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Questions and Answers
What initiates the muscle contraction according to the sliding filament mechanism?
What initiates the muscle contraction according to the sliding filament mechanism?
Which statement correctly describes the two states of crossbridges?
Which statement correctly describes the two states of crossbridges?
What is the primary role of myosin crossbridges in muscle contraction?
What is the primary role of myosin crossbridges in muscle contraction?
Why is titin significant in the context of skeletal muscle?
Why is titin significant in the context of skeletal muscle?
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In skeletal muscle metabolism, what is the main function of ATP?
In skeletal muscle metabolism, what is the main function of ATP?
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What occurs after Myosin binds to actin during muscle contraction?
What occurs after Myosin binds to actin during muscle contraction?
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In the process of muscle contraction, what role does ATP play?
In the process of muscle contraction, what role does ATP play?
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What is the initial state of myosin before the power stroke occurs?
What is the initial state of myosin before the power stroke occurs?
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What specifically enables the myosin head to swivel during contraction?
What specifically enables the myosin head to swivel during contraction?
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What happens to actin during the power stroke?
What happens to actin during the power stroke?
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How is energy generated for muscle contraction?
How is energy generated for muscle contraction?
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What results from the hydrolysis of ATP during muscle contraction?
What results from the hydrolysis of ATP during muscle contraction?
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Which type of filament moves during muscle contraction?
Which type of filament moves during muscle contraction?
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What causes the myosin head to perform a power stroke during muscle contraction?
What causes the myosin head to perform a power stroke during muscle contraction?
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What occurs immediately after the power stroke is completed?
What occurs immediately after the power stroke is completed?
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What happens when a new ATP molecule binds to the myosin head?
What happens when a new ATP molecule binds to the myosin head?
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What characterizes the rigor mortis state in muscles?
What characterizes the rigor mortis state in muscles?
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Which part of the muscle contraction process helps pull the actin filaments toward the M line?
Which part of the muscle contraction process helps pull the actin filaments toward the M line?
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In the context of the sliding filament theory, what is the role of tropomyosin?
In the context of the sliding filament theory, what is the role of tropomyosin?
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What triggers the shortening of the sarcomere during muscle contraction?
What triggers the shortening of the sarcomere during muscle contraction?
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What condition occurs if there is a lack of ATP available to the muscle?
What condition occurs if there is a lack of ATP available to the muscle?
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What is the role of Ca2+ in the contraction of skeletal muscle fibers?
What is the role of Ca2+ in the contraction of skeletal muscle fibers?
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What happens to the myosin head when ATP binds to it?
What happens to the myosin head when ATP binds to it?
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Which statement about the high-affinity sites on troponin C (TnC) is correct?
Which statement about the high-affinity sites on troponin C (TnC) is correct?
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During muscle contraction, which changes occur in the sarcomere structure?
During muscle contraction, which changes occur in the sarcomere structure?
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What does the sliding filament theory describe?
What does the sliding filament theory describe?
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What is the result of Ca2+ binding to the low-affinity sites on TnC?
What is the result of Ca2+ binding to the low-affinity sites on TnC?
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Which part of the skeletal muscle fiber is primarily involved in crossbridge formation?
Which part of the skeletal muscle fiber is primarily involved in crossbridge formation?
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What occurs immediately after ATP is hydrolyzed on the myosin head?
What occurs immediately after ATP is hydrolyzed on the myosin head?
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Which of the following conditions would prevent muscle contraction?
Which of the following conditions would prevent muscle contraction?
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What is required for the contraction cycle of skeletal muscle fibers to repeat?
What is required for the contraction cycle of skeletal muscle fibers to repeat?
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During relaxation of muscle, what happens to the calcium levels?
During relaxation of muscle, what happens to the calcium levels?
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Which molecule is responsible for initiating muscle contraction by binding to troponin?
Which molecule is responsible for initiating muscle contraction by binding to troponin?
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What happens to muscle fibers when the levels of Ca2+ decrease?
What happens to muscle fibers when the levels of Ca2+ decrease?
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What effect does tropomyosin have in a relaxed muscle state?
What effect does tropomyosin have in a relaxed muscle state?
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During excitation-contraction coupling, what is the role of acetylcholine (ACh)?
During excitation-contraction coupling, what is the role of acetylcholine (ACh)?
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What happens to the I band during muscle contraction?
What happens to the I band during muscle contraction?
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What initiates the conformational change in the troponin complex?
What initiates the conformational change in the troponin complex?
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What is the primary function of ATP in muscle contraction?
What is the primary function of ATP in muscle contraction?
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How does the transition between contracted and relaxed states occur in muscle fibers?
How does the transition between contracted and relaxed states occur in muscle fibers?
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When does the 'latent period' occur in muscle contraction?
When does the 'latent period' occur in muscle contraction?
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What substance is primarily synthesized during resting state in muscle fibers to store energy?
What substance is primarily synthesized during resting state in muscle fibers to store energy?
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How does the concentration of sarcoplasmic Ca2+ affect muscle tension?
How does the concentration of sarcoplasmic Ca2+ affect muscle tension?
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What is the primary mechanism by which muscle fibers regenerate ATP during contraction?
What is the primary mechanism by which muscle fibers regenerate ATP during contraction?
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What structural change occurs in the DHP receptor during excitation-contraction coupling?
What structural change occurs in the DHP receptor during excitation-contraction coupling?
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What occurs after myosin heads release ADP during contraction?
What occurs after myosin heads release ADP during contraction?
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How does relaxation of muscle fibers occur?
How does relaxation of muscle fibers occur?
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What must happen to Ca2+ for muscle contraction to cease?
What must happen to Ca2+ for muscle contraction to cease?
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Which part of the muscle fiber is primarily involved in the propagation of action potentials?
Which part of the muscle fiber is primarily involved in the propagation of action potentials?
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What triggers skeletal muscle contraction?
What triggers skeletal muscle contraction?
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Which sequence of structures correctly represents the pathway of action potentials necessary for skeletal muscle contraction?
Which sequence of structures correctly represents the pathway of action potentials necessary for skeletal muscle contraction?
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Which of the following correctly identifies the source of calcium release during muscle contraction?
Which of the following correctly identifies the source of calcium release during muscle contraction?
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During muscle contraction, which structure do thin filaments move toward?
During muscle contraction, which structure do thin filaments move toward?
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What process energizes the myosin head for muscle contraction?
What process energizes the myosin head for muscle contraction?
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Which of the following correctly describes the process at the neuromuscular junction?
Which of the following correctly describes the process at the neuromuscular junction?
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What happens to creatine phosphate levels during periods of high ATP demand?
What happens to creatine phosphate levels during periods of high ATP demand?
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Which enzyme is responsible for transferring a phosphate group from creatine phosphate to ADP?
Which enzyme is responsible for transferring a phosphate group from creatine phosphate to ADP?
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Study Notes
Skeletal Muscle
- Topic: Sliding filament mechanism, contraction-relaxation cycle, and muscle metabolism
- Objective 1: Detail of the sliding filament mechanism for muscle contraction and the contraction-relaxation cycle
- Objective 2: Detail of excitation-contraction coupling
- Objective 3: Muscle metabolism with respect to ATP production
Sliding Filament Mechanism for Muscle Contraction and Contraction-Relaxation Cycle
- Crossbridge formation: Myosin heads and actin filaments interlock, allowing myosin heads to bind to specific sites on actin. This is the driving force behind muscle contraction.
- Two states of crossbridges: Low-force (muscle relaxing but maintaining tone) and high-force (muscle contracting). Some crossbridge formation exists during relaxation (low-force).
- Troponin C (TnC): Within skeletal muscle, TnC has two high-affinity sites always occupied by Ca2+ (under physiological conditions). Two low-affinity sites bind and release Ca2+ as cytoplasmic [Ca2+] changes.
- High-affinity sites (structural sites) are sites with sustained activation from constant Ca2+ binding.
- Low-affinity sites located at TnC affect Tnl binding to actin. Myosin binding sites are covered by Tnl, attached to tropomyosin.
- Binding of Ca2+ to low-affinity sites leads to troponin complex conformational change. This weakens Tnl attachment to actin allowing tropomyosin to move. Also, myosin-binding sites on actin are exposed, aiding cross-bridge formation.
Excitation-Contraction (EC) Coupling
- 4 main events in excitation-contraction coupling:
- Acetylcholine (ACh) release from somatic motor neuron
- ACh initiates an action potential in the muscle fiber
- Action potential travels along the sarcolemma into T-tubules, triggering Ca2+ release from the sarcoplasmic reticulum (SR)
- Ca2+ binds to TnC, initiating muscle contraction
- Sequence of events for excitation-contraction coupling:
- Somatic motor neuron releases ACh at the neuromuscular junction.
- ACh binds to receptors on the motor end plate (muscle fiber).
- Receptor activation of Na+ channels increases Na+ permeability.
- Action potentials travel along sarcolemma.
- Muscle action potential travels along sarcolemma, into t-tubules. DHP receptors change shape.
- DHP receptors open RyRs (Ca2+ release channels) in SR. Ca2+ is released into cytoplasm.
- Ca2+ binds to TnC, allowing actin-myosin binding.
- Myosin heads execute power strokes.
- Actin filaments slide toward center of sarcomeres (contraction).
- To end a contraction, Ca2+ must be removed from sarcoplasm.
- SR pumps Ca2+ back into lumen.
- Ca2+ release from TnC: tropomyosin moves back to blocking position, blocking actin's myosin binding site (relaxation).
- Myosin heads are released, elastic elements pull filaments to their relaxed position.
Muscle Metabolism
- ATP: ATP is required for muscle contraction cycles. The available ATP reserve in skeletal muscle tissues sustains contraction for very few seconds
- Additional ATP generation: Creatine phosphate, anaerobic respiration, aerobic respiration are the three ways for muscle fibers to generate more ATP.
- Creatine Phosphate (PCr): A high energy molecule that donates a phosphate group to ADP to generate ATP. This is the initial/first source of ATP. This process is very rapid and occurs at the beginning of muscle contraction. The initial amount of ATP plus the amount released from creatine phosphate provides sufficient energy for about 15 seconds of maximum muscle contraction.
- Anaerobic Cellular Respiration: Generates 2 ATP molecules per glucose. It's used during heavy exercise, where a lack of oxygen causes pyruvic acid to be converted to lactic acid. Lactic acid diffuses into the blood and can be converted to glucose in the liver. Produces enough ATP to sustain muscle contraction for 30 to 40 seconds.
- Aerobic Cellular Respiration: Utilizes oxygen to produce 36 ATP molecules per glucose. This process utilizes pyruvic acid, fatty acids, and amino acids for aerobic ATP production. This sustained method produces energy for minutes to hours. This is critical during rest and moderate exercise.
Oxygen Debt
- Excess oxygen required after exercise is called oxygen debt.
- Oxygen debt function:
- Convert lactic acid back into glycogen.
- Resynthesize PCr (phosphocreatine) and ATP in muscle fibers.
- Replace oxygen removed from myoglobin.
- Sustain the increased chemical reactions resulting in elevated body temperature.
- Sustain the extra workload of organs (e.g., heart and lungs) after stopping exercise.
- Allow for extra energy consumption for tissue repair.
Sample Questions
- Question 1 & Answer: Contraction of myofibrils within a muscle fiber begins when calcium is released from the sarcoplasmic reticulum.
- Question 2 & Answer: The sequence of structures for action potential propagation is: somatic neuron, sarcolemma, T tubules
- Question 3 & Answer: Calcium is released from the terminal cisterns of sarcoplasmic reticulum.
- Question 4 & Answer: During muscle contractions, thin filaments are pulled toward the Z disc.
- Question 5 & Answer: ATP hydrolysis reaction energizes the myosin head.
- Question 6 & Answer: ACh is released into the neuromuscular junction, binding to receptors, stimulating the entry of sodium ions, and initiating the generation of an action potential, deep into the t-tubule.
- Question 7 & Answer: Concentration of creatine phosphate is highest during exercise.
- Question 8 & Answer: Creatine kinase catalyzes the transfer of a phosphate group.
- Question 9 & Answer: Majority of lactic acid is converted back into glucose in the liver
- Question 10 & Answer: Myoglobin has the ability to bind to oxygen.
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Description
Explore the complex processes involved in skeletal muscle contraction, focusing on the sliding filament mechanism and the contraction-relaxation cycle. Understand the role of troponin C and the excitation-contraction coupling in muscle metabolism and ATP production. This quiz will deepen your comprehension of how muscles operate and generate force.