excitation contraction Flashcards

(33 cards)

1
Q

c. Motor unit

A

one ventral horn nerve cell and all of the muscle fibers

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2
Q

skeletal muscle contracts under nervous controls and is organized in ____ each with it’s own ______

A

i. Organized in long straight parallel fibers. Each fiber has its own synapse

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3
Q

Motor neurons are located in the

A

b. Motor neurons in anterior horns of the spinal cord

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4
Q

smaller muscles have more or less motor units?

A

ii. Smaller muscles (like in our hands) have the most motor units and are best for dexterity
i. If a muscle has smaller but more numerous motor units, its capable of more different types of speeds and strengths of contraction

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5
Q

Synapse on muscle fiber occurs at the _ where nerve and muscle come together

A

Synapse on muscle fiber occurs at the _ where nerve and muscle come together

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6
Q

another name for the post-synaptic membrane

A

b. Post-synaptic membrane, also called the motor end plate

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7
Q

Invagination of muscle membrane, also called the ________

A

c. Invagination of muscle membrane, also called the synaptic gutter

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8
Q

a. Nerve terminals descend into the muscle fiber but lie outside the plasma membrane which is also known as the

A

sarcolema

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9
Q

sub-nueral folds do what for the membrane

A

d. Sub-neural folds increase surface area

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10
Q

NT at motor neuron synapse

A

Ach

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11
Q

Ach is housed in these structures before it’s release in the NMJ

A

vesicles there are approximately 125
and they are released in response to the influx of Ca at the axon terminal which occurs after the transmission of a nerve impulse

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12
Q

Ach Binds Ach receptor on motor end plate/postsynaptic membrane and binds to the receptors

A

a. Binds Ach receptor on motor end plate/postsynaptic membrane and binds to the receptors

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13
Q

Chemically gated channels on the motor end plate require binding of how many NT in order to open the channel

A

c. Chemically gated channels requiring binding of 2 Ach molecules to the external surface in order to open the channel

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14
Q

what happens after AcH binds at the motor end plate

A

when it opens, you have a flux of Na/K down their concentration gradient (so Na is entering the cell and K is leaving)

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15
Q

how does the membrane potential differ in the motor end plate compared to the axon

A

b. EPPs normally increase membrane potential 50-75mV, more than enough to pass threshold to trigger Ap
b. Resting muscle membrane potential (-80-90mV) has a larger “pull” on sodium

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16
Q

where do we get choline in the NMJ

A

breakdown from cholinesterase

Choline is then actively transported back into the presynaptic neuron and can repackaged as Ach again

17
Q

Autoimmune disease in which autoantibodies destroy Ach receptors.

A

VIII. Myasthenia Gravis

18
Q

what type of channels do we have at the NMJ

A

chemically gated channel that requires bdining of 2 Ach molecules and is a positive ion channel

5 subunits

alpha beta 2 gamma and delta)

19
Q

resting membrane potential of the muscle cell

A

-80 to 90

biggest player is sodium

20
Q

EPP trigger

A

AP

botulism toxin and curare interferes with this

21
Q

t tubules in cardiac and skeletal

A

only 1 t tubule in cardiac

2 in skeletal

22
Q

muscle stays contracted as long as

A

there is calcium present in the sarcomere

23
Q

how does atrophy of a muscle occur

A

lack of innervation

lack of activity

24
Q

dystophies

A

genetic disorders

cause combination of atrophy
hypertrophy or pseudo hypertrophy and necrosis of muscle tissue depending on the pescific defect

insidious progressive disorders with the primary symptom being weakness

25
pseudo hypertrophy
fat and fibrosis
26
duchenne MD what is it
Hertible absence of dystrophin that is required for muscle structure
27
prevalence in Duchenne MD
males and females have 50%
28
prognosis of duchenne MD
progressive weakness leading to paralysis in 3-5 years most loose the ability to walk by 12 usually heart and breathing muscles get weak and cause pneumonia or heart failure
29
becker MD
similar but less severe pt produces dystrophin but it is not fully fucntional
30
fascioscapulohumeral MD
progressive disorder seen in adults MC form is myotonic seen with cataracts and cardiac abnormalities
31
loss of trophic effect of lower motor neuron is characteristic of
Denervation atrophy
32
- slowly progressive disorder of face, arms, shoulder beginning in teens
a. Fascioscapulohumeral MD
33
MC adult form characterized by cardiac abnormalities and cataracts, swan neck (from inability to support the weight of the head), drooping eyelids
b. Myotonic adult MD