Atypical association of H1 and H2 histamine receptors with signal transduction pathways during multistage mouse skin carcinogenesis

Inflamm Res. 1997 Aug;46(8):292-8. doi: 10.1007/s000110050190.

Abstract

Objective: In the present work we studied the association of histamine receptors with second messengers during multistage carcinogenesis in Sencar mice skin.

Methods: 96 Sencar female mouse, divided into six groups were used. Tumors appeared only in the 7, 12-dimethylbenz[a]anthracene-initiated and 12-O-tetradecanoylphorbol-13-acetate-promoted group. Control groups received only TPA, or acetone or no treatment at all. Periodically during the promotion period, cAMP and inositol phosphate production were measured after stimulation with H1 or H2 agonists in samples from all groups.

Results: In non-treated skin, H1 receptors were coupled to phosphatidylinositol hydrolysis and H2 receptors mediated cAMP production. Conversely, in tumors H2 receptors were associated with phosphatidylinositol hydrolysis and H1 mediated a rise in cAMP levels. The skin among tumors and the skin from all control groups maintained the same coupling as non-treated skin. An increase in mast cell number, with a homogeneous subepithelial distribution and marked phenotypic changes, was also observed in promoted skin.

Conclusions: These findings indicate an atypical association of histamine receptors with second messengers that could be a critical feature for the postulated action of histamine in tumor growth.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 9,10-Dimethyl-1,2-benzanthracene
  • Animals
  • Cell Count
  • Cimetidine / analogs & derivatives
  • Cimetidine / metabolism
  • Cyclic AMP / metabolism
  • Female
  • Histamine H1 Antagonists / metabolism
  • Histamine H2 Antagonists / metabolism
  • Hydrolysis
  • Mast Cells / pathology
  • Mice
  • Phosphatidylinositols / metabolism
  • Pyrilamine / metabolism
  • Receptors, Histamine H1 / physiology*
  • Receptors, Histamine H2 / physiology*
  • Second Messenger Systems
  • Signal Transduction / physiology*
  • Skin Neoplasms / chemically induced
  • Skin Neoplasms / pathology
  • Skin Neoplasms / physiopathology*
  • Tetradecanoylphorbol Acetate

Substances

  • Histamine H1 Antagonists
  • Histamine H2 Antagonists
  • Phosphatidylinositols
  • Receptors, Histamine H1
  • Receptors, Histamine H2
  • 9,10-Dimethyl-1,2-benzanthracene
  • Cimetidine
  • Cyclic AMP
  • tiotidine
  • Pyrilamine
  • Tetradecanoylphorbol Acetate