Koloski Miranda Francoeur, Menon Reyana, Krasnyanskiy Victoria
Mental Health Service, VA San Diego Healthcare System, La Jolla, CA 92161, USA.
Department of Psychiatry, UC San Diego, La Jolla, CA 92093, USA.
Brain Sci. 2025 Apr 29;15(5):471. doi: 10.3390/brainsci15050471.
Brain stimulation therapies may be used to correct motor, social, emotional, and cognitive consequences of traumatic brain injury (TBI). Neuromodulation applied with anatomical specificity can ameliorate desired symptoms while leaving functional circuits intact. Before applying precision medicine approaches, preclinical animal studies are needed to explore potential neurophysiological signatures that could be modulated with neurostimulation. This review discusses potential neural signatures of cognition, particularly reward processing, which is chronically impaired after brain injury. Electrophysiology, compared to other types of biomarkers, can detect deficits missed by structural measures, holds translational potential between humans and animals, and directly informs neuromodulatory treatments. Disturbances in oscillatory activity underscore structural, molecular, and behavioral impairments seen following TBI. For instance, cortico-striatal beta frequency activity (15-30 Hz) during reward processing represents subjective value and is chronically disturbed after frontal TBI in rodents. We use the example of evoked beta oscillations in the cortico-striatal network as a putative marker of reward processing that could be targeted with electrical stimulation to improve decision making after TBI. This review highlights the necessity of collecting electrophysiological data in preclinical models to understand the underlying mechanisms of cognitive behavioral deficits after TBI and to develop targeted stimulation treatments in humans.
脑刺激疗法可用于纠正创伤性脑损伤(TBI)的运动、社交、情感和认知后果。具有解剖学特异性的神经调节可以改善预期症状,同时保持功能回路完整。在应用精准医学方法之前,需要进行临床前动物研究,以探索可能通过神经刺激调节的潜在神经生理特征。本综述讨论了认知的潜在神经特征,特别是奖励处理,这在脑损伤后会长期受损。与其他类型的生物标志物相比,电生理学可以检测到结构测量遗漏的缺陷,具有人与动物之间的转化潜力,并直接为神经调节治疗提供信息。振荡活动的紊乱突出了TBI后出现的结构、分子和行为损伤。例如,奖励处理过程中的皮质-纹状体β频率活动(15-30Hz)代表主观价值,在啮齿动物额叶TBI后会长期受到干扰。我们以皮质-纹状体网络中诱发的β振荡为例,作为奖励处理的推定标志物,可以通过电刺激来靶向改善TBI后的决策。本综述强调了在临床前模型中收集电生理数据的必要性,以了解TBI后认知行为缺陷的潜在机制,并开发针对人类的靶向刺激治疗方法。