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Synaptic tagging and capture in the living rat

机译:活大鼠的突触标记和捕获

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In isolated hippocampal slices, decaying long-term potentiation can be stabilized and converted to late long-term potentiation lasting many hours, by prior or subsequent strong high-frequency tetanization of an independent input to a common populationof neurons—a phenomenon known as ‘synaptic tagging and capture’. Here we show that the same phenomenon occurs in the intact rat. Late long-term potentiation can be induced in CA1 during the inhibition of protein synthesis if an independent input is strongly tetanized beforehand. Conversely, declining early long-term potentiation induced by weak tetanization can be converted into lasting late long-term potentiation by subsequent strong tetanization of a separate input. These findings indicate that synaptic tagging and capture is not limited to in vitro preparations; the past and future activity of neurons has a critical role in determining the persistence of synaptic changes in the living animal, thus providing a bridge between cellular studies of protein synthesis-dependent synaptic potentiation and behavioural studies of memory persistence.
机译:在分离的海马切片中,可以通过先后或随后对共同的神经元群体进行独立输入的强高频镀钛作用,使衰减的长期增强作用稳定并转换成持续数小时的晚期长期增强作用,这种现象称为“突触”标记和捕获”。在这里,我们表明在完整的老鼠中也会发生相同的现象。如果事先将一个独立的输入进行了强烈的鞣制,则可以在抑制蛋白质合成的过程中在CA1中诱导晚期长期增强作用。相反,弱的成膜作用引起的早期长期增强作用的下降可通过随后对单独输入物的强成膜作用转化为持久的后期长期增强作用。这些发现表明,突触标记和捕获不限于体外制剂。神经元的过去和未来活动在确定活体中突触变化的持久性方面起着至关重要的作用,从而在蛋白质合成依赖性突触增强作用的细胞研究与记忆持久性行为研究之间架起了桥梁。

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