Biochemistry · MU Pleven

20. Metabolism of Glycogen. Biosynthesis and Degradation of Glycogen. Importance of Glycogen in Muscles and Liver.

Covers glycogen as the animal glucose store, its branched structure, and how liver and muscle differ in holding and releasing it. Walks through glycogenesis and glycogenolysis step by step, with the hormonal controls on each, then summarises insulin, glucagon and epinephrine in a table. Ends with the energy yield of muscle glycogen and two glycogen storage diseases, von Gierke and McArdle.

Inside: 6 sections · 5 labelled pictures · 1 table · 10 flashcards · 3 min

Topic 20 of 76 in the MU Pleven syllabus for Biochemistry (Medicine, Year 2). The free AceMed note covers it in 6 sections, about 344 words (3 min of reading), with 10 flashcards.

In this note

  1. Metabolism of Glycogen. Biosynthesis and Degradation of Glycogen.
  2. Glycogen Metabolism
  3. Hormonal Control
  4. Tissue Differences: Liver vs Muscle
  5. Energetic Efficiency
  6. Clinical Correlation (Very High Yield)

Glycogen Metabolism

1. What is Glycogen?

  • Glycogen is the storage form of glucose in animals.
  • It is a highly branched polymer of α-D-glucose.
  • Stored mainly in liver (~10% of weight) and skeletal muscle (1–2%), but muscle contains more total glycogen because of larger mass.
  • Its branched structure allows rapid release of glucose when required.

2. Importance of Glycogen

A. Liver Glycogen

  • Maintains blood glucose levels between meals.
  • Liver releases glucose into blood because it has Glucose-6-phosphatase.

B. Muscle Glycogen

  • Used only inside muscle for ATP production during contraction.
  • Muscle lacks Glucose-6-phosphatase, so cannot release glucose into blood.
  • Function is local energy supply, especially during exercise.

3. Glycogenesis (Glycogen Synthesis)

Goal: Convert glucose → glycogen (storage).

Steps:

  • Glucose → Glucose-6-phosphate (by hexokinase/glucokinase).
  • Glucose-6-phosphate → Glucose-1-phosphate (via phosphoglucomutase).
  • Glucose-1-phosphate + UTP → UDP-glucose (activated glucose donor).
  • Glycogen synthase adds glucose units to a pre-existing glycogen primer (glycogenin).
  • Branching enzyme introduces α-1,6 branches, increasing solubility and synthesis rate.

Regulation:

  • Insulin activates glycogen synthase → promotes storage after meals.
  • High glucose & ATP stimulate synthesis.

4. Glycogenolysis (Glycogen Breakdown)

Goal: Convert glycogen → glucose (energy release).

Steps:

  • Glycogen phosphorylase cleaves α-1,4 bonds → forms Glucose-1-phosphate.
  • Debranching enzyme removes α-1,6 branches.
  • Glucose-1-phosphate → Glucose-6-phosphate (via phosphoglucomutase).
  • In liver: Glucose-6-phosphate → Free glucose → released into blood.
  • In muscle: Glucose-6-phosphate → enters glycolysis → ATP for contraction.

Regulation:

  • Glucagon (in fasting) activates glycogen phosphorylase in liver.
  • Epinephrine activates glycogen breakdown in both liver and muscle.
  • Ca²⁺ and AMP activate glycogen phosphorylase in muscle during exercise.

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