107
Views
8
CrossRef citations to date
0
Altmetric
Research Articles

Co-exposure to nTiO2 impairs arsenic metabolism and affects antioxidant capacity in the marine shrimp Litopenaeus vannamei

, , , , , , , , , , & show all
Pages 30-38 | Received 25 May 2018, Accepted 14 Dec 2018, Published online: 01 Jul 2019

References

  • Bagnyukova, T.V., et al., 2007. Oxidative stress and antioxidant defenses in Goldfish liver in response to short-term exposure to arsenite. Environmental and Molecular Mutagenesis, 48(8), 658–665.
  • Bitragunta, S.P., et al., 2017. Detection of TiO2 nanoparticles in municipal sewage treatment plant and their characterization using single particle ICP-MS. Bulletin of Environmental Contamination and Toxicology, 98(5), 595–600.
  • Chen, L., et al., 2018. The role of GST omega in metabolism and detoxification of arsenic in clam Ruditapes philippinarum. Aquatic Toxicology, 204, 9–18.
  • Cordeiro, L.F., et al., 2016. Evaluation of co-exposure to inorganic arsenic and titanium dioxide nanoparticles in the marine shrimp Litopenaeus vannamei. Environmental Science and Pollution Research, 23(2), 1214–1223.
  • Fan, W., et al., 2011. Nano-TiO2 enhances the toxicity of copper in natural water to Daphnia magna. Environmental Pollution (Barking, Essex : 1987), 159(3), 729–734.
  • Fan, W., et al., 2015. Bioaccumulation and oxidative stress in Daphnia magna exposed to arsenite and arsenate. Environmental Toxicology and Chemistry, 34(11), 2629–2635.
  • Fattorini, D. and Regoli, F., 2004. Arsenic speciation in tissues of the Mediterranean polychaete Sabella spallanzanii. Environmental Toxicology and Chemistry, 23(8), 1881–1887.
  • Fattorini, D., et al., 2013. Levels and chemical speciation of arsenic in representative biota and sediments of a tropical mangrove wetland, India. Environmental Science: Processes and Impacts, 15(4), 773–782.
  • Gui, S., et al., 2013. Renal injury and Nrf2 modulation in mouse kidney following chronic exposure to TiO2 nanoparticles. Journal of Agricultural and Food Chemistry, 61(37), 8959–8968.
  • Habig, N.H. and Jakoby, W.B., 1981. Assays for differentiation of glutathione S-transferases. Methods in Enzymology, 77, 398–405.
  • Halliwell, B. and Gutteridge, J. M. C., 2007. Free radicals in biology and medicine. New York: Oxford University Press Inc.
  • Hao, L., Wang, Z., and Xing, B., 2009. Effect of sub-acute exposure to TiO2 nanoparticles on oxidative stress and histopathological changes in Juvenile Carp (Cyprinus carpio). Journal of Environment Science, 21(10), 1459–1466.
  • Huang, Y.-K., et al., 2003. Arsenic species contents at aquaculture farm and in farmed mouthbreeder (Oreochromis mossambicus) in blackfoot disease hyperendemic areas. Food Chemistry and Toxicology, 41(11), 1491–1500.
  • Kaegi, R., et al., 2008. Synthetic TiO2 nanoparticle emission from exterior facades into the aquatic environment. Environmental Pollution, 156(2), 233–239.
  • Lee, B.C., et al., 2012. Oxidative stress in juvenile common carp (Cyprinus carpio) exposed to TiO2 nanoparticles. Molecular and Cellular Toxicology, 8(4), 357–366.
  • Limbach, K.L., et al., 2007. Exposure of engineered nanoparticles to human lung epithelial cells: influence of chemical composition and catalytic activity on oxidative stress. Environmental Science and Technology, 41(11), 4158–4163.
  • Lobato, R.O., et al., 2013. The role of lipoic acid in the protection against of metallic pollutant effects in the shrimp Litopenaeus vannamei (Crustacea, Decapoda). Comparative Biochemistry and Physiology, Part A, 165(4), 491–497.
  • Lobato, R.O., et al., 2018. The effect of diet enriched with lipoic acid in the accumulation and metabolization of metals in different organs of Litopenaeus vannamei. Aquaculture Research 49, 3702-3710.
  • Nagalakshimi, N. and Prasad, M.N.V., 2001. Responses of glutathione cycle enzymes and metabolism to cooper stress in Scenedesmus bijugatus. Plant Science, 160, 291–299.
  • Nigro, M., et al., 2015. n-TiO2 and CdCl2 co-exposure to titanium dioxide nanoparticles and cadmium: Genomic, DNA and chromosomal damage evaluation in the marine fish European sea bass (Dicentrarchus labrax). Aquatic Toxicology, 168, 72–77.
  • Nunes, S.M., et al., 2017. Biochemical responses induced by co-exposition to arsenic and titanium dioxide nanoparticles in the estuarine polychaete Laeonereis acuta. Toxicology, 376, 51–58.
  • Oakes, K.D. and Kraak, G.J.V., 2003. Utility of the TBARS assay in detecting oxidative stress in white sucker (Catostomus commersoni) populations exposed to pulp mill effluent. Aquatic Toxicology, 63(4), 447–460.
  • Reeves, J.F., et al., 2008. Hydroxyl radicals (•OH) are associated with titanium dioxide (TiO2) nanoparticle-induced cytotoxicity and oxidative DNA damage in fish cells. Mutation Research, 640(1–2), 113–122.
  • Sampayo-Reyes, A. and Zakharyan, R.A., 2006. Inhibition of human glutathione S-transferase omega by tocopherol succinate. Biomedicine and Pharmacotherapy, 60(5), 238–244.
  • Sarkar, S., et al., 2017. Differential modulation of cellular antioxidant status in zebrafish liver and kidney exposed to low dose arsenic trioxide. Ecotoxicology and Environmental Safety, 135, 173–182.
  • Schaumann, G.E., et al., 2015. Understanding the fate and biological effects of Ag- and TiO2 nanoparticles in the environment: the quest for advanced analytics and interdisciplinary concepts. Science of the Total Environment, 535, 3–19.
  • Saquib, Q., et al., 2012. Titanium dioxide nanoparticles induced cytotoxicity, oxidative stress and DNA damage in human amnion epithelial (WISH) cells. Toxicology in Vitro, 26(2), 351–361.
  • Thomas, D.J., 2007. Molecular processes in cellular arsenic metabolism. Toxicology and Applied Pharmacology, 222(3), 365–373.
  • Vahter, M., 2002. Mechanisms of arsenic biotransformation. Toxicology, 181–182, 211–217.
  • Ventura-Lima, J., et al., 2007. Toxicological responses in Laeonereis acuta (annelida, polychaeta) after arsenic exposure. Environment International, 33(4), 559–564.
  • Ventura-Lima, J., et al., 2009a. Effects of different inorganic arsenic species in Cyprinus carpio (Cyprinidae) tissues after short-time exposure: bioaccumulation, biotransformation and biological responses. Environment Pollution, 157(12), 3479–3484.
  • Ventura-Lima, J., et al., 2009b. Effects of arsenic (As) exposure on the antioxidant status of gills of the zebrafish Danio rerio (Cypridinae). Comparative Biochemistry and Physiology, Part C, 149, 538–543.
  • Ventura-Lima, J., et al., 2011. Accumulation, biotransformation, and biochemical responses after exposure to arsenite and arsenate in the estuarine polychaete Laeonereis acuta (Nereididae). Environmental Science and Pollution Research, 18(8), 1270–1277.
  • White, C.C., et al., 2003. Fluorescence-based microtiter plate assay for glutamate-cysteine ligase activity. Analytical Biochemistry, 318(2), 175–180.
  • Zar, J. H., 1984. Biostatistical analysis. New Jersey: Prentice Hall.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.