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鸟类两耳声级差定位神经元的突触抑制。

Synaptic Inhibition in Avian Interaural Level Difference Sound Localizing Neurons.

机构信息

Department of Anatomy and Neurobiology, College of Medicine, Northeast Ohio Medical University, Rootstown, Ohio 44272; School of Biomedical Sciences, Kent State University, Kent, Ohio 44240.

出版信息

eNeuro. 2016 Dec 20;3(6). doi: 10.1523/ENEURO.0309-16.2016. eCollection 2016 Nov-Dec.

Abstract

Synaptic inhibition plays a fundamental role in the neural computation of the interaural level difference (ILD), an important cue for the localization of high-frequency sound. Here, we studied the inhibitory synaptic currents in the chicken posterior portion of the dorsal nucleus of the lateral lemniscus (LLDp), the first binaural level difference encoder of the avian auditory pathway. Using whole-cell recordings in brain slices, we provide the first evidence confirming a monosynaptic inhibition driven by direct electrical and chemical stimulation of the contralateral LLDp, establishing the reciprocal inhibitory connection between the two LLDps, a long-standing assumption in the field. This inhibition was largely mediated by GABA receptors; however, functional glycine receptors were also identified. The reversal potential for the Cl channels measured with gramicidin-perforated patch recordings was hyperpolarizing (-88 mV), corresponding to a low intracellular Cl concentration (5.2 mm). Pharmacological manipulations of KCC2 (outwardly Cl transporter) activity demonstrate that LLDp neurons can maintain a low intracellular Cl concentration under a high Cl load, allowing for the maintenance of hyperpolarizing inhibition. We further demonstrate that hyperpolarizing inhibition was more effective at regulating cellular excitability than depolarizing inhibition in LLDp neurons.

摘要

突触抑制在听觉通路中对高频声音定位非常重要的耳间强度差(ILD)的神经计算中起着基本作用。在这里,我们研究了鸡外侧丘系背核后段(LLDp)中的抑制性突触电流,LLDp 是鸟类听觉通路中第一个双耳强度差编码器。通过脑片的全细胞膜片钳记录,我们提供了第一个证据,证实了对侧 LLDp 的直接电和化学刺激驱动的单突触抑制,从而确立了两个 LLDp 之间的相互抑制连接,这是该领域的一个长期假设。这种抑制主要是由 GABA 受体介导的;然而,也鉴定出功能性甘氨酸受体。用 gramicidin 穿孔膜片钳记录测量的 Cl 通道的反转电位为超极化(-88 mV),对应于低细胞内 Cl 浓度(5.2 mm)。对 KCC2(外向 Cl 转运体)活性的药理学操作表明,LLDp 神经元可以在高 Cl 负荷下保持低细胞内 Cl 浓度,从而允许维持超极化抑制。我们进一步证明,在 LLDp 神经元中,超极化抑制比去极化抑制更有效地调节细胞兴奋性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6dd/5168645/3a99d1fb89ca/enu0061621950001.jpg

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