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Vocabulary flashcards covering key terms, structures, proteins, physiological processes, fiber types, energy systems, contraction mechanics, clinical conditions, and muscle tissue types discussed in the Chapter 10 lecture.
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Myology
The scientific study of the muscular system.
Skeletal muscle
Voluntary, striated muscle tissue usually attached to bones.
Cardiac muscle
Involuntary, striated muscle of the heart with intercalated discs.
Smooth muscle
Involuntary, non-striated muscle found in walls of hollow organs and vessels.
Excitability
Ability of muscle to respond to chemical, stretch, or electrical stimuli.
Conductivity
Property by which a local electrical change triggers a wave of excitation along a muscle fiber.
Contractility
Capacity of muscle to shorten when stimulated.
Extensibility
Ability of muscle to be stretched between contractions.
Elasticity
Tendency of muscle to return to its original length after stretching.
Endomysium
Thin connective tissue wrapping each individual muscle fiber.
Perimysium
Connective tissue sheath surrounding a fascicle (bundle) of muscle fibers.
Epimysium
Fibrous sheath that encloses an entire muscle.
Fascia
Sheet of connective tissue that separates neighboring muscles or groups.
Fascicle
A bundle of skeletal muscle fibers wrapped together by perimysium.
Tendon
Dense regular connective tissue connecting muscle to bone.
Aponeurosis
Broad, flat tendon such as the palmar aponeurosis.
Origin
Bony attachment at the stationary end of a skeletal muscle.
Insertion
Bony attachment to the movable end of a skeletal muscle.
Muscle belly
Thick, middle region of a muscle between origin and insertion.
Innervation
Identity of the nerve that stimulates a muscle to contract.
Somatic motor neuron
Nerve cell whose axon innervates skeletal muscle fibers.
Motor unit
One motor neuron and all the muscle fibers it innervates.
Neuromuscular junction (NMJ)
Specialized synapse where a motor neuron communicates with a muscle fiber.
Synaptic knob (terminal)
Swollen axon ending at the NMJ that contains neurotransmitter vesicles.
Synaptic vesicle
Membrane sac in the synaptic knob storing acetylcholine.
Acetylcholine (ACh)
Neurotransmitter released at NMJs to excite skeletal muscle fibers.
Acetylcholinesterase
Enzyme that degrades ACh in the synaptic cleft, ending stimulation.
Resting membrane potential (RMP)
Electrical charge difference (≈ –90 mV) across the sarcolemma of a resting fiber.
Action potential
Rapid, self-propagating change in membrane voltage that travels along a muscle fiber.
Sarcolemma
Plasma membrane of a muscle fiber.
Sarcoplasm
Cytoplasm of a muscle fiber containing myofibrils, glycogen, and myoglobin.
Myofibril
Long protein cord inside a muscle fiber composed of repeating sarcomeres.
Myofilament
Protein filament (thick or thin) that slides to produce contraction.
Thick filament
Myosin-based filament found in the A band of a sarcomere.
Myosin
Motor protein whose heads bind actin and hydrolyze ATP for force.
Thin filament
Actin-based filament with associated troponin and tropomyosin.
Actin
Globular protein that forms the backbone of thin filaments.
Tropomyosin
Regulatory protein that blocks myosin-binding sites on actin at rest.
Troponin
Calcium-binding protein that moves tropomyosin to expose actin sites.
Sarcomere
Functional contractile unit of a myofibril from one Z disc to the next.
A band
Dark region of a striation where thick and thin filaments overlap.
I band
Light region containing only thin filaments, bisected by a Z disc.
H band (zone)
Central region of the A band containing thick filaments only.
Z disc
Protein plate that anchors thin and elastic filaments; marks sarcomere boundaries.
T tubule
Invagination of the sarcolemma that conducts action potentials into the fiber interior.
Sarcoplasmic reticulum (SR)
Smooth ER of muscle storing and releasing Ca²⁺ for contraction.
Triad
T-tubule flanked by two terminal cisternae of SR.
Ryanodine receptor
Calcium-release channel in the SR opened during excitation-contraction coupling.
Dihydropyridine (L-type) channel
Voltage sensor in the T-tubule that mechanically opens RyR channels.
Excitation–contraction coupling
Link between action potential on sarcolemma and sliding of filaments.
Sliding filament mechanism
Process in which myosin heads pull thin filaments toward the M line, shortening sarcomeres.
Power stroke
Flexing of a myosin head that pulls the thin filament in contraction.
Recovery stroke
Return of myosin head to cocked position after ATP binding and detachment.
ATPase
Enzyme activity of the myosin head that hydrolyzes ATP for energy.
Creatine phosphate (phosphocreatine)
High-energy storage molecule that donates phosphate to ADP for quick ATP resynthesis.
Glycogen
Stored polysaccharide of glucose within muscle fibers for energy.
Myoglobin
Red pigment that stores oxygen inside muscle fibers.
Isometric contraction
Muscle develops tension without changing length; no movement occurs.
Isotonic contraction
Muscle changes length while tension remains constant; produces movement.
Concentric contraction
Isotonic action in which muscle shortens while generating force.
Eccentric contraction
Isotonic action in which muscle lengthens while maintaining tension.
Slow-twitch fiber (Type I)
Red, fatigue-resistant muscle fiber adapted for endurance and posture.
Fast-twitch fiber (Type IIb)
White, quick-fatiguing fiber adapted for rapid, powerful contractions.
Hypertrophy
Increase in muscle fiber size due to resistance training.
Hyperplasia
Increase in muscle fiber number (limited contribution to muscle growth).
Muscle tone
Partial, involuntary contraction of resting skeletal muscles maintained by the CNS.
Length–tension relationship
Principle that muscle force depends on initial sarcomere length before stimulation.
Tetanus (state)
Sustained muscle contraction caused by rapid repetitive stimulation or toxin.
Flaccid paralysis
Loss of muscle tone and inability to contract, often from neuromuscular blockade.
Curare
Plant toxin that competes with ACh for its receptor, causing flaccid paralysis.
Botulism
Paralytic illness from Clostridium botulinum toxin that blocks ACh release.
Myasthenia gravis
Autoimmune disease where antibodies destroy ACh receptors leading to weakness.
Duchenne muscular dystrophy
Sex-linked disorder caused by lack of dystrophin leading to progressive muscle degeneration.
Intercalated disc
Specialized junction connecting cardiac muscle cells, containing gap and mechanical junctions.
Autorhythmicity
Ability of cardiac (and some smooth) muscle cells to generate spontaneous depolarizations.
Calmodulin
Calcium-binding protein that initiates smooth muscle contraction by activating MLCK.
Myosin light chain kinase (MLCK)
Enzyme that phosphorylates myosin heads in smooth muscle enabling cross-bridge cycling.
Sphincter
Ring of smooth or skeletal muscle that regulates passage of materials through openings.
Glycemic control
Role of skeletal muscle in absorbing and storing glucose to regulate blood sugar.
Heat production
Generation of up to 85 % of body heat via skeletal muscle metabolism.
Antigravity muscle
Skeletal muscle that prevents the body from falling, maintaining posture.
Connectin (Titin)
Elastic protein anchoring thick filaments to Z disc, contributing to recoil.
Myoblast
Embryonic stem cell that fuses to form a multinucleate skeletal muscle fiber.
Voltage-gated sodium channel
Membrane protein that opens during depolarization, propagating action potentials.
End-plate potential
Local depolarization at the motor end plate produced by ACh binding.
Depolarization
Reduction or reversal of membrane potential, making the interior less negative.
Repolarization
Return of membrane potential to a negative value after depolarization.
Piloerector muscle
Smooth muscle in skin that raises hairs when cold or frightened.
Autonomic nervous system
Motor division controlling involuntary effectors such as cardiac and smooth muscle.
Troponin–tropomyosin complex
Regulatory system on thin filaments controlling exposure of myosin-binding sites.
Ca²⁺ pump (SERCA)
Active transport protein returning calcium to the SR during relaxation.
Latch state
Sustained tension in smooth muscle with minimal ATP consumption.
Sarcoplasmic calcium
Ca²⁺ released into cytosol that triggers muscle contraction.
Toxin
Chemical that can disrupt normal neuromuscular function, causing tetanus or paralysis.