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Soluble Epoxide Hydrolase Inhibition for Ocular Diseases: Vision for the Future

机译:眼疾病的可溶性环氧水解酶抑制作用:未来愿景

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Ocular diseases cause visual impairment and blindness, imposing a devastating impact on quality of life and a substantial societal economic burden. Many such diseases lack universally effective pharmacotherapies. Therefore, understanding the mediators involved in their pathophysiology is necessary for the development of therapeutic strategies. To this end, the hydrolase activity of soluble epoxide hydrolase (sEH) has been explored in the context of several eye diseases, due to its implications in vascular diseases through metabolism of bioactive epoxygenated fatty acids. In this mini-review, we discuss the mounting evidence associating sEH with ocular diseases and its therapeutic value as a target. Substantial data link sEH with the retinal and choroidal neovascularization underlying diseases such as wet age-related macular degeneration, retinopathy of prematurity, and proliferative diabetic retinopathy, although some conflicting results pose challenges for the synthesis of a common mechanism. sEH also shows therapeutic relevance in non-proliferative diabetic retinopathy and diabetic keratopathy, and sEH inhibition has been tested in a uveitis model. Various approaches have been implemented to assess sEH function in the eye, including expression analyses, genetic manipulation, pharmacological targeting of sEH, and modulation of certain lipid metabolites that are upstream and downstream of sEH. On balance, sEH inhibition shows considerable promise for treating multiple eye diseases. The possibility of local delivery of inhibitors makes the eye an appealing target for future sEH drug development initiatives.
机译:眼部疾病导致视力障碍和失明,对生活质量和社会经济负担造成毁灭性影响。许多此类疾病缺乏普遍有效的药物治疗方法。因此,了解参与其病理生理的介体对于制定治疗策略是必要的。为此,在几种眼部疾病的背景下,已经探索了可溶性环氧化物水解酶(sEH)的水解酶活性,这是由于其通过生物活性环氧脂肪酸的代谢而对血管疾病有影响。在本微型综述中,我们讨论了将sEH与眼部疾病相关联的越来越多的证据及其作为靶标的治疗价值。大量数据将sEH与视网膜疾病和脉络膜新生血管形成相关的疾病(例如与年龄相关的黄斑湿性变性,早产儿视网膜病变和增生性糖尿病性视网膜病变)相关的疾病,尽管某些矛盾的结果对合成通用机制提出了挑战。 sEH在非增生性糖尿病性视网膜病和糖尿病性角膜病变中也显示出治疗意义,并且在葡萄膜炎模型中已测试了sEH抑制作用。已经实施了各种方法来评估眼睛中sEH的功能,包括表达分析,遗传操作,sEH的药理靶向以及对sEH上游和下游某些脂质代谢产物的调节。总体而言,抑制sEH显示出治疗多种眼部疾病的巨大希望。局部递送抑制剂的可能性使眼睛成为未来sEH药物开发计划的诱人目标。

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