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Division of Gastroenterology and Department of Physiology, University of Michigan, Ann Arbor, Michigan 48109
Previous evidence suggests that substance
P (SP) activates subpopulations of neurons within the dorsal motor
nucleus of the vagus (DMV). In this study we aimed at identifying these
subpopulations in relation to their gastrointestinal projection organs
or vagal branches and characterizing pharmacologically the SP response. Using whole cell patch-clamp recordings from identified
gastrointestinal-projecting vagal motoneurons, we found that SP induced
an inward current in all neuronal groups except for cecum-projecting
cells. The lowest percentage of SP-responding neurons was found in
fundus-projecting cells, where SP also had a concentration-response
curve that was shifted to the left (P < 0.05).
Independently from the projections, the SP response was reduced by
sendide and MEN 10,376 and mimicked by a combination of
[Sar9-Met(O2)11]SP and
-neurokinin. SP and
-neurokinin also increased the frequency, but
not the amplitude, of postsynaptic currents. In conclusion, we
demonstrated that SP induces both pre- and postsynaptic effects on DMV
neurons via activation of neurokinin NK1 and
NK2 receptors. The magnitude of the SP response was
correlated to the peripheral target organ.
neurokinin; electrophysiology; brain stem; gastrointestinal tract
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