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Effect of adenosine-induced changes in presynaptic release probability on long-term potentiation in the hippocampal CA1 region

机译:腺苷诱导的突触释放概率变化对海马CA1区长期增强的影响

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摘要

In the present study some characteristics of long-term potentiation (LTP) in the hippocampal CA1 region were examined under different conditions of transmitter release. Adenosine A1 agonist/antagonists, or in some instances changes in the extracellular calcium/magnesium ratio, were used to alter release probability. The overall LTP time course (onset latency, growth phase, and subsequent decay for both the non- NMDA and NMDA receptor-mediated EPSPs) following a brief tetanus was essentially the same over an almost 10-fold variation in release probability (measured as change in field EPSP magnitude). The major difference observed was a faster initial decay of LTP evoked at low levels of release probability, possibly related to impaired induction conditions. It was also observed that LTP induced at one level of release probability occluded that induced at a lower (or higher) level, and that changes in release probability induced by adenosine agonist/antagonists affected potentiated and “naive” EPSPs to an equal extent. Taken together, these data do not provide support for the notion of different locations for LTP expression at different conditions of release probability. The results are also more compatible with the notion of a single, rather than several, expression mechanism(s) within the first hour of LTP in the hippocampal CA1 region.
机译:在本研究中,在不同的递质释放条件下,研究了海马CA1区长期增强(LTP)的一些特征。腺苷A1激动剂/拮抗剂,或在某些情况下改变细胞外钙/镁比值,以改变释放的可能性。短暂的破伤风后,整个LTP时间过程(非NMDA和NMDA受体介导的EPSP的潜伏期,生长期和随后的衰变)在释放几率变化近10倍(以变化量度)上基本相同现场EPSP幅度)。观察到的主要差异是在较低的释放概​​率水平下诱发的LTP的初始衰减更快,这可能与诱导条件受损有关。还观察到,以一种释放概率水平诱导的LTP会以较低(或更高)水平诱导的LTP闭塞,并且腺苷激动剂/拮抗剂诱导的释放概率的变化在同等程度上影响了增强的和“天真的” EPSP。综上所述,这些数据不支持在不同释放概率条件下LTP表达的不同位置的概念。结果也更符合海马CA1区LTP最初一小时内单一而非多种表达机制的概念。

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