[Intervention of cetirizine on monocyte chemoattractant protein-1 in cutaneous inflammation]

Yao Xue Xue Bao. 2005 May;40(5):414-7.
[Article in Chinese]

Abstract

Aim: To study the intervention of cetirizine on monocyte chemoattractant protein-1 (MCP-1) in different cutaneous inflammation models.

Methods: Histamine and IFN-gamma stimulated dermal fibroblast cells and HaCaT cells to mimic cutaneous inflammation. Expression of MCP-1 was assessed by means of RT-PCR and ELISA.

Results: Compared with the control group of dermal fibroblast (DF) cells and HaCaT cells, MCP-1 mRNA was significantly upregulated by histamine (10 micromol x L(-1)) and IFN-gamma (20 ng x mL(-1)). The protein secretions of MCP-1 were increased 3.5 fold and 8.4 fold in DF cells, respectively. The similar tendency was observed in HaCaT cells. The enhancing effects of histamine and IFN-gamma on MCP-1 protein production were significantly inhibited by cetirizine (1 and 10 micromol x L(-1)) in DF and HaCaT cells.

Conclusion: Cetirizine may exert the anti-inflammatory effect of skin via inhibiting MCP-1 expression.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line
  • Cells, Cultured
  • Cetirizine / pharmacology*
  • Chemokine CCL2 / biosynthesis*
  • Chemokine CCL2 / genetics
  • Dermatitis / metabolism
  • Dermis / cytology
  • Fibroblasts / cytology
  • Fibroblasts / metabolism
  • Histamine / pharmacology
  • Histamine H1 Antagonists, Non-Sedating / pharmacology*
  • Humans
  • Interferon-gamma / pharmacology
  • Keratinocytes / cytology
  • Keratinocytes / metabolism
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics

Substances

  • CCL2 protein, human
  • Chemokine CCL2
  • Histamine H1 Antagonists, Non-Sedating
  • RNA, Messenger
  • Histamine
  • Interferon-gamma
  • Cetirizine