Allen Timothy A, Salz Daniel M, McKenzie Sam, Fortin Norbert J
Center for the Neurobiology of Learning and Memory, Department of Neurobiology and Behavior, University of California Irvine, Irvine, California 92697.
Center for Memory and Brain, Boston University, Boston, Massachusetts 02215, and.
J Neurosci. 2016 Feb 3;36(5):1547-63. doi: 10.1523/JNEUROSCI.2874-15.2016.
The hippocampus is critical to the memory for sequences of events, a defining feature of episodic memory. However, the fundamental neuronal mechanisms underlying this capacity remain elusive. While considerable research indicates hippocampal neurons can represent sequences of locations, direct evidence of coding for the memory of sequential relationships among nonspatial events remains lacking. To address this important issue, we recorded neural activity in CA1 as rats performed a hippocampus-dependent sequence-memory task. Briefly, the task involves the presentation of repeated sequences of odors at a single port and requires rats to identify each item as "in sequence" or "out of sequence". We report that, while the animals' location and behavior remained constant, hippocampal activity differed depending on the temporal context of items-in this case, whether they were presented in or out of sequence. Some neurons showed this effect across items or sequence positions (general sequence cells), while others exhibited selectivity for specific conjunctions of item and sequence position information (conjunctive sequence cells) or for specific probe types (probe-specific sequence cells). We also found that the temporal context of individual trials could be accurately decoded from the activity of neuronal ensembles, that sequence coding at the single-cell and ensemble level was linked to sequence memory performance, and that slow-gamma oscillations (20-40 Hz) were more strongly modulated by temporal context and performance than theta oscillations (4-12 Hz). These findings provide compelling evidence that sequence coding extends beyond the domain of spatial trajectories and is thus a fundamental function of the hippocampus.
The ability to remember the order of life events depends on the hippocampus, but the underlying neural mechanisms remain poorly understood. Here we addressed this issue by recording neural activity in hippocampal region CA1 while rats performed a nonspatial sequence memory task. We found that hippocampal neurons code for the temporal context of items (whether odors were presented in the correct or incorrect sequential position) and that this activity is linked with memory performance. The discovery of this novel form of temporal coding in hippocampal neurons advances our fundamental understanding of the neurobiology of episodic memory and will serve as a foundation for our cross-species, multitechnique approach aimed at elucidating the neural mechanisms underlying memory impairments in aging and dementia.
海马体对于事件序列的记忆至关重要,这是情景记忆的一个决定性特征。然而,这种能力背后的基本神经元机制仍然难以捉摸。虽然大量研究表明海马体神经元可以表征位置序列,但对于非空间事件之间顺序关系记忆编码的直接证据仍然缺乏。为了解决这个重要问题,我们在大鼠执行依赖海马体的序列记忆任务时记录了CA1区的神经活动。简而言之,该任务涉及在单个端口重复呈现气味序列,并要求大鼠将每个项目识别为“顺序正确”或“顺序错误”。我们报告称,虽然动物的位置和行为保持不变,但海马体活动根据项目的时间背景而有所不同——在这种情况下,即它们是按顺序呈现还是乱序呈现。一些神经元在不同项目或序列位置上表现出这种效应(一般序列细胞),而其他神经元则对项目和序列位置信息的特定组合(联合序列细胞)或特定探测类型(探测特定序列细胞)表现出选择性。我们还发现,单个试验的时间背景可以从神经元集群的活动中准确解码,单细胞和集群水平的序列编码与序列记忆表现相关,并且慢γ振荡(20 - 40赫兹)比θ振荡(4 - 12赫兹)更受时间背景和表现的强烈调制。这些发现提供了令人信服的证据,表明序列编码超出了空间轨迹的范畴,因此是海马体的一项基本功能。
记住生活事件顺序的能力取决于海马体,但潜在的神经机制仍知之甚少。在这里,我们通过在大鼠执行非空间序列记忆任务时记录海马体CA1区的神经活动来解决这个问题。我们发现海马体神经元对项目的时间背景进行编码(气味是按正确还是错误的顺序位置呈现),并且这种活动与记忆表现相关。在海马体神经元中发现这种新的时间编码形式,推进了我们对情景记忆神经生物学的基本理解,并将作为我们跨物种、多技术方法的基础,旨在阐明衰老和痴呆中记忆障碍背后的神经机制。