Why does oxygen debt develop?
Because the heart stops delivering blood during exercise
Because muscles produce excess ATP that cannot be stored
Because oxygen supply cannot meet the high demand during strenuous activity, leading to anaerobic metabolism and lactic acid buildup
Because carbon dioxide completely replaces oxygen in muscle cells
The Correct Answer is C
Oxygen debt (also called excess post-exercise oxygen consumption, EPOC) refers to the increased oxygen requirement after strenuous exercise. During intense physical activity, skeletal muscles may require more oxygen than the cardiovascular and respiratory systems can supply. When this occurs, cells temporarily rely on anaerobic metabolism to produce ATP. This leads to the accumulation of lactic acid and depletion of energy reserves, which must be corrected after exercise ends.
A. Because the heart stops delivering blood during exercise: the heart does not stop during exercise; in fact, cardiac output increases significantly to meet the heightened metabolic demands of skeletal muscles. Heart rate and stroke volume both rise to enhance oxygen delivery. Oxygen debt is not caused by cessation of blood flow but by insufficient oxygen delivery relative to demand.
B. Because muscles produce excess ATP that cannot be stored: ATP is not produced in excess during strenuous exercise; rather, ATP demand exceeds supply. Additionally, ATP is not stored in large quantities in cells and must be continuously regenerated. The issue in oxygen debt is not excess ATP production but inadequate oxygen availability for aerobic ATP synthesis.
C. Because oxygen supply cannot meet the high demand during strenuous activity, leading to anaerobic metabolism and lactic acid buildup: during intense exercise, oxygen delivery to muscles becomes insufficient for aerobic respiration. As a result, muscles shift to anaerobic glycolysis, producing ATP less efficiently and generating lactic acid as a byproduct. This lactic acid accumulation and depletion of oxygen stores (myoglobin and blood oxygen) create an oxygen deficit. After exercise, extra oxygen is required to metabolize lactic acid and restore physiological balance, which defines oxygen debt.
D. Because carbon dioxide completely replaces oxygen in muscle cells: carbon dioxide does not replace oxygen in muscle cells. Instead, carbon dioxide is a metabolic waste product of cellular respiration and is transported away via the bloodstream to the lungs for exhalation. Oxygen remains essential for aerobic ATP production whenever available. This statement is physiologically inaccurate and does not explain oxygen debt.
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Related Questions
Correct Answer is D
Explanation
Skeletal muscle contraction occurs through the sliding filament mechanism, where actin (thin filaments) and myosin (thick filaments) interact to generate force. This process is regulated by calcium ions and involves cyclic interactions between contractile proteins within the sarcomere. Cross-bridges are fundamental structures formed during contraction when myosin heads attach to binding sites on actin filaments. This interaction enables filament sliding and shortening of the muscle fiber, producing contraction.
A. Troponin binding to tropomyosin: troponin and tropomyosin are regulatory proteins, not the structures that form cross-bridges. Tropomyosin normally blocks myosin-binding sites on actin, and troponin shifts tropomyosin when calcium binds. While this regulatory system controls contraction, it does not physically generate force or form cross-bridges. This interaction facilitates contraction but is not the cross-bridge itself.
B. Calcium binding to troponin: calcium binding to troponin is an initiating regulatory step, not a structural cross-bridge. When calcium binds to troponin C, it causes a conformational change that moves tropomyosin away from actin’s binding sites. This allows myosin heads to attach to actin. However, calcium does not form the mechanical link responsible for force generation, so it is not a cross-bridge.
C. ATP binding to myosin heads: ATP binding to myosin heads is involved in detachment and energy cycling, not cross-bridge formation. ATP binding causes myosin to release from actin, and ATP hydrolysis re-energizes the myosin head for the next contraction cycle. While essential for contraction, ATP itself does not create the physical connection between filaments.
D. Myosin heads binding to actin: cross-bridges are formed when energized myosin heads attach directly to binding sites on actin filaments. This interaction is the fundamental force-generating step in muscle contraction. Once attached, the myosin heads pivot (power stroke), pulling actin filaments toward the center of the sarcomere. This repeated attachment and detachment cycle produces muscle shortening and force generation.
Correct Answer is C
Explanation
The scapula (shoulder blade) is a flat, triangular bone located on the posterior aspect of the thoracic cage. It plays a key role in upper limb movement by serving as an attachment point for muscles that stabilize and move the shoulder joint. Anatomically, it has specific borders, angles, and processes that help define its orientation and muscular attachments. Understanding these landmarks is essential for identifying scapular anatomy and its functional biomechanics in shoulder movement.
A. Acromion, coracoid, and glenoid borders: the acromion, coracoid process, and glenoid cavity are not borders of the scapula. Instead, they are specific anatomical processes and a socket. The acromion articulates with the clavicle, the coracoid serves as a muscle attachment point, and the glenoid cavity forms the shoulder joint with the humerus. These are structural features, not the three defined borders of the scapula.
B. Supraspinous, infraspinous, and subscapular borders: these terms refer to fossae (depressions) or surface regions, not borders. The supraspinous and infraspinous fossae are separated by the spine of the scapula and serve as attachment sites for rotator cuff muscles. The subscapular fossa is located on the anterior surface of the scapula. These are anatomical regions, not the structural margins of the bone.
C. Superior, medial, and lateral borders: the scapula has three distinct borders that define its triangular shape. The superior border is the shortest and contains the suprascapular notch. The medial (vertebral) border runs parallel to the spine and provides muscle attachment sites. The lateral (axillary) border is thicker and leads toward the glenoid cavity. These borders are key landmarks used in anatomical orientation and muscle attachment.
D. Inferior, anterior, and posterior borders: the scapula is not described using anterior or posterior borders. Anatomically, it is defined by superior, medial, and lateral borders instead. While the scapula does have surfaces (anterior and posterior), these are not classified as borders.
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