Haloperidol and reduced haloperidol-induced exacerbation of the dystonia produced by the κ opioid U50,488H in guinea-pigs is associated with inhibition of σ binding sites: behavioural and autoradiographical studies

Author:

Brent Paul J.

Publisher

Elsevier BV

Subject

Developmental Biology,Clinical Neurology,Molecular Biology,General Neuroscience

Reference46 articles.

1. Haloperidol treatment differentially regulates [3H]DTG and [3H](+)-3-PPP labelled σ binding sites;Bailey;Eur. J. Pharmacol.,1993

2. Metabolites of haloperidol display preferential activity at σ receptors compared to dopamine D-2 receptors;Bowen;Eur. J. Pharmacol.,1990

3. Characterization of the enantiomers of cis-N-[2-(3,4-dichlorophenyl)ethyl]-N-methyl-2-(1-pyrrolidinyl)cyclohexylamine (BD737 and BD738): novel compounds with high affinity, selectivity and biological efficacy at sigma receptors;Bowen;J. Pharmacol. Exp. Ther.,1992

4. Biochemical pharmacology of sigma receptors;Bowen,1993

5. Similar behavioural effects of sigma agonists and PCP-like non-competitive NMDA antagonists in guinea-pigs;Brent;Psychopharmacology,1991

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