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Effect of histamine, pentagastrin and theophylline on the production of cyclic AMP in isolated gastric tissue of the guinea pig

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Summary

The effect of histamine, pentagastrin and theophylline on the cyclic AMP level was studied in minced gastric tissue and isolated gastric mucosa of the guinea pig:

  1. 1.

    In the presence of high concentrations of minced tissue in the incubate theophylline (10−3 M), but not histamine (10−3 M), alone induced a significant elevation of the content of cyclic AMP.

  2. 2.

    In contrast, in the presence of low amounts of isolated gastric mucosa histamine (6×10−4 M), but not theophylline (10−3 M), alone caused an elevation of the content of cyclic AMP.

  3. 3.

    The combination of histamine (6×10−4 M or 10−3 M) and theophylline (10−3 M) caused a marked elevation in the level of cyclic AMP. However, the magnitude of this elevation was inversely related to the amount of tissue in the incubate.

  4. 4.

    The increase of the content of cyclic AMP, induced by the combination of histamine and theophylline in the isolated mucosa, was inhibited by the histamine H2-receptor antagonist burimamide, but not by the histamine H1-receptor blocking agent diphenydramine.

  5. 5.

    Pentagastrin alone or in combination with theophylline did not significantly change the level of cyclic AMP in the isolated tissue.

The results demonstrate that the histamine-induced increase of cyclic AMP in the gastric mucosa is mediated via histamine H2-receptors, the stimulation of which is also known to increase the secretion of gastric acid. Accordingly, cyclic AMP may be the intracellular mediator of the histamine-induced secretion of gastric acid. In contrast, the pentagastrin-induced secretion of gastric acid in the guinea pig does not seem to be attributable to an increase in the level of cyclic AMP.

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Karppanen, H.O., Neuvonen, P.J., Bieck, P.R. et al. Effect of histamine, pentagastrin and theophylline on the production of cyclic AMP in isolated gastric tissue of the guinea pig. Naunyn-Schmiedeberg's Arch. Pharmacol. 284, 15–23 (1974). https://doi.org/10.1007/BF00499969

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  • DOI: https://doi.org/10.1007/BF00499969

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