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The Muscular System: Structure, Function, and Physiology

Study Guide - Smart Notes

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Chapter 9: The Muscular System

Overview

This chapter provides a comprehensive overview of the muscular system, including muscle types, structure, function, physiology of contraction, energy sources, and clinical considerations. The muscular system is essential for movement, posture, joint stabilization, temperature regulation, and the control of substances within the body.

Functions of Muscle

Main Functions

  • Movement: Muscles contract to produce movement of the body and its parts.

  • Maintaining Posture: Continuous muscle contractions maintain body posture.

  • Stabilizing Joints: Muscles reinforce and stabilize joints.

  • Temperature Homeostasis: Muscle activity generates heat, helping maintain body temperature.

  • Regulation of Substances: Muscles control the movement of substances between body compartments (e.g., sphincters).

Characteristics of Muscle Tissue

Key Properties

  • Excitability: Ability to receive and respond to stimuli.

  • Contractility: Ability to shorten forcibly when stimulated.

  • Extensibility: Ability to be stretched beyond resting length.

  • Elasticity: Ability to return to original length after stretching.

Muscle Types

Classification and Features

  • Skeletal Muscle: Attached to bones, voluntary, striated, limited regeneration.

  • Cardiac Muscle: Found in heart walls, involuntary, striated, no regeneration.

  • Smooth Muscle: Located in walls of hollow organs, involuntary, non-striated, fast regeneration.

Muscle types diagram

Skeletal Muscle Structure

Connective Tissue Sheaths

  • Epimysium: Dense connective tissue surrounding the whole muscle.

  • Perimysium: Fibrous connective tissue surrounding fascicles (bundles of muscle fibers).

  • Endomysium: Fine areolar connective tissue surrounding each muscle fiber.

Skeletal muscle structure and connective tissue sheathsPhotomicrograph of skeletal muscle showing epimysium, perimysium, and fascicles

Muscle Attachments

  • Origin: Attachment to bone that does not move during contraction.

  • Insertion: Attachment to bone that moves during contraction.

  • Direct Attachment: Epimysium fused to periosteum or perichondrium.

  • Indirect Attachment: Connective tissue extends as tendon or aponeurosis; more common due to durability and size.

Biceps brachii origin and insertion

Microscopic Anatomy of Skeletal Muscle

Muscle Fiber Structure

  • Muscle Fiber: Long, cylindrical, multinucleated cell.

  • Sarcolemma: Muscle cell membrane; forms T-tubules for rapid signal transmission.

  • Sarcoplasm: Cytoplasm containing glycogen, myoglobin, and creatine phosphate for energy.

  • Nucleus: Multiple nuclei pushed to the side due to myoblast fusion.

  • Mitochondria: Numerous for energy production.

  • Sarcoplasmic Reticulum (SR): Specialized smooth ER for Ca2+ storage.

  • Triad: Structure formed by T-tubule and two terminal cisterns of SR, crucial for excitation-contraction coupling.

Muscle fiber structure showing sarcolemma, T-tubules, sarcoplasmic reticulum, and triadMuscle fiber structure showing sarcoplasm, nucleus, and mitochondria

Myofibrils and Sarcomeres

  • Myofibrils: Rod-like structures containing contractile proteins.

  • Sarcomere: Functional contractile unit formed by thick and thin filaments.

  • Thick Filaments: Composed of myosin molecules; each has a head (cross bridge) with actin and ATP binding sites.

  • Thin Filaments: Composed of actin, tropomyosin, and troponin; actin has myosin binding sites.

Myofibril and sarcomere structureLevels of muscle organizationSarcomere structureMyosin molecule structureActin filament structureTroponin and tropomyosin on actin

Muscle Physiology: Contraction

Ion Channels and Membrane Potential

  • Ion Channels: Allow ions to diffuse across the cell membrane.

  • Gated Channels: Open in response to voltage changes (voltage-gated) or ligand binding (ligand-gated).

  • Resting Membrane Potential: Maintained by Na+/K+ pump; typically -90 mV in muscle cells.

Cell membrane and ion channelsNa/K pump mechanism

Steps of Muscle Contraction

  1. Excitation: Nerve impulse triggers release of acetylcholine (ACh) at neuromuscular junction.

  2. Excitation-Contraction Coupling: Action potential travels along sarcolemma and T-tubules, causing Ca2+ release from SR.

  3. Contraction: Ca2+ binds to troponin, moving tropomyosin and exposing myosin binding sites on actin; myosin heads bind and pull actin (power stroke).

  4. Relaxation: Ca2+ is reabsorbed into SR, tropomyosin covers binding sites, and muscle returns to resting state.

Neuromuscular junction structureExcitation and membrane potential changeAction potential propagationAction potential propagationAction potential propagationAction potential graph

Sliding Filament Theory

  • ATP Hydrolysis: Myosin head hydrolyzes ATP, energizing for binding.

  • Crossbridge Formation: Myosin head binds to actin, releasing phosphate.

  • Power Stroke: Myosin head pivots, pulling actin toward sarcomere center.

  • Detachment: ATP binds to myosin, causing detachment from actin.

  • Cycle Repeats: As long as Ca2+ and ATP are available.

Equation for ATP hydrolysis:

Myosin attachment and detachmentContraction-relaxation cycle

Motor Units and Muscle Contraction

Motor Units

  • Motor Unit: A motor neuron and all the muscle fibers it innervates.

  • Size: Small motor units allow fine control; large units provide powerful contractions.

  • All-or-None Principle: Each muscle fiber contracts fully when stimulated.

  • Graded Response: Muscle contraction strength depends on number and frequency of motor units activated.

Motor unit diagramMotor unit contractionMotor units in contractionMyogram showing contraction strength

Types of Muscle Contraction

  • Isotonic: Muscle changes length, moves load (concentric: shortens; eccentric: lengthens).

  • Isometric: Tension increases, but muscle length does not change.

Smooth Muscle Contraction

Gross and Microscopic Anatomy

  • Location: Walls of hollow organs, arranged in layers.

  • Cell Structure: Small, spindle-shaped, single nucleus, no T-tubules, gap junctions, few mitochondria.

  • Myofibrils: Actin and myosin present, no sarcomeres, intermediate filaments anchor actin.

  • Regulatory Proteins: Tropomyosin present, calmodulin replaces troponin.

Smooth muscle cell anatomySmooth muscle myofibril structure

Physiology of Smooth Muscle Contraction

  • Stimulation: Can be autonomic, hormonal, or local.

  • Diffuse Junction: Neurotransmitter released from varicosities into wide cleft, affecting many cells.

  • Contraction: Slow, synchronized, resistant to fatigue, uses little energy.

Energy for Muscle Contraction

ATP and Regeneration Mechanisms

  • ATP: Direct energy source for crossbridge cycling; only enough stored for 4-6 seconds.

  • Creatine Phosphate: Regenerates ATP for short bursts (15 seconds).

  • Anaerobic Respiration (Glycolysis): Rapid ATP production, produces lactic acid, fuels muscles for up to 45 seconds.

  • Aerobic Respiration: Requires O2, produces large amounts of ATP, supports prolonged activity.

Equation for ATP regeneration:

Muscle Cell Types

  • Slow Oxidative: Thin, slow ATPases, abundant myoglobin and mitochondria, aerobic, endurance, not powerful.

  • Fast Glycolytic: Large diameter, fast ATPases, little myoglobin, few mitochondria, anaerobic, powerful, fatigues quickly.

  • Fast Oxidative: Intermediate size, fast ATPases, abundant myoglobin, uses both aerobic and anaerobic, fatigue resistant, intermediate power.

Effect of Exercise on Muscles

  • Aerobic Exercise: Increases capillaries, mitochondria, and myoglobin; converts fast glycolytic to fast oxidative.

  • Resistance Exercise: Increases muscle cell size, myofibrils, and glycogen stores; converts fast oxidative to fast glycolytic.

Clinical Considerations

Muscular Dystrophy

  • Duchenne Muscular Dystrophy (DMD): X-linked recessive disorder; lack of dystrophin protein destabilizes sarcolemma, leading to muscle degeneration and early death.

Skeletal muscle slide from DMD patient

Rigor Mortis

  • Occurs after death due to Ca2+ influx and lack of ATP, causing myosin heads to remain attached to actin, resulting in muscle rigidity.

  • Disappears as proteolytic enzymes degrade myofilaments.

Review Questions

  • What are the three muscle membranes?

  • What is the structure of skeletal muscle from the outside in?

  • What is another name for a muscle cell?

  • Name the protein filaments of the sarcomere.

  • What is the sarcomere?

  • Name the three proteins that make up actin. Which one binds calcium?

  • What is the trigger for ACh release? Where does it happen?

  • What is an action potential?

  • Where is Ca released from in the muscle cell?

  • What is a cross bridge?

  • What happens when Ca levels in the muscle cell drop?

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