Deadwyler Sam A, Hampson Robert E
Department of Physiology and Pharmacology, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.
Neuron. 2004 May 13;42(3):465-76. doi: 10.1016/s0896-6273(04)00195-3.
In this study we describe how the hippocampus and subiculum act in concert to encode information in a spatial delayed-nonmatch-to-sample (DNMS) task. This encoding was functionally partitioned between neurons within subiculum and hippocampus to uniquely identify trial-specific information accounting for both spatial and temporal constraints on performance within and between trials. Encoding by subicular neurons in the task was normally accurate and specific, but only if delays were shorter than 15 s, whereas trial-specific information encoded by hippocampal neurons was subject to strong biases from prior trial sequences and was accessible only when delays exceeded 15 s. The two structures operated in a complementary manner to encode information correctly on 75% of all trials using the above strategies. The remaining 25% of trials were at risk due to inherent idiosyncrasies by which hippocampal and subicular neurons encoded information and became errors when the random sequence of trials conflicted with these constraints.
在本研究中,我们描述了海马体和下托如何协同作用,在空间延迟非匹配样本(DNMS)任务中对信息进行编码。这种编码在功能上被划分在下托和海马体的神经元之间,以唯一地识别特定试验信息,该信息考虑了试验内和试验间表现的空间和时间限制。在该任务中,下托神经元的编码通常是准确和特异的,但前提是延迟短于15秒,而海马体神经元编码的特定试验信息则受到先前试验序列的强烈偏差影响,并且只有当延迟超过15秒时才可获取。这两个结构以互补的方式运作,使用上述策略在所有试验的75%中正确地编码信息。其余25%的试验存在风险,这是由于海马体和下托神经元编码信息的内在特性所致,当试验的随机序列与这些限制冲突时就会出现错误。