Calcium channel modulators: effects on gastric function.

Abstract

Calcium is important in stimulus-secretion coupling in the gut. We therefore examined a dihydropyridine (nitrendipine), a phenylalkylamine (verapamil) and a benzothiazepine (diltiazem) calcium channel blocker as well as a calcium channel 'agonist', CGP 28392, in several models of gastric function. Nitrendipine significantly decreased stress-induced gastric lesions, but was far less efficacious against 100% ethanol-induced lesions. The anti-ulcer effects of nitrendipine were not reversible with indomethacin, sodium meclofenamate or N-ethylmaleimide. Nitrendipine also significantly reduced basal gastric acid output. Verapamil significantly reduced stress lesions in an indomethacin and meclofenamate-reversible manner, but worsened ethanol ulcers. Verapamil also decreased basal acid secretion. Diltiazem decreased stress lesions (indomethacin- and meclofenamate-reversible), worsened ethanol lesions and slightly reduced acid secretion. CGP 28392 exerted a modest stress gastroprotective effect, decreased ethanol lesions and reduced slightly basal acid secretion. A possible clinical role for gastric calcium channel blockade is raised by these results.

• Authors: G B Glavin
• Journal: European journal of pharmacology (Eur J Pharmacol) Vol. 160 Issue 3 Pg. 323-30 (Feb 07 1989) ISSN: 0014-2999 [Print] Netherlands
• PMID: 2714365 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Calcium Channel Agonists
• Calcium Channel Blockers
• Ethanol

Topics

• Animals
• Calcium Channel Agonists (pharmacology)
• Calcium Channel Blockers (pharmacology)
• Cold Temperature
• Ethanol
• Gastric Acid (drug effects, metabolism)
• Male
• Rats
• Rats, Inbred Strains
• Restraint, Physical
• Stomach (drug effects, physiopathology)
• Stomach Ulcer (chemically induced, physiopathology)