The chronobiological regulation of the body’s processes for synthesizing, transporting, storing, and breaking down lipids in a time-of-day dependent manner. Lipid homeostasis is subject to a strong circadian rhythm, which governs the rhythmic activity of key enzymes involved in cholesterol and triglyceride metabolism. Optimizing this timing is essential for maintaining a healthy lipid profile, preventing ectopic fat deposition, and supporting cardiovascular health. Disruptions in this rhythm, such as late-night eating, contribute to dyslipidemia and metabolic syndrome.
Origin
This concept is derived from the convergence of lipidology and chronobiology, recognizing that the liver, adipose tissue, and muscle all possess internal clocks that govern lipid metabolism. The term “timing” emphasizes the critical role of the daily cycle in maintaining metabolic equilibrium. Clinical research has shown that genetic variations in clock genes can directly impact lipid panel results.
Mechanism
The core clock machinery in the liver, the central organ for lipid processing, regulates the rhythmic expression of transcription factors, such as SREBP-1c and PPARα, which control the synthesis of fatty acids and cholesterol. During the fed state, lipogenesis is promoted, while during the fasting state, lipolysis and fatty acid oxidation are favored. Misalignment of feeding and fasting cues with these intrinsic rhythms disrupts the delicate balance, leading to inappropriate fat storage and altered lipoprotein profiles.
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