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首页> 外文期刊>Investigative ophthalmology & visual science >Determination of Rod and Cone Influence to the Early and Late Dynamic of the Pupillary Light Response
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Determination of Rod and Cone Influence to the Early and Late Dynamic of the Pupillary Light Response

机译:杆和锥的确定对瞳孔光响应的早期和晚期动力学的影响

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Purpose: This study aims to identify which aspects of the pupil light reflex are most influenced by rods and cones independently by analyzing pupil recordings from different mouse models of photoreceptor deficiency. Methods: One-month-old wild type (WT), rodless (Rhoa??/a??), coneless (Cnga3a??/a??), or photoreceptor less (Cnga3a??/a??; Rhoa??/a?? or Gnat1a??/a??) mice were subjected to brief red and blue light stimuli of increasing intensity. To describe the initial dynamic response to light, the maximal pupillary constriction amplitudes and the derivative curve of the first 3 seconds were determined. To estimate the postillumination phase, the constriction amplitude at 9.5 seconds after light termination was related to the maximal constriction amplitude. Results: Rhoa??/a?? mice showed decreased constriction amplitude but more prolonged pupilloconstriction to all blue and red light stimuli compared to wild type mice. Cnga3a??/a?? mice had constriction amplitudes similar to WT however following maximal constriction, the early and rapid dilation to low intensity blue light was decreased. To high intensity blue light, the Cnga3a??/a?? mice demonstrated marked prolongation of the pupillary constriction. Cnga3a??/a??; Rhoa??/a?? mice had no pupil response to red light of low and medium intensity. Conclusions: From specific gene defective mouse models which selectively voided the rod or cone function, we determined that mouse rod photoreceptors are highly contributing to the pupil response to blue light stimuli but also to low and medium red stimuli. We also observed that cone cells mainly drive the partial rapid dilation of the initial response to low blue light stimuli. Thus photoreceptor dysfunction can be derived from chromatic pupillometry in mouse models.
机译:目的:本研究旨在通过分析来自不同光感受器缺陷小鼠模型的瞳孔记录,独立地识别瞳孔光反射的哪些方面受棒和视锥的影响最大。方法:一个月大的野生型(WT),无杆(Rhoa ?? / a ??),无锥(Cnga3a ?? / a ??)或少感光体(Cnga3a ?? / a ??; Rhoa ??)。小鼠接受了强度增加的短暂的红色和蓝色光刺激。为了描述对光的初始动态响应,确定了前3秒的最大瞳孔收缩幅度和导数曲线。为了估计后照明阶段,光终止后9.5秒时的收缩幅度与最大收缩幅度有关。结果:Rhoa ?? / a ??与野生型小鼠相比,小鼠对所有蓝光和红光刺激的收缩幅度降低,但瞳孔收缩时间延长。 Cnga3a ?? / a ??小鼠具有类似于WT的收缩幅度,但是在最大收缩之后,向低强度蓝光的早期和快速扩张减少。对于高强度蓝光,Cnga3a ?? / a ??小鼠表现出瞳孔收缩明显延长。 Cnga3a ?? / a ??; Rhoa ?? / a ??小鼠对中低强度的红光没有瞳孔反应。结论:从选择性使杆或视锥细胞功能无效的特定基因缺陷小鼠模型中,我们确定了小鼠杆感光细胞对瞳孔对蓝光刺激以及对中低红色刺激的反应有很大贡献。我们还观察到视锥细胞主要驱动低蓝光刺激的初始响应的局部快速扩张。因此,可以从小鼠模型中的彩色瞳孔测量法得出光感受器功能障碍。

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