The Eye Accessory structures or Adnexa 4 layers: 1. Skin – thinnest in the body 2. muscle – orbicularis oculi and levator palpebrae superioris 3. Connective.

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Presentation transcript:

The Eye Accessory structures or Adnexa 4 layers: 1. Skin – thinnest in the body 2. muscle – orbicularis oculi and levator palpebrae superioris 3. Connective tissue – tarsal plate contains tarsal or Meibomian glands - Chalazion

4. Conjunctiva – mucous membrane palpebral conjunctiva bulbar conjunctiva Eyelashes sebaceous ciliary glands at base of hair follicles – hordeolum or stye Lacrimal apparatus – forming and draining tears.

Strabismus – turned eye Phoria – weakness of eye muscles Eyeball – 3 layers or tunics: 1. Fibrous tunic (outer tunic) Cornea – clear - avascular Scleara – white –means “hard”

2. Vascular tunic : Uvea Choroid – blood vessels and pigment Ciliary body : ciliary processes make aqueous humor ciliary muscle - accomodation

Accommodation: Focusing the eye to see close objects Lens is thin when stretched by suspensory ligaments (low power) When round ciliary muscle contracts, tension is released from lens and it becomes thicker (higher power lens).

Lens – avascular, clear, elastic contains proteins called crystallins becomes opaque = cataract Iris – pigmented, divides anterior and posterior chamber Aqueous humor – drains into scleral venous sinus (Schlemm’s canal)  intraocular pressure - glaucoma

3. Nervous Tunic – Retina several layers “inside out” Pigmented epithelium Rods and Cones (photoreceptors) Bipolar cells Ganglion cells (vitreous humor) Light is focused by cornea and lens on the Fovea centralis (“central pit”)which is in the center of the Macula lutea (“yellow spot”) The third refractive component is the length of the eyeball.

Refractive Disorders Emmetropia – good vision 20/20 Myopia – nearsightedness Hyperopia – farsightedness Astigmatism – light does not focus to a single point on the retina Presbyopia – “old sight” – loss of ability to accommodate or see up close

Physiology of vision In the dark, Na+ channels are held open by a nucleotide called cyclic GMP (guanosine monophosphate) Inflow of sodium (“dark current”) triggers the continual release of neurotransmitter. This neurotransmitter is inhibitory- it prevents bipolar cells from firing by hyperpolarizing them.

When light strikes the retina, retinal (from vitamin A) which is bent, straightens out, and no longer fits into the opsin. The two separate – this is called bleaching. The opsin becomes an active enzyme, that activates other enzymes that break down cyclic GMP. Without cyclic GMP, the Na+ channels close.

The receptor hyperpolarizes, stopping the release of inhibitory neurotransmitter. This decrease in inhibition allows the bipolar cells to fire, and information is sent to the visual cortex. Differentiation of color is assisted by horizontal cells. In darkness, retinal isomerase converts trans- retinal back to cis-retinal, which binds with opsin forming a functional photopigment.

Color vision Uses three different photopigments : blue, green and red Wavelength of pigments may be shifted, causing color blindness Red – green color blindness most common Sex-linked trait carried on X chromosome (Males only have one gene for color vision)

Rods:Cones: Can see in dim lightRequire more light See in black and white See in color Respond to movementGive best acuity Found more in periphery More central, esp. in fovea centralis

Stereopsis Use both eyes to perceive depth – “depth perception” Nasal fibers cross at the optic chiasm Temporal fibers do not cross over Each visual cortex (R &L) receives information from both eyes so it can compare what each eye sees.