Faculty of Veterinary Medicine, Clinical Institute,Latvia University of Life Sciences and Technologies, Jelgava, Latvia.
Open Vet J. 2020 Apr;10(1):59-67. doi: 10.4314/ovj.v10i1.10. Epub 2020 Mar 14.
Cyclopentolate is not commonly used as mydriatic drug in veterinary medicine because of limited data on the local and systemic effects in animals.
To determine the effects of topical 1% cyclopentolate hydrochloride on intraocular pressure (IOP), horizontal pupil diameter (HPD) and tear production in the cat and rabbit's eye during the first hour and up to 36 hours after treatment.
One drop of 1% cyclopentolate hydrochloride was used in the left eye in 10 clinically and ophthalmologically healthy domestic cats and 10 rabbits. IOP and HPD were recorded every 5 minutes during the first hour, then every 2 hours during the following 12-hour period, and at 24 and 36 hours after application. Schirmer tear test (STT) was measured at 30 and 60 minute after treatment, then in same time points as IOP and HPD. Rebound tonometer (TonoVet) was used to assess IOP, Jameson calliper to measure HPD and STT to determine the tear production.
1% cyclopentolate increased IOP in cats, reaching a maximum (28.1 ± 5.4 mmHg) at and in rabbits at T (16.7 ± 1.3 mmHg). Maximal mydriasis in cats was observed at and lasted 24-36 hours, but in rabbits at , and returned to pre-treatment values at -. In cats, STT decreased in both eyes 30 minutes after treatment and remained lower throughout the 36-hour period. In rabbits, STT decreased in the treated eye 30 minutes after treatment, but all following STT measurements returned to normal pre-treatment levels.
Study showed novel data about the effects of 1% cyclopentolate to IOP, HPD, STT in cats and rabbits. Cyclopentolate in cats caused mydriasis 20-40 minutes after the treatment by increasing IOP, at the same time, pupil diameter reached pre-treatment values 24-36 hours after treatment. In rabbit's mydriasis occurred faster, 10-25 minutes after treatment without significant IOP increase and mydriasis lasted 10-12 hours. Significant STT decrease was recorded in cats, but more likely were connected to stress factors. This drug could be considered as a therapeutical alternative in rabbit more than in cats.
由于环戊醇在动物中的局部和全身作用数据有限,因此在兽医医学中不常将其用作散瞳药物。
确定 1%盐酸环戊醇滴眼剂在猫和兔眼的眼内压(IOP)、水平瞳孔直径(HPD)和泪液产生方面的影响,在治疗后的第一小时内直至 36 小时。
在 10 只临床和眼科健康的家猫和 10 只兔子的左眼滴用 1%环戊醇盐酸盐滴眼剂 1 滴。在最初的 1 小时内,每 5 分钟记录一次 IOP 和 HPD,然后在接下来的 12 小时内每 2 小时记录一次,在应用后 24 和 36 小时记录一次。在治疗后 30 和 60 分钟测量 Schirmer 泪液测试(STT),然后在与 IOP 和 HPD 相同的时间点测量。使用回弹眼压计(TonoVet)评估 IOP,使用 Jameson 卡尺测量 HPD,使用 STT 确定泪液产生。
1%环戊醇增加了猫的眼压,在 T 时达到最大值(28.1 ± 5.4mmHg),在兔中达到 T 时达到最大值(16.7 ± 1.3mmHg)。猫的最大散瞳作用发生在 ,持续 24-36 小时,但在兔中发生在 ,并在-时恢复到治疗前的数值。在猫中,治疗后 30 分钟双眼的 STT 下降,并且在 36 小时的过程中一直保持较低水平。在兔中,治疗后 30 分钟时治疗眼的 STT 下降,但随后的所有 STT 测量值均恢复到正常的治疗前水平。
本研究提供了有关 1%环戊醇对猫和兔的 IOP、HPD、STT 的影响的新数据。在猫中,环戊醇在治疗后 20-40 分钟内通过增加 IOP 引起散瞳,同时瞳孔直径在治疗后 24-36 小时达到治疗前的数值。在兔中,散瞳作用发生得更快,在治疗后 10-25 分钟内发生,而眼压无明显增加,散瞳作用持续 10-12 小时。在猫中记录到 STT 明显下降,但更可能与应激因素有关。与猫相比,这种药物在兔中更可被视为治疗选择。