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1 Department of Physiology and Biophysics, 2 Division of Gastroenterology and Hepatology, and 3 Department of Surgery, Mayo Clinic, Rochester, Minnesota 55905
The
neurotransmitter(s) that generates the fast component of the inhibitory
junction potential (IJP-F) in human jejunal circular smooth muscle is
not known. The aim of this study was to determine the role of ATP and
purinergic receptors in the generation of the IJP-F in human jejunal
circular smooth muscle strips. The P2-receptor antagonist suramin
(100 µM) reduced the IJP-F by 28%. Apamin (1 µM) reduced the IJP-F
by 25%. Desensitization of muscle strips with the putative
P2x-receptor agonist
,
-methylene ATP (
,
-MeATP, 100 µM) decreased the IJP-F by
44%, and desensitization with the putative
P2y-receptor agonist adenosine
5'-O-2-thiodiphosphate (ADP
S) completely abolished the
IJP-F. Desensitization with the putative
P2y-receptor agonist
2-methylthioATP had no effect on the IJP-F. Exogenous ATP evoked a
hyperpolarization with a time course that matched the IJP-F. The
ATP-evoked hyperpolarization was reduced by apamin and suramin, reduced
by desensitization with
,
-MeATP (69% decrease), and abolished by
desensitization with ADP
S. These data suggest that the IJP-F in
human jejunal circular smooth muscle is mediated in part by ATP through
an ADP
S-sensitive P2 receptor.
neurotransmission; microelectrodes; purinergic receptors
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