Laboratory of Neurophysiology, Department of Medicine, University of Patras, 26504, Rion, Greece.
Molecular Systems Biology, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Groningen, The Netherlands.
BMC Neurosci. 2019 Jul 22;20(1):35. doi: 10.1186/s12868-019-0517-5.
The functional heterogeneity of the hippocampus along its longitudinal axis at the level of behavior is an established concept; however, the neurobiological mechanisms are still unknown. Diversifications in the functioning of intrinsic hippocampal circuitry including short-term dynamics of synaptic inputs and neuronal output, that are important determinants of information processing in the brain, may profoundly contribute to functional specializations along the hippocampus. The objectives of the present study were the examination of the role of the GABA receptor-mediated inhibition, the μ-opioid receptors and the effect of stimulation intensity on the dynamics of both synaptic input and neuronal output of CA1 region in the dorsal and ventral hippocampus. We used recordings of field potentials from adult rat hippocampal slices evoked by brief repetitive activation of Schaffer collaterals.
We find that the local CA1 circuit of the dorsal hippocampus presents a remarkably increased dynamic range of frequency-dependent short-term changes in both input and output, ranging from strong facilitation to intense depression at low and high stimulation frequencies respectively. Furthermore, the input-output relationship in the dorsal CA1 circuit is profoundly influenced by frequency and time of presynaptic activation. Strikingly, the ventral hippocampus responds mostly with depression, displaying a rather monotonous input-output relationship over frequency and time. Partial blockade of GABA receptor-mediated transmission (by 5 μM picrotoxin) profoundly influences input and output dynamics in the dorsal hippocampus but affected only the neuronal output in the ventral hippocampus. M-opioid receptors control short-term dynamics of input and output in the dorsal hippocampus but they play no role in the ventral hippocampus.
The results demonstrate that information processing by CA1 local network is highly diversified between the dorsal and ventral hippocampus. Transient detection of incoming patterns of activity and frequency-dependent sustained signaling of amplified neuronal information may be assigned to the ventral and dorsal hippocampal circuitry respectively. This disparity should have profound implications for the functional roles ascribed to distinct segments along the long axis of the hippocampus.
在行为水平上,海马体沿其纵轴的功能异质性是一个既定概念;然而,神经生物学机制仍不清楚。内在海马体回路功能的多样化,包括突触输入和神经元输出的短期动力学,这些都是大脑信息处理的重要决定因素,可能会深刻地促进海马体的功能专业化。本研究的目的是检验 GABA 受体介导的抑制、μ 阿片受体以及刺激强度对背侧和腹侧海马体 CA1 区突触输入和神经元输出动力学的影响。我们使用短暂重复激活 Schaffer 侧支诱发成年大鼠海马切片的场电位记录。
我们发现,背侧海马体的局部 CA1 回路呈现出显著增加的频率依赖性短期变化的动态范围,输入和输出均从强易化到低和高刺激频率下的强烈抑制。此外,背侧 CA1 回路的输入-输出关系受到频率和时间的强烈影响。值得注意的是,腹侧海马体主要表现为抑制,在频率和时间上呈现出相当单调的输入-输出关系。GABA 受体介导的传递部分阻断(通过 5 μM 印防己毒素)深刻地影响了背侧海马体的输入和输出动力学,但仅影响了腹侧海马体的神经元输出。μ 阿片受体控制背侧海马体的输入和输出的短期动力学,但它们在腹侧海马体中不起作用。
结果表明,CA1 局部网络的信息处理在背侧和腹侧海马体之间高度多样化。传入活动模式的短暂检测和频率依赖性的放大神经元信息的持续信号传递可能分别分配给腹侧和背侧海马体回路。这种差异对赋予海马体长轴上不同节段的功能角色应该有深远的影响。