Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
45 Cards in this Set
- Front
- Back
Moderate demyelination results in a decreased what?
|
CV
|
|
Moderate demyelination results in an increased what? x2
|
1. Response latency
2. Temporal Dispersion (slowed and inconsistent AP timing) |
|
List the four categories of sensory nerve fibers.
|
Ia & Ib
II III IV |
|
Describe Ia & Ib nerve fibers.
|
Large myelinated sensory fibers
|
|
Describe II nerve fibers
|
Medium myelinated sensory fibers
|
|
Describe III nerve fibers
|
Largest unmyelinated sensory fibers
|
|
Describe IV nerve fibers
|
Smallest unmyelinated sensory fibers
|
|
Which nerve fibers are the slow pain fibers? AKA?
|
Type IV nerve fibers
AKA - C fibers |
|
Types of motor axon nerve fibers.
|
Alpha - large
Gamma - small |
|
In a mixed nerve with multiple fibers, which nerve fibers tend to be demyelinated first?
|
Largest, and fastest
|
|
Increased current threshold caused by demyelination is due to what?
|
Exposed internodal ion channels ("leakiness").
|
|
Input resistance (Rin) is affected how by demyelination?
|
Will decrease due to demyelination along with membrane resistance
|
|
Ephaptic transmission causes what?
|
Parasthesia
|
|
Ephaptic transmission is caused by what?
|
Electrical cross talk
|
|
What is electrical cross talk.
|
If nerve becomes demyelinated, another local circuit axon can transfer to that demyelinated nerve.
|
|
Severe demyelination can cause what?
|
Conduction block.
|
|
Only extensive damage causes conduction block. Why?
|
Sodium current at node of ranvier is so large.
|
|
T/F - Mammalian myelinated axons have delayed rectifier channels.
|
False
|
|
What do myelinated mammalian axons use instead of DRC?
|
Passive potassium channels.
|
|
What is responsible for repolarization?
|
Passive potassium channels
|
|
What allows for higher AP frequencies?
|
Shorter refractory period
|
|
Where is the only place to record extracellular AP currents?
|
Nodes of ranvier
|
|
For single AP, about how many nodes are active at different stages of AP cycle?
|
30
|
|
A new node becomes active every how many seconds?
|
15 microseconds
|
|
Saltatory conduction occurs in what type of axons?
|
myelinated axons
|
|
Demyelination of a few nodes typically does not cause conduction block because why? x2
|
1. Saltatory conduction
2. Safety factor |
|
What is the typical safety factor for mammalian AP?
|
5
|
|
Demyelination of where occurs in MS?
|
CNS
|
|
Demyelination of where occurs in Guillain Barre syndrome?
|
PNS
|
|
Neurophysiological symptoms of demyelination worsen when?
|
At increased body temperature
|
|
What are neurophysiological symptoms of demyelination?
|
1. Slowed CV
2. Temporal dispersion 3. Parasthesia 4. Sometimes (if bad) conduction block |
|
What is the critical hallmark of MS?
|
Multiple lesions separated by time and space
|
|
Chronic demyelination leads to what?
|
Axonal degeneration
|
|
What is the reason for progressive irreversible disability?
|
Axonal degeneration at new lesions.
|
|
Compare remyelination by schwann cells vs. remyelination in MS
|
Lasts longer
|
|
In Guillain Barre Syndrome, axonal degeneration is often associated with what organism?
|
Campylobacter jejuni
|
|
Incidence of Charcot-Marie-tooth disease?
|
1:2,500
|
|
What is the etiology of type 1b Charcot-Marie-tooth disease?
|
Point mutation in PMP (Peripheral Myelin Protein) gene
|
|
What is the etiology of type 1a Charcot-Marie-tooth disease?
|
Gene duplication causing over-expression of PMP22
|
|
What is the inheritance pattern of 1a Charcot-Marie-tooth disease?
|
AD
|
|
What is the etiology of X-linked Charcot-Marie-tooth disease?
|
Defect in gap junction protein of myelin lamellae (connexin32)
|
|
What are symptoms of Charcot-Marie-tooth disease?
|
1. Decreased CV
2. Cyclical demyelination/myelination 3. Impaired gait with deformed contracted foot. |
|
What is the long term hallmark symptom for Charcot-Marie-tooth disease?
|
Impaired gait with deformed contracted foot.
|
|
Define leukodystrophy.
|
Genetic diseases of CNS myelin
|
|
What is the etiology of Pelizaeus-Merzbacher disease?
|
Defect in proteolipid protein (PLP)
|