Fentiman Katelyn E, Rankin Amy J, Meekins Jessica M, Roush James K
Am J Vet Res. 2019 May;80(5):498-504. doi: 10.2460/ajvr.80.5.498.
To determine the effect of topical ophthalmic administration of 0.005% latanoprost solution on aqueous humor flow rate (AHFR) and intraocular pressure (IOP) in ophthalmologically normal dogs.
12 adult Beagles.
In a masked crossover design involving two 10-day experimental periods separated by a 7-day washout period, dogs were randomly assigned to first receive latanoprost or artificial tears (control) solution and then the opposite treatment in the later experimental period. Each experimental period was divided into a baseline phase (days 1 to 3), baseline fluorophotometry assessment (day 4), treatment phase (1 drop of latanoprost or artificial tears solution administered twice daily in each eye on days 5 to 9 and once on day 10), and posttreatment fluorophotometry assessment (day 10). Measured fluorescein concentrations were used to calculate baseline and posttreatment AHFRs. The IOP was measured 5 times/d in each eye during baseline and treatment (days 5 to 9) phases.
Mean baseline and posttreatment AHFR values did not differ significantly in either experimental period (latanoprost or control). In the latanoprost period, mean IOP was significantly lower during treatment than at baseline; there was no difference in corresponding IOP values during the control period. In the latanoprost period, mean IOP was significantly higher on the first day of treatment than on subsequent treatment days.
In ophthalmologically normal dogs, topical ophthalmic administration of 0.005% latanoprost solution significantly decreased IOP but did not affect AHFR. Thus, the ocular hypotensive effect of latanoprost did not appear to have been caused by a reduction in aqueous humor production. ( 2019;80:498-504).
确定局部眼用0.005%拉坦前列素溶液对眼科正常犬房水流量(AHFR)和眼压(IOP)的影响。
12只成年比格犬。
采用双盲交叉设计,包括两个为期10天的实验期,中间间隔7天的洗脱期。犬被随机分配,先接受拉坦前列素或人工泪液(对照)溶液,然后在随后的实验期接受相反的治疗。每个实验期分为基线期(第1至3天)、基线荧光光度法评估期(第4天)、治疗期(第5至9天每天每眼滴注1滴拉坦前列素或人工泪液溶液,第10天滴注1次)和治疗后荧光光度法评估期(第10天)。测量的荧光素浓度用于计算基线和治疗后的AHFR。在基线期和治疗期(第5至9天),每只眼睛每天测量5次IOP。
在两个实验期(拉坦前列素或对照)中,平均基线和治疗后的AHFR值均无显著差异。在拉坦前列素期,治疗期间的平均IOP显著低于基线;对照期相应的IOP值无差异。在拉坦前列素期,治疗第一天的平均IOP显著高于随后的治疗日。
在眼科正常犬中,局部眼用0.005%拉坦前列素溶液可显著降低IOP,但不影响AHFR。因此,拉坦前列素的降眼压作用似乎不是由房水生成减少引起的。(2019;80:498 - 504)