Abstract
We assessed the duration of the anti-cholecystokinin (CCK) action of FK480, a new non-peptide CCK-A receptor antagonist developed in Japan, in an in vivo study in rats, comparing it with CR 1505. Pancreatic exocrine secretion stimulated by intravenous infusion of CCK-8 (0.06 microgram/kg per h) was measured at intervals of 0-24 h after the oral administration of FK480 (1.5 mg/kg) and CR 1505 (30 mg/kg). FK480 significantly inhibited both CCK-stimulated pancreatic juice volume flow and amylase output 0, 4, 8, and 12 h after oral administration, whereas the inhibitory effect of CR 1505 had completely disappeared by 8 h after oral administration. It was concluded that orally administered FK480 has a prolonged anti-CCK action.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Administration, Oral
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Animals
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Benzodiazepinones / administration & dosage
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Benzodiazepinones / pharmacology*
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Hormone Antagonists / administration & dosage
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Hormone Antagonists / pharmacology*
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Indoles / administration & dosage
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Indoles / pharmacology*
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Infusions, Intravenous
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Male
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Pancreas / drug effects*
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Pancreas / metabolism
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Pancreatic Juice / drug effects
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Pancreatic Juice / metabolism
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Proglumide / administration & dosage
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Proglumide / analogs & derivatives*
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Proglumide / pharmacology
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Rats
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Rats, Wistar
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Receptors, Cholecystokinin / antagonists & inhibitors*
Substances
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Benzodiazepinones
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Hormone Antagonists
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Indoles
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Receptors, Cholecystokinin
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FR 120480
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loxiglumide
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Proglumide