Suppr超能文献

由抑制性中间神经元同步的皮质锥体细胞的模拟。

Simulations of cortical pyramidal neurons synchronized by inhibitory interneurons.

作者信息

Lytton W W, Sejnowski T J

机构信息

Salk Institute, Computational Neurobiology Laboratory, La Jolla 92037.

出版信息

J Neurophysiol. 1991 Sep;66(3):1059-79. doi: 10.1152/jn.1991.66.3.1059.

Abstract
  1. The interaction between inhibitory interneurons and cortical pyramidal neurons was studied by use of computer simulations to test whether inhibitory interneurons could assist in phase-locking postsynaptic cells. Two models were used: a simplified model, which included only 3 membrane channels, and a detailed 11-channel model. 2. The 11-channel model included most of the ion channels known to be present in neocortical pyramidal neurons as well as calcium diffusion and other membrane mechanisms. The kinetics for the channels were obtained from voltage-clamp studies in a variety of preparations. The parameters were then adjusted to produce repetitive bursting similar to that seen in some cortical pyramidal cells entrained during visual stimulation. 3. Phase-locking to a train of inhibitory postsynaptic potentials (IPSPs) located on or near the soma was observed in the 3-channel model cell subjected to random synaptic bombardment. In the 11-channel model, phase-locking due to multiple IPSPs was compared with phase-locking due to multiple excitatory postsynaptic potentials (EPSPs). Phase-locking began to occur when 20% of the IPSPs (20/100) or 40% of the EPSPs (4,000/10,000) were synchronized. The exact percentages differed with different 11-channel models, but either EPSPs or IPSPs would generally produce entrainment with approximately 40% synchronization. Thus 40 inhibitory boutons had an effect equivalent to 4,000 excitatory boutons in producing phase-locking. 4. Phase-locking with IPSPs in these models was possible because the IPSPs could cause either an increase or a decrease in firing rate over a limited range. The IPSPs served a modulatory role, increasing the rate of firing in some cases and decreasing it in others, depending on the state of the cell. 5. We examined frequency entrainment by IPSPs. In the 3-channel model, frequency entrainment of a postsynaptic cell was observed with a rapid train of strong (20-100 nS), brief, compound IPSPs. A 40-Hz compound IPSP train of 60 nS entrained cells having initial firing rates between 32 and 47 Hz. Below this range, cells could be partially entrained. Above the range, entrainment would fail. Frequency entrainment in the 3-channel model generally occurred on the first cycle after onset of the IPSPs. 6. Phase-locking and frequency entrainment were less robust in the 11-channel model. This was partly because bursts rather than individual spikes were being entrained. A 40-Hz, 90-nS compound IPSP train entrained a model cell upward from 34 Hz. Downward frequency entrainment also occurred.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 通过计算机模拟研究了抑制性中间神经元与皮质锥体细胞之间的相互作用,以测试抑制性中间神经元是否有助于使突触后细胞锁相。使用了两种模型:一种简化模型,仅包含3种膜通道;另一种详细的11通道模型。2. 11通道模型包括了已知存在于新皮质锥体细胞中的大多数离子通道,以及钙扩散和其他膜机制。通道的动力学是从各种制剂中的电压钳研究中获得的。然后调整参数以产生类似于在视觉刺激期间被夹带的一些皮质锥体细胞中所见的重复爆发。3. 在受到随机突触轰击的3通道模型细胞中,观察到对位于胞体上或附近的一串抑制性突触后电位(IPSP)的锁相。在11通道模型中,将多个IPSP引起的锁相与多个兴奋性突触后电位(EPSP)引起的锁相进行了比较。当20%的IPSP(20/100)或40%的EPSP(4000/10000)同步时,开始出现锁相。确切的百分比因不同的11通道模型而异,但EPSP或IPSP通常在约40%同步时会产生夹带。因此,在产生锁相方面,40个抑制性突触小体的作用相当于4000个兴奋性突触小体。4. 在这些模型中,与IPSP的锁相是可能的,因为IPSP可以在有限范围内引起放电率的增加或降低。IPSP起到调节作用,根据细胞状态,在某些情况下增加放电率,在其他情况下降低放电率。5. 我们研究了IPSP引起的频率夹带。在3通道模型中,用一串快速的强(20 - 100 nS)、短暂的复合IPSP观察到突触后细胞的频率夹带。60 nS的40 Hz复合IPSP串夹带了初始放电率在32至47 Hz之间的细胞。低于此范围,细胞可被部分夹带。高于此范围,夹带将失败。3通道模型中的频率夹带通常在IPSP开始后的第一个周期发生。6. 11通道模型中的锁相和频率夹带不太稳定。部分原因是被夹带的是爆发而不是单个动作电位。一串40 Hz、90 nS的复合IPSP将一个模型细胞从34 Hz向上夹带。也发生了向下的频率夹带。(摘要截断于400字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验