TY - JOUR T1 - The role of EP<sub>2</sub> receptors in mediating the ultra-long-lasting intraocular pressure reduction by JV-GL1 JF - British Journal of Ophthalmology JO - Br J Ophthalmol SP - 1610 LP - 1616 DO - 10.1136/bjophthalmol-2020-317762 VL - 105 IS - 11 AU - Jacques A Bertrand AU - David F Woodward AU - Joseph M Sherwood AU - Jenny W Wang AU - Darryl R Overby Y1 - 2021/11/01 UR - http://bjo.bmj.com/content/105/11/1610.abstract N2 - Background A single application of JV-GL1 substantially lowers non-human primate intraocular pressure (IOP) for about a week, independent of dose. This highly protracted effect does not correlate with its ocular biodisposition or correlate with the once-daily dosing regimen for other prostanoid EP2 receptor agonists such as trapenepag or omidenepag. The underlying pharmacological mechanism for the multiday extended activity of JV-GL1 is highly intriguing. The present studies were intended to determine EP2 receptor involvement in mediating the long-term ocular hypotensive activity of JV-GL1 by using mice genetically deficient in EP2 receptors.Methods The protracted IOP reduction produced by JV-GL1 was investigated in C57BL/6J and EP2 receptor knock-out mice (B6.129-Ptger2tm1Brey /J; EP2KO). Both ocular normotensive and steroid-induced ocular hypertensive (SI-OHT) mice were studied. IOP was measured tonometrically under general anaesthesia. Aqueous humour outflow facility was measured ex vivo using iPerfusion in normotensive C57BL/6J mouse eyes perfused with 100 nM de-esterified JV-GL1 and in SI-OHT C57BL/6J mouse eyes that had received topical JV-GL1 (0.01%) 3 days prior.Results Both the initial 1-day and the protracted multiday effects of JV-GL1 in the SI-OHT model for glaucoma were abolished by deletion of the gene encoding the EP2 receptor. Thus, JV-GL1 did not lower IOP in SI-OHT EP2KO mice, but in littermate SI-OHT EP2WT control mice, JV-GL1 statistically significantly lowered IOP for 4–6 days.Conclusions Both the 1-day and the long-term effects of JV-GL1 on IOP are entirely EP2 receptor dependent.All data relevant to the study are included in the article or uploaded as supplementary information. All data and analyses are available by contacting the following at their ORCID numbers, as follows: 0000-0001-9894-75150000-0002-4402-9767. ER -