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Grant: Team Grant: China-Canada Collaborative Teams in Health Research

University of Manitoba

$500,000.00

CIHR Team in Schizophrenia. Are oligodendrocytes the missing piece of the puzzle? A systematic study of the role of oligodendrocytes in schizophrenia from bench-to-bedside

EF 2009-10

Résumé
Schizophrenia is a complex disorder that affects 1% of the worldwide population, and represents a significant social and financial burden. Studies in patients with schizophrenia have found abnormalities in white matter and myelin dysfunction. Animal studies in our lab have shown that disrupting oligodendrocytes (OL), which form the myelin coating on neurons in the brain, results in schizophrenia-like behaviour and antipsychotics improve symptoms and prevent demyelination. This research project will evaluate the role of OL in patients with schizophrenia and animal models. Patients with schizophrenia will be examined for abnormalities in OL genotyping, functional and structural abnormalities in the brain using MRI(s). We will assess how gene alteration in OLs predicted the onset of symptoms, symptom profiles, brain changes, and response to treatment. Animal models of schizophrenia will parallel human studies with anatomical examination using uMRI as well as evaluating OL abnormalities using cellular techniques. We will also examine the effects of psychosocial stress on behavioural symptoms and OL damage, and the ability of antipsycotics to prevent OL damage and promote OL repair in the brain. The in vitro studies will take animal cells to the dish and look at how gene alterations change the structure and function of OLs and see if antipsychotics can regulate the gene expression and normalize OL function. This project spans many areas of expertise within the field of neuroscience and psychiatry, including human genetics, neuroimaging, animal pathology and behavioural science, cellular and molecular biology and pharmacology. This study will create a large schizophrenia database, improve screening, rationale use of treatment, drug development, and facilitate our understanding of the pathology of schizophrenia.
Programme
Team Grant: China-Canada Collaborative Teams in Health Research
Emplacement
Manitoba, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
196332
Name
Li Xin-Min
Region
Manitoba
Country
Canada
Orgtype
Institution Paid; Research Institution
Partnername
Ministry of Science and Technology of the People's Republic of China
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Team Grant: China-Canada Collaborative Teams in Health Research
Projecttitle
CIHR Team in Schizophrenia. Are oligodendrocytes the missing piece of the puzzle? A systematic study of the role of oligodendrocytes in schizophrenia from bench-to-bedside
Programtype2
Operating Grants
Orgnameinp2
University of Manitoba
Cihramount2
$500,000
Cihrequipment2
$0
Programname2
Team Grant: China-Canada Collaborative Teams in Health Research
Keyworddelim
Antipsychotics; Demyelination/Remyelination; Genetic Susceptibility; Neuroimaging; Oligodendrocytes; Schizophrenia
Abstract
Schizophrenia is a complex disorder that affects 1% of the worldwide population, and represents a significant social and financial burden. Studies in patients with schizophrenia have found abnormalities in white matter and myelin dysfunction. Animal studies in our lab have shown that disrupting oligodendrocytes (OL), which form the myelin coating on neurons in the brain, results in schizophrenia-like behaviour and antipsychotics improve symptoms and prevent demyelination. This research project will evaluate the role of OL in patients with schizophrenia and animal models. Patients with schizophrenia will be examined for abnormalities in OL genotyping, functional and structural abnormalities in the brain using MRI(s). We will assess how gene alteration in OLs predicted the onset of symptoms, symptom profiles, brain changes, and response to treatment. Animal models of schizophrenia will parallel human studies with anatomical examination using uMRI as well as evaluating OL abnormalities using cellular techniques. We will also examine the effects of psychosocial stress on behavioural symptoms and OL damage, and the ability of antipsycotics to prevent OL damage and promote OL repair in the brain. The in vitro studies will take animal cells to the dish and look at how gene alterations change the structure and function of OLs and see if antipsychotics can regulate the gene expression and normalize OL function. This project spans many areas of expertise within the field of neuroscience and psychiatry, including human genetics, neuroimaging, animal pathology and behavioural science, cellular and molecular biology and pharmacology. This study will create a large schizophrenia database, improve screening, rationale use of treatment, drug development, and facilitate our understanding of the pathology of schizophrenia.
Competitiondate
200910
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Li, Xin-Min; He, Jue; Kong, Jiming; Martin, Melanie
Approvedterm
3 ans 0 mois
Cihrcontribution2
Inst of Neurosc Mental Hlth &A~ $500,000~ $0~