Goldschleger Eye Research Institute, Tel Aviv University, 53621 Tel Hashomer, Israel.
Exp Eye Res. 2012 Oct;103:33-40. doi: 10.1016/j.exer.2012.08.004. Epub 2012 Aug 21.
Form deprivation and low illuminance of ambient light are known to induce myopia in chicks. Low concentrations of retinal dopamine, a light-driven neurohormone, was previously shown to be associated with form deprivation myopia. In the present study we examined the dependence of retinal dopamine release in chicks on illuminance during light-dark cycles and in continuous light, and the role of retinal dopamine release in illuminance dependent refractive development. Newly hatched chicks (n = 166) were divided into two experimental groups, a dopamine (n = 88) and a refraction group (n = 78). Both groups were further divided into six illumination groups for exposure of chicks to illuminances of 50, 500 or 10,000 lux of incandescent illumination (referred to throughout as low, medium, and high illuminance, respectively), either under a light-dark cycle with lights on between 7 AM and 7 PM or under continuous illumination. For the dopamine experiment, chicks were euthanized and vitreous was extracted on day 14 post-hatching at 7, 8 AM and 1 PM. Vitreal dihydroxyphenylacetic acid (DOPAC) and dopamine concentrations were quantified by high-performance liquid chromatography coupled to electrochemical detection. For the refraction experiment, chicks underwent refraction, keratometry and A-scan ultrasonography on days 30, 60 and 90 post-hatching, and each of those measurements was correlated with vitreal DOPAC concentration measured at 1 PM (representing the index of retinal dopamine release). The results showed that under light-dark cycles, vitreal DOPAC concentration was strongly correlated with log illuminance, and was significantly correlated with the developing refraction, corneal radius of curvature, and axial length values. On day 90, low vitreal DOPAC concentrations were associated with myopia (-2.41 ± 1.23 D), flat cornea, deep anterior and vitreous chambers, and thin lens. Under continuous light, vitreal DOPAC concentrations measured at 1 PM in the low, medium, and high illuminance groups did not differ from the concentrations measured at 8 AM. On day 90, low DOPAC concentrations were associated with emmetropia (+0.63 ± 3.61), steep cornea, and shallow vitreous chamber. We concluded that ambient light over a log illuminance range of 1.69-4 is linearly related to vitreal DOPAC concentration. Under both light-dark cycles and continuous light, the intensity of ambient light regulates the release of retinal dopamine. Refractive development is associated with illuminance dependent dopamine release.
形觉剥夺和环境光低照度已知可诱导小鸡近视。先前的研究表明,视网膜多巴胺(一种光驱动的神经激素)的低浓度与形觉剥夺性近视有关。在本研究中,我们研究了小鸡在光暗循环和连续光照期间视网膜多巴胺释放对光照强度的依赖性,以及视网膜多巴胺释放在光照依赖的屈光发育中的作用。将 166 只新孵化的小鸡(n=166)分为两个实验组,多巴胺组(n=88)和屈光组(n=78)。两组进一步分为六个光照组,使小鸡暴露于 50、500 或 10000 勒克斯的白炽光照度下,分别为低、中、高照度(以下简称低、中、高照度),光照时间为上午 7 点至下午 7 点,或连续光照。对于多巴胺实验,小鸡在孵化后第 14 天的上午 7 点、8 点和 1 点处死并提取玻璃体液。通过高效液相色谱法与电化学检测联用定量分析玻璃体液中二羟苯乙酸(DOPAC)和多巴胺浓度。对于屈光实验,小鸡在孵化后第 30、60 和 90 天进行屈光、角膜曲率和 A 型超声检查,将这些测量值与下午 1 点测量的玻璃体液 DOPAC 浓度(代表视网膜多巴胺释放指数)进行相关性分析。结果表明,在光暗循环下,玻璃体液 DOPAC 浓度与对数光照强度呈强相关,与发育中的屈光、角膜曲率半径和眼轴值显著相关。第 90 天,低玻璃体液 DOPAC 浓度与近视(-2.41±1.23D)、平角膜、深前房和玻璃体腔以及薄晶状体有关。在连续光照下,低、中、高照度组下午 1 点测量的玻璃体液 DOPAC 浓度与上午 8 点测量的浓度无差异。第 90 天,低 DOPAC 浓度与正视(+0.63±3.61)、陡角膜和浅玻璃体腔有关。我们得出结论,对数光照强度范围为 1.69-4 时,环境光与玻璃体液 DOPAC 浓度呈线性相关。在光暗循环和连续光照下,环境光的强度调节视网膜多巴胺的释放。屈光发育与光照依赖的多巴胺释放有关。