The effect of clozapine on extracellular dopamine levels in the shell subregion of the rat nucleus accumbens is reversed following chronic administration: comparison with a selective 5-HT(2C) receptor antagonist.

The effect of clozapine on extracellular dopamine levels in the shell subregion of the rat nucleus accumbens is reversed following chronic administration: comparison with a selective 5-HT(2C) receptor antagonist.

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Altered cortico-striatal crosstalk underlies object recognition memory deficits in the sub-chronic phencyclidine model of schizophrenia.Effectiveness of clozapine, haloperidol and chlorpromazine in schizophrenia during a five-year period.Further neurochemical and behavioural investigation of Brattleboro rats as a putative model of schizophrenia.Asenapine increases dopamine, norepinephrine, and acetylcholine efflux in the rat medial prefrontal cortex and hippocampus.Presynaptic Dopamine Capacity in Patients with Treatment-Resistant Schizophrenia Taking Clozapine: An [18F]DOPA PET Study.A systematic microdialysis study of dopamine transmission in the accumbens shell/core and prefrontal cortex after acute antipsychotics.Cyproheptadine resembles clozapine in vivo following both acute and chronic administration in rats.

P2860

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P2860

The effect of clozapine on extracellular dopamine levels in the shell subregion of the rat nucleus accumbens is reversed following chronic administration: comparison with a selective 5-HT(2C) receptor antagonist.

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http://www.wikidata.org/entity/Q45161651

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2005 nî lūn-bûn

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2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年學術文章

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name

The effect of clozapine on ext ...... mparison with a selective 5-HT

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The effect of clozapine on ext ...... 5-HT(2C) receptor antagonist.

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type

Item

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The effect of clozapine on ext ...... mparison with a selective 5-HT

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The effect of clozapine on ext ...... 5-HT(2C) receptor antagonist.

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The effect of clozapine on ext ...... mparison with a selective 5-HT

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The effect of clozapine on ext ...... 5-HT(2C) receptor antagonist.

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P1476

The effect of clozapine on ext ...... 5-HT(2C) receptor antagonist.

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P2093

Claire S Shilliam

http://www.w3.org/2001/XMLSchema#string

Lee A Dawson

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P2860

Biarylcarbamoylindolines are novel and selective 5-HT(2C) receptor inverse agonists: identification of 5-methyl-1-[[2-[(2-methyl-3-pyridyl)oxy]- 5-pyridyl]carbamoyl]-6-trifluoromethylindoline (SB-243213) as a potential antidepressant/anxiolytic agent

Intravenous cocaine, morphine, and amphetamine preferentially increase extracellular dopamine in the "shell" as compared with the "core" of the rat nucleus accumbens.

Pharmacological actions of the atypical antipsychotic drug clozapine: a review.

An integrative neuroanatomical perspective on some subcortical substrates of adaptive responding with emphasis on the nucleus accumbens.

SB-243213; a selective 5-HT2C receptor inverse agonist with improved anxiolytic profile: lack of tolerance and withdrawal anxiety.

Effect of acute and chronic administration of the selective 5-HT2C receptor antagonist SB-243213 on midbrain dopamine neurons in the rat: an in vivo extracellular single cell study.

Nonlinear relationship between impulse flow and dopamine released by rat midbrain dopaminergic neurons as studied by in vivo electrochemistry.

Morphological differences between projection neurons of the core and shell in the nucleus accumbens of the rat.

Role of serotonin(2C) receptors in the control of brain dopaminergic function.

Differential induction of neurotensin and c-fos gene expression by typical versus atypical antipsychotics.

P2888

sj.npp.1300591

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372-380

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10.1038/SJ.NPP.1300591

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English

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P921

nucleus accumbens

The effect of clozapine on extracellular dopamine levels in the shell subregion of the rat nucleus accumbens is reversed following chronic administration: comparison with a selective 5-HT(2C) receptor antagonist.

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P2860

P2860

The effect of clozapine on extracellular dopamine levels in the shell subregion of the rat nucleus accumbens is reversed following chronic administration: comparison with a selective 5-HT(2C) receptor antagonist.

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