受伤大脑的突触可塑性取决于刺激的时间模式。

IF 3.9 2区 医学 Q1 CLINICAL NEUROLOGY
Journal of neurotrauma Pub Date : 2024-11-01 Epub Date: 2024-07-23 DOI:10.1089/neu.2024.0129
Quentin S Fischer, Djanenkhodja Kalikulov, Gonzalo Viana Di Prisco, Carrie A Williams, Philip R Baldwin, Michael J Friedlander
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引用次数: 0

摘要

神经刺激方案越来越多地被用作治疗干预措施,包括治疗脑损伤。除了直接激活神经元外,这些刺激方案还可能对神经元的突触输出产生下游影响。众所周知,突触连接强度的改变(长期延时,LTP;长期抑制,LTD)对用于诱导的刺激频率很敏感,但人们对刺激的时间模式对神经刺激在损伤大脑中可能诱导的下游突触可塑性的贡献知之甚少。我们探索了正常大脑皮层和轻度创伤性脑损伤(mTBI)后神经刺激的时间模式和频率之间的相互作用,以便为加强或削弱受伤大脑神经回路的疗法提供信息,同时更好地了解这些因素在正常大脑可塑性中的作用。我们在对照组(天真鼠)、假手术鼠和 mTBI 大鼠的急性切片上进行了全细胞(WC)贴片钳记录,记录了单个神经元的诱发突触后电位(PSPs),以及场电位(FP)记录。我们比较了不同刺激方案诱导的突触可塑性,每种方案都包括特定的频率(1赫兹、10赫兹或100赫兹)、连续性(连续或不连续)和时间模式(完全规则、轻微不规则或高度不规则)。在单个神经元水平上,当使用频率为 1 赫兹或 10 赫兹的高度不规则刺激方案时,可塑性结果出现了巨大差异。与单个神经元的结果一致,同时记录 FP 的可塑性结果也很相似,这表明我们的结果可以推广到更大规模的突触网络,而不是单个 WC 记录所能采样到的。除了对照脑(幼稚脑或假脑)和损伤脑之间可塑性结果的差异外,刺激过程中突触反应的动态变化也可预测最终的可塑性结果。我们的研究结果表明,刺激的时间模式在大脑皮层诱导的突触可塑性的极性和幅度方面起着作用,同时突出了正常大脑和受伤大脑反应之间的差异。此外,这些结果可能有助于优化治疗 mTBI 和其他脑部疾病的神经刺激疗法,并为了解正常大脑的下游可塑性信号机制提供了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synaptic Plasticity in the Injured Brain Depends on the Temporal Pattern of Stimulation.

Neurostimulation protocols are increasingly used as therapeutic interventions, including for brain injury. In addition to the direct activation of neurons, these stimulation protocols are also likely to have downstream effects on those neurons' synaptic outputs. It is well known that alterations in the strength of synaptic connections (long-term potentiation, LTP; long-term depression, LTD) are sensitive to the frequency of stimulation used for induction; however, little is known about the contribution of the temporal pattern of stimulation to the downstream synaptic plasticity that may be induced by neurostimulation in the injured brain. We explored interactions of the temporal pattern and frequency of neurostimulation in the normal cerebral cortex and after mild traumatic brain injury (mTBI), to inform therapies to strengthen or weaken neural circuits in injured brains, as well as to better understand the role of these factors in normal brain plasticity. Whole-cell (WC) patch-clamp recordings of evoked postsynaptic potentials in individual neurons, as well as field potential (FP) recordings, were made from layer 2/3 of visual cortex in response to stimulation of layer 4, in acute slices from control (naive), sham operated, and mTBI rats. We compared synaptic plasticity induced by different stimulation protocols, each consisting of a specific frequency (1 Hz, 10 Hz, or 100 Hz), continuity (continuous or discontinuous), and temporal pattern (perfectly regular, slightly irregular, or highly irregular). At the individual neuron level, dramatic differences in plasticity outcome occurred when the highly irregular stimulation protocol was used at 1 Hz or 10 Hz, producing an overall LTD in controls and shams, but a robust overall LTP after mTBI. Consistent with the individual neuron results, the plasticity outcomes for simultaneous FP recordings were similar, indicative of our results generalizing to a larger scale synaptic network than can be sampled by individual WC recordings alone. In addition to the differences in plasticity outcome between control (naive or sham) and injured brains, the dynamics of the changes in synaptic responses that developed during stimulation were predictive of the final plasticity outcome. Our results demonstrate that the temporal pattern of stimulation plays a role in the polarity and magnitude of synaptic plasticity induced in the cerebral cortex while highlighting differences between normal and injured brain responses. Moreover, these results may be useful for optimization of neurostimulation therapies to treat mTBI and other brain disorders, in addition to providing new insights into downstream plasticity signaling mechanisms in the normal brain.

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来源期刊
Journal of neurotrauma
Journal of neurotrauma 医学-临床神经学
CiteScore
9.20
自引率
7.10%
发文量
233
审稿时长
3 months
期刊介绍: Journal of Neurotrauma is the flagship, peer-reviewed publication for reporting on the latest advances in both the clinical and laboratory investigation of traumatic brain and spinal cord injury. The Journal focuses on the basic pathobiology of injury to the central nervous system, while considering preclinical and clinical trials targeted at improving both the early management and long-term care and recovery of traumatically injured patients. This is the essential journal publishing cutting-edge basic and translational research in traumatically injured human and animal studies, with emphasis on neurodegenerative disease research linked to CNS trauma.
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