The dynamic, regulated process within the cell dictating which metabolic substrates—such as fatty acids, glucose, or ketone bodies—are preferentially directed toward the mitochondrial electron transport chain for ATP generation under specific physiological conditions. This allocation is tightly coupled to cellular energy demand and substrate availability. It represents key metabolic flexibility.
Origin
Emerging from cellular bioenergetics and metabolic physiology, this term describes the complex partitioning decisions made at the mitochondrial membrane interface. It reflects the cell’s need to optimize energy production efficiency based on nutrient sensing pathways. The concept underscores the metabolic flexibility required for adaptation.
Mechanism
Fuel allocation is governed by the relative abundance of substrate carriers and the activity of key regulatory enzymes like Pyruvate Dehydrogenase Kinase (PDK) and Carnitine Palmitoyltransferase I (CPT1). For instance, high insulin signaling might favor glucose oxidation, while fasting upregulates fatty acid transport via CPT1 into the matrix. This control ensures energy substrate utilization aligns with systemic requirements, optimizing ATP yield per substrate molecule.
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