Clozapine Interaction with Phosphatidyl Inositol 3-Kinase (PI3K)/Insulin-Signaling Pathway in Caenorhabditis elegans
Autor: | Raymond F. Suckow, Gregory Sliwoski, Miriam Y. Lundy, Bruce M. Cohen, Rakesh Karmacharya, Edgar A. Buttner |
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Rok vydání: | 2009 |
Předmět: |
Pharyngeal pumping
Green Fluorescent Proteins Pharmacology PI3K Article Evolution Molecular Phosphatidylinositol 3-Kinases Genes Reporter medicine Animals Insulin Caenorhabditis elegans Caenorhabditis elegans Proteins insulin signaling Clozapine Conserved Sequence PI3K/AKT/mTOR pathway biology fungi Forkhead Transcription Factors biology.organism_classification DAF-2 Growth Inhibitors Receptor Insulin schizophrenia Psychiatry and Mental health B vitamins Insulin receptor Larva Models Animal biology.protein Pharynx Daf-2 AGE-1 Signal transduction Antipsychotic Agents Signal Transduction Transcription Factors medicine.drug |
Zdroj: | Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology |
ISSN: | 1740-634X 0893-133X |
DOI: | 10.1038/npp.2009.35 |
Popis: | Clozapine has superior and unique effects as an antipsychotic agent, but the mediators of these effects are not known. We studied behavioral and developmental effects of clozapine in Caenorhabditis elegans, as a model system to identify previously undiscovered mechanisms of drug action. Clozapine induced early larval arrest, a phenotype that was also seen with the clozapine metabolite N-desmethyl clozapine but not with any other typical or atypical antipsychotic drug tested. Mutations in the insulin receptor/daf-2 and phosphatidyl inositol 3-kinase (PI3K)/age-1 suppressed clozapine-induced larval arrest, suggesting that clozapine may activate the insulin-signaling pathway. Consistent with this notion, clozapine also increased the expression of an age-1::GFP reporter. Activation of the insulin-signaling pathway leads to cytoplasmic localization of the fork head transcription factor FOXO/daf-16. Clozapine produced cytoplasmic localization of DAF-16::GFP in arrested L1 larvae, in contrast to stressors such as starvation or high temperature, which produce nuclear localization of DAF-16::GFP in arrested L1 larvae. Clozapine also inhibited pharyngeal pumping in C. elegans, an effect that may contribute to, but did not explain, clozapine-induced larval arrest. Our findings demonstrate a drug-specific interaction between clozapine and the PI3K/insulin-signaling pathway in C. elegans. As this pathway is conserved across species, the results may have implications for understanding the unique effects of clozapine in humans. |
Databáze: | OpenAIRE |
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