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Topics
1. Introduction 2. Energy and thermodynamics 3. Feeding and digestion 4. Ionic gradient, electrical potential
At resting
K+
Na+
K+
Cl P-
K+ K+ K+ -
Na+ Cl -
For all living cells, there exist an electrical potential across the plasma membrane, with inside negative relative to outside. The formation of such a potential difference is due to the facilitated diffusion of K+ from inside to the outside.
During depolarization
K+
Na+
K+
Na+
+
Cl P-
Cl -
When stimulated, the Na+ channels in the excitable membrane open and Na+ rushes in. Inside become momentarily positive relative to outside.
+55
ENa
Hyperpolarization
-60 -75 K+ + + ++ - - - -
-71
EK
Na+
K+
Na+
Ionic movement (K+) is driven by the chemical potential difference (but slightly opposed by the electric potential difference)
+55
ENa
+52.6
Depolarization
-60 -75
EK
Na+
K+
+ + ++ - - - Na+
K+
Ionic movement (Na+) is driven by both the chemical potential and electric potential differences.
Topics
1. Introduction 2. Energy and thermodynamics 3. Feeding and digestion 4. Ionic gradient, electrical potential
Topics
1. Introduction 2. Energy and thermodynamics 3. Feeding and digestion 4. Ionic gradient, electrical potential
Nerve endings
Receptor cells Elaborated structures Function 1) differential sensitivity 2) transducer and power amplification
light
electrical
sound
Mechanical
electrical
chemical
electrical
The posterior (back) of the frontal lobe consists of the premotor and motor areas. ... The parietal lobes contain the primary sensory cortex which deals with sensation.
Do our receptors measure the absolute intensity of the stimuli ?! (like a thermometer ?! Like a pressure gauge ?!)
No !!!
The Na+ channels in the receptor membrane open proportionally to the intensity of the stimulus. The signal generated is graded. There is no all or none. There is no threshold. There is no refractory period.
How can intensity of stimuli be transmitted along the axon? What is the range of intensity of stimuli that our receptor cells are sensitive to?
Characteristics
Produces relatively high Pk of resting cell
Function
Largely responsible for Vrest
Voltage-gated K+ channel
Activated by depolarization Carries current (K+ effux) but more slowly than Na+ channel; inactivated slowly and not completely if Vm remains depolarized that rapidly repolarizes the membrane to terminate the action potential
When the signal reaches the axon, the Na+ channels there open all at once after the membrane voltage reaches a threshold value.
The amplitude of the action potential generated is always the same, hence described as all or none response. Within one millisecond, the Na+ channels close and enters the refractive period for 1 - 2 milliseconds. K+ channels open up more than normal to bring the voltage back to resting.
The refractive property of the axon membrane ensures an one way traffic of neural signals.
Refractory periods
Summary video
http://www.youtube.com/watch?v=SCasruJT-DU
Watch out for the word diffusion which should be replaced with the word rush (electric or ionic current)
Because of the existence of the threshold phenomenon in the axon membrane, action potential is self - generating. There are 2 types of axon : 1) unmyelinated
2) myelinated
http://www.youtube.com/watch?v=pbg5E9GCNVE
Is there any difference between axon and the electric cable? What are their differences and similarities?
rm re
good axon = rm
re
How to make the transmission of the signal along the axon more efficient?
a. b. Re (resistance of axoplasm) Rm (resistance of membrane)
10 m
myelination
SALTATORY CONDUCTION (appear as though the action potential jumps from node to node which is not true)
Video on Schwann cells and transmission of neural signal along the axon: http://www.youtube.com/watch?v=DJe3_3XsBOg Transmission along an unmyelinated axon http://www.youtube.com/watch?v=pbg5E9GCNVE
http://www.youtube.com/watch?v=DJe3_3XsBOg
Note: the word diffusion should be replaced with electrical current for Na+ movement within the axon
Action potential
http://www.youtube.com/watch?v=HXx9qlJetSU
Action potential
Neural Zones
Figure 4.2
End