Famotidine, a histamine-2-receptor antagonist, inhibits the increase in rat gastric H+/K(+)-ATPase mRNA induced by intravenous infusion of gastrin 17 and histamine

Dig Dis Sci. 1995 Sep;40(9):2064-9. doi: 10.1007/BF02208679.

Abstract

We examined the effects of gastrin and histamine on rat gastric H+/K(+)-ATPase, the enzyme responsible for H+ secretion, gene expression in vivo. Gastrin 17 (G 17) or histamine dihydrochloride (histamine) was continuously infused through the femoral vein of anesthetized rats. Gastric H+/K(+)-ATPase mRNA levels were measured using northern blot analysis. Infusion of G 17 and histamine increased the H+/K(+)-ATPase mRNA level significantly compared with basal control level or vehicle control level (P < 0.01). However, pretreatment with famotidine, a potent histamine-2 (H2)-receptor antagonist, inhibited the increase of rat gastric H+/K(+)-ATPase mRNA following G 17 and histamine infusion. These findings indicate that both histamine and G 17 increase expression of H+/K(+)-ATPase mRNA by activating H2 receptor on the parietal cell.

MeSH terms

  • Actins / biosynthesis
  • Actins / genetics
  • Animals
  • Blotting, Northern
  • Famotidine / pharmacology*
  • Gastrins / pharmacology*
  • Gene Expression / drug effects
  • H(+)-K(+)-Exchanging ATPase / biosynthesis*
  • H(+)-K(+)-Exchanging ATPase / genetics
  • Histamine / pharmacology*
  • Histamine H2 Antagonists / pharmacology*
  • Hormones / pharmacology*
  • Infusions, Intravenous
  • Male
  • Parietal Cells, Gastric / drug effects
  • Parietal Cells, Gastric / enzymology*
  • Premedication
  • RNA, Messenger / genetics
  • Rats
  • Rats, Wistar
  • Receptors, Histamine H2 / physiology*

Substances

  • Actins
  • Gastrins
  • Histamine H2 Antagonists
  • Hormones
  • RNA, Messenger
  • Receptors, Histamine H2
  • Famotidine
  • gastrin 17
  • Histamine
  • H(+)-K(+)-Exchanging ATPase