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关于4-氨基吡啶在幼年大鼠海马CA3亚区诱导的同步活动。

On the synchronous activity induced by 4-aminopyridine in the CA3 subfield of juvenile rat hippocampus.

作者信息

Avoli M, Psarropoulou C, Tancredi V, Fueta Y

机构信息

Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada.

出版信息

J Neurophysiol. 1993 Sep;70(3):1018-29. doi: 10.1152/jn.1993.70.3.1018.

Abstract
  1. Extracellular field potential and intracellular recordings were made in the CA3 subfield of hippocampal slices obtained from 10- to 24-day-old rats during perfusion with artificial cerebrospinal fluid (ACSF) containing the convulsant 4-aminopyridine (4-AP, 50 microM). 2. Three types of spontaneous, synchronous activity were recorded in the presence of 4-AP by employing extracellular microelectrodes positioned in the CA3 stratum (s.) radiatum: first, inter-ictal-like discharges that lasted 0.2-1.2 s and had an occurrence rate of 0.3-1.3 Hz; second, ictal-like events (duration: 3-40 s) that occurred at 4-38 x 10(-3) Hz; and third, large-amplitude (up to 8 mV) negative-going potentials that preceded the onset of the ictal-like events and thus appeared to initiate them. 3. None of these synchronous activities was consistently modified by addition of antagonists of the N-methyl-D-aspartate (NMDA) receptor to the ACSF. In contrast, the non-NMDA receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX, 2-10 microM) reversibly blocked interictal- and ictallike discharges. The only synchronous, spontaneous activity recorded in this type of medium consisted of the negative-going potentials that were abolished by the GABAA receptor antagonists bicuculline methiodide (5-20 microM) or picrotoxin (50 microM). Hence they were mediated through the activation of the GABAA receptor. 4. Profile analysis of the 4-AP-induced synchronous activity revealed that the gamma-aminobutyric acid (GABA)-mediated field potential had maximal negative amplitude in s. lacunosum-moleculare, attained equipotentiality at the border between s. radiatum and s. pyramidale, and became positive-going in s. oriens. These findings indicated that the GABA-mediated field potential presumably represented a depolarization occurring in the dendrites of CA3 pyramidal cells. 5. This conclusion was supported by intracellular analysis of the 4-AP-induced activity. The GABA-mediated potential was reflected by a depolarization of the membrane of CA3 pyramidal cells that triggered a few variable-amplitude, fractionated spikes or fast action potentials. By contrast, the ictal-like discharge was associated with a prolonged depolarization during which repetitive bursts of action potentials occurred. Short-lasting depolarizations with bursts of action potentials occurred during each interictal-like discharge. 6. The GABA-mediated potential recorded intracellularly in the presence of CNQX consisted of a prolonged depolarization (up to 12 s) that was still capable of triggering a few fast action potentials and/or fractionated spikes.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 在灌注含惊厥剂4-氨基吡啶(4-AP,50微摩尔)的人工脑脊液(ACSF)期间,对10至24日龄大鼠的海马切片CA3亚区进行细胞外场电位和细胞内记录。2. 通过置于CA3辐射层的细胞外微电极,在4-AP存在下记录到三种类型的自发同步活动:第一,持续0.2至1.2秒、发生率为0.3至1.3赫兹的发作间期样放电;第二,以4至38×10⁻³赫兹发生的发作期样事件(持续时间:3至40秒);第三,在发作期样事件开始前出现的大振幅(高达8毫伏)负向电位,似乎引发了这些事件。3. 向ACSF中添加N-甲基-D-天冬氨酸(NMDA)受体拮抗剂,这些同步活动均未持续改变。相反,非NMDA受体拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX,2至10微摩尔)可逆地阻断发作间期和发作期样放电。在这种培养基中记录到的唯一同步自发活动由负向电位组成,这些电位被GABAA受体拮抗剂甲基荷包牡丹碱(5至20微摩尔)或印防己毒素(50微摩尔)消除。因此它们是通过GABAA受体的激活介导的。4. 对4-AP诱导的同步活动的剖面分析表明,γ-氨基丁酸(GABA)介导的场电位在分子层有最大负振幅,在辐射层和锥体细胞层边界达到等电位,并在原层变为正向。这些发现表明,GABA介导的场电位可能代表CA3锥体细胞树突中发生的去极化。5. 这一结论得到了对4-AP诱导活动的细胞内分析的支持。GABA介导的电位由CA3锥体细胞膜的去极化反映,该去极化触发了一些幅度可变的分离尖峰或快速动作电位。相比之下,发作期样放电与长时间去极化相关,在此期间发生动作电位的重复爆发。每次发作间期样放电期间都会出现伴有动作电位爆发的短暂去极化。6. 在CNQX存在下细胞内记录到的GABA介导的电位由长时间去极化(长达12秒)组成,该去极化仍能够触发一些快速动作电位和/或分离尖峰。(摘要截断于400字)

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