Functional assessment of neuronal cannabinoid receptors in the muscular layers of human ileum and colon

Background & aims. The notion that specific receptors account for the ability of natural and synthetic cannabinoids to alter physiological functions, prompted this study aimed at assessing their functional presence in the human gut. Methods. The effects have been studied of cannabinoids and sele...

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Veröffentlicht in:Digestive and liver disease 2002-04, Vol.34 (4), p.262-269
Hauptverfasser: Manara, L., Croci, T., Guagnini, F., Rinaldi-Carmona, M., Maffrand, J.-P., Le Fur, G., Mukenge, S., Ferla, G.
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Sprache:eng
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Zusammenfassung:Background & aims. The notion that specific receptors account for the ability of natural and synthetic cannabinoids to alter physiological functions, prompted this study aimed at assessing their functional presence in the human gut. Methods. The effects have been studied of cannabinoids and selective antagonists of their receptors on chemically or electrically evoked contractions in preparations of human intestinal smooth muscle in vitro. Results. Atropine prevented the contractions of longitudinal and circular muscle strips of ileum and colon induced by carbachol or electrical field stimulation; tetrodotoxin abolished only the latter, which suggests they do involve activation of cholinergic neurons. The synthetic cannabinoid (+)WIN 55,212-2 had no effect on carbachol contractions, but in a concentration-dependent fashion prevented those elicited by electrical field stimulation - which were insensitive to the putative endogenous cannabinoid anandamide - more potently in longitudinal than in circular strips. The selective CB, receptor antagonist SR141716, which had no effect in the absence of (+)WIN 55,212-2, competitively antagonised its inhibition of electrical field stimulation contractions, unlike the selective CB 2 antagonist SR 14452B. Conclusions. Cannabinoid CB, receptors are functionally present in the human ileum and colon; their pharmacological activation apparently results in inhibition of excitatory cholinergic pathways subserving smooth muscle contraction.
ISSN:1590-8658
1878-3562
DOI:10.1016/S1590-8658(02)80146-3