Lecture Title: Human Physiology Lecture 15: Muscle Function
Instructor: Dr. Suzanne Gray, UPEI
Semester: Winter 2025
Types and Structure of Muscle
Skeletal Muscle Contraction
Stimulation and Strength of Contraction
Types of Skeletal Muscle Fibers
Cardiac and Smooth Muscle
Skeletal Muscle
Characteristics:
Nucleus: Multiple nuclei
Striations: Present
Cardiac Muscle
Characteristics:
Striations: Present
Intercalated disk: Present
Nucleus: Central
Smooth Muscle
Characteristics:
Nucleus: Single
Striations: Absent
Skeletal Muscle
Voluntary control; striated muscle fibers
Cardiac Muscle
Involuntary control; striated muscle fibers
Smooth Muscle
Involuntary control; non-striated
Skeletal Muscle:
Represents all voluntary muscle; most abundant
Only cardiac muscle is found in the heart
Smooth muscle located primarily in digestive and circulatory vessels
Individual muscle fibers are long cells, composed of multiple fused cells.
Each muscle fiber contains many sarcomeres, the basic unit of contraction.
The boundaries of sarcomeres create striations.
Multiple nuclei present within each fiber.
Whole Muscle Structure includes:
Tendon
Muscle fiber (muscle cell)
Muscle fascicle (cell bundle)
Artery, vein, and nerve supply
Myofibrils consist of:
Z lines
M lines
Sarcolemma
Sarcoplasmic reticulum (SR)
T-tubules
Triad structures (T-tubule and terminal cisternae)
Striated Appearance:
Resulting from the arrangement of actin (thin) and myosin (thick) filaments.
I Band: Region with actin filaments
A Band: Region with both myosin and actin
H Zone: Area with only myosin
Crossbridge formation explained with myosin and actin interaction.
Initiation of contraction begins with myosin and actin interaction.
Changes in the bands and lines of the contractile apparatus during contraction.
A nerve impulse travels down an axon.
Contraction regulated via the neuromuscular junction.
The NMJ is where the axon of a motor neuron meets the muscle fiber.
ACh (acetylcholine) is released into the synaptic cleft upon nerve impulse arrival.
ACh binds to receptors, activating sodium channels.
The electrical signal passes to T-tubules of the muscle.
Calcium channels open as an electrical signal triggers them.
Calcium ions interact with actin and myosin, facilitating contraction.
Myosin filaments possess a tail and head, with:
Actin binding site
ATP binding site
Actin has additional proteins bound to it:
Tropomyosin
Troponin
Calcium ions allow binding of actin and myosin to occur.
Myosin head attachment leads to a power stroke, bending towards the center of the sarcomere, shortening it.
Myosin head attaches to actin.
ATP hydrolysis occurs when the head is unattached.
ADP release triggers position change and actin movement.
Binding of ATP causes myosin head to return to resting position.
After the power stroke:
Muscle shortens by approximately 1% but has potential to shorten up to 60%.
Cross-bridge cycle allows the power stroke to begin again after detachment.
Relaxed vs Contracted states of the sarcomere.
Thin (actin) and Thick (myosin) filaments in both states.
Review of skeletal muscle contraction through the sliding filament mechanism.
Nervous stimulation via ACh.
Ca+2 leads to conformational change of actin.
Cross-bridge formed.
Muscle cell shortens due to simultaneous contraction of all sarcomeres.
ATP is needed to detach myosin from actin, which cannot occur after death.
Results in stiff muscles until breakdown occurs.
Varying contraction strength and duration relies on the muscle twitch, which is an all-or-nothing response.
Consists of a neuron and all muscle fibers it stimulates.
Signals from the neuron activate all respective fibers.
Phases:
Latent Period: Initial milliseconds; connections between actin and myosin start forming.
Contraction: Muscle shortens.
Relaxation: Returns to original length.
Tension vs Time for a single muscular stimulus.
Latent period, contraction phase, and relaxation phase shown.
Differences in twitch speed depends on muscle fiber diameter, strength variations, and fiber types (slow vs fast twitch).
Key factors: (a) Isometric vs Isotonic contractions(b) Frequency of stimulation(c) Strength of stimulation
Isometric: Same length, changing tension.
Isotonic: Same tension, changing length (with examples).
Strength increases with higher frequency of signals; calcium availability and myosin binding site exposure increase.
High-frequency stimulation leads to muscle twitches that can overlap, resulting in tetanus where muscle relaxation diminishes.
Distinction between physiological tetanus and the disease tetanus caused by bacteria.
Muscles contract stronger as more fibers are stimulated; requires recruitment of larger fibers as force increases.
a) Slow and Fast Twitch Fibers
Different muscles exhibit varied fiber densities, such as:
Soleus: Mostly slow twitch
Gastrocnemius: Equal numbers
Slow Twitch: Efficient in using oxygen, delayed firing, fatigue-resistant.
Fast Twitch: Quick to fire, better for explosive movements, fatigue quickly.
Classification based on metabolic properties:
Glycolytic: High glycolytic enzymes, few mitochondria.
Oxidative: Rich in mitochondria, smaller diameter, efficient ATP production.
Slow oxidative fibers contract slowly using aerobic respiration.
Fast oxidative fibers contract quickly using aerobic or anaerobic respiration.
Fast glycolytic fibers primarily use anaerobic glycolysis and fatigue quickly.
Three types based on contraction speed and energy production:
Slow oxidative fibers
Fast oxidative fibers
Fast glycolytic fibers
Striated like skeletal muscle but branched and interconnected.
Intercalated discs with gap junctions, forming a single functional unit.
Location: walls of blood vessels, digestive tract, etc.
Lacks sarcomeres; has actin and myosin in a way that allows stretching.
Takes longer to initiate/terminate contractions.
Regulated by autonomic neurons; affects many cells simultaneously.
Varies in connection degree via gap junctions.
Single-unit Smooth Muscle: Linked by gap junctions, few innervating neurons.
Multi-unit Smooth Muscle: Few gap junctions, richly innervated, operates independently.
Key Takeaways:
Types and structure of muscle.
Mechanism of skeletal muscle contraction.
Control of muscle contractions.
Categories of muscle fibers.
Basic understanding of cardiac and smooth muscle.
Understanding muscle contraction mechanisms.
Preparation for upcoming topics on cardiac function.