Kim Jee Hyun, Kim Eun Joo, Kim Yeoun-Hee, Kim Yong Il, Lee Se-Hyung, Jung Jae-Chang, Lee Kyoo Won, Park Young Jeung
Cheil Eye Research Institute, Cheil Eye Hospital, Daegu, Korea.
Developmental Biology Laboratory, Department of Biology, College of Natural Sciences, Kyungpook National University, Daegu, Korea.
Korean J Ophthalmol. 2015 Aug;29(4):270-9. doi: 10.3341/kjo.2015.29.4.270. Epub 2015 Jul 21.
Chronic use of topical hypotensive agents induces several side effects caused by preservatives. The purpose of this study was to evaluate the effects of prostaglandin analogs with varying concentrations of benzalkonium chloride (BAC), preservative-free (PF), and alternative preservatives on mouse corneal tissue.
Thirty-five, 8- to 10-week-old female C57BL/6 mice (five mice for each group) were used for this study. To the control group, we applied normal saline, and to each drug-treated group we applied 0.02% BAC, bimatoprost 0.01% (with BAC 0.02%), latanoprost 0.005% (with BAC 0.02%), travoprost 0.004% (with 0.001% polyquad) or tafluprost 0.0015% with/without 0.001% BAC, once a day (9 p.m.) for 4 weeks. Corneal fluorescein staining was evaluated in all groups. After harvest, the corneal tissues were embedded in paraffin and then Hematoxylin-Eosin stain was performed for histopathological examination. Immunofluorescence staining was done against TNF-α, IL-6, HLA DR, pJNK, and pAkt.
In corneal fluorescein staining, severe punctate epithelial keratitis was seen in the groups of 0.02% BAC, 0.02% BAC containing bimatoprost 0.01% and latanoprost 0.005%. The surface desquamation, irregular surface, loss of cell borders, anisocytosis and stromal shrinkage were observed in the groups of BAC-containing eye drops. Moreover, the groups treated with BAC-containing eye drops have high inflammatory markers, significantly decreased cell viability-related signal, pAkt, and higher apoptosis-inducing signal, pJNK, than the control group. On the other hand, travoprost 0.004% and PF tafluprost 0.0015% have less cellular morphologic changes, lower inflammation, and higher cellular viability than BAC-containing formulations.
Corneal damage, increased inflammation and apoptosis and low cell viability were observed in BAC-containing groups. PF or alternatively preserved glaucoma medications seem to be a reasonable and viable alternative to those preserved with BAC.
长期使用局部降压药物会引发由防腐剂导致的多种副作用。本研究旨在评估不同浓度苯扎氯铵(BAC)、无防腐剂(PF)以及替代防腐剂的前列腺素类似物对小鼠角膜组织的影响。
本研究使用了35只8至10周龄的雌性C57BL/6小鼠(每组5只)。给对照组应用生理盐水,给每个药物治疗组分别应用0.02% BAC、0.01%比马前列素(含0.02% BAC)、0.005%拉坦前列素(含0.02% BAC)、0.004%曲伏前列素(含0.001%聚季铵盐)或0.0015%他氟前列素(含/不含0.001% BAC),每天晚上9点给药一次,持续给药4周。对所有组进行角膜荧光素染色评估。取材后,将角膜组织包埋于石蜡中,然后进行苏木精-伊红染色以进行组织病理学检查。针对肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)、人类白细胞抗原DR(HLA DR)、磷酸化c-Jun氨基末端激酶(pJNK)和磷酸化蛋白激酶B(pAkt)进行免疫荧光染色。
在角膜荧光素染色中,0.02% BAC组、含0.01%比马前列素的0.02% BAC组和含0.005%拉坦前列素的0.02% BAC组可见严重的点状上皮角膜炎。在含BAC的滴眼液组中观察到表面脱屑、表面不规则、细胞边界丧失、细胞大小不均和基质收缩。此外,与对照组相比,含BAC的滴眼液治疗组具有较高的炎症标志物、与细胞活力相关的信号pAkt显著降低以及较高的凋亡诱导信号pJNK。另一方面,0.004%曲伏前列素组和无防腐剂的0.0015%他氟前列素组比含BAC的制剂具有更少的细胞形态学变化、更低的炎症反应和更高的细胞活力。
在含BAC的组中观察到角膜损伤、炎症增加、凋亡以及细胞活力降低。无防腐剂或采用替代防腐剂的青光眼药物似乎是含BAC防腐剂药物的合理且可行的替代品。