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Abstract
Loss of Bmal1 in mice leads to swollen mitochondria that struggle to adapt to nutrient changes.
- Mitochondria in mouse liver undergo changes in response to feeding and fasting, regulated by the circadian gene Bmal1.
- Bmal1 regulates mitochondrial dynamics, including fission and the process of removing damaged mitochondria, as well as their production.
- A lack of Bmal1 results in decreased respiration rates and increased oxidative stress in liver cells.
- Mice without Bmal1 in the liver accumulate oxidative damage and develop insulin resistance.
- Restoring Bmal1 activity in mice fed a high-fat diet improves their metabolic health.
- The Bmal1-related gene AHA-1 in C. elegans can influence oxidative metabolism and lifespan, despite not being regulated by circadian rhythms.
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