Kopp-Scheinpflug Cornelia, Dehmel Susanne, Dörrscheidt Gerd J, Rübsamen Rudolf
Department of Neurobiology, University of Leipzig, 04103 Leipzig, Germany.
J Neurosci. 2002 Dec 15;22(24):11004-18. doi: 10.1523/JNEUROSCI.22-24-11004.2002.
Spherical bushy cells (SBCs) of the anteroventral cochlear nucleus (AVCN) receive their main excitatory input from auditory nerve fibers (ANFs) through large synapses, endbulbs of Held. These cells are also the target of inhibitory inputs whose function is not well understood. The present study examines the role of inhibition in the encoding of low-frequency sounds in the gerbil's AVCN. The presynaptic action potentials of endbulb terminals and postsynaptic action potentials of SBCs were monitored simultaneously in extracellular single-unit recordings in vivo. An input-output analysis of presynaptic and postsynaptic activity was performed for both spontaneous and acoustically driven activity. Two-tone stimulation and neuropharmacological experiments allowed the effects of neuronal inhibition and cochlear suppression on SBC activity to be distinguished. Ninety-one percent of SBCs showed significant neuronal inhibition. Inhibitory sidebands enclosed the high- or low-frequency, or both, sides of the excitatory areas of these units; this was reflected as a presynaptic to postsynaptic increase in frequency selectivity of up to one octave. Inhibition also affected the level-dependent responses at the characteristic frequency. Although in all units the presynaptic recordings showed monotonic rate-level functions, this was the case in only half of the postsynaptic recordings. In the other half of SBCs, postsynaptic inhibitory areas overlapped the excitatory areas, resulting in nonmonotonic rate-level functions. The results demonstrate that the sound-evoked spike activity of SBCs reflects the integration of acoustically driven excitatory and inhibitory input. The inhibition specifically affects the processing of the spectral, temporal, and intensity cues of acoustic signals.
前腹侧耳蜗核(AVCN)的球形浓密细胞(SBCs)通过大突触—— Held终球,从听神经纤维(ANFs)接收主要的兴奋性输入。这些细胞也是抑制性输入的靶点,其功能尚不清楚。本研究探讨了抑制在沙鼠AVCN低频声音编码中的作用。在体内细胞外单单位记录中,同时监测了终球终末的突触前动作电位和SBCs的突触后动作电位。对自发活动和声音驱动活动进行了突触前和突触后活动的输入-输出分析。双音刺激和神经药理学实验能够区分神经元抑制和耳蜗抑制对SBC活动的影响。91%的SBCs表现出显著的神经元抑制。抑制性边带包围了这些单位兴奋性区域的高频或低频或两侧;这表现为突触前到突触后频率选择性增加高达一个八度。抑制还影响了特征频率下的强度依赖性反应。虽然在所有单位中,突触前记录显示出单调的速率-强度函数,但在突触后记录中只有一半是这种情况。在另一半SBCs中,突触后抑制区域与兴奋性区域重叠,导致非单调的速率-强度函数。结果表明,SBCs的声音诱发尖峰活动反映了声音驱动的兴奋性和抑制性输入的整合。抑制作用特别影响声信号的频谱、时间和强度线索的处理。