JG

Nutrition and Metabolism Notes

Overview of Metabolism

  • Metabolism: All chemical reactions in an organism.
    • Produce ATP.
    • Essential cellular functions (repair, growth, secretion, etc.).
  • Catabolism: Breakdown of large molecules, releases energy (ATP).
  • Anabolism: Synthesis of new molecules, requires energy.

Carbohydrate Metabolism

  • Carbohydrates stored as glycogen.
  • Breakdown steps: glycolysis, TCA cycle, electron transport system.
  • Cellular respiration (overall reaction):
    • Glucose + oxygen \rightarrow carbon dioxide + water + energy (ATP)
    • Net gain: 36-38 ATP molecules per glucose molecule.
  • Glycolysis:
    • In cytoplasm, anaerobic.
    • Glucose (6-carbon) → 2 pyruvate (3-carbon).
    • Net yield: 2 ATP.
  • Preparatory Reaction:
    • Pyruvic acid converted to acetyl CoA.
  • TCA Cycle (Krebs cycle, citric acid cycle):
    • In mitochondria, aerobic.
    • Cyclic.
    • Products: carbon dioxide, high-energy electrons, 2 ATP.
  • Electron Transport Chain:
    • In mitochondria, aerobic.
    • Electrons transferred, energy released to make ATP.
    • Final electron acceptor: oxygen.
    • Yields 32-34 ATP.
  • Gluconeogenesis:
    • Synthesis of glucose from non-carbohydrate sources (e.g., amino acids).
    • Important for brain and RBC function during low glucose.

Lipid Metabolism

  • Triglycerides are the most abundant form used for energy.
  • Lipid Catabolism:
    • Fatty acids removed from glycerol.
    • Glycerol converted to pyruvic acid.
    • Fatty acids generate acetyl CoA.
    • Yield more ATP/gram than carbohydrates but are slower to generate energy.
  • Lipid Synthesis:
    • Excess energy stored as lipids.
  • Lipid Transport:
    • Lipoproteins (chylomicrons, VLDL, LDL, HDL) transport lipids in blood.
    • LDL: "Bad cholesterol," delivers cholesterol to tissues.
    • HDL: "Good cholesterol," transports cholesterol to liver.

Protein Metabolism

  • Proteins broken down into amino acids.
  • Amino Acid Catabolism:
    • Deamination: Removal of amino group (-NH2).
    • Ammonia (NH3) converted to urea by the liver.
  • Protein Synthesis:
    • Essential amino acids must be obtained from diet.
    • DNA dictates protein synthesis.

Metabolic Interactions

  • Liver: Focal point for metabolic control, glycogen storage.
  • Skeletal Muscle: Glycogen storage for muscle use.
  • Adipose Tissue: Triglyceride storage.
  • Neural Tissue: Requires glucose.
  • Peripheral Tissues: Use glucose or fats.

Diet and Nutrition

  • Nutrition: Absorption of nutrients.
  • Balanced Diet: Contains necessary nutrients.
  • Malnutrition: Undernutrition or overnutrition.
  • Complete Proteins: Supply all essential amino acids.
  • Incomplete Proteins: Deficient in essential amino acids.
  • Nitrogen Balance:
    • Positive: Absorption > excretion.
    • Negative: Excretion > absorption.
  • Minerals: Fluid balance, metabolic processes, enzyme cofactors.
  • Vitamins:
    • Fat-soluble (A, D, E, K): Stored in fatty tissue.
    • Water-soluble (B, C): Not generally stored.

Energy Gains and Losses

  • Metabolic Rate: Speed of chemical reactions.
  • Basal Metabolic Rate (BMR): Minimum resting energy expenditure.
  • Calorie (kilocalorie): Measure of energy (raises 1 kg of water 1°C).
  • Energy Content:
    • Carbohydrate: 4 kcal/gm
    • Protein: 4 kcal/gm
    • Lipid: 9 kcal/gm
    • Alcohol: 7 kcal/gm (empty calories).

Thermoregulation

  • Heat Transfer:
    • Radiation, conduction, convection, evaporation.
    • Insensible water loss, sensible perspiration.
  • Heat Gain/Loss:
    • Increase loss: Peripheral vasodilation, perspiration, increased respiration.
    • Promote gain: Vasoconstriction, shivering/non-shivering thermogenesis.
  • Variations:
    • Acclimatization, infants (undeveloped mechanisms), adults (adipose insulation).
  • Fever:
    • Pyrexia: Elevated body temperature (>37.2° C).