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Aging Impairs the Late Phase of Long-Term Potentiation at the Medial Perforant Path-CA3 Synapse in Awake Rats

机译:衰老损害清醒大鼠内侧穿孔路径CA3突触的长期增强后期。

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摘要

The effects of aging on long-term potentiation (LTP) in the dentate gyrus (DG) and CA1 are well documented, but LTP at the medial perforant path (MPP)-CA3 synapse of aged animals has remained unexplored. Because the MPP-DG and Schaffer-collateral-CA1 synapses account for only about 20% of total hippocampal synapses, global understanding of how aging affects hippocampal plasticity has remained limited. Much is known about LTP induction in the hippocampal formation, whereas the mechanisms that regulate LTP maintenance are less understood, especially during aging. We investigated the effects of aging on MPP-CA3 LTP induction and maintenance in awake rats. As is the case in the DG and CA1, high-frequency stimulation-induced LTP at the MPP-CA3 synapse is normal in aged rats. These data indicate that N-methyl-D-aspartate (NMDA) receptor-mediated processes are intact at the MPP-CA3 synapse in aged rats. In contrast, aging impaired the magnitude and duration of MPP-CA3 LTP over a period of days. Also, these data are consistent with reports that area CA3 is especially susceptible to age-related changes. Our data suggest that aging impairs mechanisms that regulate the late phase of MPP-CA3 LTP and contribute to a more global understanding of how aging affects hippocampal plasticity.
机译:衰老对齿状回(DG)和CA1的长期增强(LTP)的影响已有充分文献记载,但对中龄动物的内侧穿孔路径(MPP)-CA3突触处的LTP仍未进行研究。由于MPP-DG和Schaffer-侧支CA1突触仅占海马突触总数的20%,因此对衰老如何影响海马可塑性的全球理解仍然有限。关于海马形成中LTP诱导的了解很多,而调节LTP维持的机制却鲜为人知,尤其是在衰老过程中。我们研究了衰老对清醒大鼠中MPP-CA3 LTP诱导和维持的影响。与DG和CA1一样,MPP-CA3突触处的高频刺激诱导的LTP在老年大鼠中是正常的。这些数据表明,N-甲基-D-天冬氨酸(NMDA)受体介导的过程在老年大鼠的MPP-CA3突触处是完整的。相反,老化会损害MPP-CA3 LTP在几天内的强度和持续时间。而且,这些数据与区域CA3特别容易受到与年龄相关的变化的影响的报道一致。我们的数据表明,衰老会损害调节MPP-CA3 LTP晚期的机制,并有助于更全面地了解衰老如何影响海马可塑性。

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