• DocumentCode
    3040426
  • Title

    5.7: Presentation session: Neuroscience informatics: “Pathway-assisted investigation of atypical antipsychotic drugs and serotonin receptors in schizophrenia”

  • Author

    Zhao, Zhongming

  • Author_Institution
    Departments of Biomedical Informatics and Psychiatry, Vanderbilt University School of Medicine
  • fYear
    2010
  • fDate
    25-26 May 2010
  • Firstpage
    1
  • Lastpage
    1
  • Abstract
    Clozapine and its four related drugs (olanzapine, quetiapine, risperidone and ziprasidone) are the most frequently used treatments for schizophrenia in the world. The underlying mechanisms are not well understood. In this study, we investigated the features of these five drugs through their related genes at the pathway level. For each drug, we first identified the pathways that the drugs might be involved in. We found that these five drugs are all significantly involved in five pathways, i.e., G-protein coupled receptor signaling, cAMP-mediated signaling, serotonin receptor (5-HT) signaling, AMPK signaling, and cardiac hypertrophy signaling. Among these pathways, the serotonin receptor (5-HTR) pathway is an important neurotransmitter-related pathway in psychiatric disorders. Therefore, we further investigated the functional relationship between the five drugs and serotonin receptors based on the experimental data of activation, chemical-protein interaction, expression, inhabitation, and regulation of binding. We constructed a drug-5HTR network including these five drugs, serotonin receptors, and their relationships and found that clozapine has more interactors and more complicated connections with serotonin receptors than the other four drugs. Additionally, clozapine has two unique relationships with HTR2A, one of the most susceptible candidate genes for schizophrenia. These results indicated that clozapine might have a different action during the treatment process of schizophrenia from the other four drugs
  • Keywords
    Bioinformatics; Biomedical informatics; Cancer; Chemicals; Drugs; Genetics; Medical treatment; Neuroscience; Psychiatry; Psychology;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Biomedical Sciences and Engineering Conference (BSEC), 2010
  • Conference_Location
    Oak Ridge, TN, USA
  • Print_ISBN
    978-1-4244-6713-6
  • Electronic_ISBN
    978-1-4244-6714-3
  • Type

    conf

  • DOI
    10.1109/BSEC.2010.5510846
  • Filename
    5510846