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dendrites
receives signals and sends them to the axon hillock
axon hillock
the action potential begins here (if there is one)
myelin sheath
increases conduction speeds of electrical impulses & prevents ion loss
nodes of ranvier
gaps in the myelin sheath that allows for jumping of the action potential (saltatory conduction)
axon terminals (electrical vs chemical)
the end of the neuron that sends electrical or chemical signals at the synapse
electrical: directly between cells, ex: retina
chemical: communicates using chemical messengers, most common
Sensory Neurons AFFERENT
transmits action potentials in
TO spinal cord or brain
PERIPHERAL NERVOUS SYSTEM
-taste, smell, balance, etc.
Motor Neurons EFFERENT
transmits action potentials out
FROM spinal cord or brain
TO muscles, glands, visceral organs (heart, liver, intestines, etc.)
PERIPHERAL NERVOUS SYSTEM
-only the cell body is in the spinal cord
-motor nerves drive to different locations
SOMATIC & AUTONOMIC motor neurons
Interneuron
short cable that connects 2 different points
CENTRAL NERVOUS SYSTEM (spinal cord or brain)
Somatic Motor Neuron
can be controlled, VOLUNTARY
-drives skeletal muscles
Autonomic Motor Neuron
is on autopilot, INVOLUNTARY
-reflex
-drives smooth muscle, digestion, glands, cardiac muscle
2 neurons
Schwann Cells
cells responsible for producing myeline sheaths in the PERIPHERAL NERVOUS SYSTEM
Oligodendrocytes
cells responsible for producing myeline sheaths around neurons in the CENTRAL NERVOUS SYSTEM
Microglia
immune defense cells of CNS, may contribute to dementias
Central Nervous System
oligodendrocytes
microglia
astrocytes
Peripheral Nervous System
schwann cells
autonomic and somatic
Astrocytes
holds neurons in place
Ependymal Cells
line cavity, contributes to cerebral spinal fluid
Protection of Central Nervous System Tissue
Bony Structures, Meninges, Cerebrospinal Fluid, Blood-brain barrier
Bony Structures (CNS tissue Protection)
the cranium protects and encases the brain
vertebral column surrounds spinal cord
Meninges (CNS tissue protection)
membranes between bones and CNS tissue
mater tissues (3 layers of tissue)
Cerebrospinal Fluid (CNS tissue protection)
cushion against impact
Blood-brain Barrier (CNS tissue protection)
highly selective
limits access of blood-borne materials into brain tissues
separates blood from brain tissue
Diencephalon (in the brain)
Glands
Thalamus
Hypothalamus
Forebrain (in the brain)
cerebral hemispheres
right and left lobes
Brain Stem Components
Midbrain, PONS, Medulla Oblongata
Midbrain
higher level reflexes
startle reflexes
visual reflexes
PONS
bridge between midbrain and medulla oblongata
conduction tissue
Medulla Oblongata (brain stem)
blends into spinal cord
homeostatic mechanisms
respiratory and cardiovascular systems
vomiting, swallowing, coughing, sneezing
Cerebellum
located at the back of the brain, near brainstem
autopilot, subconscious
coordinates
motor signals
visual stimulu
equilibrium
produces smooth voluntary movements?
Resting Membrane Potential
1: Sodium Potassium ATPase 3:2 OUT:IN
*on all the time
*creates a gradient of high sodium (and Cl) outside and high potassium inside
*20% of the effect of creating RPM
2: Sodium Leak Channel
*RMP is far from what sodium wanted (+30)
3: Potassium Leak Channel
*there’s more potassium leak channels than sodium leak channels
*80% of the effect of creating RPM
*potassium gets its way because theres WAY more
*RPM is close to what potassium wanted (-90)
Phases of an Action Potential
1: Depolarization
2: Peak
3: Repolarization
4: Hyperpolarization
Depolarization
membrane potential is NOT ZERO
membrane potential is becoming more positive
membrane potential is LESS POLARIZED than the rest
polarized = -70mv
membrane potential becomes +30mv
VG Na+ is open
VG K+ not open yet
*if you go towards ZERO, this is depolarization
Peak
Repolarization
membrane potential returns to RESTING potential
VG K+ channels open
K+ diffuses out of the axon
membrane potential goes beyond resting state NEGATIVE
goes beyond -70mv (example: -74mv)
Hyperpolarization
membrane is MORE POLARIZED than the rest
VG K+ channels remain open
by the end of this phase ions leave through leak channels only
membrane potential returns to resting state of -70mV
*below threshold
Graded Potentials
variety gives you GRADATION hence the name GRADED POTENTIALS
short distance signals
can exist without action potentials
localized in a part of the nerve (like little sparks in a specific area)
its like a chatter that may or may not speak to an AP
come in different sizes
can go up or down (depolarization or hyperpolarization)
happens between synapses
nerves to nerves
nerves to muscle
short distance but can add up with SUMMATION
strong where it happens and decays in strength as you go away
no refractory period (they can pile up)
occurs with touch, hearing, smell, or any other STIMULI
happens at CELL BODY
the RECEIVING part of the cell
Action Potentials
gets the signal, takes it, and runs
makes it all the way to the end of an axon
doesn’t matter if its very far
the cell is trying to talk to something EXTERNALLY
taking a message somewhere
ALL or NOTHING
starts life at threshold (which is the trigger)
you go from resting to trigger by GRADED POTENTIALS
very fast
stereotype size / identical
can stack up behind each other if you need them to
will not die out from when you start
same strength all the way
VG channels must be present (they open and close)
self-regeneratory - one turns on the next like a domino
yes refractory period (absolute and relative)
only one the entire time
always depolarization to peak to repolarization
happens at the AXON hillock
Refractoriness
prevents AP from going back to where it came from
keeps a little bit of air space between AP so ots quantifiable
you can count it
may give extra info from an AP
Absolute Refractory Period
you can’t get an AP because you’re in the middle of one
due to inactivated Na+ channels
open
closed
closed and locked
Relative Refractory Period
after AP theres a dip
K+ channels take longer than usual to close and clean up
theres a possibility to have another AP
BUT you have to jump a bigger jump due to continued outward diffusion of K+
Synapses
Electrical: membranes are very close together
special channels allow current to flow
Chemical: narrow space, synaptic cleft
prevents flow of electricity
must be bridged by transmitters
theres up to 100,000 synapses for CNS
Presynaptic Cell and Postsynaptic Cells
pre: releases NT
post: receives NT
Synaptic Vesicles
membrane-bound spheres with neurotransmitters
Motor Proteins (Axonal Transport)
Kinesin: anterograde
Dynein: retrograde
they are responsible for physically walking vesicles full of material to one end and back for recycling
they move down microtubules
ACh Receptor
predominantly Na+ Channel
when you open it it allows Na+ to come in
requires ACh to bind to it to open
Acetylcholinesterase gets rid of it and it closes pretty quickly
ACh keeps it open
Acetylcholinesterase closes it
SNARE Proteins
physically takes vesicles and moves them to the membrane (docking)
it fuses them
releases NT into the synapse by exocytosis
snare proteins are well known because they are easily poisoned
toxins target snare proteins
Famous Synaptic Toxins
Tetanus: in the soil and can get into your bloodstream through a cut
Its target is to destroy snare proteins▶no vesicles▶no NT
Symptom is muscle locking up and becoming contracted
The toxin targets the inhibitory nerve (which relaxes muscle)
Botulism: another bacterial toxin that targets snare proteins
Blocks NT of activating nerves
Now you cant turn on the muscle
Muscle is tense and contracted
Think of BOTOX, no movement of face
Spider Venom: interferes with SNARE proteins
Its possible to have too much NT
Explosive paralysis because you overwhelm the synapse
Epinephrine and Norepinephrine (MONOAMINE)
alpha adrenergic: a1, a2
beta-adrenergic: b1, b2, b3
Dopamine (MONOAMINE)
Schizophrenia: excess of dopamine, can be treated with blockers
Parkinsons: deficiency of dopamine, can be treated with L-dopa
Serotonin (MONOAMINE)
affects mood, food intake, reproductive behavior
tryptophan derived
serotonin uptake blockers treats depression, lowers appetite
Glutamate (Amino Acid NT)
most common excitatory amino acid in CNS
cooperate in long-term potentiation (LEARNING!)
brain
GABA
major inhibitory NT in brain
receptors cause influx of Cl, hyperpolarizes cell
Xanax & Valium also bind to receptors
Reduces anxiety
Anti-seizure
induces sleep
Endogenous Opioids (Neuropeptides and Gases)
“good feeling”
morphine and codeine
receptors bind to opiates
b-Endorphin
possibility to stop breathing
enkephalins
Nitric Oxide (Neuropeptides and Gases)
learning and development
arousal (viagra)
dilation of blood vessels
Glycine
major inhibitory NT in spinal cord and brainstem
allows Cl in
stabilizes / hyperpolarizes membrane
especially MUSCLE
Sarcomere
Smallest structural unit of muscle contraction
Most basic unit that makes up a muscle
Items between Z discs
Myosin makes up thick filament of the sarcomere
Within each muscle fiber
Densely packed subunits
Extend in parallel rows from one end of the cell to the other
Leaving no room between for other organelles
M line
The center of the sarcomere
Attached site for thick filaments
Z disk
Anchoring point of thick filaments
Anchor the thin filaments into the cytoskeleton of the cell
Marks the edge of the sarcomere
The dark lines that can be seen in the middle of the I bands
Anchors the thin filaments into the cell
Provides the boundary of the sarcomere units
H zone
Zone of thick filaments where sarcomere shortens
A band
Area where thick and thin filaments overlap
Actin and myosin make it up
DARK bands
i band
Zone of thin filaments
LIGHT bands in skeletal muscle
Actin makes it up
Titin
Protein that stabilizes thick filament to prevent overstretching and elasticity
Actin
THIN filaments
Myosin
THICK filaments
Muscle Types
Cardiac, Skeletal, Smooth
Cardiac Muscle
Involuntary control
Only muscle found in the heart
Used for heart coordinated contractions
Skeletal Muscle
Voluntary control
Attached to muscles
Used for contraction, protection, support, homeostasis
Smooth Muscle
Involuntary control
Contracts slowly and automatically
Found in hollow organs like the intestines and stomach
Myoglobin
makes meat RED
RED vs WHITE
red = slow
white = fast
Muscle Fiber Types
Type I
Type II a
Type II x
Type II b
Type I Muscle Fiber
SLOW
oxidative (must have oxygen)
RED
little fatigue
long distance running
maintaining posture / standing
Type II a Muscle Fiber
FAST
oxidative (no oxygen)
PINK
a little of myoglobin
medium fatigue
middle distance running
moderate intense
running
Type II x Muscle Fiber
FASTER
glycolytic (no oxygen)
WHITE
more fatigue
sprinting
Type II b Muscle Fiber
FASTEST
glycolytic (no oxygen)
WHITE
rapid fatigue
not in people
Muscle Fatigue factors
Conduction Failure:
Results from excess K+ in t-tubules ▶ which will inactivate Na+ Channels because the charges are off
Lactic Acid Buildup:
Affects Ca2+ pumps and myosin
Inhibition of Cross Bridge Cycling
Because of lack of ATP
Central Command Fatigue
the brain can’t send signals properly in the CNS
What do Muscle Cells require energy for?
1: Crossbridge cycle contracting filament
2: SERCA Protein (pumping Calcium back into the SR)
3: Fiber Membrane Potential (Na+ / K+ ATPase)
Energy Sources for Muscle Contraction
1: Glycogen (60 seconds)
2: ATP (1-2 seconds)
3: Phosphocreatine (5-8 seconds)
4: Oxidative Metabolism (95% of energy)
Hypertrophy
existing muscle cells increasing in diameter (size) as a result of exercise
In adults that are fully grown
Hyperplasia
new muscle cells produced (via cell division) as a developing child
Atrophy
muscle disappears or degenerates because of disuse
Sensory Receptors in muscle
Muscle Spindle Organ: length detector
Golgi Tendon Organ: tension detector
Muscle Spindle Organ
Length Detector
Composed of intrafusal fibers
Negative Feedback prevents overstretching
Golgi Tendon Organ
Tension Detector
Kill switch based on too much pressure in tendons
Located at tendons
Negative Feedback prevents over-contraction
which is too much force that the muscle isn’t capable of producing
Twitch
Twitch - single short contraction due to a single pulse of stimulation
At or above threshold
the amount of force generated by a muscle receiving a single electrical stimulation
Tetanus
Tetanus - smooth, sustained, muscle contraction
At threshold
frequency increases ▶summation occurs until tetanus is reached
Summation: A second twitch that builds from the first due to a second pulse of stimulation right after
smooth muscle contraction which occurs when sequential summation leads to sustained muscle contraction
Summation
a second twitch that builds from the first due to a second pulse of stimulation right after
Concussion
no permanent neurological damage
Contusion
tissue destruction
Hemmorrhage
bleeding into spaces which increases pressure, may not show symptoms at first
Cerebral Edema
swelling due to fluid formation, administer anti-inflammatory
CTE
deformed and brittle brain
brain functions begin to decline
mood swings
dementia
severe depression
aggression
suicidal thoughts
What are CVAs caused by?
blood clots / blocked artery
death in initial attack
Stroke
Cerebral Vascular Accident (CVA)
blood to the brain is blocked
Causes tissue to die from lack of oxygen
Ischemia
Cerebral Vascular Accident (CVA)
deprivation of blood or nutrients from any tissue
blood thinners may remedy it
Alzheimers Progressive Nervous System Disorder
brain cells waste away and die leading to loss of important brain functions
Causes:
result of AcetylCholine DEFICIT
leads to plaque BUILDUP with brain neurons
Symptoms:
memory loss
confusion
Parkinsons Progressive Nervous System Disorder
disrupts movement
Cause:
DOPAMINE deficiency leading to lack of motor function
Symptoms:
persistent tremors
lack of facial expression
Spinal Cord
extends through vertebral canal
link for transmission of info to & from brain
connected to spinal nerves
nerves carrying sensory info to brain
nerves carrying motor info to muscles
nerves carrying autonomic nerve impulses
responsible for integration of many basic reflexes
basic unlearned
acquired or conditioned (music, sports)