Grant: Travel Awards - Institute Community Support
Direct Payment
$1,400.00
Effect of glucosamine on renin-angiotensin system under inflammatory condition
FY 2012-13
Summary
Rheumatoid arthritis (RA), a chronic progressive systemic inflammatory condition, leads to considerable pain and joint destruction, diminished function and disability. RA is associated with excess morbidity and mortality from cardiovascular complications. Evidence suggests that common pro-inflammatory cytokines, which are produced in the body in response to the disease, are involved in the development and progression of RA as well as other inflammatory diseases such as atherosclerosis. In the body, renin-angiotensin system (RAS) regulates blood pressure and fluid balance and contributes to the inflammatory response in the vascular wall. The activation of RAS by inflammation plays an important role in the physiology and pathophysiology of cardiovascular system. An important therapeutic approach in dealing with cardiovascular complications of RA, therefore, is to mitigate the process of activation of RAS. We have focused on a therapeutic intervention that may prevent cardiovascular events by inhibiting the activation of RAS caused by experimental arthritis. Glucosamine is a naturally occurring aminosugar that in our preliminary studies appears to exert anti-inflammatory effects in the heart through the RAS. We showed that inflammation activates RAS in rat heart and increases its cardiotoxic metabolites and disrupts the physiological balance of the RAS system. Administration of glucosamine, however, restored the normal balance and proved to be cardioprotective by decreasing cardiotoxic and increasing cardioprotective metabolites of RAS.
Department
Program
Travel Awards - Institute Community Support
Recipient
Location
Alberta, Canada
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
278449
Name
Aghazadeh-Habashi Ali
Region
Alberta
Country
Canada
Orgtype
Research Institution
Instname2
Circulatory and Respiratory Health
Theme2
Biomedical
Prcname2
Institute of Circulatory and Respiratory Health
Projecttitle
Effect of glucosamine on renin-angiotensin system under inflammatory condition
Programtype2
Undefined
Orgnameinp2
Direct Payment
Cihramount2
$1,400
Cihrequipment2
$0
Programname2
Travel Awards - Institute Community Support
Keyworddelim
Ace; Ace 2; Angiotensin 1-7; Angiotensin Ii; Cardiovascular Diseases; Eliza Kit; Glucosamine; Inflammation; Renin-Angiotensin System; Rheumatoid Arthritis; Western Blot
Abstract
Rheumatoid arthritis (RA), a chronic progressive systemic inflammatory condition, leads to considerable pain and joint destruction, diminished function and disability. RA is associated with excess morbidity and mortality from cardiovascular complications. Evidence suggests that common pro-inflammatory cytokines, which are produced in the body in response to the disease, are involved in the development and progression of RA as well as other inflammatory diseases such as atherosclerosis. In the body, renin-angiotensin system (RAS) regulates blood pressure and fluid balance and contributes to the inflammatory response in the vascular wall. The activation of RAS by inflammation plays an important role in the physiology and pathophysiology of cardiovascular system. An important therapeutic approach in dealing with cardiovascular complications of RA, therefore, is to mitigate the process of activation of RAS. We have focused on a therapeutic intervention that may prevent cardiovascular events by inhibiting the activation of RAS caused by experimental arthritis. Glucosamine is a naturally occurring aminosugar that in our preliminary studies appears to exert anti-inflammatory effects in the heart through the RAS. We showed that inflammation activates RAS in rat heart and increases its cardiotoxic metabolites and disrupts the physiological balance of the RAS system. Administration of glucosamine, however, restored the normal balance and proved to be cardioprotective by decreasing cardiotoxic and increasing cardioprotective metabolites of RAS.
Competitiondate
201301
Approvedterm2
0 yr 3 mths
Pinamesdelim
Aghazadeh-Habashi, Ali
Approvedterm
0 an 3 mois
Cihrcontribution2
Inst of Circ &Respiratory Hlth~ $1,400~ $0~