Moschos Marilita M, Moustafa Giannis A, Papakonstantinou Vasiliki D, Tsatsos Michael, Laios Konstantinos, Antonopoulou Smaragdi
1st Department of Ophthalmology, Medical School, University of Athens, Athens, Greece.
Biomedical Research Foundation, Academy of Athens, Athens, Greece.
Drug Des Devel Ther. 2017 Apr 19;11:1267-1272. doi: 10.2147/DDDT.S131582. eCollection 2017.
Altered platelet aggregability has been implicated in the pathogenesis of glaucoma. This study aims to investigate the anti-platelet potential of intraocular pressure lowering drops, with the possibility of establishing it as an additional mechanism of anti-glaucomatous action.
The anti-aggregating effects of a series of anti-glaucomatous eye drops were determined on human platelets in the platelet aggregation model, using four known aggregating factors (platelet activating factor [PAF], adenosine diphosphate [ADP], thrombin receptor-activating peptide [TRAP], and arachidonic acid [AA]).
Almost all of the tested samples inhibited platelet aggregation induced by PAF, ADP, TRAP, and AA, except for Alphagan, which did not demonstrate inhibition of ADP- and TRAP-induced aggregation at a wide range of concentrations. Trusopt, Betoptic, and Azarga eye drops were the most potent inhibitors of all four aggregating factors, while Alphagan was the least potent (<0.05).
This study shows that anti-glaucomatous eye drops possess anti-platelet effects, and this was shown for the first time by experimenting on human platelets.
血小板聚集性改变与青光眼的发病机制有关。本研究旨在探讨降眼压滴眼液的抗血小板潜力,有可能将其确立为抗青光眼作用的另一种机制。
在血小板聚集模型中,使用四种已知的聚集因子(血小板活化因子[PAF]、二磷酸腺苷[ADP]、凝血酶受体激活肽[TRAP]和花生四烯酸[AA]),测定一系列抗青光眼滴眼液对人血小板的抗聚集作用。
几乎所有测试样品均能抑制PAF、ADP、TRAP和AA诱导的血小板聚集,但阿法根(Alphagan)除外,在广泛的浓度范围内,它并未显示出对ADP和TRAP诱导的聚集的抑制作用。曲伏前列素(Trusopt)、倍他洛尔(Betoptic)和阿扎根(Azarga)滴眼液是所有四种聚集因子的最有效抑制剂,而阿法根的效力最低(<0.05)。
本研究表明,抗青光眼滴眼液具有抗血小板作用,这是首次通过对人血小板进行实验得到的结果。