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本文引用的文献

1
A theoretical treatment of Fuortes's observations upon eccentric cell activity in Limulus.对富尔特斯关于鲎偏心细胞活动的观察结果的理论探讨。
J Physiol. 1959 Oct;148(1):29-38. doi: 10.1113/jphysiol.1959.sp006271.
2
CHANGES IN TIME SCALE AND SENSITIVITY IN THE OMMATIDIA OF LIMULUS.鲎小眼时间尺度和敏感性的变化
J Physiol. 1964 Aug;172(2):239-63. doi: 10.1113/jphysiol.1964.sp007415.
3
EXTRACELLULAR SPACE AS A PATHWAY FOR EXCHANGE BETWEEN BLOOD AND NEURONS IN THE CENTRAL NERVOUS SYSTEM OF THE LEECH: IONIC COMPOSITION OF GLIAL CELLS AND NEURONS.水蛭中枢神经系统中细胞外空间作为血液与神经元之间交换的途径:神经胶质细胞和神经元的离子组成
J Neurophysiol. 1964 Jul;27:645-71. doi: 10.1152/jn.1964.27.4.645.
4
The routine fitting of kinetic data to models: a mathematical formalism for digital computers.动力学数据与模型的常规拟合:一种适用于数字计算机的数学形式体系。
Biophys J. 1962 May;2(3):275-87. doi: 10.1016/s0006-3495(62)86855-6.
5
Initiation of impulses in visual cells of Limulus.鲎视觉细胞中冲动的起始。
J Physiol. 1959 Oct;148(1):14-28. doi: 10.1113/jphysiol.1959.sp006270.
6
Peripheral mechanism of nervous activity in lateral eye of horseshoe crab.鲎侧眼神经活动的外周机制
J Neurophysiol. 1957 May;20(3):245-54. doi: 10.1152/jn.1957.20.3.245.
7
Steps in the production of motoneuron spikes.运动神经元动作电位产生的步骤。
J Gen Physiol. 1957 May 20;40(5):735-52. doi: 10.1085/jgp.40.5.735.
8
The ventral photoreceptor cells of Limulus. II. The basic photoresponse.鲎的腹侧感光细胞。II. 基本光反应。
J Gen Physiol. 1969 Sep;54(3):310-30. doi: 10.1085/jgp.54.3.310.
9
The site of origin of electrical responses in visual cells of the leech, Hirudo medicinalis.水蛭(药用水蛭)视觉细胞电反应的起源部位。
J Cell Biol. 1969 Jul;42(1):241-52. doi: 10.1083/jcb.42.1.241.
10
Slow and spike potentials recorded from retinula cells of the honeybee drone in response to light.从蜜蜂雄蜂小眼细胞记录到的对光反应的慢电位和锋电位。
J Gen Physiol. 1968 Dec;52(6):855-75. doi: 10.1085/jgp.52.6.855.

水蛭视觉细胞反应的分析。

Analysis of responses in visual cells of the leech.

作者信息

Fioravanti R, Fuortes M G

出版信息

J Physiol. 1972 Dec;227(1):173-94. doi: 10.1113/jphysiol.1972.sp010025.

DOI:10.1113/jphysiol.1972.sp010025
PMID:4646575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1331268/
Abstract
  1. Potentials were recorded from the cytoplasm and from the vacuole of leech photoreceptors. Since the vacuole is lined with microvilli and is connected to the outside by narrow channels, the potential drops between vacuole and outside measure the current through the microvillar membrane.2. In darkness, the potential of the cytoplasm with respect to the outside is about - 45 mV while the potential of the vacuole is approximately zero.3. Following illumination the negativity of the cytoplasm decreases and the vacuole becomes negative relative to the outside.4. For dim intensities, the response to a flash of light may grow proportionately more than the intensity of the flash. This is probably due to development of a depolarizing local response.5. The resistance from the cytoplasm to the outside was about 150 MOmega in darkness and decreased to approximately 40 MOmega at the peak of the response to a bright flash (on average). Corresponding measurements from the vacuole gave 50 MOmega in darkness and 35 MOmega at the peak of the response.6. Charging curves produced by steps of constant currents applied to the cytoplasm or to the vacuole include two time constants (about 5 and 50 msec on average). The longer time constant decreases greatly with bright illumination.7. The results are consistent with the interpretation that the response to light is brought about by an increase of conductance of the microvillar membrane.
摘要
  1. 从水蛭光感受器的细胞质和液泡记录到了电位。由于液泡衬有微绒毛,并通过狭窄通道与外部相连,液泡与外部之间的电位降测量的是通过微绒毛膜的电流。

  2. 在黑暗中,细胞质相对于外部的电位约为 -45 mV,而液泡的电位约为零。

  3. 光照后,细胞质的负性降低,液泡相对于外部变为负性。

  4. 对于暗光强度,对闪光的反应增长可能比闪光强度成比例地更多。这可能是由于去极化局部反应的发展。

  5. 在黑暗中,从细胞质到外部的电阻约为150兆欧,在对明亮闪光的反应峰值时(平均)降至约40兆欧。从液泡进行的相应测量在黑暗中为50兆欧,在反应峰值时为35兆欧。

  6. 施加到细胞质或液泡的恒定电流阶跃产生的充电曲线包括两个时间常数(平均约为5和50毫秒)。较长的时间常数在明亮光照下大大降低。

  7. 这些结果与这样的解释一致,即对光的反应是由微绒毛膜电导的增加引起的。