May Hazel G, Tsikonofilos Konstantinos, Donat Cornelius K, Sastre Magdalena, Kozlov Andriy S, Sharp David J, Bruyns-Haylett Michael
Department of Brain Sciences, Imperial College London, London W12 0NN, UK.
Department of Bioengineering, Imperial College London, London SW7 2AZ, UK.
Brain Commun. 2024 Nov 27;6(6):fcae385. doi: 10.1093/braincomms/fcae385. eCollection 2024.
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.
创伤性脑损伤是一项重大的全球健康负担,在神经系统疾病中患病率最高。即使是轻度创伤性脑损伤也可能引发细微、持久的变化,增加未来神经退行性变的风险。重要的是,通过传统的神经学评估很难检测到这些变化。这凸显了需要更敏感的诊断工具,如脑电图,来发现治疗干预的机会。该领域的进展受到了阻碍,因为缺乏将动物模型微观层面的机制见解与临床成像中观察到的宏观表型联系起来的研究。我们的研究通过对轻度爆炸创伤性脑损伤大鼠模型进行抑制性中间神经元的免疫组织化学染色和与转化相关的脑电图记录来填补这一空白。虽然我们在损伤后立即未观察到明显影响,但在慢性时间点发现了宽带兴奋性增加和连接性增强,同时抑制性中间神经元的密度降低。这种模式表明兴奋与抑制之间的平衡被破坏,为细胞机制与损伤的临床特征之间提供了关键联系。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。尽管在损伤后立即没有明显影响,但在慢性时间点脑电图异常的出现凸显了对创伤性脑损伤患者进行长期监测的重要性。观察到的抑制性中间神经元密度降低为脑电图变化提供了潜在的细胞机制,可能代表治疗干预的靶点。本研究证明了在动物模型中将细胞水平分析与宏观神经生理学记录相结合以阐明创伤性脑损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。