BackPhysiology of Muscle: Structure, Function, and Types
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Topic 2.3 - Physiology of Muscle
Overview
This section covers the microscopic structure and physiology of muscle tissue, including skeletal, cardiac, and smooth muscle. Key concepts include muscle cell anatomy, mechanisms of contraction, neuromuscular junctions, contractile properties, muscle metabolism, and comparative features of muscle types.
General Features of Muscle Cells
Muscle Cell Terminology and Structure
Muscle fibers: Elongated cells specialized for contraction.
Terminology: Prefixes myo- and sarco- refer to muscle and flesh, respectively.
Muscle contraction depends on actin and myosin myofilaments.
Comparison of Muscle Types
The three main muscle types differ in location, structure, and function.
Feature | Cardiac Muscle | Skeletal Muscle | Smooth Muscle |
|---|---|---|---|
Location | Only in heart | Attached to and covers bony skeleton | Walls of hollow, visceral organs |
Striations | Striated | Striated | Nonstriated |
Control | Involuntary | Voluntary | Involuntary |
Contraction | Pacemaker sets rate; neural input can increase rate | Can contract rapidly; tires easily & must rest; strong, adaptable | Slow, sustained contractions |
Functions and Characteristics of Muscle
Muscle Functions
Generate movement: Locomotion, manipulation, blood pressure control, respiration, propulsion of food and urine.
Maintain posture: Muscles work constantly against gravity.
Joint stabilization: Stabilize joints during movement (e.g., shoulders, knees).
Generation of heat: Maintains body temperature, especially via skeletal muscle (about 40% of body mass).
Functional Characteristics of Muscle
Excitability (Irritability): Ability to receive and respond to a stimulus, usually a chemical (neurotransmitter, hormone, pH change). Response is an action potential along the sarcolemma, leading to contraction.
Contractility: Ability to shorten forcibly when adequately stimulated.
Extensibility: Ability to be stretched or extended.
Elasticity: Ability to resume resting length after being stretched.
Microscopic Anatomy of Skeletal Muscle Fiber
Structure and Components
Skeletal muscle fiber: Cylindrical cell with multiple oval nuclei located just beneath the sarcolemma (plasma membrane).
Syncytium: Muscle cell formed by fusion of multiple cells, resulting in many nuclei.
Sarcoplasm: Cytoplasm of muscle cell, rich in glycogen and myoglobin (oxygen-binding protein).
Myofibrils: Parallel rod-like structures (~80% of cell volume) composed of myofilaments (actin, myosin) arranged in repeating units called sarcomeres.
Sarcoplasmic reticulum (SR): Specialized endoplasmic reticulum for Ca2+ storage and release.
T-tubules: Invaginations of the sarcolemma that conduct action potentials into the muscle fiber.
Connective Tissue Layers
Endomysium: Thin connective tissue surrounding each muscle fiber.
Perimysium: Connective tissue surrounding bundles of muscle fibers (fascicles).
Epimysium: Dense connective tissue surrounding the entire muscle.
Organization of Myofibrils and Sarcomeres
Sarcomere Structure
Sarcomere: The contractile unit of muscle, defined as the region between two Z discs.
Myofilaments: Actin (thin) and myosin (thick) filaments arranged in a precise pattern.
Bands and Zones:
A band: Dark band, contains thick filaments.
I band: Light band, contains thin filaments.
H zone: Central region of A band with only thick filaments.
M line: Middle of H zone, anchors thick filaments.
Z disc: Anchors thin filaments, defines sarcomere boundaries.
Myofilament Composition
Myosin (thick filament): Composed of two heavy chains (tail) and four light chains (heads). Heads have actin-binding sites and ATPase activity, forming cross-bridges with actin.
Actin (thin filament): Made of G-actin (globular) subunits polymerized into F-actin (filamentous) strands. Each G-actin has a myosin-binding site.
Tropomyosin: Rod-shaped protein that blocks myosin-binding sites on actin in resting muscle.
Troponin: Three-polypeptide complex that binds Ca2+ and regulates tropomyosin position.
Excitation-Contraction Coupling
Role of Action Potential and Ca2+
Action potential travels along sarcolemma and down T-tubules.
Triggers release of Ca2+ from sarcoplasmic reticulum.
Ca2+ binds to troponin, causing tropomyosin to move and expose myosin-binding sites on actin.
Sliding Filament Mechanism
Myosin heads attach to actin, forming cross-bridges.
Power stroke: Myosin heads pivot, pulling thin filaments toward the center of the sarcomere.
ATP binds to myosin, causing detachment from actin; ATP hydrolysis re-cocks the myosin head.
Process repeats as long as Ca2+ and ATP are available.
Muscle relaxation occurs when Ca2+ is pumped back into SR.
Key Equation:
Neuromuscular Junction (NMJ)
Structure and Function
NMJ is the synapse between a motor neuron and a muscle fiber.
Neurotransmitter acetylcholine (ACh) is released from the neuron, binds to receptors on the sarcolemma, and initiates an action potential.
ACh is broken down by acetylcholinesterase (AChE) to terminate the signal.
Contractile Properties of Skeletal Muscle
Motor Units and Graded Responses
Motor unit: One motor neuron and all the muscle fibers it innervates.
Graded muscle responses are achieved by varying the frequency of stimulation (wave summation, tetanus) and the number of motor units recruited (multiple motor unit summation).
Types of Contractions
Isotonic contraction: Muscle changes length and moves a load. Includes concentric (shortening) and eccentric (lengthening) contractions.
Isometric contraction: Muscle generates tension but does not change length.
Example: Holding up a heavy couch involves isometric contraction; lifting it involves isotonic contraction.
Muscle Metabolism and Fatigue
Energy Sources for Contraction
Stored ATP: Immediate source, lasts 4-6 seconds.
Creatine phosphate (CP): Regenerates ATP rapidly, lasts 15-20 seconds.
Anaerobic glycolysis: Produces ATP quickly without oxygen, but yields lactic acid.
Aerobic respiration: Slow, requires oxygen, produces most ATP.
Muscle Fatigue and Oxygen Debt
Muscle fatigue: Physiological inability to contract, often due to ATP depletion, ionic imbalances, or lactic acid buildup.
Oxygen debt (Excess Post-Exercise Oxygen Consumption, EPOC): Extra oxygen required after exercise to replenish reserves, convert lactic acid to pyruvic acid, restore glycogen, and resynthesize ATP and CP.
Muscle Fiber Types and Physical Activity
Classification of Muscle Fibers
Type | Features | Best for |
|---|---|---|
Slow oxidative fibers | Thin, red, high myoglobin, many mitochondria, aerobic, fatigue-resistant | Endurance activities (e.g., marathon running) |
Fast glycolytic fibers | Large, pale, low myoglobin, few mitochondria, anaerobic, powerful but fatigues quickly | Short-term, rapid, intense movements (e.g., sprinting) |
Fast oxidative fibers | Intermediate features, red/pink, aerobic, fairly fatigue-resistant | Intermediate activities (e.g., walking, middle-distance running) |
Comparison of Smooth and Skeletal Muscle
Structural Organization
Smooth muscle: Spindle-shaped cells, single central nucleus, arranged in sheets in walls of hollow organs.
No striations or sarcomeres; thick and thin filaments are present but arranged differently (ratio of thick:thin is 1:13).
Contractions are slow, sustained, and fatigue-resistant.
Regulated by autonomic nervous system, hormones, and local factors.
Contractile Response
Contraction via sliding filament mechanism; Ca2+ binds to calmodulin (not troponin).
Gap junctions allow synchronized contraction in unitary smooth muscle (e.g., gut, uterus).
Multiunit smooth muscle (e.g., large arteries, arrector pili) contracts independently.
Summary Table: Skeletal vs. Smooth Muscle
Feature | Skeletal Muscle | Smooth Muscle |
|---|---|---|
Cell shape | Long, cylindrical, multinucleate | Spindle-shaped, single nucleus |
Striations | Present | Absent |
Control | Voluntary | Involuntary |
Contraction speed | Fast, powerful, fatigues easily | Slow, sustained, fatigue-resistant |
Regulation | Somatic nervous system | Autonomic nervous system, hormones |
Additional info: Some details, such as the precise molecular steps of contraction and the role of specific proteins, have been expanded for clarity and completeness.