Lec 15 Muscle Flashcards

1
Q

What surrounds entire muscle?

A

epymysium

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2
Q

What surrounds myofiber?

A

endomysium

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3
Q

What is type 1 muscle?

A

red; slow twitch
sustained action
lots of mitochondria and myoglobin
oxidative phosphorylation

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4
Q

What is type 2 muscle?

A

white; fast twitch
less mitochondria/myoglobin
anaerobic glycolysis

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5
Q

What is a motor unit?

A

anterior horn motor neuron axon terminating in motor end plate muscle fibers that the nerve innervates

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6
Q

How is AP propagated for muscle contraction?

A

via T-tubules –> AP produces Ca efflux from SR causing muscle contraction

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7
Q

What do you see histologically with acute dennervation?

A

angular myofibers

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8
Q

What is myofiber type grouping?

A

due to partial chronic dennervation from collateral

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9
Q

What happens to muscle in stroke?

A

you are taking out the upper motor neruon but anterior horn cell still intact –> selective atrophy of type 2 fibers due to disabuse

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10
Q

When do you get type 2 myofiber atrophy?

A

when muscle isnt used [not same as dennervation]

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11
Q

What does proximal muscle disorder suggest?

A

intrinsic muscle process problem

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12
Q

What does distal muscle disorder suggest?

A

usually neurogenic

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13
Q

What do you see in Duchennes muscular dystrophy?

A

steadily progressive; onset first 5 years
X recessive
gowers sign = difficulty rising from floor
often have cardiomyopathy
lordotic posture
hypertrophy of calf muscles

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14
Q

What is pathogenesis of duchenne’s?

A

no dystrophin gene –> replace myofiber with connect tissue

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15
Q

What is beckers?

A

less severe form of duchenne

onset mid childhood; uncommon to have cardiac involvement; do have calf hypertrophy + weakness

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16
Q

What is pathogenesis of Becker?

A

normal amount of abnormal sized dystrophin protein OR markedly reduced levels of normal dystrophin

17
Q

What is myotonic dystrophy?

A

CTG repeat expansion in DMPK gene –> abnormal expression myotonin protein kinase –> myotonia, muscle wasting, frontal balding, cataracts, testicular atrophy, arrhythmia

18
Q

What is pathogenesis of myotonic dystrophy?

A

CTG repeat expansion in DMPK gene –> abnormal expression myotonin protein kinase

19
Q

What do you see in congenital myopathy

A
  • floppy infant = muscle weakness
  • symmetric proximal weakness
  • typ 1 myofiber predominance
20
Q

What is polymyositis?

A

inflammation of muscle body itself

21
Q

What are criteria for polymyositis/ dermatomyositis?

A

progressive symmetrical proximal weakness
high sarcoplasmic enzymes in serum [CK, LDH, ANA, anti-Jo-1, anti-SRP]
skin rash, periorbital edema

22
Q

What is myasthenia gravis?

A

post synaptic antibodies to ACh receptor
decrease strength w/ repetitive stimulation
assocaited w/ thymoma or thymic hyperplasia

23
Q

What is eaton-lambert?

A

presynaptic antibodies to Ca receptor
increase strength w/ repetitive stimulation
small cell lung carcinoma