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豚鼠离体蜗背侧核中对平行纤维刺激的反应

Responses to parallel fiber stimulation in the guinea pig dorsal cochlear nucleus in vitro.

作者信息

Manis P B

机构信息

Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.

出版信息

J Neurophysiol. 1989 Jan;61(1):149-61. doi: 10.1152/jn.1989.61.1.149.

Abstract
  1. Parallel fibers of the guinea pig dorsal cochlear nucleus (DCN) were electrically stimulated at the pial surface of the nucleus in a brain-slice preparation. Extracellular field potentials produced by the parallel fibers and postsynaptic cells, and the response of single units were identified and characterized. Responses were compared with those reported for stimulation of parallel fibers in the cerebellum and to those seen with electrical stimulation of the auditory nerve. 2. Stimulation of the DCN parallel fibers generates a consistent set of extracellular field potentials. In layer 1 of the DCN, a short-latency triphasic wave (P1(1)-N1(1)-P2(1)) is followed by a slower negative wave (N2(1)). The onset phase of the N2(1) often exhibits a small positive notch (P2a1). In layer 2, an initial triphasic wave (P1(2)-N1(2)-P2(2)) is followed by a short-latency negative wave (N2(2)) and a slower positive wave (P3(2)). The N1(2) is approximately coincident with the N1(1), whereas the P3(2) is coincident with N2(1). The falling phase of the P3(2) is sometimes interrupted by a brief negative deflection (N3(2)). These field potentials are similar, but not identical to those reported for parallel fiber stimulation in the cerebellum in vivo (15). These responses differ substantially from those produced in the DCN by electrical stimulation of the auditory nerve (50). 3. Low-calcium solutions and pharmacologic manipulations were used to separate pre- and postsynaptic response components in the field potential records. When the slice is bathed in a low-calcium solution the P2a1, N2(1), N2(2), P3(2), and the brief late deflections are abolished. However, the P1(1)-N1(1)-P2(1) and P1(2)-N1(2)-P2(2) remain unaffected. A similar separation of pre- and postsynaptic components can be achieved with 100 microM adenosine or 0.5 mM kynurenic acid. It is concluded that the P1(1)-M1(1)-P2(1) wave is the compound action potential of the unmyelinated parallel fibers, whereas the longer-latency field potential components are generated postsynaptically. 4. The conduction velocity of the parallel fiber volley was measured to be 0.30 m/s at the pial surface, in a line approximately parallel to the strial axis of the nucleus. Mapping experiments reveal that the spread of the P1(1)-N1(1)-P2(1) is greatest along the strial axis, and more limited in the orthogonal direction. 5. Single units were recorded in layer 2. At a distance of 500-700 microns from the stimulating electrode, the latencies of single-unit discharges fall between 2.5 and 4 ms, at the time of the N2(2).(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 在脑片标本中,对豚鼠蜗背侧核(DCN)的平行纤维在该核的软膜表面进行电刺激。确定并描述了由平行纤维和突触后细胞产生的细胞外场电位以及单个神经元的反应。将这些反应与报道的小脑平行纤维刺激的反应以及听神经电刺激所观察到的反应进行了比较。2. 刺激DCN平行纤维会产生一组一致的细胞外场电位。在DCN的第1层,一个短潜伏期的三相波(P1(1)-N1(1)-P2(1))之后是一个较慢的负波(N2(1))。N2(1)的起始阶段通常呈现一个小的正切迹(P2a1)。在第2层,一个初始的三相波(P1(2)-N1(2)-P2(2))之后是一个短潜伏期的负波(N2(2))和一个较慢的正波(P3(2))。N1(2)与N1(1)大致同时出现,而P3(2)与N2(1)同时出现。P3(2)的下降阶段有时会被一个短暂的负向偏转(N3(2))中断。这些场电位与体内小脑平行纤维刺激报道的电位相似但不完全相同(15)。这些反应与听神经电刺激在DCN中产生的反应有很大不同(50)。3. 使用低钙溶液和药理学操作来分离场电位记录中的突触前和突触后反应成分。当脑片浸泡在低钙溶液中时,P2a1、N2(1)、N2(2)、P3(2)以及短暂的晚期偏转消失。然而,P1(1)-N1(1)-P2(1)和P1(2)-N1(2)-P2(2)不受影响。用100微摩尔的腺苷或0.5毫摩尔的犬尿氨酸也可实现突触前和突触后成分的类似分离。得出结论,P1(1)-M1(1)-P2(1)波是无髓鞘平行纤维的复合动作电位,而较长潜伏期的场电位成分是突触后产生的。4. 测量到平行纤维群在软膜表面的传导速度为0.30米/秒,方向大致平行于核的纹状轴。绘图实验表明,P1(1)-N1(1)-P2(1)的传播沿纹状轴最大,在正交方向上更有限。5. 在第2层记录单个神经元。在距刺激电极500 - 700微米处,单个神经元放电的潜伏期在N2(2)出现时为2.5至4毫秒。(摘要截断于400字)

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