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Underlying mechanisms of short-term synaptic plasticity at identified central synapses

机译:在确定的中央突触的短期突触可塑性的潜在机制。

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The general goal of my project was to detect the underlying mechanisms of short-term plasticity at identified synapses in the central nervous system. I have investigated the bases of cell type-specific differences in short-term plasticity of synaptic connections of distinct types of hippocampal interneu-rons. My results showed that both the overall strength and the short-term plasticity of synapses received and established by hippocampal interneu-rons are highly regulated by persistently active presynaptic metabotropic receptors in a cell type-specific manner. Thus, in principle, cell type-specific modulation of short-term plasticity by toni-cally active presynaptic receptors may contribute to the differential functional role of distinct in-terneurons during normal and pathological hippocampal functioning.
机译:我的项目的总体目标是检测中枢神经系统中已确定的突触的短期可塑性的潜在机制。我研究了海马interneurons不同类型的突触连接的短期可塑性中细胞类型特定差异的基础。我的研究结果表明,持续激活的突触前代谢型受体以细胞类型特异性方式高度调控海马神经元接收和建立的突触的整体强度和短期可塑性。因此,原则上,通过tonically活跃的突触前受体的短期可塑性的细胞类型特异性调制可能有助于正常和病理性海马功能期间不同的内在神经元的不同功能作用。

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