Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2002-10-2
pubmed:abstractText
The present study was designed to investigate the rewarding effect, G-protein activation and dopamine (DA) release following partial sciatic nerve ligation in the rat. Here we show for the first time that morphine failed to produce a place preference in rats with nerve injury. Various studies provide arguments to support that the mesolimbic dopaminergic system, which projects from the ventral tegmental area (VTA) to the nucleus accumbens (N.Acc), is critical of the motivational effects of opioids. In the present study, there were no significant differences between sham-operated and sciatic nerve-ligated rats in the increases in guanosine-5'-o-(3-[35S]thio)triphosphate ([35S]GTPgammaS) binding to membranes of the N.Acc stimulated by either DA, the D1 receptor agonist SKF81297, the D2 receptor agonist N-propylnoraporphine or the D3 receptor agonist 7-hydroxy-2-dipropylaminotetralin (7-OH DPAT). In contrast, the increases in [35S]GTPgammaS binding to membranes of the VTA induced by either morphine or a selective micro -opioid receptor agonist [d-Ala2, NMePhe4, Gly(ol)5]enkephalin were significantly attenuated in nerve-ligated rats as compared with sham- operated rats. Furthermore, the enhancement of DA release in the N.Acc stimulated by morphine was significantly suppressed by sciatic nerve ligation. These findings suggest that attenuation of the morphine-induced place preference under neuropathic pain may result from a decrease in the morphine-induced DA release in the N.Acc with reduction in the mu-opioid receptor-mediated G-protein activation in the VTA.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0022-3042
pubmed:author
pubmed:issnType
Print
pubmed:volume
82
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1192-8
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:12358766-Animals, pubmed-meshheading:12358766-Behavior, Animal, pubmed-meshheading:12358766-Binding, Competitive, pubmed-meshheading:12358766-Disease Models, Animal, pubmed-meshheading:12358766-Dopamine, pubmed-meshheading:12358766-Extracellular Space, pubmed-meshheading:12358766-Guanosine 5'-O-(3-Thiotriphosphate), pubmed-meshheading:12358766-Hyperalgesia, pubmed-meshheading:12358766-Ligation, pubmed-meshheading:12358766-Male, pubmed-meshheading:12358766-Microdialysis, pubmed-meshheading:12358766-Morphine, pubmed-meshheading:12358766-Nucleus Accumbens, pubmed-meshheading:12358766-Pain, pubmed-meshheading:12358766-Pain Measurement, pubmed-meshheading:12358766-Rats, pubmed-meshheading:12358766-Rats, Sprague-Dawley, pubmed-meshheading:12358766-Receptors, Opioid, mu, pubmed-meshheading:12358766-Reward, pubmed-meshheading:12358766-Sciatic Neuropathy, pubmed-meshheading:12358766-Spatial Behavior, pubmed-meshheading:12358766-Ventral Tegmental Area
pubmed:year
2002
pubmed:articleTitle
Suppression of the morphine-induced rewarding effect in the rat with neuropathic pain: implication of the reduction in mu-opioid receptor functions in the ventral tegmental area.
pubmed:affiliation
Department of Toxicology, School of Pharmacy, Hoshi University, Tokyo, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't