A primary tissue type consisting of three types:
Skeletal muscle (voluntary)
Cardiac muscle (involuntary)
Smooth muscle (involuntary)
my/o
(e.g., myosatellite cells, which are stem cells for muscle tissue)
sarc/o
(e.g., sarcomere, the basic functional unit of muscle fibers)
Know the shape of each muscle type.
Note whether they are uninucleate or multinucleate.
Understand the role of intercalated discs (in cardiac muscle).
Identify whether they are striated or non-striated.
Cells are specialized for contraction via myofilaments (proteins for contraction).
Skeletal muscles move the body by pulling on bones.
Cardiac and smooth muscles control internal movements (involuntary).
Proteins of contraction include troponin and tropomyosin.
Excitability (responsiveness): Ability to respond to a stimulus, generating an action potential.
Contractility: Ability of cells to shorten when stimulated.
Extensibility: Ability to stretch.
Elasticity: Ability to recoil to the original shape.
Voluntary, controlled by the somatic nervous system.
Made of fibers containing actin and myosin for contraction.
Actin and myosin form cross-bridges during contraction.
Contains connective tissue (tendons, aponeurosis), blood vessels (O2 supply), and nerves.
Epimysium: Outermost layer.
Perimysium: Middle layer containing fascicles (bundles of muscle fibers).
Endomysium: Innermost layer.
Myoblasts fuse with myosatellite cells to form mature muscle fibers.
Some myosatellite cells remain for muscle growth and repair.
Sarcolemma
Transverse tubules (T-tubules)
Terminal cisternae
Sarcoplasmic reticulum (SR)
Sarcoplasm
Aerobic respiration: Involves O2 (cellular respiration).
Anaerobic respiration: Does not involve O2 (lactic acid fermentation, causing cramps).
Tendons (bundles)
Aponeurosis (sheets) that attach bones to other muscles. Stabilizes forces distributed across muscles.
Sprain: Overstretched or torn tendon or ligament.
Shape: Cylindrical or tubular
Appearance: Striated ("stripes")
Control: Voluntary
Nuclearity: Multinucleate (several nuclei per cell)
Cell Division: No mitosis; myosatellite cells facilitate growth via protein synthesis.
Myoblasts: Formed during embryonic development.
Combine with myosatellite cells to form mature muscle fibers.
Sarcoma or myosarcoma
Smallest functional unit of a muscle fiber.
Interactions between filaments (actin and myosin) produce contraction.
A bands: Dark bands, thick filaments (myosin).
I bands: Light bands, thin filaments (actin).
Contraction occurs when actin and myosin interact, forming cross-bridges.
Plasma membrane of a muscle fiber.
Separates the outside from the inside of the cell.
Surrounds the sarcoplasm (cytoplasm of a muscle fiber).
Changes in membrane potential initiate contractions.
Action potentials trigger contractions.
Resting membrane potential: Natural state with no contraction.
-70 MV (millivolts)
Due to differences in sodium and potassium ion concentrations.
Contraction: −70 MV resting to +30 MV
Relaxation: Returns to -70 MV.
Transmit action potentials from the sarcolemma to the inside of the cell.
Reach the sarcoplasmic reticulum (SR).
Action potentials trigger contraction via calcium release.
Contraction = Release of calcium.
Similar to smooth endoplasmic reticulum.
Two terminal cisternae plus a T-tubule form a triad.
Triad role: Coordination of calcium release and storage.
Contraction releases calcium, relaxation involves reuptake of calcium.
Thin filaments: Composed primarily of actin.
Thick filaments: Composed primarily of myosin.
Form cross-bridges during contraction.
Part of the sliding filament theory.
Titin: Allows muscles to expand and contract; contributes to elasticity and recoil.
Thin filaments made of actin: Active sites are exposed during contraction for myosin heads to bind.
Thick filaments made of myosin: Heads bind to actin.
Core of titin recoils after stretching.
Action potentials (electrical impulses).
Skeletal muscle fibers contract due to stimulation by motor neurons at neuromuscular junctions (NMJ).
They release acetylcholine (ACh), a neurotransmitter that stimulates contractions.
Depolarization: Cell becomes more positive.
Repolarization: Cell becomes more negative, returning to the resting membrane potential.
Hyperpolarization: Cell temporarily becomes more negative than the resting potential.
All neurons connected to a single muscle fiber.
Neurotransmitter: Acetylcholine (ACh).
Signal initiation.
ACh binding and sodium influx.
Action potential generation.
Calcium release (contraction).
Signal ends (relaxation).
Fixed muscular contraction after death.
Rigor = stiff
Mortis = death
Muscles stiffen after death due to a lack of ATP, preventing detachment of myosin from actin.
Onset: 2-6 hours after death, peaks around 12 hours, resolves in 1-3 days.
Used to estimate time of death.
Affected by temperature and body mass.
Maximum tension.
Incomplete tetanus: More common; occurs in voluntary muscle activities requiring sustained force.
Complete tetanus: Uncommon; occurs in high-intensity exercise or infection.
Infection = Tetanus (bacterial infection).
Muscles generate heat by using ATP.
Isotonic: Muscle changes length (e.g., lifting, pushing, pulling).
Isometric: Muscle length remains the same (e.g., posture, maintaining balance).
Myosin heads require ATP for contraction.
Three ways ATP is generated:
Creatine phosphate: For short bursts of energy (10-15 seconds).
Anaerobic metabolism: Moderate intensity, short duration activities (30 seconds to 2 minutes).
Aerobic metabolism: More common; supports everyday activities and metabolism.
Fast fibers (Type II or Fast-Twitch fibers, white):
Ideal for short bursts of power.
Primarily rely on anaerobic metabolism.
Slow fibers (Type I or Slow-Twitch fibers, red):
Designed for endurance.
Primarily rely on aerobic metabolism.
Intermediate fibers (Type IIa or Fast Oxidative fibers, pink in humans):
Intermediate speed; faster than slow fibers but not as fast as fast fibers.
Use both aerobic and anaerobic pathways.
Muscle hypertrophy: Muscle growth (e.g., weight lifting).
Muscle atrophy: Muscle wasting (e.g., paralysis, coma, cast, aging, sedentary lifestyle).
Examples of paralysis-inducing conditions: Muscular dystrophy and multiple sclerosis.
Found only in the heart.
Have excitable membranes.
Striated like skeletal muscle.
Uninucleate.
Intercalated discs.
Do not regenerate, but the heart itself can recover after a myocardial infarction (MI or heart attack).
Shape: Branched
Also called cardiocytes or cardiomyocytes.
Automaticity: Cardiac muscle can generate its own action potentials.
Due to pacemaker cells (SA node, AV node, Bundle of His, and Purkinje fibers).
Non-striated.
Involuntary.
Integumentary system: Arrector pili muscles cause hairs to erect, leading to goosebumps (vestigial trait).
Spindle-shaped.
Single central nucleus.
Non-striated.
T-tubule role: Transmits action potentials to the sarcoplasmic reticulum.