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2011 | 14 | 4 |

Tytuł artykułu

The effect of silver nanoparticles on splenocytes activity and selected cytokine levels in the mouse serum at early stage of experimental endotoxemia

Autorzy

Treść / Zawartość

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The objective of this study was to determine the effect of a nonionic silver nanocolloid administered orally for 7 or 14 days at three concentration levels (25 ppm, 2.5 ppm, and 0.25 ppm) on the phagocytic activity and mitogenic response of splenocytes and selected cytokine serum levels (IL-1β, IL-6, IL-10, IL-12 p70, TNF-α) in NMRI mice at the early stage of experimental endotoxemia induced with single 30 μg/mouse dose of bacterial LPS. Regardless of the period of administration, silver nanoparticles enhanced the production of proinflammatory cytokines and anti-inflammatory cytokine IL-10, and they inhibited IL-12 p70 levels in response to LPS challenge. The studied nanoparticles' effect on splenocyte activity was determined by the period of administration. After 7 days of use, silver nanoparticles enhanced the phagocytic activity, and doses of 2.5 ppm stimulated the mitogenic response of splenocytes. After 14 days of administration, silver nanoparticles lowered the phagocytic activity regardless of the dose applied. Although the results obtained are ambiguous, they suggest that silver nanoparticles administered via the alimentary tract are more likely to increase an inflammatory response of an organism than offer protection after LPS challenge.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

14

Numer

4

Opis fizyczny

p.597-604,ref.

Twórcy

  • Department of Microbiology and Clinical Immunology, Faculty of Veterinary Medicine, University of Warmia and Mazury,Oczapowskiego13, 10-718 Olsztyn, Poland

Bibliografia

  • Bhol KC, Alroy J, Schechter PJ (2004) Anti-inflammatory effect of topical nanocrystalline silver cream on allergic contact dermatitis in a guinea pig model. Clin Exp Dermatol 29: 282-287.
  • Bhol KC, Schechter PJ (2005) Topical nanocrystalline silver cream suppresses inflammatory cytokines and induces apoptosis of inflammatory cells in a murine model of allergic contact dermatitis. Br J Dermatol 152: 1235-1242.
  • Chung S, Secombes SJ (1988) Analysis of events occurring within teleost macrophages during the respiratory burst. Comp Biochem Physiol 89 B: 539-544.
  • Fijen JW, Kobold AC, de Boer P, Jones CR, van der Werf TS, Tervaert JW, Zijlstra JG, Tulleken JE (2000) Leukocyte activation and cytokine production during experimental human endotoxemia. Eur J Intern Med 11: 89-95.
  • Luoma SN (2008) Silver nanotechnologies and the environment: old problems or new challenges? PEN 15 (report by Project on Emerging Nanotechnologies; http://www.nanotechproject.org/publications/). http://www.nanotechproject.org/publications/
  • Małaczewska J (2011) Effect of silver nanoparticles on splenocyte activity and selected cytokine levels in the mouse serum. Bull Vet Inst Pulawy 55: 317-322.
  • Mosmann T (1983) Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods 65: 55-63.
  • Nadworny PL, Wang J, Tredget EE, Burrell RE (2008) Anti-inflammatory activity of nanocrystalline silver in a porcine contact dermatitis model. Nanomedicine 4: 241-251.
  • Nandi D, Mishra MK, Basu A, Bishayi B (2010) Protective effects of interleukin-6 in lipopolysaccharide (LPS)-induced experimental endotoxemia are linked to alteration in hepatic anti-oxidant enzymes and endogenous cytokines. Immunobiology 215: 443-451.
  • Park EJ, Bae E, Yi J, Kim Y, Choi K, Lee SH, Yoon J, Lee BC, Park K (2010) Repeated-dose toxicity and inflammatory responses in mice by oral administration of silver nanoparticles. Environ Toxicol Pharmacol 30: 162-168.
  • Park EJ, Yi J, Kim Y, Choi K, Park K (2010) Silver nanoparticles induce cytotoxicity by a Trojan-horse type mechanism. Toxicol In Vitro 24: 872-878.
  • Pelkonen KH, Heinonen-Tanski H, Hänninen OO (2003) Accumulation of silver from drinking water into cerebellum and musculus soleus in mice. Toxicology 186: 151-157.
  • Rook GA, Steele J, Umar S, Dockrell HM (1985) A simple method for the solubilisation of reduced NBT and its use as a colorimetric assay for activation of human macrophages by gamma-interferon. J Immunol Methods 82: 161-167.
  • Takemoto Y (2005) Dose effects of propofol on hemodynamic and cytokine responses to endotoxemia in rats. J Anesth 19: 40-44.
  • Takenaka S, Karg E, Mller W, Roth C, Ziesenis A, Heinzmann U, Schramel P, Heyder J (2000) A morphologic study on the fate of ultrafine silver particles: distribution pattern of phagocytized metallic silver in vitro and in vivo. Inhal Toxicol 12: 291-299.
  • Takenaka S, Karg E, Roth C, Schulz H, Ziesenis A, Heinzmann U, Schramel P, Heyder J (2001) Pulmonary and systemic distribution of inhaled ultrafine silver particles in rats. Environ Health Perspect 109: 547-551.
  • Tian J, Wong KK, Ho CM, Lok CN, Yu WY, Che CM, Chiu JF, Tam PK (2007) Topical delivery of silver nanoparticles promotes wound healing. Chem Med Chem 2: 129-136.
  • Wright JB, Lam K, Buret AG, Olson ME, Burrell RE (2002) Early healing events in a porcine model of contaminated wounds: effect of nanocrystalline silver on matrix metalloproteinases, cell apoptosis, and healing. Wound Repair Regen 10: 141-151.
  • Zhang X, Song Y, Ci X, An N, Fan J, Cui J, Deng X (2008) Effects of florfenicol on early cytokine responses and survival in murine endotoxemia. Int Immunopharmacol 8: 982-988.
  • Zimecki M, Chodaczek G, Kocięba M, Kruzel ML (2004) Lethality in LPS-induced endotoxemia in C3H/HeCr mice is associated with prevalence of proinflammatory cytokines: lack of protective action of lactoferrin. FEMS Immunol Med Microbiol 42: 167-172.

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Bibliografia

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