4.7 Article

Zinc oxide nanoparticles, a novel candidate for the treatment of allergic inflammatory diseases

Journal

EUROPEAN JOURNAL OF PHARMACOLOGY
Volume 738, Issue -, Pages 31-39

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejphar.2014.05.030

Keywords

Zinc oxide nanoparticles; Allergic inflammation; Caspase-1; Receptor interacting protein2; 1 kappa B kinase

Funding

  1. Ministry of Oceans and Fisheries of Korea [PJT200599]

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Zinc (Zn) is an essential trace metal for eukaryotes. The roles of Zn in the numerous physiological functions have been elucidated. Bamboo salt contains Zn that was shown to have anti-inflammatory effect and other health benefits. Nanoparticles of various types have found application in the biology, medicine, and physics. Here we synthesized tetrapod-like, zinc oxide nanoparticles (ZO-NP: diameter 200 nm, source of Zn) using a radio frequency thermal plasma system and investigated its effects on mast cell-mediated allergic inflammatory reactions. ZO-NP was found to inhibit the productions and mRNA expressions of inflammatory cytokines such as interleukin (IL)-1 beta, IL-6, and tumor necrosis factor-alpha on the phorbol 12-myristate 13-acetate plus A23187 (PMACI)-stimulated human mast cell line, HMC-1 cells. In these stimulated cells, caspase-1 and nuclear factor-kappa B activations were abolished by ZO-NP, and the expressions of receptor interacting protein2 (RIP2) and I kappa B kinase beta (IKK beta) induced by PAMCI were reduced. On the other hand, ZO-NP alone increased the expressions of RIP2 and IKK beta in normal condition. ZO-NP inhibited the phosphorylation of extracellular signal-regulated protein kinase in the PMACI-stimulated HMC-1 cells. Furthermore, ZO-NP significantly inhibited passive cutaneous anaphylaxis activated by anti-dinitrophenyl IgE. These findings indicate that ZO-NP effectively ameliorates mast cell mediated allergic inflammatory reaction, and suggest that ZO-NP be considered a potential therapeutic for the treatment of mast cell mediated allergic diseases. (C) 2014 Elsevier B.V. All rights reserved.

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