Abstract
Schizophrenia is one of the most common mental illnesses, with hereditary and environmental factors important for its etiology. All antipsychotics have in common a high affinity for monoaminergic receptors. Whereas hallucinations and delusions usually respond to typical (haloperidol-like) and atypical (clozapine-like) monoaminergic antipsychotics, their efficacy in improving negative symptoms and cognitive deficits remains inadequate. In addition, devastating side effects are a common characteristic of monoaminergic antipsychotics. Recent biochemical, preclinical and clinical findings support group II metabotropic glutamate receptors (mGluR2 and mGluR3) as a new approach to treat schizophrenia. This paper reviews the status of general knowledge of mGluR2 and mGluR3 in the psychopharmacology, genetics and neuropathology of schizophrenia.
| Original language | English |
|---|---|
| Pages (from-to) | 3777-3785 |
| Number of pages | 9 |
| Journal | Cellular and Molecular Life Sciences |
| Volume | 66 |
| Issue number | 23 |
| DOIs | |
| State | Published - Jan 2009 |
Keywords
- 5-HT
- Antipsychotics
- G protein-coupled receptors (GPCR)
- MGluR2
- MGluR3
- Metabotropic glutamate receptors
- Schizophrenia
- Serotonin receptors
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