Muscle Tissue Flashcards

1
Q

What’s the muscle cell hierarchy?

A

2 muscle cell types: striated and non striated

Striated: skeletal (myoglobin, voluntary direct never muscle communication) and cardiac (myoglobin, involunary, indirect nerve muscle communication)

Non striated: smooth muscle (no myoglobin, involuntary, no direct nerve-muscle communication

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2
Q

Skeletal muscle structure

A
  • point of origin and insertion (causes movement if across a joint)
  • fibres present (striated muscle cells). Can be slow oxidative, fast oxidative glycolytic or fast glycolytic
  • myofibrils in each fibre (actin and myosin)
  • muscles with similar actions grouped into compartments surrounded by fascia
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3
Q

Compare and contrast slow oxidative, fast oxidative glycolytic and fast glycolytic muscle fibres (7)

A

Slow oxidative; aerobic, lots of myoglobin, red, many mitochondria, many cytochromes, fatty acids and lots of ATP/CO2

Fast oxidative glycolytic; aerobic, lots of myoglobin, red/pink, many to intermediate mitochondria, many cytochromes, fatty acids and glycogen, initially lots of CO2 then lots of lactate

Fast glycolytic; anaerobic, little myoglobin, pale, few mitochondria, few cytpchromes, glycogen ,lots of lactate/little ATP

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4
Q

What are the four compartments of the lower leg?

A
  • anterior compartment
  • lateral compartment
  • superficial posterior compartment
  • deep posterior compartment
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5
Q

!!What’s compartment syndrome

A
  • trauma in one compartment may cause internal bleeding, placing pressure onto blood vessels and nerves
  • aggravated by passive stretch of muscle group leading to deep, poorly localised pain
  • paresthesia (pins n needles)
  • shiny, swollen skin with bruising
  • compartment feels tense and firm
  • prolonged capillary refill time
  • a fasciotomy is used to cut skin and relive pressure
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6
Q

!! What’s myasthenia gravis?

A
  • autoimmune disease
  • antibodies directed against Ach receptor (neuromuscular junction)
  • symptoms appear if more than 30% of receptors blocked
  • leads to muscle weakness

-ptosis
(Drooping of eyelid)

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7
Q

Cardiac muscle structure

A
  • caardiomyocytes
  • centrally positioned nuclei
  • intercalated disks (electrical and mechanical coupling with adjacent cells)
  • BRANCHING.
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8
Q

Structure of purkyne fibres

A
  • abundant glycogen
  • sparse myofibrils
  • extensive gap junction sites (rapid transmission)
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9
Q

Smooth muscle function

A

Slower, more sustained contraction and less ATP needed

May remain contracted hours or days

Responds to nerves, hormones, drugs or local concentrations of blood gasses.

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10
Q

Structure of smooth muscle

A
  • spindle shaped (fusiform)
  • single central large nucleus
  • forms sheets, bundles or layers
  • many caveolae (small, cave-like invaginations)
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11
Q

!!what’s muscle hypertrophy

A

Over stretching.

  • new fibrils made to replace old
  • new sarcomeres added in middle of existing ones
  • new fibres made from mesenchymal cells
  • may be present in some cardiac pathologies (eg enlarged ventricles)
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12
Q

!!Whats muscle atrophy

A
  • loss of protein, reduced fibre diameter, loss of muscle power
  • may occur due to disuse, surgery and disease
  • commonly occurs in those 30+, 50% muscle loss by 80, temp regulation
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13
Q

!!What’s duchess Muscular dystrophy?

A
  • most common muscular dystrophy
  • inheritance via X-linked recessive pattern, mutation of dystrophin gene
  • w/o dystrophin, excess calcium enters mitochondria in muscle with water causing them to burst. Muscle cells burst (rhabdomyolyis). Causes creatine kinase and myoglobin levels to inc in blood
  • muscle cells replaced by adipose tissue
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14
Q

!! Whats the botulism toxin and Botox??

A
  • botulism toxin produced by clostridium botulinum
  • prevents release of neurotransmitter
  • stops skeletal muscle contracting (flaccid paralysis)
  • clinically used to treat muscle pasms (eg cervical dystonia)
  • cosmetically used to treat wrinkles
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15
Q

!! Whats organophosphate poisoning

A
  • used as pesticides
  • Ach esterase inhibited, Ach activity at neuromuscular junction reduced
  • effects somatic and automatic signalling
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16
Q

(Toxidrome - lots of a toxin in the body)

What are the muscarinic symptoms and nicotinic symptoms of cholinergic toxidrome??

A
Muscarinic symptoms:
S-salivation
L-lacrimation
U-urination
D-defecation
G-GI cramping
E-emesis (vomiting)
Nicotinic Symptoms:
M- muscle cramps
T-tachycardia
W-weakness
T-twitching 
F-fasciculations