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泥螈视网膜神经节细胞的持续突触输入。

Sustained synaptic input to ganglion cells of mudpuppy retina.

作者信息

Belgum J H, Dvorak D R, McReynolds J S

出版信息

J Physiol. 1982 May;326:91-108. doi: 10.1113/jphysiol.1982.sp014179.

Abstract
  1. Intracellular responses were recorded from on-centre and off-centre ganglion cells in isolated eyecups of the mudpuppy, Necturus maculosus.2. Current-voltage relations were measured in darkness, during illumination of the receptive field centre, and after chemically mediated synaptic inputs were blocked by 4 mM-cobalt chloride.3. In on-centre cells the membrane potential in darkness was -56+/-6 mV (mean+/-S.D.). Addition of Co(2+) resulted in an average depolarization of 10 mV and an average decrease in conductance of 2.1 nS. These results suggest that in darkness on-centre cells are tonically inhibited by synaptic input which increases conductance and has a reversal potential more negative than the dark membrane potential. In off-centre cells the membrane potential in darkness was -46+/-5 mV. Addition of Co(2+) caused an average hyperpolarization of 6 mV and an average decrease in conductance of 1.5 nS. These results suggest that in darkness off-centre cells receive a tonic excitatory input which increases conductance and has a reversal potential more positive than the dark membrane potential.4. In on-centre cells light causes a sustained depolarization. This response involves an increase in a tonic excitatory input which increases conductance and has a reversal potential more positive than the dark membrane potential.5. In off-centre cells, light causes a sustained hyperpolarization. This response involves an increase in a sustained inhibitory input which increases conductance and has a reversal potential more negative than the dark membrane potential.6. The depolarizing off-response of off-centre cells is associated with an increase in an excitatory input which increases conductance and has a reversal potential more positive than the dark membrane potential. This response may be due to a temporary increase in the excitatory input which is tonically active in darkness or may reflect an additional excitatory input.7. It is suggested that in both on- and off-centre ganglion cells the balance of sustained excitatory and inhibitory synaptic inputs determines the resting potential in darkness. Centre illumination alters the balance of these inputs, by increasing one and decreasing the other, to produce the characteristic sustained light responses.8. The possible presynaptic sources of the sustained excitatory and inhibitory inputs are discussed.
摘要
  1. 在泥螈(Necturus maculosus)分离的视杯中,记录了中心型和周边型神经节细胞的细胞内反应。

  2. 在黑暗中、感受野中心受光照期间以及化学介导的突触输入被4 mM氯化钴阻断后,测量了电流-电压关系。

  3. 在中心型细胞中,黑暗中的膜电位为-56±6 mV(平均值±标准差)。添加Co(2+)导致平均去极化10 mV,平均电导降低2.1 nS。这些结果表明,在黑暗中,中心型细胞受到突触输入的紧张性抑制,该突触输入增加电导,且其反转电位比黑暗膜电位更负。在周边型细胞中,黑暗中的膜电位为-46±5 mV。添加Co(2+)导致平均超极化6 mV,平均电导降低1.5 nS。这些结果表明,在黑暗中,周边型细胞接受紧张性兴奋性输入,该输入增加电导,且其反转电位比黑暗膜电位更正。

  4. 在中心型细胞中,光引起持续去极化。该反应涉及紧张性兴奋性输入的增加,该输入增加电导,且其反转电位比黑暗膜电位更正。

  5. 在周边型细胞中,光引起持续超极化。该反应涉及持续抑制性输入的增加,该输入增加电导,且其反转电位比黑暗膜电位更负。

  6. 周边型细胞的去极化离反应与兴奋性输入的增加有关,该输入增加电导,且其反转电位比黑暗膜电位更正。该反应可能是由于在黑暗中紧张性活动的兴奋性输入暂时增加,或者可能反映了额外的兴奋性输入。

  7. 有人提出,在中心型和周边型神经节细胞中,持续兴奋性和抑制性突触输入的平衡决定了黑暗中的静息电位。中心光照通过增加一种输入并减少另一种输入来改变这些输入的平衡,从而产生特征性的持续光反应。

  8. 讨论了持续兴奋性和抑制性输入可能的突触前来源。

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