Premium
Cold acclimation or grapeseed oil feeding affects phospholipid composition and mitochondrial function in duckling skeletal muscle
Author(s) -
Chaînier François,
Roussel Damien,
Georges Bruno,
Meister Roger,
Rouanet JeanLouis,
Duchamp Claude,
Barre Hervé
Publication year - 2000
Publication title -
lipids
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.601
H-Index - 120
eISSN - 1558-9307
pISSN - 0024-4201
DOI - 10.1007/s11745-000-0625-8
Subject(s) - lipidology , clinical chemistry , composition (language) , function (biology) , skeletal muscle , phospholipid , chemistry , food science , biochemistry , biology , anatomy , microbiology and biotechnology , membrane , linguistics , philosophy
The phospholipid fatty acid (FA) composition and functional properties of skeletal muscle and liver mitochondria were examined in cold‐acclimated (CA, 4°C) ducklings. Phospholipid FA of isolated muscle mitochondria from CA birds were longer and more unsaturated than those from thermoneutral (TN, 25°C) reared ducklings. The rise in long‐chain and polyunsaturated FA (PUFA, mainly 20∶4n‐6) was associated with a higher State 4 respiration rate and a lower respiratory control ratio (RCR). Hepatic mitochondria, by contrast, were much less affected by cold acclimation. The cold‐induced changes in phospholipid FA profile and functional properties of muscle mitochondria were reproduced by giving TN ducklings a diet enriched in grapeseed oil (GO, rich in n‐6 FA), suggesting a causal relationship between the membrane structure and mitochondrial functional parameters. However, hepatic mitochondria from ducklings fed the GO diet also showed an enrichment in long‐chain PUFA but opposite changes in their biochemical characteristics (lower State 4, higher RCR). It is suggested that the differential modulation of mitochondrial functional properties by membrane lipid composition between skeletal muscle and liver may depend on muscle‐specific factors possibly interacting with long‐chain PUFA and affecting the proton leakiness of mitochondrial membranes.