Histamine stimulates interleukin-6 production through histamine H1 receptors in human amnion cells

Gynecol Obstet Invest. 2010;69(1):67-72. doi: 10.1159/000257663. Epub 2009 Nov 12.

Abstract

Background/aims: Previous studies have stated that maternal allergic diseases are associated with increased risk of preterm labor/delivery, but the underlying mechanisms remain unclear. This study tested the hypothesis that histamine induces interleukin (IL)-6 production in amnion cells.

Methods: Using cultured human amnion cells, we examined expression of histamine receptors and effects of histamine on IL-6 production.

Results: Reverse transcription-polymerase chain reaction and Western blotting revealed expression of histamine H1 receptor (H1R) and H2 receptor (H2R) in human amnion. Histamine stimulation significantly increased concentrations of IL-6 in conditioned medium, as did tumor necrosis factor-alpha and IL-1beta in positive controls. In addition, the H1R antagonist olopatadine significantly blocked histamine-induced production of IL-6, whereas the H2R antagonist ranitidine did not.

Conclusion: Histamine appears to induce IL-6 production through H1R in human amnion cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amnion / cytology
  • Amnion / drug effects
  • Amnion / immunology*
  • Blotting, Western
  • Dibenzoxepins / pharmacology
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Histamine / immunology
  • Histamine / pharmacology*
  • Histamine H1 Antagonists / pharmacology
  • Humans
  • Interleukin-6 / biosynthesis*
  • Interleukin-6 / immunology
  • Olopatadine Hydrochloride
  • Pregnancy
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Receptors, Histamine H1 / biosynthesis*
  • Receptors, Histamine H1 / genetics
  • Receptors, Histamine H1 / immunology
  • Receptors, Histamine H2 / biosynthesis*
  • Receptors, Histamine H2 / genetics
  • Receptors, Histamine H2 / immunology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tumor Cells, Cultured

Substances

  • Dibenzoxepins
  • Histamine H1 Antagonists
  • Interleukin-6
  • RNA, Messenger
  • Receptors, Histamine H1
  • Receptors, Histamine H2
  • Olopatadine Hydrochloride
  • Histamine