Muscular System

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Last updated 1:14 AM on 9/22/26
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85 Terms

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Skeletal muscle

Moves the skeleton

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Transverse tubules

tubules in the muscles that allow for the spreading of electrical impulses

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myofibrils

elongated strands within muscle fibers that contain the contractile proteins actin and myosin, give skeletal and cardiac muscle their striated appearance

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thick filaments

myosin filaments

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thin filaments

actin filaments

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sarcomere

repeating unit between two z-lines

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cross-bridges

basis for attachment between actin and myosin filaments

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tropomyosin

regulatory protein deciding whether actin is bound to myosin at any point

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troponin

regulatory protein allowing or denying access to binding sites by moving tropomyosin

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Sarcolemma

plasma membrane of a muscle cell

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sarcoplasm

cytoplasm of a muscle cells

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sarcoplasmic reticulum

smooth ER of a muscle cell

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Where is smooth muscle found?

lining hollow organs

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Sliding-filament mechanism

contraction produces shortening of a skeletal muscle fiber causing thick and thin filaments in each sarcomere to move past each other, propelled by the movements of the cross-bridges

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How does troponin do its job?

binds calcium reversibly and changes conformation to pull tropomyosin away from the interaction sites, allowing myosin to interact with actin

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Cross bridge cycle

  1. cross bridge binds to actin

  2. cross-bridge moves

  3. ATP binds to myosin, causing cross-bridge to detach

  4. hydrolysis of ATP energizes cross bridges


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Functions of ATP in the skeletal muscle

Na/K-ATPase pump maintains Na and K gradients to allow action potentials to be produced, Ca-ATPase provides energy for active transport of calcium ions to end the contraction, energizing cross-bridges for force generation, binding to myosin dissociates cross-bridges to repeat the cycle

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Function of the sarcoplasmic reticulum

Ca stored and released following membrane excitation

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T-tubule protein

modified voltage-sensitive Ca channel DHP receptor

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Ryanodine receptor

protein embedded in the SR membrane which forms Ca channel

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Motor unit

motor neuron and the skeletal muscle fibers it innervates

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Can a motor neuron innervate more than one muscle fiber?

yes

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Can a muscle fiber be innervated by more than one motor neuron?

no

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What does the number of innervated fibers depend on?

muscle type

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Neuromuscular junction

junction of an axon terminal with the motor end plate

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How are action potentials initiated in skeletal muscle?

Stimulation of nerve fibers

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Motor neurons

nerve cells whose axons innervate skeletal muscle

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Motor end plate

region of the muscle fiber plasma membrane directly under the terminal portion of the axon

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Tension

force generated by muscle fibers

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Load

force exerted on the muscle by an object, opposed by tension

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Isometric

tension developed without a change in length

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isotonic

lengthening

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Concentric

tension > load

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Eccentric

tension < load, only happens when external forces dictate

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Twitch

mechanical response of a muscle fiber to a single action potential

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Phases of a twitch contraction

latent period, contraction phase, relaxation phase

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Latent period

time of the action potential to the onset of contraction, happens because of excitation-contraction coupling

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Contraction phase

time tension is developing due to cross-bridge cycling

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Relaxation phase

time that tension is decreasing due to the amount of time it takes to get all the Ca sequestered

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What happens with isotonic twitches at heavier loads?

longer latent period to accumulate cross-bridges sufficient enough, shorter twitches, slower shortening

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Frequency-tension relationship

increasing the rate of action potentials fired by a motor neuron increases the tension generated by the muscle fiber

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Summation

increase in muscle tension from successive action potentials occurring during the phase of mechanical activity

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Tetanus

maintained contraction in response to repetitive stimulation

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Length-tension relationship

increased stretch causes passive tension to increaseW

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What is responsible for passive elastic properties of relaxed muscle fibers?

spring-like characteristics of titin protein

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What is the cause of the length-tension relationship?

elongation of titin filaments, if stretched fiber is released it will return to equilibrium length

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How can active tension be altered?

changing the length of the fiber. if a fiber is stretched to various lengths and tetanically stimulated at each length, the magnitude of active tension will vary with length

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Optimal length, L0

length at which the fiber develops the greatest isometric active tension

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Ways to form ATP

phosphorylation of ADP by creatine phosphate, oxidative phosphorylation of ADP in the mitochondria (terminal step of the electron transport chain), phosphorylation of ADP by the glycolytic pathway in the cytosol

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Muscle fatigue

decreased tension, shortening velocity, and rate of relaxation in the face of continuous stimulation

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Molecular causes of muscle fatigue

lower ATP, increased ADP, Pi, Mg, H+, oxygen free radicals decrease calcium release, reuptake, and storage, sensitivity of thin filament proteins to activation by calcium release, and inhibit binding and power-stroke motion of cross bridges

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Central command fatigue

fatigue at the level of the motor cortex occurs when it fails to send excitatory signals to the motor neurons which may cause a person to stop exercising even though the muscles are not fatigued

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Will to win

ability to inititate central commands to msucles during a period of increasingly distressful sensation

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How are muscle fibers classified

maximal velocities of shortening and primary pathway used to form ATP

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Oxidative muscle fibers

have a lot of mitochondria, most of the ATP produced is dependent upon blood flow to deliver oxygen and fuel molecules to muscle, contain myoglobin

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Glycolytic muscle fibers

lots of glycolytic enzyme and glycogen allows for quick bursts of activity

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Slow oxidative fibers (type I)

low myosin-ATPase activity, high oxidative capacity

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Fast oxidative glycolytic fibers (Type IIa)

high myosin ATPase activity with high oxidative capacity and intermediate glycolytic capacity

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Fast glycolytic fibers (Type IIb)

high myosin ATPase activity and high glycolytic capacity

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Recruitment

low neural activity only activates type I fibers, as it increases as it recruits each of the subsequent fiber types

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Size principle

smallest neurons require the least amount of input to depolarize, which match with smaller muscle fibers

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What does total tension depend on?

amount of tension per fiber, number of fibers contracting at a time

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What does shortening velocity of a whole muscle depend on?

load on the muscle, types of motor units in the muscle, and the number of motor units working against the load

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How does an increase in contractile activity influence muscles?

increases muscle fiber size and capacity for ATP production

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What happens to muscles that are not used?

atrophy

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Denervation atrophy

nerve damage leading to a loss of function in the muscle

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How are smooth muscle cells arranged?

not myofibrils or sarcomeres

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Does smooth muscle have troponin and tropomyosin?

only tropomyosin

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How are cross-bridge activations of smooth muscle cells controlled?

myosin light chain kinase (MLCK), a calcium regulated enzyme that phosphorylates myosin, which is the only form that can bind actin

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Myosin light-chain phosphatase (MLCP)

dephosphorylates myosin to relax smooth muscles

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Sources of cytosolic calcium

sarcoplasmic reticulum, extracellular calcium entering the cell through plasma membrane calcium channels

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Can input to smooth muscle be excitatory or inhibitory?

yes, both

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Can input to skeletal muscle be excitatory or inhibitory?

no, only excitatory

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How are smooth muscles regulated?

nerves and hormones, local factors, spontaneous activity

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How can nerves and hormones regulate smooth muscle?

neurotransmitters are released by autonomic neuron endings, no motor end-plate

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varicosities

swollen regions containing vesicles filled with neurotransmitters which are released when an action potential passes through

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Do neurotransmitters only produce one type of effect?

no, they can produce opposite effects in different muscle tissues, the type of response depends on the receptors the neurotransmitter binds to in the membrane and on the intracellular signaling mechanisms those receptors activate

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What local factors influence smooth muscle contraction?

paracrine signals, acidity, oxygen, carbon dioxide, osmolarity, ion composition of extracellular fluid

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Pacemaker potential

membrane potential change occuring during spontaneous depolarization to threshold

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Slow waves

periodic fluctuations in membrane potential due to variation in ion flux across the membrane

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Single-unit smooth muscle

cells are connected by gap junctions and respond to stimuli as a single unit

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Multi-unit smooth muscles

cells respond to stimuli independently and contain few gap junctions

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Branching cells

have intercalated discs with desmosomes and gap junctions

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Why are gap junctions important to cardiac muscle?

ability to be electrically coupled

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Automaticity/autorhythmicity

nodal cells have the ability to stimulate their own action potentials