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四种前列腺素类似物制剂对眼表细胞的影响。一项比较研究。

Effects of Four Formulations of Prostaglandin Analogs on Eye Surface Cells. A Comparative Study.

作者信息

Pérez-Roca Fernando, Rodrigo-Morales Esther, Garzón Ingrid, Oliveira Ana-Celeste, Martín-Piedra Miguel-Ángel, Carriel Víctor, Ortiz-Pérez Ana-Isabel, Sánchez-Montesinos Indalecio, Campos Antonio, Alaminos Miguel

机构信息

Hospital General Básico de Baza, E18800, Granada, Spain; PhD Program in Biomedicine, University of Granada, 18012, Granada, Spain.

Hospital La Inmaculada, Huércal Overa, 04600, Almería, Spain.

出版信息

PLoS One. 2015 Jun 12;10(6):e0129419. doi: 10.1371/journal.pone.0129419. eCollection 2015.

Abstract

We evaluated the cytotoxic effects of four prostaglandin analogs (PGAs) used to treat glaucoma. First we established primary cultures of conjunctival stromal cells from healthy donors. Then cell cultures were incubated with different concentrations (0, 0.1, 1, 5, 25, 50 and 100%) of commercial formulations of bimatoprost, tafluprost, travoprost and latanoprost for increasing periods (5 and 30 min, 1 h, 6 h and 24 h) and cell survival was assessed with three different methods: WST-1, MTT and calcein/AM-ethidium homodimer-1 assays. Our results showed that all PGAs were associated with a certain level of cell damage, which correlated significantly with the concentration of PGA used, and to a lesser extent with culture time. Tafluprost tended to be less toxic than bimatoprost, travoprost and latanoprost after all culture periods. The results for WST-1, MTT and calcein/AM-ethidium homodimer-1 correlated closely. When the average lethal dose 50 was calculated, we found that the most cytotoxic drug was latanoprost, whereas tafluprost was the most sparing of the ocular surface in vitro. These results indicate the need to design novel PGAs with high effectiveness but free from the cytotoxic effects that we found, or at least to obtain drugs that are functional at low dosages. The fact that the commercial formulation of tafluprost used in this work was preservative-free may support the current tendency to eliminate preservatives from eye drops for clinical use.

摘要

我们评估了四种用于治疗青光眼的前列腺素类似物(PGA)的细胞毒性作用。首先,我们从健康供体建立了结膜基质细胞的原代培养物。然后,将细胞培养物与不同浓度(0、0.1、1、5、25、50和100%)的比马前列素、他氟前列素、曲伏前列素和拉坦前列素商业制剂孵育不同时间(5和30分钟、1小时、6小时和24小时),并用三种不同方法评估细胞存活率:WST-1、MTT和钙黄绿素/AM-溴化乙锭同二聚体-1检测。我们的结果表明,所有PGA都与一定程度的细胞损伤有关,这与所用PGA的浓度显著相关,在较小程度上与培养时间有关。在所有培养期后,他氟前列素的毒性往往比比马前列素、曲伏前列素和拉坦前列素小。WST-1、MTT和钙黄绿素/AM-溴化乙锭同二聚体-1的结果密切相关。当计算平均致死剂量50时,我们发现细胞毒性最大的药物是拉坦前列素,而他氟前列素在体外对眼表的损伤最小。这些结果表明,需要设计出具有高效性但无我们所发现的细胞毒性作用的新型PGA,或者至少获得低剂量时仍有功能的药物。本研究中使用的他氟前列素商业制剂不含防腐剂这一事实,可能支持了目前从临床用滴眼液中去除防腐剂的趋势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23f3/4466352/5419add67b36/pone.0129419.g001.jpg

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