Abstract
Uncoupling protein 3 (UCP3) may reduce mitochondrial ROS production, and thereby protect against mitochondrial dysfunction in skeletal muscle. UCP3 has been suggested to specifically fulfill this role under high-fat conditions. Here we show that UCP3 knockout mice indeed have elevated mitochondrial ROS production after short-term (8 weeks) high-fat feeding. After 26 weeks of high-fat feeding, UCP3 knockout mice exhibited reduced mitochondrial function as measured ex vivo in isolated mitochondria. In conclusion, these data suggest that UCP3 may have a role in the protection of mitochondria against lipid-induced mitochondrial dysfunction, but only after long-term exposure to high-fat.
Original language | English |
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Pages (from-to) | 4010-4017 |
Number of pages | 8 |
Journal | Febs Letters |
Volume | 585 |
Issue number | 24 |
DOIs | |
Publication status | Published - 15 Dec 2011 |
Keywords
- UCP3
- ROS
- Mitochondria
- Mild uncoupling
- Lipotoxicity
- SKELETAL-MUSCLE MITOCHONDRIA
- ACID OXIDATION
- ROS PRODUCTION
- MICE
- OVEREXPRESSION
- METABOLISM
- LIPOTOXICITY
- RESPIRATION
- DYSFUNCTION