Muscular system Flashcards

1
Q

Skeletal muscle – Types of muscle tissue

A

attached to bones

long, cylindrical

multiple, peripherally located

no special cell to cell attachments

striations

no autorhythmic

voluntary and involuntary (reflexes)

Body movement

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2
Q

Smooth muscle – types of muscle tissue

A

Walls of hollow organs, blood vessels and glands.

spindle-shaped

single, centrally located.

gap junctions join some smooth muscle cells togehter

no striations

some smooth muscle are outorhythmic

involuntary control

Moving food through the digestive tract, emptying the urinary bladder, regulating the blood vessel diameter, contracting many gland ducts

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3
Q

Cardiac muscle – types of muscle tissue

A

Heart

Branched, cylindric

single, centrally located

intercolated disks

striations

untorhythmic

involuntary control

Pumping blood; contractions provide the major force for propelling blood through blood vessels

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4
Q

Skeletal muscle functions

A

Movement of the body;

-contraction of skeletal muscles is responsible for overall movements of the body.

-Ie/ walking, running and manipulating object with the hands

-short and lengthening of muscle (contraction) –> to initial movement.

Maintenance of posture;

-keep us sitting/standing

-hold up our body

-back and leg muscles

Respiration (ventilation);

-air in and out of lungs –> can be involuntary or voluntary.

-contraction of skeletal muscles within thoracic cage and diaphragm to help us breath.

-lungs.

Production of body heat;

-heat byproduct of muscle contraction.

-released heat is critical to maintenance of body temp.

-byproduct of muscle contraction

  • increases in exercise.
  • shivering when cold.

Communication;

-speaking, writing, typing, gesturing, and facial expressions

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5
Q

Smooth muscle functions

A

surrounds hollow organs –> to make tubes larger/smaller

constriction of organs and blood vessels

helps prople and mix food and water on digestive tract.

propel secretions from organs.

regulate blood flow through vessels

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6
Q

Cardiac muscle functions

A

Contraction of the heart

cause heart to beat, propelling blood to all parts of body.

pump blood in the correct direction

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7
Q

Organization of skeletal muscle

A

40% of body weight

also called striated muscle

tendon- where muscle attaches to bone.

skeletal muscle- attached to bone,
long, cylindrical cell shape.
multiple, peripherally located nuclei.
striated.
voluntary and involuntary control.
body movements.
Have many nuclei- produce mRNA to make protein.

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8
Q

T-tubules

A

inward folds on the sareolemma.

carry electrical impulses into center of muscle fiber so it contracts as a whole.

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9
Q

Epimysium

A

forms a connective tissue sheath that surrounds each skeletal muscle.

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10
Q

Perimysium

A

Subdiv ides each whole muscle into numerous, visible bundles and muscles fiber (cells) called fascicles

serves as a passage way for blood vessels, and nerves that supply each fascicle.

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11
Q

endomysium

A

separates individual muscle fibers within fascicle.

serves as a passage way for nerve fibers and blood vessels that supply each muscle cell.

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12
Q

Contractility

A

ability to shorten forcefully or contract.

Contraction moves bones (skeletal muscle) or structures they are attached to.

Compresses blood vessels or hollow organs (smooth muscle)

Increases pressure inside chambers of heart to pump blood (cardiac muscle)

muscle shortening is forceful, lengthening is pressure

main aspects of contraction;
1) electrical component
2) mechanical component

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13
Q

Excitability

A

ability to respond to a stimulus –> voluntary and involuntary

Action potential from motor nerves stimulates skeletal muscle contraction

Involuntary neural and hormonal signals stimulate smooth and cardiac muscle

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14
Q

Extensibility

A

ability to stretch and still be able to contract.

Skeletal muscle can produce force in various joint positions.

Blood vessels and hollow organs (stomach) are able to expand and contract to various lengths depending on blood pressure or contents

ability to stretch beyond normal resting length and still be able to contract.

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15
Q

Elasticity

A

ability to recoil to original resting length after stretch

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16
Q

The sliding-filament model of muscle contraction

A

Slide past each other to produce contraction - bring z line together (shorten sarcomere)

The sarcomere shortens during contraction. As contraction takes place, actin and myosin do not change length but instead slide past one another.

myofilliment dont change length

actin and myosin slide past each other and shorten sarcomere

the sarcomere shortens during contraction

as contraction takes place, actin and myosin do not change length but instead slide past one another

i band becomes small with contraction, a band doesn’t change

Hzone becomes smaller

Z lines get closer together as sarcomere shortens

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17
Q

I band

A

Includes z-disk and extends to the ends of the myosin myofilaments

has only actin myofilaments. - lighter staining.

–>Sarcomere – join end-end, forming myofibrils.

smallest portion of muscle that can contract.

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18
Q

A band

A

in center of each sarcomere.

darker staining.

has both actin and myosin overlapping except in the center of the A band

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19
Q

H zone

A

has only myosin

in center of A band

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20
Q

M line

A

Dark line in the middle of H zone.

has protein filaments that hold myosin myofiaments in place.

one sarcomere extends z-disk to z-disk

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21
Q

Heads

A

binds to actin molecule to form cross-bridges to contract the muscle.

break down ATP to release NRG

bend hinge region

pivot – so they can bind to actin to produce force – collectively adds to muscle production.

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22
Q

Troponin

A

3 Subnunits: a. anchors troponin to actin.
b. prevents tropomyosin from uncovering attachement site in relaxed muscle.
c. binds Ca2+

Ca2+ binds here to exposed finger holes

relationship between troponin and tropomyosin that determines when skeletal muscle will contract.

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23
Q

Tropomyosin

A

lies in active groove.

covers attachment sites on actin in relaxed muscle.

muscle cant contract until tropomyosin moves to uncover active sites

Actin strands - attachment for myosin

24
Q

Actin myofilament

A

thin

has 3 components: actin, tropomyosin, troponin.

has attachment site for myosin head.

25
myosin head
binds to actin molecule to form cross-bridges to contract the muscle break down ATP to release energy bend hinge region pivot - so they can bind to actin to produce force - collectively adds to muscle production
26
Function of NMJ
each muscle fiber is innervated by a branch of a motor neuron at the neuromuscular junction. this point of contact between axon terminal & Sarcolemma results in Ap in a muscle fiber. stimulus for this(AP) is the release of acetylcholine from the NM
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2 main aspects of muscle fibers - neuromuscular junction
Motor neuron signal transmitted to muscle cell through a specialized synapse( Neuromuscular junction) 1. electrical component 2 . mechanical component muscle fibers are electrically excitable · Aps travel from brain or spinal cord along axons to muscle fibers and cause them to contract · electrically excitable cells , like other cells are polarized. inside of most cell membranes is negatively case · voltage/electrical charge difference , exists across each cell membrane - this charge difference across cell membrane of an unstimulated cell is called RMP.
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Events that happen in neuromuscular junction
1. When an Ap reaches the terminal of a motorneuron, It causes Ca2+ channels in cell membrane of an axon to open. Ca2+ diffuses into axon terminal 2. Once inside cell , the Ca2+ causes the contents of a few synaptic vesicles to be secreted by exocytosis from the presynaptic terminal into the synaptic cleft. 3. ach molecules are released from Synaptic Vesicles. I. ach diffuse across cleft & bind to ligand-gated Na+ channels in Sarcolemma causing them to open 5. Na+ ions then diffuse into muscle fiber , causing depolarization In skeletal muscle, each AP in motor neuron causes depolarization in muscle fiber that exceeds threshold. This produces an AP in muscle fiber. 6.Ach then unbinds from gate Na+ channels, which then close. 7. Enzyme acetylcholinerase rapidly breaks down ach in synaptic cleft into acetic acid and choline. Enzyme keeps ach from accumulating within the synaptic cleft, where it would act as a constant stimulus at the mototr end-plate, producing continuous contraction in muscle fiber. 8..8 motor neurons actively absorb choline molecules into axon terminal. The choline molecules then combine with acetic acid within the neuron to produce Ach. 9. recycling choline molecules requires less NRG and is more rapid than continuously synthesizing new Ach molecules. The Ach molecules are then taken up by synaptic vesicles.
29
Action Potential in Muscle Membrane (Sarcolemma Membrane)
AP occurs when the excitable cell is stimulated reversal of RMP --> inside of cell becomes more pos, compared to outside charge reversal occurs because ion channels open when cell is stimulated. diffusion of ions through these channels changes the charge across the cell membrane and produces an AP lasts 1ms - a few ms two phases: 1.depolarization 2.repolarization before a neuron or a muscle fiber is stimulated, the gated Na+ and K+ ion channels are closed. when cell is stimulated, llgand-gated Na+ channels open & Na+ diffuses into the cell Na+ will make the inside of the cell membrane depolarized (more +) if depolarization causes the membrane potential to reach threshold, an AP triggered. A s the inside of a cell becomes more + , this voltage causes additional permeability changes in the cell membrane · this stops depolarization & starts repolarization. repolarization phase is the return of membrane potential to its resting value . occurs when when ligand-gated Nat+ channels close and gated K+ channels open K+ moves out of the cell the inside of the cell becomes more (-) AP ends and rmp is restored by Na+ K+ pump
30
Ion channels
· Phospholipid bilayer is a hydrophobic environment inhibiting the movement decrease of charged particles, particularly, across the cell membrane Ion can move across membrane through ion channels 1.leak -main ones, slow leak of ions down [ ] gradient. 2.gated - most important in stimulated cells. governs production of AP
31
Action potential and muscle contraction
AP made in sarcolemma of skeletal muscle fiber can lead to contraction of the fiber. AP is propagated along motor neuron. AP in motor neuron stimulates opening of voltage-gated Ca2+ channels The influx of Ca2+ into motor neuron causes secretion of ach. ach opens ligand-gated Na+ channels in sacrolemma AP in muscle fiber travels along entire sarcolemma. AP also moves down T-tubles.
32
Resting membrane potential
sodium potassium pump maintains the uneven distribution of Na+ & K+ across the cell membrane. · transports K+ from outside the cell to Inside & transports Na+ from inside the cell to the outside . negative inside compared to the outside. need electrical chemical gradient. electrical charge difference in an unstimulated cell. · still ready to respond in a moments notice. RMP results DC of 3 factors: 1. [] K+ inside cell>than outside 2 . 5 ) Na+ outside cell >than inside 3.Membrane more permeable to K+ than Na+ (-) charged molecules (more K+ leak channels than Na+), such as proteins are "trapped" inside the cell because cell membrane is impermeable. [ ] gradient for an ion determines if it will enter or leave a cell. K+ channels, K+ out - go towards lower [ ] of that ion Na+ channels, Na+ in - go towards lower [ ] of that ion.
33
Breakdown of ATP and cross bridge
mechanical component of muscle contraction many cycles occur per contraction ifCa+ is present this will continue 1.Exposure of active sites- Ca+ binding to troponin -myosin head stores NRG from ATP breakdown. 2.Cross bridge formation - free phosphate released - myosin head attached to actin - actin sites are exposed, myosin quickly binds. 3. Power stroke - cocking of myosin - stored NRG being used - forms cross-bridge to trigger rapid movement of myosin head called the power stroke. - Actin filament does the movement. 4. Cross-bridge release - triphosphate bind - binding of ATP to myosin head causes it to detach from myosin 5.Hydrolysis of ATP - Myosin head breaks down ATP unto ADP and P -- which remain attached to myosin head. Myosin return to their resting position
34
Regulation of muscle force production
We regulate the amount of force a muscle produces by controlling how many muscle cells (fibers) are stimulated to contract we can modify force production to vary our movements.
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Motor Unit
includes a single motor neuron and all the muscle fibers it innervates. Motor units vary in their size and their sensitivity to stimulation Small motor units have a handful of muscle fibers, while large motor units can have hundreds of muscle fibers. The muscle fibers within a motor unit are the same fiber type A muscle will contain motor units of various sizes and types Muscles tend to have motor units of a certain size, depending on their function small muscles in the hand and eye have very small motor units that allow for the fine motor control required for delicate and precise movements. Large muscles in the legs have huge motor units and produce large forces with less fine control.
36
Motor Unit Recruitment
a motor unit is recruited when an action potential is sent down its motor neuron. As indicated above the motor neuron can stimulate a few or many muscle fibers -- to get certain cells to contract. We can produce smooth, fluid movements of varying force by regulating the number and size of motor units that we recruit.
37
Muscle Fiber Types
Muscle fiber are classified into 3 specialized types based on their structural and functional characteristics. Slow oxidative to fatigue, use O2 well, have lots of mitochondria. SO – high capacity for aerobic metabolism (using oxygen) FOG – intermediate characteristics for aerobic and anaerobic metabolism FG - High capacity for anaerobic (without oxygen) force and power output Isometric and Isotonic contractions: Isometric- muscle does not shorten. - increase tension. - lifting something way to heavy. Isotonic - muscle shortens. concentric(muscle shortens) and ecccentric(increase muscle length).
38
skeletal muscle fiber types function
Functions- low-twitch oxiadative (SO) (Type-I): Maintenance of posture and performance of endurance activities. Fast-twitch oxidative glycolytic (FOG) (Type IIa): Endurance activities in endurance-trained muscles. Fast-twitch glycolytic (FG) (Type IIb): Rapid, intense movements of short duration. Will recruit all to reach maximal muscle demand.
39
skeletal muscle fiber - location where fibers are most abundant
Location where fibers are most abundant- low-twitch oxiadative (SO) (Type-I): Generally in postural muscles and more in lower limbs than upper limbs. Fast-twitch oxidative glycolytic (FOG) (Type IIa): Generally in lower limbs. Fast-twitch glycolytic (FG) (Type IIb): Generally in upper limbs.
40
skeletal muscle fiber glycogen concentration
Glycogen concentration- low-twitch oxiadative (SO) (Type-I):Low. Fast-twitch oxidative glycolytic (FOG) (Type IIa):High Fast-twitch glycolytic (FG) (Type IIb):High.
41
skeletal muscle fiber myoglobin content
Myoglobin content - Slow-twitch oxiadative (SO) (Type-I):High. Fast-twitch oxidative glycolytic (FOG) (Type IIa): High. Fast-twitch glycolytic (FG) (Type IIb): Low.
42
skeletal muscle fiber mitchondria
Mitochondria - Slow-twitch oxiadative (SO) (Type-I): Many. Fast-twitch oxidative glycolytic (FOG) (Type IIa): Many. Fast-twitch glycolytic (FG) (Type IIb): Few
43
skeletal muscle fiber capillaries
Capillaries - Slow-twitch oxiadative (SO) (Type-I): Many. Fast-twitch oxidative glycolytic (FOG) (Type IIa):Many. Fast-twitch glycolytic (FG) (Type IIb): Few.
44
skeletal muscle fiber metabolism
Metabolism - Slow-twitch oxiadative (SO) (Type-I): High aerobic capacity, low anaerobic capacity. Fast-twitch oxidative glycolytic (FOG) (Type IIa): Intermediate aerobic capacity, high anaerobic capacity. Fast-twitch glycolytic (FG) (Type IIb): Low aerobic capacity, highest anaerobic capacity.
45
skeletal muscle fiber fatigue resistance
Fatigue resistance - low-twitch oxiadative (SO) (Type-I):High. Fast-twitch oxidative glycolytic (FOG) (Type IIa):Intermediate. Fast-twitch glycolytic (FG) (Type IIb):Low, wear out quickly, cant maintain a sprint.
46
skeletal muscle fiber myosin ATPase activity
Myosin ATpose activity- low-twitch oxiadative (SO) (Type-I):Slow. Fast-twitch oxidative glycolytic (FOG) (Type IIa):Fast Fast-twitch glycolytic (FG) (Type IIb):Fast.
47
skeletal muscle fiber glycogen concentration
Glycogen concentration- low-twitch oxiadative (SO) (Type-I):Low. Fast-twitch oxidative glycolytic (FOG) (Type IIa):High Fast-twitch glycolytic (FG) (Type IIb):High.
48
Resistance training
- weight lifting – high force low duration exercise. Increases size and strength of recruited muscle fibers (all fiber types that are recruited). many different exercises are required to ensure all muscles in the body are stimulated to adapt to the training. Increase in fiber size is called hypertrophy Fiber growth requires more nuclei to be added to each muscle fiber. Resistance exercise stimulates Satellite cells to fuse with muscle fibers providing new nuclei New nuclei can sustain the higher level of protein synthesis that is needed to maintain the larger cell size. The additional protein includes: the myofilament proteins involved in force production (myosin, actin, titin). proteins needed to maintain physiological needs. enzymes for ATP re-synthesis and transporters to maintain membrane potential during relaxation. transporters to remove calcium during relaxation.
49
Endurance training
Training can increase the size and capacity of both types of muscle fibers so they can perform more efficiently. Aerobic based exercise - low force long duration exercise Increase aerobic enzymes (mitochondria) Increased capillary density (O2 uptake) Increased Cardiac Output from Heart (O2 delivery) Increased uptake and storage of fuel (carbohydrates and lipids) for aerobic metabolism Increased resistance to fatigue (reduced work capacity) Better protection against oxidative stress, inflammation and acidosis Endurance trained individuals can sustain a higher rate of aerobic metabolism, allowing them to maintain a faster running/cycling/swimming pace for much longer, improving performance in endurance events like a 10km run or triathlon. intense exercise that requires ATP production without )2 (weight + lifting, increases muscular strength and mass and cause fast - twitch muscle fibers to enlarge more than slow twitch fibers. exercise in with ATP is produced with )2 increaseing vascularity of muscle and causes slow-twitch muscles fibers to enlarge more. - throguh training with this we can run long distances. in response to exercise hypertrophy occurs --> muscle increases in size, muscle increases in strength and endurance atrophy (muscle decreases in size) --> both result from changes in size of individual muscle fibers New nuclei are added to muscle fibers because small satellite cells near skeletal muscle fibers increase in # in response to exercise and then fuse with skeletal muscle fibers, mitochondria, blood vessels and connective tissue also increase in #. athletic training increases muscle strength because in increase muscle size and # of motor units recruited simultaneous by nervous system. improved endurance is in part to increased metabolism, increased circulation to exercising muscles increase # of capillaries, more effecient respiration, and greater capacity of heart to pump blood.
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Energy Sources for Muscle Contraction
a,b. Immediate – Adenylate Kinase and Creatine Kinase(fatigue fast) - very fast but very limited quantity(cant do it often) c. Anaerobic – Partial release of energy from Glucose – fast but limited quantity d. Aerobic - Complete energy release from Glucose and Fats – slow but very large quantity Different fiber types have higher capacity for different pathways for ATP re-synthesis Different muscles will have more of specific fiber types to support their functional roles transfers on phosphate from on ADP to a second ADP resulting in one ATP and one AMP transfer of phosphate produce ATP break all glucose. Harness NRG between bonds breaking glucose in half limited, but less high net gain of ATP
51
3 layers of connective tissue
Epimysium; Perimysium; Endomysium;
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epimysium
forms connective tissue sheath that surrounds, each skeletal muscle. protein fibers gradually merge with a layer of connective tissue between adjacent muscles and connecting the skin to superficial muscles outer layers of connective tissue separate the muscles from nearby structures
53
perimysium
subdivides each who muscle into many, visible bundles of muscle fibers (cells) called fascicles. is a loose connective tissue serving as passageways for blood vessels and neurons that supply each fascicle
54
endomysium
delicate layer of connective tissue that separates the individual muscle fibers within each fascicle. serves as passageways for nerve fibers and blood vessels that supply each separate muscle fiber.
55
tendon
attach muscle to bone