Korean J Physiol Pharmacol.
1997 Feb;1(1):83-90.
Mechanism of action of pancreatic polypeptide (PP) on pancreatic
exocrine secretion in isolated rat pancreas
- Affiliations
-
- 1Department of Physiology, College of Medicine, Hallym University, Chunchon
200-702 South Korea.
Abstract
-
Aim of this study was to investigate if pancreatic polypeptide (PP)
reduced the insulin action via the intra-pancreatic cholinergic nerves
in the isolated rat pancreas. The pancreas was isolated from rats and
perfused with intra-arterial infusion of modified Krebs-Henseleit
solution containing 2.5 mM glucose at a flow rate of 1.2 ml/min.
Simultaneous intra-arterial infusion of insulin (100 nM) resulted in
potentiation of the pancreatic flow rate and amylase output which were
stimulated by cholecystokinin (CCK, 14 pM). These potentiating actions
of insulin on the CCK-stimulated pancreatic exocrine secretion were
completely abolished by administration of rat PP. Vesamicol, a potent
inhibitor of vesicular acetylcholine storage, and tetrodotoxin (TTX)
also significantly reduced the combined actions of insulin and CCK.
Administration of carbamylcholine, an acetylcholine agonist, completely
restored the vesamicol-or TTX-induced inhibition of the potentiation
between insulin and CCK. Also rat PP failed to attenuate the restoring
effect of carbamylcholine. Electrical field stimulation (15-30 V, 2
msec and 8 Hz) resulted in a significant increase in the pancreatic
flow rate and amylase output in voltage-dependent manner. Effects of
electrical field stimulation were augmented by endogenous insulin. Rat
PP also suppressed the pancreatic exocrine secretion stimulated by
electrical field stimulation. These observations strongly suggest that
PP inhibits the potentiating actions of insulin on CCK-stimulated
pancreatic exocrine secretion by suppression of the intra-pancreatic
cholinergic activity in the isolated rat pancreas.