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(Investigative Ophthalmology and Visual Science. 2007;48:4143-4147.)
© 2007 by The Association for Research in Vision and Ophthalmology, Inc.
DOI:  10.1167/iovs.07-0035
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Effect of 15-Keto Latanoprost on Intraocular Pressure and Aqueous Humor Dynamics in Monkey Eyes

Rong-Fang Wang,1 Donna J. Gagliuso,1 Thomas W. Mittag,1,2 and Steven M. Podos1,3

1From the Departments of Ophthalmology, 2Pharmacology and Systems Therapeutics, and 3Neuroscience, Mount Sinai School of Medicine of New York University, New York, New York.


   Abstract
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 Abstract
Materials and Methods
 Results
 Discussion
 References
 
PURPOSE. To compare the ocular hypotensive effects of 15-keto latanoprost (KL) with the commercial preparation of latanoprost (Xalatan; Pfizer, New York, NY) in monkey eyes with laser-induced unilateral glaucoma and to evaluate the effects of topical 0.005% KL on aqueous humor dynamics in normal monkey eyes.

METHODS. Intraocular pressure (IOP) was measured hourly for 6 hours beginning at 9:30 AM on day 1 (untreated baseline); day 2 (vehicle only); and treatment days 1, 3, and 5 (topical, 30 µL of study drug) in the glaucomatous eyes of four to eight monkeys with unilateral laser-induced glaucoma. KL concentrations of 0.0001%, 0.001%, and 0.01% and latanoprost at 0.005% were studied separately, with a minimum washout period of 2 weeks between studies. Tonographic outflow facility (C) and fluorophotometric aqueous humor flow rates (F) were measured in nine normal monkeys before and after a single topical dose of 0.005% KL in one eye, with a vehicle-only control in the fellow eye.

RESULTS. When applied once daily to glaucomatous monkey eyes, all three concentrations of KL and a 0.005% concentration of latanoprost produced significant (P < 0.05) reductions in IOP, with the maximum reduction on treatment day 5, regardless of the drug or concentration studied. The maximum reduction (P < 0.001) from vehicle-only baseline IOP was (mean ± SEM) 3.0 ± 0.3 mm Hg (9%) for 0.0001% KL, 7.6 ± 0.6 mm Hg (23%) for 0.001% KL, 6.3 ± 0.4 mm Hg (18%) for 0.01% KL, and 6.6 ± 0.6 mm Hg (20%) for 0.005% latanoprost. After application of a single dose of 0.005% KL in nine normal monkey eyes, neither C nor F was altered (P > 0.80) when compared with untreated baseline values or vehicle-treated control eyes.

CONCLUSIONS. The reduction in IOP produced by 0.001% KL was equivalent to, and at some measured time points, greater than the effect produced by 0.005% latanoprost. The IOP reduction by KL in normal monkeys appeared to have no effect on aqueous humor production or tonographic outflow facility and may thus indicate a drug-induced increase in uveoscleral outflow.

The clinically available prostaglandin analogs latanoprost, bimatoprost, travoprost,1 and isopropyl unoprostone2 are all isopropyl ester prodrugs and effective ocular hypotensive agents. The majority of receptor-binding studies indicate that the free acid metabolites of these compounds are agonists at the prostaglandin FP receptor, but with widely differing affinities.3 4 5 6 7 8 These drugs lower intraocular pressure (IOP) in part by enhancing uveoscleral outflow,9 10 11 12 13 although the precise mechanism by which this occurs is not known.14 However, recent studies in mice lacking individual PG receptor subtypes indicate that the ocular hypotensive response of these PG drugs may actually be mediated by EP3 receptors activated by endogenously produced PGs resulting from drug stimulation of FP receptors.15 16 Some studies have also shown an increase in total outflow facility after treatment with isopropyl unoprostone,17 and to some extent also with latanoprost11 12 or bimatoprost,18 in addition to their increasing uveoscleral outflow.

Three of the four clinically used PG analogs have a hydroxyl group on position 15, which is the site of potential metabolic conversion into a 15-keto analog. The exception is unoprostone, which is an analog of 15-keto PGF2{alpha} FP. We wanted to determine whether metabolic oxidation of the 15-hydroxyl function of ocular hypotensive PGF2{alpha} FP analogs produces intrinsically less active PG analogs, which is commonly believed to be the case. Therefore, the present study was designed to evaluate the ocular hypotensive effect of 15-keto latanoprost (KL) in three concentrations in glaucomatous monkey eyes compared with its clinically approved 15-hydroxy analog, Xalatan (0.005% latanoprost; Pfizer, New York, NY). The mechanism by which KL alters aqueous humor dynamics was also evaluated, by using the 0.005% concentration in normal monkey eyes.


   Materials and Methods
Top
 Abstract
 Materials and Methods
Results
 Discussion
 References
 
Animals
Twenty-one adult female cynomolgus monkeys, weighing 3 to 6 kg, were used in the studies. Twelve monkeys, in which glaucoma had been unilaterally induced by repeated diode laser photocoagulation of the mid trabecular meshwork,19 were used to evaluate the ocular hypotensive effects of 0.0001%, 0.001%, and 0.01% KL and 0.005% latanoprost. In a separate experiment, nine normal monkeys without glaucoma were used to evaluate the effect of 0.005% KL on aqueous humor dynamics. All experimental studies complied with the ARVO Statement for the Use of Animals in Ophthalmic and Vision Research and were approved by the Institutional Animal Care and Utilization Committee of Mount Sinai School of Medicine.

Preparation and Instillation of Testing Compounds
15-Keto latanoprost was obtained from two sources, termed KL-A and KL-B, and were tested at different times on different sets of monkeys. KL-A (from R-Tech Ueno, Tokyo, Japan) was used in most of the experiments. It was prepared synthetically and had analytical purity of 99.6% (batch 4, by HPLC). Solutions of 0.0001%, 0.001%, and 0.01% used for topical treatments were made up in the ophthalmic vehicle contained in Xalatan (isotonic saline containing Na EDTA and polysorbate 80, preserved with benzalkonium chloride; Pfizer) and were separately assayed (HPLC) for KL purity (95.1%, 94.2%, and 93.3%, respectively). The KL-B sample was obtained from Cayman Chemical Co. (Ann Arbor, MI) and had a purity of >98% (HPLC). The 0.001% dose was made up in the same vehicle used for the KL-A sample. The commercial preparation of 0.005% latanoprost, Xalatan, was used for comparison to KL-A. A multiple-dose study was performed in eight glaucomatous monkeys. One 30-µL drop of KL-A (0.0001%, 0.001%, and 0.01%) or latanoprost was topically applied to the glaucomatous eye at 9:30 AM for five consecutive days in a randomized, crossover design with a washout period of at least 2 weeks between studies. A single-dose test was performed with 0.001% KL-B in another group of four glaucomatous monkeys after the KL-A study was completed.

IOP Measurement
IOP was measured hourly for 6 hours, beginning at 9:30 AM on day 1 (untreated baseline), on day 2 (vehicle only), on treatment day 1 (single-dose study), and on treatment days 3 and 5 (multiple-dose study) at the same times during each day. A pneumatonometer (model 30 classic; Mentor, Norwell, MA) was used for all IOP measurements. Five minutes before each tonometry measurement, ketamine hydrochloride (2–5 mg/kg) was administered intramuscularly for sedation, and 1 drop of 0.5% proparacaine hydrochloride was applied topically to the study eye.

Outflow Facility and Aqueous Humor Flow Rates
Outflow facility was measured with an electronic indentation tonograph (EDT-130; Alcon Laboratories, Inc., Fort Worth, TX) immediately before and at the peak IOP response time (2 hours) after topical application of a single 30-µL drop of 0.005% KL-A in one eye. An equal volume of vehicle was applied to the contralateral control eye. Aqueous humor flow was measured with a scanning computerized fluorophotometer (Fluorotron; Coherent Corp., Palo Alto, CA). Fluorescein iontophoresis was performed in the central corneas of both eyes of each monkey for 7 minutes, by using 10% fluorescein in 2% agar gel at 4 PM on the day before the aqueous flow measurements on either baseline day or a treatment day. Baseline aqueous humor flow rates were measured hourly for 4 hours beginning at 9:30 AM. The following day at 8:30 AM, a 30-µL drop of 0.005% KL-A was applied to one eye of each monkey and the same volume of vehicle was applied to the contralateral control eye. One hour after drug or vehicle application, aqueous humor flow rates were measured hourly for 4 hours, beginning at 9:30 AM at the same times as the baseline measurements. Ketamine hydrochloride was used for adequate sedation before outflow facility and aqueous humor flow measurements.

Statistics
The two-tailed paired t-test was used for statistical analysis before and after single-dose treatments, and the Bonferroni t-test was used for the analysis of the multiple-dose study. P < 0.05 was considered statistically significant.


   Results
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 Abstract
 Materials and Methods
 Results
Discussion
 References
 
Comparison of Various Doses of KL and 0.005% Latanoprost on IOP
The hypotensive response of the two drug samples, KL-A and -B, were independently compared (at different times and in different sets of glaucomatous monkey eyes) at the 0.001% single-dose level. Figure 1 indicates that KL from both sources was probably equivalent: The peak response—a 15% to 20% reduction of IOP—occurred at 2 to 3 hours, and the response lasted for at least 6 hours.


Figure 1
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  		FIGURE 1. Mean percentage change in intraocular pressure (IOP) after a single-dose application of 0.001% KL-A or -B in eight and four glaucomatous monkey eyes, respectively. *Significant reduction in IOP from vehicle-only baseline (two-tailed paired t-test; P < 0.05).

 
In the multiple-dose experiments with KL-A the mean baseline and vehicle-only treated IOPs of the four treatment groups were not significantly different (P > 0.90, Table 1 ). All three concentrations of KL-A tested, (0.0001%, 0.001%, and 0.01%), and 0.005% latanoprost produced significant (P < 0.001) reductions from untreated baseline and vehicle-only IOP levels. Once-daily administration of 0.0001% KL-A for 5 days significantly (P < 0.05) reduced IOP at 2 hours after the first dose, and from 1 to 4 hours after the third and the fifth doses. Compared with vehicle-only baseline, the maximum reductions in IOP 2 hours after each morning dose for the three concentrations of KL-A are shown in Table 1 .


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  		TABLE 1. Comparison of IOP Effects of Once-Daily Administration of KL-A or Latanoprost for 5 Days

 
Both 0.001% and 0.01% KL-A significantly (P < 0.005) reduced IOP for at least 6 hours after the first dose on day 1 and for at least 24 hours after the second and fourth doses (determined before treatment on days 3 and 5; Table 1 , Fig. 2 ). The maximum reduction in IOP from vehicle-only baseline for both concentrations occurred 2 hours after each morning dose.


Figure 2
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  		FIGURE 2. Comparison of the mean change in IOP in a group of eight glaucomatous monkey eyes after once-daily administration of 0.0001%, 0.001%, or 0.01% KL-A for 5 days. Data show the mean change in IOP from vehicle-only baseline. Asterisks indicate significant difference in magnitude of IOP reduction between concentrations (two-tailed paired t-test; P < 0.01; *0.0001% vs. 0.001%; **0.001% vs. 0.01%). Arrow: drug treatment immediately after time 0 measurement.

 
Treatment with 0.005% latanoprost produced a significant (P < 0.001) reduction in IOP from vehicle treatment levels at 1 to 5 hours after the first dose on day 1. A significant (P < 0.02) ocular hypotensive effect was maintained for a minimum of 24 hours after the second dose. The peak mean reduction of IOP from vehicle treatment levels measured 4.8 ± 0.5 mm Hg (14%) on day 1, 6.0 ± 0.3 mm Hg (18%) on day 3, and 6.6 ± 0.6 mm Hg (20%) on day 5 (Table 1 , Fig. 3 ).


Figure 3
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  		FIGURE 3. Comparison of the mean change in IOP in eight glaucomatous monkey eyes after once-daily administration of either 0.001% KL-A or 0.005% latanoprost for 5 days. Values are the mean change in IOP from vehicle-only baseline. Asterisks indicate significant difference in magnitude of IOP reduction between 0.001% KL-A and 0.005% latanoprost (two-tailed paired t-test; *P < 0.05, **P < 0.005). Arrow: drug treatment immediately after time 0 measurement.

 
For all three concentrations of KL-A and for 0.005% latanoprost, the maximum reductions in IOP were increased on day 5 after repeated doses. When compared with 0.0001% KL-A, treatment with 0.001% KL-A produced a greater magnitude (23% vs. 9%, P < 0.005) and longer duration (24 hours vs. 4 hours; Fig. 2 ) of IOP reduction. Increasing the concentration to 0.01% did not further increase the magnitude of IOP reduction on days 1 and 3 (P > 0.90) but produced a slightly smaller reduction in IOP on day 5 at 0 (7% vs. 12%; P < 0.01) and 4 (14% vs. 18%; P < 0.005) hours.

Compared with 0.005% latanoprost, 0.001% KL-A produced a slightly longer duration of IOP reduction (6 hours vs. 5 hours) after the first dose on treatment day 1 and a greater (P < 0.05) IOP reduction at 4 and 6 hours on day 1 and at 0 and 4 hours on day 5 (Fig. 3) .

Effect of KL-A on Aqueous Humor Dynamics
Two hours after unilateral application of 0.005% KL-A to nine normal monkey eyes, outflow facility was unchanged compared with both vehicle-treated control eyes (P > 0.70) and baseline values (P > 0.20). IOP was significantly reduced (P < 0.01) at 2 hours in the drug-treated eyes when measured tonographically (Table 2) . For 4 hours after the administration of a single dose of 0.005% KL-A, aqueous humor flow rates were not altered compared with those in either vehicle-treated control eyes (P > 0.05) or baseline values (P > 0.80; Table 2 ).


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  		TABLE 2. Effect of a Single-Dose Application of 0.005% KL-A on Aqueous Humor Dynamics in Nine Normal Monkeys

 

   Discussion
Top
 Abstract
 Materials and Methods
 Results
 Discussion
References
 
Latanoprost and related PGF2{alpha} isopropyl ester analogs are effective ocular hypotensive agents for the treatment of patients with elevated IOP. Oxidation of the C-15 hydroxyl group by 15-hydroxy prostaglandin dehydrogenase subsequent to isopropyl ester hydrolysis introduces a 15-keto group. This metabolite of latanoprost is produced by the NADP+-dependent 15-PG dehydrogenase enzyme shown to be highly expressed in the monkey eye.20 The present comparison study on 15-keto latanoprost in a multiple-dose regimen in glaucomatous monkey eyes is the first to show a highly significant and potent ocular hypotensive effect of a 15-keto PGF2{alpha} analog that is equivalent to or even exceeds the response of its otherwise structurally identical 15-hydroxy PGF2{alpha} analog (latanoprost) at the same dose level.

Our results showed that once-daily administration of KL at concentrations as low as 0.0001% lowers IOP in glaucomatous monkey eyes. All three concentrations of KL tested and 0.005% latanoprost produced a sustained reduction in IOP for 5 days with once-daily doses. The 0.001% concentration of KL produced the greatest magnitude and longest duration of IOP reduction, whereas increasing the concentration to 0.01% caused a similar or lesser response, indicating that KL in a concentration of 0.001% is near or at the top of the dose–response curve.

In a comparison study, we showed that treatment with 0.001% KL produced an equivalent and, at some measured time points, a slightly greater reduction in IOP when compared with 0.005% latanoprost. Thus, KL at 0.001% appeared somewhat more potent (approximately fivefold by dose ratio) than latanoprost in the 0.001% to 0.005% dose range. To confirm the effect on IOP, we used KL from two different sources, prepared in the same vehicle but tested in separate groups of glaucomatous monkey eyes. The result indicated that the effect on IOP of KL-A and -B at the 0.001% dose was equivalent, with similar (P > 0.05) maximum IOP reductions of 15% to 20%.

To try to determine the mechanism of the KL response, we investigated the effect of 0.005% KL on aqueous humor dynamics in normal monkey eyes. Neither tonographic outflow facility nor aqueous humor flow rates were significantly altered in normal monkey eyes treated with 0.005% KL. Assuming that episcleral venous pressure is unchanged and pseudofacility is ignored, the primary mechanism through which KL lowers IOP appeared to be by an increase in uveoscleral outflow.

Similar to KL, the ocular hypotensive drug isopropyl unoprostone is a 15-keto PGF2{alpha} analog. It has been directly compared with latanoprost21 in the same monkey protocols as were used in the present study, with similar results. The agonist activity of isopropyl unoprostone at FP receptors is reportedly the weakest among the ocular hypotensive PG drugs,6 and in one study no FP receptor affinity was found.3 However, it has effects on ion channels and cellular Ca fluxes22 that may not be FP receptor linked. These include activation of Ca-activated potassium channels (maxi-K+ channel)23 24 and blockade of Ca-release–activated Ca flux in trabecular meshwork cells.25 Thus, it is possible that 13,14-dihydro-15-keto PGF2 analogs, such as isopropyl unoprostone and KL, lower IOP by different receptor mechanisms than does latanoprost.

In conclusion, 15-keto prostaglandin analogs that may be endogenously produced from an administered 15-hydroxy analog have the potential to contribute to the ocular hypotensive response and independently may have potential for the direct treatment of glaucoma.


   Footnotes
 
Supported in part by National Eye Institute Grant EY01867 and an unrestricted grant from Research to Prevent Blindness, Inc.

Submitted for publication January 11, 2007; revised April 27 and May 15, 2007; accepted July 9, 2007.

Disclosure: R.-F. Wang, None; D.J. Gagliuso, None; T.W. Mittag, None; S.M. Podos, R-Tech (F)

The publication costs of this article were defrayed in part by page charge payment. This article must therefore be marked "advertisement" in accordance with 18 U.S.C. §1734 solely to indicate this fact.

Corresponding author: Rong-Fang Wang, Box 1183, Mount Sinai School of Medicine, One Gustave L. Levy Place, New York, NY 10029; rong-fang.wang{at}mssm.edu.


   References
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 Abstract
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 References
 

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