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大鼠海马切片培养物中单个CA3锥体细胞对之间的长期突触可塑性。

Long-term synaptic plasticity between pairs of individual CA3 pyramidal cells in rat hippocampal slice cultures.

作者信息

Debanne D, Gähwiler B H, Thompson S M

机构信息

Brain Research Institute, University of Zurich, August Forel-Strasse 1, CH-8029 Zurich, Switzerland.

出版信息

J Physiol. 1998 Feb 15;507 ( Pt 1)(Pt 1):237-47. doi: 10.1111/j.1469-7793.1998.237bu.x.

Abstract
  1. Long-term potentiation (LTP) and depression (LTD) were investigated at synapses formed by pairs of monosynaptically connected CA3 pyramidal cells in rat hippocampal slice cultures. 2. An N-methyl-D-aspartate (NMDA) receptor-mediated component of the unitary EPSP, elicited at the resting membrane potential in response to single action potentials in an individual CA3 cell, could be isolated pharmacologically. 3. Associative LTP was induced when single presynaptic action potentials were repeatedly paired with 240 ms postsynaptic depolarizing pulses that evoked five to twelve action potentials or with single postsynaptic action potentials evoked near the peak of the unitary EPSP. LTP induction was prevented by an NMDA receptor antagonist. 4. Associative LTD was induced when single presynaptic action potentials were repeatedly elicited with a certain delay after either 240 ms postsynaptic depolarizing pulses or single postsynaptic action potentials. The time window within which presynaptic activity had to occur for LTD induction was dependent on the amount of postsynaptic depolarization. LTD was induced if single pre- and postsynaptic action potentials occurred synchronously. 5. Homosynaptic LTD was induced by 3 Hz tetanization of the presynaptic neuron for 3 min and was blocked by an NMDA receptor antagonist. 6. Depotentiation was produced with stimulation protocols that elicit either homosynaptic or associative LTD. 7. Recurrent excitatory synapses between CA3 cells display associative potentiation and depression. The sign of the change in synaptic strength is a function of the relative timing of pre- and postsynaptic action potentials.
摘要
  1. 在大鼠海马切片培养物中,研究了由单突触连接的CA3锥体细胞对形成的突触处的长时程增强(LTP)和长时程抑制(LTD)。2. 单个CA3细胞中的单动作电位在静息膜电位下引发的单位EPSP的N-甲基-D-天冬氨酸(NMDA)受体介导成分,可以通过药理学方法分离出来。3. 当单个突触前动作电位与诱发五到十二个动作电位的240毫秒突触后去极化脉冲或与在单位EPSP峰值附近诱发的单个突触后动作电位反复配对时,诱导联合LTP。LTP的诱导被NMDA受体拮抗剂阻止。4. 当单个突触前动作电位在240毫秒突触后去极化脉冲或单个突触后动作电位之后以一定延迟反复引发时,诱导联合LTD。LTD诱导所需的突触前活动发生的时间窗口取决于突触后去极化的量。如果单个突触前和突触后动作电位同步发生,则诱导LTD。5. 突触前神经元以3 Hz强直刺激3分钟诱导同突触LTD,并被NMDA受体拮抗剂阻断。6. 采用引发同突触或联合LTD的刺激方案产生去增强作用。7. CA3细胞之间的反复兴奋性突触表现出联合增强和抑制。突触强度变化的符号是突触前和突触后动作电位相对时间的函数。

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