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Action potential
o Action potentials are brief, rapid, large,
propogatory changes in membrane potentials
produced by application of adequate stimulus to
an excitable tissue.
oAction potential = “impulse”
oChanges during AP – Depolarization followed
by repolarization of membrane
stimulator
Recording
electrode
CRO
-80
-60
-40
-20
0
+20
+40
Time ( msecs. )
1 msec
Membrane
potential
(mV)
o Recording of AP in nerve fiber - monophasic
8 - after hyperpolarization
1
-70
1
2
3
Firing
level
4
5
6
7
0
- Stimulus artifact
1
2 - Latent period
- Local potentials
3
4 - Rapid depolarization
5
6 - Rapid repolarization
- After depolarization
7
- Overshoot
+30
8
Time in msec
Events during A.P. –
1) Stimulus artifact – due to leakage of electric
current from stimulating electrode to recording
electrode
2) Latent period – It is isoelectric period. Indicates
the time taken by the impulse to travel from
stim. electrode due to the recording electrode.
Duration varies with the distance between two
electrodes.
3) Local potential – slow depolarization
produced due to opening of Na+ channels
Firing level ( threshold potential ) – membrane
potential at which rapid depolarization begins –
which corresponds to 15 mV of depolarization
from RMP.(-55mV )
4)Rapid depolarization – due opening of fast
voltage gated Na+ channels which causes entry
of Na+
5) Overshoot – due to EqNa+ is + 60mV.
6) Rapid repolarization – due to closure of voltage
gated Na+ channels and opening of slow
voltage gated K+ channels which increases K+
exit & stops Na+ entry.
Afterpotentials –
7) Afterdepolarization – reduced rate of
repolarization due to accumulation of K+ on the
outer side of membrane.
8) Afterhyperpolarization – due to incomplete
closure of K+ channel causing excess efflux of K+.
Membrane potential comes to resting level by
Na+-K+ pump.
At firing level – rapid opening of activation gates of
voltage gated Na-channels.
Ionic basis of A.P.-
I. Local potentials – partial opening of Na+
channels influx of Na+ along the electrochemical
gradient causing slow depolarization
II. Rapid depolarization – influx of Na+ causes
depolarization which further increases opening of
Na channels (positive feedback mechanism)
IV.Rapid repolarization –increase in K+ efflux
along electrochemical gradient.
Peak at +30mV – Na+ entry stops because of
closure (of inactivation gates of ) Na+ channels and
opening of voltage gated K+ - channels
III.Overshoot – membrane potential becomes
+ve because Eq Na+ is + 60mV
Vb )After hyperpolarization – K-channels remain
open for longer period causing excess efflux of K+
resulting in hyperpolarization
Va ) After depolarization –slow repolarization due
to reduced rate of efflux of K+ caused by
accumulation of +ve charge on outer side, RMP is
reached
V. After potential -
VI. Hyperpolarization is corrected by Na+-K+ pump
With each AP very small difference in conc.
of Na+ & K+ in ICF & ECF.
Types of AP –
1 Spike potential- in nerve and skeletal muscle
2 Plateau potential – in cardiac muscle
3 Slow potential – in smooth muscle
Role of Ca++ in A.P. –
Ca++ is a membrane stabilizing factor .
↓Ca++ conc. → early opening of voltage
gated Na+ channels → ↑excitability

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action_potential.ppt

  • 1. Action potential o Action potentials are brief, rapid, large, propogatory changes in membrane potentials produced by application of adequate stimulus to an excitable tissue. oAction potential = “impulse” oChanges during AP – Depolarization followed by repolarization of membrane
  • 2. stimulator Recording electrode CRO -80 -60 -40 -20 0 +20 +40 Time ( msecs. ) 1 msec Membrane potential (mV) o Recording of AP in nerve fiber - monophasic
  • 3. 8 - after hyperpolarization 1 -70 1 2 3 Firing level 4 5 6 7 0 - Stimulus artifact 1 2 - Latent period - Local potentials 3 4 - Rapid depolarization 5 6 - Rapid repolarization - After depolarization 7 - Overshoot +30 8 Time in msec
  • 4. Events during A.P. – 1) Stimulus artifact – due to leakage of electric current from stimulating electrode to recording electrode 2) Latent period – It is isoelectric period. Indicates the time taken by the impulse to travel from stim. electrode due to the recording electrode. Duration varies with the distance between two electrodes.
  • 5. 3) Local potential – slow depolarization produced due to opening of Na+ channels Firing level ( threshold potential ) – membrane potential at which rapid depolarization begins – which corresponds to 15 mV of depolarization from RMP.(-55mV )
  • 6. 4)Rapid depolarization – due opening of fast voltage gated Na+ channels which causes entry of Na+ 5) Overshoot – due to EqNa+ is + 60mV. 6) Rapid repolarization – due to closure of voltage gated Na+ channels and opening of slow voltage gated K+ channels which increases K+ exit & stops Na+ entry.
  • 7. Afterpotentials – 7) Afterdepolarization – reduced rate of repolarization due to accumulation of K+ on the outer side of membrane. 8) Afterhyperpolarization – due to incomplete closure of K+ channel causing excess efflux of K+. Membrane potential comes to resting level by Na+-K+ pump.
  • 8. At firing level – rapid opening of activation gates of voltage gated Na-channels. Ionic basis of A.P.- I. Local potentials – partial opening of Na+ channels influx of Na+ along the electrochemical gradient causing slow depolarization II. Rapid depolarization – influx of Na+ causes depolarization which further increases opening of Na channels (positive feedback mechanism)
  • 9. IV.Rapid repolarization –increase in K+ efflux along electrochemical gradient. Peak at +30mV – Na+ entry stops because of closure (of inactivation gates of ) Na+ channels and opening of voltage gated K+ - channels III.Overshoot – membrane potential becomes +ve because Eq Na+ is + 60mV
  • 10. Vb )After hyperpolarization – K-channels remain open for longer period causing excess efflux of K+ resulting in hyperpolarization Va ) After depolarization –slow repolarization due to reduced rate of efflux of K+ caused by accumulation of +ve charge on outer side, RMP is reached V. After potential - VI. Hyperpolarization is corrected by Na+-K+ pump
  • 11. With each AP very small difference in conc. of Na+ & K+ in ICF & ECF. Types of AP – 1 Spike potential- in nerve and skeletal muscle 2 Plateau potential – in cardiac muscle 3 Slow potential – in smooth muscle
  • 12. Role of Ca++ in A.P. – Ca++ is a membrane stabilizing factor . ↓Ca++ conc. → early opening of voltage gated Na+ channels → ↑excitability