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75 Cards in this Set

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What is the first and second strongest attachments of the vitreous to the retina?
Firmest-vitreous base
second firmest-(Ligamentum hyaloide capsulare) or Optic disk
What happens to the composition of the vitreous as people age?
becomes more liquid and less gel. and more soluble proteins in vitreous as we age
Where does liquidification begin in the vitreous?
in the central vitreous
What happens to the collagen in vitreous as we age
The total collagen amount doesn't change but increase in collagen in the gel component and reduction in liquid
what happens to Hyaluronic acid in vitreous as we age
HA conc doesn't change after 20 but the amount in the liqu. increases and the gel HA decreases
PVD happens in what percentage of people? Do you have to have symptoms?
70% for 65+
Macular holes are most prevalent in who?
What causes them?
elderly women

Shrinkage of prefoveal vitreous cortex

Bloodsupply of the retina
outer 1/3-diffusion from the choriocap form short post ciliary art.
inner 2/3- central ret art.
What is the difference between the two?
outer-high flow and oversupply the retina can only utilize a small amount of O2,metabolites pass
Inner-slow flow, best utilization of O2
Difference between structure of choriocapillaries and ret blood vessels
chorio- fenestrated
ret vessels-not fen. tight jxn

What does this mean
chorio cap will leak flourescien
leaking in ret photo-due to ret. arteries should
Blood vessels in the ciliary body
Blood vessels in the cil. body. pars plicata and pars plana are fenestrated.
But in the ciliary muscle they aren't!!!
Iris blood vessels
not fenestrated, major and minor art. circle, only minor venous circle
not innervated or surrounded by sm. muscle
contracts by PERICYTES
Auto regulation of retinal blood flow in eye
the ret blood vessels and the onh have myogenic and metabolic autoreg of blood vessels but the choroid doesn't
it allows metabolite to still enter even when central ret flow is reduced
Visual pigment consists of
Chromophore and Opsin
LOCATED IN OUTER DISKS

(chromophore-> retinal
Dark Current
cGMP bound channels in the outer segment are open in dark.
Na and other cations are transported in while
K is transported out
-40--50
depolarized
(-70=rmp)
What happens is levels of cGMP greatly decrease?
How is this caused?
The channels close and the membrane becomes polarized. Less glutamate is transmitted.
PDE converts cGMP to 5'GMP
What is the initial step of phototransduction?
(Initialization)
photon absorbtion causes the 11-cis retinal to be isomerized in to all trans metarodopsin
R->R*
What are the two gains in phototransduction?
1. R* activates over 100 tranducins.
2. PDE hydrolyzes many cGMP and the rate is set by diffusion
What is significant about the two gains in phototrans?
These two gains cause a very high amplification that make the rods very sensitive even to one photon.
How is restoration of cGMP controlled?
1. PDE* hydrolysis
2. Guanylate cyclase (GC) mediated synthesis
In dark low Ca conc. so GCAP is formed and inhibits GC
Inside of the RPE what is the name of the storage form?
11-cis-retinal
What are the fxn of the RPE
to absorb scattered light, transmit substances between chorio. and ret.
What does the RPE transport from the blood to the retina
1. Glucose, GLUT1 and GLUT3
2.all trans ret
3.DHA from liver
What does the RPE transport from the retina to blood?
1. maintains water and electrolytes
Na, K, and Cl and H20
2. Lactic Acid
3. Bicarbonate (NA/HC3O, Na gradient)
(an increase in LA increases bicarb.)
4. Phagocytosis of photoreceptor outer pigments
5. secretion of certain factors (immune)
How is the transport of water driven from the retina to the choriocapilaries driven across the rpe?
by active trans of cl from ret to blood
In the visual cycle,what proteins carry the chromaphore between the RPE and the retina and what form is it in?
1. from ret to RPE: all trans retinOL bount to IRBP goes in to RPE
2. from RPE to retina: 11-cis retinal is transported attached to IRBP
How often is the entire length of the outer segment of a photoreceptor renewed.
11 days
6 FXNS of the RPE
1. Phagocytosis
2. epithelial transport
3. light absorbtion
4. Glia (Phagocytosis)
5. Visual Cycle
6. Secretion
Secretion of substances from the RPE is mediated by ________?
Voltage dependent Calcium Channels
What are the principle supporting cells of the retina? What is their fxn?
Mueller Cells, ilm->olm
1.structural support
2.electrolyte homeostasis
3. neuroactive substances
4. Recycle transmitters
what 2 transmitters are recycled by the Mueller cells
glutamate and CA!
what type of cells are astrocytes derived from
progenitor cells outside the ret
Astrocytes fxn. where found?
NFL and GCL1/4 ILM and in optive nerve. protect bvs
Microglia
mononuc. phago.
defence
Metabolic processes inside the retina and how glial cells participate?
Glycolysis is performed inside Mueller glia and than Lactate or alaline
Ox. metab inside photoreceptor
Than Glutamate is a waste and is signal to glia cell
For metabolism of glucose in ret. what goes from glial cell to PR back to glial?
1. lactate or alanine goes to PR
2. GLU from PR to glia
3. glia turn to GLN it goes back to PR
How do glia regulate bloodvessels dilation?
their endfoot is in contact with vascular wall of retinal arteries (have sm and endothelium)
Endfoot->**L-Lactate->release of NO endothel/glia->arteolar vasodilation-> increase in ret blood flow
What cells produce the precursor to NO and what is it?
Mueller cells->L-Arginine from glucose
how is L arginine made in to NO
l-arginine+O2-NOS->NO +L citrulin
Mechanism of Glaucoma?
1. sped up ganglion cell loss -GC suseptibility, aging, high iop, large disk?
2.myopic suseptibility - Connective tissue in optic nerve head, sugessing somekind of altered scleral ridgity deformation of post.
3. weak laminar pores in the outer portions of the lamina cribosa
4.IOP levels
5.low vascular nutrition of the optic disk-poor perfusion- sys. htn, peripheral vasoplasm, PV
6. deficient Autoregulation of blood flow
7. focal areas of filling defects
8. zone between ohn and peripapillary choroid suseptible to ischemia
These usually read lower IOPs.
thinner corneas--myopia
In descending order, where is the neuroretinal rim broadest
ISNT
Inferior, superior, Nasal, Temporal
Glacoma can lead to what affecting the neuroret. rim.
neuroret rim loss: it, st, th, ni, ns
Which is circular the vertical disk or the horizontal cup?
Neither are circular
What are the zones in PERIPAPILLARY CHORORETINAL ATROPHY?
1. alpha (peripherally)-thinning of chorioret area with hypo and hyperpigmentation
2. beta (centrally)-visible scleral and large choroidal vessels
3. sceral ring- inner to beta exaggerated in myopia and tited dics

APBC
When zone beta completely surrounds the ONH.
Halo Glacomatosus
What are the fxns of the conjunctiva?
movement of eyelids
maitance and drainage of tear film
protective fxns-trapping microbes
defensive-lymph tisue
contol of microflora
supplies the corneal epithelial cells
*it does all these things with the help of the lacrimal system
Distribution of mast cells in the conjunctiva.
adenoid layer, numorous in conj. stroma, norm. not in epi.
Which have blood vessels? Papillae or follicles?
Papilla
What is produced inside the goblet cells of the conj?
MUC5AC
Main neural inputs to conjunct. for goblet cell secretion.
parasympathetic
Basal secretion of tears:
sympathetic inn., sup cervical gang. accessory lacrimal gland
reflex tear secretion by stimulation of cornea
cn V parasym. sphengopal. gang.
lacrimal gland
PERIPHERAL ORIGIN
Light or psychogenic reflex tears
cortical, brain stem, parasym, spengopal gang.
CENTRAL ORIGIN
Tear turnover
5-6 min.
basal tear secretion rate
1.2mL/min
tear turnover rate
16% of total tear volume per minute
total tear film
7mL
max capacity of lacrimal lake
30mL
What MUC is found most in tears?
MUC16
Regulated proteins increase with tear secreation. What are they?
lactoferrin, lipocalin,lysozyme
Jones I test. Typical results
florescein retrieved from through nasal pass. etc. 5 min after

under 45 pass within 6 min average 3
over 45 pass within 12 min avg 6
Jones II Test
instill florescein in lacrimal lake after 5 min of test I,
1. Dye recovery-NORMAL
2.Recovery of only saline-UPPER SYSTEM IS FAULTY
3. No recovery-COMPLETE OBSTRUCTION
partial pressure of the o2 in AH
55
Strength stiffness of Bowman's Layer
the ant 1/3 is much stiffer and stronger due to its woven nature
**Damage usually starts posteriorly and moves anteriorly
Polymodal receptors respond to
mechanical higher temp and chemical
large receptive field-code for intensity and duration
Cold receptors in cornea
small recept. field and respond to amperage
more abundant in the periphery
don't respond to heat, basal firing rate
short delay, good discrimination threshold
mechano-nociceptors
limited ability to respond to coding of a stimulus

acute sharp sensations
Corneal sensitivity
more in apex less in perifery,
less in morning,
the cornea is less sens. j/ b4 menstruation
Regeneration of cornea at descemet's membreane and endothelium
descemet's membrane gets regenerated by endotheial
But damage to endothelial cells doesn't repair
Where does Cloquet's Canal come from? Where is it?
It is formed when the primary vitreous gets compressed by the secondary vitreous.
S shaped optically empty space between mittendorf (ant lens) to bergmeister's papilla at optic disk
Vitreous boy composition
99% water, 1%type II collagen, some soluable protiens, and HA
The collagen content of the collagen is highest when?
it is a gel
Where is the collagen concentrated in the vitreous?
in the ant
concentration of phosphates in the vitreous
Low conc of Phosphates in vit.
Glucose conc. in vitreous?
half the amount in vitreous or plasma