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Characterization of the in vitro effects of 5‐hydroxytryptamine (5‐HT) on identified neurones of the rat dorsal motor nucleus of the vagus (DMV)
Author(s) -
Browning Kirsteen N,
Travagli R Alberto
Publication year - 1999
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/sj.bjp.0702908
Subject(s) - dorsal motor nucleus , ketanserin , inhibitory postsynaptic potential , neurotransmission , solitary nucleus , biology , medicine , agonist , 5 ht receptor , endocrinology , pylorus , antrum , vagus nerve , stimulation , neuroscience , chemistry , receptor , serotonin , stomach
Whole cell patch clamp techniques were used on thin brainstem slices to investigate the effects of 5‐hydroxytryptamine (5‐HT) on gastrointestinal‐projecting dorsal motor nucleus of the vagus (DMV) neurones. Neurones were identified as projecting to the stomach ( n =122) or intestine ( n =84) if they contained the fluorescent tracer Dil after it had been applied to the gastric fundus, corpus or antrum/pylorus or to the duodenum or caecum. A higher proportion of intestinal neurones (69%) than gastric neurones (47%) responded to 5‐HT with a concentration‐dependent inward current which was antagonized fully by the 5‐HT 2A receptor antagonist ketanserin (1 μ M ). Stimulation of the nucleus tractus solitarius (NTS) induced inhibitory synaptic currents that were reduced in amplitude by application of the 5‐HT 1A receptor agonist 8‐OHDPAT (1 μ M ) or the 5‐HT 1A/1B receptor agonist TFMPP (1 μ M ) in 61% and 52% of gastric‐ and intestinal‐projecting neurones, respectively. 5‐HT also significantly reduced the frequency but not the amplitude of spontaneous inhibitory currents. These data show that 5‐HT excites directly a larger proportion of intestinal projecting neurones than gastric‐projecting neurones, as well as inhibiting synaptic transmission from the NTS to the DMV. These data imply that the response to DMV neurones to 5‐HT may be determined and classified by their specific projections.British Journal of Pharmacology (1999) 128 , 1307–1315; doi: 10.1038/sj.bjp.0702908

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