脑电图过度兴奋和超连接性与脑外伤后 GABA 能抑制性中间神经元缺失有关。

IF 4.1 Q1 CLINICAL NEUROLOGY Brain communications Pub Date : 2024-11-27 eCollection Date: 2024-01-01 DOI:10.1093/braincomms/fcae385
Hazel G May, Konstantinos Tsikonofilos, Cornelius K Donat, Magdalena Sastre, Andriy S Kozlov, David J Sharp, Michael Bruyns-Haylett
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引用次数: 0

摘要

脑外伤给全球健康造成了巨大负担,是神经系统疾病中发病率最高的一种。即使是轻微的脑外伤也会引起微妙而持久的变化,从而增加未来神经变性的风险。重要的是,这很难通过传统的神经系统评估发现。这就强调了需要更灵敏的诊断工具,如脑电图,以发现治疗干预的机会。由于缺乏将动物模型微观层面的机理见解与临床成像中观察到的宏观表型联系起来的研究,该领域的研究进展一直受到阻碍。我们的研究利用抑制性中间神经元的免疫组化染色和翻译相关的脑电图记录研究了轻度爆炸性脑外伤大鼠模型,从而弥补了这一空白。虽然我们没有观察到损伤后立即出现的明显影响,但长期的时间点显示出宽带过度兴奋和连接性增加,同时抑制性中间神经元的密度下降。这种模式表明兴奋和抑制之间的平衡被打破,为细胞机制和损伤的临床特征之间提供了重要的联系。我们的发现对创伤性脑损伤的诊断、监测和治疗具有重要意义。尽管没有直接影响,但在长期时间点出现的脑电图异常突显了对脑外伤患者进行长期监测的重要性。所观察到的抑制性中间神经元密度下降为脑电图变化提供了潜在的细胞机制,并可能成为治疗干预的目标。这项研究证明了在动物模型中结合细胞水平分析和宏观神经电生理记录来阐明脑外伤病理生理学的价值。未来的研究应侧重于将这些发现转化为人体研究,并探索针对创伤性脑损伤中兴奋-抑制失衡的潜在治疗策略。
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EEG hyperexcitability and hyperconnectivity linked to GABAergic inhibitory interneuron loss following traumatic brain injury.

Traumatic brain injury represents a significant global health burden and has the highest prevalence among neurological disorders. Even mild traumatic brain injury can induce subtle, long-lasting changes that increase the risk of future neurodegeneration. Importantly, this can be challenging to detect through conventional neurological assessment. This underscores the need for more sensitive diagnostic tools, such as electroencephalography, to uncover opportunities for therapeutic intervention. Progress in the field has been hindered by a lack of studies linking mechanistic insights at the microscopic level from animal models to the macroscale phenotypes observed in clinical imaging. Our study addresses this gap by investigating a rat model of mild blast traumatic brain injury using both immunohistochemical staining of inhibitory interneurons and translationally relevant electroencephalography recordings. Although we observed no pronounced effects immediately post-injury, chronic time points revealed broadband hyperexcitability and increased connectivity, accompanied by decreased density of inhibitory interneurons. This pattern suggests a disruption in the balance between excitation and inhibition, providing a crucial link between cellular mechanisms and clinical hallmarks of injury. Our findings have significant implications for the diagnosis, monitoring, and treatment of traumatic brain injury. The emergence of electroencephalography abnormalities at chronic time points, despite the absence of immediate effects, highlights the importance of long-term monitoring in traumatic brain injury patients. The observed decrease in inhibitory interneuron density offers a potential cellular mechanism underlying the electroencephalography changes and may represent a target for therapeutic intervention. This study demonstrates the value of combining cellular-level analysis with macroscale neurophysiological recordings in animal models to elucidate the pathophysiology of traumatic brain injury. Future research should focus on translating these findings to human studies and exploring potential therapeutic strategies targeting the excitation-inhibition imbalance in traumatic brain injury.

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