Grant: Operating Grant
University of Toronto
$880,985.00
Drug Metabolism in the Brain: CYP2D and Neuroprotection
FY 2013-14
Summary
Recently we have shown that proteins in our brain, specific types of enzymes, can metabolically inactivate environmental neurotoxins (e.g. pesticides, drugs); these toxins cause a number of brain diseases, more often in men, and older people. This project uses an animal model to investigate the impact of having lower (like people with common genetic variants of this enzyme) or higher (due to some common drugs increasing them) brain levels of this enzyme on toxicity from neurotoxins associated with Parkinson's disease, tardive dyskinesia and essential tremor. This project both establishes, for the first time, a role for these brain enzymes in neurotoxicity, which may explain some of the variability among people in their risk for these diseases, and importantly, provides the basis for future development of novel prevention and treatment approaches.
Department
Program
Operating Grant
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
305059
Name
Tyndale Rachel F
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Pharmacology & Toxicology
Projecttitle
Drug Metabolism in the Brain: CYP2D and Neuroprotection
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$880,985
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Biotransformation; Cytochrome P450s; Neurotoxicity
Abstract
Recently we have shown that proteins in our brain, specific types of enzymes, can metabolically inactivate environmental neurotoxins (e.g. pesticides, drugs); these toxins cause a number of brain diseases, more often in men, and older people. This project uses an animal model to investigate the impact of having lower (like people with common genetic variants of this enzyme) or higher (due to some common drugs increasing them) brain levels of this enzyme on toxicity from neurotoxins associated with Parkinson's disease, tardive dyskinesia and essential tremor. This project both establishes, for the first time, a role for these brain enzymes in neurotoxicity, which may explain some of the variability among people in their risk for these diseases, and importantly, provides the basis for future development of novel prevention and treatment approaches.
Competitiondate
201403
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Tyndale, Rachel F
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $880,985~ $0~