PD 158771, a potential antipsychotic agent with D2/D3 partial agonist and 5-HT1A agonist actions. I. Neurochemical effects-Reference-Cited by-同舟云学术

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PD 158771, a potential antipsychotic agent with D2/D3 partial agonist and 5-HT1A agonist actions. I. Neurochemical effects

Published:2000-06 Issue:7 Volume:39 Page:1197-1210
ISSN:0028-3908
Container-title:Neuropharmacology
language:en
Short-container-title:Neuropharmacology

Author:

Akunne H.C,Zoski K.T,Davis M.D,Cooke L.W,Meltzer L.T,Whetzel S.Z,Shih Y.H,Wustrow D.J,Wise L.D,MacKenzie R.G,Georgic L.M,Heffner T.G,Pugsley T.A

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Pharmacology

Reference48 articles.

1. Characterization of binding of [3H]PD 128907, a selective D3 receptor agonist ligand, to CHO-K1 cells;Akunne;Life Sci.,1995

2. Differential inhibition of serotonin release by 5-HT and NA reuptake blockers after systemic administration;Auerbach;Neuropharmacol.,1995

3. Functional localization in the brain in schizophrenia;Berman,1991

4. Characterization of the binding of [3H]SCH 23390, a selective D-1 receptor antagonist ligand, in rat striatum;Billard;Life Sci.,1984

5. Efficacy and safety of a putative anxiolytic agent: ipsapirone;Borison;Psychopharmacol. Bull.,1990

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1. Update on the Mechanism of Action of Aripiprazole: Translational Insights into Antipsychotic Strategies Beyond Dopamine Receptor Antagonism;CNS Drugs;2015-09

2. In vivo effects of pardoprunox (SLV308), a partial D2/D3 receptor and 5-HT1A receptor agonist, on rat dopamine and serotonin neuronal activity;Synapse;2011-05-03

3. Action of novel antipsychotics at human dopamine D3 receptors coupled to G protein and ERK1/2 activation;Neuropharmacology;2007-08

4. KKHA-761, a potent D3 receptor antagonist with high 5-HT1A receptor affinity, exhibits antipsychotic properties in animal models of schizophrenia;Pharmacology Biochemistry and Behavior;2005-10

5. Neurotoxins and medicinals for the treatment of Parkinson’s disease. Part 2: dopamine receptors and their agonists;Pharmaceutical Chemistry Journal;2005-10

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