Grant: Project Grant
University of Toronto
$791,775.00
Molecular and cellular mechanisms of dopamine transporter pharmacological chaperones.
EF 2018-19
Résumé
Dopamine transmission in the brain is a tightly regulated process, and alterations in dopamine
signaling result in several disease with enormous human and economic burden, including
schizophrenia, ADHD, Bipolar disorder, Parkinson's disease and dyskinesias. One of the key
regulators of dopamine transmission is the plasma membrane dopamine transporter, DAT,
which transports released dopamine back into the neuron. In addition to the above prevalent
diseases, there is also a rare, fatal disease caused by mutations in the dopamine transporter,
called dopamine transporter deficiency syndrome. We hypothesize that several disease
states could be corrected by increasing the protein levels of the dopamine transporter. Drug
that increase dopamine transporter activity could potentially treat conditions such as such as
dopamine transporter deficiency syndrome. We have worked to identify drugs that would
increase the levels and activity of the dopamine transporter, and have discovered that the
prescribed drug bupropion increases dopamine transporter levels and activity. Our proposed
research is designed to uncover the mechanism by which bupropion is able to increase
dopamine transporter levels, and help determine whether bupropion would be an effective
treatment for dopamine transporter deficiency syndrome. This work involves studying the
pharmacological and biochemical effects of bupropion. The studies could be quickly
translated into the clinic, since bupropion is already an approved drug for the treatment of
depression.
Programme
Project Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
389034
Name
Salahpour Ali
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Pharmacology & Toxicology
Projecttitle
Molecular and cellular mechanisms of dopamine transporter pharmacological chaperones.
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$791,775
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Bupropion; Dopamine Transporter Deficiency Syndrome; Dopamine Transporter,; Ibogaine; Pharmacological Chaperones; Protein Trafficking
Abstract
Dopamine transmission in the brain is a tightly regulated process, and alterations in dopamine
signaling result in several disease with enormous human and economic burden, including
schizophrenia, ADHD, Bipolar disorder, Parkinson's disease and dyskinesias. One of the key
regulators of dopamine transmission is the plasma membrane dopamine transporter, DAT,
which transports released dopamine back into the neuron. In addition to the above prevalent
diseases, there is also a rare, fatal disease caused by mutations in the dopamine transporter,
called dopamine transporter deficiency syndrome. We hypothesize that several disease
states could be corrected by increasing the protein levels of the dopamine transporter. Drug
that increase dopamine transporter activity could potentially treat conditions such as such as
dopamine transporter deficiency syndrome. We have worked to identify drugs that would
increase the levels and activity of the dopamine transporter, and have discovered that the
prescribed drug bupropion increases dopamine transporter levels and activity. Our proposed
research is designed to uncover the mechanism by which bupropion is able to increase
dopamine transporter levels, and help determine whether bupropion would be an effective
treatment for dopamine transporter deficiency syndrome. This work involves studying the
pharmacological and biochemical effects of bupropion. The studies could be quickly
translated into the clinic, since bupropion is already an approved drug for the treatment of
depression.
Competitiondate
201809
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Salahpour, Ali
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $791,775~ $0~