IB SEHS Unit 4

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41 Terms

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Label a diagram of a neuron
Dendrite- Allows transfer of info

Cell body- Provides structure

Nucleus- Cells control center

Axon- Main component of nerve signal transmission

Motor end plate- Where the neuron is unmyelinated and joins with a muscle

Synapse- The gap between the muscle and the MEP

Muscle- Receives the message
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Acetylcholines role in neuromuscular junctions
A small molecule that acts a chemical messenger that triggers the firing of motor neurons and affecting voluntary movements (contracts)
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Cholinesterase role in neuromuscular junctions
Breaks down the acetylcholine (relaxes)
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SFT steps

1. action potential arrives at the neuromuscular junction
2. cell membrane is depolarized, acetylcholine is released, sodium goes into cell
3. calcium is released from sarcoplasmic reticulum into muscle
4. calcium binds to troponin (on tropomyosin) causes movement and revealing myosin binding sites on actin
5. ATP is hydrolyzed to form ADP + phosphate
6. myosin head binds to actin and forms cross bridges (stays there until ATP molecule releases it) - if calcium is still there cross bridge is still there
7. ADP is released causing myosin heads to activate and move towards center of sarcomere (Power stroke)
8. power stroke is continued till z lines are pulled toward H zone
9. calcium is transported back causing termination of cross bridge.
10. myosin binding sites covered by tropomyosin and troponin (returns to original state)
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Myofibril
Elongated contractile threads found in striated muscle cells
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Myofilament
The structure that makes up the myofibril, examples include Actin and Myosin
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Sarcomere
 Structural unit of a myofibril consisting of a dark band and near a pale band
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Actin (I band)
thin filaments only, The protein that forms the contractile filaments of muscle cells
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H zones
Contains only thick filaments and shortens during contraction
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Myosin (A band)
The fibrous protein that forms the contractile filaments of muscle cells, Thick bands
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Z line
end of sarcomere
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Tropomyosin
Found in actin, blocks muscle contraction
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Sarcoplasmic reticulum
Contains and releases calcium
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Calcium ions
Bonds to troponin and reveals the binding sites on the actin
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ATP
Fuel for muscle contraction, splits into ADP and P
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Type I
Activity- Light activity

Glycogen- Low
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Type IIa
Activity- Long duration low intensity

Glycogen- High
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Type IIb
Activity- Short duration high intensity

Glycogen- High
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Flexion
Decrease the angle of a joint
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Extension
Increase the angle of a joint
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Abduction
movement away from the midline of the body
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Adduction
Movement toward the midline of the body
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Pronation
Rotation of Forearm where the palm of the hand is facing down
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Supination
Rotation of Forearm where the palm of the hand is facing up
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Elevation
Raising of the shoulder girdle
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Depression
Lowering of the shoulder girdle
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Rotation
Movement around a pivotal point
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Circumduction
A circular movement/direction resembling a cone
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Dorsiflexion
Raising of the foot/toes towards the body \n - Decreasing angle between tibia and foot
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Plantar flexion
Pointing of the toes/ foot towards the body \n - increasing angle between tibia and foot
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Eversion
Turning of the sole of the foot outwards
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Inversion
Turning of the sole of the foot inwards
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Isotonic
when the muscles either shortens or lengthens during contraction
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Isometric
When a muscle contracts with no resulting movement
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Isokinetic
A muscle contraction with constant speed
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Concentric vs Eccentric
Muscle shortens, muscle lengthens
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Agonist
Prime mover - contracts to cause movement
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Antagonist
Relaxes to allow movement
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DOMS
delayed onset muscle soreness (24-72 hours after eccentric muscle contraction) and is associated with structural muscle damage, inflammatory reactions in the muscle, overstretching and overtraining. \n \n DOMS is prevented/minimized by reducing the eccentric component of muscle actions during early training, starting training at a low intensity and gradually increasing the intensity, and warming up before exercise, cooling down after exercise.
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Fixator
Stabilizes the origin of a prime mover
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Synergist
Neutralizer, whom contract isometrically to prevent unwanted actions against the agonist/ antagonist