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MUSCLE TYPES. Skeletal. Smooth. Cardiac. OVERVIEW. Skeletal and smooth muscle cells are elongated
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1. MUSCLES AND MUSCLE TISSUE
2. MUSCLE TYPES Skeletal Smooth
3. OVERVIEW Skeletal and smooth muscle cells are elongated
“Muscle fibers”
Muscle contraction depends on two kinds of myofilaments
Actin fibers
Myosin fibers
4. SKELETAL MUSCLES Skeletal muscles
Tissue packaged into organs
Skeletal muscle fibers longest muscle cells
Striated
Obvious stripes due to overlapping of filaments
Contraction involves movement of filaments
Voluntary control
Voluntary muscles
Only type of muscle subject to conscious control
5. CARDIAC MUSCLES Cardiac muscles
Tissue packaged into organs
Present only in heart
Constitutes bulk of heart wall
Striated
Obvious stripes due to overlapping of filaments
Contraction involves movement of filaments
Involuntary
Involuntary muscles
Not subject to conscious control
6. SMOOTH MUSCLES Smooth muscles
Tissue packaged into organs
Present in walls of hollow visceral organs
Forces substances through internal body channels
Nonstriated
Filaments present, but no stripes apparent
Involuntary
Involuntary muscles
Not subject to conscious control
7. MUSCLE CHARACTERISTICS Excitability (Irritability)
Ability to receive and respond to a stimulus
e.g., chemical, pH change, etc.
Response is generation of an electrical impulse
Contractility
Ability to shorten forcibly when stimulated
Extensibility
Ability to be stretched/extended when relaxed
Elasticity
Ability of muscle fiber to recoil and resume resting length after being stretched
8. MUSCLE FUNCTIONS Produce movement
Most movements result of muscular contraction
Movement of body and within body
Maintain posture
Muscles continuously active
Stabilize joints
Major force stabilizing many joints
Generate heat
Contraction generates heat
Heat required to maintain constant body temperature
9. SKELETAL MUSCLE Gross Anatomy
Each skeletal muscle is a discrete organ
Composed of several kinds of tissues
Skeletal muscle fibers
Blood vessels
Nerve fibers
Connective tissue
10. SKELETAL MUSCLE Gross Anatomy: Nerve & Blood Supply
Muscle served by
Single nerve
Single artery
One or more veins
All branch profusely through connective tissue sheaths
11. SKELETAL MUSCLE Gross Anatomy: Connective Tissue Sheaths
Individual muscle fibers wrapped and held together by multiple connective tissue sheaths
Endomysium
Perimysium
Epimysium
Support each cell and reinforce muscle
12. SKELETAL MUSCLE Gross Anatomy: Connective Tissue Sheaths
Endomysium
Surround each individual muscle fiber
Fibers mainly reticular fibers
13. SKELETAL MUSCLE Gross Anatomy: Connective Tissue Sheaths
Perimysium
Fibrous connective tissue
Surrounds bundles wrapped muscle fibers
Endomysium-wrapped bundles are “fasicles”
14. SKELETAL MUSCLE Gross Anatomy: Connective Tissue Sheaths
Epimysium
Dense irregular connective tissue
Surrounds entire muscle
15. SKELETAL MUSCLE Gross Anatomy: Connective Tissue Sheaths
All connective tissue sheaths are continuous with each other and with tendons
Muscle fibers contract ?
Contraction pulls on sheaths ?
Sheaths transmit force to bones ?
Bones move
Contribute to natural elasticity of muscle tissue
16. SKELETAL MUSCLE Gross Anatomy: Muscle Attachments
Skeletal muscles span joints
Attachment to bones in two places
Insertion
More movable bone
Origin
Less movable bone
17. SKELETAL MUSCLE Gross Anatomy: Muscle Attachments
Direct attachments
Epimysium is attached to the bone’s periosteum
Indirect attachments
More common than direct attachments
Smaller, more durable
Connective tissue sheaths extend beyond the muscle
Rope-like tendon
Sheet-like aponeurosis
Anchors muscle to the connective tissue covering of a bone, cartilage, or the fascia of another muscle
18. SKELETAL MUSCLE Microscopic Anatomy: Skeletal Muscle Fiber
Long, cylindrical cell
10 – 100 mm width
~10X that of average body cell
Up to 30 cm length
Plasma membrane is termed “sarcolemma”
Cytoplasm is termed “sarcoplasm”
19. SKELETAL MUSCLE Microscopic Anatomy: Skeletal Muscle Fiber
Sarcoplasm
Large amounts of stored glycogen
“Glycosomes”
Large amount of myoglobin
Oxygen-storing pigment similar to hemoglobin
Hemoglobin genes descended from duplicated ancestral myoglobin gene
“Molecular evolution”
What is the function of these two components?
20. SKELETAL MUSCLE Microscopic Anatomy: Skeletal Muscle Fiber
Organelles
The usual organelles are present
Multiple nuclei beneath sarcolemma
Skeletal muscles are syncytia, fusions of hundreds of embryonic cells
Myofibrils
Sarcoplasmic reticulum
T-tubules
21. SKELETAL MUSCLE Microscopic Anatomy: Skeletal Muscle Fiber
Myofibrils
Many myofibrils densely packed in each muscle cell
More than 105 per cell
80% of cell volume
Run parallel to length of cell
Diameter of 1-2 mm
Contain contractile elements
22. SKELETAL MUSCLE Microscopic Anatomy: Myofibrils
Striations
Repeating pattern of dark and light bands
Dark “A bands”
Light “I bands”
Near-perfect alignment of bands between myofibrils gives entire cell striped appearance
23. SKELETAL MUSCLE Microscopic Anatomy: Myofibril Striations
A-bands (dark bands)
Lighter stripe in center
“H-zone”
Bisected by M line
I-bands (light bands)
Bisected by Z disc
Sarcomere
Region of a myofibril between two Z discs
24. SKELETAL MUSCLE Microscopic Anatomy: Myofibril Striations
Sarcomere
Region of a myofibril between two Z discs
A band flanked by half of an I band on each end
~2 mm long
Smallest contractile unit of a muscle fiber
Myofibril consists of linked sarcomeres
25. SKELETAL MUSCLE Microscopic Anatomy: Myofibril Striations
Banding pattern results from an orderly arrangement of thick (myosin) and thin (actin) filaments
Thick filaments extend entire length of A band
Thick filaments absent across I band
Z disc composed of the protein nebulin
Anchors thin filaments
M line in H zone darker due to protein strands linking adjacent thick filaments
26. SKELETAL MUSCLE Microscopic Anatomy: Thick Filaments
Composed mainly of ~200 myosin molecules
Rod-like tail
Two interwoven polypeptide chains
Form central part of thick filament
Globular heads
Present on ends of thick filaments
“Business end” of myosin
Cross bridges linking thick filaments to thin filaments during contraction
27. SKELETAL MUSCLE Microscopic Anatomy: Thin Filaments
Composed mainly of the protein actin
Possess sites to which myosin heads bind during contraction
Also contains regulatory proteins
Tropomyosin
Surround and stiffen actin core
Block myosin binding sites in relaxed muscle
Troponin
Three-polypeptide complex
TnI: inhibitory subunit
TnT: helps position tropomyosin on actin
TnC: binds to Ca2+
28. SKELETAL MUSCLE Microscopic Anatomy: Other Filaments
Elastic filaments
Comprised of the giant protein titin
Extends from Z disc to the thick filament
Functions
Holds thick filaments in place
Resists excessive stretching
Assists the muscle cell in springing back into shape after being stretched
29. SKELETAL MUSCLE Microscopic Anatomy: Sarcoplasmic Reticulum
Elaborate smooth endoplasmic reticulum
Interconnecting tubules loosely surround each myofibril
Regulates intracellular Ca2+ levels
Stores Ca2+
Ca2+ released on demand during stimulation
30. SKELETAL MUSCLE Microscopic Anatomy: T Tubules
Invagination of plasma membrane (sarcolemma)
Elongated tube penetrating cell interior
Intimate contact with SR
Electrical impulses traveling along sarcolemma also travel along T tubules
Conduct impulses to deepest regions of muscle
Transmit to every sarcomere
Impulses signal Ca2+ release from SR
31. SKELETAL MUSCLE Sliding Filament Model of Contraction
During contraction, thin filaments slide past thick filaments
Involves activation of myosin’s cross bridges
Increases overlap between actin and myosin
Relaxed muscle: slight overlap
Stimulated muscle: increased overlap
32. SKELETAL MUSCLE Sliding Filament Model of Contraction
How do filaments slide?
Each myosin cross bridge attaches and detaches several times during a contraction
Ratcheting action generates tension
Thin filaments propelled toward center of sarcomere
Occurs simultaneously in all sarcomeres throughout the cell
Not all cells of the muscle
Cell shortens
33. MUSCLE PHYSIOLOGY Excitation - Contraction Coupling
Muscle contraction requires stimulation by nerve
Electrical current is propagated
“Action potential”
Intracellular Ca2+ rises
Contraction is triggered
34. MUSCLE PHYSIOLOGY Neuromuscular Junction
Skeletal muscles stimulated by motor neurons
Components of somatic nervous system
Nerves “reside” in brain or spinal cord
Threadlike extensions travel to muscle cells
“Axon”
Divides profusely as it enters the muscle
Each axonal ending forms branching neuromuscular junction with a single muscle fiber
Only one neuromuscular junction per muscle fiber
35. MUSCLE PHYSIOLOGY Neuromuscular Junction
Axonal ending and muscle fiber very close
Not touching
1 – 2 nanometers (nm) apart
Separating space termed “synaptic cleft”
Gel-like extracellular substance rich in glycoproteins
36. MUSCLE PHYSIOLOGY Neuromuscular Junction
Axonal ending contains synaptic vesicles
Membrane-enclosed sacs
Contain neurotransmitter acetylcholine (Ach)
Ach can be released into synaptic cleft by exocytosis
37. MUSCLE PHYSIOLOGY Neuromuscular Junction
Nerve impulse reaches end of axon
Voltage-gated Ca2+ channels in axonal membrane open
Ca2+ enters axon from extracellular fluid
Ca2+ influx signals exocytosis
Synaptic vesicles fuse with axonal membrane
ACh enters synaptic cleft
38. MUSCLE PHYSIOLOGY Neuromuscular Junction
Muscle cell’s sarcolemma highly infolded
“Junctional folds”
Increased surface area
Membrane rich with ACh receptors
39. MUSCLE PHYSIOLOGY Neuromuscular Junction
Released ACh diffuses across synaptic cleft
ACh binds to sarcolemma’s ACh receptors
ACh ? acetic acid and choline
Catalyzed by the enzyme acetylcholinesterase
Sarcolemma-bound enzyme
Binding triggers electrical events
Muscle ultimately contracts
40. MUSCLE PHYSIOLOGY Homeostatic Imbalance: Myasthenia Gravis
Disease characterized by a shortage of ACh receptors
Autoimmune disease
Body destroys its own Ach receptors
Interferes with neuromuscular junction events
Drooping eyelids, difficulty swallowing & talking, generalized weakness
41. MEMBRANE POTENTIAL A voltage exists across the plasma membrane
“Membrane potential”
Due to separation of oppositely charged ions
Resting potential exhibited in cell’s resting state
From -5 to -100 millivolts (mV)
Inside of cell is negative relative to outside
Cells are “polarized”
42. MUSCLE PHYSIOLOGY Neuromuscular Junction: Depolarization
Resting sarcolemma is polarized
“Resting potential”
Interior face slightly negatively charged
Binding of ACh to receptors opens ligand-gated Na+ channels
Na+ enters myofibril
K+ exits cell, but to lesser degree
Interior face of sarcolemma becomes less negative
“Depolarization”
“End plate potential” is formed
43. MUSCLE PHYSIOLOGY Action Potential
Depolarization is initially a local electrical event
End plate potential becomes action potential, which spreads rapidly along sarcolemma
Membrane areas adjacent initial depolarization become depolarized
Voltage-gated Na+ channels are activated
Na+ enters cell, initiation action potential
Depolarization wave spreads to adjacent areas, opening additional Na+ channels
Action potential results in contraction
44. MUSCLE PHYSIOLOGY Action Potential
Repolarization wave quickly follows depolarization wave
Na+ channels close
Voltage-gated K+ channels open
K+ rapidly exits myofibril
Electrical conditions of cell restored
Na+-K+ pump will restore ionic conditions
Several contractions can occur before ionic imbalances adversely impact contractile activity
45. MUSCLE PHYSIOLOGY Action Potential
Muscle cannot be stimulated again until repolarization is complete
“Refractory period”
46. MUSCLE PHYSIOLOGY Excitation-Contraction Coupling
Action potential propagates along sarcolemma
Transmitted down T tubules
Brief (1-2 milliseconds [ms])
Ends prior to visible signs of contraction
AP triggers SR to release Ca2+ into sarcoplasm
Ca2+ channels opened
47. MUSCLE PHYSIOLOGY Excitation-Contraction Coupling
Ca2+ binds to troponin TnC
Shape altered, blocking action of tropomyosin removed
Myosin heads attach to thin filaments
“Ratcheting” pulls thin filaments toward center of sarcomere
48. MUSCLE PHYSIOLOGY Excitation-Contraction Coupling
Ca2+ actively pumped back into SR
Ca2+ signal ends within ~30 ms
Tropomyosin blockade reestablished
Cross bridge activity ends
Relaxation occurs
49. MUSCLE PHYSIOLOGY Excitation-Contraction Coupling
Repeat
Requires additional nerve impulse
When nerve impulses are delivered rapidly
Ca2+ levels increase greatly
Muscle cells do not completely relax between stimuli
Contraction is stronger and more sustained
50. MUSCLE PHYSIOLOGY Sarcoplasmic Ca2+ Concentrations
Sarcoplasmic Ca2+ levels are very low
Phosphate levels in sarcoplasm are higher
Ca2+ and PO43- react to form crystals
These crystals would kill the cell
Ca2+ and PO43- must be kept separated
Intracellular Ca2+ is tightly regulated by proteins
e.g., calsequestrin, calmodulin
51. MUSCLE PHYSIOLOGY Muscle Fiber Contraction
Cross bridge attachment of actin requires Ca2+
Low intracellular Ca2+
Muscle cell is relaxed
Myosin binding sites on actin are physically blocked by tropomyosin molecules
Rising Ca2+ levels
Ca2+ ions bind to regulatory sites on troponin TnC
TnC shape changes
Tropomyosin removed from binding site
Binding sites on actin are exposed
52. MUSCLE PHYSIOLOGY Muscle Fiber Contraction
Once binding sites on actin are exposed:
Myosin head is already “cocked”
Cocking fueled by hydrolysis of bound ATP molecule
ADP & Pi remain covalently bound to myosin
53. MUSCLE PHYSIOLOGY Muscle Fiber Contraction
Once binding sites on actin are exposed:
Cross bridge formation
Myosin heads attach to binding sites
Approximately half of the myosin heads on a given thick filament are bound at any given time
54. MUSCLE PHYSIOLOGY Muscle Fiber Contraction
Once binding sites on actin are exposed:
Power stroke
Myosin head pivots, moving through 70o angle
ADP & Pi released from myosin
55. MUSCLE PHYSIOLOGY Muscle Fiber Contraction
Once binding sites on actin are exposed:
Cross bridge detachment
New ATP molecule covalently binds to myosin head
Myosin and actin disassociate
56. MUSCLE PHYSIOLOGY Muscle Fiber Contraction
Once binding sites on actin are exposed:
Myosin head is again “cocked”
Repeat ~30 times or more during a muscle contraction
Continues as long as Ca2+ and ATP concentrations are sufficient
57. MUSCLE PHYSIOLOGY Muscle Fiber Relaxation
As Ca2+ pumps of the SR reclaim Ca2+
Troponin again changes shape
Myosin binding sites on actin again blocked by tropomyosin
Contraction ends
Muscle fiber relaxes
58. MUSCLE PHYSIOLOGY Muscle Fiber Contraction: Rigor Mortis
Muscles begin to stiffen 3 – 4 hours after death
Peak rigidity at ~12 hours
Dying cells are unable to exclude Ca2+
Intracellular [Ca2+] normally low
Ca2+ influx promotes formation of cross bridges
What step requires ATP binding?
How much ATP is made by dead cells?
Why don’t the muscles relax?
59. MUSCLE PHYSIOLOGY Contraction of a Skeletal Muscle
A skeletal muscle consists of many muscle cells
Principles governing the contraction of a muscle fiber and of a skeletal muscle are similar
All contractions are not equal
In response to different stimuli, muscles contract
With varying force
For varying periods of time
60. MUSCLE PHYSIOLOGY Contraction of a Skeletal Muscle
Muscle tension
The force exerted by a contracting muscle
Load
The opposing force exerted by the weight of the object being moved
Isometric contraction
Muscle tension develops, but load is not moved
Isotonic contraction
Muscle tension developed overcomes the load
Muscle shortening occurs
61. MUSCLE PHYSIOLOGY Each muscle is served by one or more motor nerves
Consist of axons of hundreds of motor neurons
The axon of each motor neuron branches upon entering muscle
Each branch ends at a neuromuscular junction
62. MUSCLE PHYSIOLOGY Motor Unit
A single motor neuron and its associated muscle fibers
From four to hundreds of muscle fibers per motor unit
Multiple motor units per muscle
Not clustered within muscle
Firing of motor neuron causes contraction of all muscle fibers in motor unit
Not all muscle fibers of muscle
Entire muscle contracts
More motor units = stronger contraction
63. MUSCLE TWITCH Response of motor unit to single action potential
Three phases
Latent period
Few msec following stimulation
Muscle tension begins to increase
Period of contraction
10 – 100 msec
Cross bridges are active
Tension develops, muscle may shorten
Period of relaxation
10 – 100 msec
Initiated by reentry of Ca2+ into SR
Muscle tension decreases to zero
64. MUSCLE TWITCH Twitch contractions of some muscles are rapid and brief
e.g., muscles controlling eye movement
Some muscles contract more slowly and remain contracted for longer periods
e.g., calf muscles
65. GRADED RESPONSES Normal muscle contractions
Not jerky
Relatively smooth
Vary in strength based on demand
“Graded muscle responses”
Graded muscle responses achieved by
Altering the frequency of stimulation
Altering the strength of the stimulus
66. GRADED RESPONSES Changes in Stimulation Frequency
Two stimuli in rapid succession
Second twitch will be stronger than the first
Appears to “ride on shoulders” of first
“Wave summation”
Second contraction occurs before the muscle is completely relaxed following the first contraction
Second contraction causes more shortening that first
67. GRADED RESPONSES Changes in Stimulation Frequency
Multiple stimuli in rapid succession
Relaxation time between twitches shortens
Sarcoplasmic [Ca2+] increases
Degree of summation increases
Quivering contraction termed “incomplete tetanus”
a.k.a., “unfused tetanus”
68. GRADED RESPONSES Changes in Stimulation Frequency
Multiple stimuli in rapid succession
Relaxation time between twitches shortens
Sarcoplasmic [Ca2+] increases
Degree of summation increases
Quivering contraction termed “incomplete tetanus”
Ultimately fused into smooth “complete tetanus”
69. GRADED RESPONSES Response to Stronger Stimuli
Wave summation increases contractile force
Main function is to produce smooth, continuous contractions
Force of contraction increased by “multiple motor unit summation”
Threshhold stimulus recruits first motor units
Maximal stimulus recruits all of a muscle’s motor units
70. GRADED RESPONSES Smallest motor units
Fewest and smallest muscle fibers
Controlled by small, highly excitable motor neurons
Tend to get activated first
Larger motor units
Contain large, coarse muscle fibers
Controlled by larger, less excitable motor neurons
Activated only when a stronger contraction is necessary
DON’T REALLY DO THIS, JUST PRETEND!!!!!
Caress your neighbor, then slap him/her.
What motor units are you activating?
71. GRADED RESPONSES Treppe
Why do muscle contractions become slightly stronger with each successive stimulus during the initial phases of muscle activity?
Increasing sarcoplasmic [Ca2+]
More binding sites exposed
More heat liberated
Enzymes work more efficiently
Muscles become more pliable
72. MUSCLE TONE Relaxed skeletal muscles are always slightly contracted
This state is termed “muscle tone”
Stretch receptors in muscles and tendons are activated
Spinal reflexes continually activate an alternating subset of motor neurons
No active movement produced
Mucles kept firm, healthy, and ready to respond to stimulation
Helps stabilize joints and maintain osture
73. ISOTONIC CONTRACTIONS Muscle length changes and moves the load
Cross bridges are moving thin filaments
Once tension is sufficient to move load, tension remains relatively constant
Two types
Concentric contractions
Muscle shortens and does work
Eccetric contractions
Muscle contracts as it lengthens
e.g., calf muscle while walking up a hill
More forceful than concentric contractions
74. ISOMETRIC CONTRACTIONS Tension builds but muscle length remains constant
Muscle attempts to move a load greater than the force the muscle is able to develop
(Try to lift your car or push this building over)
Cross bridges are generating force but are not moving the thin filaments
75. MUSCLE METABOLISM Muscular contraction requires energy
Actually, they require TONS of energy
Energy for the movement of the cross bridges
Energy for the operation fo the calcium pump
Energy sources
Stored ATP
Creatine phosphate
Aerobic respiration
Fermentation
76. MUSCLE METABOLISM Stored ATP
ATP provides the energy for
Movement of the cross bridges
Operation of the calcium pump
ATP reserves provide this ATP for a little while
Reserves depleted in 4 – 6 seconds at most
How is this ATP get regenerated?
77. MUSCLE METABOLISM Phosphorylation of ADP by Creatine Phosphate
Creatine phosphate is a high-energy molecule stored in muscle
Amount stored exceeds ATP reserves
Phosphate readily transferred to ADP
ADP + creatine-P ? ATP + creatine
(A-P-P + creatine-P ? A-P-P-P + creatine)
Creatine phosphate provides ATP for a while
Creatine phosphate deplete in up to 10 – 15 seconds
Now what do we do?
78. MUSCLE METABOLISM Aerobic Respiration
Provides most of the ATP during rest and light to moderate exercise
Sugar +O2 ? ATP + CO2 + H2O
Provides ~36 ATP molecules per glucose
Sugar
Easily liberated from glycogen stored in muscle
Present in blood
Can be replaced by other fuels (e.g., fatty acids, amino acids)
Oxygen
Carried by hemoglobin in blood
Stored by myoglobin in muscle
Ultimately limits aerobic respiration
79. MUSCLE METABOLISM Fermentation
Does not require O2
Aerobic respiration does require O2
Much less efficient than aerobic respiration
2 ATP per sugar as opposed to 30-something
Faster than aerobic respiration
Important early in strenuous exercise
Glycolysis occurs as usual
Glucose ? 2 pyruvate + 2 ATP + 2 NADH
Pyruvate is reduced to form lactic acid
Process regenerates NAD+ (which is required for glycolysis)
Pyruvate + 2 NADH ? lactic acid + 2 NAD+
80. MUSCLE METABOLISM Order of use of the various energy sources
Stored ATP
Creatine phosphate
Fermentation
Aerobic respiration
Fermentation
81. MUSCLE FATIGUE O2 ultimately becomes limiting
ATP use exceeds ATP production
Intracellular [lactic acid] increases
Intracellular pH drops
Ionic imbalances occur (e.g., K+, Ca2+)
Muscles contract less effectively
Muscles ultimately become physiologically unable to contract even when receiving stimuli
“Muscle fatigue”
Do cardiac muscles experience fatigue?
Why or why not?
82. OXYGEN DEBT For a muscle to return to its resting state
Lactic acid must be removed
O2 reserves must be replenished
ATP reserves must be replenished
Creatine phosphate must be replenished
The amount of oxygen required for these processes is termed the oxygen debt
Represents the difference between the amount of O2 needed for aerobic muscle activity and the amount of O2 actually used
All non-aerobic sources of ATP contribute to debt
83. HEAT PRODUCTION Heat production is an incidental consequence of muscle contraction
~40% of the energy released during muscle contraction is converted to useful work
Remainder is given off as heat
This heat is used to maintain a constant body temperature
Excess heat is shed
Do you remember how?
Shivering produces additional heat when required
84. FORCE OF CONTRACTION Force of muscle contraction is affected by
Number of muscle fibers stimulated
More motor units = greater force
Relative size of fibers
Larger fibers produce greater force
Regular exercise causes muscle fiber hypertrophy
Frequency of stimulation
Force transferred from muscle to load
Repeated stimulations produce sustained contraction
Transfer more complete during sustained contractions
Degree of muscle stretch
Greatest force when muscle is slightly stretched
85. CONTRACTION Velocity and Duration of Contraction
Affected by load
Faster contractions with no added load
Greater load causes:
Longer latent period
Slower contraction
Shorter contraction duration
Affected by recruitment
More motor units ? faster & more prolonged contractions
Affected by muscle fiber type
Detailed on next image
86. CONTRACTION Velocity and Duration of Contraction
Classification of muscle type by major ATP formation pathways
Oxidative fibers
Rely mainly on aerobic pathways for ATP generation
Glycolytic fibers
Rely mainly on fermentation for ATP generation Classification of muscle type by speed of contraction
Slow fibers vs. fast fibers
Differences reflect speed enzymatic hydrolysis of ATP
Slow oxidative fibers
Fast oxidative fibers
Fast glycolytic fibers
87. EFFECTS OF EXERCISE Muscles change in response to the amount of work they do
e.g., active muscles may increase in size and strength
e.g., inactive muscles atrophy
88. EFFECTS OF EXERCISE Effects of aerobic (endurance) exercise
(e.g., swimming, jogging, etc.)
Increased # of capillaries surrounding muscle fibers
Increased number of mitochondria in muscle fibers
Increased myoglobin synthesis
Most dramatic changes in slow oxidative fibers
Changes result in
More efficient muscle metabolism
Greater endurance and strength
Greater resistance to fatigue
NO significant muscle hypertrophy
89. EFFECTS OF EXERCISE Effects of resistance exercise
(e.g., weight lifting, etc.)
Significant muscle hypertrophy
Individual muscle fibers increase in size
Increase in number of mitochondria in muscle fibers
Increase in number of myofilaments in muscle fibers
Increased amount of connective tissue in muscle
90. SMOOTH MUSCLE Present in the walls of all hollow organs
(Not including the heart)
Contractions similar to those of skeletal muscle
Smooth muscle has several differences
91. SMOOTH MUSCLE Spindle-shaped cells
Smaller than skeletal muscle cells
2 – 5 micrometer diameter
100 – 400 micrometer length
Single, centrally located nucleus
Lack coarse connective tissue sheaths
Possess small amount of fine connective tissue (endomysium) secreted by muscle cells
Vascular, innervated
92. SMOOTH MUSCLE Generally organized into two sheets
Fibers organized perpendicular to each other
Why are no striations visible?
Alternating contraction and relaxation of opposing layers mixes and moves substances in organ’s lumen
“Peristalsis”
93. SMOOTH MUSCLE Lacks highly structured neuromuscular junctions
Possess “diffuse junctions”
Neurotransmitter released into wider area
Sarcoplasmic reticulum less developed
T-tubules absent
Sarcolemma posesses Ca2+-containing infoldings
“Caveoli”
94. SMOOTH MUSCLE Organization of filaments differs
No sarcomeres
Thick:thin ratio 1:13, not 1:2
Thick filaments longer than skeletal counterparts
Myosin heads on entire length of thick filaments
Tropomyosin present, troponin absent
Filaments arranged diagonally *
Contain noncontractile intermediate filaments
Resist tension
Attach to “dense bodies”
95. SMOOTH MUSCLE Slow, synchronized contractions
Entire sheet responds to stimulus in unison
Electrically coupled via gap junctions
Some fibers in stomach and small intestine act as “pacemakers”
Set contraction pace for other cells
Some are self-excitatory
Contract even without external stimulus
Contract in response to neuronal or hormonal stimuli