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电鳗电器官活动期间的光散射和双折射变化。

Light scattering and birefringence changes during activity in the electric organ of electrophorus electricus.

作者信息

Cohen L B, Hille B, Keynes R D

出版信息

J Physiol. 1969 Aug;203(2):489-509. doi: 10.1113/jphysiol.1969.sp008876.

Abstract
  1. In an attempt to obtain information about structural changes related to electrical activity in Electrophorus electroplates, we have determined the size and time course of the changes in light scattering and in bire-fringence that occur during and after the discharge of the electric organ.2. The changes in light intensity detected with a photomultiplier were never greater than 0.2% for a single discharge, and were often much smaller than this, but records with an acceptable ratio of signal to noise could be obtained by signal-averaging techniques.3. A single stimulus led to a decrease, then an increase, and finally another decrease in the light scattered by slices of the main electric organ. These three phases were designated E1, E2 and E3.4. E1 started at the beginning of the action potential, and its peak was reached at the same time as the completion of repolarization, even when the repolarization was delayed by cooling or hastened by drawing larger currents from the tissue.5. E2 was proportional to the integral of the current flowing through the slice of electric organ, and may arise from the swelling and shrinking of the tubules that stud the faces of the electroplates. It developed within a millisecond or two of the start of an applied current, and lasted for about 100 msec.6. E3 was a variable decrease in scattering that lasted for some seconds.7. A stimulus also led to a transient increase in the birefringence of the electric organ. The optical change followed the change in electrical potential across the innervated faces of the electroplates with a delay of somewhat under 50 musec.8. This voltage-dependent change in birefringence may arise from a Kerr effect (electric birefringence) in the membrane or from compression of the membrane.
摘要
  1. 为了获取与电鳗电板中电活动相关的结构变化信息,我们测定了电器官放电期间及之后发生的光散射和双折射变化的大小及时间进程。

  2. 用光电倍增管检测到的光强度变化,单次放电时从未超过0.2%,且通常比这小得多,但通过信号平均技术可获得信噪比可接受的记录。

  3. 单个刺激会导致主电器官切片散射光先减少,然后增加,最后再次减少。这三个阶段分别命名为E1、E2和E3。

  4. E1在动作电位开始时启动,其峰值在复极化完成时达到,即使复极化因冷却而延迟或因从组织中引出更大电流而加速也是如此。

  5. E2与流经电器官切片的电流积分成正比,可能源于密布在电板表面的小管的肿胀和收缩。它在施加电流开始后的一两毫秒内出现,持续约100毫秒。

  6. E3是散射的可变减少,持续数秒。

  7. 刺激还会导致电器官的双折射短暂增加。光学变化跟随电板受神经支配表面跨膜电位的变化,延迟略小于50微秒。

  8. 这种双折射的电压依赖性变化可能源于膜中的克尔效应(电双折射)或膜的压缩。

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