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乌龟光感受器中的光路和光子捕获。

Light path and photon capture in turtle photoreceptors.

作者信息

Baylor D A, Fettiplace R

出版信息

J Physiol. 1975 Jun;248(2):433-64. doi: 10.1113/jphysiol.1975.sp010983.

DOI:10.1113/jphysiol.1975.sp010983
PMID:1151792
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1309531/
Abstract
  1. The directional selectivity of individual cones was examined by intracellular recording in the eye of the turtle. Sensitivites were determined from linear responses to dim flashes of monochromatic light incident on a cell over a range of angles to its long axis. 2. With light near the optimum wave-length, some red- and green-sensitive cones showed a high sensitivity for light entering axially and lower sensitivities for light entering obliquely. In contrast, other cells had lower peak sensitivities and less pronounced directional selectivities. The highest axial sensitivities observed in red receptors were about 320 muV photon(-1) mu2; in these cells, the sensitivity declined to half for rays 6-9 degrees off the axis as measured in the retina. Green receptors had lower axial sensitivities and broader angular profiles. 3. On the assumption that rays at all angles contribute independently to the over-all sensitivity, the sensitivity of a cell to large cones of rays was successfully predicted from the angular selectivity determined with a narrow pencil of rays. The shape of small responses to dim stimuli delivered on and off the axis of the cell was invariant, implying that a cone signals the number of photons absorbed but not their angle of incidence. 4. Short wave-lengths have previously been shown to be filtered out by the oil droplets present in turtle cones. At short wave-lengths, the angular profiles showed a depression in axial sensitivity consistent with this filtering action. 5. Diameters of inner segments, oil droplets, and outer segments were measured in red-, green-, and blue-sensitive cones, since these dimensions are expected to influence the cones' angular acceptances and ability to collect light. The diameters of the structure were in approximately the same proportions for each type of receptor, but the absolute values of the diameters were found to be scaled in relation to the wave-length of maximum sensitivity. 6. Optical determinations of the efficiency with which axial rays are concentrated by red receptors gave a mean value of 55%. 7. Receptors in histological sections of the whole eye were found to be oriented with their long axes directed approximately toward the pupil. 8. The observed directional selectivities and collecting efficiencies agree well with the behaviour of a model retinal cone developed by Winston & Enoch (1971) on a geometrical optical treatment. 9. Effective collecting areas are derived for red-, green- and blue-sensitive cones; these permit conversion of observed flash sensitivities into the mean peak hyperpolarization produced by isomerization of a visual pigment molecule. The figure obtained is about 25 muV for red-sensitive cones and 21muV for green-sensitive cones.
摘要
  1. 通过对海龟眼睛进行细胞内记录来检测单个视锥细胞的方向选择性。灵敏度是根据细胞对在其长轴的一系列角度上入射的单色暗光闪烁的线性反应来确定的。2. 在接近最佳波长的光下,一些对红色和绿色敏感的视锥细胞对轴向入射的光表现出高灵敏度,而对斜向入射的光灵敏度较低。相比之下,其他细胞的峰值灵敏度较低,方向选择性也不那么明显。在红色感受器中观察到的最高轴向灵敏度约为320 μV光子⁻¹μm²;在这些细胞中,如在视网膜中测量的那样,对于偏离轴6 - 9度的光线,灵敏度下降到一半。绿色感受器的轴向灵敏度较低,角度分布较宽。3. 假设所有角度的光线对总体灵敏度的贡献是独立的,根据用窄光束确定的角度选择性成功预测了细胞对大光线锥的灵敏度。在细胞轴上和轴外施加的对暗光刺激的小反应形状不变,这意味着视锥细胞信号吸收的光子数量,而不是它们的入射角。4. 先前已表明,短波被海龟视锥细胞中存在的油滴滤除。在短波下,角度分布显示轴向灵敏度降低,这与这种滤光作用一致。5. 测量了对红色、绿色和蓝色敏感的视锥细胞内段、油滴和外段的直径,因为预计这些尺寸会影响视锥细胞的角度接受度和收集光的能力。每种类型感受器的结构直径大致成相同比例,但发现直径的绝对值与最大灵敏度波长相关。6. 对红色感受器集中轴向光线效率的光学测定给出的平均值为55%。7. 在整个眼睛的组织学切片中发现感受器的长轴大致指向瞳孔。8. 观察到的方向选择性和收集效率与温斯顿和伊诺克(1971年)在几何光学处理基础上建立的视网膜视锥细胞模型的行为非常吻合。9. 得出了对红色、绿色和蓝色敏感的视锥细胞的有效收集面积;这些允许将观察到的闪光灵敏度转换为视觉色素分子异构化产生的平均峰值超极化。对于红色敏感视锥细胞得到的数值约为25 μV,对于绿色敏感视锥细胞为21 μV。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af35/1309531/5b4276ac61a4/jphysiol00895-0224-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af35/1309531/fc5d549bd656/jphysiol00895-0221-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af35/1309531/4396844e1073/jphysiol00895-0222-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af35/1309531/c74859478a35/jphysiol00895-0223-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af35/1309531/5b4276ac61a4/jphysiol00895-0224-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af35/1309531/fc5d549bd656/jphysiol00895-0221-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af35/1309531/4396844e1073/jphysiol00895-0222-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af35/1309531/c74859478a35/jphysiol00895-0223-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af35/1309531/5b4276ac61a4/jphysiol00895-0224-a.jpg

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