Serotonergic mechanisms in schizophrenia: Evolution and current concepts

Herbert Y. Meltzer*, Zhu Li, Mei Huang, Adam Prus

*Corresponding author for this work

Research output: Contribution to journalReview article

1 Citation (Scopus)

Abstract

Serotonin (5-HT) was once thought to have a role in visual hallucinations based on the findings that lysergic acid diethylamide was found to be a serotonin agonist. This led to a search for endogenous indole hallucinogens in schizophrenia, which ultimately proved unsuccessful. Studies of 5-HT receptor subtypes opened up the issue in several ways, with the 5-HT2A, 5-HT2C, and 5-HT1A receptors seeming to be of greatest importance, and 5-HT6 and 5-HT7 receptors of secondary importance. Linkages between 5-HT, dopamine (DA), glutamate, acetylcholine, and brain-derived neurotrophic factor, have provided some important leads as to how 5-HT may be involved in schizophrenia. It has been found that 5-HT2A rather than 5-HT2C receptor stimulation is the most likely basis for the hallucinogenic effects of lysergic acid diethylamide, but recent neurochemical and genetic studies have raised the possibility that the 5-HT2C receptor may also be important in psychosis based on its ability to regulate tonic dopaminergic function. The discovery that 5-HT2A receptor blockade was an important component of the action of clozapine and other atypical antipsychotic drugs also restored interest in a primary role of 5-HT2A receptors in the etiology of psychosis. 5-HT1A receptors also have been found to enhance DA release in the cortex and hippocampus and are primary factor in the regulation of DA release in both of these regions. Postmortem studies have found some evidence of non-drug-induced increased density of 5-HT1A receptors. Genetic studies are ongoing to link single nucleotide polymorphisms of the 5-HT2A, 5-HT2C, and 5-HT1A receptors to some schizophrenia phenotypes. It is likely that serotonergic function will become even more important in developing genetic and other markers for schizophrenia novel therapies, particularly for psychosis and cognition.

Original languageEnglish (US)
Pages (from-to)12-19
Number of pages8
JournalCurrent Psychosis and Therapeutics Reports
Volume4
Issue number1
DOIs
StatePublished - Mar 1 2006

Fingerprint

Receptor, Serotonin, 5-HT1A
Serotonin
Schizophrenia
Psychotic Disorders
Receptor, Serotonin, 5-HT2C
Receptor, Serotonin, 5-HT2A
Lysergic Acid Diethylamide
Dopamine
Hallucinogens
Serotonin Receptor Agonists
Aptitude
Clozapine
Serotonin Receptors
Hallucinations
Brain-Derived Neurotrophic Factor
Genetic Markers
Cognition
Antipsychotic Agents
Acetylcholine
Single Nucleotide Polymorphism

ASJC Scopus subject areas

  • Phychiatric Mental Health
  • Psychiatry and Mental health

Cite this

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title = "Serotonergic mechanisms in schizophrenia: Evolution and current concepts",
abstract = "Serotonin (5-HT) was once thought to have a role in visual hallucinations based on the findings that lysergic acid diethylamide was found to be a serotonin agonist. This led to a search for endogenous indole hallucinogens in schizophrenia, which ultimately proved unsuccessful. Studies of 5-HT receptor subtypes opened up the issue in several ways, with the 5-HT2A, 5-HT2C, and 5-HT1A receptors seeming to be of greatest importance, and 5-HT6 and 5-HT7 receptors of secondary importance. Linkages between 5-HT, dopamine (DA), glutamate, acetylcholine, and brain-derived neurotrophic factor, have provided some important leads as to how 5-HT may be involved in schizophrenia. It has been found that 5-HT2A rather than 5-HT2C receptor stimulation is the most likely basis for the hallucinogenic effects of lysergic acid diethylamide, but recent neurochemical and genetic studies have raised the possibility that the 5-HT2C receptor may also be important in psychosis based on its ability to regulate tonic dopaminergic function. The discovery that 5-HT2A receptor blockade was an important component of the action of clozapine and other atypical antipsychotic drugs also restored interest in a primary role of 5-HT2A receptors in the etiology of psychosis. 5-HT1A receptors also have been found to enhance DA release in the cortex and hippocampus and are primary factor in the regulation of DA release in both of these regions. Postmortem studies have found some evidence of non-drug-induced increased density of 5-HT1A receptors. Genetic studies are ongoing to link single nucleotide polymorphisms of the 5-HT2A, 5-HT2C, and 5-HT1A receptors to some schizophrenia phenotypes. It is likely that serotonergic function will become even more important in developing genetic and other markers for schizophrenia novel therapies, particularly for psychosis and cognition.",
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Serotonergic mechanisms in schizophrenia : Evolution and current concepts. / Meltzer, Herbert Y.; Li, Zhu; Huang, Mei; Prus, Adam.

In: Current Psychosis and Therapeutics Reports, Vol. 4, No. 1, 01.03.2006, p. 12-19.

Research output: Contribution to journalReview article

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