Muscle - Lectures 10-11-12 Flashcards

(67 cards)

1
Q

what are the 3 types of muscle
- 2 similarities

A
  1. Skeletal muscle
  2. cardiac muscle
  3. smooth muscle
    SIMILARITIES:
    - excitability! membrane potential can be changed
    - all use actin and myosin –> 2 major proteins responsible for contractability
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2
Q

describe each type of skeletal muscles:
- size?
- pattern/striation?
- how many nucleus?
- intercalated disk?
- T-tubules?

A

SKELETAL:
- large fibers
- striped or striated
- multiple nuclei –> advantage = can produce many proteins
- no intercalated disks
- T-tubules
CARDIAC:
- smaller than skeletal, branched
- striations
- 1 nucleus per cell
- cells are joined in series by intercalated disks (to squeeze at the same time)
- T-tubules!
SMOOTH:
- small
- no striations
- 1 nucleus per cell
- no intercalated disks
- no T-tubules

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3
Q

how can there be multiple nuclei in one muscle cell?

A

stem cells during embryonic development form myoblasts (1 nucleus per cell) –> merge together to form myocytes/muscle fibers = many nuclei per cell

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4
Q

what are antagonistic muscles?
- what are the 2 movements?

A
  • move bones in opposite directions
  • flexion moves bones closer together (arm curl)
  • extension moves bones away from each other (push-up)
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5
Q
  • muscle cells are called muscle _______- –> shape (2)
  • what kind of cells differentiate into muscle for growth and repair?
  • amount of muscle cells already decided at birth? what changes?
  • muscle ____A____ –> bundle into _______ which bundle into _______
  • connective tissues hold muscle to bone with _______
A
  • muscle fibers –> long and cylindrical
  • satellite cells/stem cells
  • yes! when you exercise, you change diameter and length BUT stem cells can repair and replace damaged muscles
  • muscle fibers bundle into fascicles which bundle into entire muscle
  • tendon
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6
Q

what are the 3 layers of connective tissue that surround muscle vs fascicles vs myocytes?
- what does the connective tissue provide? (3)

A
  • myocytes surrounded by endomysium
  • fascicles surrounded by perimysium
  • entire muscle surrounded by epimysium
  • fluid, blood, nerves
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7
Q

Z-line vs M-line vs A band vs I-band vs H-zone
- dark or light?

A
  • Z line/Z-disk: separates each sarcomere (btw 2 actins of different sarcomeres)
  • M-line: middle of myosin
  • A-band: entire length of myosin, has some overlap with actin –> dArk
  • I-band: only covers actin (from 2 sarcomeres ish) –> light!
  • H-zone: only myosin! bit lighter than A band
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8
Q

what is a sarcomere?

A

functional unit of muscle

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9
Q

muscle fiber anatomy:
- sarcolemma?
- sarcoplasm?
- sarcoplasmic reticulum? describe structure + function?

A
  • sarcolemma: cell membrane
  • sarcoplasm: cytoplasm
  • sarcoplasmic reticulum: endoplasmic reticulum: longitudinal tubes with enlarged ends called terminal cisternae
  • concentrates and sequesters Ca2+
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10
Q

What are t-tubules?
- what forms a triad?
- function?

A
  • continuous with the sarcolemma, invaginations of the sarcolemma that allows action potentials to get closer to SR
  • t-tubule + 2 flanking terminal cisternae = triad
  • allow AP to penetrate nearer to the internal structures of the fiber
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11
Q

muscle fibers also contain
1. all sarcomeres linked together
2. energy source
3. powerhouse

A
  1. myofibrils
  2. glycogen granules
  3. mitochondria
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12
Q
  • thin filament = which protein?
  • thick filament = which protein? heavy vs light chains
  • regulatory proteins (2)
  • accessory proteins (2)
  • crossbridges
A
  • thin = actin –> each can interact with 3 myosin
  • thick = myosin –> each can interact with 6 actin: heavy chains = motor domain = myosin ATPase VS light chains = regulatory fcts
  • reg proteins: tropomyosin and troponin
  • acces: titin and nebulin
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13
Q

myosin heads contain 3 parts

A
  1. actin binding site
  2. ATP or ADP/P+ binding site
  3. ATPase enzyme –> break down ATP into ADP + P
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14
Q

what are the 3 subunits of troponin?
- when troponin binds with ____ –> 2 things happen
- repeated as long as what?

A
  1. troponin I –> binds with actin
  2. troponin C –> binds with Ca2+
  3. troponin T –> binds with tropomyosin
    - when troponin C binds with Ca2+ released by SR (from terminal cisternae), troponin pulls tropomyosin from myosin-binding sites of actin –> myosin binds tightly to and moves actin
    - repeated as long as binding sites are uncovered and ATP is available
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15
Q

what is the important component of actin?
- actins are all linked together by _______

A
  • myosin binding site! binds with myosin head and forms crossbridge
  • myosin binding site usually covered by tropomyosin when not a lot of calcium
  • linked together by tropomyosin ish (which covers myosin binding sites)
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16
Q

when myosin binds with actin, myosin heads move towards _______ –> sarcomere becomes longer/shorter
- A-band, H-zone, I band stay the same lengths?

A
  • M-line –> sarcomere becomes shorter
  • A band stays same
  • I band and H-zone become shorter
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17
Q
  • titan spans distance from _______ to the neighbouring ________
  • nebulin attaches to a _______ but does not extend to the ________
  • role of titn?
A
  • from Z-disk to M-line (ie half a sarcomere)
  • Z-disk but doesn’t extend to M-line
  • titin provides elasticity and stabilizes myosin
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18
Q
  • muscle tension = what?
  • load = what?
  • contraction = what?
  • relaxation = what?
A
  • muscle tension = force created by muscle
  • load = weight or force opposing contraction
  • contraction = creation of tension in muscle
  • relaxation = release of tension
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19
Q

5 major steps leading up to skeletal muscle contraction

A
  1. events at the neuromuscular junction
  2. excitation-contraction (E-C) coupling
  3. Ca2+ signal
  4. contraction-relaxation cycle
  5. muscle twitch + sliding filament theory
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20
Q

do length or thick and thin filament change during contraction? –> what is this theory called?

A
  • no!
  • sliding filament theory of contraction –> overlapping actin and myosin fibrils
  • fibrils are fixed length
  • slide past each other in energy-dependant process
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21
Q
  • what is a powerstroke?
  • what happens at the end of a powerstroke (2)
A
  • myosin crossbrige swivels and pulls actin toward M-line
    1. myosin releases actin and resets and binds another actin
    2. heads are not released in unison
  • then powerstroke is repeated many times
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22
Q

rigor state vs rigor mortis

A
  • rigor state = occurs when no ATP or ADP are bound to myosin –> very brief
  • rigot mortis: muscle freezes if no ATP is available to release myosin
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23
Q

Start: rigor state where myosin is tightly bound to ______ after a ______ _______ (needs what to detach?)
1. ATP binds and myosin ________ –> ATP increases/decreases myosin affinity to actin
2. _______ of ATP provides energy for myosin head to do what?
- how is energy provided?
3. ______ _______
- begins in response to ____ binding ______
- release of ____ allows head to swivel, pulling ____ toward ______
4. myosin releases ____ –> makes room for next ____
*CHECK SCHÉMA!

A

start: myosin bound to actin after a power stroke (needs ATP to detach!)
1. ATP binds to ATP binding site on myosin head and myosin detaches –> ATP decreases myosin affinity to actin
2. hydrolysis of ATP provides E for myosin head to rotate and weakly bind to actin
- E is provided by myosin ATPase that breaks down ATP into ADP and Pi
3. Power stroke
- to Ca2+ binding to troponin
- release of Pi allows head to pull actin towards M-line
4. myosin releases ADP –> makes room for next ATP

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24
Q

explain steps from neuron to contraction of muscle to relaxation (10 steps)

A
  1. somatic motor neuron releases Ach at neuromuscular junction
  2. ACh binds to Nm receptor –> opens Na+ channels –> depolarization -> EPP –> Action potential into T-tubules!
  3. AP in T-tubules alters conformation of DHP (L-type Ca2+ channel) receptor (voltage gated channel)
  4. DHP receptor opens RYR (Ca2+ channel on SR) in SR and Ca2+ from SR is released and enters cytoplasm
  5. Ca2+ binds to troponin C + expose myosin binding site
  6. myosin heads execute power stroke
  7. actin filament slides toward center of sarcomere
  8. sarcoplasmic Ca2+ ATPase pumps Ca2+ back into SR
  9. decrease in [Ca2+] in cytosol causes Ca2+ to unbind from troponin
  10. tropomyosin recovers binding site. when myosin heads release, elastic elements pull filaments back to their relaxed position
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25
Timing of Excitation-Contraction coupling --> 3 steps
1. motor neuron AP --> releases ACh --> binds Nm --> induces 2 2. muscle fiber action potential --> Ca2+ released --> induces 3 3. development of tension during 1 muscle twitch (latent period + contraction phase + relaxation phase)
26
skeletal muscle contraction requires a steady supply of ____ - what breakdown produces short burst of energy? using what enzyme? - ________ are the most rapid and efficient store of energy?
- ATP! - phosphocreatine breakdown --> creatine kinase - carbohydrates (glucose)
27
1. anaerobic glycolysis produces (2) - quick or slow? - oxygen required? - quantity of energy released? 2. aerobic respiration (biochemistry pathways (2)) - quick or slow? - oxygen required? - quantity of energy released?
1. anaerobic glycolysis produces lactate and acid - quick! - no oxygen - small amount of E released 2. aerobic respiration (TCA cycle + ETC) - slow - oxygen required - large amount of E released
28
what are the 3 types of skeletal muscles?
- slow-twich fibers (ST or type 1) - fast twitch oxidative-glycolytic fiber fibers (FOG or type IIA) - fast twitch glycolytic fibers (FG or type IIB/X)
29
SLOW TWITCH FIBERS: - rely primarily on what? - ie what type of activity? - increase (3) FAST TWITCH FIBERS: - does 3 things faster - 2 types? difference?
SLOW TWITCH FIBERS: - oxidative phosphorylation - marathon running - increases mitochondria, myoglobin and blood vessels/capillaries to muscle FAST TWITCH FIBERS: - develop tension faster + split ATP more rapidly + pumps Ca2+ into sarcoplasmic reticulum more rapidly - oxidative-glycolytic --> uses oxidative AND glycolytic metabolism (ie weightlifting) - glycolytic fiber --> relies primarily on anaerobic glycolysis
30
oxidative fibers have more _________ --> why?
- myoglobin! - because myoglobin binds oxygen in muscle so it is readily available for aerobic processes
31
how to visually differentiate slow twitch vs fast twitch?
- slow twitch oxidative has large amounts of red myoglobin, numerous mitochondria + extensive capillary blood supply - fast twitch: larger diameter, pale color, easily fatigued
32
what affects tension in muscle? - sarcomeres contract with optimum force if it is at optimum _________ before contraction begins - tension generated directly proportional to number of __________
- resting fiber length! - optimum force at optimum length - tension proportional to number of crossbridges!
33
force of contraction increases with _____A____ --> what is ____A_____ - what is tetanus?
- with summation! - summation = stronger contraction when the muscle does not relax completely btw action potentials - tetanus = maximal contraction
34
what is a motor unit? small or big? examples - contraction depends on the ______ and _________ of motor units --> explain (2)
- motor unit = one motor neuron and its muscle fibers - can be small (ie eyelids) = good control, or big (ie back muscle) = less precise - depends on type and number of motor units 1. recruitment of additional motor units increases contraction force (increase load = increase motor units mobilized) 2. asynchronous recruitment of motor units helps avoid fatigue (ie not all leg muscles are contracted when standing to avoid fatigue)
35
length-tension relationship: - very big overlap between thick and thin filament = what? - almost no overlap btw thick and thin = what? - optimal resting length = what?
- BIG overlap = less tension - NO overlap = no crossbridges can be formed = no contraction - optimal length = maximum force
36
can AP have summations? can graded potentials have summations? can contractions have summations? + explain! - 1 EPP = 1 what?
- AP --> no - graded potential --> yes! spatial and temporal - contractions --> yes! stimuli closer together do not allow muscle to relax fully - 1 EPP = 1 contraction/twitch/power stroke
37
summation leading to unfused tetanus VS leading to complete tetanus
- unfused: stimuli are far enough apart to allow muscle to relax slightly between stimuli - complete tetanus: muscle reaches steady tension = complete tetanus --> if muscle fatigues, tension decreases rapidly
38
isotonic contractions vs isometric contractions? - what stays the same? - 2 types of isotonic contractions - what allows isometric contractions?
ISOTONIC contractions move loads! - muscle force stays the same ish - concentric action = shortening action - eccentric action = lengthening action ISOMETRIC contractions create force without movement --> load does NOT move --> tetanus below the force required to move load - muscle length stays the same - sarcomeres shorten while elastic elements (ie tendons) stretch, resulting in little change in overall length
39
- in an isometric contraction, sarcomeres lengthen/shorten, generating ______, but elastic elements ________, allowing muscle length to ________ _________ - in isotonic contractions, sarcomeres lengthen/shorten more, but because elastic elements are ________ _______, the muscles _______
- isometric --> sarcomeres shorten, generating force, but elastic elements stretch, allow muscle length to remain the same - isotonic --> sarcomeres shorten more --> elastic elements are already stretched --> muscle shortens
40
bones and muscles around joints form ___A___ and _______ - what is a ____A______ - what forms ____A____ and what forms _____B_____
- form levers and fulcrums - lever = rigid bar that pivots around a point called a fulcrum - bones = lever - flexible joints = fulcrums
41
human forearms = lever - what is the fulcrum? - what is the lever? - where is the applied force? - where is the load?
- fulcrum = elbow joint - lever = forearm bone - applied force = bicep attached to forearm bone - load = in your hand/ gravity acting on mass of forearm and hand
42
to lift up a 2 kg book using your bicep (bicep curl), is more than 2kg of bicep force needed? - what is advantageous of the human body?
- yes! 6kg! - small movement of the biceps becomes a much larger movement of the hand! --> biceps contracts and shortens 1 cm, hand moves upward 5 cm!
43
Golgi tendon organs (GTO) - where are they found (2) - composed of what?
- found in junction of tendons and muscle fibers (so between tendons and muscle fibers) - composed of free nerve endings that wind between collagen fibers inside connective tissue capsule
44
what is the role of golgi tendon organs? - how does it do it? (4)
- goal = prevents too much contraction of muscle - when a muscle contracts, its tendons act as a series elastic element during isometric phase --> activates GTO --> GTO sends sensory info to CNS/spinal cord --> spinal cord sends back signal to muscle to decrease muscle contraction
45
- what are muscle spindles? - muscle spindle capsule encloses a group of what? known as what? - innervation of muscle spindles from what neurons?
- muscle spindles = stretch receptors that encode signals about muscle length and changes in muscle length - group of small muscle fibers known as intrafusal fibers - from gamma moror neurons
46
what is alpha-gamma coactivation? - def - 3 steps - result
- simultaneous activation of alpha and gamma motor neurons 1. alpha motor neurons fire, innervates extrafusal muscle fibers = muscle shortens, tension released 2. gamma motor neurons fire, intrafusal fibers contract, maintains stretch ---> sends info to spinal cord/CNS 3. spinal cords sends back signal to contract extrafusal fibers but not TOO much stretching - result: spindle remains active
47
what is the role of muscle spindles vs golgi tendon organs?
- muscle spindles: prevents too much stretching - GTO: prevents too much contraction
48
why do intrafusal fibers contract if they cannot generate force?
because they keep muscle fibers sensitive to stretch! to prevent too much stretching!
49
3 different ways to classify smooth muscles 1. by location (6) 2. by contraction pattern: 2 types + examples 3. by their communication with neighboring cells (2 types)
1. vascular, gastrointestinal, urinary, respiratory, reproductive, ocular 2. phasic smooth muscles --> alternate contraction and relaxation (mostly GI tract) VS tonic smooth muscles --> always a bit of contraction (esophageal and urinary bladder sphincters + blood vessels) 3. single-unit smooth muscle or unitary smooth muscle or visceral smooth musche --> around empty cavities + contract together! function as 1 unit through gap junctions! VS multiunit smooth muscles --> each muscle cell receive different neuron signals
50
do multi-unit smooth muscle cells have gap junctions? - how are they stimulated?
- no! - stimulated independently through neurotransmitters released by caricosities
51
smooth vs skeletal vs heart muscle --> which has fastest/slowest muscle twitch duration? - how fast depends on (2)
- skeletal = fastest (less than 0.5sec) - cardiac = middle (1 sec) - smooth = really slow! (5 sec) --> slow contraction AND slow relaxation! 1. ATPase (actin-myosin dissociation) 2. amount of Ca2+ --> how fast it can go in/out
52
smooth muscles lack _________ ACTIN: - ratio with myosin? - associated with _______ but not _________ MYOSIN: - filaments are _________ - myosin heads along what? SR: - amount of SR _______ and is more/less organized - no _________ but has _________
- sarcomeres! ACTIN: - 10-15 actin for 1 myosin (vs 6 actin per myosin for skeletal) - with tropomyosin (blocks myosin binding site) but not troponin MYOSIN: - longer! - entire surface of filament covered with myosin heads SR: - amount varies and is less organized - no t-tubules but has caveolae (indentation in plasma membrane, has lots of Ca2+)
53
how do smooth muscles hold integrity if no sarcomeres?
have an extensive cytoskeleton --> intermediate filaments and dense bodies
54
do smooth muscles have a z-line? where do actins attach?
no z-line - actins attach to dense bodies which links to plasma membrane
55
explain contraction of smooth muscle (5 steps)
1. Autonomic nervous system --> AP opens Ca2+ channels on plasma membrane 2. increase in cytosolic Ca2+ initiates contraction (Ca2+ comes from SR and extracellular fluid) 3. Ca2+ binds calmodulin 4. Ca2+-calmodulin activates myosin light chain kinase (MLCK) --> MLCK phosphorylates Myosin light chain which enhances myosin ATPase activity (myosin become active) 5. phosphorylated MLC can remove tropomyosin --> myosin can bind actin and induce contraction = increase muscle tension
56
Explain relaxation in smooth muscle (10)
1. free Ca2+ in cytolsol decreases when Ca2+ is pumped out of cell or back into SR 2. Ca2+ unbinds from calmodulin. MLCK activity decreases 3. myosin phosphatase/myosin light chain phosphorylase (MLCP) removes phosphate from myosin light chains, which decreases myosin ATPase activity --> dephosphorylated myosin may remain attached to actin for a period of time during latch state 5. less myosin ATPase activity results in decreased muscle tension = relaxation
57
what controls Ca2+ sensivity in smooth muscle contraction? - low vs high = sensitize or desensitizes myosin?
myosin light chain phosphorylase (MLCP) (same as phosphatase) - low phosphatase activity sensitizes myosin --> needs less calcium to generate force - high phosphatase activity desensitizes myosin --> needs more calcium to generate force
58
what is calmodulin?
a calcium binding protein that binds to calcium and activates myosin light chain kinase
59
4 channels to release sarcoplasmic Ca2+
1. ryanodine receptor (RyR) calcium release channel 2. IP3 - receptor channel 3. calcium-induced calcium release (CICR) --> Ca from outside cell can induce Ca release from SR 4. store-operated Ca2+ channels (on plasma membrane)
60
electromechanical coupling vs pharmacomechanical coupling
- electromechanical coupling --> contraction caused by electrical signaling - pharmacomechanical coupling --> contraction caused by chemical signaling
61
3 ways for calcium to enter cell membrane (from extracellular fluid)
1. voltage-gated Ca2+ channels (opens when AP from ANS comes) 2. ligand gated Ca2+ channels (opens when hormones come) or receptor-operated calcium channels (ROCC) 3. stretch activated calcium channels --> open when pressure or other force distorts cell membrane (ie blood vessel stretching) --> myogenic contraction
62
what are 2 types of unstable membrane potentials?
1. slow wave potential --> not stable resting membrane potential --> once it reaches threshold, activates AP 2. pacemakker potentials: unstable but will always reach threshold and induce AP (mostly in cardiac muscle)
63
where does the extra Ca2+ go after contraction? - consequence? (3 steps)
- goes back to extracellular fluid (and not SR) - SO we need to replenish depleted Ca2+ stores of SR --> use store-operated Ca2+ channels that are on plasma membrane --> will increase Ca2+ entry from ECF and replenish SR
64
- 2 similarities between cardiac and skeletal muscle (shape/structure) - 3 differences between cardiac and skeletal muscle
SIMILARITIES: - striated - sarcomere structure DIFFERENCES: - cardiac muscle fibers are shorter - cardiac muscles may be branched - cardiac muscle have single nucleus
65
- 3 similarities btw cardiac and smooth muscles (function/properties) - 1 difference
SIMILARITIES: - electrically linked to one another (just like single unit smooth muscles --> gap junctions! - some exhibit pacemaker potentials - under sympathetic and parasympathetic control as well as hormone control DIFFERENCES: - cardiac muscle: gap junctions in intercalated disks!
66
desmosome vs gap junction vs intercalated disk?
- desmosome = connecting junction --> links 2 cells together, allows some flow of (nutrients/water?) between cells - gap junction: forms channel between 2 muscle cells to electrical signal can quickly move between cells - intercalated disk --> junction between 2 cells --> contains desmosome and gap junctions!
67
excitation-contraction coupling in cardiac contractile cells (7 steps)
1. AP in cardiac contractile cell --> travels down T-tubules 2. entry of small amount of Ca2+ from ECF through L-type Ca2+ channels --> induces release of large amount of Ca2+ from SR through ryanodine Ca2+ release channels 3. increase cytosolic Ca2+ 4. troponin-tropomyosin complex in thin filaments pulled aside 5. cross-bridge cycling between thick and thin filaments 6. thin filaments slide inwards between thick filaments 7. contraction