Guanine nucleotides and pertussis toxin reduce the affinity of histamine H3 receptors on AtT-20 cells

Agents Actions. 1993 Nov;40(3-4):129-34. doi: 10.1007/BF01984051.


Agonist occupancy of high affinity histamine H3 receptors on AtT-20 cells induces increased ACTH release. However, the signal transduction process by which this occurs is presently unknown. As a first step in characterizing this pathway, we have examined the effects of a variety of nucleotides and nucleotide analogs on Na-methylhistamine binding to these receptors. Nonhydrolyzable guanine nucleotide analogs inhibit up to 40% of the [3H]Na-methylhistamine binding by increasing the dissociation rate of the ligand from the receptor and, thereby, reducing receptor affinity. Pertussis toxin also decreases the affinity of the H3 receptors and ADP ribosylates a 41 kDa protein. Neither GTP gamma S nor pertussis toxin change Bmax. These data indicate that the H3 receptors on these cells are coupled to a G protein of the Gi subclass.

MeSH terms

  • Adenosine Diphosphate Ribose / metabolism
  • Animals
  • Cell Line
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Guanine Nucleotides / pharmacology*
  • Guanosine 5'-O-(3-Thiotriphosphate) / pharmacology
  • Histamine Agonists / pharmacokinetics
  • Methylhistamines / pharmacokinetics
  • Mice
  • NAD / metabolism
  • Pertussis Toxin*
  • Phosphorus Radioisotopes
  • Pituitary Gland / metabolism
  • Receptors, Histamine H3 / drug effects
  • Receptors, Histamine H3 / metabolism*
  • Signal Transduction / drug effects
  • Virulence Factors, Bordetella / pharmacology*


  • Guanine Nucleotides
  • Histamine Agonists
  • Methylhistamines
  • Phosphorus Radioisotopes
  • Receptors, Histamine H3
  • Virulence Factors, Bordetella
  • NAD
  • Adenosine Diphosphate Ribose
  • Guanosine 5'-O-(3-Thiotriphosphate)
  • Pertussis Toxin
  • N-methylhistamine