4A. Action Potentials Flashcards

1
Q

Graded Potential–Spread by ____ current flow

Graded potentials die over ___ distances

A

Passive

short

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2
Q

Examples of graded potentials

A
  1. Postsynaptic potentials
  2. Receptor potentials
  3. End-plate potentials
  4. Pacemaker potentials
  5. Slow-wave potentials
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3
Q

Action potentials do not decrease in strength as they ____ from their site of ____ throughout the remainder of the cell membrane.

As long as that region of the cell membrane the AP is traversing contains ____ Na+ or ___channels which can be activated (that is they are not in the gate shut inactivated state)

A
  • travel
  • initiation
  • voltage-gated
  • Ca++
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4
Q

When the membrane reaches threshold potential:

  • Voltage gated Na+ channels in _____ undergo conformational changes.
  • Flow of Na+ ions into the ICF reverses the membrane potential from -70mV to ___
  • Flow of K+ ions into the ECF restores the membrane potential to the ___ state
A
  • membrane
  • +30mV
  • resting -70mV
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5
Q

Action Potentials

•Additional characteristics
–Na+ channels open during depolarization by ____.
–When the Na channels become inactive, the channels for open.

** This repolarizes the membrane.**

–the action potential develops at ___in the plasma membrane, it regenerates an identical action potential at the next ___in the membrane.

–So it travels along the plasma membrane undiminished.

A
    • feedback
  • K+
  • one point
  • point
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6
Q

Action Potentials: Ion Permeability Changes and Fluxes

Name this step.

A
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7
Q

Action Potentials: Ion Permeability Changes and Fluxes

Name this step.

A
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8
Q

Action Potentials: Ion Permeability Changes and Fluxes

Name this step.

A
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9
Q

Action Potentials: Ion Permeability Changes and Fluxes

Name this step.

A
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10
Q

Steps to an Action Potential

When membrane reaches threshold potential:

  • 1.Initiation: Voltage-gated SODIUM (OR CALCIUM) channels in the membrane undergo conformational changes (S4 segment) and the channel rapidly OPENS
  • 2.Upstroke: Extrordinarily rapid flow of sodium (or calcium) ions into the ICF rapidly reverses (< msecs) the membrane potential from -70 mV to +30 mV
  • 3.Repolarization I: At the peak of the AP, VG channels rapidly INACTIVATE and
A
  1. Repolarization II: Voltage gated K+ channels also rapidly activate causing strong outward current of K+ that drives Vm negative to toward EK
  2. Afterhyperpolarization: This overshoot of the RMP past normal and more negative is due to the combined permeability of both the Kir (resting RMP) channels and the VGKCs (which repolarize after APs)
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11
Q
A
  • VGICs provide the selective permeability for Na/K/Ca which underlie the different types of APs in excitable tissues
  • Multiple types of VGICs exist for Na+, K+ and Ca++
  • All derived from main ancestor and share basic structure
  • VG Na channels – simplest
  • VG Ca channels more diverse
  • VG K channels REALLY diverse
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12
Q
A

Na+/Ca++ channels:

  • very similar structurally
  • Main alpha subunits shown all have accessory subunits as well
  • 4 cassettes of 6 (S1-6) transmembrane regions which form the main channel
  • Thus, 24 tm regions on a single peptide required
  • P-regions form the actual ion pore
  • S4 region (red) has a net + charge and is the main voltage sensor
  • S4 is displaced when the membrane depolarizes and induces the conformational change required for channel opening
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13
Q
A
  • 4 cassettes of 6 (S1-6) transmembrane regions which form the main channel
  • Thus, 24 tm regions on a single peptide required
  • P-regions form the actual ion pore
  • S4 region (red) has a net + charge and is the main voltage sensor

•S4 is displaced when the membrane depolarizes and induces the conformational change required for channel opening

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14
Q

K+ channels:

  • VERY, VERY diverse
  • Not all are voltage-gated
  • may have 2-8 tm regions
  • These are:
  • IKir – inward-rectifier (not VG)
  • IKdr – delayed-rectifier (VG)
  • A-type – transient (VG)
  • Ca++-activated K+ channels (+/- VG)
  • ATP – inhibited by ATP (VERY sig in diabetes)
A
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15
Q

Voltage-gated sodium channels:

  • all are ____
  • very high degree sequence homology
  • by convention currents are _____ of movement of + CHARGES (eg Na+)
  • by convention downward currents flow ___ the cell
  • these inward currents are depolarizing and underlie initiation of APs
A

voltage-gated

drawn in the direction

INTO

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16
Q

Voltage-gated calcium channels:

  • 3 functionally distinct types – __
  • distinct activation and inactivation voltages and kinetics across different types

•3 major types that differ by:

  1. Vm range that activates S4-
    • (gating Vm, as in high or low Vm,
    • HVA, High-Vm Activated or Low VA) and
  2. open time – slow persistent or fast inactivating
A
  • all VG
17
Q

A plethora of potassium channels

A
  • 6/7 TM: numerous diff types of
    • VG (Kdr),
    • non-VG and
    • Ca++-activated K channels
  • 2 TM: Kir – sets resting Vm (RMP)
  • 2 TM: K(ATP) – site of oral hypoglycemic agents
18
Q

Ion Channel Differentiation
Electrical interactions between ions and water create a hydrated radius around the ion

  • Potassium is a diffuse point source (large radius, delocalized charge) and has less hydrated water, so it has smaller hydration radius that sodium (even though K+ is larger)
  • Sodium is a conc point sources with more hydrated water, leading to a larger hydration radius than potassium
A

This radius can then be filtered

  • Potassium channel does not strip hydration, so it accepts the smaller hydrated potassium and blocks the larger hydrated sodium
  • Sodium channel does strip hydration, so it accepts the smaller sodium ion and blocks the larger potassium ion
19
Q
A