Wulff Katharina, Foster Russell G
University of Oxford, Sleep and Circadian Neuroscience Institute, Sir William Dunn School of Pathology (OMPI), South Parks Road, Oxford, OX1 3RE. United Kingdom.
Sleep and Circadian Neuroscience Institute (SCNi), Nuffield Laboratory of Ophthalmology, University of Oxford, Oxford, OX1 3RE. United Kingdom.
Curr Alzheimer Res. 2017;14(10):1022-1029. doi: 10.2174/1567205014666170523095231.
Light exerts influences on many physiological and behavioural functions in humans. These functions can be described as image-forming (IF) and non-image forming (NIF) visual processes, both originating in the retina of the eye. Image-forming refers to vision; the process of detecting and distinguishing shapes and colour of objects. Non-image forming refers to detecting level of light intensity or brightness of ambient space, which affects basal physiology such as cycles of rest and activity or the endocrine system. Rod and cone photoreceptors in the outer retinal layer are most important for imageforming vision, while non-image forming functions depend upon additional input from the photopigment melanopsin, which is expressed in retinal ganglion cells (RGC) that makes these cells photosensitive (pRGC). Projections of these pRGCs convey light-induced electrical impulses to a number of brain regions. Visual acuity and colour contrast naturally diminishes with age but dementia often has major effects on the visual processing systems, which impact on the quality of life. The ability of humans to manipulate their light exposure has the immediate potential to either create problems with human physiology (as in shift workers) or to compensate physiological disadvantages (of IF and NIF visual impairment). This mini-review describes the impact of aging on the function of the eye with respect to nonimage forming effects of light, summarises light intervention studies for sleep and neuropsychiatric symptoms and considers implications from photoreceptor-weighted light intensities for biologically effective light intervention and lighting solutions for patients with dementia.
光对人类的许多生理和行为功能都有影响。这些功能可被描述为成像(IF)和非成像(NIF)视觉过程,二者均起源于眼睛的视网膜。成像指的是视觉,即检测和区分物体形状与颜色的过程。非成像则指检测环境空间的光强度或亮度水平,这会影响诸如休息和活动周期或内分泌系统等基础生理功能。视网膜外层的视杆和视锥光感受器对成像视觉最为重要,而非成像功能则依赖于视色素黑素视蛋白的额外输入,黑素视蛋白在视网膜神经节细胞(RGC)中表达,使这些细胞具有光敏感性(pRGC)。这些pRGC的投射将光诱导的电冲动传递到多个脑区。视力和颜色对比度会随着年龄的增长自然下降,但痴呆症通常会对视觉处理系统产生重大影响,进而影响生活质量。人类控制自身光照暴露的能力有可能立即引发人体生理问题(如轮班工作者),也有可能弥补生理缺陷(成像和非成像视觉障碍)。本综述描述了衰老对眼睛功能在光的非成像效应方面的影响,总结了针对睡眠和神经精神症状的光干预研究,并探讨了光感受器加权光强度对生物有效光干预的意义以及为痴呆症患者提供的照明解决方案。