Carbohydrate Metabolism in Sports and Exercise

Relevance of Carbohydrates in Sports and Exercise

  • Carbohydrates (CHO) are a critical energy source for performance.

  • The right dose of carbohydrates is essential, as excess can cause damage and disease.

    • Paracelsus (1493-1541): "All substances are poisons; the right dose differentiates a poison and a remedy."

Relevance of Carbohydrate for Metabolism

  • Instantaneous energy source: 4 kcal/g, with or without oxygen.

  • Protein sparing: Preserves protein by providing an alternative energy source.

  • Stored as glycogen in muscle and liver.

    • Liver glycogen stores are about 5x higher than in skeletal muscle.

  • Can be converted to fat for energy storage.

  • Keeps the gastrointestinal (GI) tract healthy.

Importance of CHO for Exercise

  • CHO is the most important energy source for athletic performance.

  • Increasingly important in competition at >85% VO2max.

  • CHO fuels about 70% of exercise at this intensity.

Four Steps of Carbohydrate Metabolism

  • Step 1: Glycolysis

  • Step 2: The Link Reaction

  • Step 3: The Krebs Cycle

  • Step 4: The Electron Transport Chain (ETC)

Step 1: Glycolysis

  • Breakdown of glucose to two molecules of pyruvate.

  • Occurs in the cytoplasm.

Step 2: The Link Reaction

  • Breakdown of pyruvate to Acetyl CoA.

  • Pyruvate is transported into the mitochondria.

Step 3: Krebs Cycle

  • Hans Krebs: Pioneer of cellular respiration (Nobel Prize in 1953).

  • >75% of the original energy in glucose is still present in two molecules of pyruvate.

  • If oxygen is present, pyruvate is completely metabolized to CO_2.

  • Takes place in the mitochondria.

  • Acetate from acetyl CoA combines with oxaloacetic acid (OAA) to form citrate (citric acid).

  • Each turn of the cycle produces:

    • 1 ATP by substrate-level phosphorylation

    • 3 NADH

    • 1 FADH_2

  • Purpose is to 'steal' electrons (with H) from carbon molecules to NADH and FADH_2.

Krebs Cycle Summary (Per Pyruvate )
  • 3 CO_2

  • 4 NADH + H^+

  • 1 FADH_2

  • 1 ATP

Krebs Cycle Summary (Per Glucose)
  • 6 CO_2

  • 8 NADH + H^+

  • 2 FADH_2

  • 2 ATP

Step 4: Electron Transport and Oxidative Phosphorylation

  • Most ATP comes from the energy of electrons carried by NADH and FADH_2.

  • Energy in electrons powers ATP synthesis.

  • The electron transport chain has thousands of copies in the cristae of the mitochondria.

Step 4 Sub-Processes
  • Electron transport

  • Chemiosmosis

Step 4i: Electron Transport
  • NADH and FADH_2 donate electrons to the ETC.

  • Electrons are passed along the ETC in a series of oxidation-reduction (redox) reactions.

    • Oxidation: Loss of electrons (LEO)

    • Reduction: Gain of electrons

  • NADH excites complex 1, pumping H^+ into the intermembrane space.

  • Complex 1 passes the electron to CoQ.

  • FADH_2 hands its electron to complex 2; no H^+ pumping.

  • Complex 2 passes electrons to CoQ.

  • Complex 3 pumps H^+ ions into the intermembrane space.

  • H^+ ions flow down their concentration gradient through ATP synthase (complex 5) via chemiosmosis.

Step 4ii: Chemiosmosis
  • Peter Mitchell: Nobel Prize in Chemistry in 1978.

  • Energy from electron transport is used to pump H^+ across the inner mitochondrial membrane.

  • This creates a proton concentration gradient.

  • Backflow of H^+ through ATP synthase synthesizes ATP from ADP and Pi.

  • Chemiosmosis converts a H^+ gradient into ATP, which is critical for fueling muscle contractions during extended periods of exercise.

  • Uses potential energy of H^+ to induce backflow through ATP synthase.

  • ATP synthase is a molecular machine converting released energy into ATP.

Complexes and Supercomplexes
  • Electron transport complexes are not simply arranged in series

  • They form supercomplexes where individual complexes associate with each other.

Measuring Changes in Carbohydrate Metabolism

Respiratory Quotient (RQ) and Respiratory Exchange Ratio (RER)

  • RER of 0.7 indicates burning fat; RER of 1.0 indicates burning 100% CHO.

  • CHO RER = 1.0 because:

    • 6 molecules of O2 are used in glucose oxidation producing 6 molecules of CO2.

    • C6H{12}O6 + 6 O2 6 CO2 + 6 H2O + 38 ATP

  • Fat is oxidized with an RQ/RER of 0.70.

    • 23 molecules of O2 are used for fat oxidation, producing 16 molecules of CO2 (16/23 = RQ = 0.70).

    • C{16}H{32}O2 + 23 O2 \rightarrow 16 CO2 + 16 H2O + 130 ATP

Control of Blood Glucose and Glucose Uptake

Pancreas and Liver Control

  • Alpha-cells: Glucagon (stimulates liver breakdown of glycogen to release glucose into blood).

  • Beta-cells: Insulin (stimulates muscle and fat cells to absorb glucose).

Insulin vs. Contraction-Induced Glucose Uptake

  • Insulin uses a PI3k-dependent mechanism to induce GLUT-4 translocation.

  • Exercise acts independently of PI3k, likely through Ca^{2+} release.

  • Exercise-stimulated glucose uptake is preserved in insulin-resistant muscle.

  • Therefore, good therapy in type II diabetes.

Adaptations to Carbohydrate Metabolism with Training

Substrate Utilization

  • With training, there is a rightward shift of the CHO utilization curve.

  • CHO is spared at higher exercise intensities (both relative and absolute intensities).

  • More use of fats.

Molecular Adaptations

  • Endurance training increases aerobic enzymes.

Molecular Adaptations Examples
  • Swimming training:

    • Significant increase in Citrate Synthase activity (mmol .kg-1. min-1) and Succinate dehydrogenase activity (\mu$$mol/g) with training distance (m/day) and duration (months).

  • Aerobic vs. Anaerobic Training:

    • Significant increase in select aerobic enzymes (Succinate dehydrogenase, Malate dehydrogenase) with Aerobic Training.