P19-derived neuronal cells express H1, H2, and H3 histamine receptors: a biopharmaceutical approach to evaluate antihistamine agents

Amino Acids. 2023 Jun;55(6):821-833. doi: 10.1007/s00726-023-03273-6. Epub 2023 May 12.

Abstract

Histamine is a biogenic amine implicated in various biological and pathological processes. Convenient cellular models are needed to screen and develop new antihistamine agents. This report aimed to characterize the response of neurons differentiated from mouse P19 embryonal carcinoma cells to histamine treatment, and to investigate the modulation of this response by antihistamine drugs, vegetal diamine oxidase, and catalase. The exposure of P19 neurons to histamine reduced cell viability to 65% maximally. This effect involves specific histamine receptors, since it was prevented by treatment with desloratadine and cimetidine, respectively, H1 and H2 antagonists, but not by the H3 antagonist ciproxifan. RT-PCR analysis showed that P19 neurons express H1 and H2 receptors, and the H3 receptor, although it seemed not involved in the histamine effect on these cells. The H4 receptor was not expressed. H1 and H2 antagonists as well as vegetal diamine oxidase diminished the intracellular Ca2+ mobilization triggered by histamine. The treatment with vegetal diamine oxidase or catalase protected against mortality and a significant reduction of H2O2 level, generated from the cells under the histamine action, was found upon treatments with desloratadine, cimetidine, vegetal diamine oxidase, or catalase. Overall, the results indicate the expression of functional histamine receptors and open the possibility of using P19 neurons as model system to study the roles of histamine and related drugs in neuronal pathogenesis. This model is less expensive to operate and can be easily implemented by current laboratories of analysis and by Contract Research Organizations.

Keywords: Antihistamine drugs; Biogenic amine; Catalase; Cimetidine; Ciproxifan; Copper-containing diamine oxidase; Desloratadine; Histamine; Histamine receptors; P19 embryonic carcinoma cells.

MeSH terms

  • Amine Oxidase (Copper-Containing)*
  • Animals
  • Biological Products* / pharmacology
  • Catalase
  • Cimetidine / pharmacology
  • Histamine / metabolism
  • Histamine / pharmacology
  • Histamine Antagonists / pharmacology
  • Histamine H1 Antagonists / pharmacology
  • Hydrogen Peroxide / pharmacology
  • Mice
  • Neurons / metabolism
  • Receptors, Histamine / genetics

Substances

  • Histamine
  • Cimetidine
  • Catalase
  • Amine Oxidase (Copper-Containing)
  • desloratadine
  • Hydrogen Peroxide
  • Histamine Antagonists
  • Receptors, Histamine
  • Histamine H1 Antagonists
  • Biological Products