Literature DB >> 2905626

Enhancement of dopamine metabolism in rat brain frontal cortex: a common effect of chronically administered antipsychotic drugs.

I N Mefford1, K A Roth, H Agren, J D Barchas.   

Abstract

Administration of 4 antipsychotic drugs, haloperidol, chlorpromazine, thioridazine and clozapine, for 21 days elicited increased dopamine metabolism in frontal cortex of rat brain. Only clozapine failed to decrease the apparent firing rate of dopamine neurons in the striatum, as indexed by [homovanillic acid]/[dopamine]. These data support the hypotheses that frontal cortex dopamine neurons may be a common site for antipsychotic action while decreased release of dopamine in the striatum may be associated with the development of extrapyramidal side effects.

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Year:  1988        PMID: 2905626     DOI: 10.1016/0006-8993(88)90630-0

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  6 in total

1.  Regulatory aspects of nigrostriatal dopaminergic neurons.

Authors:  P Miu; F Karoum; G Toffano; J W Commissiong
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

Review 2.  TNF in the era of immune checkpoint inhibitors: friend or foe?

Authors:  Allen Y Chen; Jedd D Wolchok; Anne R Bass
Journal:  Nat Rev Rheumatol       Date:  2021-03-08       Impact factor: 20.543

3.  Endogenous homovanillic acid levels differ between rat and rabbit caudate, hippocampus, and cortical regions.

Authors:  T A Reader; K M Dewar
Journal:  Neurochem Res       Date:  1989-11       Impact factor: 3.996

Review 4.  Clozapine: new research on efficacy and mechanism of action.

Authors:  H Y Meltzer; B Bastani; L Ramirez; S Matsubara
Journal:  Eur Arch Psychiatry Neurol Sci       Date:  1989

5.  Risperidone: a novel antipsychotic with many "atypical" properties?

Authors:  P Stathis; K Antoniou; Z Papadopoulou-Daifotis; M N Rimikis; D Varonos
Journal:  Psychopharmacology (Berl)       Date:  1996-10       Impact factor: 4.530

6.  Effects of chronic administration of ondansetron (GR38032F), a selective 5-HT3 receptor antagonist, on monoamine metabolism in mesolimbic and nigrostriatal dopaminergic neurons and on striatal D2-receptor binding.

Authors:  M Koulu; J Lappalainen; J Hietala; B Sjöholm
Journal:  Psychopharmacology (Berl)       Date:  1990       Impact factor: 4.530

  6 in total

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