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Biochemistry Integration of Metabolism and Metabolism in Starvation

Overview of Integrated Metabolism

Topic overview

Start with the big picture

After a meal, insulin favors glucose use and storage, fat synthesis, and protein synthesis. As fasting begins, lower insulin and higher glucagon promote liver glycogen breakdown and release of fatty acids and glycerol from adipose tissue. With glycogen depletion, the liver makes glucose from lactate, glycerol, and alanine; muscle and red blood cells contribute substrates through lactate and alanine pathways. During prolonged starvation, fatty-acid oxidation supports hepatic energy needs while ketone production rises. The brain increasingly uses ketones, helping reduce reliance on muscle protein. The kidney also contributes to glucose production and acid buffering. These coordinated shifts illustrate how fuel priorities and organ roles change over time.

Learning objectives

What you'll learn

  • Compare the principal metabolic responses in the fed state, early fasting, and prolonged starvation.
  • Explain how insulin and glucagon influence fuel storage and mobilization.
  • Describe the liver’s roles in glycogen breakdown, gluconeogenesis, fatty-acid oxidation, and ketogenesis.
  • Identify how muscle, adipose tissue, brain, red blood cells, and kidney contribute during fasting.
  • Summarize how ketone use changes fuel priorities during prolonged starvation.
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