Muscle Contraction Mechanisms and Cellular Energy
Essential Concepts in Muscle Physiology
Skeletal Muscle Anatomy: The Sarcomere
- A sarcomere (The basic contractile unit)
- Myofibril (A bundle of myofilaments)
- T-tubule; terminal cistern (Components of the Triad)
Sarcomere Components Defined
- Thin filaments
- I band: (Light band containing only thin filaments; spans from the Z line into the sarcomere.)
- Z line: (Anchors thin filaments and defines the boundary of a sarcomere.)
- H band: (Central part of the A band where only thick filaments are present—no overlap with thin filaments.)
- M line: (The center of the sarcomere, within the H zone, where thick filaments are linked.)
Excitation-Contraction Mechanisms
- None of these: The correct answer is the Nicotinic ACh receptor, which was not listed.
- Sarcoplasmic reticulum (The primary source of intracellular calcium)
- Depolarization (The electrical event initiating contraction)
- Ryanodine receptors (Calcium release channels on the sarcoplasmic reticulum)
Missing Protein in E-C Coupling
The missing protein is the voltage-gated sodium channel. These channels are essential for starting and spreading an action potential. Without them, the signal cannot travel—it just fades out before triggering a full muscle contraction.
Myosin Cross-Bridge Cycling Steps
- Troponin (The calcium binding protein in skeletal muscle)
- Myosin (The motor protein that forms cross-bridges)
- ADP and Pi (Required for the high-energy, cocked state of myosin)
- Hydrolysis of ATP (The process that powers the cocking of the myosin head)
- In rigor (The state of sustained binding when ATP is absent)
- Sequence of Events (4, 3, 2, 1):
- Binding to actin
- Loss of Pi (Inorganic Phosphate)
- Loss of ADP
- Return of the myosin head (Requires new ATP binding)
Muscle Contraction Dynamics and Types
- One twitch (The response to a single action potential)
- 10 ms (Typical duration of a muscle action potential)
- Fused tetanus (A sustained, maximal contraction with no relaxation)
- Fewer muscle fibers in each motor unit (Characteristic of muscles requiring fine motor control)
- Type IIx (Fast glycolytic muscle fibers)
- False (Regarding a statement about muscle fiber characteristics or recruitment)
- B and C (Factors influencing muscle force generation)
Cellular Energy Production
- Linking step and Krebs cycle (Key stages in aerobic metabolism)
- Thirty-two (Likely referring to the net ATP yield per glucose molecule)
- Three (Likely related to ATP yield per specific metabolic intermediate)
- About 112 (Likely related to the total ATP yield from fatty acid oxidation)
Smooth Muscle Regulation and Function
- Smooth muscle does not rely on tropomyosin to stop contractions (Regulation is primarily via myosin light chain phosphorylation)
- Cardiac muscle and Skeletal muscle (Muscle types that rely on the troponin-tropomyosin complex)
- Cardiac muscle (Muscle type found in the heart)
- Around tubes (digestive, blood, etc.) (Location of smooth muscle tissue)
- Calmodulin (The calcium binding protein in smooth muscle)
- Myosin light-chain phosphatase (The enzyme responsible for smooth muscle relaxation)
- Single-unit smooth muscle (Muscle type characterized by electrical coupling)
Single-Unit vs. Multi-Unit Smooth Muscle
Single-unit smooth muscle acts like a team—the cells contract together because they are linked by gap junctions, which let electrical signals pass directly from one cell to the next.
In contrast, multi-unit smooth muscle cells work solo. They do not share signals, so each one needs its own nerve input to contract.
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