Brierley M J, Yeoman M S, Benjamin P R
Sussex Centre for Neuroscience, School of Biological Sciences, University of Sussex, Brighton, East Sussex BN1 9QG, United Kingdom.
J Neurophysiol. 1997 Dec;78(6):3396-407. doi: 10.1152/jn.1997.78.6.3396.
We aimed to show that the paired N2v (N2 ventral) plateauing cells of the buccal ganglia are important central pattern generator (CPG) interneurons of the Lymnaea feeding system. N2v plateauing is phase-locked to the rest of the CPG network in a slow oscillator (SO)-driven fictive feeding rhythm. The phase of the rhythm is reset by artificially evoked N2v bursts, a characteristic of CPG neurons. N2v cells have extensive input and output synaptic connections with the rest of the CPG network and the modulatory SO cell and cerebral giant cells (CGCs). Synaptic input from the protraction phase interneurons N1M (excitatory), N1L (inhibitory), and SO (inhibitory-excitatory) are likely to contribute to a ramp-shaped prepotential that triggers the N2v plateau. The prepotential has a highly complex waveform due to progressive changes in the amplitude of the component synaptic potentials. Most significant is the facilitation of the excitatory component of the SO --> N2v monosynaptic connection. None of the other CPG interneurons has the appropriate input synaptic connections to terminate the N2v plateaus. The modulatory function of acetylcholine (ACh), the transmitter of the SO and N1M/N1Ls, was examined. Focal application of ACh (50-ms pulses) onto the N2v cells reproduced the SO --> N2v biphasic synaptic response but also induced long-term plateauing (20-60 s). N2d cells show no endogenous ability to plateau, but this can be induced by focal applications of ACh. The N2v cells inhibit the N3 tonic (N3t) but not the N3 phasic (N3p) CPG interneurons. The N2v --> N3t inhibitory synaptic connection is important in timing N3t activity. The N3t cells recover from this inhibition and fire during the swallow phase of the feeding pattern. Feedback N2v inhibition to the SO, N1L protraction phase interneurons prevents them firing during the retraction phase of the feeding cycle. The N2v --> N1M synaptic connection was weak and only found in 50% of preparations. A weak N2v --> CGC inhibitory connection prevents the CGCs firing during the rasp (N2) phase of the feeding cycle. These data allowed a new model for the Lymnaea feeding CPG to be proposed. This emphasizes that each of the six types of CPG interneuron has a unique set of synaptic connections, all of which contribute to the generation of a full CPG pattern.
我们旨在证明,淡水螺颊神经节中的成对N2v(N2腹侧)平台化细胞是椎实螺进食系统重要的中枢模式发生器(CPG)中间神经元。在由慢振荡器(SO)驱动的虚构进食节律中,N2v平台化与CPG网络的其余部分相位锁定。通过人工诱发N2v爆发可重置节律的相位,这是CPG神经元的一个特征。N2v细胞与CPG网络的其余部分、调制性SO细胞和脑巨细胞(CGC)有着广泛的输入和输出突触连接。来自伸展相中间神经元N1M(兴奋性)、N1L(抑制性)和SO(抑制 - 兴奋性)的突触输入可能有助于形成触发N2v平台的斜坡形预电位。由于组成突触电位幅度的逐渐变化,该预电位具有高度复杂的波形。最显著的是SO→N2v单突触连接的兴奋性成分的易化作用。其他CPG中间神经元均没有合适的输入突触连接来终止N2v平台。我们研究了乙酰胆碱(ACh)的调制功能,它是SO和N1M/N1L的神经递质。向N2v细胞局部施加ACh(50毫秒脉冲)可重现SO→N2v双相突触反应,但也会诱导长期平台化(20 - 60秒)。N2d细胞没有内源性的平台化能力,但可通过局部施加ACh来诱导。N2v细胞抑制N3紧张性(N3t)而非N3相位性(N3p)CPG中间神经元。N2v→N3t抑制性突触连接在确定N3t活动的时间方面很重要。N3t细胞从这种抑制中恢复并在进食模式的吞咽阶段放电。N2v对SO、N1L伸展相中间神经元的反馈抑制可防止它们在进食周期的回缩阶段放电。N2v→N1M突触连接较弱,仅在50%的标本中发现。N2v→CGC的微弱抑制性连接可防止CGC在进食周期的锉磨(N2)阶段放电。这些数据使得我们能够提出一个新的椎实螺进食CPG模型。这强调了六种类型的CPG中间神经元中的每一种都有一组独特的突触连接,所有这些连接都有助于产生完整的CPG模式。