Bio 207 Exam 2

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123 Terms

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dendrites

receives signals and sends them to the axon hillock

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axon hillock

the action potential begins here (if there is one)

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myelin sheath

increases conduction speeds of electrical impulses & prevents ion loss

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nodes of ranvier

gaps in the myelin sheath that allows for jumping of the action potential (saltatory conduction)

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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

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Sensory Neurons AFFERENT

transmits action potentials in

TO spinal cord or brain

PERIPHERAL NERVOUS SYSTEM

-taste, smell, balance, etc.

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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

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Interneuron

short cable that connects 2 different points

CENTRAL NERVOUS SYSTEM (spinal cord or brain)

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Somatic Motor Neuron

can be controlled, VOLUNTARY

-drives skeletal muscles

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Autonomic Motor Neuron

is on autopilot, INVOLUNTARY

-reflex

-drives smooth muscle, digestion, glands, cardiac muscle

2 neurons

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Schwann Cells

cells responsible for producing myeline sheaths in the PERIPHERAL NERVOUS SYSTEM

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Oligodendrocytes

cells responsible for producing myeline sheaths around neurons in the CENTRAL NERVOUS SYSTEM

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Microglia

immune defense cells of CNS, may contribute to dementias

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Central Nervous System

  • oligodendrocytes

  • microglia

  • astrocytes

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Peripheral Nervous System

  • schwann cells

  • autonomic and somatic

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Astrocytes

holds neurons in place

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Ependymal Cells

line cavity, contributes to cerebral spinal fluid

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Protection of Central Nervous System Tissue

Bony Structures, Meninges, Cerebrospinal Fluid, Blood-brain barrier

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Bony Structures (CNS tissue Protection)

  • the cranium protects and encases the brain

  • vertebral column surrounds spinal cord

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Meninges (CNS tissue protection)

  • membranes between bones and CNS tissue

  • mater tissues (3 layers of tissue)

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Cerebrospinal Fluid (CNS tissue protection)

  • cushion against impact

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Blood-brain Barrier (CNS tissue protection)

  • highly selective

  • limits access of blood-borne materials into brain tissues

  • separates blood from brain tissue

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Diencephalon (in the brain)

  • Glands

  • Thalamus

  • Hypothalamus 

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Forebrain (in the brain)

  • cerebral hemispheres

  • right and left lobes

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Brain Stem Components

Midbrain, PONS, Medulla Oblongata

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Midbrain

  • higher level reflexes

  • startle reflexes

  • visual reflexes

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PONS

  • bridge between midbrain and medulla oblongata

  • conduction tissue

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Medulla Oblongata (brain stem)

  • blends into spinal cord

  • homeostatic mechanisms

  • respiratory and cardiovascular systems

  • vomiting, swallowing, coughing, sneezing

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Cerebellum

  • located at the back of the brain, near brainstem

  • autopilot, subconscious

  • coordinates

    • motor signals

    • visual stimulu

    • equilibrium

  • produces smooth voluntary movements?

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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)

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Phases of an Action Potential

1: Depolarization

2: Peak

3: Repolarization

4: Hyperpolarization

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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

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Peak

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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)

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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

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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

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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

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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

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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

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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+

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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

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Presynaptic Cell and Postsynaptic Cells

pre: releases NT

post: receives NT

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Synaptic Vesicles

membrane-bound spheres with neurotransmitters

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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

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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

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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

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Famous Synaptic Toxins

Tetanus: in the soil and can get into your bloodstream through a cut

  • Its target is to destroy snare proteinsno vesiclesno 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

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Epinephrine and Norepinephrine (MONOAMINE)

alpha adrenergic: a1, a2

beta-adrenergic: b1, b2, b3

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Dopamine (MONOAMINE)

Schizophrenia: excess of dopamine, can be treated with blockers

Parkinsons: deficiency of dopamine, can be treated with L-dopa

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Serotonin (MONOAMINE)

affects mood, food intake, reproductive behavior

  • tryptophan derived

  • serotonin uptake blockers treats depression, lowers appetite

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Glutamate (Amino Acid NT)

  • most common excitatory amino acid in CNS

  • cooperate in long-term potentiation (LEARNING!)

  • brain

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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

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Endogenous Opioids (Neuropeptides and Gases)

  • “good feeling”

  • morphine and codeine

  • receptors bind to opiates

  • b-Endorphin

  • possibility to stop breathing

  • enkephalins

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Nitric Oxide (Neuropeptides and Gases)

  • learning and development

  • arousal (viagra)

  • dilation of blood vessels

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Glycine

  • major inhibitory NT in spinal cord and brainstem

  • allows Cl in

    • stabilizes / hyperpolarizes membrane

  • especially MUSCLE

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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

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M line

  • The center of the sarcomere

  • Attached site for thick filaments

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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

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H zone

  • Zone of thick filaments where sarcomere shortens

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A band

  • Area where thick and thin filaments overlap

  • Actin and myosin make it up

  • DARK bands

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i band

  • Zone of thin filaments

  • LIGHT bands in skeletal muscle

  • Actin makes it up

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Titin

  • Protein that stabilizes thick filament to prevent overstretching and elasticity

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Actin

THIN filaments

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Myosin

THICK filaments

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Muscle Types

Cardiac, Skeletal, Smooth

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Cardiac Muscle

  • Involuntary control

  • Only muscle found in the heart

  • Used for heart coordinated contractions

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Skeletal Muscle

  • Voluntary control

  • Attached to muscles

  • Used for contraction, protection, support, homeostasis

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Smooth Muscle

  • Involuntary control

  • Contracts slowly and automatically

  • Found in hollow organs like the intestines and stomach

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Myoglobin

makes meat RED

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RED vs WHITE

red = slow

white = fast

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Muscle Fiber Types

  • Type I

  • Type II a

  • Type II x

  • Type II b

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Type I Muscle Fiber

  • SLOW

  • oxidative (must have oxygen)

  • RED

  • little fatigue

  • long distance running

  • maintaining posture / standing

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Type II a Muscle Fiber

  • FAST

  • oxidative (no oxygen)

  • PINK

  • a little of myoglobin

  • medium fatigue

  • middle distance running

  • moderate intense

  • running

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Type II x Muscle Fiber

  • FASTER

  • glycolytic (no oxygen)

  • WHITE

  • more fatigue

  • sprinting

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Type II b Muscle Fiber

  • FASTEST

  • glycolytic (no oxygen)

  • WHITE

  • rapid fatigue

  • not in people

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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

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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)

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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)

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Hypertrophy

existing muscle cells increasing in diameter (size) as a result of exercise

  • In adults that are fully grown

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Hyperplasia

new muscle cells produced (via cell division) as a developing child

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Atrophy

muscle disappears or degenerates because of disuse

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Sensory Receptors in muscle

Muscle Spindle Organ: length detector

Golgi Tendon Organ: tension detector

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Muscle Spindle Organ

Length Detector

  • Composed of intrafusal fibers

  • Negative Feedback prevents overstretching

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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

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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

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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

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Summation

a second twitch that builds from the first due to a second pulse of stimulation right after

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Concussion

no permanent neurological damage

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Contusion

tissue destruction

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Hemmorrhage

bleeding into spaces which increases pressure, may not show symptoms at first

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Cerebral Edema

swelling due to fluid formation, administer anti-inflammatory

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CTE

  • deformed and brittle brain

  • brain functions begin to decline

  • mood swings

  • dementia

  • severe depression

  • aggression

  • suicidal thoughts

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What are CVAs caused by?

  • blood clots / blocked artery

  • death in initial attack

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Stroke

  • Cerebral Vascular Accident (CVA)

  • blood to the brain is blocked

    • Causes tissue to die from lack of oxygen

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Ischemia

  • Cerebral Vascular Accident (CVA)

  • deprivation of blood or nutrients from any tissue

    • blood thinners may remedy it

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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

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Parkinsons Progressive Nervous System Disorder

disrupts movement

Cause:

  • DOPAMINE deficiency leading to lack of motor function

Symptoms:

  • persistent tremors

  • lack of facial expression

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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)