Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
1995-10-3
pubmed:abstractText
1. Whole-cell and intracellular recordings were made from neurons in slices of guinea-pig spinal trigeminal nucleus pars caudalis. 2. 5-Hydroxytryptamine (5-HT) hyperpolarized 70% of neurons by activating 5-HT1A receptors. The effect was mimicked by 5-carboxamidotryptamine (5-CT) and (+/-)-2-dipropylamino-8-hydroxy-1,2,3,4-tetrahydronapthalene hydrobromide (8-OH-DPAT) and antagonized by 1-(2-methoxyphenyl)-4-[4-(2-phthalimido)-butyl]-piperazine hydrobromide (NAN 190) and pindobind-5-HT1A. Nine per cent of the neurons were depolarized by 5-HT. 3. In about 20% of recordings, 5-HT also evoked repetitive inhibitory postsynaptic potentials that were mediated by glycine. 4. Noradrenaline (NA) hyperpolarized 71% of neurons. This effect was mediated by activation of alpha 2-adrenoceptors, since 5-bromo-N-(4,5-dihydro-1H-imidazol-2-yl)-6-quinoxalinamine (UK14304) also caused a hyperpolarization and idazoxan (1 microM) blocked the hyperpolarization to both NA and UK14304. Phenylephrine depolarized a subset of neurons and this depolarization was blocked by prazosin, suggesting an action mediated by activation of alpha 1-adrenoceptors. 5. NA also evoked repetitive GABAA-mediated inhibitory postsynaptic potentials in about 20% of recordings. The increase in synaptic activity was mimicked by phenylephrine and blocked by prazosin. 6. These results indicate that there are at least two mechanisms through which 5-HT and NA inhibit neurons: (i) in many cells both 5-HT and NA mediate a hyperpolarization through an increase of a potassium conductance; (ii) 5-HT and NA also activated GABA- and glycine-containing interneurons to cause IPSPs in separate groups of cells.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-1000295, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-1354394, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-14067768, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-1578363, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-1832328, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-1884202, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-2087262, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-2141079, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-2175924, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-2337803, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-2358549, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-2370323, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-2566681, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-2861606, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-2868781, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-2872283, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-2901110, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-2996695, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-3025380, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-3171686, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-3343395, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-3427477, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-3764416, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-4052776, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-447880, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-581884, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-6110767, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-6115759, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-6145790, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-6162863, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-6259218, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-6384280, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-659668, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-7083306, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-8101640, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-8126561, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-8350989, http://linkedlifedata.com/resource/pubmed/commentcorrection/7658366-8381444
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0022-3751
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
485 ( Pt 1)
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
113-20
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed:year
1995
pubmed:articleTitle
Inhibition by 5-hydroxytryptamine and noradrenaline in substantia gelatinosa of guinea-pig spinal trigeminal nucleus.
pubmed:affiliation
Vollum Institute, Oregon Health Sciences University, Portland 97201, USA.
pubmed:publicationType
Journal Article, In Vitro, Research Support, U.S. Gov't, P.H.S.