excitation contraction Flashcards

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
Q

pseudo hypertrophy

A

fat and fibrosis

26
Q

duchenne MD what is it

A

Hertible absence of dystrophin that is required for muscle structure

27
Q

prevalence in Duchenne MD

A

males and females have 50%

28
Q

prognosis of duchenne MD

A

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
Q

becker MD

A

similar but less severe

pt produces dystrophin but it is not fully fucntional

30
Q

fascioscapulohumeral MD

A

progressive disorder seen in adults

MC form is myotonic seen with cataracts and cardiac abnormalities

31
Q

loss of trophic effect of lower motor neuron is characteristic of

A

Denervation atrophy

32
Q
  • slowly progressive disorder of face, arms, shoulder beginning in teens
A

a. Fascioscapulohumeral MD

33
Q

MC adult form characterized by cardiac abnormalities and cataracts, swan neck (from inability to support the weight of the head), drooping eyelids

A

b. Myotonic adult MD