Muscle Tissue Types, Structure & Function

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Questions and Answers

Which of the following scenarios would most likely involve the predominant use of fast glycolytic (Type IIb) muscle fibers?

  • A cyclist riding at a moderate intensity for an extended period.
  • A marathon runner maintaining a steady pace for several hours.
  • A weightlifter performing a single, maximal lift. (correct)
  • A yoga instructor holding a static pose for several minutes.

Smooth muscle contraction relies on troponin to initiate cross-bridge formation, similar to skeletal muscle contraction.

False (B)

Explain how the absence of ATP would prevent muscle relaxation, even if calcium ions were actively being pumped back into the sarcoplasmic reticulum.

ATP is required for the detachment of myosin from actin. Without ATP, the cross-bridges remain bound, preventing relaxation.

In smooth muscle, calcium ions bind to ______, leading to the activation of a kinase enzyme that initiates muscle contraction.

<p>calmodulin</p>
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Match the muscle fiber type with its primary energy source during sustained activity:

<p>Slow Oxidative (Type I) = Aerobic metabolism of glucose and fatty acids Fast Oxidative (Type IIa) = Aerobic metabolism and glycolysis Fast Glycolytic (Type IIb) = Anaerobic glycolysis</p>
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During muscle contraction, what is the direct role of ATP hydrolysis?

<p>To re-energize the myosin head into a 'cocked' position. (B)</p>
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The A-band in a sarcomere decreases in length during muscle contraction as the actin filaments slide over the myosin filaments.

<p>False (B)</p>
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Explain why a buildup of lactic acid during intense exercise can lead to muscle fatigue.

<p>Lactic acid increases muscle acidity, which interferes with the proteins involved in muscle contraction, impairing function and causing fatigue.</p>
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The ______ is the area within the sarcomere that contains only myosin filaments and is visible when the muscle is relaxed.

<p>H-zone</p>
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Match the following components of muscle tissue with their respective functions:

<p>Sarcoplasmic Reticulum = Stores and releases calcium ions T-tubules = Transmits action potentials deep into the muscle fiber Sarcolemma = Muscle cell membrane Myofibrils = Contain sarcomeres, the contractile units</p>
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What would be the immediate consequence if the enzyme acetylcholinesterase were inhibited at the neuromuscular junction?

<p>ACh would continuously stimulate the muscle fiber, causing prolonged contraction. (D)</p>
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Cardiac muscle relies on external nerve stimulation for each contraction.

<p>False (B)</p>
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Describe the role of troponin and tropomyosin in preventing continuous muscle contraction when calcium levels are low.

<p>Tropomyosin physically blocks the myosin-binding sites on actin. Troponin, when not bound to calcium, holds tropomyosin in this blocking position.</p>
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The process by which an action potential in the muscle fiber leads to the release of calcium ions from the sarcoplasmic reticulum is known as ______.

<p>excitation-contraction coupling</p>
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Match the type of muscle tissue with its unique structural feature:

<p>Skeletal Muscle = Striations and multiple nuclei per fiber Cardiac Muscle = Intercalated discs Smooth Muscle = Lack of striations</p>
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Why is the presence of ATP necessary for muscle relaxation?

<p>ATP is used to pump calcium back into the sarcoplasmic reticulum and to detach myosin from actin. (D)</p>
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Increasing the frequency of motor neuron stimulation always results in complete tetanus, where the muscle achieves a state of maximal and sustained contraction with no relaxation.

<p>False (B)</p>
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Explain why rigor mortis occurs after death in terms of ATP availability and muscle contraction.

<p>After death, ATP production ceases. Without ATP, myosin heads cannot detach from actin, resulting in a state of continuous cross-bridging and muscle stiffness known as rigor mortis.</p>
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The neurotransmitter released at the neuromuscular junction that initiates muscle contraction is ______.

<p>acetylcholine</p>
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Match the type of muscle tissue with its primary function:

<p>Skeletal Muscle = Movement and stabilization of the skeleton Cardiac Muscle = Pumping blood throughout the body Smooth Muscle = Regulating the diameter of blood vessels and moving substances through internal organs</p>
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Which of the following events directly triggers the release of calcium ions from the sarcoplasmic reticulum in skeletal muscle?

<p>The arrival of an action potential along the T-tubules. (B)</p>
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Smooth muscle cells have sarcomeres, which give them a striated appearance similar to skeletal and cardiac muscle.

<p>False (B)</p>
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Explain how the length-tension relationship affects the force a muscle can generate.

<p>Muscle force is optimal when the muscle is at its resting length. Too short or too long, and the overlap between actin and myosin filaments and the number of cross-bridges decrease, reducing the force generated.</p>
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The regulatory protein that blocks myosin-binding sites on actin when calcium levels are low is ______.

<p>tropomyosin</p>
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Match the zone/band of the sarcomere with its compositional change during muscle contraction:

<p>I-band = Decreases in length H-zone = Decreases in length A-band = Remains the same length</p>
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What is the function of the calcium ATPase pump in muscle relaxation?

<p>To pump calcium ions back into the sarcoplasmic reticulum to promote relaxation. (D)</p>
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Increasing the number of activated motor units will decrease the force of muscle contraction.

<p>False (B)</p>
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Describe how the arrangement of actin and myosin filaments within a sarcomere contributes to the striated appearance of skeletal muscle.

<p>The alternating pattern of actin (thin) and myosin (thick) filaments creates distinct light (I-bands) and dark (A-bands) regions, resulting in the striated appearance.</p>
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The connection between a motor neuron and a muscle fiber is called the ______.

<p>neuromuscular junction</p>
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Match each muscle type with its type of control:

<p>Skeletal = Voluntary Cardiac = Involuntary Smooth = Involuntary</p>
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Which statement accurately describes the role of the Z-line in a sarcomere?

<p>It anchors the actin filaments and defines the boundaries of the sarcomere. (D)</p>
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Smooth muscle fatigue occurs more rapidly than skeletal muscle fatigue due to its higher energy requirements.

<p>False (B)</p>
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Explain how the sodium-potassium pump contributes to maintaining the resting membrane potential in muscle cells and its importance for muscle excitability.

<p>The sodium-potassium pump maintains the ion gradients necessary for the resting membrane potential by pumping sodium ions out of the cell and potassium ions into the cell. This polarization is essential for generating action potentials and muscle excitability.</p>
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The ability of muscle tissue to return to its original length after stretching is known as ______.

<p>elasticity</p>
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Match the term with its accurate definition related to muscle contraction.

<p>Motor Unit = A motor neuron and all the muscle fibers it innervates Tetanus = Sustained muscle contraction due to high-frequency stimulation Hypertrophy = Increase in muscle fiber size Atrophy = Decrease in muscle fiber size</p>
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Which of these properties is NOT a characteristic that differentiates muscle tissue from other cell types?

<p>Excitability (D)</p>
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Skeletal muscles are primarily responsible for controlling the movement of internal organs and blood vessels?

<p>False (B)</p>
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Within muscle tissue, what is the name given to the cytoplasm and the cell membrane, respectively?

<p>sarcoplasm; sarcolemma</p>
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The functional unit of a muscle fibre responsible for contraction composed of actin and myosin proteins is called a ________

<p>sarcomere</p>
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Match the muscle tissue types with their primary characteristics:

<p>Skeletal Muscle = Attaches to bones and is responsible for voluntary movement Smooth Muscle = Lines the walls of internal organs and blood vessels, responsible for involuntary movements Cardiac Muscle = Found only in the heart, responsible for pumping blood</p>
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Which statement accurately describes the arrangement of contractile filaments within a sarcomere?

<p>Actin and myosin filaments overlap in the A band, with actin filaments extending into the I band. (B)</p>
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During muscle contraction, the length of both actin and myosin filaments decreases, resulting in the shortening of the sarcomere?

<p>False (B)</p>
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Explain the role of the myosin head in muscle contraction, including its binding sites and enzymatic activity.

<p>The myosin head contains binding sites for both actin and ATP. It uses the energy from ATP hydrolysis to pivot and pull the actin filament toward the center of the sarcomere, which causes muscle contraction.</p>
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The energy required for the power stroke during muscle contraction is provided by the hydrolysis of _______, while the detachment of the myosin head from actin requires the binding of _______.

<p>ATP; ATP</p>
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Match the following statements with whether they are associated with muscle tension or muscle load:

<p>Muscle Tension = Force exerted by a contracting muscle on an object Muscle Load = Force exerted by an object on the muscle</p>
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What is the primary function of the motor neuron in initiating muscle contraction?

<p>Releasing neurotransmitters that depolarize the muscle fibre. (B)</p>
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A single action potential in a motor neuron always results in a maximal, sustained contraction of all muscle fibres within its motor unit?

<p>False (B)</p>
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Describe the sequence of events at the neuromuscular junction that leads to muscle fibre depolarization.

<p>The motor neuron releases acetylcholine (ACh), which binds to nicotinic receptors on the muscle fiber. This binding opens ion channels, allowing sodium ions to flow in, causing depolarization of the muscle fiber membrane.</p>
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The enzyme __________ is responsible for breaking down acetylcholine in the synaptic cleft, which terminates the signal and allows the muscle fibre to relax

<p>acetylcholinesterase</p>
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Each of the following descriptions lists a component of a muscle, match the component to its correct function:

<p>T-tubules = Invaginations of the sarcolemma that transmit action potentials deep into the muscle fibre. Sarcoplasmic Reticulum = Stores and releases calcium ions to regulate muscle contraction. Ryanodine Receptors = Calcium release channels in the sarcoplasmic reticulum membrane. Dihydropyridine (DHP) Receptors = Voltage sensors in the T-tubule membrane that trigger calcium release.</p>
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Which of the following correctly explains the role of tropomyosin and troponin in skeletal muscle contraction?

<p>Troponin blocks myosin-binding sites on actin in resting muscle, and tropomyosin moves to uncover these sites when calcium binds troponin. (C)</p>
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An increase in intracellular calcium levels always leads to muscle contraction regardless of the presence of ATP or the position of tropomyosin?

<p>False (B)</p>
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Explain the two distinct roles of ATP in muscle contraction.

<p>ATP hydrolysis provides energy for the myosin head to pivot and perform the power stroke, while ATP binding to myosin causes the myosin head to detach from actin, allowing the cycle to repeat.</p>
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In excitation-contraction coupling, the action potential in the T-tubule membrane causes the DHP receptors to trigger the opening of __________ channels in the sarcoplasmic reticulum, leading to calcium release

<p>ryanodine</p>
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Match the following statements with whether they are associated with low or high cytosolic calcium, in relaxed or activated muscle:

<p>Low Cytosolic Calcium = Relaxed muscle: Tropomyosin blocks myosin-binding sites. High Cytosolic Calcium = Activated muscle: Cross-bridge binding sites exposed, contraction occurs.</p>
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What happens during the latent period of muscle contraction?

<p>The action potential propagates across the sarcolemma and T-tubules. (D)</p>
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During concentric contraction, muscle tension is less than the load?

<p>False (B)</p>
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Describe the role of titin in the sarcomere and its impact on muscle function.

<p>Titin anchors myosin filaments to the Z-line, maintaining sarcomere structure and contributing to muscle elasticity. It ensures proper alignment and prevents over-stretching.</p>
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The A band of the sarcomere contains __________ filaments, while the I band contains __________ filaments.

<p>myosin; actin</p>
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For each muscle fiber type, match its corresponding role:

<p>Type 1 = Endurance; fatigue resistant Type IIa = Fast contractions; fatigue-resistant Type IIx = Powerful; fast fatigue</p>
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Which of the following best describes the function of the $Ca^{2+}$-ATPase pump in muscle relaxation?

<p>Actively transporting calcium back into the sarcoplasmic reticulum. (B)</p>
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After death, rigor mortis occurs because the myosin heads are permanently bound to actin filaments due to the lack of ATP to unbind them?

<p>True (A)</p>
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Briefly explain what role the Z-lines play in muscle contraction and relaxation.

<p>Z-lines mark the boundaries of each sarcomere, and they move closer together during muscle contraction as the actin filaments slide toward the center of the sarcomere.</p>
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Motor neurons form specialized junctions with muscle fibres called __________, across which __________ is released to initiate muscle contraction.

<p>neuromuscular junctions; acetylcholine</p>
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Match the type of muscle contraction wth the statement that best describes the scenario:

<p>Concentric Contraction = A muscle shortens while generating force Eccentric Contraction = A muscle lengthens while generating force Isometric Contraction = The muscle does not change in length.</p>
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How does the frequency of action potentials in a motor neuron affect the force of muscle contraction?

<p>Higher frequency causes summation, increasing the duration of calcium release and muscle tension. (A)</p>
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Smooth muscle cells are striated due to the highly regular arrangement of contractile filaments into sarcomeres?

<p>False (B)</p>
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Describe the role of troponin in the mechanism of muscle contraction, including calcium binding and conformational changes.

<p>Troponin binds calcium ions, causing a conformational change that moves tropomyosin away from the myosin-binding sites on actin, allowing for cross-bridge formation and muscle contraction.</p>
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Changes in ______ ______ in the skeletal muscle cell will determine the number of cross-bridges that form, directly affecting the force of muscle contraction.

<p>calcium; levels</p>
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Match the definitions to the corresponding type of filaments present in a sacromere:

<p>Myosin filaments = Thick filament Actin Filaments = Thin filaments</p>
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Which of the following structural changes occurs within the sarcomere during muscle contraction, supporting the sliding filament theory?

<p>The I band and H zone shorten as the actin filaments slide toward the center of the sarcomere. (D)</p>
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Muscle tension refers to the passive resistance of a muscle to stretching, while load is the force generated by the muscle contraction?

<p>False (B)</p>
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Describe the role of the transverse tubules (T-tubules) in excitation-contraction coupling within skeletal muscle fibres.

<p>T-tubules are invaginations of the sarcolemma that conduct action potentials deep into the muscle fiber, facilitating the rapid and uniform release of calcium from the sarcoplasmic reticulum.</p>
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The process of excitation-contraction coupling relies on an ______ ______ that depolarizes the motor endplate in the muscle fibre

<p>action; potential</p>
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Match each of following terms with a function:

<p>Acetylcholine = An ACH (neurotransmitter) being released by the motor terminal. acetylcholinesterase = breaks down ACH</p>
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Which statement best describes the primary role of ATP in muscle contraction?

<p>It provides the energy for the power stroke of the myosin head and disrupts the actin-myosin bond. (D)</p>
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The shortening of myosin during muscle contraction primarily drives the sliding filament theory.

<p>False (B)</p>
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Describe the critical event initiated by the action potential that directly leads to the release of Calcium ions ($Ca^{2+}$) from the sarcoplasmic reticulum.

<p>The action potential in the T-tubule membrane causes $Ca^{2+}$ release channels to open.</p>
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The ______ is defined as the force created by a contracting muscle, while the ______ is the weight or force that opposes muscle contraction.

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Which of the following statements accurately describes the structural arrangement within a sarcomere during muscle contraction, according to the sliding filament theory?

<p>The length of both the actin and myosin filaments remains constant as they slide past each other. (B)</p>
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In skeletal muscle, a motor neuron forms multiple synapses with a single muscle fiber, allowing for a greater degree of control over contraction.

<p>False (B)</p>
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Explain the crucial roles of ATP (adenosine triphosphate) in muscle contraction, focusing on the specific interactions with myosin and the stages of the cross-bridge cycle.

<p>ATP is required for both dissociating the myosin head from actin and providing energy for the myosin head to return to its high-energy conformation, enabling the next cross-bridge cycle. It also plays a role in calcium transport.</p>
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The influx of ______ ions into the muscle fiber triggers the release of acetylcholine.

<p>sodium</p>
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Match the following muscle fiber components with their function in muscle contraction:

<p>Tropomyosin = Blocks myosin-binding sites on actin in relaxed muscle Troponin = Binds calcium ions, causing a conformational change that exposes myosin-binding sites on actin Myosin = Forms cross-bridges with actin to generate force Actin = Forms thin filaments and provides binding sites for myosin</p>
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Which of the following is the most accurate description of the role of T-tubules in excitation-contraction coupling?

<p>They transmit action potentials from the sarcolemma to the interior of the muscle fiber. (D)</p>
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Smooth muscle contraction is primarily regulated by the troponin-tropomyosin complex, similar to skeletal muscle.

<p>False (B)</p>
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Describe the structural differences between actin and myosin filaments and how these differences facilitate muscle contraction.

<p>Actin filaments are thin filaments composed of globular actin (G-actin) monomers that polymerize to form filamentous actin (F-actin). Myosin filaments are thick filaments composed of myosin molecules, each with a head and tail region. The myosin heads bind to actin, forming cross-bridges that generate force during muscle contraction.</p>
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The enzyme ______ catalyzes the breakdown of acetylcholine in the synaptic cleft, terminating its effect on the motor endplate.

<p>acetylcholinesterase</p>
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According to the sliding filament theory, what happens to the H zone during muscle contraction?

<p>It disappears as the actin filaments slide over the myosin filaments. (C)</p>
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The 'latent period' in muscle contraction refers to the time it takes for calcium ions to bind to troponin and initiate cross-bridge cycling.

<p>True (A)</p>
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Describe the role of ryanodine receptors in excitation-contraction coupling.

<p>Ryanodine receptors are calcium release channels located on the sarcoplasmic reticulum (SR) membrane. In response to an action potential, they open, allowing calcium ions to flow from the SR into the cytoplasm, initiating muscle contraction.</p>
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The force created by a contracting muscle is termed ______, while the opposing force is termed ______.

<p>muscle tension, load</p>
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Which of the following is responsible for generating the power stroke during muscle contraction?

<p>The release of ADP and inorganic phosphate from the myosin head. (A)</p>
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The A band of the sarcomere shortens during muscle contraction due to the movement of myosin filaments.

<p>False (B)</p>
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Which of the following features distinguishes smooth muscle from skeletal muscle?

<p>Presence of sarcomeres (C)</p>
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Smooth muscle relies primarily on the sarcoplasmic reticulum (SR) as its sole source of calcium ions for contraction.

<p>False (B)</p>
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Which metabolic adaptation allows skeletal muscle to continue functioning during short periods of oxygen deprivation?

<p>Anaerobic glycolysis and lactate production (B)</p>
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The process by which a voluntary action transitions into an automatic one through repeated execution primarily involves changes in the ______ control level of the motor hierarchy.

<p>local</p>
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Match each fatigue mechanism with its primary site of impact:

<p>Central Fatigue = Decreased neural drive from the motor cortex Peripheral Fatigue = Impaired excitation-contraction coupling in muscle fibers</p>
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In smooth muscle, what is the immediate consequence of calcium binding to calmodulin?

<p>Phosphorylation of myosin light chain (C)</p>
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Skeletal muscle fatigue always results from a complete depletion of ATP within the muscle fibers.

<p>False (B)</p>
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How does the arrangement of actin and myosin filaments in smooth muscle differ structurally from that in skeletal muscle, and how does this difference affect the contractile mechanism?

<p>Smooth muscle lacks sarcomeres and has actin and myosin arranged in an X-shape, which allows for contraction across multiple axes, unlike the unidirectional contraction in striated muscle.</p>
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Which characteristic is most indicative of a fast glycolytic (Type IIx) skeletal muscle fiber?

<p>High force-generating capacity (A)</p>
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In the excitation-contraction coupling of smooth muscle, the influx of extracellular Ca2+ through ______-gated channels is often a crucial initial step that triggers further Ca2+ release from intracellular stores.

<p>ligand</p>
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Which of the following statements accurately describes the role of caveolae in smooth muscle cells?

<p>They are invaginations of the sarcolemma that concentrate calcium channels and receptors. (C)</p>
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Creatine phosphate provides a sustainable, long-term source of ATP for prolonged muscle activity.

<p>False (B)</p>
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How do muscarinic receptors play a role in the contraction of smooth muscle, and what intracellular signaling pathways are involved?

<p>Muscarinic receptors, when activated, can trigger IP3/DAG signaling, leading to calcium release and smooth muscle contraction.</p>
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Why is the ability to sustain tension over a broad range of muscle lengths particularly important in smooth muscle?

<p>It accommodates volume changes in organs such as the bladder and blood vessels. (D)</p>
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Unlike skeletal muscle, smooth muscle contraction relies on the enzyme ______ to phosphorylate myosin, enabling it to bind with actin and initiate cross-bridge cycling.

<p>myosin light-chain kinase</p>
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Match each type of muscle fiber with its primary characteristic:

<p>Slow Twitch (Type I) = High resistance to fatigue Fast Twitch (Type IIx) = High force-generating capacity</p>
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Which of the following statements best explains central fatigue?

<p>It involves a reduction in neural drive from the motor cortex to the muscles. (A)</p>
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In both skeletal and smooth muscle, the binding of calcium to troponin directly initiates the cross-bridge cycle.

<p>False (B)</p>
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Describe the key differences in the sarcoplasmic reticulum (SR) between skeletal and smooth muscle cells, and explain how these differences impact the regulation of muscle contraction.

<p>Skeletal muscle SR is extensive with well-defined t-tubules, facilitating rapid calcium release. Smooth muscle SR is less developed, relying more on caveolae for calcium regulation.</p>
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During high-intensity exercise, what is the primary mechanism by which glycolysis contributes to muscle fatigue?

<p>Accumulation of lactic acid, causing a decrease in muscle pH. (A)</p>
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The hierarchical organization of motor control starts in the ______, proceeds through intermediate brainstem and spinal cord circuits, and culminates in the activation of motor neurons.

<p>brain</p>
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Match each muscle type with its description:

<p>Skeletal Muscle = Striated, voluntary control Smooth Muscle = Non-striated, involuntary control Cardiac Muscle = Striated, involuntary control</p>
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How does extracellular fluid contribute to the increase of calcium during smooth muscle excitation?

<p>Ligand-gated channels allow intial Ca2+ entry, which triggers Voltage-gated Ca2+ channels allowing further Ca2+ entry (A)</p>
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Slow twitch, type 1, fibers are fast oxidative

<p>False (B)</p>
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What is the definition of central fatique?

<p>Central fatigue refers to a decrease in the ability of the central nervous system (CNS) to send signals to the muscles, leading to a reduction in voluntary activation and performance.</p>
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During muscle activity, what happens to energy?

<p>Energy is used at peak activity (E)</p>
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Central fatigue refers to a decrease in the ability of the ______ to send signals to the muscles.

<p>central nervous system</p>
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Link runner type to muscle fiber.

<p>Sprinter = Fast twitch muscle fiber Marathon runner = Slow twitch muscle fiber</p>
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What type of channels are invovled in calcium entry?

<p>All of the above (D)</p>
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Muscles often run out of ATP during excercise.

<p>False (B)</p>
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List three differences between slow oxidative fibers and fast oxidative fibers

<p>Resistance to fatigue, fiber diameter, and force-generating capacity are some of the primary differences.</p>
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Which of these features is not involved in mechanisms of central fatigue?

<p>Failure of neuromuscular transmission (E)</p>
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Activation of ______ receptors can stimulate G-protein coupled receptors, leading to the production of IP3 and DAG, which then impact calcium levels and contraction

<p>muscarinic</p>
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Match the function to the location or muscle.

<p>Smooth Muscle - respiratory passage = Controls diameter of respiratory passages Smooth Muscle - blood vessels = Controls vasodilation and circulation</p>
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Which is not a difference between skeletal and smooth muscle?

<p>Ca2+ binding initiates contraction (D)</p>
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T-tubules is not needed for smooth muscle function.

<p>True (A)</p>
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How do different percentages of muscle fiber types affect activites such as running?

<p>WORLD-CLASS SPRINTER BRIAN LEWIS of the U.S. has a larger proportion of so-called fast muscle fibers in his legs than a marathoner.</p>
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Which is true about voluntary movement?

<p>voluntary but gradually become automatic (B)</p>
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______ is stored during rest/recovery, and used during activity.

<p>energy</p>
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Match the function to central or peripheral fatigue

<p>Central Fatigue = Decreased frequency and synchronization of motoneurons Peripheral Fatigue = Muscle bioenergetics</p>
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Flashcards

Muscle Tissue

Specialized tissue with the ability to contract and generate force for movement.

Skeletal Muscle

Attached to bones, striated, and under voluntary control for movement and heat production.

Cardiac Muscle

Found in the heart, striated, involuntary, and responsible for pumping blood.

Smooth Muscle

Found in hollow organ walls, non-striated, involuntary, and regulates blood vessel diameter and movement of substances.

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Sarcoplasm

The cytoplasm of a muscle cell, containing components for energy production and muscle function.

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Sarcolemma

The cell membrane surrounding a muscle fiber.

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Myofibrils

Long, threadlike structures within muscle fibers composed of sarcomeres.

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Sarcomere

The basic unit of muscle contraction, containing actin and myosin filaments.

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Myosin

Thick strands of protein with heads that bind to actin.

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Actin

Thin strands of protein that act as tracks for myosin to grab and pull.

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Z-line

The boundary of each sarcomere.

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H-Zone

The middle part of the sarcomere where only myosin filaments are found.

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A-Band

The full length of the myosin filaments within the sarcomere.

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I-Band

Area containing only actin filaments, which gets smaller during muscle contraction.

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Motor Neuron

A messenger from the brain that sends an electrical signal to muscles.

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Neuromuscular Junction

The connection between a motor neuron and a muscle fiber.

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Acetylcholine (ACh)

A chemical released by motor neurons at the neuromuscular junction that binds to receptors on the muscle cell.

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T-Tubules

Tiny tubes inside muscle cells that transmit electrical signals.

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Sarcoplasmic Reticulum (SR)

The organelle that stores and releases calcium ions in muscle cells.

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Sliding Filament Theory

The theory that muscle contraction occurs when actin filaments slide past myosin filaments.

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Cross-Bridge Formation

The process where myosin heads attach to actin filaments.

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Power Stroke

The movement of myosin heads pulling on actin filaments.

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Slow Oxidative Fibers (Type I)

Fibers that use oxygen to produce energy and are good for endurance activities.

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Fast Oxidative Fibers (Type IIa)

Fibers that can use oxygen but work faster and are used for strength and endurance activities.

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Fast Glycolytic Fibers (Type IIb)

Fibers that don't rely much on oxygen and are used for short, explosive activities.

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Calmodulin

A protein used in smooth muscle to control contraction when calcium binds to it.

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Kinase Enzyme

The enzyme activated by calmodulin that phosphorylates myosin, allowing it to bind to actin in smooth muscle.

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Muscle Fatigue

The point when a muscle can no longer generate force due to depletion of ATP, lactic acid buildup, or ion imbalance.

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Tropomyosin

A protein that blocks myosin-binding sites on actin, preventing contraction when calcium levels are low.

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Troponin

A protein with a binding site for calcium that controls the position of tropomyosin.

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Depolarization

The influx of sodium ions into the muscle fiber, caused by ACh binding, leading to membrane depolarization.

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Excitation-Contraction Coupling

The process linking the electrical signal to the mechanical contraction of muscle.

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Hydrolysis of ATP

The breakdown of ATP into ADP and inorganic phosphate, providing energy for myosin movement.

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Muscle tension

Force created by a contracting muscle.

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Load

Weight or opposing force that hinders muscle contraction.

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Action potential

The change in muscle fiber membrane potential that initiates contraction.

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Latent period

Period between action potential and start of muscle contraction.

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Cross-bridge cycling

A repeating cycle during muscle contraction where myosin heads bind to actin, pull, release, and reset.

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Acetylcholinesterase

An enzyme that breaks down acetylcholine, terminating its action at the neuromuscular junction.

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Smooth Muscle Cells

Elongated and smaller compared to skeletal muscle cells, lacking sarcomeres.

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Caveolae

Specialized invaginations in the smooth muscle sarcolemma, located close to the sarcoplasmic reticulum.

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Source of Ca2+ in Smooth Muscle

Primarily from extracellular fluid, with intracellular sarcoplasmic reticulum (SR) stores contributing.

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Ca2+ Release in Smooth Muscle

Calcium entry through extracellular fluid and release from the sarcoplasmic reticulum.

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Smooth Muscle Contraction

Process of muscle contraction initiated by cytosolic calcium associating with calmodulin.

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Energy Use in Muscle

Energy is predominantly stored, and less energy is used at peak activity. Energy stores are rebuilt during recovery.

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Central Fatigue

The central nervous system's (CNS) reduced ability to send signals to muscles.

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Peripheral Fatigue

Changes or impairments in the neuromuscular system, including the neuromuscular junction, muscle fibers, or muscle metabolism.

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Slow Twitch Fibers

Fibers with high oxidative capacity, low glycolytic capacity, and slow contraction speed.

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Fast Twitch Fibers

Fibers with high oxidative and glycolytic capacity, and fast contraction speed.

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Motor Control Hierarchy

Hierarchical system of the brain for controlling movements, from high-level planning to local execution.

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Study Notes

  • Muscle tissue contracts to generate force, enabling voluntary (skeletal) and involuntary (cardiac/smooth) movements.
  • Muscle tissues possess different properties from other cells.
  • Contraction is muscle tissue's specialization, resulting in becoming shorter and tighter, allowing movement.

Types of Muscle Tissue

  • Skeletal muscle is attached to bones via tendons, has a striated appearance, and is under voluntary control.
  • Skeletal muscle functions include movement, joint stabilization, heat production, organ protection, and control of body entrances/exits.
  • Cardiac muscle is located in the heart, striated, with cells connected by intercalated discs, and is under involuntary control.
  • Cardiac muscle pumps blood, maintains blood pressure via heartbeats.
  • Smooth muscle is found in hollow organ walls, lacks striations and is under involuntary control.
  • Smooth muscle regulates vessel diameter for circulation and moves substances in digestive, urinary, reproductive, and respiratory systems.
  • Different muscle types have different structures and functions in the body.
  • There are 3 types of muscle tissue in the body: skeletal, cardiac and smooth.
  • Skeletal and cardiac muscle tissue is striated, while smooth muscle is non-striated.

Muscle Fiber Structure and Sarcomere

  • A skeletal muscle is made of muscle fibers (cells), myofibrils, and sarcomeres.
  • Muscle fibers contain sarcoplasm (cytoplasm), a sarcolemma (cell membrane), and myofibrils (contractile units).
  • The sarcoplasm is the cytoplasm of a muscle cell with the cell membrane being the sarcolemma.
  • Sarcomeres are the functional units within myofibrils.
  • Each myofibril contains sarcomeres.
  • Each sarcomere contains myosin and actin.
  • Myosin (thick filament) consists of strands of protein with tiny hooks.
  • Myosin has a tail and a head.
  • Myosin heads stick out at an angle of 120 degrees, and myosin includes an ATPase site.
  • Myosin heads have affinity for actin, and myosin tails have affinity for myosin.
  • Actin (thin filament) comprise thinner strands that act as tracks for myosin.
  • F-actin consists of helical filaments made of two strands of fibrous actin.
  • F-actin is polymer of ~200 globular actins, called G-actins with myosin-head binding sites.
  • Myosin and actin filaments overlap in the sarcomere, surrounded by each other.
  • The Z-line marks the boundary of each sarcomere.
  • The H-zone is the central region of the sarcomere containing only myosin, visible when the muscle is relaxed.
  • The A-band spans the entire length of the myosin filaments and remains constant during contraction.
  • The I-band contains only actin filaments and shortens during contraction.
  • Skeletal muscle is striated, because of the highly regular arrangements of contractile filaments which overlap.
  • Smooth muscle cells are elongated and smaller than skeletal muscle cells.
  • Actin and myosin in smooth muscle overlap in an X-shape.
  • Smooth muscle does not have sarcomeres or Z lines.

Muscle Contraction

  • Muscle tension is the force created by a contracting muscle.
  • Load is the weight or force opposing muscle contraction.
  • A motor neuron stimulates a muscle fibre to contract.
  • An action potential causes the muscle fibre to contract, which generates tension.
  • Study of the sarcomere via electron microscopy led to the sliding filament theory of muscle contraction.
  • During muscle contraction, Z-lines move closer to the center.
  • Myosin bands do not change in length.
  • Thin actin filaments slide toward the center of the sarcomere along thick myosin filaments during contraction.

How Muscle Contraction Happens: The Sliding Filament Theory

  • A motor neuron sends an action potential (electrical signal).
  • Acetylcholine (ACh) is released at the neuromuscular junction, binding to muscle cell receptors and allowing sodium ions to enter, which spreads an electrical signal.
  • This process occurs at the motor endplate.
  • Each axon forms a synapse with one or more muscle fibres, collectively known as the neuromuscular junction (NMJ).
  • Neuronal action potential depolarizes the motor endplate in the muscle fibre.
  • Action potential is released (ACh, neurotransmitter).
  • ACh binds to nicotinic acetylcholine receptors (nAChR; ligand-gated ion channels), which causes the nAChRs to open.
  • Sodium ions flow into the muscle fibre, causing local depolarisation of motor endplate.
  • Action of acetylcholine is terminated by acetylcholinesterase, which breaks down ACh.
  • Ligand-gated ion channels allow Na+ ions to flow through into the muscle.
  • Excitation-contraction coupling involves the signal traveling along T-tubules, causing the sarcoplasmic reticulum (SR) to release calcium ions (Ca²⁺).
  • The latent period is when the action potential happens.
  • Calcium binds to troponin on actin, exposing myosin binding sites.
  • Cross-bridge cycling involves myosin heads attaching to actin (cross-bridge formation).
  • Myosin heads are bound to actin to form cross-bridges.
  • The power stroke occurs when myosin heads pull actin filaments closer, requiring ATP.
  • The Sliding Filament Theory can be viewed in action at https://www.youtube.com/watch?v=BVcgO4p88AA between 0m0sec – 0m40sec.
  • ATP binds to myosin heads to release them from actin.
  • ATP is used to re-cock myosin heads and pull the actin with it.
  • Repeated cycles shorten the muscle, generating movement.
  • Excitation-contraction coupling in smooth muscle has similarities to skeletal muscle as Ca2+ binding initiates contraction and cross-bridge cycling (of myosin and actin) produces contraction.
  • Excitation-contraction coupling in smooth muscle differs to skeletal muscle in with the source, release , and use of Ca2+ in contraction

Cross-Bridge Cycling

  • Cross-bridge cycling refers to the action of myosin, actin, troponin, tropomyosin, calcium, and ATP.
  • ATP provides energy for cross-bridge cycling.
  • ATP has two distinct roles in muscle contraction: binding to musing and hydrolisis.
  • ATP binding to myosin disrupts the actin-myosin link.
  • ATP hydrolysis produces energy for cross-bridge movement ('resets' the myosin head).

Muscle Relaxation

  • Brain signals stop, and calcium ions are pumped back into the sarcoplasmic reticulum.
  • Tropomyosin covers actin filaments, blocking myosin attachment, thus halting contraction.

Different Muscle Fiber Types

  • Slow oxidative fibers (Type I) use oxygen aerobically for endurance, do not produce much power, and resist fatigue.
  • Fast oxidative fibers (Type IIa) use oxygen, work faster, suitable for strength and endurance, and fatigue quicker than Type I.
  • Fast glycolytic fibers (Type IIb) use glycolysis, contract quickly/powerfully, fatigue rapidly, suitable for short/explosive activities.
  • Different types of physical activity lead to different percentages of muscle fibre types in skeletal muscle.
  • There are different types of skeletal muscle fibre.
  • Slow twitch fibers (ST I) are slow oxidative.
  • Fast twitch fibers (FTa or FTb, or IIa/IIb) are fast oxidative / fast glycolytic.
  • Muscle fibre types differ in metabolism, speed of rapid shortening, and resistance to fatigue.
  • Muscle fibre types allow muscles to carry out different types of movement.

Smooth Muscle Contraction

  • Smooth muscle contracts slowly and sustains contraction longer.
  • Calmodulin (not troponin) controls contraction.
  • Calcium binds to calmodulin, activating a kinase enzyme that phosphorylates myosin, enabling actin binding.
  • This process is slower and more controlled than in skeletal muscle.
  • Cytosolic Ca2+ associates with calmodulin to initiate contraction.
  • SR (sarcoplasmic reticulum) is in caveolae, which are close to the sarcolemma.
  • Contraction leads to quick depolarisation.

Muscle Fatigue

  • Muscle fatigue occurs when the muscle cannot generate force.
  • Causes include ATP depletion.
  • Causes include lactic acid build up.
  • Causes include ion imbalance.
  • Smooth muscle resists fatigue due to lower energy use and prolonged contraction ability.
  • Usually 30% of ATP available is used in strenuous exercise.

Muscle Contraction Overview:

  • Actin and myosin filaments slide past each other (cross-bridge cycling).
  • Myosin heads bind to actin.
  • ATP provides energy.
  • Calcium ions (Ca²⁺) control contraction.
  • Troponin and tropomyosin regulate access to binding sites for myosin on actin.
  • ATP binds to myosin heads, causing them to detach from actin (if previously bound).
  • When ATP is hydrolyzed, the myosin head "re-energizes".
  • Myosin then attaches to specific binding sites on the actin filament, forming a cross-bridge.
  • Myosin heads pivot, pulling the actin filament during the power stroke.

Regulation:

  • Tropomyosin blocks myosin-binding sites on actin.
  • Troponin has a binding site for calcium.
  • When calcium levels are low, tropomyosin blocks the myosin-binding sites on actin, preventing contraction.
  • Rising calcium levels cause tropomyosin to shift, exposing the binding sites and allowing myosin to bind to actin.

What Triggers Contraction?

  • The contraction is triggered by an increase in intracellular calcium (Ca²⁺).
  • A motor neuron sends a signal (action potential) to the muscle fiber.
  • Acetylcholine (ACh) is released.
  • Action potential spreads along the muscle fiber and through the T-tubules.
  • The sarcoplasmic reticulum (SR) releases calcium into the muscle fiber's cytoplasm.
  • Calcium ions bind to troponin, which causes tropomyosin to shift, exposing the binding sites on actin for myosin.
  • Troponin changes shape, which causes tropomyosin to move and expose the binding sites on actin.
  • Once the action potential ends, calcium is pumped back into the sarcoplasmic reticulum (SR).
  • As calcium levels drop, troponin goes back to its original shape, causing tropomyosin to block the binding sites on actin again.

ATP and Its Role:

  • Binding to Myosin: When ATP binds to myosin, it breaks the bond between myosin and actin.
  • Hydrolysis of ATP: ATP is broken down into ADP and inorganic phosphate (Pi), which provides the energy for the myosin head to move (reset) and perform the power stroke.

Excitation Contraction Coupling Relies On:

  • T-tubule and sarcoplasmic reticulum.
  • Linkage between the structures: Dihydropyridine (DHP) and ryanodine receptors.
  • Increase in intracellular calcium.
  • Ca2+ ATPase lowers intracellular calcium.
  • Action occurs for Myosin, actin, troponin, tropomyosin, calcium and ATP between 0m40sec – 2m00.
  • Action potential in T-tubule membrane causes SR Ca2+ release channels to open.
  • Ryanodine receptors (foot structures) open Ca2+ release channels.
  • Ca2+ is pumped back into the SR by Ca2+ ATPase.
  • There needs increased intracellular Ca2+ for contraction.
  • Source of Ca2+ sarcoplasmic reticulum (SR).
  • SR membrane contains Ca2+ release channels that are voltage sensitive.
  • Channels are closed at 'rest'.
  • T-tubules are needed for quick depolarisation.
  • There are no T-Tubules in smooth muscle cells.

Smooth Muscle Information

  • In the smooth muscle, actin and myosin do not form sarcomeres
  • Sarcoplasmic reticulum is situated close to the plasma membrane
  • Calcium source can be extracellular and from the SR
  • The sarcoplasmic reticulum is situated close to the plasma membrane
  • Ca²⁺ enters from extracellular fluid and ligand-gated channels initial Ca2+ entry, which triggers voltage-gated Ca2+ channels allowing further Ca2+ entry
  • “Second messenger” signalling in the cell triggers Ca2+ release from the sarcoplasmic reticulum
  • This is by muscarinic ACh receptor stimulation, G-protein coupled receptors, and inosital
  • If IP3/DAG is involved contraction of smooth muscle takes place.
  • Smooth muscle uses Myosin light-chain kinase (MLCK), and calcium

Metabolism In Muscle

  • ATP is available from multiple sources in muscle: creatine phosphate, glycogen, and fatty acids/amino acids
  • Energy is stored during rest/recovery and used during activity
  • Fatigue is not caused by a lack of ATP
  • At rest energy is stored, while at peak activity energy is used
  • During recovery, energy stores are re-built

Fatigue

  • Central fatigue is a decrease in the ability of the central nervous system (CNS) to send signals to the muscles, leading to a reduction in voluntary activation and performance.
  • Central fatigue relates to the motor cortex as mechanisms involve reduced neural drive, decreased frequency/synchronization of motoneurons, and impaired motivation/effort perception
  • Peripheral fatigue refers to changes or impairments in the neuromuscular system, including the neuromuscular junction, muscle fibers, or muscle metabolism.
  • Peripheral fatigue is caused by mechanisms such as muscle bioenergetics (e.g., ATP depletion, lactate accumulation), muscle damage, impaired excitation-contraction coupling, or neuromuscular transmission failure.

Control Of Movement

  • The motor control hierarchy controls movement from the brain.
  • Flexion and extension of antagonistic muscles moves joints.
  • Voluntary movements involve conscious awareness and involuntary movements involve unconscious or automatic actions.
  • Learned actions start as voluntary but gradually become automatic
  • The brain controls most movement through something called the motor control hierarchy
  • Movements are of two types
    • Voluntary – conscious awareness
    • Involuntary – unconscious or automatic

Additional Resources:

  • Recommended reading: Human Physiology: An Integrated Approach by Dee Unglaub Silverthorn.

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