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Grant: Catalyst Grant: Bone Health

Université du Québec à Montréal

$90,079.00

Redox-dependent regulation of osteoblast and osteoclast function during haemolytic anaemia

FY 2010-11

Summary
Low bone mass density (BMD) with osteoporosis is commonly observed in patients with haemolytic anaemia (HA), but its causes remain unknown. The enhanced destruction of red blood cells (RBC) responsible for HA leads to the release and accumulation of free haemoglobin and heme in the plasma. Heme and haemoglobin are iron-containing molecules with important oxidant properties, and generate systemic oxidative stress in patients with HA. We want to understand the links between free heme, oxidative stress and bone fragility in these patients. For this, we aim to set up an in vivo experimental model in mice to study the effects of heme injection on their bone structure. In parallel, we will also study whether free heme further contributes to the destruction of oxidised RBC, whether free heme leads to inflammation, and whether these factors act in combination to render bones more fragile. As the capacity of our tissues to defend themselves against oxidants diminishes with age, with hormonal changes or with disease, and as all these conditions may lead to bone fragility, we believe that our study will contribute to understand how failure in antioxidant defences progressively modifies the function of bone cells.
Program
Catalyst Grant: Bone Health
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
207733
Name
Moreau Robert
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Musculoskeletal Health and Arthritis
Theme2
Biomedical
Prcname2
Catalyst Grant: Bone Health
Projecttitle
Redox-dependent regulation of osteoblast and osteoclast function during haemolytic anaemia
Programtype2
Operating Grants
Orgnameinp2
Université du Québec à Montréal
Cihramount2
$90,079
Cihrequipment2
$0
Programname2
Catalyst Grant: Bone Health
Keyworddelim
Haemolytic Anaemia; Heme; Hemin; Inflammation; Microtomography; Osteoblast; Osteoporosis; Oxidative Stress
Abstract
Low bone mass density (BMD) with osteoporosis is commonly observed in patients with haemolytic anaemia (HA), but its causes remain unknown. The enhanced destruction of red blood cells (RBC) responsible for HA leads to the release and accumulation of free haemoglobin and heme in the plasma. Heme and haemoglobin are iron-containing molecules with important oxidant properties, and generate systemic oxidative stress in patients with HA. We want to understand the links between free heme, oxidative stress and bone fragility in these patients. For this, we aim to set up an in vivo experimental model in mice to study the effects of heme injection on their bone structure. In parallel, we will also study whether free heme further contributes to the destruction of oxidised RBC, whether free heme leads to inflammation, and whether these factors act in combination to render bones more fragile. As the capacity of our tissues to defend themselves against oxidants diminishes with age, with hormonal changes or with disease, and as all these conditions may lead to bone fragility, we believe that our study will contribute to understand how failure in antioxidant defences progressively modifies the function of bone cells.
Competitiondate
201006
Approvedterm2
1 yr 0 mth
Pinamesdelim
Moreau, Robert
Approvedterm
1 an 0 mois
Cihrcontribution2
Inst of Musculoskel Hlth &Arth~ $90,079~ $0~
Université du Québec à Montréal - $90,079 Grant (2010… | Canada Spends