Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
1982-5-21
|
pubmed:abstractText |
Flupenthixyl chloride (FPT-Cl), a derivative of the dopamine (DA) receptor antagonist and neuroleptic alpha-flupenthixol possessing a chloroethyl side chain, has been prepared and evaluated for use in vivo in affinity labeling of DA receptors. Binding of [3H]spiperone to rat striatal DA receptors was markedly altered up to 12 h after intraventricular injection of FPT-Cl as compared with controls, while Scatchard plots of [3H]spiperone binding obtained on rat striatal homogenates 24 and 48 h after injection of FPT-Cl had values of Bmax significantly lower than in controls. The results suggest that the administration of FPT-Cl leads to irreversible and possibly covalent blockade of a portion of the spiperone binding sites in rat striatum. A second population of receptors appears to be blocked reversibly and presumably noncovalently by FPT-Cl, and these spiperone binding sites are partially reactivated in vivo after 48 h.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
0014-2999
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
5
|
pubmed:volume |
77
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
313-6
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:7060641-Animals,
pubmed-meshheading:7060641-Corpus Striatum,
pubmed-meshheading:7060641-Flupenthixol,
pubmed-meshheading:7060641-Male,
pubmed-meshheading:7060641-Rats,
pubmed-meshheading:7060641-Rats, Inbred Strains,
pubmed-meshheading:7060641-Receptors, Dopamine,
pubmed-meshheading:7060641-Thioxanthenes
|
pubmed:year |
1982
|
pubmed:articleTitle |
Irreversible blockade of striatal dopamine receptors in vivo by a derivative of alpha-flupenthixol.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
|