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In the human eye, the aqueous fluid, which is a complex mixture of electrolytes, growth factors,
and other proteins that nourish the non-vascularized tissue of the anterior chamber, is secreted by
the ciliary body into the posterior chamber of the eye and then flows into the anterior chamber.
The aqueous fluid outflow is from the anterior chamber, through a sieve-like trabecular
meshwork into the Schlemms canal (a canal that is at the junction of the iris and cornea), and
then into the venous system of the eye. If the aqueous outflow is obstructed, there is a pressure
increase in the anterior chamber, which then exerts pressure in the posterior chamber on the
retina and the optic nerve. The resultant damage to the retina and optic nerve tissue from
elevated intraocular pressure is called glaucoma. In this study, we look at the aqueous outflow
pathway in mice under Scanning Electron Microscope. This allows the examination of the
anatomy of the structures like Schlemms canal, collector channel orifices and aqueous veins in
the mouse eye. We use C57BL6 mice of either sex, weighing around 30g. Mice will be killed by
CO2 inhalation. Both eyes from each mouse will be removed, fixed and stored by immersion in
3% glutaraldehyde. The eye tissue will be dehydrated in graded ethanol, dried with
Hexamethyldisilazane, and examined by SEM. We expect the mouse aqueous outflow pathway
to be similar to that described in humans. Schlemms canal, collector channel orifices, the
collector channels and the aqueous veins in the mouse eye will be much smaller in scale in
comparison to the human eye. Examining the anatomy of the Schlemms canal and the outflow