ROLE OF VIP1 PACAP RECEPTORS IN POSTOPERATIVE ILEUS IN RATS/

Citation
By. Dewinter et al., ROLE OF VIP1 PACAP RECEPTORS IN POSTOPERATIVE ILEUS IN RATS/, British Journal of Pharmacology, 124(6), 1998, pp. 1181-1186
Citations number
26
Categorie Soggetti
Pharmacology & Pharmacy",Biology
ISSN journal
00071188
Volume
124
Issue
6
Year of publication
1998
Pages
1181 - 1186
Database
ISI
SICI code
0007-1188(1998)124:6<1181:ROVPRI>2.0.ZU;2-0
Abstract
1 Vasoactive intestinal polypeptide (VIP) is an inhibitory neurotransm itter in the enteric nervous system. We investigated the role of VIP1/ PACAP receptors in postoperative ileus in rats. 2 Different degrees of inhibition of the gastrointestinal transit, measured by the migration of Evans blue, were achieved by skin incision, laparotomy or laparoto my plus mechanical stimulation of the gut. 3 The transit after skin in cision or laparotomy was not altered by the VIP1/PACAP receptor antago nist Ac-Hisl,D-Phe(2), K-15, R-16, VIP(3-7), GRF(8-27)-NH2 nor by the VIP1/PACAP receptor agonist K-15, R-16, VIP(I-7), GRF(8-27)-NH2 and th e VIP2/PACAP receptor agonist RO 25-1553 (5 mu g kg(-1)). 4 However, t he transit after laparotomy plus mechanical stimulation was significan tly enhanced by the VIP1/PACAP receptor antagonist, whereas it was fur ther inhibited by the VIP1/PACAP receptor agonist. The combination of the VIP1/PACAP receptor agonist and antagonist counteracted the effect of both drugs alone. The VIP2/PACAP receptor agonist did not after th e effect of the VIP1/PACAP receptor antagonist. 5 The combination of t he VIP1/PACAP receptor antagonist plus the nitric oxide (NO) synthase inhibitor L-nitroarginine had no effect on the transit after laparotom y plus mechanical stimulation, while the transit after skin incision w as significantly decreased. 6 These findings suggest the involvement o f VIP1/PACAP receptors, next to NO, in the pathogenesis of postoperati ve ileus. However, the combination of the VIP1/PACAP antagonist and th e NO synthase inhibitor abolished the beneficial effect of each drug a lone, suggesting the need for one of the inhibitory neurotransmitters to enable normal gastrointestinal transit.