Electrical properties of neuron Flashcards

(25 cards)

1
Q

Bases of neuronal excitability

A
  • Regulated Ion movement
    across the membrane
    (ion channels and pumps)
  • Existence of membrane
    ionic gradients as quickly
    releasable energy stores
  • Existence of an electric
    resting potential
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2
Q

Resting Membrane Potential

A
  • Controlled permeability of
    the neuronal membrane
  • maintained by sodium potassium pump
  • resting K+ channels
  • -70mV
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3
Q

Ions involved in neuronal excitablity:

A

Sodium Na+
* Chloride Cl-
* Potassium K+
* Calcium Ca+2
* Magnesium Mg+2
* Bicarbonate HCO3-

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4
Q

Channel ion selectivity classification

A

Channels are selectively permeable to specific ion species
- Cationic (negative charge filter) - excitory
- Anionic (positive charge filter) - inhibitory
- K+ channels
- Na+ channels (smaller than K+)
- Ca+2 channels (synaptic transmission/modulation of AP)
- Cl- channels (

**Selectivity is not absolute (some other ions may transit as well)
**

- Ions are part of hydration spheres, so diff hsapes of water wrap around ion
- channels remove shells of water in diff way

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5
Q

Channels may also be classified according to the
stimulus that induces their opening (gating)….

A
  • changes in transmemb voltage
  • Voltage changes
  • Ligands (small organic mol e.g GABA/glutamate/Ach) (desensitization) - made of 5/4 subunits
  • Pressure
  • pH
  • light
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6
Q

Channel gating (opening and
closing) requires a specific event:

A
  • Voltage change
  • Ligand binding
  • Phosphorylation
  • Sensory stimulus
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7
Q

Channels agonists, antagonists, and allosteric modulators

A
  • Complex molecular
    interactions account for
    competitive OR non
    competitive antagonism
  • from endogenous or
    exogenous ligands
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8
Q

Channel biophysics:
Closure vs. Inactivation

A

Different strategies bring about
the closure of a channel:

* Subunit movement
* Ball and chain

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9
Q

Ion Channel Inactivation

The stimulus for
opening the channel is
still present.

Nonetheless, after a
while the channel
tends to close:

A

Inactivation
(V-gated channels)
or
Desensitization
(ligand-gated channels

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10
Q

Function, Structure, and Pharmacology of the Na-K pump

A
  • Stoichiometric transport of ion
    (different from channels, non
    stoichiometric)
  • Pumps use energy to move some
    ions across the membrane
  • Different from channels, whose
    ion movement is passive)

Energy source:
- ATP (ATPases)
- Gradient of (other) ions
(exchangers)

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11
Q

pumps vs. exchangers

A
  • Exchange pumps differ from ATPases as they exploit a ion gradient to move a different ion against its gradient (no ATP involved)
  • Pumps use ATP
    for creating ion
    gradients across
    the membrane
  • move ions in a stochimetric function = specific number of ions going in and out
  • Exchangers use
    pre-existing ionic
    gradients to
    transport other
    ions against their
    gradient (most
    often they use
    the Na gradient)
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12
Q

Nernst potential

A
  • equilibrium potential
  • reversal potential

Nernst potential is the membrane voltage at which the net entropic force moving permeable ions along their conc gradient is equal + opposite to the electrostatic attraction/repulsion for the other side of the cell memb

-LOOK AT EQUATION

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13
Q

Ohm’s law regulates ion flow

A

In general, Ohm’s law
V = RI
or I = 1 V/R
or I = g x V (where g = 1/R)

**describes the flow of a current I through a conductance (1/r) g
- The opening of a selectively permeable channel induces a passive flow of current in the channels according to a modified Ohm’s law

I = gion (Vm – Eion)
g ion = conductance to that ion
Vm = actual transmembrane voltage
Eion = Nernst potential for that ion

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14
Q

Ionic current through a membrane channel

A

1)The transmembrane (resting) potential is the result of active ion movements (ATP-
driven) and of a high resting permeability to K+ ions
2) Channel opening is consequent to a specific stimulus or set of stimuli (voltage, ligand)
3) The flow of ions through a channel depends on the selective ion permeability of that
channel, and on the actual driving force at a particular time:

**I = gion (Vm – Eion)*
(Vm – Eion) = DRIVING FORCE for a particular permeant ion
g ion = conductance to that ion
Vm = actual transmembrane voltage
Eion = Nernst potential for that ion

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15
Q

Nernst potential for
biologically relevant ions

A
  • Ionic gradients store energy
  • The ionic gradient
  • (Concentration Outside/Concentration Inside)
  • Determine the strength of ionic currents
  • (measure of energy stored)
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16
Q

Steps in the generation of the resting potential

A
  • pumps create an ionic gradient using ATP to force out Na from the cell and to insert K into the cytosol
  • K leakage channels allow K to freely cross the membrane
  • The outflow of K+ creates a negatively charged cell interior
  • This process originates the resting potential
17
Q

Concentration difference
creates membrane potential

A

left = neuronal inside
right = cytosol

INITIAL CONDITION: MORE K INSIDE
* The movement of K ions creates accumulation of + electric charges to the right
* This is equivalent to an excess of negative charge in the inside
* THIS IS THE EXQUIVALENT OF THE MEMBRANE (NEGATIVE) POTENTIAL

18
Q

Goldman Equation for the resting potential

A
  • If K was the only permeable ion at resting, the resting
    potential would be the Nernst potential for K.
  • Since we also have other ions (slightly) permeable at
    resting, the following is the more complete expression for the resting potential
19
Q

Summarize these cards

A
  1. The transmembrane (resting) potential is the result of active
    ion movements (ATP-driven) and of a high resting permeability
    to K+ ions
  2. Channel opening is consequent to a specific stimulus or set of
    stimuli (voltage, ligand, pressure, chemical factors)
  3. The flow of ions through a channel depends on the selective
    ion permeability of that channel, and on the actual driving
    force at a particular time
  4. Once opened, every membrane channel displays peculiar time dependent opening and closure properties (kinetic)
  5. Channels greatly differ in their closure kinetic (de-sensitization)
20
Q

glycosylation

A
  • attatchement of a sugar group attached to proteins/lipids
21
Q

if excess sugar in blood..

A
  • increased glycosolation
  • increased inflammation
  • nerve neuropathy
22
Q

Alpha subunit is where..

23
Q

Ligand gated channels 2 examples

A

Glutumate exciatory
Gaba inhibitory

24
Q

NMDA channel needed for..

A
  • learning pathway
  • high permeability to calcium ions and induces plasticity
  • cell death
  • NMDA associated neurotoxicity
  • R1,R2A,R2B subunits –> A an B have developmeet expression w variability, in adults its R2A and in infant is R2B (difference = diff permebaility to calcium)
25