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N-甲基-D-天冬氨酸在小脑浦肯野细胞和中间神经元中的突触前效应。

Presynaptic effects of NMDA in cerebellar Purkinje cells and interneurons.

作者信息

Glitsch M, Marty A

机构信息

Arbeitsgruppe Zelluläre Neurobiologie, Max-Planck-Institut für biophysikalische Chemie, 37077, Göttingen, Germany.

出版信息

J Neurosci. 1999 Jan 15;19(2):511-9. doi: 10.1523/JNEUROSCI.19-02-00511.1999.

Abstract

NMDA receptors (NMDARs) are generally believed to mediate exclusively postsynaptic effects at brain synapses. Here we searched for presynaptic effects of NMDA at inhibitory synapses in rat cerebellar slices. In Purkinje cells, application of NMDA enhanced the frequency of miniature IPSCs (mIPSCs) but not that of miniature EPSCs (mEPSCs). This increase in frequency was dependent on the external Mg2+ concentration. In basket and stellate cells, NMDA induced an even larger mIPSC frequency increase than in Purkinje cells, whereas mEPSCs were again not affected. Moreover, NMDA induced an inward current in both types of interneuron, which translated into a small depolarization (approximately 10 mV for 30 microM NMDA) under current-clamp conditions. In paired recordings of connected basket cell-Purkinje cell synapses, depolarizations of 10-30 mV applied to the basket cell soma enhanced the frequency of postsynaptic mIPSCs, suggesting that somatic depolarization was partially transmitted to the terminals in the presence of tetrodotoxin. However, this effect was small and unlikely to account fully for the effects of NMDA on mIPSCs. Consistent with a small number of dendritic NMDARs, evoked EPSCs in interneurons had a remarkably small NMDA component. Evoked IPSCs at interneuron-interneuron synapses were inhibited by NMDA, and the rate of failures was increased, indicating again a presynaptic site of action. We conclude that activation of NMDARs in interneurons exerts complex presynaptic effects, and that the corresponding receptors are most likely located in the axonal domain of the cell.

摘要

一般认为,N-甲基-D-天冬氨酸受体(NMDARs)仅介导脑突触的突触后效应。在此,我们探寻了NMDA在大鼠小脑切片抑制性突触处的突触前效应。在浦肯野细胞中,应用NMDA可提高微小抑制性突触后电流(mIPSCs)的频率,但对微小兴奋性突触后电流(mEPSCs)的频率无影响。这种频率增加依赖于细胞外Mg2+浓度。在篮状细胞和星状细胞中,NMDA诱导的mIPSC频率增加甚至比在浦肯野细胞中更大,而mEPSCs同样不受影响。此外,NMDA在这两种中间神经元中均诱导出内向电流,在电流钳制条件下,这转化为小的去极化(对于30 microM的NMDA约为10 mV)。在相连的篮状细胞 - 浦肯野细胞突触的配对记录中,施加于篮状细胞胞体的10 - 30 mV去极化增强了突触后mIPSCs的频率,这表明在存在河豚毒素的情况下,胞体去极化部分传递到了终末。然而,这种效应较小,不太可能完全解释NMDA对mIPSCs的影响。与少量树突状NMDARs一致,中间神经元中诱发的兴奋性突触后电流(EPSCs)的NMDA成分非常小。中间神经元 - 中间神经元突触处诱发的抑制性突触后电流(IPSCs)受到NMDA抑制,且失败率增加,再次表明作用位点在突触前。我们得出结论,中间神经元中NMDARs的激活发挥复杂的突触前效应,且相应受体很可能位于细胞的轴突区域。

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