Fluids, Electrolytes & Nutrition: Energy Production
Metabolism
Aerobic Respiration
- ATP Generation Through the Use of Oxygen
- Steps:
- Glycolysis
- Converts Glucose to Pyruvate & ATP
- Occurs in Cell Cytoplasm
- Oxidative Decarboxylation
- Pyruvate is Oxidized to Acetyl-CoA & CO2
- Occur in Cell Mitochondria
- Citric Acid (Krebs) Cycle
- Acetyl-CoA is Oxidized to CO2
- Produces NADH & FADH2
- Occur in Cell Mitochondria
- Oxidative Phosphorylation
- Electron Transport Chain – Oxidizes NADH to Establish a Proton Gradient
- Proton Gradient Used to Phosphorylate ADP & Produce ATP
- Occur in Cell Mitochondria
- Electron Transport Chain – Oxidizes NADH to Establish a Proton Gradient
- Glycolysis
- Produces 30-32 ATP Per Glucose Molecule
Cori (Lactic Acid) Cycle
- ATP Generation Without the Use of Oxygen
- Steps:
- Glycolysis
- Same as in Aerobic Respiration
- Converts Glucose to Pyruvate & ATP
- Occurs in Cell Cytoplasm
- Fermentation
- Pyruvate is Converted to Waste Products & Removed from the Cell
- Converted to Lactic Acid in Skeletal Muscle
- Occurs in Cell Cytoplasm
- Pyruvate is Converted to Waste Products & Removed from the Cell
- Gluconeogenesis
- Lactic Acid (From Fermentation in Muscle) is Converted Back to Glucose
- Occurs in the Liver
- Prevents Lactic Acidosis
- Glycolysis
- Produces Muscle ATP Faster than Aerobic Respiration for Short Bursts
- Net Body Consumption of 4 ATP Molecules Per Cycle
- Only Produces 2 ATP Per Glucose Molecule Through Glycolysis
- Consumes 6 ATP Through Gluconeogenesis
- Lactic Acidosis:
- Buildup of Lactic Acid Causing Acidosis
- Cohen-Woods Classification:
- Type A: Caused by Tissue Hypoxia
- Type B: Non-Hypoxic Causes
- B1: From Underlying Disease
- B2: From Medication or Intoxication
- B3: From Inborn Errors of Metabolism
Energy Source After Meals
Immediately After a Meal
- Primary Energy Source: Carbohydrates (Used Rapidly)
- Excess Stored as Fatty Acids or Glycogen
6-24 Hours After Last Meal
- Primary Energy Source: Glycogenolysis
- Glycogen Stores:
- Muscle (2/3 of Stores)
- Only Available Locally
- Liver (1/3 of Stores)
- Available Systemically
- Liver Stores Last 16-36 Hours
- Muscle (2/3 of Stores)
Days After Last Meal
- Glycogen Stores are Depleted
- Primary Energy Source: Breakdown of Muscle & Lipids
- Largest Source: Free Fatty Acids
- Gluconeogenesis
- Occurs Primarily in Liver Early & Kidney Later
- Primary Substrate: Alanine in Liver
- Glutamine in Kidney Once Hepatic Alanine Exhausted
Starvation (6-8 Days After Last Meal)
- Primary Energy Source: Gluconeogenesis
- From Muscle Protein Breakdown to Amino Acids
- Primary Substrate: Ketone Bodies
Stress vs Starvation
Stress | Starvation | |
Primary Energy Source | Fat & Protein (Mixed) | Fat |
Basal Metabolic Rate | Increased | Decreased |
Inflammatory Mediators | Increased | Decreased |
Ketone Production | Unchanged | Increased |
Gluconeogenesis | Greatly Increased | Increased |
Protein Metabolism & Negative Nitrogen Balance | Greatly Increased | Increased |
Muscle Proteolysis | Greatly Increased | Increased |
Hepatic Protein & Urea Synthesis | Greatly Increased | Increased |
Cell-Specific Energy Sources
Cell-Specific Sources
- Cells Only Able to Use Glucose for Energy:
- Red Blood Cells (RBC)
- White Blood Cells (WBC)
- Adrenal Medulla
- Peripheral Nerves
- Brain Cells Normally Use Glucose but Can Use Ketones if Needed
- Primary Energy Source of Neoplastic Cells: Glutamine
Bowel Energy Sources
- Small Intestine Enterocytes: Glutamine
- Colonocytes: Short-Chain Fatty Acids