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Vol. 287, Issue 3, 832-838, December 1998
Department of Pharmacology (M.R., M.D., L.B.),
INRA, BP3, F-31931
and Laboratory of Digestive Motility (M.D., J.F.), CHU Rangueil,
F-31054 Toulouse, France
Distension of the small intestine can play a role in the
pathogenesis of various functional intestinal disorders. This study determined the role of vasoactive intestinal polypeptide (VIP) in the
adaptative response of intestinal smooth muscle to acute and chronic
distension of the ileum in vivo. Several in vitro experiments were performed to identify the mechanism of receptor regulation. Distension was applied by a balloon inflated with air in
the ileum either during a single episode in anesthetized or repeatedly
in conscious guinea pigs. Then, muscle cells were isolated by enzymatic
digestion from the distended and nondistended adjacent ileal segments.
In addition, in vitro experiments were performed on freshly
dispersed cells for determination of mechanisms. Control cells
maximally relaxed (Cmax) at 1 µM VIP (EC50 = 50 pM) and
100 µM isoproterenol (EC50 = 7 nM). Both acute and
chronic distensions triggered a right-ward shift of the
concentration-response curves for VIP (Cmax = 100 µM,
EC50 = 10 nM). A desensitization of the relaxing effect of
VIP receptors was also observed when cells were preincubated for 30 min
in vitro with VIP. By contrast, the relaxing effect of
isoproterenol was affected neither by in vivo distension nor
by in vitro incubation with isoproterenol. Desensitization
of VIP receptors was prevented by in vitro incubation of
cells with VIP plus a VIP antagonist
[(D-P-Cl-Phe6,Leu17)VIP] and by
intraluminal perfusion of the VIP antagonist during acute distention
in vivo. Moreover, desensitization of VIP receptors did not
occur after 30 min preincubation with either forskolin or
8-Bromo-cyclic AMP. These results indicate that mechanical distension
of the ileum induces a homologous desensitization of VIP receptors on
circular smooth muscle cells, which requires the occupation of its
receptors by VIP.
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