Adi Tzameret, Ifat Sher, Victoria Edelstain, Michael Belkin, Ofra Kalter-Leibovici, Arieh S Solomon, Ygal Rotenstreich
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Four-week-old RCS rats presented a significantly shorter mean latency to dismount the stage compared with 6-week-old rats (mean ± standard error, 13.7 ± 1.68 vs. 20.85 ± 6.5 s, P = 0.018). Longer latencies were recorded as rats aged, reaching 45.72 s in 15-week-old rats (P < 0.00001 compared with 4-week-old rats). All rats at the age of 4 weeks placed their first foot on the table side. By contrast, at the age of 8 weeks, 28.6% rats dismounted on the cliff side and at the age of 10 and 15 weeks, rats randomly dismounted the stage to either table or cliff side. LE rats dismounted the stage faster than 4-week-old RCS rats, but the difference was not statistically significant (7 ± 1.58 s, P = 0.057) and all LE rats dismounted on the table side. The latency to dismount the stage in RCS rats correlated with maximal electroretinogram b-wave under dark and light adaptation (Spearman's rho test = -0.603 and -0.534, respectively, all P < 0.0001), outer nuclear layer thickness (Spearman's rho test = -0.764, P = 0.002), and number of S- and M-cones (Spearman's rho test = -0.763 [P = 0.002], and -0.733 [P = 0.004], respectively). 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引用次数: 6
摘要
视觉保存是视觉研究的主要目标。本研究使用深度知觉测试评估了皇家外科学院(RCS)大鼠视觉功能的保存。老鼠被放置在一个舞台上,其中一侧有一个虚幻的陡峭的下降(“悬崖”),另一侧有一个最小的下降(“桌子”)。测定了下马潜伏期和第一次踏上“悬崖”一侧的大鼠百分比。以非营养不良大鼠Long-Evans (LE)为对照。视网膜电图和组织学分析测定视网膜功能和结构。4周龄RCS大鼠平均下马潜伏期明显短于6周龄大鼠(平均±标准误差,13.7±1.68 vs 20.85±6.5 s, P = 0.018)。大鼠年龄越大潜伏期越长,15周龄大鼠潜伏期达到45.72 s (P <0.00001(与4周龄大鼠比较)。所有4周大的大鼠将第一只脚放在桌子边。相比之下,在8周龄时,28.6%的大鼠在悬崖边下马,在10和15周龄时,大鼠随机下马到桌子或悬崖边。LE大鼠下马速度快于4周龄RCS大鼠,但差异无统计学意义(7±1.58 s, P = 0.057),且均为桌侧下马。RCS大鼠下马潜伏期与暗适应和光适应下视网膜电图b波最大值相关(Spearman’s rho检验分别= -0.603和-0.534,P <0.0001)、外核层厚度(Spearman’S rho检验= -0.764,P = 0.002)、S锥和m锥数量(Spearman’S rho检验分别= -0.763 [P = 0.002]和-0.733 [P = 0.004])。悬崖躲避实验是一种客观、快速、简便的测定RCS大鼠视觉功能的方法。
Evaluation of visual function in Royal College of Surgeon rats using a depth perception visual cliff test.
Preserving of vision is the main goal in vision research. The presented research evaluates the preservation of visual function in Royal College of Surgeon (RCS) rats using a depth perception test. Rats were placed on a stage with one side containing an illusory steep drop ("cliff") and another side with a minimal drop ("table"). Latency of stage dismounting and the percentage of rats that set their first foot on the "cliff" side were determined. Nondystrophic Long-Evans (LE) rats were tested as control. Electroretinogram and histology analysis were used to determine retinal function and structure. Four-week-old RCS rats presented a significantly shorter mean latency to dismount the stage compared with 6-week-old rats (mean ± standard error, 13.7 ± 1.68 vs. 20.85 ± 6.5 s, P = 0.018). Longer latencies were recorded as rats aged, reaching 45.72 s in 15-week-old rats (P < 0.00001 compared with 4-week-old rats). All rats at the age of 4 weeks placed their first foot on the table side. By contrast, at the age of 8 weeks, 28.6% rats dismounted on the cliff side and at the age of 10 and 15 weeks, rats randomly dismounted the stage to either table or cliff side. LE rats dismounted the stage faster than 4-week-old RCS rats, but the difference was not statistically significant (7 ± 1.58 s, P = 0.057) and all LE rats dismounted on the table side. The latency to dismount the stage in RCS rats correlated with maximal electroretinogram b-wave under dark and light adaptation (Spearman's rho test = -0.603 and -0.534, respectively, all P < 0.0001), outer nuclear layer thickness (Spearman's rho test = -0.764, P = 0.002), and number of S- and M-cones (Spearman's rho test = -0.763 [P = 0.002], and -0.733 [P = 0.004], respectively). The cliff avoidance test is an objective, quick, and readily available method for the determination of RCS rats' visual function.
期刊介绍:
Visual Neuroscience is an international journal devoted to the publication of experimental and theoretical research on biological mechanisms of vision. A major goal of publication is to bring together in one journal a broad range of studies that reflect the diversity and originality of all aspects of neuroscience research relating to the visual system. Contributions may address molecular, cellular or systems-level processes in either vertebrate or invertebrate species. The journal publishes work based on a wide range of technical approaches, including molecular genetics, anatomy, physiology, psychophysics and imaging, and utilizing comparative, developmental, theoretical or computational approaches to understand the biology of vision and visuo-motor control. The journal also publishes research seeking to understand disorders of the visual system and strategies for restoring vision. Studies based exclusively on clinical, psychophysiological or behavioral data are welcomed, provided that they address questions concerning neural mechanisms of vision or provide insight into visual dysfunction.