pubmed-article:11438603 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:11438603 | lifeskim:mentions | umls-concept:C0007634 | lld:lifeskim |
pubmed-article:11438603 | lifeskim:mentions | umls-concept:C0025148 | lld:lifeskim |
pubmed-article:11438603 | lifeskim:mentions | umls-concept:C0001629 | lld:lifeskim |
pubmed-article:11438603 | lifeskim:mentions | umls-concept:C0006121 | lld:lifeskim |
pubmed-article:11438603 | lifeskim:mentions | umls-concept:C1550278 | lld:lifeskim |
pubmed-article:11438603 | lifeskim:mentions | umls-concept:C0027796 | lld:lifeskim |
pubmed-article:11438603 | lifeskim:mentions | umls-concept:C0066908 | lld:lifeskim |
pubmed-article:11438603 | lifeskim:mentions | umls-concept:C0021467 | lld:lifeskim |
pubmed-article:11438603 | lifeskim:mentions | umls-concept:C0547070 | lld:lifeskim |
pubmed-article:11438603 | lifeskim:mentions | umls-concept:C0021469 | lld:lifeskim |
pubmed-article:11438603 | pubmed:issue | 14 | lld:pubmed |
pubmed-article:11438603 | pubmed:dateCreated | 2001-7-4 | lld:pubmed |
pubmed-article:11438603 | pubmed:abstractText | Neurons in the rostroventromedial medulla (RVM) project to spinal loci where the neurons inhibit or facilitate pain transmission. Abnormal activity of facilitatory processes may thus represent a mechanism of chronic pain. This possibility and the phenotype of RVM cells that might underlie experimental neuropathic pain were investigated. Cells expressing mu-opioid receptors were targeted with a single microinjection of saporin conjugated to the mu-opioid agonist dermorphin; unconjugated saporin and dermorphin were used as controls. RVM dermorphin-saporin, but not dermorphin or saporin, significantly decreased cells expressing mu-opioid receptor transcript. RVM dermorphin, saporin, or dermorphin-saporin did not change baseline hindpaw sensitivity to non-noxious or noxious stimuli. Spinal nerve ligation (SNL) injury in rats pretreated with RVM dermorphin-saporin failed to elicit the expected increase in sensitivity to non-noxious mechanical or noxious thermal stimuli applied to the paw. RVM dermorphin or saporin did not alter SNL-induced experimental pain, and no pretreatment affected the responses of sham-operated groups. This protective effect of dermorphin-saporin against SNL-induced pain was blocked by beta-funaltrexamine, a selective mu-opioid receptor antagonist, indicating specific interaction of dermorphin-saporin with the mu-opioid receptor. RVM microinjection of dermorphin-saporin, but not of dermorphin or saporin, in animals previously undergoing SNL showed a time-related reversal of the SNL-induced experimental pain to preinjury baseline levels. Thus, loss of RVM mu receptor-expressing cells both prevents and reverses experimental neuropathic pain. The data support the hypothesis that inappropriate tonic-descending facilitation may underlie some chronic pain states and offer new possibilities for the design of therapeutic strategies. | lld:pubmed |
pubmed-article:11438603 | pubmed:language | eng | lld:pubmed |
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pubmed-article:11438603 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:11438603 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11438603 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11438603 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11438603 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11438603 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11438603 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11438603 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:11438603 | pubmed:month | Jul | lld:pubmed |
pubmed-article:11438603 | pubmed:issn | 1529-2401 | lld:pubmed |
pubmed-article:11438603 | pubmed:author | pubmed-author:LamFF | lld:pubmed |
pubmed-article:11438603 | pubmed:author | pubmed-author:LappiD ADA | lld:pubmed |
pubmed-article:11438603 | pubmed:author | pubmed-author:PorrecaFF | lld:pubmed |
pubmed-article:11438603 | pubmed:author | pubmed-author:VanderahT WTW | lld:pubmed |
pubmed-article:11438603 | pubmed:author | pubmed-author:OssipovM HMH | lld:pubmed |
pubmed-article:11438603 | pubmed:author | pubmed-author:MalanT PTPJr | lld:pubmed |
pubmed-article:11438603 | pubmed:author | pubmed-author:BurgessS ESE | lld:pubmed |
pubmed-article:11438603 | pubmed:author | pubmed-author:GardellL RLR | lld:pubmed |
pubmed-article:11438603 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:11438603 | pubmed:day | 15 | lld:pubmed |
pubmed-article:11438603 | pubmed:volume | 21 | lld:pubmed |
pubmed-article:11438603 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:11438603 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:11438603 | pubmed:pagination | 5281-8 | lld:pubmed |
pubmed-article:11438603 | pubmed:dateRevised | 2008-7-12 | lld:pubmed |
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pubmed-article:11438603 | pubmed:year | 2001 | lld:pubmed |
pubmed-article:11438603 | pubmed:articleTitle | Inhibition of neuropathic pain by selective ablation of brainstem medullary cells expressing the mu-opioid receptor. | lld:pubmed |
pubmed-article:11438603 | pubmed:affiliation | Departments of Pharmacology and Anesthesiology, University of Arizona, Tucson, Arizona 85724, USA. frankp@u.arizona.edu | lld:pubmed |
pubmed-article:11438603 | pubmed:publicationType | Journal Article | lld:pubmed |
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