Module 3 - Neuromechanics Flashcards

(83 cards)

1
Q

Central nervous system (CNS)

A

Brain + spinal cord protected by boney structures

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2
Q

Peripheral nervous system (PNS)

A
  • Nerves outside the CNS
  • Somatic component includes sensory (senses) + motor (movement, muscle cells) nerves
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3
Q

Autonomic nervous system (ANS)

A
  • Control system of body functions such as breathing, cardiovascular function, etc.
  • Sympathetic + parasympathetic
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4
Q

Components of brain

A
  • Cerebrum (bulk of grey matter, neuron cell bodies)
  • Diencephalon
  • Cerebellum
  • Brain stem
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5
Q

Cerebrum (components + function)

A
  • Cerebral cortex
  • Hippocampus + amygdala (long-term memory)
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6
Q

Diencephalon (components + function)

A
  • Thalamus (sensory)
  • Hypothalamus (homeostasis)
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7
Q

Brain stem (components + function)

A
  • Midbrain
  • Pons
  • Medulla (cardiovascular function)
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8
Q

Spinal cord

A

Runs through vertebra, connects to peripheral on the sides of each vertebra

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9
Q

Grey matter

A
  • Cell bodies, dendrites, axon terminals
  • Areas of synaptic connections
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10
Q

White matter

A
  • Axons
  • Pathways between grey matter areas
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11
Q

Spinal cord to PNS

A

Grey + white matter of spinal cord –> ventral + dorsal roots (projections coming out of vertebra) –> go on to form PNS

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12
Q

Peripheral nerves

A
  • Nerve –> collection of many neurons (cells)
  • Motor nerves: efferent neurons –> control effectors such as skeletal muscles
  • Sensory nerves: afferent neurons –> detect stimuli + relay that info to CNS
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13
Q

Neurons

A
  • Basic information processing unit: receives input, process info, + provides output
  • Neurons are excitable cells; send/stop action potential
  • In a balancing act (tug-of-war) between “turn on” (depolarize + receive info from other neurons) + “turn off” (stay at -70mV)
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14
Q

Neuron anatomy

A
  • Processing section: nucleus, soma (cell body), dendrites (receive info from other neurons)
  • Communication section: axon (where AP transmitted, can be very long), axon terminal (where synapses form w/ other neurons)
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15
Q

Axon hillock

A
  • Where processing section connects to communication section (via axon)
  • Decides if AP is transferred to axon (is there enough AP?)
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16
Q

Membrane potential

A
  • Negative at rest (-70mV)
  • Depolarization = membrane potential becomes +ve (+20mV) (once AP surpasses thershold)
  • Repolarization/hyperpolarization = membrane potential becomes negative (-70mV)
  • Has a refractory period (opening/closing of ion channels) –> then resting state
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17
Q

Glial cells

A

Provide support to neuron function (helps with structure, metabolism, + repair) (helper/support cells)

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18
Q

Synapse

A
  • Structure permitting communication b/w 2 neurons
  • Where neuron interacts w/ another neuron/cell type
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19
Q

Action potential

A

Change in electrical potential that can travel along a cell membrane (-ve to +ve –> depolarization)

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20
Q

Neurotransmitter

A

A chemical messenger that transmits a message b/w cells

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21
Q

Cell to cell communication

A
  • Action potential travelling down an axon is an electrical signal
  • This electrical signal converted to chemical signal at axon terminals
  • Chemical signal converted to electrical signal at post-synaptic neuron
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22
Q

Measuring the nervous system

A
  • Structure: structural imaging –> MRI
  • Function: neuronal activity –> functional imaging, electroencephalography (EEG) –> measures electrical activity of brain, electrophysiology
  • Behaviour: times (e.g. reaction time), non-timed (errors, response)
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23
Q

Biopotential

A
  • Electrical potential measured between 2 points in living cells, tissues, and organisms (electrical diff. b/w 2 points) –> e.g. neurons, skeletal muscles
  • Electrodes, amplifiers, + electrical activity
  • EMG, ECG, EEG
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24
Q

Electroencephalography (EEG)

A
  • Measuring electrical activity (biopotentials) arising from the CNS
  • What is being measured? –> neuronal activity –> APs (de/repolarization)
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25
Muscle
- Tissue made up of many muscle cells + associated connective tissue - 3 main types: skeletal, cardiac, smooth
26
Skeletal muscle cell
- Muscle fibre/myocyte --> individual cell that when activated produced force that can lead to motion
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Sarcomere
Fundamental unit of skeletal + cardiac muscle. MANY sarcomeres arranged in sequence within single myofibril + many myofibrils make up a muscle cell
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Myofilaments
Sarcomeres are composed of highly organized arrangement of myofilaments (composed mainly of actin + myosin) that interact w/ each other to generate force (slide across each other)
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Skeletal muscle structure (levels of organization)
- Full, highly organized, full of machinery used to generate force (proteins, structures, etc.) - Fascicle: unit of a muscle cell - Muscle fibre: unit of a fascicle - Myofibril: unit of a muscle fibre (long strands of sarcomere) - Sarcomere: unit of myofibril (ends are Z-lines) - Sarcolemma: cell membrane
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Cross bridge
- Binding of actin to myosin myofilaments + change in confirmation of myosin - Cross bridge cycle: process involving attachment, conformation change + detachment (with ATP) that generates force
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Sliding filament theory
Theory explaining mechanism of muscle contraction associated with cross bridge cycling + sliding of myofilaments past each other to generate force
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Cross bridge cycle overview
- Sarcomere shortens when myosin heads in thick myofilaments form cross bridges w/ actin in thin filament - Formation of cross bridge --> initiated when Ca2+ released from sarcoplasmic reticulum bind to troponin --> changes shape - Tropomyosin moves away from myosin binding site on actin --> myosin head binds to actin + forms cross bridge (myosin head must also be activated before cycle can begin --> ATP hydrolysis provides energy to activate into cocked position) - Ends when Ca2+ is actively transported back to SR, troponin returns to original shape --> tropomyosin covers myosin binding site on actin
33
Cross bridge cycle steps
1) Cross bridge formation: myosin head binds to actin, inorganic P released, bond is stronger 2) Power stroke: ADP released + activated myosin head pivots, sliding thing myofilament toward centre of sarcomere 3) Cross bridge detachment: another ATP binds to myosin head --> link b/w myosin head + actin weakens --> myosin head detaches 4) Reactivation of myosin head: ATP hydrolyzed --> energy reactivates myosin head --> cocked position As long as actin binding sites exposed --> cross bridge cycle repeats --> thin myofilaments pulled towards each other --> sarcomere shortens
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Motor neuron
Neuron that synapses w/ skeletal muscle cells
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Motor unit
Motor neuron + ALL muscle cells it innervates (neuron interacts w/ diff. cell type) --> 100s-1,000s-100,000s
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Neuromuscular junction
Synapse b/w motor neuron + a skeletal muscle cell
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Muscle action potential
Action potential (depolarization --> repolarization on membrane of skeletal muscle cell)
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Neuromuscular activation
- Electrical: depolarization of motor neuron (neuronal AP) - Chemical: neurotransmitter (acetylcholine (ACH)) release at neuromuscular junction - Electrical: depolarization of muscle fibre - Mechanical: cross-bridge formation + sarcomere shortening
39
How can you control the amount of force a whole muscle generates?
- Muscle fibres activate in an ALL or NONE manner (1 motor neuron --> all muscle cells it innervates/AP arrives at one muscle --> ACH released --> muscle contracts) 1) Motor unit recruitment 2) AP frequency In general: increase in AP frequency --> increase in force
40
What determine the maximum isometric force a whole muscle cell could generate (assume maximal potential frequency and recruitment + optimal length)?
- Bigger muscle --> more sarcomere --> more force - Cross-sectional area of a muscle --> more muscle cells --> more sarcomeres --> more cross bridges --> more force
41
Electromyography (EMG)
Technique to measure electrical activity produced by muscles (muscle APs) that occurs when muscle is stimulated
42
Surface EMG
- Skin prep + electrode placement --> very important - Need to know direction of muscle fibres - Pro: relatively easy technique, less risk of damage/infection - Con: limited to superficial muscle, unsure of which muscle is producing electrical activity (risk of interference)
43
Intramuscular EMG
- Small needle is inserted into a muscle + electrical activity is recorded directly - Pro: specific choice of muscle - Con: invasive (skilled technician needed)
44
Axes of EMG graph
- y-axis: mV, V - x-axis: time
45
Relationship b/w EMG amplitude + muscle force
- Positive relationship b/w RAW (unfiltered, no mathematical manipulation) EMG + muscle force - As EMG increases, force increases - CANNOT compare RAW EMG b/w diff. muscles (e.g. diff. size) OR b/w people - Slight delay/lag time w/ force production compared to EMG
46
Stimulus response
- Series of events that req. afferent info + involve some sort of efferent response/effect - Stimulus presented --> SENSORY: info going to CNS through afferent neurons --> CORTICAL: neural info is processed (combined with prior behavioural instructions) --> MOTOR: an effect is determined + is transported through efferent neurons --> muscles activated to perform task - ALL steps take time (short time)
47
Reaction time
- Time it takes CNS to sense, process, + initiate response to stimulus (from stimulus to onset of response) - Afferent --> processing --> efferent
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Movement time
- Time it takes person to execute specific movement (does not include reaction time) - Time from onset muscle activation (EMG) to end of response - From muscle activated (start) to end of response
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Response time
- Reaction time + movement time - Total time from stimulus detection --> end of stimulus response
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What factors is reaction time dependent on?
Stimulus intensity + modality (type) - Cognitive/neural impairment - Age - Presence/absence of neurological disease + inheritence - Medications/drugs - Environment (distractions) - Sex SRT: simple reaction time CRT: choice reaction time
51
Simple reaction time (SRT)
- Only 1 stimulus + 1 response - e.g. "Hear something --> push a button"
52
Choice reaction time (CRT)
- Number of diff. stimuli presented each required diff. response - Reaction time gets longer w/ more stimuli - e.g. various pitch sounds --> press diff. button for each
53
Dual-task interference
- Simultaneous performance of 2 tasks often leads to performance deficits in component tasks - Thought to be proof of capacity limitation in cognition - Can't to Z things at the same time as fast is if they were separate Multi-tasking: - Possible, some people better than others - Aspect of learning + practice
54
Agonist
Muscle primarily responsible for a movement (e.g. biceps brachii in bicep curl)
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Antagonist
Muscle that opposes the movement of agonist (e.g. triceps brachii in bicep curl)
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Agonist + antagonist dependency
- Dependent on posture + movement - e.g. Knee flexion + extension while sitting vs lying down - Gravity always affects body --> posture + movement change agonist vs antagonist
57
Reciprocal contraction (/activation) + benfits
- Simultaneous activation of agonist + inactivation (relaxation) of antagonist - Maximizes amount of force it can produce (does not need to overcome agonist)
58
Co-contraction + benefits
- Simultaneous activation of agonist + antagonist - Stabilizes joint - e.g. Carrying heavy load --> stability of joint needed to support weight + prevent injury
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Graphing joint kinematics + EMG
CANNOT graph without kinematics (EMG only) --> don't know what's going on
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Biomechanics
Study of effects + control of forces that act on + are produced by living beings
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Kinematics
Study of MOTION of objects (w/out reference to the FORCES that caused the motion)
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Kinetics
Study of FORCES that cause motion
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Linear kinematics terms
- Displacement (m) - Velocity (m/s) - Acceleration (m/s^2)
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Angular kinematics terms
*ROTATIONAL* - Angular displacement (rad) - Angular velocity (rad/s) - Angular acceleration (rad/s^2)
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Force
*LINEAR* - Action/influence that moves body or influences movement of the body - UNIT: newtons (N) - Internal forces: created primarily by skeletal muscles - External forces: created by ground (ground reaction force), external loads, other individuals, + from passive sources (e.g. wind resistance)
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Moment
*ANGULAR* - "Moment of force" - Force that tends to change the rotational motion of an object - UNIT: Nxm - M +ve: counter-clockwise - M -ve: clockwise
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Vectors
- Have magnitude (length) + direction - Tail and head - A non vertical/horizontal vector is a sum of its vertical + horizontal components
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Moment arm
- Perpendicular distance from application of force - Distance b/w point of rotation + application of force - Larger moment arm --> larger moment of force (rotational)
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Centre of mass (COM)
Point in centre of object where all of the mass of object is equally distributed in all directions
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Centre of mass (COM) and gravity
Force of gravity acts in downward direction (-y) through the centre of mass (COM) of an object
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Force of gravity
- Mass x acceleration due to gravity (9.8m/s^2) F = m x a F = 5kg x -9.8m/s^2 F = -49N
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Moment calculation
M = F x d Approach 1: - F = force applied - d (moment arm) = perpendicular distance b/w axis of rotation + line of force - No 90 degree angle --> trig Approach 2: - F = force vector component that is perpendicular to segment - d (moment arm) = distance from axis of rotation to point of application of force - USING THIS ONE
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Muscle force and moments
- Must consider all moments acting on a segment --> must consider the sum of the moments - If a segment is stationary --> sum of M = 0
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Kinematics measurement
- Visual observation - Goniometer (instrument to measure angles): hand held/electronic - Inertial sensors: measure acceleration - Optical/magnet motion capture: gold standard for measuring kinematics
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Goniometer types + pros/cons
Hand held: - Pro: can do everywhere on anyone - Con: guess, estimate, not very accurate, stuck with static Electronic: - Pro: mobile - Con: may not be as accurate Potentiometer: - Pro: accurate joint angle - Con: tethered to one spot, immobile
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Inertial sensors pros/cons
High-end: - Pro: accurate - Con: expensive Personal (e.g. Apple Watch): - Pro: affordable in comparison, easy to use - Con: not as accurate
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Optical motion capture
- Gold standard (one of best techniques, go-to, reliable) of measuring kinematics - Cameras tracking dots: know exactly where each joint is in 3D (inertia + joint angle), can calc. displacement, velocity, acceleration, etc. - Pro: really accurate/gold standard - Con: expensive, software + trained people required
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Kinetics measurement
- Manual assessment - Dynamometer: device to measure force, moment, or power (hand held/electronic) - Force plates: instrument to measure ground reaction forces
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Manual muscle testing pros/cons
- Want to understand where deficits in body are through comparison w/ healthy parts - Pro: can do it anywhere - Con: lots of training required, not very accurate (subjective, don't know how many N)
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Dynamometer types + pros/cons
Hand held, hand grip: - Pro: objective (N, kg), measures amount of force - Con: have to be able to brace yourself to oppose the force Isokinetic dynamometer: - Pro: can test most joints, can control many variables (joint angle, speed (fixed/variable), resistance), completely adjustable, 360 degree rotation - Con: Expensive
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Force plates
- Gold standard in measuring kinetics (forces) - Can get a sense of interaction w/ environment while doing things - Need kinematics to go with kinetics for full picture - Pro: can measure force in all 6 directions + moments, really accurate - Con: alone --> no idea of kinematics, really sensitive, some are anchored into ground/others mobile
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What is included in the foundation of biomechanical research?
- EMG (muscle activation) - Kinematics (movement) - Kinetics (forces) Combined = full picture
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Gold standards of biomechanics
- Optical motion capture: kinematics - Force plates: kinetics