Effect of pancreatic polypeptide on gastric accommodation and gastric emptying in conscious rats

• Published in: American journal of physiology: Gastrointestinal and liver physiology 2014-07, Vol.307 (1), p.G122-G128
• Main Authors: Verschueren, Sofie, Janssen, Pieter, Van Oudenhove, Lukas, Hultin, Leif, Tack, Jan
• Format: Article
• Language: English
• Subjects: Animals; Cells; Consciousness; Eating; Energy Intake; Enzyme Inhibitors - administration & dosage; Gastric Emptying - drug effects; Male; Muscarinic Antagonists - administration & dosage; Nitric oxide; Nitric Oxide - metabolism; Nitric Oxide Synthase - antagonists & inhibitors; Nitric Oxide Synthase - metabolism; Nitrous oxide; Pancreas; Pancreatic Polypeptide - administration & dosage; Polypeptides; Pressure; Rats; Rats, Wistar; Rodents; Stomach - drug effects; Stomach - enzymology; Stomach - innervation; Time Factors; Vagotomy
• ISSN: 0193-1857; 1522-1547
• DOI: 10.1152/ajpgi.00043.2014

Pancreatic polypeptide (PP) is an anorexigenic hormone released from pancreatic F cells upon food intake. We aimed to determine the effect of PP on gastric accommodation and gastric emptying in conscious Wistar HAN rats to investigate whether effects on motor function could contribute to its anorexigenic effects. Intragastric pressure (IGP) was measured through a chronically implanted gastric fistula during the infusion of a nutrient meal (Nutridrink; 0.5 ml/min). Rats were treated with PP (0, 33 and 100 pmol·kg(-1)·min(-1)) in combination with N(G)-nitro-L-arginine methyl ester (L-NAME; 180 mg·kg(-1)·h(-1)), atropine (3 mg·kg(-1)·h(-1)), or vehicle. Furthermore, the effect of PP was tested after subdiaphragmal vagotomy of the stomach. Gastric emptying of a noncaloric and a caloric meal after treatment with 100 pmol·kg(-1)·min(-1) PP or vehicle was compared using X-rays. PP significantly increased IGP during nutrient infusion compared with vehicle (P < 0.01). L-NAME and atropine significantly increased IGP during nutrient infusion compared with vehicle treatment (P < 0.005 and 0.01, respectively). The effect of PP on IGP during nutrient infusion was abolished in the presence of L-NAME and in the presence of atropine. In vagotomized rats, PP increased IGP compared with intact controls (P < 0.05). PP significantly delayed gastric emptying of both a noncaloric (P < 0.05) and a caloric (P < 0.005) meal. PP inhibits gastric accommodation and delays gastric emptying, probably through inhibition of nitric oxide release. These results indicate that, besides the well-known centrally mediated effects, PP might decrease food intake through peripheral mechanisms.