Gut dysbiosis and 5-HT2A dysregulation in a preclinical schizophrenia model

Information

  • Research Project
  • 10242023
  • ApplicationId
    10242023
  • Core Project Number
    F30MH116550
  • Full Project Number
    5F30MH116550-04
  • Serial Number
    116550
  • FOA Number
    PA-18-673
  • Sub Project Id
  • Project Start Date
    9/10/2018 - 6 years ago
  • Project End Date
    9/9/2022 - 2 years ago
  • Program Officer Name
    DRISCOLL, JAMIE
  • Budget Start Date
    9/10/2021 - 3 years ago
  • Budget End Date
    9/9/2022 - 2 years ago
  • Fiscal Year
    2021
  • Support Year
    04
  • Suffix
  • Award Notice Date
    8/24/2021 - 3 years ago

Gut dysbiosis and 5-HT2A dysregulation in a preclinical schizophrenia model

Project Summary/Abstract The pathophysiology of schizophrenia is complex and, despite significant advances in understanding the development of this disorder, available treatments will not produce a response in a significant subset of patients. This fact, combined with the significant morbidity associated with currently available antipsychotics, highlights a need for novel approaches to understanding schizophrenia pathophysiology and developing new treatments. The gut microbiome has emerged as a contributor to neuropsychiatric disorders in humans and behavioral alterations in rodents, but has not been extensively investigated within the context of schizophrenia. Interestingly, the microbiome has been demonstrated to affect expression of the serotonin 5-HT2A receptor, which has been well implicated within human schizophrenia as well as animal models of the disorder. Our group has demonstrated that both antipsychotic-free postmortem samples from human schizophrenia patients and offspring mice within a maternal immune activation model of schizophrenia display increased density of the receptor in the prefrontal cortex. Mice within this model also display increased rates of the psychosis-like, 5-HT2A receptor-dependent head twitch response. Other groups have demonstrated association of the receptor with schizophrenia-related phenotypes such as altered function of cortical pyramidal neurons and sensorimotor gating deficits. We therefore propose to investigate the role of the gut microbiome in the development of 5-HT2A receptor alterations and subsequent schizophrenia-like phenotypes in an influenza virus-induced maternal immune activation model of schizophrenia in mice. Transgenic mice, molecular biology techniques, rodent behavioral assays, and microscopy will be used to accomplish these goals. Our results have the potential to further understanding of the pathophysiology of schizophrenia and implication of the gut microbiome in schizophrenia would allow for investigation into new targets for therapy and prevention. The training plan proposes to develop the applicant?s scientific and clinical abilities via introduction to experimental techniques relevant to molecular biology, mouse behavior, dendritic spine analysis, and manipulation of the gut microbiome; development of essential skills such as scientific communication, statistical analysis, hypothesis generation and testing, and ethics; enhancement of clinical skills during medical school clerkships; and addition of scientific knowledge through venues such as seminars and journal clubs. The environment in which the proposed research will take place possesses the equipment necessary to conduct the work, a wealth of core facilities including the Microscopy and Transgenic Mouse cores, and faculty with expertise in a breadth of areas including psychiatric genetics, microscopy, and neuroscience.

IC Name
NATIONAL INSTITUTE OF MENTAL HEALTH
  • Activity
    F30
  • Administering IC
    MH
  • Application Type
    5
  • Direct Cost Amount
    38622
  • Indirect Cost Amount
  • Total Cost
    38622
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    242
  • Ed Inst. Type
    SCHOOLS OF MEDICINE
  • Funding ICs
    NIMH:38622\
  • Funding Mechanism
    TRAINING, INDIVIDUAL
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    VIRGINIA COMMONWEALTH UNIVERSITY
  • Organization Department
    PHYSIOLOGY
  • Organization DUNS
    105300446
  • Organization City
    RICHMOND
  • Organization State
    VA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    232980568
  • Organization District
    UNITED STATES