Muscle Physiology: Thick Filaments Quiz

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Questions and Answers

Which of the following statements about thick filaments is true?

  • Thick filaments have myosin heads present only in areas of myosin-actin overlap. (correct)
  • Thick filaments are composed entirely of actin.
  • Thick filaments do not play a role in muscle contraction.
  • Thick filaments consist of two strands of actin subunits.

Troponin is one of the proteins found in thin filaments.

True (A)

What are the primary components of a thick filament?

Many myosin molecules with heads protruding from opposite ends.

Each thin filament consists of two strands of ______ subunits twisted into a helix.

<p>actin</p> Signup and view all the answers

Match the following components with their respective functions or characteristics:

<p>Myosin heads = Bind to actin during contraction Troponin = Regulates muscle contraction Actin = Forms the core structure of thin filaments Tropomyosin = Blocks myosin binding sites on actin</p> Signup and view all the answers

What is the primary structure that generates force during muscle contraction?

<p>Cross bridges (B)</p> Signup and view all the answers

Thin filaments slide past thick filaments during muscle contraction.

<p>True (A)</p> Signup and view all the answers

Name the two types of filaments involved in the sliding filament model.

<p>Actin and myosin</p> Signup and view all the answers

The _____ disc marks the boundary of a sarcomere.

<p>Z</p> Signup and view all the answers

Match the following parts of a muscle fiber with their functions:

<p>I band = Region of thin filaments only A band = Region of overlap of thick and thin filaments H zone = Zone of thick filaments only M line = Middle of the sarcomere</p> Signup and view all the answers

What must occur for muscle fiber shortening to happen?

<p>Tension generated by cross bridges must exceed opposing forces (C)</p> Signup and view all the answers

In a relaxed muscle state, thin and thick filaments completely overlap.

<p>False (B)</p> Signup and view all the answers

During contraction, actin and myosin _____ more.

<p>overlap</p> Signup and view all the answers

What initiates the sliding filament mechanism of muscle contraction?

<p>Binding of myosin heads to actin (D)</p> Signup and view all the answers

During muscle contraction, the A bands shorten.

<p>False (B)</p> Signup and view all the answers

What is the role of intracellular Ca2+ levels during muscle contraction?

<p>They must rise briefly to trigger contraction.</p> Signup and view all the answers

The action potential is propagated along the ______ after it is generated.

<p>sarcolemma</p> Signup and view all the answers

Match the following components with their functions in muscle contraction:

<p>Z discs = End points of the sarcomere H zone = Region without thin filaments I band = Region containing only thin filaments A band = Region containing both thick and thin filaments</p> Signup and view all the answers

What happens to the Z discs during muscle contraction?

<p>They are pulled closer to the M line (C)</p> Signup and view all the answers

Excitation-contraction coupling does not involve ion permeability changes.

<p>False (B)</p> Signup and view all the answers

How do cross bridges contribute to muscle contraction?

<p>They form and break, ratcheting thin filaments toward the center.</p> Signup and view all the answers

What ion primarily enters the cell during the depolarization phase of action potential generation?

<p>Na+ (C)</p> Signup and view all the answers

During the action potential, voltage-gated K+ channels open before Na+ channels.

<p>False (B)</p> Signup and view all the answers

What generates the end plate potential at the neuromuscular junction?

<p>Acetylcholine (ACh) binding to receptors.</p> Signup and view all the answers

The spread of local depolarization current along the sarcolemma opens __________ channels.

<p>voltage-gated sodium</p> Signup and view all the answers

Match the following channels with their states during an action potential:

<p>Na+ Channel = Open during depolarization K+ Channel = Open during repolarization Ca2+ Channel = Open at the axon terminal Voltage-gated Channel = Triggered by local depolarization</p> Signup and view all the answers

What follows the opening of voltage-gated sodium channels in action potential generation?

<p>K+ exits the cell (B)</p> Signup and view all the answers

The local depolarization wave is responsible for starting new action potentials in adjacent areas of the sarcolemma.

<p>True (A)</p> Signup and view all the answers

What is the role of acetylcholine (ACh) in muscle cell activation?

<p>It binds to receptors and initiates depolarization.</p> Signup and view all the answers

What causes the detachment of the cross bridge in the cross bridge cycle?

<p>The attachment of ATP to the myosin head (D)</p> Signup and view all the answers

The myosin head pivots and bends to pull the actin filament toward the M line.

<p>True (A)</p> Signup and view all the answers

What happens to the myosin head during the 'cocking' phase of the cross bridge cycle?

<p>It moves into a high-energy state</p> Signup and view all the answers

In the absence of ATP, myosin heads will not detach, causing __________.

<p>rigor mortis</p> Signup and view all the answers

Match the following steps of the cross bridge cycle with their descriptions:

<p>Cross bridge formation = Energized myosin head attaches to actin Power stroke = Myosin head pivots and pulls actin filament Cocking of myosin head = Myosin head moves to high-energy state Cross bridge detachment = ATP binds to myosin head</p> Signup and view all the answers

Which molecule is hydrolyzed to provide energy for the myosin head to move to a high-energy state?

<p>ATP (D)</p> Signup and view all the answers

What triggers the release of Ca2+ from the sarcoplasmic reticulum?

<p>Change in shape of sarcoplasmic reticulum (D)</p> Signup and view all the answers

Troponin prevents myosin from binding to actin until calcium binds to it.

<p>True (A)</p> Signup and view all the answers

ADP and Pi are released during the cocking phase of the cross bridge cycle.

<p>False (B)</p> Signup and view all the answers

What is the role of calcium ions (Ca2+) in the cross bridge cycle?

<p>To expose binding sites on actin filaments</p> Signup and view all the answers

What happens when calcium binds to troponin?

<p>Troponin changes shape and removes the blocking action of tropomyosin.</p> Signup and view all the answers

The process where myosin binds to actin to form ___________ is known as contraction.

<p>cross bridges</p> Signup and view all the answers

Match the components in muscle contraction with their roles:

<p>Ca2+ = Signals release of troponin Troponin = Binds calcium and moves tropomyosin Tropomyosin = Blocks active sites on actin Myosin = Forms cross bridges with actin</p> Signup and view all the answers

What is the outcome of myosin binding to exposed active sites on actin?

<p>Cross bridge cycling and contraction (D)</p> Signup and view all the answers

The contraction process occurs before E-C coupling is complete.

<p>False (B)</p> Signup and view all the answers

What does the term E-C coupling refer to?

<p>The process of excitation-contraction coupling in muscle fibers.</p> Signup and view all the answers

Flashcards

Myosin

A protein found in muscle fibers that forms the thick filaments within a sarcomere.

Actin

The protein that forms the thin filaments within a sarcomere. These filaments contain binding sites for myosin heads.

H-Zone

Located at the center of the sarcomere, this zone lacks myosin heads, allowing for efficient muscle contraction.

Myosin Head

The part of the myosin molecule that binds to actin and facilitates the sliding process of filaments during muscle contraction.

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Actin Binding Site

The area on the actin filament where the myosin head binds.

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Myofibril

A protein filament that forms the backbone of a muscle fiber, made up of repeating units called sarcomeres.

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Sarcolemma

The plasma membrane of a muscle cell.

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Sarcomere

The basic unit of muscle contraction. It is the repeating unit of a myofibril.

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I band

The light band in a sarcomere, containing only thin filaments (actin).

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A band

The dark band in a sarcomere, containing both thick (myosin) and thin (actin) filaments.

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Thick filament (Myosin)

A protein filament involved in muscle contraction, responsible for generating force. It has 'heads' which bind to actin.

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Thin filament (Actin)

A protein filament involved in muscle contraction, it serves as a 'track' for myosin heads to bind to.

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Sliding Filament Model

Model of muscle contraction explaining how muscle fibers shorten. It describes how the thin filaments (actin) slide past the thick filaments (myosin) due to interactions of myosin heads with actin.

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Neuromuscular Junction

The point where a motor neuron connects to a muscle fiber, transmitting signals for contraction.

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Excitation-Contraction Coupling

The process of converting a nerve impulse into muscle contraction. This involves the release of calcium ions and the interaction of actin and myosin.

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Troponin

A protein found in muscle fibers that binds to calcium ions, triggering muscle contraction.

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Synaptic cleft

The space between the axon terminal of a motor neuron and the sarcolemma of a muscle fiber.

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Motor end plate

A specialized region of the sarcolemma that's directly beneath the axon terminal of a motor neuron.

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End plate potential (EPP)

A localized depolarization of the sarcolemma at the motor end plate, caused by the binding of acetylcholine to receptors.

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Action potential (AP)

A rapid rise and fall in membrane potential that spreads along the sarcolemma, triggered by an EPP.

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Refractory period

The period during which the muscle fiber is unable to generate another action potential.

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Depolarization

The movement of ions across the sarcolemma, causing a change in membrane potential.

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Repolarization

The return of the membrane potential to its resting value.

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Excitation-Contraction Coupling (E-C Coupling)

The process where an action potential in a motor neuron triggers the release of calcium ions (Ca2+) from the sarcoplasmic reticulum (SR) into the muscle fiber's cytosol.

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Terminal Cisternae

The specialized region of the SR that lies close to the transverse tubules (T-tubules) in a muscle fiber.

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Tropomyosin

A protein that wraps around actin filaments and blocks myosin binding sites in relaxed muscle.

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Active Sites

The location on an actin filament where the myosin head binds.

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Cross Bridge Cycling

The process where myosin heads bind to actin, forming cross-bridges, and pull the actin filaments towards the center of the sarcomere, causing muscle contraction.

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Troponin Shape Change

The change in shape of troponin caused by calcium binding, which exposes the active sites on actin filaments.

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Calcium Reuptake

The process of calcium ions (Ca2+) being pumped back into the SR after a contraction, allowing the muscle to relax.

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Cross bridge formation

The stage when the energized myosin head binds to an actin filament, forming a connection. This is the starting point of the muscle contraction cycle.

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Power Stroke

The myosin head pivots and bends, pulling the actin filament towards the center of the sarcomere. This generates the force behind muscle contraction.

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Cross bridge detachment

The myosin head detaches from the actin filament. This allows the cycle to repeat.

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Cocking of the myosin head

An energized state of the myosin head, ready to bind to actin. This is achieved by the hydrolysis of ATP.

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ATP's role in the cross bridge cycle

The molecule that powers the cross bridge cycle. Hydrolysis of ATP provides the energy for the myosin head to move and detach from actin.

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High-energy state of Myosin

The state of the myosin head after it has hydrolyzed ATP. This high-energy state allows the head to bind to actin and initiate the power stroke.

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Rigor mortis

When ATP is absent, the myosin head stays attached to the actin filament, causing muscle stiffness. This typically occurs during death.

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Study Notes

Muscular System Overview

  • Muscles comprise nearly half of the body's mass.
  • Muscles transform chemical energy (ATP) into directed mechanical energy, creating force.
  • Muscles are classified into three types: skeletal, cardiac, and smooth.
  • Prefixes like "myo," "mys," and "sarco" are frequently used in muscle-related terminology.

Muscle Tissue Types

Skeletal Muscle

  • Skeletal muscles are attached to bones and skin.
  • Their cells are elongated, called muscle fibers, and are striated (striped).
  • Skeletal muscle contractions are voluntary (consciously controlled).
  • These muscles contract quickly but tire easily.
  • They require nervous system stimulation for contraction.

Cardiac Muscle

  • Found only in the heart, forming the bulk of its walls.
  • Cardiac muscle cells are striated.
  • These muscles can contract without nervous system stimulation.
  • Contraction of cardiac muscle is involuntary.

Smooth Muscle

  • Found in the walls of hollow organs (e.g., stomach, urinary bladder, airways).
  • Smooth muscle cells lack striations.
  • Smooth muscle contractions are involuntary.
  • Smooth muscle can contract without nervous system stimulation.

Muscle Tissue Comparisons

  • A table comparing characteristics of skeletal, cardiac, and smooth muscle is provided.
    • Key distinctions include body location, cell shape/appearance, myofibrils/sarcomeres, and presence of T tubules and/or gap junctions.
    • Different types also have various contraction regulation mechanisms.

Special Characteristics of Muscle Tissue

  • Excitability (responsiveness): The ability to receive and respond to stimuli.
  • Contractility: The ability to shorten forcibly when stimulated.
  • Extensibility: The ability to be stretched.
  • Elasticity: The ability to recoil to resting length.

Muscle Functions

  • Movement: Movement of bones or fluids (e.g., blood).
  • Maintaining posture and body position.
  • Stabilizing joints.
  • Heat generation: Primarily skeletal muscles.
  • Additional functions: Protecting organs, forming valves, controlling pupil and lumen size, and causing "goosebumps."

Skeletal Muscle Structure and Function

  • Each skeletal muscle is served by one nerve, one artery, and one or more veins.
  • The connective tissue sheaths (epimysium, perimysium, and endomysium) surround and support muscle fibers.
  • Muscles attach in at least two places:
    • Insertion (movable bone)
    • Origin (immovable or less movable bone)
    • Some attachments are direct, others indirect (tendons or aponeuroses).

Skeletal Muscle Fiber Structure

  • Skeletal muscle fibers are long, cylindrical, multinucleate cells with peripheral nuclei.
  • Sarcolemma: The plasma membrane of the muscle fiber.
  • Sarcoplasm: The cytoplasm of the muscle fiber containing glycosomes and myoglobin (oxygen-binding protein).
  • Myofibrils: Contractile organelles within the muscle fiber, containing sarcomeres (the functional units of contraction).
  • Sarcoplasmic reticulum: Specialized smooth endoplasmic reticulum that regulates calcium ion levels within the muscle fiber.
  • T tubules: Tubular infoldings of the sarcolemma that penetrate through the muscle fiber, bringing the action potential from the surface membrane into the interior of the cell.

Myofibrils and Sarcomeres

  • Myofibrils are densely packed, rod-like elements that compose roughly 80% of the muscle cell volume.
  • They are composed of repeating subunits called sarcomeres.
  • Sarcomeres exhibit striations (alternating light and dark bands).
  • The structure of thick and thin filaments within sarcomeres accounts for the banding patterns.

Sliding Filament Model of Contraction

  • In a relaxed muscle, thin and thick filaments overlap only at the ends of the A band.
  • During contraction, thin filaments slide past thick filaments, causing the sarcomere to shorten.
  • Myosin heads bind to actin, forming cross bridges, pulling the thin filaments toward the center of the sarcomere.
  • ATP is crucial for cross-bridge detachment and myosin head recocking.

Physiology of Skeletal Muscle Fibers

  • Excitation: A nervous system signal is required before contraction can occur.
  • Excitation-contraction coupling: The events that connect the nerve signal to the muscle contraction.
  • AP propagated along the sarcolemma and down into T tubules, which eventually causes SR to release calcium ions.

Neuromuscular Junction (NMJ)

  • A specialized area where a motor neuron synaptic terminal meets a muscle fiber.
  • Synaptic vesicles contain acetylcholine, a neurotransmitter involved in signal transmission across the synapse.

Events at the Neuromuscular Junction

  • Nerve impulse arrives at the axon terminal.
  • ACh is released into the synaptic cleft.
  • ACh diffuses across the cleft and binds to receptors on the sarcolemma.
  • This binding triggers a local electrical event (end-plate potential).
  • The end-plate potential triggers an action potential in the muscle fiber.

Destruction of Acetylcholine

  • Acetylcholinesterase breaks down ACh in the neuromuscular junction.
  • This termination of ACh activity prevents continuous muscle fiber contraction.

Channels in Muscle Contraction

  • Voltage-gated channels are central to the process.
  • ACh binds to receptors, opening ligand-gated channels allowing Na+ and K+ flow.
  • Voltage-gated Na+ channels open leading to depolarization (action potential).
  • Voltage-sensitive proteins in T tubules help trigger Ca2+ release.

Role of Calcium in Contraction

  • At low Ca2+ levels, tropomyosin blocks active sites on actin, preventing myosin from binding.
  • At higher Ca2+ levels, Ca2+ binds to troponin, moving tropomyosin away, exposing active sites, and allowing myosin binding.

Cross Bridge Cycle

  • The cycle of cross-bridge formation, working stroke, and detachment continually pulls thin filaments inward.
  • Requires energy from ATP.
  • Crucial to muscle contraction.

Muscle Mechanics

  • Isometric contractions: Muscle tension increases but does not exceed the load, no shortening occurs.
  • Isotonic contractions: Muscle shortens because muscle tension exceeds the load.
  • Force and duration of contraction vary: Based on stimulus frequency and intensity.
  • Motor units: A motor neuron and all the muscle fibers it supplies. Smaller motor units enable fine control

Homeostatic Imbalances

  • Myasthenia gravis: Autoimmune disease where antibodies block ACh receptors leading to progressive muscle weakness.
  • Rigor mortis: When death occurs, muscle fibers run out of ATP causing cross-bridge detachment failure, resulting in muscle stiffening.

Muscular Dystrophies

  • Duchenne muscular dystrophy (DMD): Inherited sex-linked disorder, characterized by a deficiency or absence of dystrophin that supports the sarcolemma.

Polio

  • Polio is a viral infection that destroys motor neurons.

Muscle Action Types

  • Agonists: Main movers in joint actions
  • Antagonists: Muscles that oppose or reverse agonist actions
  • Synergists: Aid agonists in a movement
  • Fixators: Stabilize bones involved in the movement.

Muscle Names

  • Location: Reflecting the muscles' location (e.g., frontalis, pectoralis).
  • Size: Indicating muscle size (e.g., maximus, minimus).
  • Shape: Based on muscle shape (e.g., deltoid, trapezius).
  • Direction of fibers: Muscle fibers' orientation (e.g., rectus, oblique).
  • Number of origins: Based on the number of attachments to the bone (e.g., bicep, tricep).
  • Attachments: The location and attachment points on bones.
  • Movement actions: The type of movement the muscle performs (e.g., flexors, extensors).

Muscle Fiber Types

  • Speed of contraction (slow/fast twitch): Classified based on the speed of myosin ATPase activity.
  • Metabolic pathways: Classified based on how they generate ATP (aerobic vs. anaerobic).
  • Oxidative fibers: Use aerobic pathways to generate ATP, suited for endurance activities.
  • Glycolytic fibers: Use anaerobic glycolysis to generate ATP, more suited for short, powerful bursts of activity.

Exercise Types

  • Isotonic: Muscles change in length during contraction (e.g., lifting weights).
  • Isometric: Muscle tension increases but no change in length (e.g., holding a heavy object).
  • Anaerobic: Respiration without oxygen, can result in lactic acid buildup.
  • Aerobic: Respiration using oxygen, a longer term energy source.

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