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首页> 外文期刊>Journal of ocular pharmacology and therapeutics: The official journal of the Association for Ocular Pharmacology and Therapeutics >Effect of topical olopatadine and epinastine in the botulinum toxin B-induced mouse model of dry eye.
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Effect of topical olopatadine and epinastine in the botulinum toxin B-induced mouse model of dry eye.

机译:局部用奥洛他定和淫羊tine碱在肉毒杆菌毒素B引起的干眼小鼠模型中的作用。

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PURPOSE: The aim of this study was to compare the effect of topical olopatadine, epinastine, and lubricant eye drops on dry eye ocular surface disease in the botulinum toxin B (BTX-B)-induced mouse model of keratoconjunctivitis sicca. METHODS: CBA/J mice were randomized into 3 experimental groups of 10 animals each. All mice received a transconjunctival injection of 0.05 mL of 20-mU BTX-B solutions into the left lacrimal gland. Three (3) days after intralacrimal gland injections, each group received treatment with twice-daily topical lubricant as a control, 0.1% olopatadine, or 0.05% epinastine eye drops. To monitor the progression of dry eye tear production, an ocular surface fluorescein staining score was evaluated in each of the 3 experimental groups. RESULTS: Three (3) days after the intralacrimal gland injection of BTX-B, aqueous tear production was significantly decreased (1.95+/-0.64 mm), compared to baseline level (2.69+/-0.66 mm; P<0.001). Similarly, there was a statistically significant increase in the proportion of mice with a corneal staining score of 2 or greater at 3 days postinjection, compared to the preinjection value (P<0.001). There were no statistically significant differences in aqueous tear production between the 3 different medication groups at all time points. Aqueous tear production in neither the olopatadine nor the epinastine-challenged groups was further decreased compared to the lubricant-treated group. Difference in the proportion of mice with a low- and high corneal staining score between the control and study groups did not reach statistical significance throughout the 4-week experimental period. In addition, changes in corneal fluorescein staining of the olopatadine group versus the epinastine group did not show a statistically significant difference. CONCLUSIONS: Topical olopatadine and epinastine do not cause significantly additional damage to the compromised ocular surface secondary to dry eye after continuous 4-week, twice-daily application. Topical olopatadine andepinastine appear to have comparable effects on aqueous tear-production and corneal-surface changes in this mouse model.
机译:目的:本研究的目的是比较肉毒杆菌毒素B(BTX-B)引起的干燥性角膜结膜炎小鼠模型中局部用奥洛他定,表皮碱和润滑性滴眼液对干眼眼表面疾病的影响。方法:将CBA / J小鼠随机分为3组,每组10只。所有小鼠均接受了结膜腔注射,将0.05 mL 20 mU BTX-B溶液注入左泪腺。泪腺内注射后三(3)天,每组均接受每日两次局部润滑剂作为对照,0.1%的奥洛他定或0.05%的淫羊tine滴眼液治疗。为了监测干眼泪产生的进程,在3个实验组的每一个中评估了眼表荧光素染色评分。结果:在泪腺内注射BTX-B后三(3)天,与基准水平(2.69 +/- 0.66 mm; P <0.001)相比,泪液产生明显减少(1.95 +/- 0.64 mm)。类似地,与注射前的值相比,注射后3天角膜染色评分为2或更高的小鼠比例有统计学上的显着增加(P <0.001)。在所有时间点上,三个不同药物组之间的泪液产生量在统计学上均无统计学差异。与润滑剂治疗组相比,奥洛他定和受氯霉素治疗的组的泪液产生均没有进一步降低。在整个4周的实验期间,对照组和研究组之间角膜染色评分低和高的小鼠比例的差异没有达到统计学意义。此外,奥洛他定组与依那西汀组的角膜荧光素染色变化未显示统计学上的显着差异。结论:连续4周,每天2次应用后,外用的olopatadine和epinastine不会对继发于干眼的受损眼表造成明显的额外损害。在该小鼠模型中,局部用奥洛他定和依哌那汀对水性泪液产生和角膜表面变化具有类似的作用。

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