Linsenmeier Robert A, Zhang Hao F
Biomedical Engineering Department, Northwestern University, 2145 Sheridan Road, Evanston 60208-3107, IL, USA; Neurobiology Department, Northwestern University, 2205 Tech Drive, Evanston 60208-3520, IL, USA; Ophthalmology Department, Northwestern University, 645 N. Michigan Ave, Suite 440, Chicago 60611, IL, USA.
Biomedical Engineering Department, Northwestern University, 2145 Sheridan Road, Evanston 60208-3107, IL, USA; Ophthalmology Department, Northwestern University, 645 N. Michigan Ave, Suite 440, Chicago 60611, IL, USA.
Prog Retin Eye Res. 2017 May;58:115-151. doi: 10.1016/j.preteyeres.2017.01.003. Epub 2017 Jan 18.
This article discusses retinal oxygenation and retinal metabolism by focusing on measurements made with two of the principal methods used to study O in the retina: measurements of PO with oxygen-sensitive microelectrodes in vivo in animals with a retinal circulation similar to that of humans, and oximetry, which can be used non-invasively in both animals and humans to measure O concentration in retinal vessels. Microelectrodes uniquely have high spatial resolution, allowing the mapping of PO in detail, and when combined with mathematical models of diffusion and consumption, they provide information about retinal metabolism. Mathematical models, grounded in experiments, can also be used to simulate situations that are not amenable to experimental study. New methods of oximetry, particularly photoacoustic ophthalmoscopy and visible light optical coherence tomography, provide depth-resolved methods that can separate signals from blood vessels and surrounding tissues, and can be combined with blood flow measures to determine metabolic rate. We discuss the effects on retinal oxygenation of illumination, hypoxia and hyperoxia, and describe retinal oxygenation in diabetes, retinal detachment, arterial occlusion, and macular degeneration. We explain how the metabolic measurements obtained from microelectrodes and imaging are different, and how they need to be brought together in the future. Finally, we argue for revisiting the clinical use of hyperoxia in ophthalmology, particularly in retinal arterial occlusions and retinal detachment, based on animal research and diffusion theory.
本文通过聚焦于两种用于研究视网膜中氧的主要方法所进行的测量,来探讨视网膜氧合作用和视网膜代谢:在具有与人类相似视网膜循环的动物体内,使用氧敏感微电极测量氧分压(PO);以及血氧测定法,该方法可在动物和人类中无创地测量视网膜血管中的氧浓度。微电极具有独特的高空间分辨率,能够详细绘制氧分压图,并且当与扩散和消耗的数学模型相结合时,它们可提供有关视网膜代谢的信息。基于实验的数学模型也可用于模拟不适于实验研究的情况。血氧测定的新方法,特别是光声眼科检查和可见光光学相干断层扫描,提供了深度分辨方法,能够分离来自血管和周围组织的信号,并且可以与血流测量相结合以确定代谢率。我们讨论了光照、缺氧和高氧对视网膜氧合的影响,并描述了糖尿病、视网膜脱离、动脉阻塞和黄斑变性中的视网膜氧合情况。我们解释了从微电极和成像获得的代谢测量结果有何不同,以及它们未来需要如何整合。最后,基于动物研究和扩散理论,我们主张重新审视高氧在眼科临床中的应用,特别是在视网膜动脉阻塞和视网膜脱离方面。