Zhou Xiangtian, Pardue Machelle T, Iuvone P Michael, Qu Jia
School of Ophthalmology and Optometry, Eye Hospital, Wenzhou Medical University, 270 Xueyuan Road, Wenzhou, Zhejiang 325003, China; State Key Laboratory of Ophthalmology, Optometry and Vision Science. 270 Xueyuan Road, Wenzhou, Zhejiang, 325003, China.
Department of Biomedical Engineering, Georgia Institute of Technology, 313 Ferst Dr, Atlanta, GA 30332, United States; Center for Visual and Neurocognitive Rehabilitation, Atlanta VA Medical Center, 1670 Clairmont Rd, Decatur, GA 30033, United States.
Prog Retin Eye Res. 2017 Nov;61:60-71. doi: 10.1016/j.preteyeres.2017.06.003. Epub 2017 Jun 7.
In the face of an "epidemic" increase in myopia over the last decades and myopia prevalence predicted to reach 2.5 billion people by the end of this decade, there is an urgent need to develop effective and safe therapeutic interventions to slow down this "myopia booming" and prevent myopia-related complications and vision loss. Dopamine (DA) is an important neurotransmitter in the retina and mediates diverse functions including retina development, visual signaling, and refractive development. Inspired by the convergence of epidemiological and animal studies in support of the inverse relationship between outdoor activity and risk of developing myopia and by the close biological relationship between light exposure and dopamine release/signaling, we felt it is timely and important to critically review the role of DA in myopia development. This review will revisit several key points of evidence for and against DA mediating light control of myopia: 1) the causal role of extracellular retinal DA levels, 2) the mechanism and action of dopamine D1 and D2 receptors and 3) the roles of cellular/circuit retinal pathways. We examine the experiments that show causation by altering DA, DA receptors and visual pathways using pharmacological, transgenic, or visual environment approaches. Furthermore, we critically evaluate the safety issues of a DA-based treatment strategy and some approaches to address these issues. The review identifies the key questions and challenges in translating basic knowledge on DA signaling and myopia from animal studies into effective pharmacological treatments for myopia in children.
在过去几十年中近视呈“流行”式增长,预计到本十年末近视患病率将达到25亿人,因此迫切需要开发有效且安全的治疗干预措施,以减缓这种“近视激增”现象,并预防与近视相关的并发症和视力丧失。多巴胺(DA)是视网膜中的一种重要神经递质,介导多种功能,包括视网膜发育、视觉信号传导和屈光发育。鉴于流行病学和动物研究均支持户外活动与近视发生风险呈负相关,且光照与多巴胺释放/信号传导之间存在密切的生物学关系,我们认为及时且重要的是,批判性地审视多巴胺在近视发展中的作用。本综述将重新审视支持和反对多巴胺介导近视的光控作用的几个关键证据要点:1)细胞外视网膜多巴胺水平的因果作用,2)多巴胺D1和D2受体的机制和作用,以及3)细胞/视网膜回路途径的作用。我们研究了通过药理学、转基因或视觉环境方法改变多巴胺、多巴胺受体和视觉通路来证明因果关系的实验。此外,我们批判性地评估了基于多巴胺的治疗策略的安全性问题以及解决这些问题的一些方法。本综述确定了将动物研究中关于多巴胺信号传导和近视的基础知识转化为儿童近视有效药物治疗的关键问题和挑战。