Muscles Part 2 Fitz Flashcards

1
Q

Isotonic twitch contractions

A

Generate force by changing the length of the muscle.

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2
Q

Tension differences are based on

A

The recruitment of more muscle fibers (more sarcomeres). With each sarcomere recruited, tension is increased.

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3
Q

Unfused tetanus

A

Spastic muscle movement. Action potentials causing a lot of contractions. Ex: working out in reps. Taking breaks.

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4
Q

Fused tetanus

A

Fully contracted muscle and stays contracted. This is what happens when a muscle cramps.

Why we get tetanus shots.

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5
Q

Optimal length of a fiber

A

The length at which the fiber develops the greatest isometric active tension.

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6
Q

Passive vs active tension

A

Passive (elastic) is due to titan elastic filament. Can be stretched and springs back into place.As you stretch it, passive tension increases.

Active tension of a muscle fibers develops during contraction and can be altered by changing the muscle length. As you stretch it, it reaches isometric, then decreases in tension due to too much overlap.

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7
Q

Fatigue resistant fibers vs fatigue prone

A

Fatigue resistant- oxidative fibers

Fatigue prone- glycolytic.

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8
Q

Three ways a muscle fiber can form ATP

A
  1. Create ATP from creatine phosphate (reserve ATP source)
  2. Oxidative phosphorylation of ADP in mitochondria
  3. Substrate level phosphorylation of ADP in the cytosol via glycolysis
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9
Q

Fast twitch fibers

A

Rapid contraction but short lived. Extra ocular muscles.

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10
Q

Slow twitch fibers

A

Very slow to reach max tension, but doesn’t fatigue as quickly.

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11
Q

Diameters to determine slow oxidative, fast oxidative and fast glycolytic

A

Slow oxidative- small and dark
Fast oxidative- medium size and lighter
Fast glycolytic- largest and lightest

Larger diameter= faster signal

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12
Q

Rates of fatigue for slow oxidative, fast oxidative and fast glycolytic

A

Rates of fatigue from fastest fatigue to slowest fatigue
Fastest- fast glycolytic
Fast oxidative
Slowest- Slow glycolytic

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13
Q

What gives oxidative fibers its red color

A

Myoglobin, which is only seen in lives muscles. Due to a higher need for blood supply.

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14
Q

4 parts of twitch contraction

A
  1. Latent period (2m sec when ca2+ is being released froM SR)
  2. Contraction period. Filaments slide past each other.
  3. Relaxation period. Active transport of Ca2+ back in SR
  4. Refractory period. Muscles cannot respond until it can reset.
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15
Q

Isotonic contraction

A

A load is moved by changing the length of a muscle.

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16
Q

Two types of isotonic contraction

A

Concentric- a muscle shortens to produce force and movement. Lifting book towards chest.

Eccentric- a muscle lengthens while maintaining force and movement. Lowering book towards legs with arms extended.

17
Q

Isometric

A

No movement occurs. Tension is generated without muscle shortening. Holding a book out straight. Arms not bent.

18
Q

Myogram measures

A

Muscle fibers

19
Q

Summation

A

When a new contraction occurs before the muscle had fully relaxed, tension will add which is called summation.

20
Q

Sensory feedback from the muscle is by

A

Muscle spindles (Activated by stretch) and golgi tendon organ (activated by tension)

21
Q

A muscle spindle consists of ___

A

of a collection of specialized fibers that lie within a connective tissue capsule.

22
Q

The muscle spindle is innervated by

A

Its own gamma motor neuron and is supplied by 2 afferent sensory terminals- primary and secondary. Both are activated by stretch.

23
Q

The golgi tendon organ

A

Monitors change in muscle tension.

Located where muscle attaches to bone.

24
Q

Patellar tendon reflex (stretch reflex)

A

Tapping on the tendon causes extension response from the golgi tendon and muscle spindles.

25
Q

Atrophy

A

Happens primarily from not using a msuscle.

26
Q

Which virus destroys motor neurons

A

Polio

27
Q

ALS

A

Excitotixic disease- too much calcium in the cytoplasm results in the cell killing itself. In ALS, the neurons that have paravalbumin die last. Makes sense since paravalbumin is a calcium regulator.

Stephen hawking

28
Q

Muscular dystrophy is more present in males or females

A

Males.

29
Q

Muscular dystrophy is a disorder in which

A

Costamers (which hold the myofibrils to the sarcomere) rip and no longer support the muscle. Death usually occurs because the diaphragm can’t contract.

30
Q

Dystrophin

A

A type of costumer, which is a protein that holds the myofibrils to the sarcomere.

31
Q

Myasthenia graves

A

Body attacks ach receptors in muscles. Patient has diplopia- should use neostigmine to increase muscle contractions.

32
Q

Muscular sclerosis is related to which polyneuropathy syndrome?

A

Guillaian barre- body attacks nerves. weakness and tingly.

33
Q

Myofibrils of smooth muscles interact with ___, instead of Z, M lines

A

Dense bodies.

34
Q

Is there a solid NMJ in smooth muscle

A

No

35
Q

Receptors on smooth muscles

A

Variscocities. Little beads. Chemicals from nervous system can bind anywhere on the varicosities.

They are attached to the axon of the postganglionic autonomic neuron.

36
Q

In smooth muscle, calcium binds to ___

In skeletal muscle, calcium binds to ___

A

Calmodulin

Troponin

37
Q

What type of cell communication occurs in smooth muscle

A

Gap junctions/connexons. Wave of contractions. Systolic Ca2+ from extracellular fluid stimulates the smooth muscles.

38
Q

Gap junctions are found in which two muscles

A

Cardiac and smooth

39
Q

action potentials in cardiac muscles have a long plateau period due to which channel

A

The L calcium channel