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1. The effects of intracameral injections of prostaglandins E1, E2, Fia, F2a, and A1 were studied on.the intraocular pressure (IOP) of rabbits anaesthetized with urethane.2. With the exception of prostaglandin F,a, all the prostaglandins studied were found to be capable of producing a large, sustained rise in IOP, accompanied in many cases by miosis. 3. A marked decrease in response to repeated injections was found with all the prostaglandins studied; this effect was more pronounced following a large initial response to the prostaglandin. 4. The descending order of potency in their ability to raise IOP was as follows: prostaglandin Ei-E2>F2a>Al>Fia.5. Intracameral injections of prostaglandins E1 and E2 resulted in an increase in the protein content of the aqueous humour, which was related to the magnitude of the sustained increase in IOP. 6. Stabilization of the blood-aqueous barrier with polyphloretin phosgphate markedly reduced both the IOP response and the effect of prostaglandin E2 on the protein content of the aqueous humour. 7. It is concluded that the production of local vasodilatation and increased permeability of the blood-aqueous barrier play an important part in the effect of prostaglandins on the IOP. The involvement of prostaglandins in the response of the rabbit eye to irritation is discussed.Injections of prostaglandins into rabbit eyes have been shown by Waitzman & King (1967) to produce a sustained rise in intraocular pressure (IOP). This effect on the IOP was thought to result from an action of prostaglandins on the metabolic processes involved in aqueous humour production, rather than from vascular or permeaibility changes (Waitzman, 1968), although it was well known that many prostaglandins are powerful vasodilators. Moreover, it had been shown earlier that the response of the rabbit eye to irritation is associated with the release into the aqueous humour of irin, an ether-soluble spasmogen with vasodilator activity consisting of unsaturated hydroxy fatty acid(s)

Myeloperoxidase (MPO) activity was measured in rabbit cornea and iris-ciliary body to quantitate the infiltration and accumulation of polymorphonuclear leucocytes (PMN's) following an inflammatory stimulus. Following injection of clove oil into the cornea, MPO activity could be detected in the cornea at 6 hr, reaching a maximum at 12 hr, and falling to non-detectable levels at 72 hr. MPO activity was only detected in the iris-ciliary body 24 hr after intracorneal clove oil injection. MPO activity in the iris-ciliary body increased in a dose-dependent manner following intravitreal injection of endotoxin. No MPO activity could be detected in cornea. Topical administration of dexamethasone inhibited MPO activity in cornea and iris-ciliary body 24 hr after intracorneal clove oil and intravitreal endotoxin injection, respectively. Measurement of MPO activity in ocular tissues could provide a useful tool to quantitatively evaluate the severity and time course of inflammation.

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