Metabolism and Energy Production

Nutrients

  • Definition: Essential substances needed for cells to generate energy in the form of ATP.

  • Functions: Support cell growth, division, contraction, secretion, etc.

Metabolism

  • Definition: All chemical reactions in the body.

  • Divisions:

    • Catabolism: Breakdown of organic molecules.

    • Anabolism: Synthesis of new organic molecules.

Interstitial Fluid and Cell Functions

  • Key Functions:

    • Maintenance and repairs.

    • Growth.

    • Secretion.

    • Stored nutrient reserves.

Nutrient Pool

  • Components: Organic molecules including amino acids, lipids, and simple sugars.

  • Anabolic Activities: Require amino acids, some lipids, and few carbohydrates.

  • Catabolic Reactions:

    • Break down carbohydrates first, followed by lipids, and rarely amino acids.

Types of Metabolism

  • Anaerobic Catabolism: Limited to small ATP production under unusual conditions.

  • Aerobic Metabolism (Cellular Respiration): Occurs in mitochondria and accounts for 40% of the energy produced.

Energy Expenses in ATP Usage

  • Other ATP Expenses: Includes locomotion, contraction, intracellular transport, cytokinesis, endocytosis, and exocytosis.

Overview of Carbohydrate Metabolism

  • Cellular Respiration Equation: C6H12O6+6O2ightarrow6CO2+6H2O+36ATPC_6H_{12}O_6 + 6O_2 ightarrow 6CO_2 + 6H_2O + 36 ATP

    • Aerobic: Requires oxygen and occurs in mitochondria.

    • Anaerobic: Does not require oxygen.

Redox Reactions

  • Definitions:

    • Oxidation: Remove electrons, making the particle more positive (e.g., Na+Na^+).

    • Reduction: Add electrons, making the particle less positive (e.g., ClCl^-).

  • Redox Reactions: Electron transfer between materials.

Cellular Respiration Overview

  • Processes:

    • Glucose is oxidized.

    • Oxygen is reduced.

  • Detailed Equation:
    C6H12O6+6O2<br>ightarrow6CO2+6H2O+36ATP+extheatC_6H_{12}O_6 + 6 O_2 <br>ightarrow 6 CO_2 + 6 H_2O + 36 ATP + ext{heat}

Glycolysis

  • Definition: Breakdown of glucose into two molecules of pyruvate (CH3COCOOHCH_3—CO—COOH).

  • Process:

    • Enters mitochondria to harvest high-energy electrons.

    • NAD+ conversion: NAD++2e<br>ightarrowNADHNAD^+ + 2 e^- <br>ightarrow NADH.

    • Initial ATP investment: 2 ATP yields 4 ATP for a net gain of 2 ATP.

Steps in Glycolysis

  1. Glucose is phosphorylated twice (costs 2 ATP).

  2. The six-carbon chain splits into two three-carbon molecules.

  3. Harvest energy and produce 2 ATP and NADH.

Mitochondrial Structure

  • Composition:

    • Surrounded by two membranes:

    • Outer Membrane: Permeable to pyruvate.

    • Inner Membrane: Uses carrier proteins to transport pyruvate into the mitochondrial matrix.

  • Key Cycles: Citric Acid Cycle and Oxidative Phosphorylation.

The Citric Acid Cycle (Krebs Cycle)

  • Pyruvate Conversion: To acetyl-CoA (2 carbon sugar).

  • Energy Harvesting: Produces 2 ATP from GTP, 8 NADH, 2 FADH2, and releases six CO2.

  • Electron Transport System: NADH and FADH2 feed into it.

Electrons Carriers in Cellular Respiration

  • Types:

    • NAD+ (Nicotinamide adenine dinucleotide) + 2 electrons = NADHNADH.

    • FAD (Flavin adenine dinucleotide) + 2 electrons = FADH2FADH_2.

Oxidative Phosphorylation

  • Electron Transport System (ETS):

    • Embedded in the inner mitochondrial membrane.

    • Provides 95% of all cellular energy.

    • Series of protein-pigment cytochromes facilitate stepwise electron energy release.

Electron Transport and ATP Formation

  • Key Process: Protons from NADH and FADH2 are split, leading to a proton gradient and ATP synthesis through ATP synthase, a process termed "chemiosmosis".

Summary of Energy Yield from Carbohydrates

  • Energy Outputs:

    • Glycolysis: 2 ATP

    • Citric Acid Cycle: 2 ATP

    • Electron Transport System: 32 ATP

  • Total ATP from one glucose molecule: 36 ATP (primarily produced in mitochondria).

Mitochondrial Diseases

  • Symptoms may include:

    • Poor growth

    • Developmental delay

    • Muscle weakness

    • Gastrointestinal disorders

    • Neurological issues (e.g., seizures)

    • Increased infection susceptibility.

Gluconeogenesis

  • Definition: The synthesis of "new" glucose from non-carbohydrate sources.

  • Intermediates Used: Lactate, glycerol, and specific amino acids with different enzymes than those for glycolysis.

Alternate Catabolic Pathways

  • Scenarios without Oxygen:

    • Fermentation occurs; otherwise cells will die.

  • Without Glucose: Cells can utilize lipids and proteins for energy, while nucleic acids are rarely used.

Lipid Catabolism (Fat Metabolism)

  • Definition: Lipolysis, the hydrolysis of triglycerides into components like glycerol and fatty acids.

  • Energy Yield: 18-carbon fatty acid can yield 144 ATP via beta-oxidation.

Beta-Oxidation Process

  • Occurs in mitochondria, breaking down fatty acids in two-carbon units.

  • Produces FADH2, NADH, and Acetyl-CoA.

Diabetes Type I Warning Signs

  • Presence of ketones in blood/breath due to insulin deficiency, high blood sugar levels, with blood sugars often exceeding 250 mg/dl.

  • Risk of diabetic ketoacidosis and pH imbalance.

Lipids and Energy Production

  • Storage: Lipids stored in fat droplets; present a challenge for water-soluble enzymes.

  • Energy Access:

    • Skeletal muscle fibers primarily access glucose for quick energy and fatty acids during rest.

Lipid Synthesis (Lipogenesis)

  • Sources: Glycerol derived from glycolysis products and acetyl-CoA used to build steroids and fatty acids.

  • Essential Fatty Acids: Must be obtained from diet, including omega-3 and omega-6 fatty acids.

Lipoproteins and Lipid Transport

  • Composition: Contain triglycerides, cholesterol, wrapped in phospholipids and proteins.

  • Types:

    • Chylomicrons: Largest, transport fat from intestines to body.

    • Low-Density Lipoproteins (LDLs): Carry cholesterol from liver to tissues (often termed as “bad cholesterol”).

    • High-Density Lipoproteins (HDLs): Transport cholesterol from tissues back to liver (termed as “good cholesterol”).

Cholesterol Transport Mechanism

  • Hyperlipidemia Consequences: Cholesterol re-entering bloodstream from peripheral tissues to be transported back to the liver by HDLs, sorted for reuse or excretion with bile.

Questions

  • Open floor for questions before proceeding to discuss amino acids.