014 muscle histology Flashcards

You may prefer our related Brainscape-certified flashcards:
1
Q

what are the 3 connective tissue sheets on muscle?

A
  • epimysium = outside of muscle
  • perimysium = around each muscle bundle/fasicle
  • endomysium = around each individual muscle fibre/cell
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what does the epimysium cover?

A
  • outside of muscle
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what does the perimysium cover?

A
  • each muscle bundle/fascicle
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what does the endomysium cover?

A
  • each individual muscle cell/fiber
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what is the breakdown of the structure of skeletal muscle?

A
  • myofilaments (actin, myosin) —>
  • sarcomere —>
  • myofibril —>
  • muscle cell/fibre —>
  • muscle fascicle —>
  • skeletal muscle
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

give 7 key features of skeletal muscle cells

A
  • 1 muscle cell = 1 muscle fibre
  • very wide, 100 micrometers diameter
  • very long 30cm
  • many nuclei on periphery
  • no special junctions between cells
  • many mitochondria
  • sarcolemma, sarcoplasm, sarcoplasmic retitculum
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

where are the nuclei in skeletal muscle?

A
  • on periphery of muscle cells
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what does this transmssion electron micrograph (TEM) show?

A
  • skeletal muscle fibres
  • you can see the sarcomeres Sa
  • SR = sarcoplasmic reticulum
  • ZL = Z line
  • A = dark A band = myosin and actin overlap
  • I = light I band = actin
  • Hzone = myosin only
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what happens to the sarcomere during contraction?

A
  • myosin pulls the actin filaments towards each either
  • Z lines get closer together
  • light I band shortens
  • dark A band = same
  • sarcomere shortens
  • sliding filament theory
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what is A?

A

sarcolemma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what is b?

A

terminal cisternae

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what is c?

A

transverse tubules / T-tubules

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what is d?

A

sarcoplasmic reticulum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what is e?

A

mitochondria

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what is f?

A

myofibrils

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what is g?

A
  • dark A band myosin
17
Q

what is h?

A
  • light I band actin
18
Q

what is i?

A
  • Z line
19
Q

what is j?

A
  • nucleus
20
Q

what is the triad in skeletal muscle?

A
  • 1 T tubule and 2 terminal cisternae
21
Q

what are the 2 different muscle fibre types?

A
  • type 1 = slow
  • type 2 = fast
22
Q

what colour do type 1 muscle fibres appear?

A
  • red = rich in myoglobin
23
Q

what colour do type 2 muscle fibres appear?

A
  • white = rich in glycogen, less myoglobin
24
Q

what are type 1 muscle fibers used for?

A
  • small, slow, aerobic exercise
  • e.g. marathon
  • related to continuous weak contractions e.g. postural muscles
25
Q

what are type 2 muscle fibres used for?

A
  • large fast anaerobic exercise
  • e.g. sprint
  • related to intense sporadic contraction, e.g. biceps
26
Q

what does this image show?

A
  • neuromuscular junction
  • motor unit with multiple motor end plates on different myofibrils
27
Q

what does this image demonstrate?

A
  • muscle spindles
28
Q

what do muscle spindles detect?

A

stretch

29
Q

what do golgi tendon organs detect?

A

tension

30
Q

what is myasthenia gravis and what is its pathophysiology?

A
  • rare autoimmune disease that causes weakness of muscles
  • caused by auto-anitbodies attacking ACh receptors on post-synaptic membrane of muscle
  • also flattens junctional folds
    = weaker less frequent nerve transmission = wealer muscle contractions
31
Q

what is Duchenne’s muscular dystrophy?

A
  • genetic disorder characterized by progressive muscle degeneration and weakness due to the alterations of a protein called dystrophin that helps keep muscle cells intact
32
Q

what is Duchenne’s muscular dystrophy caused by?

A
  • mutation in dystrophin gene which is responsible for connecting cytoskeleton of each muscle fibre to the basal lamina
  • when dystrophin is mutated, excess Ca can penetrate the sarcolemma = excess water entry = cells burst and die
    = muscles waste away
33
Q

what does this picture show in terms of Duchenne muscular dystrophy?

A

dystrophin immunofluorescence stain shows absence of functional dystrophin in muscle membrane in MD

34
Q

what are satellite cells?

A
  • stem cells of the muscle
    = proliferate to form new muscle fibres or replace damaged muscle fibres
35
Q

where are satellite cells found in muscle?

A
  • on the outside of skeletal muscle cells/fibres
36
Q

what are satellite cells activated/stimulated by?

A
  • muscle cells breaking/over stretching
37
Q

what is this a picture of ?

A

satellite cell