Advances in drug therapy for peptic ulcer disease.
Recently, three new drug types have emerged to treat peptic ulceration. We compared the mechanism of action of omeprazole and somatostatin-14, both inhibitors of gastric acid, with that of tetraprenylacetone, a drug thought to be cytoprotective in the upper gut. Omeprazole and somatostatin-14 caused potent inhibition of meal-stimulated acid secretion in the dog (92% +/- 6% and 97% +/- 1%, respectively). On the other hand, tetraprenylacetone had no significant inhibitory effect on acid secretion (4% +/- 17%). In separate studies, tetraprenylacetone was shown to be a stimulant of gastric bicarbonate secretion in the rabbit, increasing bicarbonate secretion from a basal level of 0 to 86 +/- 28 pmol/2 h. Tetraprenylactone was also found to be a strong stimulant of canine pancreatic bicarbonate secretion. The ability of tetraprenylacetone to stimulate endogenous bicarbonate secretion may explain its ability to heal ulcers both experimentally and clinically.
Duke Scholars
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Related Subject Headings
- Surgery
- Statistics as Topic
- Somatostatin
- Rabbits
- Peptic Ulcer
- Pancreas
- Omeprazole
- Gastric Mucosa
- Gastric Acid
- Dogs
Citation
Published In
DOI
ISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- Surgery
- Statistics as Topic
- Somatostatin
- Rabbits
- Peptic Ulcer
- Pancreas
- Omeprazole
- Gastric Mucosa
- Gastric Acid
- Dogs