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

  • Min Ho Kim
  • , Jun Ho Seo
  • , Hyung Min Kim
  • , Hyun Ja Jeong*
  • *Corresponding author for this work
  • Jeonbuk National University
  • Kyung Hee University
  • Hoseo University

Research output: Contribution to journalJournal articlepeer-review

Abstract

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)-1β, IL-6, and tumor necrosis factor-α 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-κB activations were abolished by ZO-NP, and the expressions of receptor interacting protein2 (RIP2) and IκB kinaseβ (IKKβ) induced by PAMCI were reduced. On the other hand, ZO-NP alone increased the expressions of RIP2 and IKKβ 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.

Original languageEnglish
Pages (from-to)31-39
Number of pages9
JournalEuropean Journal of Pharmacology
Volume738
DOIs
StatePublished - 2014.09.5

Keywords

  • Allergic inflammation
  • Caspase-1
  • IκB kinase
  • Receptor interacting protein2
  • Zinc oxide nanoparticles

Quacquarelli Symonds(QS) Subject Topics

  • Pharmacy & Pharmacology

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