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207 Cards in this Set

  • Front
  • Back
types of cell in retina (front to back)
ganglion cells (form nerve fibers)
amacrine cells
bi-polar cells
horizontal cells
receptor cells (rods and cones)
rods
night vision (low light conditions)
abundant in periphery
black and white
cones
color vision
daytime vision (bright light conditions)
abundant in fovea
transduction
the conversion of physical energy to an electrochemical pattern in the neurons
resting state of receptor cells
- constant influx of Na+
- resting potential of -20 mV
- inhibitory synapse inhibits bi-polar cells from firing
types of receptor cells
rods and cones
state of events when light strikes photoreceptors
- 11-cis-retinal is transformed to all-trans-retinal
- Na+ channels close, causing hyperpolarization (-70mV)
- receptor stops firing inhibitory signals to bi-polar cells
- bi-polar cells can fire
2 types of cells with on-center off-surround receptive fields
ganglion and bipolar cells
Bipolar cells (function)
Connects photoreceptors to ganglion cells
ganglion cells
- fire action potentials in response to light
- only source of output from retina
Horizontal Cells
- Receive input from the photoreceptors and project neurites laterally to influence surrounding bipolar cells and photoreceptors
Amacrine cells
- Receive input from bipolar cells and project laterally to influence ganglion cells, bipolar cells, and other amacrine cells
ganglion and bipolar cells
similar response properties except ganglion cells fire and bipolar cells only have graded potentials (center surround receptive fields)
Center- surround receptive fields
Center (on)- spikes per second increases when stimulus hits it

Surround (off)- spikes per second increases when stimulus is removed
Ganglion cells (center surround receptive fields)
- light hits rod cell, inhibiting it
- leads to less inhibition of bipolar cell
- bipolar cell is excited and fires onto ganglion cell
- ganglion cell is excited
lateral inhibition
light hits rod (r) and rod (l), inhibiting them. horizontal cells (r and l) are inhibited. horizontal cells fire to rod (m), which cause excitation (increased inhibition onto bipolar cells). Bipolar cells are then inhibited and so are the ganglion cells
benefit of center surround receptive fields
contour and edge detection
types of ganglion cells
parvocellular and magnocellular (both have on and off receptors
parvocellular ganglion cells
smaller cell bodies, small recpetive fields, respond to details, located near fovea, input from cone cells
magnocellular
larger cell bodies and receptive fields, respond to transient and moving stimuli, spread throughout retina, input from cone and rod cells
types of cone cells
red, green, blue (detect different wavelengths)
three theories of color vision
the trichromatic (young-helmholtz) theory, the opponent process theory, the retinex theory
Trichromatic (Young-Helmholtz) theory
colors are encoded through the relative activity of three classes of cones (RGB)
Opponent Process Theory
We perceive color in terms of paired opposites (R-G, B-Y
The Retinex Theory
Color vision in terms of spatial comparison, explains color constancy
what is color deficiency caused by?
A missing subset of cones
chemosensory systems
olfactory, gustatory, vemeronasal
Flavor
a combination of input from taste and smell
taste recpetors (location)
located in taste buds, which are located on folds of skin called papillae on the tongue and throat (mostly along sides and back of tongue)
how many receptors per taste bud
50
how many taste buds per papillae
10 or more
types of papillae
Fungiform
vallate (circumvallate)
foliate
filiform
Fungiform
mushroom shaped, front half of tongue
vallate/ circumvallate
back of tongue
Foliate
like folds, sides of tongue
Filiform
fill in middle of tongue. No tastebuds on these
parts of a taste bud
capsule cells, taste pores, sensory receptor cells, basal stem cells, microvilli
Capsule cells of taste buds
outer protective layer
taste pores of taste buds
surface through which tastants enter
sensory receptor cells of taste buds
endode which tastants enter, where transduction occurs
basal stem cells of taste buds
create new receptor cells
microvilli of taste buds
increase surface area for detecting tastants where transduction occurs
taste receptor cells
specialized epithelial cells, innervated with cranial nerves
what happens if taste buds lose innervation?
they disappear but can regenerate with new innervation and stem cell differentiation
taste bud innervation
innervated by cranial nerves VII, IX, and X
facial nerve innervation
anterior tongue
glossopharyngeal nerve innervation
posterior tongue
Vagus nerve
innervates epiglottis
how many nerve fibers innervate each taste bud
approx. 50
Sensory System theories
labelled line, across fiber pattern
Labelled line Theory
each receptor responds to a limited range of stimuli with a direct line to the brain
Across- Fiber Pattern Theory
each receptor responds to a range of stimuli that contribute to the perception of each of them (context of responses)
taste qualities
sweet, salty, bitter, sour, umami

different parts of the tongue respond to all taste qualities
fiber innervation and taste quality
fibers can respond to more than one taste quality, but each responds best to one specific quality
taste fiber responses
across-fiber pattern is dominant form of response, but labelled line is a component as well because there is no cross-adaptation
Adaptation
if a receptor is exposed to a particular taste quality for an extended period of time, it will lose its sensitivity and the taste will not be as strong
cross-adaptation
if a receptor is exposed to a particular taste quality for an extended period of time, it will lose its sensitivity to other taste qualities and they will also be less strong (DOES NOT OCCUR IN HUMANS)
substances that modify taste qualities
Miracle fruit, toothpaste

caused by different transduction methods
salty taste interpretation
availability of salts, essential to life
sweet taste interpretation
substances that are safe to eat and provide energy
bitter taste interpretation
poisons (like alkaloids in plants)
sour taste interpretation
acidic substances, characteristic of spoiled foods
taste pathways
-Cranial nerves VII, IX, X
-solitary tract
-nucleus of the solitary tract (NTS) in medulla
-Discrimination pathway OR motivation and emotion pathway
Discrimination Pathway of taste
-Ventral Posterior Medial Nucleus (VPM) in thalamus
-Primary gustatory cortex (near somatosensory)
-Secondary Gustatory Cortex (insular cortex)
Motivation and Emotion Pathway of taste
Limbic System
-lateral hypothalamus
-Central Nucleus of the Amygdala
what is the taste discrimination pathway
goes through a thalamic relay nucleus before reaching cortex
what do the motivational and emotional pathways mean
involved with emotional associations
taste reflex pathway
goes to brainstem for gagging responses
olfaction (definition)
the detection of odorants (volatile chemicals) through specialized epithelium in the nose

some detection is through the trigeminal nerve (ammonia)
Components of olfactory epithelium
olfactory knobs
microvilli
mucus layer
supporting cells
bipolar neuron (receptor cells)
basal stem cell
bowmans gland
Bipolar neurons (of olfactory system)
receptor cells with cilia that contain receptor proteins for detecting odorants
basal stem cells
capable of continuously generating new neurons
supporting cells
provide nourishment for receptor cells, produce some mucus
what happens if cribiform plate breaks?
Can still recover
what happens if all neurons are removed?
it becomes difficult to find the correct targets so sense of smell never fully recovers
olfactory transduction
-odorant binding proteins carry odorants to receptors
-bind to receptors
-G protein (Golf) releases 2nd messenger
-2nd messenger causes ion channels to open
Taste transduction
different for different tastes

Uses G protein gustducin
Olfactory bulb
receptor axons synapse directly onto the olfactory bulbs
components of olfactory bulb
-glomeruli
-perglomerular cells
-mitral cells
-granual cells
function of Glomeruli
where the receptors synapse
function of peroglomerular cells
connect different glomeruli
function of mitral cells
send info out of olfactory bulb
function of granual cells
modulate processing and can be regenerated
Olfactory bulb mapping
each type of odorant receptor projects to the same glomerulus
Olfactory pathways
-olfactory receptor neurons (Cranial never I)
- olfactory bulb
-discrimination pathway OR endocrine and emotional pathway (both lead to hypothalamus)
Discrimination pathway of olfactory system
-primary olfactory cortex (ventral frontal lobe)
-Dorsal medial thalamus OR hypothalamus
-Association olfactory cortex (orbitofrontal cortex)
Endocrine and Emotional Pathway (taste)
Limbic System
-Central nucleus of the Amygdala
-Lateral Hypothalamus
What is the discrimination pathway for olfaction?
Goes directly to the primary cortex before the thalamus and then further processing in the cortex
What does the endocrine and emotional pathway mean (olfaction)?
Amygdala processes emotions
Pheromones (definition)
chemicals that are released by a member of a species which have behavioral or physiological affects on a different member of the same species
detection of pheromones
through olfactory or vomeronasal system
hypothalamus and pheromones
connections to the hypothalamus mediate endocrine effects produced by pheromone stimulation
Vomeronasal system
(found in most terrestrial vertebrates except birds and old world primates)
-specialized behaviors bring chemicals into mouth
-receptor neurons on roof of mouth
-chemicals are brought into receptors through suction
Vomeronasal system and olfactory system
-vomeronasal neurons can be generated through lifelike olfactory receptor neurons
-separate from olfactory neurons
-mediate different behaviors
Vomeronasal system higher functioning
-labelled line
-no adaptation
-no primary cortex
-no conscious perception is thought to occur
Vomernasal behaviour in rodents
-Lee-Boot effect
-Whitten Effect
-Vandenbergh Effect
-Bruce effect
Lee-Boot Effect
Groups of female rodents housed together cause the estrous (reproductive) cycles of the females to slow down and eventually stop.
Whitten Effect
Groups of non-cycling females exposed to a male odor begin to cycle again and become synchronized.
Vandenbergh Effect
Male odors accelerate the onset of puberty in female rodents.
Bruce Effect
If a pregnant female encounters a male (or his odor) that is different from her mate, she will spontaneously abort.
pathway from eye to brain
-eye
-retina
-optic nerve
-optic chiasm
-lateral geniculate Nucleus (LGN) in thalamus
-superior colliculi
-Visual cortex (V1) in occipital lobe
visual field in retina
-each eye processes both right and left visual field (backward)
-ex. right visual field is on the left side of each eye
-the left visual field is on the right side of each eye
optic chiasm
-info from right side of the left eye (LEFT VISUAL FIELD) crosses
-info from left side of right eye (RIGHT VISUAL FIELD) crosses
-"nasal nerves" cross
mapping of visual fields in cortex
-left visual field is on the right side of the brain
-right visual field is on the left side of the brain
optic radiations
neurons that lead from LGN to V1
function of LGN
-relay station towards cortex, helps process both magno and parvo info
-center surround receptive fields
structure of LGN
-6 layers (4 parvo, 2 magno)
-forms retinotopic map (2 neighboring neurons will have neighboring receptive fields)
-each neuron receives info from 1 or more ganglion cell and sends an axon to V1 (optic radiations)
magno
motion, dynamic events
parvo
details, static events
LGN oddity
-80% of afferent neurons to LGN are NOT from retina, unknown source
Structure of V1
-has 6 layers
-when stained it looks dark because layer IV is densely packed with neurons because it receives input
Layer IV of V1
-axons from LGN connect to layer IV
-info comes in
-Layer IV connects to layers II and III
Layer II and III
-send info to layer V, which sends it back
-sends info to V2
Layer V and VI
sends info to subcortical structures
Retinotopic map in V1
-Map is vastly distorted, with most of the map covering the fovea
retinotopic map and fovea
-high resolution from the fovea
-almost 1:1 correspondence between receptor cells and ganglion cells
-HUGE part of ganglions come from fovea
do we notice that we don't see periphery?
No, because we compensate by moving our eyes a lot (about 3x per sec!)
function of V1
basic visual analysis including movement and oriented contours
Receptive fields in V1
-receptive fields are elongated rectangles
-simple and complex cells
Simple receptive field
-sub-regions with on and off regions
complex cells
-anywhere in receptive field can get on or off response
simple cell functioning
-tells us what the contour is
-on and off cancel each other out
-if the bar is in a certain place and has a certain orientation the cell will not fire
-population code
population code
-functions through a large number of different types of cells
-true for almost EVERY function in the brain
Tuning curve
a graph that shows us the orientation of a contour and the fire rate of a receptive field at each orientation
Complex cell functioning
-makes up for simple cell
-can detect the bar anywhere because there are on and off cells everywhere
hypercomplex cell
-if the bar is too long, the firing rate can be reduced or even stop altogether
-explained by cell curvature
columnar organization (vision)
Columns are grouped together by function
-ex. cells within the same column respond best to a single orientation
hemianopia
type of V1 lesion

causes cortical blindness
Where/ How Pathway (Mainly magno)
V1, V2, MST/MT, PPC, Motor Cortex
MST/MT
Process depth and motion
PPC
-Posterior Parietal Cortex
-motor intent
-object localization
-spatial attention
-decision making
What pathway (mainly parvo)
V1, V2, V4, IT
IT
-Infero Temporal Complex
-object recognition
-cells respond to complex objects (faces, scenes)
-lesions lead to visual agnosia and prosopagnosia
fMRI
-functional MRI
-measures neural activity
monkey brain vs. human brain (for vision)
-humans have a much smaller visual cortex in order to make room for other functions
Illusory contours
-Occurs in V2
-V2 responds as if there is a contour even when there is not, which creates the illusion that there is
Motion selectivity
-Occurs in MT
-Cells respond to direction and speed of motion
-lesions lead to motion blindness
hemineglect
-caused by lesions to PPC
-if there is a lesion on the right side, person will neglect everything in the left visual field
Color selectivity
-V4
-cells respond to color and exhibit color constancy
depth perception, shape from shading
-occurs in V1, V4, and MT
mechanical senses
-cutaneous senses
-senses about body movement and position
cutaneous senses
-touch
-temperature
-pain
senses about body movement and position
-proprioception
-vestibular sense
general rule 1 for somatosensory system
somatosensory systems are organized somatotopically
general rule 2 for somatosensory system
primary sensory neurons are located outside the CNS (in a ganglion)
general rule 3 for somatosensory system
information from one side of the body crosses the midline to the contralateral thalamus and somatosensory cortex
sensory info from body
-travels through dorsal root ganglion neurons
sensory info from head and neck
-travels through cranial nerves
skin receptors
many types
separate into:
-touch/pressure/vibration
-temperature/pain
Corpuscles
-process vibration and pressure
-include:
-meissner's corpuscles
-pacinian corpuscles
Meissner's corpuscles
low-frequency vibrations
Pacinian corpuscles
high frequency vibrations
Merkel's disks
light pressure
transduction in skin receptors
-bend membranes which opens Na+ channels
Dorsal Column pathway
-carries info from body to brain
-also called Medial Lemniscal Pathway
Trigeminal nerve
carries information from head
spinal cord pathways
-ipsilateral for touch
-contralateral side for pain
function of dorsal column pathway
-processes fine, tactile discrimination
order of dorsal column pathway
-ascend to medulla on ipsilateral side of spinal cord
-info crosses in medulla
-synapses in ventral posterior lateral nucleus (VPL) in thalamus
-goes to primary somatosensory cortex
Somatotopic organization
-dorsal root ganglion organized by dermatome
-somatosensory map in VPL and S1
Nocioception means
pain
pain is subjective
-measured by withdrawal response
skin receptors- pain
-free nerve ending
-temperature
-pain
temperature transduction
-temperature gated ion channels (specialized for different ranges)
pain transduction
-tactile
-temperature
-chemical (capsaicin)
interaction of thermoreceptor and nociceptor
-at a maximum temperature, activity of thermoreceptor levels off, because it cannot respond any more strongly
-at this point, nociceptors start firing and their activity increases over time if the thermoreceptor is not altered
Nociceptors
2 kinds of pain
-fast pain (pinprick, cut)
-slow pain (burning)
A-delta fibers
-small, myelinated fibers
-carry fast pain
C fibers
-unmyelinated
-carry slow pain
spinothalamic pathway
-(anterolateral pathway)
-carry pain and temperature to the brain
order of spinothalamic pathway (carries pain and temperature)
-sensory neurons synapse in dorsal horn of spine
-info immediately crosses to contralateral side
-travels to many nuclei in thalamus and other locations
-goes to S1
analgesia (definition)
decreased sensitivity to pain
types of analgesia
-opoids
-stress
-mating
Opiate induced analgesia
-drugs:morphine, vicodin, heroin
-endogenous opiates: endorphins
-FUNCTION BY BLOCKING RELEASE OF SUBSTANCE P (neurotransmitter)
stress induced analgesia
-times of severe stress (war, abuse)
-2 ways:
-release of stress hormones increases level of endogenous opiates
-release of endogenous cannabinoids in CNS
mating induced analgesia
-during pregnancy and vaginal stimulation
-increased levels of estrogen and progesterone cause release of endogenous opiates
referred pain
-pain receptors are only in skin
-organs signal pain to closest dermatomes
phantom limb
-after amputation, cortex is reorganized to accommodate change, but does not occur immediately
Proprioception
-knowing where your body is in space
-(follows dorsal columnpathway w/ other somatosensory info)
-2 types of receptors
-muscle spindles
-golgi tendon organ
muscle spindle
responds to stretch
Golgi tendon organs
-respond to increases in muscle tension
-prevent contractions that are too strong
Vestibular system (functions)
-sense of balance
-head movements in all directions
location of vestibular system
-receptors in inner ear
-types of receptors
-saccule
-utricle
-semicircular canals
receptor functioning
-work by displacement of hairs
-info carried by auditory nerve
Saccule and Utricle
-sense head tilt and acceleration
-tilt or acceleration shifts otoliths, which bends hair cells
-bending hairs opens or closes K+ channels
-confusion between tilt and accerleration
Semicircular canals
-head rotation
-uses differences between the 2 sides to know which direction head is turning
-can be fooled (warm h2o, turning toward that side)
Nystagmus
-reflexive eye movement
-counteracts head turn
application of nystagmus
-check to see if vestibular system is functioning correctly
amplitude
loudness
frequency
pitch
amplitude measurement
10-90 dB
frequency measurement
number of waves/second 15-20,000 Hz
pure sound waves
sound artificial b/c speech is made of multiple frequencies
purpose of eustcian tube
adjust for air pressure
three chambers of cochlea
scala vestibuli
scala tympani
scala media
three bones of ear
hammer
anvil
stirrup
structure of cochlea
-oval window where stirrup connects to cochlea
-fluid filled
-basilar membrane is covered in specialized hair cells
-auditory nerve collects info from hair cells and leaves cochlea
function of semicircular canals
balance and orientation
function of bones of middle ear
bones mechanically amplify vibrations from tympanic membrane
method of transmission in hair cells
neurotransmitters, no axons
tectorial membrane
parallel to basilar membrane, senses movement of hair cells
trigeminal nerve
carries sensory information from head
mechanism of salty taste receptor
permit sodium ions to cross membrane
mechanism of sour taste receptor
H+ ions in, K+ ions out

detects presence of acids
mechanism of sweet receptor
-tastant binds to receptor
-causes release of gustducin
-releases 2nd messenger cAMP
-closes K+ channel
-build up of positive charge causes opening opening of Ca+ channels
-release of neurotransmitter
mechanism of bitter receptor
-2nd messenger is IP3
-causes influx of Ca+
mechanism of umami receptor
-2nd messenger cAMP
-influx of Ca+