Reversal of subchronic PCP-induced deficits in attentional set shifting in rats by sertindole and a 5-HT6 receptor antagonist: comparison among antipsychotics. (Q46840298)

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English	Reversal of subchronic PCP-induced deficits in attentional set shifting in rats by sertindole and a 5-HT6 receptor antagonist: comparison among antipsychotics.	scientific article

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30 December 2019

Reversal of subchronic PCP-induced deficits in attentional set shifting in rats by sertindole and a 5-HT6 receptor antagonist: comparison among antipsychotics (English)

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30 December 2019

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Joshua S Rodefer

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30 December 2019

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Tuyet N Nguyen

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30 December 2019

Jens-Jakob Karlsson

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30 December 2019

Jørn Arnt

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30 December 2019

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19 December 2007

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30 December 2019

Neuropsychopharmacology

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30 December 2019

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30 December 2019

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30 December 2019

2657-2666

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30 December 2019

https://scigraph.springernature.com/pub.10.1038/sj.npp.1301654

0 references

Sub-chronic psychotomimetic phencyclidine induces deficits in reversal learning and alterations in parvalbumin-immunoreactive expression in the rat.

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The effect of atypical and classical antipsychotics on sub-chronic PCP-induced cognitive deficits in a reversal-learning paradigm

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A double-blind, controlled study of sertindole versus risperidone in the treatment of moderate-to-severe schizophrenia

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Aged rats are impaired on an attentional set-shifting task sensitive to medial frontal cortex damage in young rats.

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Central blockade of muscarinic cholinergic receptors disrupts affective and attentional set-shifting

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Induction of metabolic hypofunction and neurochemical deficits after chronic intermittent exposure to phencyclidine: differential modulation by antipsychotic drugs

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The 5-HT(6) receptor antagonist SB-271046 selectively enhances excitatory neurotransmission in the rat frontal cortex and hippocampus

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Dissociation in prefrontal cortex of affective and attentional shifts

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Effects of antipsychotics on cognitive behaviour in rats using the delayed non-match to position paradigm.

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Sertindole, in contrast to clozapine and olanzapine, does not disrupt water maze performance after acute or chronic treatment.

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5-HT6 receptor binding sites in schizophrenia and following antipsychotic drug administration: autoradiographic studies with [125I]SB-258585.

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Impairment in perceptual attentional set-shifting following PCP administration: a rodent model of set-shifting deficits in schizophrenia

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Gestational methylazoxymethanol acetate treatment impairs select cognitive functions: parallels to schizophrenia

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Clozapine. A review of its pharmacological properties, and therapeutic use in schizophrenia

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Olanzapine. A review of its pharmacological properties and therapeutic efficacy in the management of schizophrenia and related psychoses

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Course of recovery of cognitive impairment in patients with schizophrenia: a randomised double-blind study comparing sertindole and haloperidol.

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Cognitive improvement after treatment with second-generation antipsychotic medications in first-episode schizophrenia: is it a practice effect?

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What are the functional consequences of neurocognitive deficits in schizophrenia?

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Treatment of cognitive impairment in early psychosis: a comparison of risperidone and haloperidol in a large long-term trial

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5-HT6 receptor antagonists improve performance in an attentional set shifting task in rats

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SB-399885 is a potent, selective 5-HT6 receptor antagonist with cognitive enhancing properties in aged rat water maze and novel object recognition models.

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Recent advances in the phencyclidine model of schizophrenia

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The neuropsychopharmacology of phencyclidine: from NMDA receptor hypofunction to the dopamine hypothesis of schizophrenia

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Sertindole (Serdolect): preclinical and clinical findings of a new atypical antipsychotic

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5‐HT6 receptor antagonist SB‐271046 enhances extracellular levels of monoamines in the rat medial prefrontal cortex

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5-HT6 receptor antagonist SB-399885 potentiates haloperidol and risperidone-induced dopamine efflux in the medial prefrontal cortex or hippocampus

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5-HT(2A) receptor antagonism potentiates haloperidol-induced dopamine release in rat medial prefrontal cortex and inhibits that in the nucleus accumbens in a dose-dependent manner

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Orbital prefrontal cortex mediates reversal learning and not attentional set shifting in the rat.

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The effects of clozapine, risperidone, and olanzapine on cognitive function in schizophrenia

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PDE10A inhibition reverses subchronic PCP-induced deficits in attentional set-shifting in rats

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