Sakurai M, Araie M, Oshika T, Mori M, Masuda K, Ueno R, Takase M
Department of Ophthalmology, University of Tokyo School of Medicine, Japan.
Jpn J Ophthalmol. 1991;35(2):156-65.
The mechanism underlying the intraocular pressure (IOP) lowering effect of a prostaglandin-related compound, isopropyl 20-ethyl-9 alpha,11 alpha-dihydroxy-15-keto-cis-delta 5-prostanoate (UF-021), and its possible adverse effects in long-term use were studied in normal human eyes. A single instillation of 0.12% UF-021 significantly lowered IOP without affecting aqueous flow rate, tonographic C value or episcleral venous pressure. Protein concentration in the anterior chamber and corneal endothelial permeability to fluorescein remained unaffected. It was suggested that UF-021 lowers IOP mainly by increasing uveoscleral outflow. Twice daily application of 0.12% UF-021 for 4 weeks caused no significant changes in aqueous protein concentration, aqueous flow rate or corneal endothelial permeability. Neither single nor long-term use of topical UF-021 induced irritative responses in the outer segment of the eye. The present study suggests that UF-021 has potential as a safe and effective ocular hypotensive drug with a mechanism of action different from other drugs currently available for the treatment of glaucoma.
在正常人类眼睛中研究了前列腺素相关化合物20-乙基-9α,11α-二羟基-15-酮-顺式-δ5-前列腺酸异丙酯(UF-021)降低眼压(IOP)的作用机制及其长期使用可能产生的不良反应。单次滴注0.12%的UF-021可显著降低眼压,而不影响房水流量、眼压描记C值或巩膜静脉压。前房中的蛋白质浓度和角膜内皮对荧光素的通透性未受影响。提示UF-021主要通过增加葡萄膜巩膜外流来降低眼压。每天两次应用0.12%的UF-021,持续4周,房水蛋白质浓度、房水流量或角膜内皮通透性均无显著变化。局部使用UF-021无论是单次还是长期使用,均未在眼的外段引起刺激性反应。本研究表明,UF-021有潜力成为一种安全有效的降眼压药物,其作用机制与目前用于治疗青光眼的其他药物不同。