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Mindmap

Action Potentials (L6-12)

J J Englisch

Action Potentials (L6-12)

Inhalt der Mindmap

Action Potentials (L6-12)

  1. Resting Membrane Potential

    • Nernst Equation for equilibrium potential
      • Ek = -90mV
        • Means you need to apply -90mV to the cell to keep K from following concentration gradient out
      • ENa = +60mV
      • ECl = -70mV
    • Goldman Equation for RMP combines all EP
      • Typically -70mV
        • So K diffuses out, Na diffuses in, no net Cl diffusion
  2. Action Potential

    • @ threshold -55mV
      • Na+ voltage gated channel opens, depolarizing membrane to +45mV
        • K+ voltage gated channel opens (0.5ms delay), repolarizing membrane to -70mV
          • Hyperpolarizes below -70 as it reequilibriates
        • positive feedback loop
        • Inactivation gate closes, enters refractory period
        • Tetrodoxin blocks Na+ VG channel
          • Reaches threshold but no depolarization
        • Greyanotoxin blocks Na+ inactivation gate
          • Resists repolarization
        • Tetraethylammonium (TEA) & Dendrotoxin inhibits K+ VG channel preventing repolarization
        • Local anaesthetics act on the Na+ activation gate
      • Cell maintains homeostasis up to -55mV
        • Na/K pump
        • K leaks out of cell
        • Cl leaks into cell
        • Depolarizing subthreshold = EPSP
          • Hyperpolarizing subthreshold = IPSP
    • Neurons 1-2ms, Heart 300ms
  3. AP Propagation

    • Local + charge inside axon is attracted to proximal - charge
      • Initially can move any direction but once directionality is established refractory period keeps it moving forward
    • Myelin prevents ion leakage, speeding up AP
      • AP channels at Nodes of Ranvier
        • Thicker axons = faster AP propagation
      • MS demyelinates axons
  4. Skeletal Muscle

    • Neuromuscular Junction
      • AP in alpha-motor neuron
        • Depolarization of neuron terminal
          • Voltage-gated Ca channels open, Ca enters terminal
            • Acetylcholine (Ach) vesicles in terminal fuse to membrane, releasing Ach
              • Ach diffuses to muscle folded endplates
                • 2 Ach bind to Ach-Nicotinic (n1) receptors, opening channel for K and Na to pass through
                  • Muscle membrane depolarizes, opening VG channels
                    • AP propagates through muscle from endplate
                      • Acetylcholinesterase breaks down Ach, closing channels
                      • AP spreads over sarcolemma and down T-tubules
                        • DHP receptor on T-tubule changes conformation
                          • Ryanodine receptor/Ca release channel on SR opens, Ca diffuses to thin filaments (fast)
                            • Ca binds to troponin C, pulls tropomyosin off actin's myosin binding sites and myosin binds to actin forming crossbridges
                              • Myosin head power stroke
                                • Sarcomere shortens
                                  • Ca pumped back into SR by Ca-ATPase (slow)
                                    • Tropomyosin covers Actin's myosin sites again
                                      • Muscle relaxes (slow)
                                • Actin
                                  • Actin
                                    • Actin + Myosin + ADP + Pi
                                • Myosin + ATP
                                  • Myosin + ADP + Pi
                                    • Actin + Myosin + ADP + Pi
                                      • Actin + Myosin
                                  • 1. ATP Hydrolyzed. Rate limiting step
                                    • 2. AP on muscle cell releases Ca to expose myosin binding site on Actin
                                      • 3. Crossbridge formation. Pi ejected, triggering power stroke. ADP released after power stroke
                                        • 4. Crossbridge remains until new ATP binds to Myosin, releasing actin
                                          • Continues until ATP runs out (Rigor mortis) or Ca is gone (pumped back into SR)
      • 1 AP in neuron = 1 AP in muscle
      • Botulin blocks release of Ach, leads to muscular paralysis
      • Nerve gas blocks acetylcholinesterase, keeping channels open and muscles contracted
      • Myasthenia Gravis autoimmune disease that blocks Ach receptors. Treated with Neostigmine - competes with antibodies for Ach binding sites
    • Fascicles --> Muscle cells --> Myofibrils --> Myofilaments - thin and thick
      • Membrane = Sarcolemma
        • T-tubules = sarcolemma inside the muscle
          • Sarcoplasmic Reticulum (SR) between, Ca reservoir
      • Thick filaments
        • Myosin
          • 2 long chains forming tail, arm, hinge, and 1 head
          • Head contains 2 light protein chains - binding ATP and Actin
        • Titin
          • Holds thick filaments in place, prevents overstretching
        • M-line
          • Down middle of thick filaments, holding them in place
      • Thin filaments
        • G-Actin
          • 2 alpha-helices, myosin binding site
        • Tropomyosin
          • alpha helix that covers myosin binding sites
        • Troponin
          • Holds tropomyosin over myosin binding site. Has a Ca binding site that releases the tropomyosin
        • Z-lines
          • Connects thin filaments keeping them in place
          • Sarcomere is distance between Z-lines
    • Motor units
      • 1 alphamotor neuron and all the muscles it innervates
        • each muscle has 1 neuron, but multiple muscles per neuron
          • Small diameter = small # of muscles
      • More motor units = stronger twitch
        • Varying AP frequency can cause multiple twitches that sum without time for the muscle to relax
          • No relax = complete tetanic contraction ~30 Hz
    • Muscle fiber types
      • Type I - slow-oxidative
        • Marathoners
          • Low myosin ATPase. 100ms contraction
            • High myoglobin (dark)
              • Small motoneurons
                • Recruited first
      • Type IIa - fast-oxidative
      • Type IIb - fast-glycolytic
        • Sprinters
          • High myosin ATPase. 10ms contraction
            • Glycolysis - easily fatigued
              • Low myoglobin (light)
                • Large motoneurons
                  • Recruited last

Bilder und Dateien der Mindmap

  • Action Potentials (L6-12)
  • Action Potentials (L6-12)
  • Action Potentials (L6-12)
  • Action Potentials (L6-12)
  • Action Potentials (L6-12)
  • Action Potentials (L6-12)

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Beschreibung
Mindmap am Action Potentials (L6-12), erstellt von J J am 14/11/2018.
Erstellt von
J J
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