Grant: Project Grant
University of Alberta
$757,350.00
Cardiac sodium channels as novel targets for the SGLT2 inhibitors
FY 2021-22
Summary
In Canada it is estimated that 1 in 60 individuals live with heart failure (HF) and rates are increasing. Importantly, HF patients have poor quality of life and are 6X more likely to die prematurely, in part through an increased risk of life-threatening arrhythmias which are the predominant cause of sudden cardiac death (SCD) in HF patients. Recent evidence indicates that the SGLT2 inhibitor class of drug, which are used to lower blood glucose in diabetes, is protective against HF and life-threatening arrhythmias. However, precisely how these drugs provide this unexpected effect is not fully understood. We have recently discovered a novel target in the heart, the cardiac sodium channel, that may explain how these drugs work to provide protection against HF and SCD. The overall goal of this project grant is to better understand the molecular mechanisms, cellular consequences and translational implications of our exciting initial observations. It is anticipated that this research will provide a rationale for using this class of drug in HF and also allow development of newer and even more effective drugs for HF.
Department
Program
Project Grant
Recipient
Location
Alberta, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
461364
Name
Light Peter E
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Circulatory and Respiratory Health
Theme2
Biomedical
Prcname2
Cardiovascular System - A: Cells and Tissues
Projecttitle
Cardiac sodium channels as novel targets for the SGLT2 inhibitors
Programtype2
Operating Grants
Orgnameinp2
University of Alberta
Cihramount2
$757,350
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Heart Failure; Ion Channels; Long Qt Syndrome 3; Sglt2 Inhibitors; Sodium Channel
Abstract
In Canada it is estimated that 1 in 60 individuals live with heart failure (HF) and rates are increasing. Importantly, HF patients have poor quality of life and are 6X more likely to die prematurely, in part through an increased risk of life-threatening arrhythmias which are the predominant cause of sudden cardiac death (SCD) in HF patients. Recent evidence indicates that the SGLT2 inhibitor class of drug, which are used to lower blood glucose in diabetes, is protective against HF and life-threatening arrhythmias. However, precisely how these drugs provide this unexpected effect is not fully understood. We have recently discovered a novel target in the heart, the cardiac sodium channel, that may explain how these drugs work to provide protection against HF and SCD. The overall goal of this project grant is to better understand the molecular mechanisms, cellular consequences and translational implications of our exciting initial observations. It is anticipated that this research will provide a rationale for using this class of drug in HF and also allow development of newer and even more effective drugs for HF.
Competitiondate
202203
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Light, Peter E
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $757,350~ $0~