Physiology Exam 2

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Last updated 9:27 PM on 10/8/26
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144 Terms

1
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<p>describe the different parts of a neuron</p>

describe the different parts of a neuron

A = dendrites

B = cell body

C = Axon Hillock

D = Axon

F = axon terminal

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nervous system organization

Central nervous system — brain + spinal cord (integration center)

Peripherial nervous system — crainal & spinal nerves

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define afferent neuron, efferent neuron, & interneuron

afferent = SENSORY

  • conduct impulses INTO CNS →

efferent = MOTOR (2 types)

  • conduct impulses ← OUT CNS

  • 1. somatic — voluntary / reflex

  • 2. autonomic — involuntary

interneuron = CNS neuron in between afferent & efferent

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the flow of information in a neuron

  1. sensory receptor detects something is happening

  2. sends a information up the AFFERENT neuron

  3. signal reaches CNS thru an interneuron

  4. CNS sends signal down the EFFERENT neuron

  5. reaches effector organ to carry out the movement


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what are the effects of myelination on a neuron

can send signal much faster

allows it to skip thru axon in nodes of ranvier

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different types of neurons & functions

  1. afferent

  2. efferent

    1. somatic

    2. autonomic

  3. interneurons


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different types of neuroglial cells & functions

supporting cells

  1. shwann cells — PNS & MYELINATE PNS

  2. oligodendrocytes — CNS & MYELINATE CNS

  3. astrocytes

  4. microglia — phagocytic

  5. ependymal cells — line the CNS


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difference in the PNS & CNS for neural regeneration

CNS — doesnt regenerate

PNS — can regenerate from schwann cells

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how is an AP produced

excitable tissue

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compare & contrast action potentials & graded potentials

graded: doesnt reach threshold

A.P.: able to reach threshold and continue w/ stimulus

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characteristics of graded potentials

can be either depolarizing or hyperpolarizing

never reaches threshold

decremental (decreases)

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how are action potentials conducted & characteristics of them

they reach threshold (-50 @ axon hillock)

not decremental (always the same magnitude)

all or none

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describe the refractory period

absolute: cannot make more AP

  • either when Na+ channels are open / inactivated

  • prevents overlap of signals

relative: can send another AP

  • but you need a STRONGER stimulus & to get this you need higher frequencies of AP

  • hyperpolarized, more difficult to get it to threshold


<p><strong><u>absolute</u></strong>: cannot make more AP</p><ul><li><p>either when Na+ channels are open / inactivated</p></li><li><p>prevents overlap of signals </p></li></ul><p><strong><u>relative</u></strong>: can send another AP</p><ul><li><p>but you need a STRONGER stimulus &amp; to get this you need higher frequencies of AP</p></li><li><p>hyperpolarized, more difficult to get it to threshold</p></li></ul><p></p>
14
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define depolarization

less negative (than -70)

Na+ channels opening → Na+ rushes IN

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define repolarization

returning back to RMP (-70)

Na+/K+ pumps maintain this process

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define overshoot

when the membrane potential goes above 0 mV & becomes POSITIVE

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define hyperpolarization

more negative (than -70)

Na+ channels inactivated & K+ channels activate → K+ rushes out

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permeability of K+ & Na+ during AP & how does this change affect membrane potential

depolarization = Na+ most permeable & K+ least permeable

repolarization = Na+ least permeable & K+ most permeable

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Na+ v. K+ gating channels

Na+ VOLTAGE gated channels

  • open: during depolarization

  • inactivated: during peak of AP

  • closed: at rest

K+ Voltage gated channels

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what does “all or none” principle for AP

its either at threshold or it is not

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what is saltatory conduction

when action potentials jump thru rodes of Rav.

dont happen in myleine

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electrical v. chemical synapses

Electrical synapse

  • Cells are directly connected

  • Signal passes straight from cell to cell

  • Very fast

  • Uses gap junctions

  • Electrical = direct + fast

Chemical synapse

  • Cells are NOT directly connected

  • One cell releases a neurotransmitter

  • Neurotransmitter crosses the small gap to the next cell

  • Slower than electrical


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what does propagation mean

moving down the axon

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what is the sequence of events in neural communication across a synapse

  1. Action potential reaches terminal end of the presynaptic neuron

  2. triggers Ca2+ to rush IN thru Ca2+ voltage gated channels

  3. Ca2+ triggers neurotransmitters to get exocytosed out synaptic vesicles

  4. neurotransmitters bind to ligand gated channels on the POSTsynaptic neuron

  5. induces synaptic potential & causes Na+ to rush in

    1. can cause the next neuron to send or inhibit AP


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excitatory v. inhibitory postsynaptic potentials

EPSP — less negative / depolarize (Na+ rushes IN)

  • can be strong enough to reach threshold & AP forms on postsynaptic cell

IPSP — more negative / hyperpolarizes (Cl- rushses IN)

  • more difficult to send AP and reach threshold

  • GABA opens ligand gated channels


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differentiate: temporal v. spatial summation

WILL ALWAYS BE EXCITATORY

temporal: if 1 presynaptic input sends multiple outputs to reaches threshold

spatial: if +2 send a signal at SAME TIME, they get added together to reach threshold

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what is a ligand gated channel

where neurotransmitter binds to

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compare: actions of an excitatory neurotransmitter & an inhibitory neurotransmitter on the POST synaptic neuron

mechanically gated channel:

excitatory — opens Na+ channels & rushes in → depolarize & can reach AP

inhibitatory — opens Cl- channgels & rushes in → hyperpolarize & cannot reach AP

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action of acetylcholinesterase

breaks down acetyl choline & found in synaptic cleft

contains neurotransmitter reuptake receptor

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how do G protein coupled signal pathways produce synaptic potentials

polar molecule binds to receptor

G proteins released

G protein binds to channel

opens channel

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describe protection of the CNS

bone is the thickest layer & outermost layer

meninges: 3 layers

  • dura mater by bone = solid matter

  • arachnoid matter = middle

    • subarachnoid space

  • pia mater = directly on the brain


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what is the function of cerebral spinal fluid (CSF)

buoyancy

protection

maintenance of chemical environment

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what produces CSF

epidenmal cells

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what connects the right & left hemisphere

corpus callosum

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what are the 5 lobes of the cerebral cortex

what are the function of all of them

  1. occipital — VISUAL

    1. perception and interpretation of visual images

  2. temporal — AUDITORY

    1. perception & interpretation of auditory info

  3. parietal — SENSORY

    1. somatosensory — receives info

    2. perception of senses

  4. frontal — MOTOR

    1. voluntary movements

    2. executive reasonings

  5. insula — VISCERAL RESPONSES

    1. deepest layer / on inside


<ol><li><p>occipital — <strong><u>VISUAL</u></strong></p><ol><li><p>perception and interpretation of visual images </p></li></ol></li><li><p>temporal — <strong><u>AUDITORY</u></strong> </p><ol><li><p>perception &amp; interpretation of auditory info</p></li></ol></li><li><p>parietal — <strong><u>SENSORY</u></strong></p><ol><li><p>somatosensory — receives info</p></li><li><p>perception of senses</p></li></ol></li><li><p>frontal — <strong><u>MOTOR</u></strong> </p><ol><li><p>voluntary movements </p></li><li><p>executive reasonings</p></li></ol></li><li><p>insula — <strong><u>VISCERAL RESPONSES</u></strong></p><ol><li><p>deepest layer / on inside </p></li></ol></li></ol><p></p>
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what divides the frontal and parietal lobe

precentral gryus — frontal

postcentral gryus — parietal

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functions of the right hemisphere v. functions of the left hemisphere

which one is dominant

Right — depth perception (visuospatial) & patterns/reading maps

Left — language & analytical ability

  • THE MOST DOMINANT


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what is the difference between broca’s area v. wernicke’s area

brocas area: frontal lobe

  • fine motor functions involved in speech

wenickes area: in between pariteal/occipital/temporal region

  • hearing & understanding language

  • formulating words


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what is aphasia?

  • broca’s aphasia

  • wernicke’s aphasia


aphasia: a brain-related language disorder that makes it hard to speak/understand speech/read/write

  • Broccas Aphasia: cannot talk/difficult responding BUT can understand what is spoken

  • Wernickes Aphasia: cannot understand spoken/written language BUT can speak using made up words


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what are the different types of memory

Memory:

  1. short term: <30 sec

  2. long term: >30 sec

    1. non-decalarative: memory of simple skills (ex: tying shoes)

    2. declarative: memory of facts & events (ex: where were you…?)


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what are the different types of memory consolidation

temporal lobes (amygdala & hippocampus) involved in converting short term → long term

  • sleep is needed for this

STRESS IMPAIRS THIS

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locations & functions of the thalamus & hypothalamus

location: diencephalon

functions:

  • body temp

  • thirst & urine

  • food intake

  • pituitary hormone

  • circadian rhythm

  • control ANS


43
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what are the structures & functions of the midbrain

motor movements of the eye

auditory processing

44
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what are the 2 proteins that impact alzheimers disease

  1. beta amyoild plaques

  2. tau

these both inhibit & alter movement of ions

45
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what are the structures & functions of the brainstem

critical link between between spinal cord & higher brain regions

vegetative funcitons = involuntary functions that keep you alive

made up of:

  1. midbrain (top) — eye movement

  2. pons — relay information station

  3. medulla (bottom) — basal survival functions (breathing, heartbeat, dilation of blood)


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function of the cerebellum?

planning, initiating, & timing motor movements

learning skilled motor tasks

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ataxia

damage to cerebellum

UNCOORDINATED MOVEMENT

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function of the limbic system

hippocampus + amygdala

  • emotions

  • aggression

  • fear

  • smell

  • goal directed behavior


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what are the structures & functions of the reticular activating system

Structure: midbrain, pons, medulla

Fire to keep you awake & brain awake

  • inhibited: brain isnt awake


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phases of sleep?

REM — rapid eye movement // eyes moving very fast

  • brain is buidling memories

Stages:

  1. go into sleep

  2. longer & deeper stage & body temp drops

  3. GOLDEN STAGE = want to be here& body is repairing

  4. cycling back to REM


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what is the difference between: ascending v. descending tracts of the spinal cord

ascending: dorsal root

  • carry sensory information UP to brain (afferent)

ascending: ventral root

  • carry motor information DOWN to effector (efferent)


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structures of the spinal nerve v. neural pathways of the reflex arc

PNS

all are mixed nerves: sensory & motor

  • dorsal root = sensory (afferent pathway)

  • ventral root = motor (efferent pathway)

Pathway:

  1. stimulus is detected thru receptor neuron →

  2. receptor sends singal thru dorsal root

  3. signal enters intregating center (interneuron)

  4. response gets sent thru ventral root

  5. signal gets to effector & a response happens


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what are the components of the withdrawal reflex

nociceptor detects pain

AP goest thru afferent pathway

hits integration center

AP sent by integration center thru efferent pathway

stimulates motor control

  • stimulate flexors

  • inhibits extensors


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classification of cranial nerves

part of the PNS

12 pairs

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what are the divisions of the efferent division of the PNS

  1. somatic nervous system — voluntary

    1. pre&postsynaptic

  2. autonomic nervous system — involuntary

    1. pre&postganglionic


56
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organization of the AUTOnomic motor neurons

both are on, but which one is innervating MORE

sympathetic: stress

parasympathetic: rest

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what is the structure of the sympathetic nervous system

  • ganglia

  • preganglionic v. post ganglionic

  • pathway


thoracolumbar region

SHORT pre & LONG post

preganglionic release acetyl choline & bind to nicotinic receptors on post

Postganglionic release norepinenorepinephrinephrine into adrenergic receptors on effector

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what is the relationship between the sympathetic nervous system & adrenal medulla

modified part of the sympathetic system

preganglionic fibers secrete hormones into BLOOD

  • more epinephrine > compared to norepinephrine


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structure & innervation pathways of the parasympathetic division of the ANS

craniosacral region

LONG pre & SHORT post

preganglionic release acetyl choline & bind to nicotinic receptors on post

Postganglionic release acetyle choline into muscarinic receptors on effector

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cholinergic receptors v. adrenergic receptors

cholinergic receptors = nicotinic & muscrainic

  • parasympathetic

adrenergic receptors = nicotinic & adrenergic

  • sympathetic


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what are the effects of adrenergic stimulation on different organs & what are the different types of receptors involved

Alpha & beta receptors on SYMPATHETIC

  • release NE & epinephrine


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how does albuterol work in ANS

b2 agonist = BETA = sympathetic

inhaling N.E.

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how does atropine work in ANS

blocks muscrainic receptors = parasympathetic

dilate pupils

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how does beta-blockers work in ANS

block beta-adrenergic receptors

  • sympathetic


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antagonistic & cooperative actions of the sympathetic & parasympathetic divisions of the ANS

parasympathetic & sympathetic work in OPPOSITION = ANTAGONISTIC

  • EX: parasympathetic = increase heart rate & sympathetic = decrease heart rate


cooperative effects: saliva & urination

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what innervates an organ without dual innervation

ONLY SYMPATHETIC (increase or decrease)

EX: sweat glands

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explain the term sensory transduction

converting a stimulus into an electrical signal (AP) so the brain can understand it

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phasic v. tonic receptors

tonic: CNS is continually getting info

  • dont adapt

  • or adapt slowly

  • you know & understand the stimulus is there


phasic: you forget the stimulus is there once applied, but remember its there when its gone

  • constantly adapt

  • touch receptors in the skin


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describe the nature & significance of the receptor potential

electrical change that happens in a sensory receptor when it senses a stimulus

can lead to an AP

influx of Na+ can produce receptor potentials

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differentiate between sensation v. perception

sensation: collection of info (RECEPTORS)

perception: interpretation of what is sensed (where AP are sent)

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4 steps of perception

  1. stimulus

  2. transduction: converting stimulus → AP

  3. conduction: axons; conducting AP/electrical signals

  4. perception: integrating center


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define sensory acuity & explain factors that affect acuity

sensory: ability to tell two things apart when touching you

high: able to tell very specifics

low: able to tell general area

affect:

  • field size

  • # of receptors

  • area of somatosensory


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what are the different types of sensory receptors

  • photoreceptors - light

  • mechanoreceptors - mechanical energy

  • thermoreceptors - temp regulation

  • osmoreceptors - osmolarity

  • chemoreceptors - specific chemicals

  • nociceptors - pain

  • proprioceptors - position of your body

  • externoreceptors - outside your body

  • interoreceptors - inside your body


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what are cutaneous sensations

temp, touch, pressure, pain

contralateral - terminates here

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what are the modalities of taste

chemoreceptors detect taste — housed in taste buds

tastant: taste chemical that dissolves thru salvia

  1. salty — caused by chemical salts (NaCl)

  2. sour — caused by acids

  3. sweet — caused by glucose

  4. bitter — caused by chemically diverse group of tastants

  5. umami — savory taste


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how is taste produce + conveyed in the brain

produce: binding of tastant w/ receptor cell & produces receptor potential

brain: insula detects gustatory & somatosensory cortex moves tongue

<p>produce: binding of tastant w/ receptor cell &amp; produces receptor potential </p><p>brain: insula detects gustatory &amp; somatosensory cortex moves tongue </p>
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how do odorant molecules stimulate their receptors (polarity?) & how the information is conveyed to the brain

odorants — chemcial molecules that can be smelled

  • POLAR = water soluble solvents that dissolve into mucus layer & stimulate the olfactory bulb by binding to MEMBRANE bound receptors

smell reaches the limbic system & thats how you form memories w/ smells

<p>odorants — chemcial molecules that can be smelled </p><ul><li><p>POLAR = water soluble solvents that dissolve into mucus layer &amp; stimulate the olfactory bulb by binding to MEMBRANE bound receptors </p></li></ul><p>smell reaches the limbic system &amp; thats how you form memories w/ smells </p>
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describe hertz

number of cycles / second

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what are the structures of the vestibular apparatus & how do they function to produce a sense of:

  • balance

  • equilibrium

  • position of the head


  1. semicircular canals - ROTATIONAL MOVEMENT

    1. anterior canals: head moves forward / back (nodding)

    2. posterior canals: head is tilting left / right

    3. lateral canals: spinning

  2. otolithic organs - LINEAR MOVEMENT

    1. utricle: left & right

    2. saccule: up & down


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what are the semicircular canals

bending of hair cells embedded in cupula = KINOCILIUM

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what are the otolithic organs

utricle - horizontal (moving forward/backward) or left/right

saccule - vertical (up/down)

contain otoliths - crystals found in gelatinous substance that provides mass & helps move against gravity

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neural pathways of the vestibular system

input: goes to vestibular nuceli in brain

cerebellum helps w/ balance

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how do sound waves result in movements of the oval window & the basilar membrane

sound wave travels thru → hits the tympanic membrane → malleus → incus → stapes → hits oval window → oval window causes perilymph fluid to move in cochlea → fluid causes basilar membrane to deflect → the hairs on the basilar membrane move → sends AP

<p>sound wave travels thru → hits the tympanic membrane → malleus → incus → stapes → hits oval window → oval window causes perilymph fluid to move in cochlea → fluid causes basilar membrane to deflect → the hairs on the basilar membrane move → sends AP </p>
84
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low pitch v. high pitch

  • higher frequency (#) = higher pitch

  • lower frequency (#) = lower pitch


<ul><li><p>higher frequency (#) = higher pitch</p></li><li><p>lower frequency (#) = lower pitch </p></li></ul><p></p>
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soft sound v. loud sound

  • soft sound = smaller amplitude (height)

  • louder sound = larger amplitude (height)


<ul><li><p>soft sound = smaller amplitude (height)</p></li><li><p>louder sound = larger amplitude (height)</p></li></ul><p></p>
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how are loudness & pitch discrimminated

pitch:

  • low = distal (further) = helicotrema

  • high = against oval window (closer)


loudness

  • soft = hairs bent softer & closer

  • louder = hairs bent harder & further away = helicotrema


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what are the structures of the eye

sclera - white portion of eye

cornea

iris - colored portion

pupil - black

vitreous humor - makes the shape & inside cell

aqueous humor - carries nutrients for cornea & lens

retina - rods & cones

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how do the structures of the eye focus light onto the retina

  1. cornea - where light first enters thru and bends

  2. iris - controls the amount of light entering eye by changing pupil size

    1. circular muscle

    2. radial muscle

  3. pupil - light passes thru here; doesnt move,, hte iris around it moves & adjusts the size

  4. lens - changes shape helps to refract light on retina

    1. flattens - near

    2. rounder - far

  5. retina - rods and cones


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what is refraction

bending of light as it moves thru areas

cornea does this

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what is accomodation

changing shape of lens for near/far away items

how to direct the bent light into eye

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how is accommodation at different distances accomplished?

is this parasympathetic, sympathetic, or dual innervation?

REFRACTION OF LIGHT THRU ACCOMMODATION

near items: lens becomes rounder → parasympathetic INCREASES

  • ciliary muscles contract

  • suspensory ligaments slacken

far away items: lens becomes flatter → parasympathetic DECREASES

  • ciliary muscles relax

  • suspensory ligaments get pulled


<p>REFRACTION OF LIGHT THRU ACCOMMODATION</p><p>near items: lens becomes rounder <strong><u>→ parasympathetic <mark data-color="#2fff00" style="background-color: rgb(47, 255, 0); color: inherit;">INCREASES</mark></u></strong></p><ul><li><p>ciliary muscles contract </p></li><li><p>suspensory ligaments slacken</p></li></ul><p>far away items: lens becomes flatter <strong><u>→ parasympathetic <mark data-color="#f60b0b" style="background-color: rgb(246, 11, 11); color: inherit;">DECREASES</mark></u></strong></p><ul><li><p>ciliary muscles relax</p></li><li><p>suspensory ligaments get pulled</p></li></ul><p></p>
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how does the iris innervate & change

HOW MUCH LIGHT ENTERS

contains 2 muscles

  • circular muscle: CONSTRICT via parasympathetic nervous system

    • INNERMOST AREA

    • becomes smaller in bright light

  • radial muscle: DILATES via sympathetic nervous system

    • OUTERMOST AREA

    • becomes larger in dim light


<p>HOW MUCH LIGHT ENTERS </p><p>contains 2 muscles </p><ul><li><p>circular muscle: CONSTRICT via parasympathetic nervous system </p><ul><li><p>INNERMOST AREA</p></li><li><p><strong><u>becomes smaller in bright light</u></strong></p></li></ul></li><li><p>radial muscle: DILATES via sympathetic nervous system</p><ul><li><p>OUTERMOST AREA</p></li><li><p><strong><u>becomes larger in dim light </u></strong></p></li></ul></li></ul><p></p>
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common disorders of:

  • refraction

  • glaucoma

  • cataracts


cataracts: opacity of lens

glaucoma: increased pressure of built up aqueous humor in eye, causes damage to optic nerve

refraction:

  • myopia: nearsighted

    • unable to see far things

    • lens is too long, you need concave lens

  • hyeropia: farsighted

    • unable to see close up things

    • lens is too short, you need convex lens

  • presbyopia: stiffness of lens as you age

    • decrease in accomodation


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what are the 3 layers of the retina

  1. outermost layer = RODS & CONES

  2. middle layer = bipolar cells

  3. inner layer = ganglion cells


<ol><li><p>outermost layer = RODS &amp; CONES</p></li><li><p>middle layer = bipolar cells</p></li><li><p>inner layer = ganglion cells </p></li></ol><p></p>
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how does light affect rods & cones

outer segment detects light, inner segment = mitochondria, & synaptic terminal is where they release neurotransmitter

  • rods = night/gray colors

  • cones = day/color


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describe dark & light adapatation

DARK:

  • AT PHOTORECEPTOR:

    • Na+ channels open

    • release neurotransmitter = GABA

  • GABA inhibits bipolar cell

  • No EPSP

  • No AP sent = cannot view anything in dark


LIGHT:

  • AT PHOTORECEPTOR

    • light closes Na+ channels

    • membrane becomes hyperpolarized & doesnt allow GABA to be sent

  • because GABA isnt sent, bipolar & ganglion cells can send messages

  • become EPSP →

  • there is AP in visual cortex & you are able to see light


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compare the functions of rods & cones

(photopigments)

similarities:

  • consists of 2 components — opsin & retinal

    • opsin = protein that retinal binds to

    • retinal = absorbs light

      • cis or trans


Differences:

  • 4 different types of photopigments

    • rods (1) = rhodopsin

      • absorbs all visible wavelengths

      • gray colors

    • cone (3) = red, green, blue


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rods v. cones:

  • which has higher sensitivity & lower sensitivity

  • which has higher acuity & lower acuity


Rods: higher sensitivity because it has more receptors & low acuity

  • receptors CONVERGE into 1 pathway

  • larger number of receptors but they all converge

Cones: higher acuity because each cone has their own receptor / does not converge & low sensitivity

  • no convergence happening

  • receptors are their own individual one

  • smaller # of receptors


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what is the importance of the fovea centralis

contains rods and cones

vision is best at fovea centralis

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how is color perceived

depends on the amount of cones you have

  • red is the longest wavelength

  • green is middle

  • blue is shortest wavelength

the color you see is the light that is being reflected