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海马体长期抑制的两种形式,即长期增强的对应形式。

Two forms of hippocampal long-term depression, the counterpart of long-term potentiation.

作者信息

Manabe T

机构信息

Department of Neurophysiology, Faculty of Medicine, University of Tokyo, Japan.

出版信息

Rev Neurosci. 1997 Jul-Dec;8(3-4):179-93. doi: 10.1515/revneuro.1997.8.3-4.179.

Abstract

In the hippocampus there are two distinct forms of long-term depression (LTD) of excitatory synaptic transmission. In the CA1 region, prolonged low-frequency stimulation induces LTD by activating postsynaptic NMDA receptors, which causes a moderate rise in Ca2+ concentrations. In mossy fiber synapses of the CA3 region, similar low-frequency stimulation also gives rise to LTD. However, this form of LTD (mossy fiber LTD) does not require activation of NMDA receptors, but is mediated by activation of presynaptic metabotropic glutamate receptors. Induction of mossy fiber LTD is not dependent on postsynaptic depolarization or activation of postsynaptic ionotropic glutamate receptors, thus it is likely to be mediated by purely presynaptic mechanisms. This conclusion is confirmed by the analysis of mutant mice lacking presynaptic mGluR2, in which mossy fiber LTD is almost absent. Since long-term potentiation at mossy fiber synapses is also induced presynaptically, the synaptic efficacy may be regulated through common mechanisms bidirectionally, which may contribute to neural information processing in the hippocampus.

摘要

在海马体中,兴奋性突触传递存在两种不同形式的长时程抑制(LTD)。在CA1区域,长时间的低频刺激通过激活突触后NMDA受体诱导LTD,这会导致Ca2+浓度适度升高。在CA3区域的苔藓纤维突触中,类似的低频刺激也会引发LTD。然而,这种形式的LTD(苔藓纤维LTD)并不需要激活NMDA受体,而是由突触前代谢型谷氨酸受体的激活介导的。苔藓纤维LTD的诱导不依赖于突触后去极化或突触后离子型谷氨酸受体的激活,因此它很可能是由纯粹的突触前机制介导的。对缺乏突触前mGluR2的突变小鼠的分析证实了这一结论,在这些小鼠中几乎不存在苔藓纤维LTD。由于苔藓纤维突触处的长时程增强也是由突触前诱导的,突触效能可能通过共同机制进行双向调节,这可能有助于海马体中的神经信息处理。

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