[Effects of erythromycin on hydrogen peroxide-induced interleukin-8 synthesis and regulation of glutathione in human bronchial epithelial cells]

Zhonghua Yi Xue Za Zhi. 2005 Apr 13;85(14):976-80.
[Article in Chinese]

Abstract

Objective: To study the effects of erythromycin on Hydrogen peroxide (H2O2)-induced interleukin-8 synthesis and regulation of glutathione in human bronchial epithelial cells.

Methods: Human bronchial epithelial (16HBE) growth curve was recorded by MTT, cells were divided into three groups (1) control (incubation for 24, 36, 48) (2) H2O2 (Pre-incubation for 24, 36, 48 h before adding H2O2 (3) H2O2 + EM (Pre-incubation EM for 24, 36, 48 h before adding H2O2). IL-8 levels were measured in culture supernatants by ELISA, activation of transcription factor NF-kappaB and AP-1 in HBE was evaluated by Electrophoretic mobility shift assay (EMSA). Intracellular GSH and Gamma-GCS concentrations were measured by spectrophotometric assay, gamma-GCS-HS protein were determined by Western blot.

Results: Erythromycin (1 microg/ml, 10 microg/ml) and H2O2 (0.01 mM, 0.1 mM) have no effects on cell growth, Preincubation with EM (5 microg/ml) for 36 h and 48 h significantly inhibit H2O2 (0.01 mmol/L) induced increase of IL-8 levels in HBE supernatants, in the mean time decrease the expression of NF-kB and AP-1. Preincubation with EM (5 microg/ml) for 48 h significantly inhibit H2O2 (0.01 mmol/L) induced increase of gamma-GCS levels, gamma-GCS-HS protein expression and AP-1 binding of gamma-GCS-HS promoter in HBE. However GSH and gamma-GCS-HS protein expression in EM + H2O2 group significantly higher than those in control group.

Conclusion: Erythromycin inhibits oxidant-mediated IL-8 levels through down-regulation of NF-kB and AP-1 binding in HBE, which can further influence the synthesis of GSH and expression gamma-GCS in HBE.

Publication types

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

MeSH terms

  • Bronchi / cytology*
  • Cells, Cultured
  • Epithelial Cells / cytology*
  • Erythromycin / pharmacology*
  • Glutathione / biosynthesis*
  • Glutathione / genetics
  • Humans
  • Hydrogen Peroxide
  • Interleukin-8 / biosynthesis*
  • Interleukin-8 / genetics
  • NF-kappa B / biosynthesis
  • NF-kappa B / genetics
  • Transcription Factor AP-1 / biosynthesis
  • Transcription Factor AP-1 / genetics

Substances

  • Interleukin-8
  • NF-kappa B
  • Transcription Factor AP-1
  • Erythromycin
  • Hydrogen Peroxide
  • Glutathione