Exam 2 Flashcards

Chapter 9 Part 1

1
Q

major functions of muscles

A
  1. body movement
  2. posture
  3. respiration
  4. body heat production
  5. communication
  6. constriction of blood vessels and organs
  7. heart contraction
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2
Q

characteristics of muscles

A

excitable
contractable
extensible
elasticity

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3
Q

excitable =

A

responds to stimuli

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4
Q

contractable=

A

shortens with height, muscles pull, not push

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5
Q

extensible=

A

stretch, beyond original resting length

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6
Q

elasticity=

A

recoil

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7
Q

3 muscle types

A

smooth, skeletal, cardiac

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8
Q

each myoblast has its own

A

nucleus

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9
Q

long, cylindrical cells formed by fusion of hundreds of embryonic cells =

A

myoblasts in myogenesis

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10
Q

Stem cells in Skeletal muscle, Usually Quiescent, Activate by Muscle damage
Stimulated to divide and fuse with existing muscle fibers

A

satellite cells

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11
Q

hypertrophy=

A

enlarge

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12
Q

what do skeletal muscles not do

A

undergo mitosis

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13
Q

what control localized region

A

nuclear domains

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14
Q

muscular compositon consists of

A

75% water
20% protein (actin, myosin, troponin, tropomyosin)
5% organic and inorganic compounds

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15
Q

muscular hierachy is

A

muscle fibers= muscle cell= myocyte

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16
Q

parallel and connect to one another by

A

endomysium

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17
Q

endomysium is what kind of CT

A

loose areolar

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18
Q

wrapped into unit called

A

fascicle

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19
Q

fascicles are connected by

A

perimysium

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20
Q

perimysium is what CT

A

dense irregular CT

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21
Q

entire unit is wrapped in a CT overcoat called

A

epimysium

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22
Q

epimysium is what CT

A

dense irregular CT

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23
Q

joins with deep muscular fascia=

A

separate structures

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24
Q

muscle anchored to bone via tendon (strap) or

A

aponeurosis (sheet)

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25
Q

can direct or indirect muscle to bone withstand more friction

A

indirect

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26
Q

what surround each muscle fiber and fascicle

A

bv and nerves

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27
Q

each what has its own nerve ending that control activity

A

muscle fiber

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28
Q

Specialized nerve cells that stimulate skeletal muscle contraction

A

motor neurons

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29
Q

each muscle fiver surrounded by plasma membrane=

A

sarcolemma

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30
Q

cytoplasm with xs glycogen and myoglobin=

A

sarcoplasm

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31
Q

Each Muscle Fiber (Cell) consists of Bundled
Contractile Elements

A

myofibrils

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32
Q

each myofibril is surrounded by

A

sarcoplasmic reticulum

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33
Q

the sarcoplasmic reticulum is highly

A

modified er

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34
Q

highly modified er regulates

A

calcium

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35
Q

Each Myofibril consists of Bundles Contractile
Elements ….. in sarcomere units

A

myofilaments

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36
Q

smallest contractile unit

A

sarcomere

37
Q

sarcomere stretches from

A

z line to z line

38
Q

dark band =

A

a band

39
Q

light band=

A

I band

40
Q

2 contractile proteins=

A

myofilaments

41
Q

thick A vand connect at m line =

A

myosin

42
Q

thin I band connect at z line

A

actin

43
Q

globular=

A

polypeptide subunits

44
Q

atp binding site is

A

myosin atpase

45
Q

Rod Shape, Stiffens F actin. Spans 7 Actin, Blocks Myosin – Actin Interaction

A

tropomyosin

46
Q

3 Polypeptide subunits = 3 Binding Sites

A

troponin

47
Q

Tnl=

A

actin

48
Q

TnT=

A

tropomyosin

49
Q

TnC=

A

calcium

50
Q

what does troponin do

A

interact with calcium to regulate tropomyosin’s position of blocking of actin-myosin interaction

51
Q

when calcium moves tropomyosin away, actin and myosin=

A

cross bridge and power stroke begins

52
Q

holds thick filaments in place and are extensible. composed of protein= titan

A

elastic filament

53
Q

Helps Muscle cell spring back into shape after stretching

A

elastic filament

54
Q

Stiffens as Uncoils to Resist Excessive Stretch. Largest Protein in Humans.

A

elastic filament

55
Q

Links Thin Filaments to Integral Proteins on Sarcolemma

A

dystrophin

56
Q

Mechanical Support to keep Sarcolemma Intact, NO Calcium Leak

A

dystrophin

57
Q

defective gene (sex linked recessive)=

A

duchenne muscular dystrophy

58
Q

S&S of duchenne muscular dystrophy

A

Frequent Falls, NOT rise from Lying/Sitting, Waddling Gait, Walk on toes

59
Q

treatment for duchenne muscular dystrophy

A

to sustain mobility & Respiratory function. OT, PT.
Steroids
no cure

60
Q

when do people with duchenne muscular dystrophy usually die

A

in 30s, respiratory failure

61
Q

weakening if skeletal muscles and adipose is what

A

duchenne muscular dystrophy

62
Q

when are you Dx for duchenne muscular dystrophy, and due to what

A

at birth

due to elevated CK levels, genetic tests

63
Q

what does elevated CK levels indicate

A

damage to muscle fibers

64
Q

in duchenne muscular dystrophy what tears during contraction and excessive calcium enters and damages contractile fibers

A

sarcolemma

65
Q

does the muscle regenerate in duchenne muscular dystrophy

A

no

66
Q

muscle fiber’s PM
transmits electrical impulses to muscle interior

A

sarcolemma

67
Q

tubelike infold of sarcolemma.
carry electrical impulses into center or muscle fiber- every muscle fiber sarcomere contracts together

A

transverse tubules

68
Q

SER in skeletal muscle fibers that store calcium

A

sarcoplasmic retuculum

69
Q

temrinal cisternae- t tubule- terminal cisternae

A

triad

70
Q

nervous stimulation

A

quick response

71
Q

motor neuron does what

A

message to muscle; voltage regulated calcium channels open and influx

72
Q

where do muscular contractions meet

A

neuromuscular junction

73
Q

ACh released from vesicles at synapse

A

stimulation

74
Q

what diffuses across synaptic cleft and binds to receptors

A

ACh

75
Q

muscular contraction stimulates what release

A

Na

76
Q

Na release and depolarization past threshold generate

A

action potential

77
Q

action potential goes along sarcolemma and down what

A

t tubule

78
Q

calcium release from

A

sarcoplasmic reticulum

79
Q

what binds troponin

A

calcium

80
Q

binding of calcium on troponin causes

A

conformational change

81
Q

after the conformational change

A

troponin attaches to tropomyosin

82
Q

after troponin attaches to tropomyosin what happens

A

tropomyosin moves no longer locking actin and myosin

83
Q

once tropomyosin moves

A

actin and myosin interact

84
Q

once actin and myosin interact

A

myosin pulls actin to center of sarcomere

85
Q

after myosin pulls actin to the center of the sarcomere

A

it shortens sarcomere length and muscle fiber length

86
Q

once sarcomere and muscle fiber length shorten what happens

A

Ca goes back to SR

87
Q

once Ca goes back to SR

A

troponin and tropomyosin go back to resting position

88
Q

power stroke steps

A
  1. myosin head cocks into position
  2. myosin binds to actin
  3. power stroke (push actin)
  4. detach from actin and new atp binds
  5. repeat

Need calcium and atp