Ultrastructural hepatocytic alterations induced by silver nanoparticle toxicity

References

• Rai MK, Deshmukh SD, Ingle AP, et al. Silver nanoparticles: The powerful nanoweapon against multidrug resistant bacteria. J Appl Microbiol 2012;112:841–52.
   PubMed Web of Science ®Google Scholar
• Chou WL, Yu DG, Yang MC. The preparation and characterization of silver loading cellulose acetate hollow fiber membrane for water treatment. Polym Adv Technol 2005;16:600–7.
   Web of Science ®Google Scholar
• Kalantzi OI, Biskos G. Methods for assessing basic particle properties and cytotoxicity of engineered nanoparticles. Toxics 2014;2:79–91.
   Google Scholar
• Qin Y. Silver-containing alginate fibers and dressing. Int Wound J 2005;2:172–6.
   PubMedGoogle Scholar
• Jain J, Arora S, Rajwade J, et al. Silver nanoparticles in therapeutics: Development of an antimicrobial gel formulation for topical use. Mol Pharm 2009;2:1388–1401.
   Google Scholar
• Vigneshwaran N, Kathe AA, Varada PV, et al. Functional finishing of cotton fabrics using silver nanoparticles. J Nanosci Nanotechnol 2007;7:1893–7.
   PubMed Web of Science ®Google Scholar
• Turtle GR. Size and Surface Area Dependent Toxicity of Silver Nanoparticles in Zebrafish Embryo (Danio rerio). Master Thesis in toxicology submitted to Oregon State University, USA, 2012.
   Google Scholar
• Ahamed M, Alsalhi MS, Siddiqui MK. Silver nanoparticle applications and human health. Clin Chem Acta 2010;411:1841–8.
   PubMed Web of Science ®Google Scholar
• Faraj AH, Wipf P. Nanoparticles in cellular drug delivery. Bioorg Med Chem 2009;17:2950–2962.
   Google Scholar
• Attia AA. Evaluation of the testicular alterations induced by silver nanoparticles in male mice: Biochemical, histological and ultrastructural studies. RJPBSC 2014;5(4): 1558–9.
   Google Scholar
• Asharani PV, Hande MP, Valiyaveettil S. Anti-proliferative activity of silver nanoparticles. BMC Cell Biol 2009;10(65): 1–14.
   PubMed Web of Science ®Google Scholar
• Liu J, Hurt RH. Ion release kinetics and particle persistence in aqueous non-silver colloids. Environ Sci Technol 2010;44:2169–75.
   Web of Science ®Google Scholar
• Ahamed M, Posgai R, Gorey TJ, et al. Silver nanoparticles induced heat shock protein 70, oxidative stress and apoptosis in Drosophila melanogaster. Toxicol Appl Pharmacol 2010; 242: 263–9.
   PubMed Web of Science ®Google Scholar
• Lim D, Roh JY, Eom HJ, et al. Oxidative stress-related PMK- 1 P38 MAPK activation as a mechanism for toxicity of silver nanoparticles to reproduction in the nematode Caenorhabditis elegans. Environ Toxicol Chem 2012;31:585–92.
   PubMed Web of Science ®Google Scholar
• Park EJ, Bae E, Yi J, et al. Repeated-dose toxicity and inflammatory responses in mice by oral administration of silver nanoparticles. Environ Toxicol Phar 2010;30:162–8.
   PubMed Web of Science ®Google Scholar
• Park EJ, Yi J, Kim Y, et al. Silver nanoparticles induce cytotoxicity by a Trojan horse type mechanism. Toxicol In Vitro 2010;24:872–8.
   PubMed Web of Science ®Google Scholar
• Ma RC, Levard C, Marinakos SM, et al. Size-controlled dissolution of organic-coated silver nanoparticles. Environ Sci Technol 2012;46:752–759.
   PubMed Web of Science ®Google Scholar
• Schrand AM, Bradich-Stolle LK, Schlager JJ, et al. Can silver nanoparticles be useful as potential biological labels? Nanotechnology 2008;19:1–13.
   PubMed Web of Science ®Google Scholar
• Schrand AM, Rahman MF, Hussain SM, et al. Metal-based nanoparticles and their toxicity assessment. WIREs Nanomed Nanobiotechnol 2010;2:544–68.
   PubMed Web of Science ®Google Scholar
• Hsin YH, Chen CF, Huang S, et al. The apoptotic effect of nanosilver is mediated by a ROS- and JNK-dependent mechanism involving the mitochondrial pathway in NIH3T3 cells. Toxicol Lett 2008;179:130–9.
   PubMed Web of Science ®Google Scholar
• Carlson C, Hussian SM, Schrand AM, et al. Unique cellular interaction of silver nanoparticles: Size-dependent generation of reactive oxygen species. J Phys Chem B 2008;112:13608–19.
   Google Scholar
• Kim TH, Kim M, Park HS, et al. Size-dependent cellular toxicity of silver nanoparticles. J Biomed Mater Res 2012;100:1033–43.
   Google Scholar
• Cedervall T, Lynch I, Lindman S, et al. Understanding the nanoparticle-protein corona using methods to quantify exchange rates and affinities of proteins for nanoparticles. Proc Natl Acad Sci USA 2007;104:2050–5.
   PubMed Web of Science ®Google Scholar
• Duran N, Silveira CP, Marcela Duran M, et al. Silver nanoparticle protein corona and toxicity: A mini-review. J Nanobiotechnol 2015;13:55.
   PubMed Web of Science ®Google Scholar
• Asharani PV, Hande MP, Valiyaveettil S. Anti-proliferative activity of silver nanoparticles. BMC Cell Biol 2009;10: 65.
   PubMed Web of Science ®Google Scholar
• Dawson KA, Salvati A, Lynch I. Nanotoxicology: Nanoparticles reconstruct lipids. Nat Nanotechnol 2009;4:84–85.
   PubMed Web of Science ®Google Scholar
• Oberdörster G, Sharp Z, Atudorei V, et al. Translocation of inhaled ultrafine particles to the brain. Inhal Toxicol. 2004;16:437–45.
   PubMed Web of Science ®Google Scholar
• Jarrar Q. Silver Nanoparticles Toxicity: Size Effects. Thesis was submitted for Master Degree in Analytical Toxicology for the University of Jordan, 2013.
   Google Scholar
• Sharma HS, Hussain S, Schlager J, et al. Influence of nanoparticles on blood–brain barrier permeability and brain edema formation in rats. Acta Neurochir Suppl 2010;106:359–364.
   PubMedGoogle Scholar
• Dziendzikowska K, Gromadzka-Ostrowska J, Lankoff A, et al. Time‐dependent biodistribution and excretion of silver nanoparticles in male Wistar rats. J Appl Toxicol 2012;32:920–8.
   PubMed Web of Science ®Google Scholar
• Jarrar Q, Battah A, Obeidat F et al. Biochemical changes induced by the toxicity of variable sizes of silver nanoparticles. Brit J Pharmac Res 2014;4(24): 2670–8.
   Google Scholar
• Trop M, Novak M, Rodl S, et al. Silver-coated wound dressing acticoat caused raised liver enzymes argyria-like symptoms in burn patient. J Trauma 2006;60:648–52.
   PubMed Web of Science ®Google Scholar
• Almansour M, Jarrar Q, Battah A, et al. Histomorphometric alterations induced in the testicular tissues by variable sizes of silver nanoparticles. J Rep Med 2016; manuscript accepted for publication.
   Google Scholar
• Seiffert J, Hussain F, Wiegman C, et al. Pulmonary toxicity of instilled silver nanoparticles: Influence of size, coating and rat strain. Plos One. 2015. doi:10.1371/journal.pone.0119726
   Google Scholar
• Hussain SM, Hess KL, Gearhart JM, et al. In vitro toxicity of nanoparticles in BRl 3A rat liver cells. Toxicol In Vitro 2005;19:975–83.
   PubMed Web of Science ®Google Scholar
• Oberdörster G, Stone V, Donaldson K. Toxicology of nanoparticles: A historical perspective. Nanotoxicology 2007;1:2–25.
   Web of Science ®Google Scholar
• Kim YS, Song MY, Park JD, et al. Subchronic oral toxicity of silver nanoparticles. Part Fibre Toxicol. 2010;7: 20.
   PubMed Web of Science ®Google Scholar
• Johnston HJ, Hutchison G, Christensen FM, et al. A review of the in vivo and in vitro toxicity of silver and gold particulates: Particle attributes and biological mechanisms responsible for the for the observed toxicity. Crit Rev Toxicol. 2010;40:328–46.
   PubMed Web of Science ®Google Scholar
• Xue Y, Zhang S, Huang Y, et al. Acute toxic effects and gender-related biokinetics of silver nanoparticles following an intravenous injection in mice. J Appl Toxicol 2012;32:890–9.
   PubMed Web of Science ®Google Scholar
• Austin CA, Umbreit TH, Brown KM, et al. Distribution of silver nanoparticles in pregnant mice and developing embryos. Nanotoxicology 2011;6:912–922.
   Google Scholar
• Farkas B, Geretovszky ZS. On determining the spot size for laser flounce measurements. Appl Surf Sci 2006;252:4728–32.
   Web of Science ®Google Scholar
• Bozzola, JJ, Russell LD. Electron Microscopy: Principles and Techniques for Biologists. 2nd ed. Boston: Jones and Bartlett, 1999.
   Google Scholar
• Mascorro JA, Bozzola JJ. Processing biological tissues for ultrastructural study. In: Electron microscopy, methods and protocols. Methods in molecular biology. Ed. John Kuo. Human Press, 2007, pp. 19–34.
   Google Scholar
• Ayache J, Beaunier L, Boumendil J, et al. Sample preparation handbook for transmission electron microscopy, methodology. London: Springer Press, 2010.
   Google Scholar
• Hayat MA. Principles and techniques of electron microscopy, biological applications. 4th ed. Cambridge: Cambridge University Press, 2000.
   Google Scholar
• El-Shenawy NS. Oxidative stress responses of rats exposed to roundup and its active ingredient glyphosate. Environ Toxicol Pharmacol 2009;28:379–85.
   PubMed Web of Science ®Google Scholar
• Braydich-Stolle L, Hussain S, Schlager JJ, et al. In vitro cytotoxicity of nanoparticles in mammalian germline stem cells. Toxicol Sci 2005;88:412–9.
   PubMed Web of Science ®Google Scholar
• Singh A, Bhat T, Sharma OP. Clinical biochemistry and hepatotoxicity. J Clin Toxicol 2011;4:11–8.
   Google Scholar
• Gurabi M, Ali D, Alkahtani S, et al. In vivo DNA and apoptotic potential of silver nanoparticles in Swiss albino mice. Onco Targets Ther 2015;8:295–302.
   PubMed Web of Science ®Google Scholar
• Shlan MG, Mostafa MS, Hassouna MM, et al. Elrafaie. Amelioration of lead toxicity on rat liver with vitamin C and silymarin supplements. Toxicology 2005;206(1): 1–15.
   PubMed Web of Science ®Google Scholar
• Sioutas C, Delfino RJ, Singh M. Exposure assessment for atmospheric ultrafine particles (UFPs) and implications in epidemiologic research. Environ Health Perspec 2005;113(8): 947–55.
   PubMed Web of Science ®Google Scholar
• Xia T, Kovochich M, J. Brant, et al. Comparison of the abilities of ambient and manufactured nanoparticles to induce cellular toxicity according to an oxidative stress paradigm. Nano Lett 2006;6(8): 1794–807.
   PubMed Web of Science ®Google Scholar
• Lenaz G. The mitochondrial production of reactive oxygen species: Mechanisms and implications in human pathology. IUBMB Life 2001;52(3–5): 159–64.
   PubMed Web of Science ®Google Scholar
• Buko V, Ergov A, Karput S, et al. Mitochondrial respiration and oxidative phosphorylation in thioacetamide-induced liver necrosis. Toxicol Lett 1998;95:162–162.
   Google Scholar
• Shannahan JH, Lai X, Ke PC, et al. Silver nanoparticle protein corona composition in cell culture media. Plos One 2013;8: e74001
   PubMed Web of Science ®Google Scholar
• Stern ST, Adiseshaiah PP, Crist RM. Autophagy and lysosomal dysfunction as emerging mechanisms of nanomaterial toxicity. Part Fibre Toxicol 2012;9: 20
   Google Scholar
• Eom E, J. Choi J. p38 MAPK activation, DNA damage, cell cycle arrest and apoptosis as mechanisms of toxicity of silver nanoparticles in Jurkat T cells. Environ Sci Technol 2010;44(21): 8337–42.
   PubMed Web of Science ®Google Scholar
• Serhan OM, Hussein RM. Effects of intraperitoneally injected silver nanoparticles on histological structures and blood parameters in the albino rat. Int J Nanomed 2014;9:1505–16.
   PubMed Web of Science ®Google Scholar
• Kim S, Kim S, Lee S, et al. Characterization of the effects of silver nanoparticles on liver cell using HR-MAS NMR spectroscopy. Bull Korean Chem Soc 2011;32(6):2021–6.
   Web of Science ®Google Scholar
• Asharani, PV, Wu YL, Gong Z, et al. Toxicity of silver nanoparticles in zebra fish models. Nanotechnology 2008;19(25): 255102.
   PubMed Web of Science ®Google Scholar
• Bouwmeester H, Poortman J, Peters RJ et al. Characterization of translocation of silver nanoparticles and effects on whole-genome gene expression using an in vitro intestinal epithelium coculture model. ACS Nano 2011;5:4091–103.
   Google Scholar
• Song MF, Li YS, Kasai H, et al. Metal nanoparticle-induced micronuclei and oxidative DNA damage in mice. J Clin Biochem Nutr 2012;50(3): 211–6.
   PubMed Web of Science ®Google Scholar
• Urich RG, Cramer CT. Potential to induce lamellar bodies and acute cytotoxicity of 6’-alkyl analogues of spectinomycin in primary cultures of rat hepatocytes. Toxicol In Vitro 1991;5(3): 239–245.
   PubMed Web of Science ®Google Scholar
• Schmitz G, Muller G. Structure and function of lamellar bodies, lipid-protein complexes involved in storage and secretion of cellular lipids. J Lipid Res 1991;32:1539–70.
   Google Scholar
• Anderson N, Borlak J. Drug-induced phospholipidosis. FEBS Lett 2006;580(23):5533–40.
   PubMed Web of Science ®Google Scholar
• Kegel V, Pfeiffer E, Burkhardt B, et al. Subtoxic concentrations of hepatotoxic drugs lead to Kupffer cell activation in a human in vitro liver model: An approach to study DILI. Mediat Inflamm 2015; Article ID 640631.
   Google Scholar