TY - JOUR
T1 - The Ocular Hypotensive Effect of the Topical Carbonic Anhydrase Inhibitor L-671,152 in Glaucomatous Monkeys
AU - Wang, Rong Fang
AU - Serle, Janet B.
AU - Podos, Steven M.
AU - Sugrue, Michael F.
PY - 1990/4
Y1 - 1990/4
N2 - L-671,152, a new potent water-soluble inhibitor of human carbonic anhydrase II in vitro, was applied topically to cynomolgus monkey eyes in which glaucoma had been produced by argon laser photocoagulation of the trabecular meshwork. Intraocular pressure was measured at 0 hours, 0.5 hours, and hourly for 8 hours in eight eyes for 2 baseline days, 1 day receiving the vehicle and 5 days receiving therapy with 2% L-671, 152 twice a day, after initial single-dose trials of various concentrations. Intraocular pressure was not significantly different comparing baseline and vehicle-treated days. Significant intraocular pressure reductions occurred from 1 to 8 hours after the first dose, and lasted for at least 16 hours after the second dose. The reduction in intraocular pressure became more pronounced from day 1 to day 5 at each time interval. The mean (± SEM) maximum reduction in intraocular pressure was 7.8 ± 2.1 mm Hg on day 1 and 10.1 ± 2.4 mm Hg on day 5 at 3 hours after administration, comparing the intraocular pressure in drug-treated and vehicle-treated eyes. L-671,152 has a longer duration of action than does previously studied MK-927 in glaucomatous monkeys. It appears to have great clinical potential.
AB - L-671,152, a new potent water-soluble inhibitor of human carbonic anhydrase II in vitro, was applied topically to cynomolgus monkey eyes in which glaucoma had been produced by argon laser photocoagulation of the trabecular meshwork. Intraocular pressure was measured at 0 hours, 0.5 hours, and hourly for 8 hours in eight eyes for 2 baseline days, 1 day receiving the vehicle and 5 days receiving therapy with 2% L-671, 152 twice a day, after initial single-dose trials of various concentrations. Intraocular pressure was not significantly different comparing baseline and vehicle-treated days. Significant intraocular pressure reductions occurred from 1 to 8 hours after the first dose, and lasted for at least 16 hours after the second dose. The reduction in intraocular pressure became more pronounced from day 1 to day 5 at each time interval. The mean (± SEM) maximum reduction in intraocular pressure was 7.8 ± 2.1 mm Hg on day 1 and 10.1 ± 2.4 mm Hg on day 5 at 3 hours after administration, comparing the intraocular pressure in drug-treated and vehicle-treated eyes. L-671,152 has a longer duration of action than does previously studied MK-927 in glaucomatous monkeys. It appears to have great clinical potential.
UR - http://www.scopus.com/inward/record.url?scp=0025269576&partnerID=8YFLogxK
U2 - 10.1001/archopht.1990.01070060059049
DO - 10.1001/archopht.1990.01070060059049
M3 - Article
C2 - 2322152
AN - SCOPUS:0025269576
SN - 0003-9950
VL - 108
SP - 511
EP - 513
JO - Archives of Ophthalmology
JF - Archives of Ophthalmology
IS - 4
ER -