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视杆信号的大小。

The size of rod signals.

作者信息

Alpern M, Rushton W A, Torii S

出版信息

J Physiol. 1970 Jan;206(1):193-208. doi: 10.1113/jphysiol.1970.sp009006.

Abstract
  1. This investigation is based upon Alpern's (1965) contrast flash observations. The threshold for the test flash lambda (Fig. 2a) is raised if a second flash varphi falls on the annular surround. Moreover, if lambda excites rods at threshold, it is only the rods in the surround that contribute to the threshold rise.2. The possibility that the rise in lambda threshold might be due to light physically scattered from surround to centre we exclude by several different experiments. We conclude (Fig. 1b) that the varphi flash sets up a nerve signal N which is conducted to some place C where it inhibits the signal from the centre.3. If the luminous surround, instead of being a full circle (Fig. 2a) consists only of the sectors shown black in Fig. 2b, that occupy 1/m of the surround area, it is found (in the physiological range) that the light/area on those sectors must be m times as great to produce the same threshold rise at centre, i.e. the total surround illumination must remain the same.4. This result would obviously follow if N, the inhibitory nerve signal, were proportional to the total surround illumination. We have established the converse; the signal must be proportional to the quantum catch.5. Light can be increased indefinitely, nerve signals cannot. When varphi increases sufficiently, N saturates in the same way that S-potentials and receptor potentials saturate, namely according to N = varphi/(varphi + sigma) where sigma, the semi-saturation constant is about 200 td sec, or 800 quanta absorbed per rod per flash.6. Thus the nerve signal N is proportional to the quantum catch over 4 log units in the physiological range, namely from 1 quantum per 100 rods to 100 quanta per rod per flash. Above this for another 2 log units N continues to increase, but now more slowly, after the manner of S-potentials and receptor potentials.
摘要
  1. 本研究基于阿尔珀恩(1965年)的对比闪光观察。如果第二个闪光φ落在环形周边区域,测试闪光λ(图2a)的阈值会升高。此外,如果λ在阈值时激发视杆细胞,那么只有周边区域的视杆细胞会导致阈值升高。

  2. 通过几个不同的实验,我们排除了λ阈值升高可能是由于光从周边区域物理散射到中心区域的可能性。我们得出结论(图1b),闪光φ会产生一个神经信号N,该信号传导到某个位置C,在那里它会抑制来自中心区域的信号。

  3. 如果发光周边区域不是完整的圆形(图2a),而是仅由图2b中黑色显示的扇形组成,这些扇形占据周边区域的1/m,那么(在生理范围内)发现这些扇形上的光/面积必须增大m倍,才能在中心区域产生相同的阈值升高,即周边区域的总光照度必须保持不变。

  4. 如果抑制性神经信号N与周边区域的总光照度成正比,那么显然会得出这个结果。我们已经证实了相反的情况;该信号必须与量子捕获量成正比。

  5. 光可以无限增加,而神经信号不能。当φ充分增加时,N会饱和,其方式与S电位和感受器电位饱和相同,即根据N = φ/(φ + σ),其中半饱和常数σ约为200td秒,或每个视杆细胞每次闪光吸收800个量子。

  6. 因此,在生理范围内,神经信号N在4个对数单位上与量子捕获量成正比,即从每100个视杆细胞1个量子到每个视杆细胞每次闪光100个量子。在此之上的另外2个对数单位,N继续增加,但现在增加得更慢,其方式与S电位和感受器电位相同。

相似文献

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The size of rod signals.视杆信号的大小。
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引用本文的文献

6
Signals from cones.来自视锥细胞的信号。
J Physiol. 1970 Apr;207(2):463-75. doi: 10.1113/jphysiol.1970.sp009073.
7
The attenuation of rod signals by bleachings.视杆细胞信号因漂白作用而衰减。
J Physiol. 1970 Apr;207(2):449-61. doi: 10.1113/jphysiol.1970.sp009072.
8
The attenuation of rod signals by backgrounds.背景对视杆细胞信号的衰减作用。
J Physiol. 1970 Jan;206(1):209-27. doi: 10.1113/jphysiol.1970.sp009007.
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On the retinal basis of visual adaptation.
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本文引用的文献

1
THE SENSITIVITY OF RODS UNDER ILLUMINATION.光照下视杆细胞的敏感性。
J Physiol. 1965 May;178(1):141-60. doi: 10.1113/jphysiol.1965.sp007620.
3
ROD-CONE INDEPENDENCE IN THE AFTER-FLASH EFFECT.后闪光效应中的视杆-视锥细胞独立性
J Physiol. 1965 Feb;176(3):462-72. doi: 10.1113/jphysiol.1965.sp007561.
4
8
Glare: its measurement by cone thresholds and by the bleaching of cone pigments.
J Opt Soc Am. 1966 Jan;56(1):104-10. doi: 10.1364/josa.56.000104.
9
Computer assisted analysis of S-potentials.S电位的计算机辅助分析
Biophys J. 1969 Jun;9(6):845-59. doi: 10.1016/S0006-3495(69)86422-2.

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