Does stimulation of 5-HT1A receptors improve cognition in schizophrenia?

Herbert Y. Meltzer*, Tomiki Sumiyoshi

*Corresponding author for this work

Research output: Contribution to journalReview article

119 Citations (Scopus)

Abstract

Cognitive impairment is a key feature of schizophrenia and may be the most important determinant of outcome in schizophrenia. This impairment is diffuse and may reflect abnormalities in frontal cortex, hippocampus and other brain regions. While deficits in glutamatergic, GABAergic, dopaminergic and cholinergic impairment have received the most attention as the basis of this impairment, there are many reasons for considering the role of serotonin (5-HT) in contributing to these deficits. This may be via its influence on dopaminergic, cholinergic, glutamatergic and GABAergic function, as well as various growth factors that have been implicated in schizophrenia. Of the 14 known serotonin receptors, the 5-HT1A receptor is a key candidate for mediating at least some of the influence 5-HT has on cognition. 5-HT1A receptors are upregulated in postmortem specimens from patients with schizophrenia, suggesting a deficit in 5-HT1A function in this disorder. Atypical but not typical antipsychotic drugs stimulate the efflux of dopamine from cortex by a 5-HT1A-dependent mechanism. A series of studies from this laboratory involving the 5-HT1A partial agonists tandospirone and buspirone have reported a modest ability of these agents to improve some domains of cognition in patients receiving typical or atypical antipsychotic drugs. Preclinical studies have been mixed in regard to the ability of 5-HT1A partial agonists to improve cognition in various paradigms; some studies report that 5-HT1A antagonists are effective to improve cognition. Aripiprazole, clozapine, olanzapine, perospirone, quetiapine risperidone, and ziprasidone are examples of atypical antipsychotic drugs which are either direct or indirect 5-HT1A agonists which have been shown to improve cognitive function in patients with schizophrenia. Further study is needed to determine the role of the 5-HT1A receptor to improve cognitive function in schizophrenia.

Original languageEnglish (US)
Pages (from-to)98-102
Number of pages5
JournalBehavioural Brain Research
Volume195
Issue number1
DOIs
StatePublished - Dec 16 2008

Fingerprint

Receptor, Serotonin, 5-HT1A
Cognition
Schizophrenia
Serotonin 5-HT1 Receptor Agonists
Antipsychotic Agents
Serotonin
Aptitude
olanzapine
Cholinergic Agents
Serotonin 5-HT1 Receptor Antagonists
Buspirone
Risperidone
Clozapine
Serotonin Receptors
Frontal Lobe
Hippocampus
Dopamine
Intercellular Signaling Peptides and Proteins
Brain

Keywords

  • 5-HT1A
  • Cognition
  • Dopamine
  • Schizophrenia
  • Serotonin

ASJC Scopus subject areas

  • Behavioral Neuroscience

Cite this

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title = "Does stimulation of 5-HT1A receptors improve cognition in schizophrenia?",
abstract = "Cognitive impairment is a key feature of schizophrenia and may be the most important determinant of outcome in schizophrenia. This impairment is diffuse and may reflect abnormalities in frontal cortex, hippocampus and other brain regions. While deficits in glutamatergic, GABAergic, dopaminergic and cholinergic impairment have received the most attention as the basis of this impairment, there are many reasons for considering the role of serotonin (5-HT) in contributing to these deficits. This may be via its influence on dopaminergic, cholinergic, glutamatergic and GABAergic function, as well as various growth factors that have been implicated in schizophrenia. Of the 14 known serotonin receptors, the 5-HT1A receptor is a key candidate for mediating at least some of the influence 5-HT has on cognition. 5-HT1A receptors are upregulated in postmortem specimens from patients with schizophrenia, suggesting a deficit in 5-HT1A function in this disorder. Atypical but not typical antipsychotic drugs stimulate the efflux of dopamine from cortex by a 5-HT1A-dependent mechanism. A series of studies from this laboratory involving the 5-HT1A partial agonists tandospirone and buspirone have reported a modest ability of these agents to improve some domains of cognition in patients receiving typical or atypical antipsychotic drugs. Preclinical studies have been mixed in regard to the ability of 5-HT1A partial agonists to improve cognition in various paradigms; some studies report that 5-HT1A antagonists are effective to improve cognition. Aripiprazole, clozapine, olanzapine, perospirone, quetiapine risperidone, and ziprasidone are examples of atypical antipsychotic drugs which are either direct or indirect 5-HT1A agonists which have been shown to improve cognitive function in patients with schizophrenia. Further study is needed to determine the role of the 5-HT1A receptor to improve cognitive function in schizophrenia.",
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Does stimulation of 5-HT1A receptors improve cognition in schizophrenia? / Meltzer, Herbert Y.; Sumiyoshi, Tomiki.

In: Behavioural Brain Research, Vol. 195, No. 1, 16.12.2008, p. 98-102.

Research output: Contribution to journalReview article

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T1 - Does stimulation of 5-HT1A receptors improve cognition in schizophrenia?

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AU - Sumiyoshi, Tomiki

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