Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
21
pubmed:dateCreated
2003-10-13
pubmed:abstractText
We have previously proposed that haloperidol's debilitating extrapyramidal symptoms (EPS) may be associated with its quaternary BCPP+ (an MPP+ like species) metabolite formed in vivo. However, recent work on D2 knock out mice suggests that haloperidol's EPS may be related to its potent D2 binding (K(i)=0.9 nM). In this study, we explore this question by synthesizing and testing an analogue (DS-27) that binds to D2 receptors with higher affinity than haloperidol, but cannot form quaternary metabolites. This study suggests that D2 affinity may be the primary underlying mechanism for acute catalepsy induction by haloperidol.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0960-894X
pubmed:author
pubmed:issnType
Print
pubmed:day
3
pubmed:volume
13
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3779-82
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:14552778-Acetyl-CoA Carboxylase, pubmed-meshheading:14552778-Animals, pubmed-meshheading:14552778-Antipsychotic Agents, pubmed-meshheading:14552778-Apomorphine, pubmed-meshheading:14552778-Basal Ganglia Diseases, pubmed-meshheading:14552778-Carrier Proteins, pubmed-meshheading:14552778-Catalepsy, pubmed-meshheading:14552778-Dopamine Agonists, pubmed-meshheading:14552778-Fatty Acid Synthetase Complex, Type II, pubmed-meshheading:14552778-Haloperidol, pubmed-meshheading:14552778-Humans, pubmed-meshheading:14552778-Male, pubmed-meshheading:14552778-Mice, pubmed-meshheading:14552778-Psychomotor Performance, pubmed-meshheading:14552778-Radioligand Assay, pubmed-meshheading:14552778-Rats, pubmed-meshheading:14552778-Rats, Sprague-Dawley, pubmed-meshheading:14552778-Receptors, Dopamine D2, pubmed-meshheading:14552778-Stereotyped Behavior
pubmed:year
2003
pubmed:articleTitle
The acute EPS of haloperidol may be unrelated to its metabolic transformation to BCPP+.
pubmed:affiliation
College of Pharmacy & Pharmaceutical Sciences, Florida A & M University, Tallahassee, FL 32307, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't