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."
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.
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.
Step 1: Glycolysis
Step 2: The Link Reaction
Step 3: The Krebs Cycle
Step 4: The Electron Transport Chain (ETC)
Breakdown of glucose to two molecules of pyruvate.
Occurs in the cytoplasm.
Breakdown of pyruvate to Acetyl CoA.
Pyruvate is transported into the mitochondria.
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.
3 CO_2
4 NADH + H^+
1 FADH_2
1 ATP
6 CO_2
8 NADH + H^+
2 FADH_2
2 ATP
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.
Electron transport
Chemiosmosis
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.
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.
Electron transport complexes are not simply arranged in series
They form supercomplexes where individual complexes associate with each other.
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
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 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.
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.
Endurance training increases aerobic enzymes.
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.