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135 Terms

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Skeletal Muscle Tissue
smallest to largest: myofilaments (actin and myosin) bundled to make myofibrils -\> bundles of myofibrils wrapped in sarcolemma and wrapped in endomysium make up muscle fibers -\> bundles of muscle fibers wrapped in perimysium make up fascicles -\> bundles of fascicles wrapped in epimysium make up skeletal muscles (organs).
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Myofibril
contractile organelle that runs the length of the myocyte
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Thick filament
Myosin
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Thin filament
Actin
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T tubule
Runs around and in between myofibrils
Invagination of the sarcolemma as it is diving down into the cell's interior
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Sarcoplasmic Reticulum
Network, membrane bound organelle that surrounds the myofibrils
Function: stores calcium
Terminal cisternae: enlarged regions of the SR that make contact with the T-tubules
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Triad
T tubule, and lateral sacs
2 terminal cisternae and an individual T-tubule cutting between \= triad
2 triads for every sarcomere
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Sarcomere
The functional unit of organization of the myofibril and its overlapping arrangement of actin and myosin given the striated appearance
Goes from one Z disc to other Z disc
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How many actin encircle each myosin thick filament?
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M line (midline)
Chunk of proteins running straight down the middle of sarcomere
Ends of myosin thick filaments are holding on to each other (end to end)
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A band
length of myosin
no change in contraction
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I band
only have actin myofilaments
on either side of Z line
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H zone
represented by length of myosin
in the middle of A band, immediately surrounding M line
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Z disc
Actin extending from one sarcomere to the next
Zippered seam between adjacent sarcomeres
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Contractile Proteins
Actin and myosin
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Regulatory proteins
Tropomyosin and troponin
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Contractile proteins: the thin myofilament (actin)
Double helix structure, each strand made up of individual globular-looking protein structures called G actins
Each G actin has a specific myosin-binding site
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Strand of G actin
F actin
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Two strands of F actin with a double helix
actin thin myofilament
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Tropomyosin
Long strand that lays on top of myosin binding site
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Tropomyosin v Troponin
Tropomyosin: long, fibrous type of protein
Troponin: a complex of several smaller globular proteins
Function: keep myosin binding sites covered or exposed
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What uncovers tropomyosin?
Calcium
When it is released from the sarcoplasmic reticulum, It will bind to one of the proteins in the troponin complex.
When calcium binds you get conformational change in that troponin.
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When myosin sites are exposed
Myosin and actin can come together and you get contraction every time
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Contractile Protein: the Thick Myofilament (myosin)
Fibrous double helix tail that terminates as double headed globular structure
Final structure: 300 double helixed strands
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Bare zone of myosin
Tails of strands
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Titin
At end of myosin, attaches myosin to Z disc
Large, highly elastic protein
Allows recoil
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Head of myosin
Actin binding site
ATPase site- hydrolyze ATP, dephosphorylate them
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Sarcomere is
smallest functional unit of skeletal muscle contraction
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The Sliding-Filament Mechanism of Contraction
actin filament and myosin filament overlap during contraction
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How do we initiate muscle contraction?
-Somatic motor neurons release ACh onto the sarcolemma
-Somatic motor neurons always activate muscle cells to contract
-Muscle cells are electrically excitable, so they can also generate action potentials...called end plate potentials
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Excitation-contraction coupling
series of events that link the end-plate potential to muscle contraction
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The motor unit
One somatic motor neuron and all the muscle fibers it innervates
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Large motor unit
dependent on how many muscle fibers the neuron innervates
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The muscle twitch
the mechanical response of a muscle cell, or a motor unit, or a whole muscle to a single end-plate potential
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Latent period of muscle twitch
millisecond time delay between the action potential and initiation of contraction (time for ECC)
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Contraction phase of muscle twitch
crossbridge cycling is occurring and cytosolic Calcium levels are rising
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Relaxation phase
cytosolic Calcium is returned to the SR and the number of crossbridges decline
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Not all twitches are equal
Variability in speed of contraction and amount of force generated
Depends on diameter of the muscle cell
Depends on type of myosin ATPase
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Isotonic twitch/ contraction
muscle generates a force that just exceeds the load resulting in muscle length change
-concentric
-eccentric
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Isometric twitch/ contraction
muscle generates a force that does not exceed the load and results in no change in muscle length
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limited muscle to decrease in length causing a maximal contraction
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Isometric contraction
Muscle contracts but does not shorten because contractile element decreased in length but elastic element increased in length (accommodated change)
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Concentric contraction
Both contractile and elastic element shorten, shortening entire length of muscle
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Treppe
Warming up phase for the myocyte
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smaller motor units
activate smaller fibers
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when ATP utilization increases
ATP decreases
ADP increases
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The creatine-phosphate system
CP+ADP yields ATP + Creatine
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slow oxidative fibers
red
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fast oxidative-glycolytic
pink
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fast glycolytic
white
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Endurance exercise enhances the oxidative capacity
fast glycolytic transitions to fast oxidative glycolytic
more mitochondria, bigger mitochondria
increased capillary density
fiber diameter decreases
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High intensity exercise enhances glycolytic capacity
fast oxidative-glycolytic transitions into fast glycolytic
less mitochondria, smaller mitochondria
decreased capillary density
increased concentration of glycolytic enzymes
fiber diameter increases
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myosatellite cells
cells that hang out along the periphery of the cell that fuse themselves into the skeletal muscle, adding their nuclei and organelles to the structure
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biceps brachii
elbow flexion
attaches in front of elbow
agonist
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triceps brachii
attaches behind elbow
elbow extension
antagonist
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muscle spindles
detect length
combo of intrafusal fibers with their sensory axons
type 1 and type 2 afferent
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golgi tendon organs
detect tension
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alpha motor neurons
type of axons innervating skeletal muscle cells (somatic)
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gamma motor neuron
synapse on intrafusal fibers
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muscle spindle stretch
stretched: lots of action potential
relaxed: still some action potential
contracted: very few
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atria
receive blood
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ventricles
pump blood out
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wall of left ventricle
very thick because blood is going to entire rest of body
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wall of right ventricle
not as thick as left ventricle
because blood is going to lungs that are close
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arteries
carry blood away from heart
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endothelium
simple squamous epithelial
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arterie structure
endothelium-smooth muscle-connective tissue
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arteriole
lots of smooth muscle tissue
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capillary
endothelium-basement membrane (thin CT)
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venule
small vein
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vein vs artery
artery-more smooth muscle
vein-larger lumen
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venous valves
like semilunar valves
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blood anatomy
plasma- 55% of blood volume
Buffy coat (leukocytes and platelets)- less than 1%
Erythrocytes- 45% HCT
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Erythrocytes (RBCs)
red because of hemoglobin
biconcave disc imparts flexibility and increased surface area
slightly larger diameter than capillaries- go through one by one single file
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pulmonary circuit
associated with lungs
arteries bring deox blood
veins bring ox blood
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veins
bring blood back to heart
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in series blood flow
pulmonary- systemic
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right heart
pulmonary
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left heart
systemic (rest of body)
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why is parallel blood flow necessary
same blood delivered to all organs
-same nutrients/oxygen
-same capacity to remove wastes
regional control of blood distribution
-decrease blood to one organ
-increase blood to another organ
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GI tract and liver
Kidneys
have parallel and series blood flow
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heart has myogenic contractile activity
skeletal muscle has neurogenic contractile activity
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autorhythmic cells
specialized cardiac myocytes
-pacemaker cells:
-conduction fibers
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pacemaker cells
spontaneously generate action potentials and establish heart rhythm
-located in high concentration at SA node and AV node
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Conduction fibers
transmit action potentials
larger diameter cardiac myocytes
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SA node
high posterior wall of right atrium where the superior vena cava opens
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AV node
interatrial septum, floor of right atrium
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ECG
non invasive technique for recording ELECTRIC activity in the heart
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reflects patterns of action potential firing in the entire population of cells that make up the myocardium
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P-wave
Atrial depolarization
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QRS complex
ventricular depolarization
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T wave
ventricular repolarization
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Lead 2
LL-RA
down and towards left
atria to ventricle
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systole
ventricular contraction
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diastole
ventricular relaxation
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systolic blood pressure
maximal aortic pressure occurs during systole
blood entering the aorta from the left ventricle
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diastolic blood pressure
minimum aortic pressure occurs during diastole
spend more time in DP
blood leaving aorta as it moves downstream
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mean arterial pressure
average aortic pressure during a cardiac cycle
overall driving force for blood to reach organs
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end diastolic volume
volume when blood is about to be pushed out of ventricles
avg- 130ml
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end systolic volume
volume when all blood has been pushed out of ventricles
avg- 60ml