Histamine-induced inositol phosphate accumulation in type-2 astrocytes

Biochem Biophys Res Commun. 1991 Jun 14;177(2):734-8. doi: 10.1016/0006-291x(91)91849-8.

Abstract

Histamine elicited dose-dependent accumulation of [3H]inositol phosphates in type-2 astrocytes, but not in type-1 astrocytes. The ED50 was about 2.4 x 10(-6) M and the maximal response was obtained at 10(-4) M. This response was dose-dependently inhibited by H1-antagonists, mepyramine and D- and L-chlorpheniramine. Furthermore, D- and L-chlorpheniramine showed stereoselectivity in the inhibition. On the other hand, an H2-antagonist, famotidine, and an H3-antagonist, thioperamide, did not inhibit the response. These results indicate that histamine stimulates accumulation of inositol phosphates in type-2 astrocytes via H1-receptors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astrocytes / drug effects
  • Astrocytes / metabolism*
  • Cells, Cultured
  • Chlorpheniramine / pharmacology
  • Famotidine / pharmacology
  • Histamine / pharmacology*
  • Inositol Phosphates / metabolism*
  • Piperidines / pharmacology
  • Pyrilamine / pharmacology
  • Rats
  • Rats, Inbred Strains
  • Receptors, Histamine / metabolism

Substances

  • Inositol Phosphates
  • Piperidines
  • Receptors, Histamine
  • Chlorpheniramine
  • Famotidine
  • Histamine
  • Pyrilamine
  • thioperamide