pubmed-article:7680798 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:7680798 | lifeskim:mentions | umls-concept:C0035820 | lld:lifeskim |
pubmed-article:7680798 | lifeskim:mentions | umls-concept:C0027793 | lld:lifeskim |
pubmed-article:7680798 | lifeskim:mentions | umls-concept:C1882864 | lld:lifeskim |
pubmed-article:7680798 | lifeskim:mentions | umls-concept:C0682680 | lld:lifeskim |
pubmed-article:7680798 | lifeskim:mentions | umls-concept:C0080093 | lld:lifeskim |
pubmed-article:7680798 | lifeskim:mentions | umls-concept:C1533691 | lld:lifeskim |
pubmed-article:7680798 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:7680798 | pubmed:dateCreated | 1993-4-15 | lld:pubmed |
pubmed-article:7680798 | pubmed:abstractText | The rat spinal cord with connected dorsal root ganglia was used to study neurokinin and N-methyl-D-aspartate receptors involved in the sensory synaptic transmission of dorsal horn cells. Selective C-fibre excitation was produced by capsaicin (200-500 nM) administered to the dorsal root ganglions. Sixty-nine per cent of dorsal horn cells responded with a postsynaptic depolarization and enhanced synaptic activity, recorded via intracellular electrodes, to capsaicin-activated primary afferent input. Dorsal horn neurons activated by the capsaicin-evoked input were also excited by a 1-min perfusion of the neurokinin-1 receptor agonists substance P methyl ester or GR73 632 and by the neurokinin-2 agonist neurokinin-A. These cells were also depolarized by N-methyl-D-aspartate. Responses to substance P methyl ester and GR73 632 were selectively reduced by the neurokinin-1 receptor antagonist CP96,345, and responses to neurokinin-A were completely blocked by the neurokinin-2 receptor antagonist MEN10 376. The depolarization evoked by N-methyl-D-aspartate was not altered by either of the antagonists, but was completely blocked by the selective N-methyl-D-aspartate receptor antagonist (-)-2-amino-5-phosphonovaleric acid. Capsaicin-evoked responses in the dorsal horn were inhibited by MEN10,376 (63 +/- 13% inhibition) but no significant change was observed with CP96,345. The N-methyl-D-aspartate receptor antagonist (-)-2-amino-5-phosphonovaleric acid consistently inhibited the capsaicin-induced response by 76 +/- 14%. Combination of (-)-2-amino-5-phosphonovaleric acid and MEN10,376 produced an almost complete abolition of the capsaicin-evoked depolarization.(ABSTRACT TRUNCATED AT 250 WORDS) | lld:pubmed |
pubmed-article:7680798 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7680798 | pubmed:language | eng | lld:pubmed |
pubmed-article:7680798 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7680798 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:7680798 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7680798 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7680798 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7680798 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7680798 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7680798 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7680798 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7680798 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7680798 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7680798 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7680798 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7680798 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7680798 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7680798 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:7680798 | pubmed:month | Feb | lld:pubmed |
pubmed-article:7680798 | pubmed:issn | 0306-4522 | lld:pubmed |
pubmed-article:7680798 | pubmed:author | pubmed-author:DrayAA | lld:pubmed |
pubmed-article:7680798 | pubmed:author | pubmed-author:NagyII | lld:pubmed |
pubmed-article:7680798 | pubmed:author | pubmed-author:WoolfC JCJ | lld:pubmed |
pubmed-article:7680798 | pubmed:author | pubmed-author:MaggiC ACA | lld:pubmed |
pubmed-article:7680798 | pubmed:author | pubmed-author:UrbanLL | lld:pubmed |
pubmed-article:7680798 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:7680798 | pubmed:volume | 52 | lld:pubmed |
pubmed-article:7680798 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:7680798 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:7680798 | pubmed:pagination | 1029-37 | lld:pubmed |
pubmed-article:7680798 | pubmed:dateRevised | 2009-9-29 | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:meshHeading | pubmed-meshheading:7680798-... | lld:pubmed |
pubmed-article:7680798 | pubmed:year | 1993 | lld:pubmed |
pubmed-article:7680798 | pubmed:articleTitle | The role of neurokinin and N-methyl-D-aspartate receptors in synaptic transmission from capsaicin-sensitive primary afferents in the rat spinal cord in vitro. | lld:pubmed |
pubmed-article:7680798 | pubmed:affiliation | Department of Anatomy, University Medical School, Debrecen, Hungary. | lld:pubmed |
pubmed-article:7680798 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:7680798 | pubmed:publicationType | In Vitro | lld:pubmed |