Effects of Prepubertal Exposure to Silver Nanoparticles on Reproductive Parameters in Adult Male Wistar Rats

REFERENCES

• Allan , D. , Harmon , B. and Roberts , S. A. 1992 . Spermatogonial apoptosis has three morphologically recognizable phases and shows no circadian rhythm during normal spermatogenesis in the rat . Cell Proliferat , 25 : 241 – 250 .
   PubMed Web of Science ®Google Scholar
• Asare , N. , Instanes , C. , Sandberg , W. J. , Refsnes , M. , Schwarze , P. , Kruszewski , M. and Brunborg , G. 2012 . Cytotoxic and genotoxic effects of silver nanoparticles in testicular cells . Toxicology , 291 : 65 – 72 .
   PubMed Web of Science ®Google Scholar
• AshaRani , P. V. , Low Kah Mun , G. , Hande , M. P. and Valiyaveettil , S. 2009 . Cytotoxicity and genotoxicity of silver nanoparticles in human cells . ACS Nano , 3 : 279 – 290 .
   PubMed Web of Science ®Google Scholar
• Braydich-Stolle , L. , Hussain , S. , Schlager , J. J. and Hofmann , M. C. 2005 . In vitro cytotoxicity of nanoparticles in mammalian germline stem cells . Toxicol. Sci , 88 : 412 – 419 .
   PubMed Web of Science ®Google Scholar
• Braydich-Stolle , L. K. , Lucas , B. , Schrand , A. , Murdock , R. C. , Lee , T. , Schlager , J. J. , Hussain , S. M. and Hofmann , M. C. 2010 . Silver nanoparticles disrupt GDNF/Fyn kinase signaling in spermatogonial stem cells . Toxicol. Sci , 116 : 577 – 589 .
   PubMed Web of Science ®Google Scholar
• Carlson , C. , Hussain , S. M. , Schrand , A. M. , Braydich-Stolle , L. K. , Hess , K. L. , Jones , R. L. and Schlager , J. J. 2008 . Unique cellular interaction of silver nanoparticles: Size-dependent generation of reactive oxygen species . J. Phys. Chem. B , 112 : 13608 – 13619 .
   PubMed Web of Science ®Google Scholar
• Dhawan , A. and Sharma , V. 2010 . Toxicity assessment of nanomaterials: Methods and challenges . Anal. Bioanal. Chem , 398 : 589 – 605 .
   PubMed Web of Science ®Google Scholar
• Drake , P. L. and Hazelwood , K. J. 2005 . Exposure-related health effects of silver and silver compounds: A review . Ann. Occup. Hyg , 49 : 575 – 585 .
   PubMed Web of Science ®Google Scholar
• Durán , N. , Marcato , P. D. , Conti , R. , Alves , O. L. , Costa , F. T. M. and Brocchi , M. 2010 . Potential use of silver nanoparticles on pathogenic bacteria, their toxicity and possible mechanisms of action . J. Braz. Chem. Soc , 21 : 11
   Google Scholar
• Gagne , F. , Auclair , J. , Turcotte , P. and Gagnon , C. 2013 . Sublethal effects of silver nanoparticles and dissolved silver in freshwater mussels . J. Toxicol. Environ. Health A , 76 : 479 – 490 .
   PubMed Web of Science ®Google Scholar
• Garcia-Alonso , J. , Khan , F. R. , Misra , S. K. , Turmaine , M. , Smith , B. D. , Rainbow , P. S. , Luoma , S. N. and Valsami-Jones , E. 2011 . Cellular internalization of silver nanoparticles in gut epithelia of the estuarine polychaete . Nereis diversicolor. Environ. Sci. Technol , 45 : 4630 – 4636 .
   PubMed Web of Science ®Google Scholar
• García-Contreras , R. , Argueta-Figueroa , L. , Mejía-Rubalcava , C. , Jiménez-Martínez , R. , Cuevas-Guajardo , S. , Sánchez-Reyna , P. A. and Mendieta-Zeron , H. 2011 . Perspectives for the use of silver nanoparticles in dental practice . Int. Dental J , 61 : 297 – 301 .
   PubMed Web of Science ®Google Scholar
• Hadrup , N. , Loeschner , K. , Mortensen , A. , Sharma , A. K. , Qvortrup , K. , Larsen , E. H. and Lam , H. R. 2012.The . similar neurotoxic effects of nanoparticulate and ionic silver in vivo and in vitro . Neurotoxicology , 33 : 416 – 423 .
   PubMed Web of Science ®Google Scholar
• Hess , R. A. 1990 . Quantitative and qualitative characteristics of the stages and transitions in the cycle of the rat seminiferous epithelium: Light microscopic observations of perfusion-fixed and plastic-embedded testes . Biol. Reprod , 43 : 525 – 542 .
   PubMed Web of Science ®Google Scholar
• Horie , M. , Kato , H. , Fujita , K. , Endoh , S. and Iwahashi , H. 2012 . In vitro evaluation of cellular response induced by manufactured nanoparticles . Chem. Res. Toxicol , 25 : 605 – 619 .
   PubMed Web of Science ®Google Scholar
• Jeong , G. , Jo , U. , Ryu , H. , Kim , Y. , Song , K. and Yu , I. 2010.Histochemical . study of intestinal mucins after administration of silver nanoparticles in Sprague–Dawley rats . Arch. Toxicol , 84 : 63 – 69 .
   PubMed Web of Science ®Google Scholar
• Kim , Y. S. , Song , M. Y. , Park , J. D. , Song , K. S. , Ryu , H. R. , Chung , Y. H. , Chang , H. K. , Lee , J. H. , Oh , K. H. , Kelman , B. J. , Hwang , I. K. and Yu , I. J. 2010 . Subchronic oral toxicity of silver nanoparticles . Part. Fibre Toxicol , 7 : 7 – 20 .
   PubMedGoogle Scholar
• Korenbrot , C. C. , Huhtaniemi , I. T. and Weiner , R. I. 1977 . Preputial separation as an external sign of pubertal development in the male rat . Biol. Reprod , 17 : 298 – 303 .
   PubMed Web of Science ®Google Scholar
• Lucas , B. , Fields , C. and Hofmann , M. C. 2009 . Signaling pathways in spermatogonial stem cells and their disruption by toxicants . Birth Defects Res. C , 87 : 35 – 42 .
   PubMed Web of Science ®Google Scholar
• Meistrich , M. L. and Hess , R. A. 2013 . Assessment of spermatogenesis through staging of seminiferous tubules . Methods Mol. Biol , 927 : 299 – 307 .
   PubMedGoogle Scholar
• Panacek , A. , Prucek , R. , Safarova , D. , Dittrich , M. , Richtrova , J. , Benickova , K. , Zboril , R. and Kvitek , L. 2011 . Acute and chronic toxicity effects of silver nanoparticles (NPs) on Drosophila melanogaster. Environ . Sci. Technol , 45 : 4974 – 4979 .
   PubMed Web of Science ®Google Scholar
• Robb , G. W. , Amann , R. P. and Killian , G. J. 1978 . Daily sperm production and epididymal sperm reserves of pubertal and adult rats . J. Reprod. Fertil , 54 : 103 – 107 .
   PubMedGoogle Scholar
• Robert , J. R. , McKinney , W. , Kan , H. , Krajnak , K. , Frazer , D. G. , Thomas , T. A. , Waugh , S. , Kenyon , A. , MacCuspie , R. I. , Hackley , V. A. and Castranova , V. 2013 . Pulmonary and cardiovascular responses of rats to inhalation of silver nanoparticles . J. Toxicol. Environ. Health A , 76 : 651 – 668 .
   PubMedGoogle Scholar
• Romano , M. A. , Romano , R. M. , Santos , L. D. , Wisniewski , P. , Campos , D. A. , Souza , P. B. , Viau , P. , Bernardi , M. M. , Nunes , M. T. and Oliveira , C. A. 2012 . Glyphosate impairs male offspring reproductive development by disrupting gonadotropin expression . Arch. Toxicol , 86 : 663 – 673 .
   PubMed Web of Science ®Google Scholar
• Romano , R. M. , Romano , M. A. , Bernardi , M. M. , Furtado , P. V. and Oliveira , C. A. 2010 . Prepubertal exposure to commercial formulation of the Arch . Toxicol , 84 : 309 – 317 .
   Google Scholar
• Samberg , M. E. , Oldenburg , S. J. and Monteiro-Riviere , N. A. 2010 . Evaluation of silver nanoparticle toxicity in skin in vivo and keratinocytes in vitro . Environ. Health Perspect , 118 : 407 – 413 .
   PubMed Web of Science ®Google Scholar
• Savithramma , N. R. , Rao , M. L. , Rukmini , K. and Devi , P S. 2011 . Antimicrobial activity of silver nanoparticles synthesized by using medicinal plants . Int. J. Chem. Tech. Res , 3 : 9
   Google Scholar
• Schluesener , J. K. and Schluesener , H. J. 2013 . Nanosilver: Application and novel aspects of toxicology . Arch. Toxicol , 87 : 569 – 576 .
   PubMed Web of Science ®Google Scholar
• Shahare , B. and Yashpal , M. 2013 . Toxic effects of repeated oral exposure of silver nanoparticles on small intestine mucosa of mice . Toxicol. Mech. Methods , 23 : 161 – 167 .
   PubMed Web of Science ®Google Scholar
• Skinner , M. K. and Anway , M. D. 2005 . Seminiferous cord formation and germ-cell programming: Epigenetic transgenerational actions of endocrine disruptors . Ann. NY Acad. Sci , 1061 : 18 – 32 .
   PubMed Web of Science ®Google Scholar
• Snyder-Talkington , B. N. , Qian , Y. , Castranova , V. and Guo , N. L. 2012 . New perspectives for in vitro risk assessment of mutiwalled carbon nanotubes: Application of coculture and bioinformatics . J. Toxicol. Environ. Health B , 15 : 468 – 492 .
   PubMed Web of Science ®Google Scholar
• Stoker , T. E. , Parks , L. G. , Gray , L. E. and Cooper , R. L. 2000 . Endocrine-disrupting chemicals: prepubertal exposures and effects on sexual maturation and thyroid function in the male rat. A focus on the EDSTAC recommendations. Endocrine Disrupter Screening and Testing Advisory Committee . Crit. Rev. Toxicol , 30 : 197 – 252 .
   PubMed Web of Science ®Google Scholar
• Win-Shwe , T. T. and Fujimaki , H. 2011 . Nanoparticles and neurotoxicity . Int. J. Mol. Sci , 12 : 6267 – 6280 .
   PubMed Web of Science ®Google Scholar