Grant: Doctoral: Vanier Canada Graduate Scholarships
University of Alberta
$150,000.00
Investigating Sex-Based Differences in Neutrophil Response Following Ischemic Stroke: Assessing the Efficacy of NTS-104, a Progesterone Agonist, in Enhancing Treatment Outcomes
FY 2024-25
Summary
Dr. Ian Winship, University of Alberta. Stroke is a leading cause of death and long-term disability worldwide. Ischemic stroke is a severe medical condition that occurs when blood flow to the brain is blocked, often by a clot. This blockage prevents the brain from getting essential nutrients, resulting in brain damage. Although stroke treatments exist to help restore blood flow to the brain, over half of the patients who receive this therapy still suffer from significant health issues and poor recovery. One factor contributing to this problem is the behaviour of neutrophils, a type of blood and immune cell that arrives at the injury site to aid in repair. However, these cells can clog small blood vessels in the brain after treatment, causing more damage. Our research aims to explore a potential new treatment that could reduce the damage caused by neutrophils following a stroke. We aim to investigate how progesterone, a female sex hormone, may influence neutrophil activity. Early experiments in rats have shown that a new drug, NTS-104, which activates progesterone, might help protect the brain after a stroke. We hypothesize that NTS-104 may reduce the harmful effects of neutrophils and enhance recovery outcomes. Using a mouse model of ischemic stroke, we will assess several key factors, including the number of neutrophils in the brain, the size of the stroke-affected area, and the improvement in blood flow after treatment with NTS-104. Our research helps better understand neutrophil behaviour and the potential protective effects of progesterone. By testing this new treatment, we aim to improve stroke recovery and the quality of life for survivors, particularly those with limited options and poor outcomes from existing therapies. Additionally, our work could pave the way for new research avenues, ultimately contributing to better healthcare solutions for stroke patients.
Department
Program
Doctoral: Vanier Canada Graduate Scholarships
Recipient
Location
Alberta, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
517175
Name
Bui Truong An
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Vanier Canada Graduate Scholarships CIHR
Projecttitle
Investigating Sex-Based Differences in Neutrophil Response Following Ischemic Stroke: Assessing the Efficacy of NTS-104, a Progesterone Agonist, in Enhancing Treatment Outcomes
Programtype2
Studentship Programs
Orgnameinp2
University of Alberta
Cihramount2
$150,000
Cihrequipment2
$0
Programname2
Doctoral: Vanier Canada Graduate Scholarships
Keyworddelim
Basic Science Research; Genetics; Imaging; Ischemic Stroke; Novel Therapeutic Drugs; Sex Differences; Stroke Treatment; Translational Research
Abstract
Dr. Ian Winship, University of Alberta. Stroke is a leading cause of death and long-term disability worldwide. Ischemic stroke is a severe medical condition that occurs when blood flow to the brain is blocked, often by a clot. This blockage prevents the brain from getting essential nutrients, resulting in brain damage. Although stroke treatments exist to help restore blood flow to the brain, over half of the patients who receive this therapy still suffer from significant health issues and poor recovery. One factor contributing to this problem is the behaviour of neutrophils, a type of blood and immune cell that arrives at the injury site to aid in repair. However, these cells can clog small blood vessels in the brain after treatment, causing more damage. Our research aims to explore a potential new treatment that could reduce the damage caused by neutrophils following a stroke. We aim to investigate how progesterone, a female sex hormone, may influence neutrophil activity. Early experiments in rats have shown that a new drug, NTS-104, which activates progesterone, might help protect the brain after a stroke. We hypothesize that NTS-104 may reduce the harmful effects of neutrophils and enhance recovery outcomes. Using a mouse model of ischemic stroke, we will assess several key factors, including the number of neutrophils in the brain, the size of the stroke-affected area, and the improvement in blood flow after treatment with NTS-104. Our research helps better understand neutrophil behaviour and the potential protective effects of progesterone. By testing this new treatment, we aim to improve stroke recovery and the quality of life for survivors, particularly those with limited options and poor outcomes from existing therapies. Additionally, our work could pave the way for new research avenues, ultimately contributing to better healthcare solutions for stroke patients.
Competitiondate
202410
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Bui, Truong An
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $150,000~ $0~