Intro to skeletal muscle Flashcards

1
Q

What is skeletal muscle tissue?

A
  • Skeletal : Attach and move skeleton
  • 40% of body weight
  • Fibres are multinucleate cells
  • Cells with obvious striations
  • Contractions are voluntary
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2
Q

What is cardiac tissue?

A
  • Wall of the heart
  • Striated walls
    -Involuntary contractions
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3
Q

What is smooth tissue?

A
  • Walls of hollow organs
  • Lack striations
  • Involuntary contractions
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4
Q

What are the functions of skeletal muscle tissue?

A
  • Designed to contract
  • Generate mechanical force
  • Heat generation (shivering, involuntary contractions etc)
  • Locomotion/ external movements
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5
Q

Descrive how skeletal muscle is connected to the skeleton

A
  • connected via tendons
  • attached to immobile bone at one end (origin)
  • Other end attached to insertion (moveable bone)
  • Non-contractile parts (elastic elements) of the muscle and tendons are stretched before tension where attachment occurs
  • Contracting muscles - typically pull on attachment points to move insertion toward origin
  • Elastic elements allow muscle to elastically recoil back to its original resting length when contraction is completed
  • Antagonistic (Synergistic) pairs
  • Contraction of one does the opposite to counterpart (biceps and triceps)
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6
Q

What are myofibres?

A
  • Elongated cells
  • Arranged parallel to one another and bundled by connective tissue into fascicles
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7
Q

What are sacrolemma?

A

cell membrane
- Striated (banded)

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8
Q

What are the different components of skeletal muscle in connective tissue (layers) ?

A
  • Superficial fascia = loose connective tissue underlying skin
  • Deep fascia = dense connective tissue around muscle
  • Epimysium - surrounds whole muscle
  • Perimysium - surrounds bundles (fascicles) of muscle cells
  • Endomysium - separates individual muscle cells
  • Connective tissue layers extend beyond muscle bellly to form the tendon = aponeuroses and MTJ
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9
Q

What are myofibrils?

A
  • Long bundles of protein, made up of thick and thin filaments
  • myofilaments arranged in sacromeres
  • Repeated units
  • From one Z disc to the next
  • Thick filaments ar center, thin filaments at either end attached to the z-discs
  • I band near either end - only thin myofilaments
  • A band at midsection - thick filaments
  • H zone at centre - only thick fialments (no overlap with thin)
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10
Q

What is myosin?

A
  • composes thick filaments
  • held in place by the M line proteins
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11
Q

What is Actin?

A
  • Composed thin filaments alongside troponin and tropomyosin
  • Myosin-binding site on each actin molecule - covered by tropomyosin in relaxed muscle
  • Thin filaments held in place by Z lines. From one Z line to the next = sacromere
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12
Q

What is the sliding filament mechanism?

A
  • Movement of thin filaments over thick
  • sacromere shorterning
  • Thick filaments = stationary; thin are dragged over thick
  • length of the filaments do not change
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13
Q

What is the anatomy of a nerve-muscle

A
  • extensive blood supply for every muscle
  • Specialised nerve cell = motor neuron = associated with muscles- every muscle fibre receieves innervation from a nerve
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14
Q

What events link muscle excitation / action potentials to muscle contraction (cross bridge cycling)?

A
  • Action potential - propagates down the sacrolemma
  • Transverse tubules conduct AP into the cell’s interior
  • Ca 2+release channels open in Sarcoplasmic reticulum
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15
Q

How are muscle contractions activated by action potentials?

A
  • APs induce the release of Ca 2+ into the sarcoplasm
  • When Ca 2+ binds to troponin on thin filament, troponins changes
  • Shifts tropomyosin off myosin binding sites
  • Enables myosin to bidn to actin
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16
Q

What is Cross-bridge cycling?

A

Cross-bridge
Cycling
Myosin head binds to actin
Power Stroke
— Globular head bends
toward center of
sarcomere
— thin filaments pulled
toward center of sarcomere
- Cross bridge link broken and head unbends
- Myosin binds to next actin molecule on the thin filament
- Repeats, shortening length of the sarcomere

17
Q

What are contractile properties?

A
  • Twitch = single contraction and relaxation of a muscle in response to a single bried stimulus
  • Strength of twitch contraction can be modifed
    In vitro (isolated) - increasing stimulus strength induces large numbers of myofibres to contract
    In vivo ( in the body) - activation of additional motor units (motor unit recruitment) increases contraction strength
  • Henneman’s size principle motor units - genrally recruited in order of smallest to largest (fewest fibres to most fibres ) as contraction increases
18
Q

What is the length-tension relationship?

A
  • Normal resting length for skeletal muscles ( sacromere ~ 2.0 micrometeres) - for generation of max tension
  • If length decreased ( sacromere length < 2.0 micrometers ) - tension reduced as fluid pressure builds, thin filaments from either end of the sacromere collide
19
Q

Wnat are the types of muscle contraction?

A
  • Summation : when a muscle is stimulated multiple times in rapid succession
  • Complete tetanus - muscle stimulates at high frequency so that no relaxation occurs (Steady state of tension)
  • In vitro - high rate of stimulation prevents muscle fibres from relaxing
  • In vivo - different motor units activated in rapid succession to generate sustained contraction
20
Q

What is an isometric contraction?

A
  • Muscle does not shorten,remains at the same length
  • Force generated by the contraction is equal to the load applied
21
Q

What are isotonic contractions?

A
  • Muscle changes length
22
Q

What are concentric contractions?

A
  • Force generated is greater than load applies
  • Muscle shortens as it contracts
23
Q

What are eccentric contractions?

A
  • Force generated is less than load applied
  • Muscle lengthens even though it is contracting
24
Q

What do muscle contraction require?

A
  • ATP
  • Cross bridge cycling
    -Ca 2+ pump activity
    Sources available:
  • cytosolic ATP
  • Phosphocreatine (PCr)
  • Aerobic respiration (oxidative phosphorylation)
  • Anaerobic respiration (fermentation)
25
Q

Describe ATP and Creatine Phosphate in muscle

A

ATP - limited stores (used up in a few contractions)
- Phosphocreatine (creatine phosphate)
- Storage of high energy phosphate bonds
- Used to quickly regenerate ATP from ADP
- Limited supply in cells

26
Q

What is anaerobic respiration?

A
  • Glycolysis + lactate fermentation
  • breakdown of glucose
  • Stored as glycogen in muscle cells
  • Does not require O2
    -Generates ATP quickly (faster than aerobic respiration)
  • Used during intense exercise - O2 supply cannot keep up with demand
  • Lactate produced - associated with muscle soreness and fatigue
27
Q

What is aerobic respiration?

A
  • Occurs in mitochondria
  • Requires O2 to form ATP
  • Fatty acids = primary nutrient source
  • Contain lots of energy, but requires O2 to release it
  • Aerobic exercise - light to moderate exercise (walking, jogging, swimming)
  • Max O2 uptake
  • Max rate of O2 delivery to the muscles
  • Max level of aerobic activity
28
Q

How is skeletal muscle developed and regenerated (via postmitotic nuclei) ?
- where are they located?

A

-Adult SKM fibres have 100-1000s of postmitotic nuclei that are located at the periphery of the fibres

29
Q

What are satellite cells?
Active in young growin.. and … in older muscles
Donate … into growing…
Repair…

A
  • active in young growing muscle and quiescent in older muscles
  • donate myonuclei into growing muscle fibres
  • Satellire cells - repair muscle damage
30
Q

What is myogenesis?
- Reg by … reg factors
- Appear at different.. during… development
- … MRFs regulate ….. {MYOD-r Myf-5),
- Secondary MRFS regulate fusion of … and terminal differentiation (MRF4)

A
  • The muscle making process
  • Regulated by myogenic regulatory factors (MRFS)
  • They appear at different times during muscle development
  • Primary MRFs regulate determination ( MyoD or Myf-5), Secondary MRF’S regulate fusion of myoblasts and terminal differentiation (MRF4)

Somite cells to Myoblasts then Proliferation then Fusion = muscle fibres

31
Q

What are the two ways that muscle tissue can grow?

A
  1. Cells can double their nuclei/DNA and contents in a process called cell cycle and then split - HYPERPLASIA - most common form of muscle growth during development
  2. Adult muscle cells can also grow in size = HYPERTROPHY. Hyperplasia does not occur in adulthood. Cellular hypertrophy limited because the DNA concentration within a cell with one nucleus will be diluted due to their post-mitotic nature
32
Q

What are the two possible outcomes of hypertrophy?

Hypertrophy with … dilution
(increase in nuclear number)
DNA: … is kept … during hypertrophy

A
  • Hypertrophy with DNA dilution (only protein synthesis)
  • Mechanism for increase in nuclear number
  • DNA - to muscle volume is kept constant during hypertrophy
33
Q

What is the role of satellite cells in hypertrophy?

A
  • Satellite cell proliferation and differentation
  • Hypertrophy stimulus
  • Nucleus donated by satellte cell
  • Fusion of some satellite cells with muscle fibres