![]() |
|
|
Vol. 288, Issue 2, 389-398, February 1999
Gastroenterology Unit 1 (C.S., G.R., G.D.F.) and
Department of
Cellular Biotechnology and Haematology (R.S.), University "La
Sapienza," Rome, Italy; and
Department of Biomedical Sciences and
Technology (V.C., A.D.G., A.B., A.O.), University of L'Aquila,
L'Aquila, Italy
Acute desensitization of contraction and its relative mechanisms have
been studied in smooth muscle cells isolated from guinea pig stomach.
Desensitization was induced by pre-exposure of the cells to one of the
excitatory neuropeptides linked to the phospholipase C
intracellular cascade, i.e., cholecystokinin (CCK), gastrin-releasing peptide, and Substance P. Desensitization was homologous after a 30-s
pre-exposure and heterologous if pre-exposure lasted for 5 min or
longer. Homologous desensitization was studied in a more detailed way
after pre-exposure to CCK. Preincubation with increasing concentrations
of CCK (10 pM-1 µM) induced a progressive rightward shift of the
dose-response curves associated with both a decrease in potency
(ED50 4.5 pM-2.2 nM) and a maximum response that were not
related to a modification of response kinetics. After brief pre-exposure to 1 nM CCK (Dmax), an inhibition
of contraction was observed in response to an identical dose of CCK
(45.1 ± 8.6%), the decreased response being associated with an
inhibition of inositol phosphates and [Ca++]i
mobilization. Both inositol trisphosphate (InsP3)-induced
contraction and [Ca++]i mobilization were
inhibited to a lesser extent than CCK-induced responses. Any longer
pre-exposure of cells to one of the above-mentioned neuropeptides
caused heterologous desensitization, with an observed inhibition of
contraction in response to all tested agonists (CCK, 60.3 ± 5.9%; gastrin-releasing peptide: 56.7 ± 3.5%; Substance P,
60.6 ± 6.5%). A similar decrease was observed in
InsP3-induced contractions resulting in a desensitization
of the InsP3 response as well. Full recovery of contractile
responses appeared within 30 min from the end of preincubation, thus
indicating that degradation of membrane receptors did not occur.
Although pre-exposure of the cells to protein kinase C inhibitor
GF109203X did not modify CCK-induced homologous desensitization, it
blocked CCK-induced heterologous desensitization. This study
demonstrates that excitatory phospholipase C-coupled enteric
neuropeptides induce a time-dependent homologous as well as
heterologous desensitization of smooth muscle contraction occurring at
receptor and postreceptor levels.