finals study - all topics Flashcards

1
Q

what is the muscle breakdown

A

whole muscle -> fascicle -> fibre or M cell -> myofibril

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2
Q

what is the epimysium

A

surrounds the muscle tissue

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3
Q

what are the 3 roles of skeletal muscle

A

stores protein (metabolism)
movement and generates force
thermogenesis

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4
Q

what are the 4 unique properties of muscle

A

excitability/irritability, contractility, extensibility, and elasticity

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5
Q

what is excitability/irritability

A

developing and propagating (sustaining) a transient electrical event (action potential)

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6
Q

what is contractility

A

ability to shorten

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7
Q

what is extensibility

A

stretched without damage

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8
Q

what is elasticity

A

tends to return to original state after extensibility and contractility

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9
Q

what are the 8 factors that affect torque

A
  1. activation history
  2. elasticity/passive stiffness
  3. cross-bridge functions and energetics/ATP availability
  4. muscle size
  5. mechanics
  6. innervation/neural activation
  7. fibre type composition
  8. antagonist balance
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10
Q

what factors determine muscle phenotypic properties

A
  1. cell lineage/genetic determinants
  2. epigenetics
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11
Q

what makes up epigenetics

A
  • motoneurons, hormones, load/stretch
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12
Q

what are the 2 components of structure <–> function contraction

A
  1. contractile components
  2. support and connecting protein components
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13
Q

what makes up the contractile components

A

muscles that shorten (actin and myosin)

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14
Q

what makes up the support and connecting protein components

A
  • collagen and elastin form connective tissue at many levels
  • epimysium (whole muscle separation)
  • perimysium (fascicles)
  • endomysium (fibre level)
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15
Q

what are the roles of structural proteins at the sub-cellular level

A
  • support contractile components
  • transmit force to tendons
  • resist injurious stretch by wide distribution of forces
  • mechanotransducers
  • promote gene transcription
  • involved in protein metabolism
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16
Q

what is the Hill (1938) model

A
  1. passive elements (CT, tendons and titin)
  2. active elastic elements (rotation of myosin heads during actin attachment)
    - parallel elastic elements (PE)
    - series elastic elements (SE)
    - contractile element (sarcomere)
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17
Q

what are the determinants of muscle force output

A
  • size, shape, composition
  • increased size = increased force
  • shape
  • slow twitch vs fast twitch
  • adaptability
  • variations of muscle shape/architecture
  • pennation
  • extrinsic factors
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18
Q

what makes up size, shape and composition

A

mass, geometry and fibre type

19
Q

what makes up increased size = increased force

A

muscle force is proportional to cross-sectional area (CSA) or more correctly, physiological cross-sectional area (PCSA)

20
Q

what makes up shape

A

compartments, length of fibres, and pennation arrangement -> pennation affects PCSA

21
Q

what makes up slow twitch vs fast twitch

A

fibre type composition affects speed and endurance of muscle contraction

22
Q

what makes up adaptability of skeletal tissue

A

muscle atrophy aligns with adipose tissue/subcutaneous fat buildup

23
Q

what makes up variations of muscle shapes and architecture

A

different pennation types, and length of fibre architecture of fibre

24
Q

what are the different types of pennation

A
  • unipennate = linear from end-to-end (fastest)
  • bipennate = angular to central tendon (large fibre length to muscle length ratio)
  • multipennate = many angles to central tendon (highest pennation = most force, low muscle to fibre ratio)
25
what makes up length of fibres
varies within and among different muscles, but usually does not span the length of the muscle (tendon-to-tendon) --> ratio of FL:ML = <1 (0.2-0.8)
26
what makes up muscle fibre architecture
- affects contractile properties of whole muscle - a combination of series and parallel (not 100% of either) - in series -> contractile length and shortening velocity, greater ROM, and faster force produced and greater shortening - in parallel -> total force generating capacity, lower ROM, higher force produced total, shortens less
27
what makes up the affect of pennation
- more fibres = more force - not a 1:1 ratio of force to fibre # - force is lost with angle but more in total - PCSA = CSA x cosB (greater angle from horizontal = more force lost, small loss of force per fibre, but great increase in packing density of fibres and overall greater force potential) - specific tension of fibres (F/PCSA ~15-20N/cm^2 or 2kg/cm^2) - larger PCSA = greater overall force capacity - can assess angle with an ultrasound - PCSA and ACSA (anatomical) are equal in non-pennated muscle -> therefore less force
28
what are the extrinsic determinants of muscle force output
neural control, activation history, antagonist function
29
what are the components of the motoneuron
soma, synapse, spinal cord regionalization, axon, axon hillock, dendrites
30
what is the soma
- aka cell body - the ventral portion of gray matter in SC. > 100/muscle (may be several hundred) - hard to maintan (large SA) - very active cells - post-mitotic after birth - loss with aging - alpha exrafusal fibres and gamma intrafusal fibres (spindles) - small soma supports may long processes
31
what is the different between alpha extrafusal fibres and gamma intrafusal fibres (spindles)
- alpha = what we will focus on, the main fibres of skeletal muscles - spindles = proprioception for length changes (feedback)
32
what is the synapse
- electrical or chemical junction between neural tissues - transmission point between2 cells (same or different cells) - differential control - the site of information control (positive (excitatory) or negative (inhibitory) signal types -> need a balance
33
what is the spinal cord regionalization of motoneurons
- regionalization meaning not randomized - the motoneurons span more than one lumbar level so paralysis at L2 won't necessarily make lost function completely
34
what is the axon
- for efferent traffic (out of cell) -> toward the muscle - covered by organized myelin (lipid); nodes of ranvier
35
what is the axon hillock
- for afferent traffic (into cell) - dendritic tree - > receiving information via synaptic connections (control points) - 1 axon = many dendrites - electrical or chemical
36
what is the membrane potential pump
the pump requires energy which moves sodium and potassium in and out of the membrane -> potassium into cell and sodium out
37
what are the steps to action potential
1. negative membrane potential inside the cell 2. threshold of excitation is reached 3. Na into cell 4. Na into cell and K out (depolarization) 5. K out of cell, at a big positive membrane potential 6. K out of cell causing membrane potential to return to normal (repolarization) 7. K channels and Na channels close and reset 8. extra K diffuses away -> overshoots (afterhyperpolarization) because wants to ensure the negative point is reached (for a few ms) -> if negative point isn't reached, can't send another
38
what is the normal resting membrane potential
~-70mV -> if reached a rapid change in ionic concentration causes a reversal of the membrane potential to positive (+30 to 50mV) -> spike potential
39
what is Na conductance
abrupt/rapid/big (lower than membrane potential, higher than K conductance)
40
what is K conductance
(lower than both membrane potential and Na conductance)
41
what is refractory
determines the number of action potentials that can be sent per millisecond -> includes absolute (can't produce) and relative (harder to produce)
42
what are synaptic pots
not all input will reach threshold and cause action potential, not enough input so forgotten, small hyperpolarizing afterpotential -> smaller periods = less time between action potentials
43
what is action potential
- AP amplitude is invariant and all-or-nothing - neural information is encoded by the frequency and pattern of impulses (rate coding) - refractory periods variable among different motoneuron types and determines basic firing rates - net charge of synaptic potentials - ~10K synapses generates an action potential at the axon hillock if critical threshold is reached (excitatory > inhibitory)
44
what are nerve conduction velocities