Aqueous humor production:
Flow: Ciliary process (posterior chamber) → anterior chamber → trabecular network (canal of Schlemm)
*β1-adrenergic receptors increase production
1. β1-adrenergic antagonists block AH production
2. Carbonic anhydrase inhibitors block AH production
3. α2 agonists (apraclonidine): decrease AH production; also increase uveoscleral drainage
Uveoscleral Flow:
1. α2 agonists (apraclonidine): decrease AH production; also increase uveoscleral drainage?
2. Prostaglandin agonists PGF2α (latanoprost): als increase uveoscleral drainage
3. α agonists (epinephrine): increase uveoscleral flow
Trabecular Tone:
1. Muscarinic agonists (carbachol, pilocarpine) cause miosis → incresed trabecular tone & porosity
2. Acetylchoinesterase inhibitors (physostigmine, echothiophate) cause miosis → incresed trabecular tone & porosity
Osmotic:
1. Mannitol: removal of H2O from eye
Notes:
1. Miosis (constriction) → ↑ trabecular tone & porosity → ↑ drainage
*M3 receptors on pupillary sphincter
2. Mydriasis (dilation) → ↓ trabecular tone & porosity → ↓ drainage
*α1-agonists are on pupillary dilator muscle
3. Cycloplegia (accomodation) → Muscarininc receptors
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