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Rhodopsin kinetics in the human eye

机译:人眼中的视紫红质动力学

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摘要

1. Rhodopsin has been measured by Rushton's method of reflexion densitometry in a retinal region 18° temporal to the fovea, using a wavelength of measuring light (555 nm) so far into the long wave part of the spectrum that possible blue absorbing intermediates (e.g. transient orange) do not interfere.2. Rhodopsin was bleached by a strong light for 10 sec and then held steady by a weaker light. During a 10 sec bleach, no regeneration occurs and the rate of bleaching is proportional to the quantum catch. The proportionality constant is about 10-7 (td sec)-1.3. From 2, the rate of photolysis at equilibrium produced by the steady light was calculated. Since conditions were at equilibrium, photolysis matched regeneration. It was found that the rate of generation was proportional to the amount of pigment still bleached. The proportionality constant was about 0·0025 sec-1.4. It was found by several different methods that the constant in 3 is the same in the light or dark and hence regeneration occurs independently of bleaching.5. Therefore, the results from bleaching and regeneration experiments can be combined to give the general equation [Formula: see text], where p is the fraction of rhodopsin, t is time in sec and I is the retinal illuminance.6. This equation describes the results of partial bleaching and regeneration experiments under a variety of different exposure intensities of moderately long (at least 10 min) exposure durations.7. The dark adaptation curve in a peripheral region of the rod monochromat's retina where there are few cones follows a simple exponential course over nearly 7 log10 units. Rhodopsin regeneration and log threshold for this region are described by the same curve with a time constant of about 400 sec. Each log unit fal in threshold is accompanied by 0·835% increase in rhodopsin. This time constant is in agreement with Rushton's (1961) finding, but appreciably longer than that reported by Ripps & Weale (1969a).8. The Ripps & Weale result was, however, obtained by bleaching with a very short bright xenon flash (as they did). Under these conditions, blue absorbing intermediate(s) is (are) formed, the time constant of regeneration of rhodopsin is much faster than after long tungsten bleaches, and the kinetic equation is not valid.9. The general equation, together with the relation found in 7, successfully accounts for results previously published by others of the effect of duration and intensity of bleaching on the recovery of rod threshold in the dark, provided only that more than 5% of the rhodopsin was bleached at the beginning of dark adaptation.
机译:1.视紫红质已通过Rushton反射密度测定法在距中央凹18°的视网膜区域中进行了测量,使用的是测量到光谱的长波部分的波长(555 nm)的波长,这可能是蓝色吸收中间体(例如瞬态橙色)请勿干扰2。将视紫红质在强光下漂白10秒,然后在弱光下保持稳定。在10秒的漂白过程中,没有再生发生,并且漂白的速度与量子捕获成正比。比例常数约为10 -7 (td sec) -1 .3。从2计算出稳定光在平衡状态下产生的光解速率。由于条件处于平衡状态,因此光解与再生相匹配。发现生成速率与仍被漂白的颜料量成比例。比例常数约为0·0025 sec -1 .4。通过几种不同的方法发现,亮或暗中3的常数相同,因此再生独立于漂白而发生。5。因此,可以将漂白和再生实验的结果结合起来,得到一个总的方程式[公式:见正文],其中p是视紫红质的分数,t是以秒为单位的时间,I是视网膜的照度。6。该方程式描述了在中等持续时间(至少10分钟)的各种暴露强度下,部分漂白和再生实验的结果。7。视杆单色器视网膜的周围区域中的视锥很少的暗适应曲线遵循简单的指数过程,超过了7 log10个单位。该视紫红质的再生和对数阈值由同一条曲线描述,时间常数约为400秒。视阈值的每对数单位均伴随着视紫红质增加0·835%。这个时间常数与Rushton(1961)的发现是一致的,但是比Ripps&Weale(1969a).8报道的时间长得多。但是,Ripps&Weale的结果是通过用非常短的明亮氙气闪光灯进行漂白获得的(就像他们所做的那样)。在这种条件下,形成了吸收蓝的中间体,视紫红质的再生时间常数比长的钨漂白后要快得多,动力学方程式无效。9。该通用方程以及在7中找到的关系,成功解释了其他人先前发表的结果,即漂白的持续时间和强度对黑暗中杆阈值恢复的影响,但前提是视紫红质的含量不得超过5%。在黑暗适应的开始就被漂白了。

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