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111 Cards in this Set

  • Front
  • Back
Visual System
One of the most important special senses in human and other mammals

In addition to audition, vision is needed for human communication

Detects and interprets photic stimuli

Visible light
photic stimuli are electromagnetic waves between 400 and 750 nM long
Layers of eye
Sclera

Cornea

Choroid

Retina
Sclera
avascular (light impeded), dense, white, opaque protective coat covers 85%
Cornea (Layer)
avascular (light impeded), covers 15%, lined by a thin tear film
Choroid
vascular
Retina
1. neuronal layer

2. outer pigmented layer - absorb light
Cornea (Transparent)

Aqueous Humor (Transparent)
Has refractive power - (change in direction or bending of light rays)

AH- has refractive power as well
Vitreous Homor (Transparent)
90% volume of eye
structural support
shock absorber
Last transparent part of eye
Retina
Cornea - general info
Is the clear tissue at the front of the eye

Protective barrier

Serves as the main refractive element of the visual system, directing incoming light through the lens for precise focusing on the retina.

Refractive power is measured in diopters

2/3 of the 59 diopters of refractive power of the eye - ability to bend light

A normal cornea is round, with even curves from side to side and top to bottom.
Lens
focus incoming images into the retina
1/3 refractive power
avascular
transparent elastic
convex anterior and posterior sides
Accommodation
The ability increase the lens refractive power

Zonules are radial ligaments that connects the lens to the ciliary body

contraction of the muscles in the ciliary body
Contraction of the muscles in the ciliary body
relaxes the lens ligaments

lens become spherical, convex and thicker

lens refractive power increases

shape for near vision

contraction controlled by parasympathetic nerve signals - gives ability to bend light more
Presbyopia
Loss in power of accommodation

Eye remains focused on distant objects

Wears bifocal glasses
Upper segment for far-seeing
Lower segment for near-seeing (reading)
Lacrimal system:
lacrimal gland - produces tears

puncta and tear sac - collects tears

nasolacrimal duct - empties tears into the nasal cavity

Disorder: dry eyes
Tears - composition
98% H2O,
1.5% NaCl
potassium
albumin
glucose
lysozymes
immunoglobulin
Tears - function
wet and protect cornea and conjunctiva
cleans and provides nutrients to cornea
protects against infection
Conjunctiva
A thin layer of mucous membrane that lines the outer surface of eye and the anterior surface of the eyelids.

Disorders: conjunctivitis (inflammation of the conjunctiva)

bacteria, virus, chlamydia, allergens
Aqueous humor
Fluid
Produced by ciliary process epithelium
Na,K-ATPase
ion carriers
co-transporters

Plasma
Provides nutrients to lens and cornea
(glucose) b/c avascular
Na,K-ATPase Function
Na,K-ATPase
localized in the plasma membrane of the cell.

See pg 8
What regulates Na, K-ATPase?
Acetylcholine and NO

See pg 8
Aqueous humor outflow
Trabecular meshwork
Schlemn’s canal (under trabecular meshwork)
Cellular mechanisms of Aqueous humor Regulation
Agents that decrease cell volume increase the rate of aqueous humor outflow:
-Nitric oxide & cGMP

Agents that disrupt the actin cytoskeleton increases aqueous humor outflow.
-Ouabain
If trabecular meshwork is clogged
Build up of pressure

The spaces in meshwork get smaller as pressure increases
Intraocular pressure
Rates of secretion of aqueous humor
Rates of outflow of aqueous humor

Improper regulation of IOP is a risk factor for glaucoma
Receptor and Neuronal Function of the Retina
Light captured by rods and cones and sent to horizontal cells. Then synapse with rods and cones or bipolar cells that synapse with rods and cones. Biploar cells synapse with amacrine and ganglion cells. Axons of ganglion cells from optic nerve that take signal from eye to brain.
Neuronal Retina
central to the visual process

light absorbed by photoreceptors
rods – black/white
cones - color

converted to electrical signal in a process called phototransduction.
CONES
Light sensitive portion of cone – cone pigment

High density of cones in the fovea (located in the macula lutea)

Detect color vision

Three types of cones
respond to the blue, green and red portions of the visible electromagnetic spectrum
RODS
A visual pigment called rhodopsin traps light retinal (vitamin A-derived pigment) and opsin

Rhodopsin
Is a membrane protein
Rhodopsin
Contains a chromophore called 11-cis retinal which is covalently bound to opsin

Photon capture converts 11-cis-retinal to all-trans retinal

Opsin is activated
Metarhodopsin II – activated rhodopsin
Metarhodopsin II
Relays activating changes to the G protein, transducin

GTP binds to transducin α subunit

Activates phosphodiesterase (PDE)

PDE degrades cGMP to GMP

The decrease in cGMP concentration leads to closure of cyclic-nucleotide-gated (CNG) channels
Effects of Metarhodopsin II
resulting in two effects:
a decrease in Ca2+ influx
hyperpolarization of the membrane potential

Lowered [Ca2+]i concentration disinhibits guanylate-cyclase-activating protein (GCAP), leading to activation of guanylate cyclase (GC) and resynthesis of cGMP.


Light that is not absorbed by rhodopsin is absorbed by retinal pigment melanin (keeps light from scattering)
Optic Nerve
Primary Visual Center of Brain

axons of the retinal ganglion cells form the optic nerve
Visual Cortex
located in the occipital lobe neuronal circuitry provides for visual sensation and perception
Re-formation of Rhodopsin
all-trans retinal revert to 11-cis form conversion catalyzed by retinal isomerase

Vitamin A in cytoplasm of rods and pigment of retinal

Reduced sensitivity to light – deficiency in vitamin A
Re-formation of Rhodopsin
(cont)

rod vision, light adaptation, dark adaptation
Rod vision adapted for night and low-level illumination

Light adaptation - decreased sensitivity to light
bright light causes concentrations of photosensitive chemicals in rods and cones to be reduced
sensitivity of eye to light also reduced

Dark adaptation increase in light sensitive pigments
remains in darkness retinal and opsin combine also vitamin A is converted into retinal
Errors of Refraction
The refractive process is similar to the way a camera takes a picture.
The cornea and lens in your eye act as the camera lens.
The retina is similar to the film. If the image is not focused properly, the film (or retina) receives a blurry image
Hyperopia
(farsightedness )
decreased refractive power
eyeball too short
distant objects are clear, and close-up objects appear blurry
images focus on a point beyond the retina
corrected with convex lens
Myopia
(nearsightedness)
refractive surfaces have too much refractive power
the eye is too long
faraway objects appear blurry because they are focused in front of the retina
affects over 25 percent of all adult Americans.
corrected with concave lens
Astigmatism
uneven curvature of the cornea
blurs and distorts both distant and near objects.
the cornea is shaped more like the back of a spoon, curved more in one direction than in another.
light rays to have more than one focal point and focus on two separate areas of the retina, distorting the visual image.
Two-thirds of Americans with myopia also have astigmatism.
Refractive errors
are usually corrected by eyeglasses or contact lenses.
refractive surgeries are becoming an increasingly popular option.
Cataracts
lens opacity (does not allow the transmission of light)

most common cause of visual loss
treated with lens replacement (surgery)
RETINAL DEFECTS
Color blindness – confuse or mismatch colors

Retinitis Pigmentosa - degeneration of the retinal photoreceptors

Diabetic Retinopathy – 3rd cause of blindness involves thickening of the retinal capillary walls, hemorrhages, formation of fragile blood vessels

Treatment - Scatter laser treatment helps to shrink the abnormal blood vessels
Age-related macular degeneration (AMD)
is a disease associated with aging that gradually destroys sharp, central vision.
Wet AMD
abnormal blood vessels behind the retina start to grow under the macula.
blood raise the macula from its normal place at the back of the eye

early symptom of wet AMD is that straight lines appear wavy.
Dry AMD
light-sensitive cells in the macula slowly break down

blurred central vision
blurred spot in the center of your vision.

Treatment include:
argon laser photocoagulation of extrafoveal choroidal neovascularisation (CNV) and photodynamic therapy of selected sub-foveal CNV
Understanding IOP regulation
is important in identifying potential treatments for individuals with high IOP and glaucoma
Glaucoma
Optic neuropathy

characterized by:
optic disk cupping (increasing in size and depth) as result of
axonal loss
visual field loss - area in which objects can be seen while the eye is focused on a central point.
Hearing
EARS:

The external ear, the middle ear, and the cochlea of the inner ear are concerned with hearing.

The receptors for hearing are hair cells in the cochlea.

Level of sound is measured in decibels sound pressure level or dB SPL
Structures of the Ear
See pg 2
Outer ear
Auricle –
corrugated surface acts as a reflector that collects sounds from different directions and frequency
captures the mechanical energy (sound)
focus mechanical energy

External Auditory Meatus
transmits the mechanical energy to the tympanic membrane (eardrum)
Structures in the middle ear
See pg 3
Middle ear
The middle ear is an air-filled cavity in the temporal bone
The auditory (eustachian) tube connects the middle ear to the nasopharynx
The three auditory ossicles, the malleus, incus, and stapes, are located in the middle ear .
The malleus
manubrium, (handle of the malleus)
head
short process
The incus interacts with the head of the stapes.
The stapes (foot plate )is attached to the walls of the oval window.
The inner ear: tubes of the cochlea
See pg 4
Cochlea
The cochlear portion is a coiled tube
Throughout its length, the basilar membrane and Reissner's membrane divide the cochlea into three chambers or scalae:
**scala vestibuli
scala media
**scala tympani
**contain perilymph and communicate with each other at the apex of the cochlea through a small opening called the helicotrema
Cochlea cont
The scala vestibuli ends at the oval window
The scala tympani ends at the round window
The scala media contain endolymph
Basilar membrane
Fibrous membrane
Length of the fibers increase progressively from the oval window to the helicotrema
Diameter of the fibers decrease progressively from oval window to the helicotrema
High-frequency resonance occur near the oval window
Low-frequency resonance occur at the helicotrema
Organ of Corti
See pg 5
Organ of Corti cont
Located on the basilar membrane
contains the hair cells, which are the auditory receptors.
outer hair cells
inner hair cells
Tectorial membrane cover the rows of hair cells
Organ of Corti cont
The axons of the afferent neurons that innervate the hair cells form the auditory (cochlear) division of the eighth cranial nerve.
The processes of the hair cells are bathed in endolymph
Basilar membrane is relatively permeable to perilymph in the scala tympani and the bases of the hair cells are bathed in perilymph.
Function of the external ear
The external ear funnels sound waves to the external auditory meatus .
The external auditory meatus funnels sound waves to the tympanic membrane (eardrum).
Function of the middle ear
Air filled cavity
The tympanic membrane receives sound from the external auditory meatus
The tympanic membrane transmits sounds to the ossicles; malleus, incus and stapes
Ossicles conducts sounds to the cochlea
Function of the inner ear
Fluid filled cavity
Converts mechanical sound into electrical signals
Hair cells located in organ of Corti generates nerve impulses in response to vibration
Sound waves
A is the record of a pure tone.

B has a greater amplitude = louder

C greater frequency = higher
pitch

D is a complex wave that is
regularly repeated= musical sound

E have no regular pattern=
noise
Sound
Sound is produced when vibrations of the molecules in the external environment strike the tympanic membrane.

Level of sound is measured in decibels sound pressure level or dB SPL.

The waves travel through air at a speed of approximately 344 m/s (770 mph) at 20 °C at sea level (1450 m/s at 20 °C in fresh water and is even greater in salt water).

The loudness of a sound is correlated with the amplitude of a sound wave.
Sound (cont)
The pitch of a sound is correlated with the frequency (number of waves per unit of time).
Sound waves that have repeating patterns are perceived as musical sounds
Harmonic vibrations (overtones) that give the sound its characteristic timbre (quality).
Aperiodic nonrepeating vibrations cause a sensation of noise
Tympanic Reflex
Loud sounds initiate a reflex contraction called tympanic reflex.
Contraction of the tensor tympani and stapedius decreases sound transmission.
Its function is protective, preventing strong sound waves from causing excessive stimulation of the auditory receptors.
Sound Transmission
Sound waves produce pressure changes on the external surface of the tympanic membrane

In response to the pressure changes the tympanic membrane moves in and out.

The motions of the tympanic membrane are imparted to the malleus.

The malleus moves and transmits the vibrations to the incus.
Sound Transmission (cont)
The incus moves and transmits vibrations to the stapes. Movements of the stapes vibrates along the oval window against the fluid in the scala vestibuli.

The basilar and tympani membranes move in the same direction, so a shearing motion bends the hairs. The hairs of the inner hair cells are not attached to the tectorial membrane, but they are apparently bent by fluid moving between the tectorial membrane and the underlying hair cells.
Sound Transmission (cont)
The inner hair cells are the primary sensory cells that generate action potentials in the auditory nerves.

The outer hair cells increase the amplitude and clarity of sounds.

Prestin is a membrane protein (the motor protein of outer hair cells)
Sound Transmission (cont)
Cochlea transduces sound energy into electrical signals and sends them to the brain
Hearing begins:
The hair cells in the organ of Corti generate changes in membrane potential proportional to the direction and distance the hair moves.
Electrical signals are sent via the nerve fibers
Uncoiled cochlea and flow of stimulus energy
See Pg
Frequency resonance of basilar membrane
See Pg
Central Pathway
Nerve fibers from the spiral ganglion of Corti enter the cochlear nuclei and synapse
Second-order neurons pass to the opposite side of the brain stem
From there, auditory impulses pass by various routes to the:
inferior colliculi
medial geniculate body
auditory cortex.
The primary auditory cortex is Brodmann's area 41.
Auditory cortex (AC)
Discriminate different sound pitches and patterns of sound (AC)
Detect direction of sound (AC)
Meaning of sound (AAC)
Deafness
Conductive (conduction) deafness
impaired sound transmission in the external or middle ear
impacts all sound frequencies.
causes of conduction deafness
are plugging of the external auditory canals with wax (cerumen) or foreign bodies,

otitis externa (inflammation of the outer ear, "swimmer's ear")

otitis media (inflammation of the middle ear) causing fluid accumulation ( in the inner ear)
Sensorineural deafness
is most commonly the result of loss of cochlear hair cells
problems with the cochlear nerve or within central auditory pathways.

It often impairs the ability to hear certain pitches while others are unaffected.
Causes of Sensorineural deafness
Aminoglycoside antibiotics such as streptomycin and gentamicin obstruct the mechanosensitive channels in the hair cells and can cause the cells to degenerate

Damage to the outer hair cells by prolonged exposure to noise

Tumors of the eighth cranial nerve

Audiometer-used to determine hearing disabilities
Olfactory epithelium
Receptor cells for smell sensation are olfactory cells

Olfactory sensory neurons are embedded within the olfactory epithelium

These neurons project axons to the olfactory bulb of the brain.
Cell types in olfactory epithelium
There are three cell types:

olfactory sensory neurons

supporting cells (sustentacular)
Secretes mucus
that bathes the odorant receptors on the cilia and
provides the appropriate molecular and ionic environment for odor detection.

basal stem cells
Produce new olfactory sensory neurons
Olfactory sensory neuron: dendrite
Dendrite
projects into the nasal cavity
terminates in a knob containing 10 to 20 cilia
Odorants bind to specific odorant receptors on the cilia
initiate a cascade of events
leading to generation of action potentials in the sensory axon.
Olfactory sensory neuron: axon
A single axon projects from each neuron to the olfactory bulb.

The axons of the olfactory sensory neurons pass through the cribriform plate and enter the olfactory bulbs.
Odorant receptor
See Pg
Signaling mechanism
See Pg
Odorant receptors
The olfactory system mediates discrimination of more than 10,000 different odors.

The genes code for about 1000 different types of odorant receptors

All the odorant receptors are coupled to heterotrimeric G proteins.

Odorant molecule binds to its receptor
Odorant receptors (cont)
The G protein subunits (a, b, g ) dissociate.

The a-subunit activates adenylate cyclase to catalyze the production of cAMP,

Open cation channels - causing an inward-directed Ca2+ current.

This produces the graded receptor potential, which then leads to an action potential in the olfactory nerve.
Basic neural circuits in the olfactory bulb
Note that olfactory receptor cells with one type of odorant receptor project to one olfactory glomerulus (OG) and olfactory receptor cells with another type of receptor project to a different olfactory glomerulus.

CP, cribriform plate; PG, periglomerular cell; M, mitral cell; T, tufted cell; Gr, granule cell.
Olfactory Bulbs
In the olfactory bulbs
olfactory glomeruli - axonal synapse of the olfactory sensory neurons with primary dendrites of the mitral cells and tufted cells

Axons of mitral cells and tufted cells go into the olfactory cortex
Olfactory Bulbs (cont)
periglomerular cells- are inhibitory neurons connecting one glomerulus to another
granule cells have no axons and make reciprocal synapses with the lateral dendrites of the mitral and tufted cell

the mitral or tufted cell excites the granule cell by releasing glutamate,

granule cell inhibits the mitral or tufted cell by releasing GABA.
Regions of the Olfactory Cortex
The axons of the mitral and tufted cells pass through the lateral olfactory stria to terminate on dendrites of pyramidal cells:
Anterior olfactory nucleus
Olfactory tubercle
Piriform cortex
Amygdala – emotional response
Entorhinal cortex - memories
Then to the frontal or orbitofrontal cortex -discrimination of odors
Vomeronasal Organ
Vomeronasal organ in olfactory epithelium of rodents and various other mammals
perception of odors that act as pheromones.

sensory neurons project to the accessory olfactory bulb and from there primarily to areas in the amygdala and hypothalamus
concerned with reproduction and ingestive behavior.

Vomeronasal input has major effects on these functions.
Vomeronasal Organ (cont)
The vomeronasal organ has about 100 G protein-coupled odorant receptors that differ in structure from those in the rest of the olfactory epithelium.

The organ is not well developed in humans,
There is evidence for the existence of pheromones in humans

There is a close relationship between smell and sexual function
Primary sensations of smell
Musky
Floral
pepperminty
pungent
putrid
Adaptation
Perception of the odor decreases and eventually ceases when continuously exposed.
rapid adaptation, or desensitization,
mediated by Ca2+ acting via calmodulin on cyclic nucleotide-gated (CNG) ion channels.
When the CNG A4 subunit is knocked out, adaptation is slowed.
Threshold for smell
Minute quantity of stimulating agent in the air that can elicit a smell sensation
Methylmercaptan
1/25 trillionth of a gram is in milliliter of air (low threshold
Abnormalities in odor detection
anosmia -inability to smell

hyposmia or hypesthesia -diminished olfactory sensitivity

Due to nasal congestion
damage to the olfactory nerves
due to fractures of the cribriform plate
tumors
infections (such as abscesses).
Alzheimer disease
Abnormalities in odor detection (cont)
Aging - 75% of humans over the age of 80 have an impaired ability to identify smells

Hyperosmia - enhanced olfactory sensitivity Dysosmia - distorted sense of smell

can be caused by sinus infections,
partial damage to the olfactory nerves
poor dental hygiene.
Primary sensations of taste
Sour
Caused by acids; hydrogen ion concentration
Salty
Caused by sodium (cations) ion concentration
Sweet
Not caused by any one class of compound (sugars, glycols, alcohols, amino acids)
Bitter
_ Not caused by any one class of compound (alkaloids and organic substances containing nitrogen)
Umami
Food containing L-glutamate such as meat extracts and aging cheese.
Threshold for taste
Humans sensitivity to:
Bitter > sour> sweet = salty
The salty taste:
is triggered by NaCl.
Na+-selective channel called amiloride-sensitive epithelial sodium channel (ENaC).
The entry of Na+ into the salt receptors depolarizes the membrane, generating the receptor potential.
Other unknown receptors involved
Sour taste
The sour taste is triggered by protons (H+ ions).
Protons enter the ENaCs
The H+ ions block K+-sensitive channel.
The fall in K+ permeability can depolarize the membrane.
Hyperpolarization-activated cyclic nucleotide-gated cation channel (HCN),
Other unknown mechanisms
Umami taste
is due to activation of
metabotropic glutamate receptor (mGluR4).
ionotropic glutamate receptors

produces depolarization
Bitter taste
is produced by a variety of unrelated compounds
Many of these are poisons
bitter taste serves as a warning to avoid them.
Receptors include:
K+-selective channels.
T2R family of receptors
heterotrimeric G protein, gustducin.
decreased cAMP
increases the formation of inositol phosphates
depolarization.
Some bitter compounds are membrane permeable, quinine is an example.
Sweet taste
Substances that taste sweet
T1R3
act via the G protein gustducin.
sweet-responsive receptors act via cyclic nucleotides and inositol phosphate metabolism.
Taste receptors
See Pg
Taste buds located in papillae of the human tongue
Papilla – nipple-shaped projection

3 major types

Taste buds innervated by the
chorda tympani branch of the facial nerve
lingual branch of the glossopharyngeal nerve
Ventral posterior medial nucleus of thalamus
Gustatory cortex (anterior insula frontal operculum)
Cells in taste bud
See Pg
Neural pathway
See Pg
Abnormalities in taste
Ageusia - absence of the sense of taste

Hypogeusia diminished taste sensitivity
Causes:
damage to the lingual or glossopharyngeal nerve.
Neurological disorders
certain infections (eg, primary amoeboid meningoencephalopathy)
side effect of various drugs including cisplatin and captopril
vitamin B3 or zinc deficiencies.
Aging and tobacco abuse also contribute to diminished taste.
Abnormalities in taste (cont)
Dysgeusia or parageusia - unpleasant perception of taste
causes a metallic, salty, foul, or rancid taste.

temporary problem