LeBeau Fiona E N, Towers Stephen K, Traub Roger D, Whittington Miles A, Buhl Eberhard H
School of Biomedical Sciences, University of Leeds, Leeds LS2 9NQ, UK.
J Physiol. 2002 Jul 1;542(Pt 1):167-79. doi: 10.1113/jphysiol.2002.015933.
Brief pressure ejection of solutions containing potassium, caesium or rubidium ions into stratum radiatum of the CA1 or CA3 regions of the hippocampal slice evoked a fast network oscillation. The activity evoked lasted approximately 3-25 s with the predominant frequency component being in the gamma frequency range (30-80 Hz), although beta frequency (15-30 Hz) and ultrafast (> 80 Hz) components could also be seen. The gamma frequency component of the oscillation remained constant, even when large changes in power occurred, and was synchronous across the CA1 region. Measurements with potassium ion-sensitive electrodes revealed that the network oscillation was accompanied by increases (0.5 to 2.0 mM) in the extracellular potassium concentration [K+]o. Bath application of the N-methyl-D-aspartate (NMDA) receptor antagonists D(-)-2-amino-5-phosphonopentanoic acid (D-AP5; 50 microM) had no significant effect but the alpha-amino-3-hydroxy-5-methyl-4-isooxazolepropionic acid (AMPA)/kainate receptor antagonist 2,3,-dioxo-6-nitro-1,2,3,4-tetrahydrobenzo[f]quinoxaline-7-sulphonamide disodium (NBQX; 20 microM) caused a significant reduction (86.7 +/- 4.5 %) in the power in the gamma frequency range. Residual rhythmic activity, presumably arising in the interneuronal network, was blocked by the GABA(A) receptor antagonist bicuculline. The putative gap junction blocker octanol caused a decrease in the power of the gamma frequency component of 75.5 +/- 5.6 %, while carbenoxolone produced a reduction of only 14 +/- 42 %. These experiments demonstrate that a modest increase in exogenous [K+]o in the hippocampus in vitro is sufficient to evoke a fast network oscillation, which is an emergent property of the synaptically and electrically interconnected neuronal network.
将含有钾离子、铯离子或铷离子的溶液短暂压力喷射到海马切片CA1或CA3区的辐射层中,会诱发快速的网络振荡。诱发的活动持续约3 - 25秒,主要频率成分在γ频率范围(30 - 80赫兹),不过也能看到β频率(15 - 30赫兹)和超快(> 80赫兹)成分。即使功率发生大幅变化,振荡的γ频率成分仍保持恒定,且在整个CA1区是同步的。用钾离子敏感电极测量发现,网络振荡伴随着细胞外钾离子浓度[K + ] o的升高(0.5至2.0毫摩尔)。浴用N - 甲基 - D - 天冬氨酸(NMDA)受体拮抗剂D( - ) - 2 - 氨基 - 5 - 磷酸戊酸(D - AP5;50微摩尔)没有显著影响,但α - 氨基 - 3 - 羟基 - 5 - 甲基 - 4 - 异恶唑丙酸(AMPA)/海人藻酸受体拮抗剂2,3 - 二氧代 - 6 - 硝基 - 1,2,3,4 - 四氢苯并[f]喹喔啉 - 7 - 磺酰胺二钠(NBQX;20微摩尔)使γ频率范围内的功率显著降低(86.7±4.5%)。推测起源于中间神经元网络的残余节律性活动被GABA(A)受体拮抗剂荷包牡丹碱阻断。公认的缝隙连接阻滞剂辛醇使γ频率成分的功率降低75.5±5.6%,而甘草次酸仅使功率降低14±42%。这些实验表明,体外海马中外源性[K + ] o的适度升高足以诱发快速的网络振荡,这是突触和电连接的神经元网络的一种涌现特性。