INTERACTION BETWEEN CCK AND OPIOIDS IN THE MODULATION OF THE RECTOCOLONIC INHIBITORY REFLEX IN RATS

Citation
M. Gue et al., INTERACTION BETWEEN CCK AND OPIOIDS IN THE MODULATION OF THE RECTOCOLONIC INHIBITORY REFLEX IN RATS, American journal of physiology: Gastrointestinal and liver physiology, 32(2), 1995, pp. 240-245
Citations number
36
Categorie Soggetti
Physiology
ISSN journal
01931857
Volume
32
Issue
2
Year of publication
1995
Pages
240 - 245
Database
ISI
SICI code
0193-1857(1995)32:2<240:IBCAOI>2.0.ZU;2-K
Abstract
The effects of cholecystokinin octapeptide (CCK-8) as well as the invo lvement of opioid system were evaluated in rectal distension (RD)-indu ced colonic motor inhibition in rats. Rats were surgically prepared wi th electrodes implanted on the proximal colon, and a catheter was impl anted in lateral ventricle of the brain. RD was performed by inflation (0.0-1.6 mi) of a balloon rectally inserted. RD 1.6 ml of induced an inhibition of the colonic spike bursts (3.1 +/- 0.5 per 5 min vs. 8.1 +/- 0.4 before RD). Intracerebroventricular but not intravenous inject ion of CCK-8 and A-71623 (50 and 100 ng/kg) reduced the RD-induced col onic motor inhibition, whereas A-63387 was ineffective. PD-135,158 (10 mu g/kg icv) suppressed the inhibitory reflex caused by RD. Devazepid e (100 mu g/kg icv) had no effect in this reflex function. Devazepide (1 mu g/kg), naloxone (0.1 mg/kg), and nor-binaltorphimine (nor-BNI; 1 0 mg/kg) reversed the blocking effect of CCK-8, whereas PD-135,158 (0. 1 mu g/kg) and naltrindole (1 mg/kg) have no effect. In conclusion, CC K-8 acts on central alimentary cholecystokinin receptors to modulate t he RD-induced inhibition of colonic motility through pathways involvin g activation of endogenous kappa-receptors.