[Zafirlukast inhibition of leukotriene C4 induced endothelin-1 expression in human airway structural cell]

Zhonghua Jie He He Hu Xi Za Zhi. 2000 Oct;23(10):617-20.
[Article in Chinese]

Abstract

Objective: To investigate the effects of a cysteinyl leukotriene receptor antagonist (zafirlukast) on endothelin-1(ET-1) expression in human airway epithelial cell line (16-HBE) and airway smooth muscle cells (ASMC) in response to leukotriene C4(LTC4) stimulation.

Methods: 16-HBE or ASMC was incubated with 10(-8) mol/L LTC4 and graded concentrations of zafirlukast. ET-1 level in supernatant was determined by ELISA and ET-1 mRNA expression was assessed by RT-PCR.

Results: (1) LTC4 induced ET-1 mRNA expression in 16-HBE and ASMC was significantly inhibited by zafirlukast (10(-8) mol/L) 0.23 +/- 0.10 vs. 0.10 +/- 0.03 (16-HBE), t = 3.698, P = 0.034; 0.13 +/- 0.04 vs. 0.04 +/- 0.02 ASMC, t = 4.629, P = 0.019. (2) When graded concentrations of zafirlukast (0, 10(-12) mol/L, 10(-10) mol/L, 10(-8) mol/L, 10(-6) mol/L) were added to the LTC4 cultured 16-HBE and ASMC, a significant inhibition of ET-1 production was observed in both groups cultured with 10(-8) mol/L or more zafirlukast [(12.7 +/- 1.3) ng/L vs (5.5 +/- 2.6) ng/L 16-HBE, t = 4.693, P = 0.019; (7.5 +/- 1.0) ng/L vs (4.4 +/- 0.9) ng/L ASMC (t = 5.003, P = 0.007)]. (3) There was a significant negative linear correlation between ET-1 levels and zafirlukast concentrations in LTC4-treated 16-HBE and ASMC (16-HBE: r = -0.9177, P = 0.0289; ASMC: r = -0.9451, P = 0.0153).

Conclusions: These data suggest that zafirlukast inhibit LTC4-induced ET-1 over-expression 16-HBE and ASMC, which may be one of the anti-inflammatory mechanism of LTs receptor antagonists.

MeSH terms

  • Endothelin-1 / biosynthesis*
  • Endothelin-1 / genetics
  • Enzyme-Linked Immunosorbent Assay
  • Epithelial Cells / cytology
  • Gene Expression
  • Humans
  • Indoles
  • Leukotriene Antagonists / pharmacology*
  • Leukotriene C4 / pharmacology*
  • Muscle, Smooth / cytology
  • Muscle, Smooth / metabolism*
  • Phenylcarbamates
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Respiratory System / cytology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sulfonamides
  • Tosyl Compounds / pharmacology*

Substances

  • Endothelin-1
  • Indoles
  • Leukotriene Antagonists
  • Phenylcarbamates
  • RNA, Messenger
  • Sulfonamides
  • Tosyl Compounds
  • Leukotriene C4
  • zafirlukast