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Myelin increases resistance across the cell membrane

 
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Sep23-08, 05:43 PM   #18
 
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Myelin increases resistance across the cell membrane


Quote by DaleSpam View Post
Thanks for the info. They do appear to propagate. In number 5 they do mention varying degrees of demyleination, so I am not sure if it still propagates with complete demyleination, but there is at least some "extra" mylein than is strictly needed.
The reference I cited earlier also measured propagation in demyelinated neurons. Nonetheless, this is why I advised caution in comparing the concept of DEmyelinated to NONmyelinated, because I'm not sure that all else is equal if you remove the myelin, either via pathological or experimental mechanisms.
 
Sep24-08, 04:12 AM   #19
 
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Quote by atyy View Post
Yes, it is. But Prof C Koch is a nice guy, so he won't hit me, although he might punish me by discussing consciousness.
That's fine but there is another problem!
If the capacitance is effectively 50 time less with the wrapping of myelin, you forgot a crucial parameter in your computation: length => area.
if a node is 2.2 pF for 0.5 µm then an internode (1 mm) is (2.2/50)*2000= 88 pF.
Did I said Divergence?
 
Sep24-08, 06:25 AM   #20
 
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Quote by Moonbear View Post
I advised caution in comparing the concept of DEmyelinated to NONmyelinated, because I'm not sure that all else is equal if you remove the myelin, either via pathological or experimental mechanisms.
I agree.
 
Sep24-08, 06:52 AM   #21
 
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Quote by DaleSpam View Post
Thanks for the info. They do appear to propagate. In number 5 they do mention varying degrees of demyleination, so I am not sure if it still propagates with complete demyleination, but there is at least some "extra" mylein than is strictly needed.
I agree.
But what about this?
http://www.physicsforums.com/showpos...8&postcount=19
 
Sep24-08, 08:40 AM   #22
 
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Quote by somasimple View Post
It doesn't really matter as long as you are consistent. If you measure resistance in ohms*cm² and capacitance in farads/cm² then you have the same time constant as if you measure resistance in ohms and capacitance in farads. You just have to be consistent.
 
Sep24-08, 09:26 AM   #23
 
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I have some difficulty with your reply:
A cylindrical resistance is proportional to volume => proportional to length.
http://en.wikipedia.org/wiki/Electrical_resistance
A plane capacitor is proportional to area => proportional to length.
http://en.wikipedia.org/wiki/Capacitor#Capacitance
See computations =>
http://butler.cc.tut.fi/~malmivuo/bem/bembook/21/21.htm
I'm consistent.

Where did you find a unit of ohm*cm²?
 
Sep24-08, 04:16 PM   #24
 
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Quote by somasimple View Post
A cylindrical resistance is proportional to volume
No, resistance is proportional to length/area. Volume is length*area. So, resistance is not proportional to volume.

Quote by somasimple View Post
Where did you find a unit of ohm*cm²?
The "area specific resistance" is in ohm*cm². It is the appropriate "normalized" resistance for current through a membrane. To the best of my knowledge it is used primarily for characterizing fuel cell membranes and neuron membranes.

Note Gm listed in your last reference (http://butler.cc.tut.fi/~malmivuo/bem/bembook/21/21.htm). Conductance/unit area is simply the inverse of area specific resistance and is, IMO, more convenient.
 
Sep24-08, 08:41 PM   #25
 
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Quote by somasimple View Post
That's fine but there is another problem!
If the capacitance is effectively 50 time less with the wrapping of myelin, you forgot a crucial parameter in your computation: length => area.
if a node is 2.2 pF for 0.5 µm then an internode (1 mm) is (2.2/50)*2000= 88 pF.
Did I said Divergence?
Yes, my solution is problematic. I am completely baffled as to how the "standard answer" would be justified quantitatively with all holes in the argument filled in. Koch mentions numerical computations and a "precise" argument called dimensional scaling, which he does not describe. In short, I do not think his text contains the details which would enable one to reach his conclusions firmly.
 
Sep24-08, 11:44 PM   #26
 
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Quote by atyy View Post
Yes, my solution is problematic. I am completely baffled as to how the "standard answer" would be justified quantitatively with all holes in the argument filled in. Koch mentions numerical computations and a "precise" argument called dimensional scaling, which he does not describe. In short, I do not think his text contains the details which would enable one to reach his conclusions firmly.
Atyy,
I bought the book of Koch. I'll see.
I'll ask Ted Carnevale...
Edit:
I'm unable to draw the equivalent circuit since the capacitor must be oriented to the external milieu but connected to the internal one. The resistance must be longitudinal.
It gives a worst solution than before.
 
Sep24-08, 11:52 PM   #27
 
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Quote by DaleSpam View Post
No, resistance is proportional to length/area. Volume is length*area. So, resistance is not proportional to volume.
You're right. So resistance is still proportional to length. So is Capacitance
 
Sep25-08, 12:29 AM   #28
 
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Quote by atyy View Post
Yes, my solution is problematic. I am completely baffled as to how the "standard answer" would be justified quantitatively with all holes in the argument filled in. Koch mentions numerical computations and a "precise" argument called dimensional scaling, which he does not describe. In short, I do not think his text contains the details which would enable one to reach his conclusions firmly.
See table 2
http://www.pubmedcentral.nih.gov/pic...8&blobtype=pdf
http://www.ncbi.nlm.nih.gov/pubmed/1...ubmed_RVDocSum
The time constant is already 10 fold too high.
 
Sep25-08, 06:33 AM   #29
 
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Quote by somasimple View Post
You're right. So resistance is still proportional to length. So is Capacitance
Yes for resistance.

Capacitance is proportional to area/distance. So capacitance is inversely proportional to length if you wish to say it that way. (Although "distance" is a better description of the separation between plates than "length" since "length" connotes the largest dimension of an object and the separation between the plates is the smallest dimension)
 
Sep25-08, 06:50 AM   #30
 
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we are speaking about the area of the plates, here.
the distance between the plates, d was already implied.
two plates of an area of A and separated by a distance d.
C is proportional to A and inversely proportional to d since C =e*A/d

Thus if A is augmented (internode), even if d is augmented, C is augmented
since a node has a length of L1= 0.5 µ => area = 2*pi*R*L1 => 2.2 pf

the same plates where d is *50 => C/50
an internode is 2000 time longer
2*pi*R*L1*2000 => (2.2/50)*2000 = 88 pf
and the computation is simplified since the perimeter augments with each wrap => C>88pf
 
Sep25-08, 07:05 AM   #31
 
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Quote by somasimple View Post
C is proportional to A and inversely proportional to d since C =e*A/d
Yes.

Quote by somasimple View Post
Thus if A is augmented (internode), even if d is augmented, C is augmented
That depends entirely on which is augmented more. If they are both doubled then C is unchanged. If A is doubled and d is tripled then C is reduced to 2/3 of its original value. On the other hand if A is tripled and d is doubled then C is augmented to 3/2 of its original value.
 
Sep25-08, 07:10 AM   #32
 
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DaleSpam,
Give the results in our example.
50 turns of myelin (50*d) and a length that is 2000 time longer (2000*A).
 
Sep25-08, 07:55 AM   #33
 
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Quote by somasimple View Post
50 turns of myelin (50*d) and a length that is 2000 time longer (2000*A).
This is not correct. The presence or absence of the mylein doesn't change the length at all. It may slightly change A by a small increase in the circumference.
 
Sep25-08, 08:54 AM   #34
 
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Quote by DaleSpam View Post
This is not correct. t may slightly change A by a small increase in the circumference.
Thats is not a result at all!
Please give us your result (and computation)?

Quote by DaleSpam View Post
The presence or absence of the mylein doesn't change the length at all.
Where did I said the length was modified?
 
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