Muscular System

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6 Functions of Skeletal Muscle

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6 Functions of Skeletal Muscle

-Producing movement

-Maintaining Posture

-Supports Soft Tissue

-Guards entrances and Exits

-Generates heat

-Stabilizes joints

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Producing Movement

-Skeletal muscle contractions pull on tendons and move the bones of the skeleton

-The effects range from simple motions such as extending the arm or breathing to the highly coordinated movements

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Maintaining Posture

-Tension in our skeletal muscles maintains body posture

-holding your head in position when you read a book or balancing your body weight above your feet when you walk

-Without constant muscle tension, we would not sit up straight

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Supporting Soft Tissues

-The abdominal wall and the floor of the pelvic cavity consist of layers of skeletal muscle

-These muscles support the weight of visceral organs and shield internal tissues from injury

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Guarding Exits and Entrances

-The openings of the digestive and urinary tracts are encircled by skeletal muscles

-provide voluntary control over swallowing, defecation, and urination

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Generating Heat (Maintaining Homeostasis)

-Muscle contractions require energy; whenever energy is used in the body, some of it is converted to heat

-The heat released by working muscles keeps our body temperature in the range required for normal functioning

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Joint Stabilization

Combination of movement & posture to prevent too much movement in a joint, especially in joints where bones don’t articulate well like the shoulder girdle (tendons play a vital role in this function)

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Origin

Part of muscle attached to the immovable or less movable bone

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Insertion

-part attached to the movable bone

-insertion moves toward the origin

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Prime Mover

Muscles that has the major responsibility for causing a particular movement

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Antagonist

-muscles that oppose or reverse a movement

-Biceps to the triceps, or triceps to the biceps

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Synergists

help prime movers by producing same movements

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Fixators

hold a bone still or stabilize the origin of a prime mover so all the tension can be used to move the insertion bone (Postural muscles)

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Direction of the muscle fibers

usually a reference to a midline or long axis of a limb (i.e. – rectus = straight; oblique = at a slant to)

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Relative size of muscle

maximus, minimus, longus

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Location of Muscle

-named for bone associated with the muscle (i.e. – temporalis, tibialis)

-Only gives 1 location

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Number of Origins

biceps brachii, triceps brachii

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Location of muscle’s origin & insertion

-sternocleidomastoid (originates on sternum & clavicle, inserts on mastoid process of temporal bone)

-Will give 2 or more locations

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Action of the muscle

flexor, extensor, adductor, etc.

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Skeletal Muscle Contains

-Connective Tissue

-Blood vessels and nerves

-muscle tissue (cells or fibers)

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Connective tissues

-Endomysium

-Perimysium

-Epimysium

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Endomysium

delicate connective tissue sheath that encloses each muscle fiber

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Perimysium

coarser fibrous sheath that surrounds muscle fiber bundles called fascicles

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Epimysium

covers bundle of fasciculi (entire muscle); blends into either tendons or aponeurosis

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Tendon

cord of dense, fibrous tissue attaching a muscle to a bone

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Aponeurosis

fibrous or membranous sheet connecting a muscle and the part it moves (usually found on torso)

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Sarcolemma

-plasma membrane of muscle fiber

-under the endomysium

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Sarcoplasma

cytoplasm of muscle fiber

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Peripheral nuclei

nuclei are pushed aside by myofibrils

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Myofibrils

long rope-like organelles made of tiny contractile units called sarcomeres

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2 myofilaments in Sarcomeres

-Myosin (Thick)

-Actin (Thin)

-Form a banding pattern (Striations)

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Z Line

thin filaments at either end attached to interconnecting proteins, thin filaments extend from Z line

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M Line

-zone of overlap of thick and thin filaments

-In the middle of the sarcomere

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A Band

area containing thick filaments including some overlap with thin filaments (appears dark)

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H Zone

area containing only thick filaments in center of A band

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I Band

area containing only thin filaments, including Z line (appears Light)

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Transverse Tubules (T Tubules)

-Openings along the sarcolemma that form passageways through the muscle fiber

-Transmit action potential through cell and allow entire muscle fiber to contract simultaneously

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Sarcoplasmic reticulum (SR)

-Specialized form of smooth endoplasmic reticulum that forms a tubular network around each myofibril

-Releases Ca2+ into sacromeres to begin muscle contraction and helps transmit action potential to myofibril

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Terminal cisternae

are expanded chambers of SR on either side of T-tubule

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Triad

A T-tubule sandwiched between 2 terminal cisternae

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Actin (Thin) Filaments

-Consists of twisted strand of actin molecules

-Each actin molecule has an active site that interacts with myosin

-Resting muscle, actin molecules covered with the protein tropomyosin which is held in position by troponin

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Myosin (Thick) Filaments

-Composed of myosin molecules with a tail and globular head

-Myosin heads attach to actin molecules during contraction (can’t happen until troponin changes position revealing the active sites)

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Sliding Filament Theory

-I band gets smaller Z lines move closer together

-H bands decrease Zones of overlap get larger

-Width of the A bands does not change

-Actin filaments slide toward center of the sarcomere aside of stationary myosin filaments

-Cross bridges are created when myosin heads connect to active sites on actin filaments

-Power Stroke- myosin heads drag actin filaments in towards the center

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Power Stroke

attach, pivot, detach, and return

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Irritability

the ability to receive and respond to a stimulus

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Contractility

the ability to shorten (forcibly) when an adequate stimulus is received

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Nerve stimulus and action potential

one motor neuron may stimulate a few muscle cells or hundreds of them, depending on the particular muscle and the work it does

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Motor unit

one neuron and all the skeletal muscle cells it stimulates

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Neuromuscular junction

where the axon (synaptic) terminals form junctions with the sarcolemma

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Step 1 Action Potential

-When the nerve impulse reaches the axon terminals, a neurotransmitter travels across the synaptic cleft

-acetylcholine (ACh) – neurotransmitter that stimulates skeletal muscle

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Step 2 Action Potential

Ach attaches to receptors which makes the membrane more permeable to Na+

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Step 3 Action Potential

Na+ diffuses in and K+ rushes out, generating an action potential (electrical impulse), which travels over the entire surface of the sarcolemma

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Step 10 Action Potential

ACh is removed by acetylcholinesterase (AChE) to stop contraction

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Step 4 Muscle Contraction

AP travels down T-tubules, which causes Ca2+ to be released from the lateral sacs of the sarcoplasmic reticulum

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Step 5 Muscle Contraction

Ca2+ binds to tropinin, causing the troponin-tropomyosin complex to move out of the way – exposing the active site on the actin filament

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Step 6 Muscle Contraction

Myosin heads swing back and attach to the active site on actin, forming cross-bridges

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Step 7 Muscle Contraction

Myosin heads perform a power stroke – move toward the center of the sarcomere pulling actin filaments towards the center of the sarcomere

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Step 8 Muscle Contraction

ATP is broken down to provide energy for the myosin heads to release the active site; leftover energy is stored for the next power stroke

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Step 9 Muscle Contraction

Myosin heads grab further & further back each time, whole muscle shortens

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Tension

-an active force produced when muscle cells contract, pulling on collagen fibers

-Tension must be greater than resistance in order to move

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Resistance

a passive force that opposes movement, needs to be overcome before movement can occur

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Compression

-a push applied to an object

-muscle fibers can’t do this, they only contract

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All or None Law

-a muscle fiber will contract to its fullest extent when it is stimulated adequately

-it never partially contracts

-is true of muscle cells only (not whole muscle)

-Muscle cells react to stimuli with graded responses or different degrees of shortening

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2 Ways graded responses are produced

-By changing number of muscle cells being stimulated

-By changing frequency of muscle stimulation

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Changing the number of cells stimulated

-How forcefully a muscle contracts depends largely on the number of muscle cells stimulated

-when only a few cells are stimulated, contractions will be slight

-when all cells are stimulated, contraction is strong

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Muscle Twitch

a single, brief contraction (7-100 msec)

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Latent Period

-Where there is no tension yet

-AP moves through the Sarcolemma

-Ca2+ released

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Contraction Phase

-Maximum tension released

-Cross-bridges interact with active site

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Relaxation Phase

-Tension falls to resting

-Ca2+ levels fall

-Active sites covered, number of cross-bridges decline

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Nerve Impulses

delivered to the muscle at a very rapid rate, so rapid that muscle does not get a chance to relax completely between stimuli as a result, the effects of the successive contractions are added together (summation)

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Incomplete Tetanus

when a muscle produces almost peak tension during rapid cycles of contraction and relaxation

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Complete Tetanus

when maximum tension has been reached

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Recruitment

the activation of more and more motor units, results in smooth steady increase in tension

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Muscle Tone

some motor units are always active, but do not produce enough tension to cause movement

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Atrophy

occurs when skeletal muscle is not regularly stimulated, muscle fibers become smaller and weaker

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Isotonic Contraction

when myofilaments are successful in sliding movement and muscle shortens

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Isometric Contraction

when muscles do not shorten b/c muscles are pitted against some more or less immovable object, but tension keeps building but never exceeds the resistance

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Direct phosphorylation of ADP by creatine phosphate

-a phosphate group transfers from CP to ADP, regenerating more ATP regulated by creatine phosphokinase - CPK CP supplies exhaust in about 20 seconds

-Phosphate breaks off of CP and joins with ADP

-P is broken off by the CPK

-One creatine is left, which will go bond with other phosphate

-Lasts for roughly 20 seconds

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Slow Twitch Muscle Fibers (Type 1)

-Mostly aerobic

-Smaller diameter

-Take longer to contract

-Can contract for extended periods of time

-Oxygen supply greater due to more extensive capillary network

-Can store oxygen because of red myoglobin pigment that binds with oxygen

-Contain more mitochondria

-Due to capillaries and myoglobin, appear reddish

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Fast twitch muscle fibers (Type 2)

-Mostly anaerobic

-Large diameter with densely packed myofibrils and large glycogen reserves

-Quick to contract (good for quick bursts of strength or speed)

-Fatigue quickly, few mitochondria

-Appear pale so termed white muscles or “white meat”

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Type 2a Fibers

-Also known as intermediate fast-twitch fibers

-They can use both aerobic and anaerobic metabolism almost equally to create energy

-They are a combination of Type I and Type II muscle fibers.

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Type 2b (2x) Fibers

-use anaerobic metabolism to create energy

-the "classic" fast twitch muscle fibers that excel at producing quick, powerful bursts of speed.

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Anaerobic glycolysis

-No oxygen required, occurs in cytoplasm

-Glucose is converted to pyruvic acid where energy is captured in ATP bonds

-Get 2 ATP/1 glucose If oxygen, go to aerobic respiration If no oxygen (i.e. – intense muscle activity), go to lactic acid fermentation

-Glycolysis = Breaking down glucose

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Aerobic respiration

-provides 95% of ATP at rest and during light exercise

-occurs in mitochondria & involves a series of metabolic pathways that use oxygen – called oxidative phosphorylation

-2 Pyruvic Acids + O2 →Kreb’s Cycle →CO2 + H20 + 34 ATP

-36 ATP from each glucose molecule

-The extra 2 come from Glycolysis

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Stored ATP

Lasts 4-6 Seconds

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Anaerobic respiration & Lactic acid fermentation

-No oxygen

-When we need quicker (short term) energy

Only lasts a few minutes

-2 Pyruvic Acids + 2 ATP →Lactic Acid + 4 ATP

-Net Gain is 2 ATP for each glucose

- causes muscle soreness and fatigue (muscle fatigue occurs when the muscle can no longer contract despite still being stimulated because ATP is depleted).

-It results from oxygen debt which must be “paid back” (recovery period) by taking deep breaths

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