Mechanism of action of pancreatic polypeptide (PP) on pancreatic exocrine secretion in isolated rat pancreas.
- Author:
Yun Lyul LEE
1
;
Hyeok Yil KWON
;
Hyung Seo PARK
;
Hyoung Jin PARK
Author Information
1. Department of Physiology, College of Medicine, Hallym University, Chunchon 200-702 South Korea.
- Publication Type:Original Article
- Keywords:
Pancreatic polypeptide;
Electrical field stmulation;
Cholecystokinin;
Insulin
- MeSH:
Acetylcholine;
Amylases;
Animals;
Carbachol;
Cholecystokinin;
Cholinergic Agonists;
Glucose;
Infusions, Intra-Arterial;
Insulin;
Pancreas*;
Pancreatic Polypeptide*;
Rats*;
Tetrodotoxin
- From:The Korean Journal of Physiology and Pharmacology
1997;1(1):83-90
- CountryRepublic of Korea
- Language:English
-
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.
