Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1984 Sep;327(2):139-42.
doi: 10.1007/BF00500908.

Evidence for two opposite effects of clonidine on gastric acid secretion in the dog

Evidence for two opposite effects of clonidine on gastric acid secretion in the dog

G Soldani et al. Naunyn Schmiedebergs Arch Pharmacol. 1984 Sep.

Abstract

The effects of clonidine on gastric acid secretion were studied in conscious dogs with both gastric fistulae and Heidenhain pouches. Clonidine infused systemically at graded doses under basal conditions produced a significant increase in acid secretion from both gastric fistulae and Heidenhain pouches. Acid secretion from gastric fistulae submaximally stimulated by pentagastrin was dose-dependently reduced by clonidine while 2-deoxy-D-glucose-induced secretion was completely suppressed. Under these conditions a significant enhancement of secretion from Heidenhain pouches was recorded. An increase in acid secretion from both main stomachs and Heidenhain pouches was observed for clonidine with submaximal doses of bethanechol and histamine as stimulants, though clonidine showed no effect on maximal stimulation by histamine. The stimulant effect of clonidine from gastric fistulae and Heidenhain pouches under basal conditions was fully prevented by cimetidine, while the inhibitory effect of clonidine on acid secretion stimulated by pentagastrin from gastric fistulae was reversed by yohimbine. The present results suggest that clonidine displays two simultaneous yet opposite effects on dog gastric secretion. The inhibitory effect might be mediated through a decrease of vagally released acetylcholine following the activation of alpha 2-adrenoceptors both at central and peripheral sites, while the stimulatory effect probably depends on the histamine-like properties of the drug.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Eur J Pharmacol. 1982 Jul 9;81(2):255-61 - PubMed
    1. J Pharm Pharmacol. 1983 Oct;35(10):671-3 - PubMed
    1. Rev Physiol Biochem Pharmacol. 1981;88:199-236 - PubMed
    1. Gastroenterology. 1975 May;68(5 Pt 1):1340-3 - PubMed
    1. Eur J Pharmacol. 1970;10(3):369-77 - PubMed

Publication types