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1
Detection and resolution of visual stimuli by turtle photoreceptors.乌龟光感受器对视觉刺激的检测与分辨
J Physiol. 1973 Oct;234(1):163-98. doi: 10.1113/jphysiol.1973.sp010340.
2
Light path and photon capture in turtle photoreceptors.乌龟光感受器中的光路和光子捕获。
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3
Properties of centre-hyperpolarizing, red-sensitive bipolar cells in the turtle retina.乌龟视网膜中中心超极化、红敏双极细胞的特性
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4
Functional characteristics of lateral interactions between rods in the retina of the snapping turtle.鳄龟视网膜中视杆细胞间侧向相互作用的功能特性
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5
Electrical responses of double cones in the turtle retina.龟视网膜中双锥细胞的电反应。
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6
Colour-dependence of cone responses in the turtle retina.龟视网膜中视锥细胞反应的颜色依赖性。
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7
Spectral sensitivities of seven morphological types of photoreceptors in the retina of the turtle, Geoclemys reevesii.乌龟(Geoclemys reevesii)视网膜中七种形态类型光感受器的光谱敏感性。
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Interactions leading to horizontal cell responses in the turtle retina.导致海龟视网膜水平细胞反应的相互作用。
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Cones excite rods in the retina of the turtle.视锥细胞刺激海龟视网膜中的视杆细胞。
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Temporal and spatial characteristics of the voltage response of rods in the retina of the snapping turtle.鳄龟视网膜中视杆细胞电压响应的时空特性
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Biophysical neural adaptation mechanisms enable artificial neural networks to capture dynamic retinal computation.生物物理神经适应机制使人工神经网络能够捕获动态视网膜计算。
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Front Ophthalmol (Lausanne). 2024 Apr 8;4:1340692. doi: 10.3389/fopht.2024.1340692. eCollection 2024.
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Homeostasis at different backgrounds: The roles of overlayed feedback structures in vertebrate photoadaptation.不同背景下的稳态:脊椎动物光适应中重叠反馈结构的作用。
PLoS One. 2023 Apr 28;18(4):e0281490. doi: 10.1371/journal.pone.0281490. eCollection 2023.
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The evolutionary history and spectral tuning of vertebrate visual opsins.脊椎动物视蛋白的进化历史和光谱调谐。
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本文引用的文献

1
Absorption spectra of retinal oil globules in turkey, turtle and pigeon.火鸡、海龟和鸽子视网膜油滴的吸收光谱。
Exp Cell Res. 1963 Jan;29:349-55. doi: 10.1016/0014-4827(63)90389-6.
2
S-potentials from colour units in the retina of fish (Cyprinidae).鱼类(鲤科)视网膜中颜色单元的S电位。
J Physiol. 1966 Aug;185(3):536-55. doi: 10.1113/jphysiol.1966.sp008001.
3
Spectroscopic properties of porphyropsins.视紫蓝质的光谱特性。
Vision Res. 1967 May;7(5):349-69. doi: 10.1016/0042-6989(67)90044-2.
4
A nomogram for retinene-2-based visual pigments.基于视黄醛-2的视觉色素列线图。
Vision Res. 1967 Mar;7(3):111-20. doi: 10.1016/0042-6989(67)90078-8.
5
Receptive fields of cones in the retina of the turtle.海龟视网膜中视锥细胞的感受野。
J Physiol. 1971 Apr;214(2):265-94. doi: 10.1113/jphysiol.1971.sp009432.
6
Microspectrophotometric measurements of visual pigments in two species of turtle, Pseudemys scripta and Chelonia mydas.对两种海龟(伪彩龟和绿海龟)视觉色素的显微分光光度测量。
Vision Res. 1971 Feb;11(2):105-14. doi: 10.1016/0042-6989(71)90227-6.
7
Physiological and morphological identification of horizontal, bipolar and amacrine cells in goldfish retina.金鱼视网膜中水平细胞、双极细胞和无长突细胞的生理与形态学鉴定
J Physiol. 1970 May;207(3):623-33. doi: 10.1113/jphysiol.1970.sp009084.
8
Dark current and photocurrent in retinal rods.视网膜视杆细胞中的暗电流和光电流。
Biophys J. 1970 May;10(5):380-412. doi: 10.1016/S0006-3495(70)86308-1.
9
Kinetics of the photocurrent of retinal rods.视网膜视杆细胞光电流的动力学
Biophys J. 1972 Aug;12(8):1073-94. doi: 10.1016/S0006-3495(72)86145-9.
10
Electrical activity of vertebrate photoreceptors.脊椎动物光感受器的电活动。
Q Rev Biophys. 1970 May;3(2):179-222. doi: 10.1017/s0033583500004571.

乌龟光感受器对视觉刺激的检测与分辨

Detection and resolution of visual stimuli by turtle photoreceptors.

作者信息

Baylor D A, Hodgkin A L

出版信息

J Physiol. 1973 Oct;234(1):163-98. doi: 10.1113/jphysiol.1973.sp010340.

DOI:10.1113/jphysiol.1973.sp010340
PMID:4766219
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1350657/
Abstract
  1. Hyperpolarizing responses up to 30 mV in amplitude were recorded from cones and from certain cells believed to be rods in the isolated retina of the swamp turtle, Pseudemys scripta elegans.2. The responses evoked by weak flashes of light reach their maximum in 100-140 msec in red-sensitive cones, 140-180 msec in green-sensitive cones, and 300-600 msec in the rod-like cells (20 degrees C).3. The cone response evoked by weak flashes of light is linearly related to light intensity and obeys the superposition principle in that the response to a very weak step of light is the integral of the response to a very weak flash.4. On the basis of their spectral sensitivities cones can be divided into three distinct classes, namely red-sensitive cones whose relative quantum sensitivity is maximal at 630 nm, green-sensitive cones with a maximal sensitivity at 550 nm and blue-sensitive cones with a maximum at 460 nm.5. The difference between the spectral sensitivity of rods with a maximum at about 520 nm and green-sensitive cones (lambda(max) = 550 nm) is consistent with the view that both receptors contain a 518(2) retinal pigment as reported by Liebman & Granda, but that light is filtered by an orange oil droplet in green-sensitive cones.6. The spectral sensitivities of both red- and green-sensitive cones agree well amongst themselves at long wave-lengths but differ markedly in the extent of the reduction at short wave-lengths. This variation is attributed to differences in the extent to which light is filtered through the coloured oil droplets.7. There is a significant positive correlation between the absolute sensitivity of red- and green-sensitive cones and the reduction in sensitivity at short wave-lengths. This would be explained if a greater fraction of the light passes through the oil droplet in the most sensitive cells.8. The absolute flash sensitivities of the most sensitive receptors were about 250 muV photon(-1) mum(2) in red- and green-sensitive cones, 120 muV photon(-1) mum(2) in blue-sensitive cones, and 1300 muV photon(-1) mum(2) in rods.9. If the effective collecting area (which includes factors for absorption etc.) is taken as 10 mum(2) in a red-sensitive cone the peak hyperpolarization produced by 1 photon would average 25 muV.10. Provided that small spots of light are used, individual receptors obey the ;univariance principle' and the response produced by light of strength I', and wave-length lambda(1) can be matched by a light of strength kI' and wave-length lambda(2), where k is the same for all values of I'.11. A small proportion of cones behave like isolated units in that they have very sharp sensitivity-profiles and obey the univariance principle with respect to the position as well as to the wave-length of light.12. The majority of red and green cones have more diffuse sensitivity-profiles, sometimes with bumps on the descending limb, and behave as though cones with the same spectral sensitivity were electrically coupled to one another.13. The relation between the area of illumination and flash sensitivity agreed approximately with that calculated from the spatial profile.
摘要
  1. 在黄腹彩龟(Pseudemys scripta elegans)离体视网膜的视锥细胞以及某些被认为是视杆细胞的细胞中,记录到了幅度高达30 mV的超极化反应。

  2. 弱闪光诱发的反应在红色敏感视锥细胞中100 - 140毫秒达到最大值,绿色敏感视锥细胞中140 - 180毫秒达到最大值,杆状细胞中300 - 600毫秒达到最大值(20摄氏度)。

  3. 弱闪光诱发的视锥细胞反应与光强度呈线性关系,并遵循叠加原理,即对非常弱的阶跃光的反应是对非常弱的闪光反应的积分。

  4. 根据其光谱敏感性,视锥细胞可分为三个不同类别,即相对量子敏感性在630 nm处最大的红色敏感视锥细胞、在550 nm处具有最大敏感性的绿色敏感视锥细胞以及在460 nm处具有最大值的蓝色敏感视锥细胞。

  5. 最大波长约为520 nm的视杆细胞与绿色敏感视锥细胞(λ(max)=550 nm)的光谱敏感性差异与以下观点一致,即如Liebman和Granda所报道,两种感受器都含有518(2)视网膜色素,但在绿色敏感视锥细胞中,光是通过橙色油滴进行过滤的。

  6. 红色和绿色敏感视锥细胞的光谱敏感性在长波长处彼此吻合良好,但在短波长处的降低程度明显不同。这种变化归因于光通过有色油滴的过滤程度的差异。

  7. 红色和绿色敏感视锥细胞的绝对敏感性与短波长处敏感性的降低之间存在显著的正相关。如果在最敏感的细胞中有更大比例的光通过油滴,这一点就能得到解释。

  8. 最敏感感受器的绝对闪光敏感性在红色和绿色敏感视锥细胞中约为250 μV photon⁻¹ μm²,蓝色敏感视锥细胞中为120 μV photon⁻¹ μm²,视杆细胞中为1300 μV photon⁻¹ μm²。

  9. 如果在红色敏感视锥细胞中有效收集面积(包括吸收等因素)取为10 μm²,那么1个光子产生的峰值超极化平均为25 μV。

  10. 只要使用小光斑,单个感受器遵循“单变量原则”,强度为I'、波长为λ₁的光产生的反应可以由强度为kI'、波长为λ₂的光匹配,其中k对于所有I'值都是相同的。

  11. 一小部分视锥细胞表现得像孤立单元,它们具有非常尖锐的敏感性分布,并在光的位置以及波长方面遵循单变量原则。

  12. 大多数红色和绿色视锥细胞具有更弥散的敏感性分布,有时在下降支上有凸起,并且表现得好像具有相同光谱敏感性的视锥细胞彼此电耦合。

  13. 光照面积与闪光敏感性之间的关系大致与根据空间分布计算出的关系相符。