Bito L Z
College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.
Surv Ophthalmol. 1997 Feb;41 Suppl 2:S1-14. doi: 10.1016/s0039-6257(97)80002-1.
This introductory overview considers the advantages of a class of local hormones-the prostaglandins (PGs)-for the management of intraocular pressure (IOP) in glaucoma, over agonists and antagonists of neurotransmitters that dominated this field in the 20th century. PGs and PG analogues, in particular esterified prodrug forms of PGF2 alpha, are effective ocular hypotensive agents, but cause some conjunctival hyperemia and corneal sensory irritation at higher concentrations. Based on structure-activity studies, a 17-phenyl PGF2 alpha prodrug, latanoprost (PhXA41), was found to have a greatly improved therapeutic index, without compromising the ocular hypotensive potency of PGF2 alpha prodrugs. The IOP lowering mechanism of such PGF2 alpha s, increased uveoscleral outflow, can be expected to have great physiologic advantages, especially with respect to normal tension glaucoma, over most currently used ocular hypotensive drugs. The introduction of this new approach has already led to a new insight into the control and clinical significance of this outflow route. Similarly, the newly discovered ocular side effect, PG-induced increase in iridial pigmentation, can be expected to provide insight into the oculo-protective role of iridial melanocytes and into the punative association between a decline in the ocular melanin system and the vulnerability of the eye to some age-related diseases.
本介绍性概述探讨了一类局部激素——前列腺素(PGs)——在青光眼眼压(IOP)管理方面相对于20世纪主导该领域的神经递质激动剂和拮抗剂的优势。PGs及其类似物,特别是PGF2α的酯化前药形式,是有效的降眼压药物,但在较高浓度时会引起一些结膜充血和角膜感觉刺激。基于构效关系研究,发现一种17-苯基PGF2α前药拉坦前列素(PhXA41)具有大大改善的治疗指数,同时不损害PGF2α前药的降眼压效力。这种PGF2α降低眼压的机制是增加葡萄膜巩膜外流,与目前大多数使用的降眼压药物相比,预计在生理方面具有很大优势,尤其是对于正常眼压性青光眼。这种新方法的引入已经为这条外流途径的控制和临床意义带来了新的见解。同样,新发现的眼部副作用,即PG诱导的虹膜色素沉着增加,有望为虹膜黑素细胞的眼保护作用以及眼部黑素系统下降与眼睛对某些年龄相关性疾病的易感性之间的惩罚性关联提供见解。