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组织培养中大鼠海马体的兴奋性突触及阿尼西坦的作用。

Excitatory synapse in the rat hippocampus in tissue culture and effects of aniracetam.

作者信息

Ozawa S, Iino M, Abe M

机构信息

Department of Physiology, School of Medicine, Gunma University, Maebashi, Japan.

出版信息

Neurosci Res. 1991 Oct;12(1):72-82. doi: 10.1016/0168-0102(91)90101-4.

Abstract

Excitatory synaptic connections between rat hippocampal neurons were established in tissue culture. The electrophysiological and pharmacological properties of these synapses were studied with the use of the tight-seal whole-cell recording technique. The excitatory postsynaptic current (EPSC) in a dissociated CA1 neuron evoked by stimulation of an explant from the CA3/CA4 region of the hippocampus had two distinct components in Mg(2+)-free medium. The fast component was abolished by the non-NMDA receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) (2 microM), whereas the slow component was abolished by the N-methyl-D-aspartate (NMDA) receptor antagonist D-2-amino-5-phosphonovalerate (D-APV) (50 microM). In solution containing 1 mM Mg2+, the peak amplitude of the fast component was almost linearly related to the membrane potential. In contrast, the conductance change underlying the slow component of the EPSC was voltage-dependent with a region of negative-slope conductance in the range of -80 to -20 mV. A nootropic drug, aniracetam, increased both the amplitude and duration of the fast component of the EPSC in a concentration-dependent manner in the range of 0.1-5 mM, whereas it had no potentiating effect on the slow component. Aniracetam (0.1-5 mM) similarly increased current responses of the postsynaptic neuron to alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA). Current responses to quisqualate and glutamate in the presence of D-APV were also potentiated by aniracetam. However, neither NMDA- nor kainate-induced current was potentiated by 1 mM aniracetam.

摘要

大鼠海马神经元之间的兴奋性突触连接在组织培养中得以建立。利用紧密封全细胞记录技术研究了这些突触的电生理和药理学特性。在无镁培养基中,刺激海马CA3/CA4区的外植体诱发的离体CA1神经元中的兴奋性突触后电流(EPSC)有两个不同的成分。快速成分被非NMDA受体拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)(2微摩尔)消除,而慢速成分被N-甲基-D-天冬氨酸(NMDA)受体拮抗剂D-2-氨基-5-磷酸戊酸(D-APV)(50微摩尔)消除。在含有1毫摩尔镁离子的溶液中,快速成分的峰值幅度几乎与膜电位呈线性相关。相比之下,EPSC慢速成分背后的电导变化是电压依赖性的,在-80至-20毫伏范围内存在负斜率电导区域。一种益智药阿尼西坦在0.1-5毫摩尔范围内以浓度依赖性方式增加了EPSC快速成分的幅度和持续时间,而对慢速成分没有增强作用。阿尼西坦(0.1-5毫摩尔)同样增加了突触后神经元对α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)的电流反应。在存在D-APV的情况下,对quisqualate和谷氨酸的电流反应也被阿尼西坦增强。然而,1毫摩尔阿尼西坦对NMDA或海人藻酸诱导的电流均无增强作用。

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