wang, Y. Fan, Q. Feng and F.Z. Cui. 2012. Biocompatibility and toxicity of nanoparticles and nanotubes. J. Nanomaterials. 1-19
-Magdolenova Z., A. Collins, A. Kumar, A. Dhawan, V. Stone and M. Dusinska. 2014. Mechanisms of genotoxicity. A review of in vitro and in vivo studies with engineered nanoparticles. Nanotoxicology. 8: 233–278
-Moreau, R., K. Dabrowski, S. Czesny and F. Chila. 1999. Vitamin C-vitamin E interaction in juvenile lake sturgeon (Acipenser fulvescens), a fish able synthesize ascorbic acid. J. Appl. Ichthyol. 15: 205-257
-Musalmah, M., A.H. Fairuz, M.T. Gapor and W.Z.W. Ngah. 2002. Effect of vitamin E on plasma malondialdehyde, antioxidant enzyme levels and the rates of wound closures during wound healing in normal and diabetic rats. Asia Pac. J. Clin. Nutr. 11: S448–S451
-Mustafa, S. A and A. J. Al-Rudainy. 2021. Impact of mercury chloride exposure on some of immunological and biochemical assays of common carp, Cyprinus carpio. Iraqi J. Agric. Sci. 52(3):547-551
-Mustafa, S. A., S. N. Al-Subiai, S. J. Davies and A. N. Jha. 2011. Hypoxia-induced oxidative DNA damage links with higher level biological effects including specific growth rate in common carp, Cyprinus carpio L. Ecotoxicology, 20(6):1455–1466
-Mustafa, S. A., S. S. Karieb, S. J. Davies and A. N. Jha. 2015. Assessment of oxidative damage to DNA, transcriptional expression of key genes, lipid peroxidation and histopathological changes in carp Cyprinus carpio L. following exposure to chronic hypoxic and subsequent recovery in normoxic conditions. Mutagenesis. 30(1):107–116
-Mustafa, S.A. 2012. An Integrated Approach to Assess Impact of Environmental Stress in Carp, Cyprinus carpio L.: Biochemical, Genotoxic, Histopathological and Individual Level Effects, Ph.D. Dissertation,. Dept. Biomed. Biol. Sci. Fac. Sci. Uni. Plymouth. pp. 74
-Nakano T., M. Sato, and M. Takeuchi. 1992. Partial purification and properties of glutathione peroxidase from carp hepatopancreas. Comp. Biochem. Physiol 102: 31-35
-Nussey, G., J. H. J. Vanvuren and H. H. du preez. 2000. Bioaccumulation of chromium, manganese, nickel and lead in the tissues of the moggel, Labeo umbratus (cyprindae), from wit bank dam, MPU – Malanga Watu Sa. 26: 268-248
-Olurin, K.B., E.A.A. Olojo and O.B. Tijani. 2012. Effect of Zinc on Hematological Parameters of African catfish (Clarias gariepinus). Asian. J. Pharmacol. Health. Sci. 2: 266‒272
-Oti, E.E. and D.A. Avoaja. 2005. Haematological assessment of freshwater catfishes, Clarias gariepinus (Burch) and “Heteroclarias” (hybrid) exposed to sublethal concentrations of zinc. Pak. J. Zool. 37: 101‒ 105
-Sampath, K., R. James and K.M. Akbar Ali. 1998. Effects of copper and zinc on blood parameters and prediction of their recovery in Oreochromis mossambicus. Ind. J. Fish. 45: 129-139
-Shahzad, K., M. N. Khan, F. Jabeen, N. Kosour, A. S. Chaudhry, M. Sohail and N. Ahmad. 2018. Toxicity of zinc oxide nanoparticles (ZnO-NPs) in tilapia (Oreochromis mossambicus): tissue accumulation, oxidative stress, histopathology and genotoxicity. Inter. J. Environ. Sci. Technol. 16(1):1-13
-Singh, N., B. Manshian and G.J. Jenkins, et al. 2009. NanoGenotoxicology: the DNA damaging potential of engineered nanomaterials. Biomaterials. 30(23–24):3891–3914
-Surendran, D.K., M.M. Xavier and V.P. Viswanathan. 2017. Synthesis of a ternary Ag/RGO/ZnO nanocomposite via microwave irradiation and its application for the degradation of Rhodamine B under visible light. Environ. Sci. Pollut. Res. 24: 15360–15368
- Swati, S. K. and D. S. Mahendra. 2015. Optical and structural properties of zinc oxide nanoparticles, Inter. J. Advan. Res. Physi. Sci. (IJARPS) 2 (1):14-18
-Taheri S., M. Banaee, H.B. Nemadoost and M. Mohiseni. 2017. Effects of dietary supplementation of zinc oxide nanoparticles on some biochemical biomarkers in common carp (Cyprinus carpio). Inter. J. Aqua. Biol. 5(5): 286- 294
-Van Gaal, L., I. Mertens and C. De Block. 2006. Mechanisms linking obesity with cardiovascular disease. Nature. 444 (7121): 875–880
-Verlhac, V. and J. Gabaudan. 1997. The effect of vitamin C on Fish Health. Roche Technical Buletin, Hoffmann-La Roche Ltd, Basel, Switzerland, 30 pp
-Winston, G. W. and R. T. Di Giulio. 1991. Prooxidant and anti- oxidant mechanisms in aquatic organisms. Aquat. Toxicol. 19: 137-161
-Xiong, D.T., Y.L.X. Fangm and W. Zhu. 2011. Effect of nano-scale TiO2, ZnO and their bulk counter parts on zebrafish: Acute toxicity, oxidative stress and oxidative damage. Science of Total Environment. 409(8):1444-1452
-Zhu, X.S., L. Zhu, Y. Li, and Y.P. Lang. 2008. Comparative toxicity of several metal oxide nanoparticles aqueous suspensions to zebrafish (Danio rerio) early developmental stage. J. Environ. Sci. Health 43:278-284
-Zorriehzahra, M.E.J., T. Nakai, I. Sharifpour, D.K. Gomes, S.C. Chi, M. Soltani, D. Mohd, H. Hj, M. Sharif Rohani, and A.A. Saidi. 2005. Mortality of wild golden mullet (Liza auratus) in Iranian waters of the Caspian Sea associated with viral nervous necrosis like agent. Iranian J.Fisheries Sci.45: 43-58
Downloads
Published
Issue
Section
License
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.