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Match the following terms with their definitions:
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Insertion = Attachment to movable bone Origin = Attachment to immovable or less movable bone Aponeurosis = Sheet-like fibrous tissue connecting muscles Fleshy attachment = Epimysium fused to periosteum of bone
Match the following terms with their associated connective tissue sheath in skeletal muscle:
Match the following terms with their associated connective tissue sheath in skeletal muscle:
Epimysium = Surrounds the entire muscle Perimysium = Wraps around fascicles Endomysium = Surrounds individual muscle fibers Fascicle = Bundle of muscle fibers
Match the following muscles with their functions:
Match the following muscles with their functions:
Occipitofrontalis = Responsible for raising eyebrows Auricular muscles = Responsible for moving the ears Fascicles = Structural units of muscle tissue Aponeurosis = Connects muscles to other body parts
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Match the following characteristics with their corresponding connective tissue wrapping:
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Match the steps at the neuromuscular junction with their descriptions:
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Match the process with its description during muscle excitation:
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Match the structures in skeletal muscle with their roles:
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Match the description of the neuromuscular junction with the action performed:
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Match the ion involved in muscle function with its role:
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Match the neurotransmitter with its function in muscle activation:
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Match the following steps of the neuromuscular transmission process with their descriptions:
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Match the following components of the neuromuscular junction with their roles:
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Match the following events with their sequence in neuromuscular transmission:
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Match the following structures with their functions in the neuromuscular junction:
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Match the following terms with their definitions in the context of neuromuscular transmission:
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Match the following ions involved in neuromuscular transmission with their roles:
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Match the neuromuscular junction terms with their definitions:
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Match the following terms related to neuromuscular transmission with their correct pairs:
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Match the following phrases with their corresponding actions during neuromuscular transmission:
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Match the diseases with their characteristics:
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Match the ions involved in action potential generation with their roles:
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Match the phases of action potential with their descriptions:
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Match the types of synaptic vesicles with their contents:
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Match the mechanisms of muscle contraction with their descriptions:
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Match the following steps with their corresponding descriptions in the neuromuscular junction process:
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Match the terms with their respective descriptions regarding excitation-contraction coupling:
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Match the terms with their definitions in the context of nerve impulses:
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Match the steps of the cross bridge cycle with their correct order:
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Match the following mechanisms with their roles in muscle contraction:
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Match the intracellular events with their resulting outcomes:
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Match the following elements with their locations in the neuromuscular junction:
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Match the components of the muscle contraction process with their roles:
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Match these steps of muscle activation with their order:
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Match the muscle contraction terms with their definitions:
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Match the following ions with their actions in the neuromuscular junction:
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Study Notes
Chapter 09 Part A: Muscles and Muscle Tissue
- Muscles make up nearly half of the body's mass
- Muscles transform chemical energy (ATP) into mechanical energy, capable of exerting force
- To understand muscles, consider:
- Types of muscle tissue
- Characteristics of muscle tissue
- Muscle functions
Types of Muscle Tissue
- Terminologies: Myo, mys, and sarco are prefixes for muscle. Example: sarcoplasm (muscle cell cytoplasm)
- Three types: Skeletal, Cardiac, Smooth
-
Skeletal muscle:
- Packaged into skeletal muscles (organs attached to bones/skin)
- Longest of all muscle fibers
- Striated (striped)
- Voluntary (consciously controlled)
- Contracts rapidly; tires easily; powerful
- Key words: skeletal, striated, voluntary
-
Cardiac muscle:
- Found only in the heart
- Makes up most of the heart walls
- Striated
- Involuntary (cannot be controlled consciously)
- Contracts at a steady rate, controlled by the heart's own pacemaker, but the nervous system can increase rate
- Key words: cardiac, striated, involuntary
-
Smooth muscle:
- Found in the walls of hollow organs (e.g., stomach, urinary bladder, airways)
- Not striated
- Involuntary (cannot be controlled consciously)
- Key words: visceral, nonstriated, involuntary
Table 9.3-1 Comparison of Skeletal, Cardiac, and Smooth Muscle
- Provides a comparison table of skeletal, cardiac, and smooth muscle, detailing body location, cell shape/appearance, and other characteristics.
Characteristics of Muscle Tissue
- All muscles share four main characteristics:
- Excitability (responsiveness): ability to receive and respond to stimuli
- Contractility: ability to shorten forcibly when stimulated
- Extensibility: ability to be stretched
- Elasticity: ability to recoil to resting length
Muscle Functions
- Produce movement: responsible for all locomotion and manipulation (e.g., walking, digesting, pumping blood)
- Maintain posture and body position
- Stabilize joints
- Generate heat as they contract
Skeletal Muscle Anatomy
- Skeletal muscle is an organ made up of several tissues with these features:
- Nerve and blood supply
- Connective tissue sheaths
- Attachments
Nerve and Blood Supply
- Each muscle receives a nerve, artery, and veins
- Control skeletal muscle activity by supplying nerves to each fiber
- Contraction requires oxygen and nutrients, thus needing quick removal of waste products.
Connective Tissue Sheaths
- Each muscle and muscle fiber is covered by connective tissue
- Support cells and reinforce the whole muscle
- Three layers from external to internal:
- Epimysium (surrounds entire muscle or blends with fascia)
- Perimysium (surrounds fascicles or groups of muscle fibers)
- Endomysium (surrounds each muscle fiber)
Skeletal Muscle Attachments
- Muscles span joints and attach to bones in at least two places.
- Two points of attachment:
- Origin: attachment to immovable or less movable bone
- Insertion: attachment to movable bone
- Types of attachments:
- Direct (fleshy): epimysium fused to periosteum of bone or perichondrium of cartilage
- Indirect: connective tissue wrappings extend beyond muscle as ropelike tendon or sheetlike aponeurosis
Aponeuroses
- Sheet-like, pearly-white tissues similar to tendons
- Connect sheet-like muscles, providing wide areas of attachment to other body parts (bones, cartilage, other muscles)
9.3 Muscle Fiber Microanatomy and Sliding Filament Model
- Skeletal muscle fibers are long, cylindrical cells with multiple nuclei
- Sarcolemma: muscle fiber plasma membrane
- Sarcoplasm: muscle fiber cytoplasm
-
Myofibrils: densely packed, rod-like elements within muscle fiber, responsible for ~ 80 % of muscle volume
- Contains many glycosomes (for glycogen storage) and myoglobin (for O2 storage)
- Sarcoplasmic reticulum: network of smooth endoplasmic reticulum surrounding each myofibril
- T (transverse) tubules: formed by sarcolemma protrusions into the muscle fiber, increasing surface area and allow electrical nerve transmission to reach deep into the fiber.
Myofibrils (1 of 7): Features and Composition
- Myofibrils are packed, rod-like elements within muscle fibers.
- Key features include striations (striped pattern), sarcomeres (functional units), and myofilaments (actin and myosin).
Myofibrils (2 of 7): Striations and Structural Components
- Striations are formed by repeating series of dark (A bands) and light (I bands) bands along the length of each myofibril.
- Components within each myofibril include: A bands, H zone, M line, I bands, and Z discs.
Myofibrils (3 of 7): Sarcomere (Functional Unit)
- Sarcomeres are the smallest contractile units of a muscle fiber.
- Each sarcomere is the region between two Z discs.
- Sarcomeres align end to end along a myofibril, similar to boxcars.
Myofibrils (4 of 7): Myofilaments (Actin and Myosin)
- Myofilaments (protein fibers) are responsible for muscle contraction.
- Thin filaments (primarily actin) extend across the I band and partway into the A band.
- Thick filaments (primarily myosin) extend the entire length of the A band.
Myofibrils (5 of 7): Molecular Composition of Myofilaments (Thick Filaments)
- Thick filaments are made of myosin protein.
- Myosin contains two heavy and four light polypeptide chains.
- Heavy chains form the myosin tail.
- Light chains form the myosin globular head..
- Myosin heads bind to actin during contraction forming cross bridges.
Myofibrils (6 of 7): Molecular Composition of Myofilaments (Thin Filaments)
- Thin filaments are made up of actin protein.
- G actin subunits bear active sites for myosin head attachment.
- F actin is a filamentous actin consisting of two strands of G actin twisted together.
- Tropomyosin and troponin are regulatory proteins bound to actin.
Myofibrils (7 of 7): Additional Proteins
- Elastic filaments (titin): hold thick filaments in place, recoil after stretch, resist excessive stretching.
- Dystrophin: links thin filaments to proteins of sarcolemma.
- Nebulin, myomesin, C proteins: bind filaments/sarcomeres together; maintain alignment.
9.1 Overview of Muscle Tissue (cont.): Muscle Fiber Microanatomy
- Muscle fiber microanatomy: Describes the internal structure of muscle fibers (cells), including myofibrils, sarcomeres, and the proteins involved in contraction.
Clinical – Homeostatic Imbalance 9.1 (Duchenne Muscular Dystrophy)
- Duchenne muscular dystrophy (DMD) is a sex-linked recessive disease, affecting primarily males.
- Symptoms start in childhood, progressively affecting muscles (from extremities upward) and can lead to cardiac muscle issues.
- Caused by defective gene for dystrophin, a protein linking thin filaments with extracellular matrix/sarcolemma
- Muscle fibers tear easily, allowing excess calcium entry, causing damage to contractile fibers, inflammation, and increased apoptosis (cell death) leading to muscle loss and disease progression.
Sarcoplasmic Reticulum and T Tubules
- Sarcoplasmic reticulum (SR): network of smooth endoplasmic reticulum surrounding each myofibril.
- Terminal cisterns: form perpendicular cross channels at A-I junction. Important for regulating intracellular Ca2+ levels. Stores/releases Ca2+ during contraction
- T tubules are extensions of the sarcolemma, traveling deep into the muscle fiber. Increase membrane surface area and allow electrical nerve transmissions to reach deep into fiber.
Sarcoplasmic Reticulum and T Tubules (Triad Relationships)
- Triad is the junction formed by t tubule and two terminal cisterns
- T tubule and SR integral protein interactions trigger Ca release from SR cisterns.
- When electrical impulse passes through t-tubules, SR proteins are affected causing Calcium release into the cytoplasm causing muscle contraction.
Sliding Filament Model of Contraction (1 of 3)
- Contraction: Activation of cross-bridges generate force. Shortening occurs when tension generated on thin filaments exceeds opposing forces. The contraction ends when cross-bridges become inactive.
- Sliding filament model: In a relaxed state, thin and thick filaments slightly overlap. During contraction, thin filaments slide past thick filaments causing more overlap. Lengths of filaments do not change.
Sliding Filament Model of Contraction (2 of 3)
- Nervous system stimulation allows myosin heads to bind to actin.
- This binding causes the sliding process to begin.
Sliding Filament Model of Contraction (3 of 3)
- Cross-bridges attach and detach, pulling thin filaments towards the center of sarcomeres.
- I bands shorten, Z disks become closer together, H zones disappear, A bands move closer together.
9.4 Muscle Fiber Contraction: Background
- Decision to move is activated by brain, signal transmitted down spinal cord
- Neurons activate muscle fibers by generating action potentials
- AP crosses from neuron to muscle cell via the neurotransmitter acetylcholine (ACh)
Ion Channels
- Play a major role in changing membrane potentials
- Two types:
- Chemically gated channels: opened by chemical messengers (e.g., neurotransmitters, like ACh)
- Voltage-gated channels: open or close in response to membrane potential changes
Anatomy of Motor Neurons and the Neuromuscular Junction / Motor End Plate
- Skeletal muscles are stimulated by somatic motor neurons via axonal projections (long extensions) called axon.
- Each axon branches into many branches as it goes into the muscle
- Axon branches end on muscle fiber, forming neuromuscular junction (or motor end plate)
- Each muscle fiber has one neuromuscular junction with one motor neuron
Overview of Skeletal Muscle Contraction
- Signal from brain travels down spinal cord to motor neuron, triggering axon release of neurotransmitter Acetylcholine
- ACh binds receptors on muscle fiber surface
- Resulting depolarization triggers an action potential and muscle contraction through steps of excitation, contraction coupling, and cross-bridge cycling.
Events at Neuromuscular Junction
- Action potential arrives at axon terminal
- Voltage-gated Ca2+ channels open, Ca2+ enters axon terminal.
- Ca2+ entry causes ACh release into synaptic cleft.
- ACh diffuses across synaptic cleft, binds to ACh receptors
- ACh binding opens ion channels in muscle fiber membrane, leading to end-plate potential.
- Acetylcholinesterase degrades ACh, causing termination of signal.
Clinical – Homeostatic Imbalance 9.2 (Myasthenia Gravis)
- Myasthenia gravis is a disease characterized by muscle weakness (drooping eyelids, difficulty swallowing/talking).
- Involves a shortage of ACh receptors due to the immune system attacking the receptors.
- Suggests it is an autoimmune disease, based on ACh receptor shortage.
Generation of an Action Potential Across the Sarcolemma
- Resting sarcolemma is polarized (negative inside, positive outside)
- Action potential is caused by changes in electrical charges (generation of end plate potential, depolarization, and repolarization)
Generation of an Action Potential Across the Sarcolemma (End Plate Potential)
- ACh released from motor neuron binds to ACh receptors
- Neurotransmitter binding opens chemically gated ion channels (Na+ channels open)
- Na+ diffuses into muscle fiber, causing interior of sarcolemma to become less negative (more positive)
- This local depolarization is called end-plate potential (EPP), leading to action potential.
Generation of an Action Potential Across the Sarcolemma (Depolarization)
- If end-plate potential causes enough change in membrane voltage to reach threshold (a critical level), voltage-gated Na+ channels open.
- Large Na+ influx triggers unstoppable action potential, leading to muscle fiber contraction.
- The action potential spreads from one voltage-gated Na+ channel to the next, depolarizing adjacent areas.
Generation of an Action Potential Across the Sarcolemma (Repolarization)
- Voltage-gated Na+ channels close, and voltage-gated K+ channels open.
- K+ efflux out of the cell rapidly returns membrane to its initial resting potential.
- Ionic conditions (Na+/K+) of resting state are restored by the Na+/K+ pump.
Excitation-Contraction (E-C) Coupling
- Events that transmit AP along sarcolemma (excitation) are coupled to the sliding of myofilaments (contraction).
- AP is propagated along sarcolemma and down T-tubules.
- Voltage-sensitive proteins in T-tubules stimulate Ca2+ release from SR.
- Ca2+ release leads to contraction but AP ends before contraction actually starts.
Muscle Fiber Contraction: Cross Bridge Cycling
- At low intracellular Ca2+ concentration, tropomyosin blocks active sites on actin, preventing contraction. Myosin heads cannot attach to actin, and the muscle fiber remains relaxed.
- Voltage-sensitive proteins in T tubules change shape, triggering SR release of Ca2+ into the cytosol.
Muscle Fiber Contraction: Cross Bridge Cycling (cont.)
- At higher intracellular Ca2+ concentrations, Ca2+ binds to troponin, causing tropomyosin to move away from myosin-binding sites on actin.
- Myosin heads can then bind to actin, initiating the cross-bridge cycle, which leads to sarcomere shortening and muscle contraction.
- When nervous stimulation ceases, Ca2+ is pumped back into the SR, contraction ends, and tropomyosin returns to block active sites.
Muscle Fiber Contraction: Cross Bridge Cycling (Four Steps)
- Four steps of the cross-bridge cycle:
- Cross-bridge formation: Energized myosin head attaches to actin.
- Power (working) stroke: Myosin head pivots and bends, pulling actin toward M line.
- Cross-bridge detachment: ATP attaches to myosin, causing detachment.
- Cocking of myosin head: Energy from ATP hydrolysis "cocks" myosin into high-energy state, preparing for the next cycle.
Clinical – Homeostatic Imbalance 9.3 (Rigor Mortis)
- Rigor mortis: Stiffening of muscles after death, lasting 3-4 hours after death, peaking about 12 hours postmortem.
- Caused by the lack of ATP synthesis, preventing calcium from being pumped back into the SR.
- This leads to continued cross-bridge formation, resulting in muscle contraction until muscle proteins break down and myosin is released.
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Test your knowledge on the terms, structures, and functions associated with skeletal muscle. This quiz covers connective tissue sheaths, muscle attachment concepts, and the steps involved in muscle contraction. Perfect for students studying anatomy or physiology!