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发现用于治疗青光眼的新型抑制剂。

Discovery of novel inhibitors for the treatment of glaucoma.

作者信息

Cholkar Kishore, Trinh Hoang M, Pal Dhananjay, Mitra Ashim K

机构信息

University of Missouri-Kansas City, School of Pharmacy, Division of Pharmaceutical Sciences , 5258 Health Science Building, 2464 Charlotte Street, Kansas City, MO 64108-2718 , USA +1 816 235 1615 ; +1 816 235 5779 ;

出版信息

Expert Opin Drug Discov. 2015 Mar;10(3):293-313. doi: 10.1517/17460441.2015.1000857. Epub 2015 Jan 9.

DOI:10.1517/17460441.2015.1000857
PMID:25575654
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4589152/
Abstract

INTRODUCTION

Glaucoma is a neurodegenerative disease with heterogeneous causes that result in retinal ganglionic cell (RGC) death. The discovery of ocular antihypertensives has shifted glaucoma therapy, largely, from surgery to medical intervention. Indeed, several intraocular pressure (IOP)-lowering drugs, with different mechanisms of action and RGC protective property, have been developed.

AREAS COVERED

In this review, the authors discuss the main new class of kinase inhibitors used as glaucoma treatments, which lower IOP by enhancing drainage and/or lowering production of aqueous humor. The authors include novel inhibitors under preclinical evaluation and investigation for their anti-glaucoma treatment. Additionally, the authors look at treatments that are in clinics now and which may be available in the near future.

EXPERT OPINION

Treatment of glaucoma remains challenging because the exact cause is yet to be delineated. Neuroprotection to the optic nerve head is undisputable. The novel Rho-associated kinase inhibitors have the capacity to lower IOP and provide optic nerve and RGC protection. In particular, the S-isomer of roscovitine has the capacity to lower IOP and provide neuroprotection. Combinations of selected drugs, which can provide maximal and sustained IOP-lowering effects as well as neuroprotection, are paramount to the prevention of glaucoma progression. In the near future, microRNA intervention may be considered as a potential therapeutic target.

摘要

引言

青光眼是一种病因多样的神经退行性疾病,可导致视网膜神经节细胞(RGC)死亡。眼用降压药的发现极大地改变了青光眼的治疗方式,从手术治疗转向了药物干预。事实上,已经开发出了几种作用机制不同且具有RGC保护特性的降低眼压(IOP)的药物。

涵盖领域

在本综述中,作者讨论了用作青光眼治疗的主要新型激酶抑制剂类别,这些抑制剂通过增强房水引流和/或降低房水生成来降低眼压。作者纳入了正在进行临床前评估和研究以用于抗青光眼治疗的新型抑制剂。此外,作者还探讨了目前正在临床应用以及可能在不久的将来可用的治疗方法。

专家观点

青光眼的治疗仍然具有挑战性,因为确切病因尚未明确。对视神经乳头的神经保护作用是无可争议的。新型Rho相关激酶抑制剂有降低眼压并对视神经和RGC提供保护的能力。特别是,罗斯考维汀的S-异构体有降低眼压并提供神经保护的能力。选择能够提供最大且持续的眼压降低效果以及神经保护作用的药物组合,对于预防青光眼进展至关重要。在不久的将来,微小RNA干预可能被视为一种潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6270/4589152/14f6b437ec41/nihms722996f8.jpg
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