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Skeletal muscle
Appearance: Striated (striped)
Nuclei: Many nuclei per cell (multinucleated), nuclei at periphery
Location: Attached to bones
Special features:
Long, cylindrical fibers
Voluntary control
No branching
Cardiac muscle
Appearance: Striated
Nuclei: Usually 1 (sometimes 2), central nucleus
Location: Heart only
Special features:
Branched cells
Intercalated discs (gap junctions + desmosomes)
Involuntary, rhythmic contraction
Smooth muscle
Appearance: Non-striated (smooth)
Nuclei: Single, central nucleus
Location: Walls of organs (intestines, blood vessels, bladder)
Special features:
Spindle-shaped cells
Involuntary
No branching or intercalated discs
levels of muscle organization
Muscle (organ level) → made of bundles of fascicles
Fascicle → bundle of muscle fibers (cells)
Muscle fiber / muscle cell → a single long muscle cell
Myofibril → thread-like structures inside a muscle fiber; made of repeating units
Sarcomere → basic contractile unit of a myofibril (repeats along the myofibril)
Myofilament → protein filaments inside sarcomeres (actin + myosin)
Why Striations Exist
Striations come from the repeating pattern of sarcomeres:
A bands (dark): thick + thin overlap
I bands (light): thin only
Z lines: boundaries of sarcomeres
👉 The aligned arrangement of actin and myosin creates visible stripes.
Thick vs Thin Filaments
Thick filament (myosin)
Made of myosin protein
Has:
Head: binds actin + uses ATP
Tail: structural support
Function:
Pulls actin during contraction
Thin filament
Made of:
Actin (F-actin): binding site for myosin
Tropomyosin: blocks binding sites
Troponin: calcium-binding switch protein
Function:
Regulates contraction + provides binding sites
Steps of Muscle Contraction (from neuron to relaxation)
Action potential reaches motor neuron terminal
Acetylcholine (ACh) released
ACh binds receptors on muscle fiber
Muscle membrane depolarizes → muscle action potential
Signal travels along T-tubules
Sarcoplasmic reticulum releases Ca²⁺
Ca²⁺ binds troponin → moves tropomyosin
Myosin binds actin (cross-bridge forms)
Power stroke pulls actin → contraction
ATP binds myosin → detaches actin
Calcium is pumped back into SR
Muscle relaxes
role of calcium in contraction of a skeletal muscle.
Calcium is the ON switch for contraction:
Stored in sarcoplasmic reticulum
Released when muscle is stimulated
Binds troponin
Causes tropomyosin to move
Exposes actin binding sites
👉 Without Ca²⁺ → no contraction
Role of ATP
ATP is required for:
Detaching myosin from actin
ATP binds myosin → breaks cross-bridge
Powering the myosin head
ATP hydrolysis “cocks” myosin head
Calcium removal
ATP pumps Ca²⁺ back into SR
👉 Without ATP → muscle stays locked (rigor)
Effects of Sarcomere Contraction
During event:
I band gets smaller
H zone disappears
Z lines move closer together
A band stays the same length
👉 Filaments do NOT shorten— they slide past each other (sliding filament theory)
Identify the phases of a muscle twitch and match them to the events of contraction.
1. Latent period
Action potential spreads
Ca²⁺ released
No visible contraction yet
2. Contraction phase
Cross-bridges form
Myosin pulls actin
Muscle shortens
3. Relaxation phase
Ca²⁺ pumped back into SR
Cross-bridges stop forming
Muscle returns to resting length
Wave (twitch) summation
Repeated stimuli before full relaxation
Ca²⁺ stays elevated → stronger contraction
👉 Force increases with each stimulus
Tetanus
Rapid, continuous stimulation
No relaxation between twitches
👉 Results in sustained, maximal contraction
Recruitment
(multiple motor unit summation)
Increasing number of motor units activated
👉 More fibers contracting = stronger force
Isotonic contraction
muscle changes length but tentnus is constant (normal)
Concentric
Muscle shortens
Example: lifting a weight
(Isotonic)
Eccentric
Muscle lengthens while contracting
Example: lowering a weight slowly (Isotonic)
Isometric contraction
Muscle does NOT change length
Tension increases but no movement
Example: holding a weight still
Wave summation
tapping a muscle repeatedly → stronger contractions
Tetanus
holding a heavy object steady (continuous contraction)
Concentric isotonic
lifting a dumbbell
Eccentric isotonic
lowering a dumbbell
Isometric
plank, wall sit, holding a book still
Isometric
plank, wall sit, holding a book still
Motor Unit
One motor neuron + all the muscle fibers it controls
Gradation of Muscle Tension
You control strength in 2 main ways:
1. Recruitment
Activate more motor units → stronger force
2. Frequency of stimulation
Increase impulse rate → summation → tetanus
👉 Light tap = few motor units + low frequency
👉 Strong hit = many motor units + high frequency
Direct phosphorylation
Very fast
Uses creatine phosphate (CP)
Lasts ~10–15 seconds
No oxygen needed
(Energy Production)
Anaerobic glycolysis
Breaks down glucose → lactic acid
No oxygen required
Produces small ATP
Supports ~30–40 seconds of activity
(Energy Production)
Aerobic respiration
Uses oxygen
Occurs in mitochondria
Produces large ATP
Supports long-duration activity
(Energy Production)
Causes of Muscle Fatigue
ATP depletion
Lactic acid buildup → ↓ pH
Ion imbalances (Na⁺, K⁺, Ca²⁺)
Decreased Ca²⁺ release
Oxygen debt
Nervous system fatigue
👉 Fatigue = reduced ability to contract
(Skeletal Muscle Fibers)
Slow Oxidative (Type I)
Feature | ????? |
Speed | Slow |
Fatigue resistance | High |
Mitochondria | Many |
Blood vessels | Many |
Myoglobin | High |
Diameter | Small |
Color | Red |
Metabolism | Aerobic |
Function | Endurance (marathon) |
(Skeletal Muscle Fibers)
Fast Glycolytic (Type IIb)
Feature |
Speed |
Fatigue resistance |
Mitochondria |
Blood vessels |
Myoglobin |
Diameter |
Color |
Metabolism |
Function |
??? (Type IIa) |
Fast |
Moderate |
Moderate |
Moderate |
Moderate |
Medium |
Pink |
Aerobic + anaerobic |
Mixed activity |
(Skeletal Muscle Fibers)
Fast Glycolytic (Type IIb)
Feature |
Speed |
Fatigue resistance |
Mitochondria |
Blood vessels |
Myoglobin |
Diameter |
Color |
Metabolism |
Function |
Fast Glycolytic (Type IIb) |
Very fast |
Low |
Few |
Few |
Low |
Large |
White |
Anaerobic |
Power (sprinting, lifting) |
(Skeletal Muscle Fibers)
Fast Glycolytic (Type IIb)
Feature |
Speed |
Fatigue resistance |
Mitochondria |
Blood vessels |
Myoglobin |
Diameter |
Color |
Metabolism |
Function |
Fast Glycolytic (Type IIb) |
Very fast |
Low |
Few |
Few |
Low |
Large |
White |
Anaerobic |
Power (sprinting, lifting) |
Skeletal Muscle
Feature | ??? |
Structure | Long, cylindrical, striated, multinucleated |
Location | Attached to bones |
Energy production | All 3 (CP, anaerobic, aerobic) |
Innervation | Somatic nervous system |
Initiation of contraction | Motor neuron releases ACh |
Role of Ca²⁺ | Binds troponin |
Presence of T-tubules | Present, well-developed |
Sarcoplasmic reticulum (SR) | Highly developed |
Source of Ca²⁺ | SR only |
Mechanism of Ca²⁺ action | Ca²⁺ → troponin → moves tropomyosin → exposes actin sites |
Means of gradation (force control) | Recruitment + frequency (summation) |
Cardiac Muscle
Feature |
Structure |
Location |
Energy production |
Innervation |
Initiation of contraction |
Role of Ca²⁺ |
Presence of T-tubules |
Sarcoplasmic reticulum (SR) |
Source of Ca²⁺ |
Mechanism of Ca²⁺ action |
Means of gradation (force control) |
Cardiac Muscle |
Branched, striated, 1–2 nuclei, intercalated discs |
Heart |
Mostly aerobic |
Autonomic nervous system |
Pacemaker cells + autonomic input |
Binds troponin |
Present, less developed |
Moderately developed |
SR + extracellular fluid |
Same as skeletal |
Frequency of Ca²⁺ entry + hormonal control |
Smooth Muscle (Single Unit)
Smooth Muscle (Single Unit) |
Non-striated, spindle-shaped, single nucleus, gap junctions |
Walls of organs (intestines, uterus) |
Mostly aerobic |
Autonomic + self-excitable |
Stretch, hormones, pacemaker activity |
Binds calmodulin |
Absent |
Poorly developed |
Mostly extracellular fluid |
Ca²⁺ → calmodulin → activates MLCK → phosphorylates myosin |
Degree of stretch + Ca²⁺ levels + hormones |
Feature |
Structure |
Location |
Energy production |
Innervation |
Initiation of contraction |
Role of Ca²⁺ |
Presence of T-tubules |
Sarcoplasmic reticulum (SR) |
Source of Ca²⁺ |
Mechanism of Ca²⁺ action |
Means of gradation (force control) |
function of the muscular system
Movement of the body
Maintenance of posture
Respiration
Production of body heat
Communication
Constriction of organs and vessels
Contraction of the heart
General Properties of Muscle
Contractility
Elasticity:
Excitability:
Conductivity:
Extensibility:
Contractility:
ability of muscle to recoil to original resting length after stretched
Excitability
capacity of muscle to respond to a stimulus (from our nerves)
Conductivity:
ability to propogate
Extensibility
muscle can be stretched to its normal resting length and beyond to a limited degree
Skeletal Muscle Structure
highly vascular
well innervated
Fascia (hypodermis)
around individual muscle = epimysium
holds blood vessels and nerves
Skeletal Muscle Structure
Composed of muscle cells (fibers), connective tissue, _______, and _______.
Fibers are long, cylindrical, multinucleated
Striated appearance
Sarcomeres
highly ordered repeating units of myofilaments
Actin (Thin) Myofilaments
attached to the Z-discs on each end. Fibrous (F) actin forms a double helix attached at sarcomere.
Tropomyosin
Troponin
Actin (Thin) Myofilaments
forms a double helix attached at sarcomere.
Composed of G actin monomers each of which has an active site
Actin site can bind myosin during muscle contraction.
Tropomyosin
winds along the groove of the F actin.
Troponin
three subunits:
one binds to actin
second that binds to tropomyosin
third that binds to calcium ions.
The tropomyosin/troponin regulates the interaction actin and myosin.
Tropomyosin
winds along the groove of the F actin.
Myosin (Thick) Myofilament
Myosin heads
Can form cross-bridges.
Attached to the rod portion by a hinge region.
Are ATPase enzymes: Part of the energy from breaking down ATP is used to bend the hinge region of the myosin.
Sarcomere
The fundamental, repeating contractile unit of striated muscle fibers, bordered by Z-lines.
generates force through the sliding of actin (thin) and myosin (thick) filaments
Z disk
filamentous network of protein. Serves as attachment for actin
I bands
from Z disks to start of thick filaments
A bands:
length of thick filaments
H zone
region in A band where actin and myosin do not overlap
M line
middle of H zone; delicate filaments holding myosin in place
Motor neurons
stimulate muscle fibers to contract.
Axons branch so that each muscle fiber is innervated
Contact is neuromuscular junction
motor end plate
specialized area, part of neuromuscular junction
transverse (T) tubules
tube-like invaginations of plasma membrane that penetrate to deep part of fiber
conduct impulse rapidly through cell
Capillary beds
surround muscle fibers
Neuromuscular junction (NMJ)
axon terminal resting in an invagination of the sarcolemma
Calcium and Muscle Contraction (Skeletal Muscle)
1. Sarcoplasmic reticulum stores calcium
The sarcoplasmic reticulum (SR) stores a large amount of Ca²⁺ (calcium) inside the muscle cell.
2. Calcium is released
When the muscle receives a signal, Ca²⁺ floods out of the sarcoplasmic reticulum into the cytoplasm of the muscle cell.
3. Calcium binds troponin
The Ca²⁺ binds to a protein called troponin.
4. Troponin moves tropomyosin
When calcium binds troponin changes shape.
This pulls tropomyosin away from the binding sites on actin.
5. Actin binding sites are exposed
Normally tropomyosin blocks the actin binding sites.
When it moves away, the myosin-binding sites on actin become exposed.
6. Cross-bridge formation
Myosin heads attach to the exposed actin sites.
This attachment is called a cross-bridge.
Cross-bridges allow the muscle to contract.
Cross-Bridge Movement
The myosin head has ATP attached, which is split into ADP + a phosphate group (Pi).
The phosphate group is released, which activates the myosin head and causes it to bend.
This bending creates the power stroke, where the myosin pulls on the actin filament.
After the power stroke, ATP binds to the myosin head.
The binding of ATP causes myosin to detach from actin.
The ATP is then broken down again, which re-cocks (straightens) the myosin head so it is ready for another cycle.
This cycle repeats as long as calcium is present and ATP is available
do filaments chnage length?
Filaments do NOT change length — they slide past each other.
This causes the sarcomere to shorten, which contracts the muscle.
Sarcomere shortens during when
contraction.
what happnes to Z disks during contraction
move closer together.
what happnes to Z disks during contraction
they get closer together
what happnes to i band during contraction
I band shortens.
what happnes to H band during contraction
shortens or disappears.
What Happens to a bands during contraction
stays the same length.
Muscle Relaxation
Ca2+ moves back into sarcoplasmic reticulum by active transport. Requires atp
Ca2+ moves away from troponin-tropomyosin complex
Complex re-establishes its position and blocks binding sites.
Motor unit
a single motor neuron and all muscle fibers innervated by it
Motor Unit numbers
Large muscles have motor units with many muscle fibers.
Small muscles that make delicate movements contain motor units with few muscle fibers
Regulation of Smooth Muscle
Innervated by autonomic nervous system
Neurotransmitters are acetylcholine and norepinephrine
Hormones are epinephrine and oxytocin
Receptors present on plasma membrane
Excitation–Contraction Coupling
Excitation–Contraction Coupling is the process that links a nerve signal to muscle contraction.
Muscle Twitch
muscle contraction in response to a stimulus that causes action potential in one or more muscle fibers
Phases of Twitch
Lag or latent: Ca2+ must be released from SR
Contraction: contraction occurs
Relaxation: Ca2+ is taken up into SR
Electrical Properties of Smooth Muscle
Slow waves of depolarization and repolarization transferred from cell to cell
Depolarization caused by spontaneous diffusion of Na+ and Ca2+ into cell
Does not follow the all-or-none law
May have pacemaker cells
Contraction regulated by nervous system and by hormones
Regulation of Smooth Muscle
Innervated by autonomic nervous system
Neurotransmitters are acetylcholine and norepinephrine
Hormones are epinephrine and oxytocin
Receptors present on plasma membrane
All-or-none
law for muscle fibers;Contraction of equal force in response to each action potential
Sub-threshold stimulus
no action potential; no contraction
Multiple motor unit summation
strength of contraction depends upon recruitment of motor units. A muscle has many motor units
Submaximal stimuli
Maximal stimulus
Supramaximal stimuli
Strength of contraction is graded
ranges from weak to strong depending on stimulus strength
Treppe
Graded response
Occurs in rested muscle
Each subsequent contraction is stronger than previous until all equal after few stimuli
More and more Ca2+ remains in sarcoplasm and is not all taken up into the sarcoplasmic reticulum
Incomplete tetanus
muscle fibers partially relax between contraction
Complete tetanus
no relaxation between contractions
Multiple-wave summation
muscle tension increases as contraction frequencies increase
Maxium tension
produces maxium tension in reponse to maxium stimulus at sacomores optional length
lever systems
Muscles and their tendons and bones act together,to move either parts of the body or the whole body.
Lever
rigid shaft or bone
Fulcrum:
pivot point or joint
Weight or resistance
(force of gravity either in the form of the weight of the body parts or the weight of an object being lifted, pulled, or pushed)
Active tension
force applied to an object to be lifted when a muscle contracts
Stretched muscle
not enough cross-bridging
Crumpled muscle
myofilaments crumpled, cross-bridges can't contract
Passive tension
tension applied to load when a muscle is stretched but not stimulated
Total tension
active plus passive
Muscle Tone
Alternating contractions in motor units stimulated by spinal reflexes
gives firmness to relaxed muscle without movement
keeps muscle healthy, ready to respond
important to posture