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 Excitability
 Conductivity
 Unfatigability
 Refractive period
 All or none response
 Summation
 Accommodation
 Excitability:
› nerve fibres are highly excitable tissue
› respond to various stimuli
› Capable of generating electrical impulse
 Conductivity:
› action potential is generated in the nerve fibre,
which is propagated along its entire length to the
axon terminal.
 Refractive period:
 during action potential the excitability of a
nerve become reduced
 i.e a new impulse cannot be generated
during a AP
 Types:
› a. Absolute refractory period (ARP)
› b. Relative refractory period( RRP)
 Note :- once initiated moving impulse wont
depolarize the area behind it
 Unfatiguability :
› Nerve fibres can not be fatigued even when they
are stimulated continuously.
 All or none response:
› Either all of the action potential is seen or none
at all
› If a stimulus of threshold strength is applied AP
will be generated
› Further increase in strength of stimulus or
duration has no effect on amplitude of AP
› But can affect frequency
 Summation:
› Application of a sub threshold stimulus does not
evoke an action potential. However if sub
threshold stimuli are applied in rapid succession
they are added and they produce an action
potential.
 Accommodation:
› Application of continuous stimuli may
decrease the excitability of nerve fibre.

Fiber
Type
Function
Fiber
Diameter
(μm)
Conduction
Velocity
(m/s)
Aα Proprioception; somatic
motor
12-20 70-120
Aβ Touch, pressure 5-12 30-70
Aγ Motor to muscle
spindles
3-6 15-30
Aδ Pain, cold, touch 2-5 12-30
Fiber Type
Function
Fiber
Diameter
(μm)
Conduction
Velocity
(m/s)
B Preganglionic
autonomic
<3 3-15
Dorsal root
(C)
Pain, temperature,
some Mechano-
reception, reflex
responses
0.4-1.2 0.5-2
Sympathetic Postganglionic 0.3-1.3 0.7-2.3
 Pressure – A> B > C
 Hypoxia – B > A > C
 Local Anesthesia – C > B > A
 It’s a protective insulator covering of the axon
 Formed by schwann cells
 Double layer membrane of a single schwann cell
wraps itself several times around axon
 1 mm in length , 8 -10 micrometer in thickness
 Layers stick to each other due to protein p0
 Schwann cell nucleus lies in the outermost layer
 Orthodromic
 Antidromic
 Axoplasmic Transport
› Fast antegrade – 400mm/day (kinesin)
› Fast retrograde – 200mm/day (dynein)
› Slow antegrade
 Distal fragment degenerates fully
 Proximal frag. Until previous node of Ranvier
 Swollen myelin sheath – (appear as beads )
 Schwan cells does not die
 Debris taken by macrophages
 Soma swells and become round
 Extrusion of nuclei
 Disintegration of Nissle granules – Chromolysis
 Disappearance of golgi apparatus
 Completed by 3 – 4 weeks
 Soma tries to repair by synthesizing new
protein (axonal reaction)
 Chromatolysis reversible
 Axonal sprouts may form
 Axonal cone (growth 1-4 mm/day)
 Schwan cells myelinate new axon
 Nucleus occupy center , RER , GA reappears
 Denervation hypersensitivity seen in target
organ
Properties of nerve fibre

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Properties of nerve fibre

  • 1.
  • 2.  Excitability  Conductivity  Unfatigability  Refractive period  All or none response  Summation  Accommodation
  • 3.  Excitability: › nerve fibres are highly excitable tissue › respond to various stimuli › Capable of generating electrical impulse  Conductivity: › action potential is generated in the nerve fibre, which is propagated along its entire length to the axon terminal.
  • 4.  Refractive period:  during action potential the excitability of a nerve become reduced  i.e a new impulse cannot be generated during a AP  Types: › a. Absolute refractory period (ARP) › b. Relative refractory period( RRP)  Note :- once initiated moving impulse wont depolarize the area behind it
  • 5.
  • 6.
  • 7.  Unfatiguability : › Nerve fibres can not be fatigued even when they are stimulated continuously.  All or none response: › Either all of the action potential is seen or none at all › If a stimulus of threshold strength is applied AP will be generated › Further increase in strength of stimulus or duration has no effect on amplitude of AP › But can affect frequency
  • 8.  Summation: › Application of a sub threshold stimulus does not evoke an action potential. However if sub threshold stimuli are applied in rapid succession they are added and they produce an action potential.  Accommodation: › Application of continuous stimuli may decrease the excitability of nerve fibre.
  • 9.  Fiber Type Function Fiber Diameter (μm) Conduction Velocity (m/s) Aα Proprioception; somatic motor 12-20 70-120 Aβ Touch, pressure 5-12 30-70 Aγ Motor to muscle spindles 3-6 15-30 Aδ Pain, cold, touch 2-5 12-30
  • 10. Fiber Type Function Fiber Diameter (μm) Conduction Velocity (m/s) B Preganglionic autonomic <3 3-15 Dorsal root (C) Pain, temperature, some Mechano- reception, reflex responses 0.4-1.2 0.5-2 Sympathetic Postganglionic 0.3-1.3 0.7-2.3
  • 11.  Pressure – A> B > C  Hypoxia – B > A > C  Local Anesthesia – C > B > A
  • 12.  It’s a protective insulator covering of the axon  Formed by schwann cells  Double layer membrane of a single schwann cell wraps itself several times around axon  1 mm in length , 8 -10 micrometer in thickness  Layers stick to each other due to protein p0  Schwann cell nucleus lies in the outermost layer
  • 13.
  • 14.
  • 15.  Orthodromic  Antidromic  Axoplasmic Transport › Fast antegrade – 400mm/day (kinesin) › Fast retrograde – 200mm/day (dynein) › Slow antegrade
  • 16.  Distal fragment degenerates fully  Proximal frag. Until previous node of Ranvier  Swollen myelin sheath – (appear as beads )  Schwan cells does not die  Debris taken by macrophages  Soma swells and become round  Extrusion of nuclei  Disintegration of Nissle granules – Chromolysis  Disappearance of golgi apparatus  Completed by 3 – 4 weeks
  • 17.
  • 18.
  • 19.
  • 20.  Soma tries to repair by synthesizing new protein (axonal reaction)  Chromatolysis reversible  Axonal sprouts may form  Axonal cone (growth 1-4 mm/day)  Schwan cells myelinate new axon  Nucleus occupy center , RER , GA reappears  Denervation hypersensitivity seen in target organ