EXAM 2 Module 4 Flashcards

1
Q

striated muscles (striped pattern perpendicular to their long axis)

A

skeletal and cardiac

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

skeletal muscle structures

A

connective tissue
blood vessels
striated muscle fiber (single muscle cell)
sarcomere between two Z lines

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

thick filament

A

myosin

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

thin filament

A

actin

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

muscle contraction:
thick filament cross bridges are composed of ______ proteins

A

myosin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

muscle contraction:
myosin proteins contact thin filaments and use the energy of ______ to pull on the thin filaments

A

ATP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

muscle contraction:
in the absence of ATP, myosin attaches to _____

A

actin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

explains what happens at sarcomere level

A

sliding-filament mechanism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

in the sliding filament mechanism at the sarcomere level, the ______ move closer together

A

Z lines

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

sliding filament mechanism:
- the lengths of the thick filaments (A band) and thin filaments ______ change
- rather, the thin filaments are ________ around the thick filaments
- this does reduce the length of the _____ and ____

A

do not;
pulled in closer;
H zone; I band

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

cross-bridge cycling in skeletal and cardiac muscle:
- when Ca2+ inside the cell is low, _______ keeps the tropomyosin in a position that blocks cross-bridge binding to the ______
- muscle is ______

A

troponin; actin;
relaxed

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

cross-bridge cycling in skeletal and cardiac muscle:
- when Ca2+ inside the cell is high, it binds to troponin, which allows ________ to move away from the cross-bridge binding sites
- cross-bridges ______ and muscle is _______

A

tropomyosin;
form; contracted

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

3 sources of ATP production in muscle (in general order in which they are used during muscle contraction)

A
  1. creatine phosphate
  2. oxidative phosphorylation
  3. glycolysis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

synapse where motor neuron AP communicates with muscle fiber to trigger muscle contraction

A

neuromuscular junction

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

EC coupling in skeletal muscle pathway

A

AP motor neuron
T tubules
DHP receptors
muscle contraction

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

after ______ flows into the cytoplasm, it binds troponin to allow cross-bridge formation and subsequent muscle contraction

A

Ca2+

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

EC coupling in cardiac muscle pathway

A

difference to skeletal muscle is no DHP receptors, instead there are voltage-gated L-type Ca2+ channels

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

muscle type with no striations

A

smooth muscle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

smooth muscle structures

A

thick myosin filaments
thin actin filaments (anchored to plasma membrane or dense bodies)
tropomyosin
NO troponin

20
Q

in smooth muscle, the thick and thin filaments slide past each other, and when the contraction happens, the entire cell ______ and ______

A

shortens; thickens

21
Q

smooth muscle specialized structures

A

relaxed spindle-shaped
contracted blob

22
Q

smooth muscles that respond to stimuli as a single unit, cells are connected by gap junctions

A

single-unit smooth muscles

23
Q

smooth muscles that respond to stimuli independently, fewer gap junctions

A

multi-unit smooth muscles

24
Q

two things that are lacking in smooth muscle contraction

A

troponin
sarcomere

25
smooth muscle contraction pathway: 1. increased cytosolic Ca2+ binds and activates _____ 2. active calmodulin activates _______ 3. myosin light-chain kinase ________ smooth muscle myosin 4. _______ can form 5. cross-bridge cycling can occur as long as _______ is phosphorylated
calmodulin; myosin light-chain kinase; phosphorylates; cross-bridges; myosin
26
thick and thin filaments
skeletal, smooth, cardiac
27
sarcomeres - banding pattern
skeletal, cardiac
28
transverse (T) tubules
skeletal, cardiac
29
sarcoplasmic reticulum
high skeletal, low smooth, medium cardiac
30
gap junctions between cells
smooth (more in single-unit, few in multi-unit), cardiac
31
source of activating Ca2+
skeletal: SR smooth: SR and extracellular cardiac: SR and extracellular
32
site of Ca2+ regulation
skeletal: troponin smooth: myosin cardiac: troponin
33
speed of contraction
skeletal: fast-slow smooth: very slow cardiac: slow
34
spontaneous production of action potentials by pacemakers
single-unit smooth, few specialized cardiac
35
tone (low levels of maintained tension in the absence of external stimuli)
single-unit smooth
36
effect of nerve stimulation
skeletal: excitation smooth: excitation or inhibition cardiac: excitation or inhibition
37
physiological effects of hormones on excitability and contraction
smooth, cardiac
38
stretch of cell produces contraction
single-unit smooth
39
once-common viral disease that can destroy motor neurons, leading to paralysis of skeletal muscle
poliomyelitis
40
involuntary tetanic contraction of skeletal muscles
muscle cramps
41
involuntary tetanic contraction of skeletal muscles that occurs when the extracellular Ca2+ concentration decreases to about 40% of its normal value
hypocalcemia tetany
42
common genetic disease, associated with progressive degeneration of skeletal and cardiac muscle fibers, more common in men
muscular dystrophy
43
what causes muscular dystrophy
the absence or defect of one or more proteins that make up the costameres in striated muscle
44
sex-linked recessive disorder caused by a mutation in a gene on the X chromosome that codes for the protein dystrophin
Duchenne muscular dystrophy
45
neuromuscular disorder characterized by muscle fatigue and weakness that progressively worsen as the muscle is used
myasthenia gravis