Exploring the Effects of Prefrontal Transcranial Direct Current Stimulation on Brain Metabolites: A Concurrent tDCS-MRS Study

IF 3.5 2区 医学 Q1 NEUROIMAGING Human Brain Mapping Pub Date : 2024-12-17 DOI:10.1002/hbm.70097
Gizem Vural, Aldo Soldini, Frank Padberg, Berkhan Karslı, Artyom Zinchenko, Stephan Goerigk, Alexander Soutschek, Eva Mezger, Sophia Stoecklein, Lucia Bulubas, Antonia Šušnjar, Daniel Keeser
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Abstract

Transcranial Direct Current Stimulation (tDCS) is a non-invasive brain stimulation technique used to modulates cortical brain activity. However, its effects on brain metabolites within the dorsolateral prefrontal cortex (DLPFC), a crucial area targeted for brain stimulation in mental disorders, remain unclear. This study aimed to investigate whether prefrontal tDCS over the left and right DLPFC modulates levels of key metabolites, including gamma-aminobutyric acid (GABA), glutamate (Glu), glutamine/glutamate (Glx), N-acetylaspartate (NAA), near to the target region and to explore potential sex-specific effects on these metabolite concentrations. A total of 41 healthy individuals (19 female, M_age = 25 years, SD = 3.15) underwent either bifrontal active (2 mA for 20 min) or sham tDCS targeting the left (anode: F3) and right (cathode: F4) DLPFC within a 3 Tesla MRI scanner. Magnetic resonance spectroscopy (MRS) was used to monitor neurometabolic changes before, during, and after 40 min of tDCS, with measurements of two 10-min intervals during stimulation. A single voxel beneath F3 was used for metabolic quantification. Results showed a statistically significant increase in Glx levels under active tDCS compared to the sham condition, particularly during the second 10-min window and persisting into the post-stimulation phase. No significant changes were observed in other metabolites, but consistent sex differences were detected. Specifically, females showed lower levels of NAA and GABA under active tDCS compared to the sham condition, while no significant changes were observed in males. E-field modeling showed no significant differences in field magnitudes between sexes, and the magnitude of the e-fields did not correlate with changes in Glx levels between active and sham stimulation during the second interval or post-stimulation. This study demonstrates that a single session of prefrontal tDCS significantly elevates Glx levels in the left DLPFC, with effects persisting post-stimulation. However, the observed sex differences in the neurochemical response to tDCS were not linked to specific stimulation intervals or variations in e-field magnitudes, highlighting the complexity of tDCS effects and the need for personalized neuromodulation strategies.

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探索前额叶经颅直流电刺激对脑代谢物的影响:同时进行的 tDCS-MRS 研究。
经颅直流电刺激(tDCS)是一种用于调节大脑皮层活动的非侵入性脑刺激技术。然而,其对背外侧前额叶皮层(DLPFC)内脑代谢物的影响尚不清楚,DLPFC是精神障碍中脑刺激的关键区域。本研究旨在探讨左、右DLPFC上的前额叶tDCS是否调节靶区附近的关键代谢物水平,包括γ -氨基丁酸(GABA)、谷氨酸(Glu)、谷氨酰胺/谷氨酸(Glx)、n -乙酰天冬氨酸(NAA),并探讨对这些代谢物浓度的潜在性别特异性影响。共有41名健康个体(19名女性,M_age = 25岁,SD = 3.15)在3特斯拉MRI扫描仪内接受双额活动(2 mA,持续20分钟)或针对左(正极:F3)和右(正极:F4) DLPFC的假tDCS。磁共振波谱(MRS)用于监测tDCS之前、期间和之后40分钟的神经代谢变化,并在刺激期间进行两次10分钟间隔的测量。F3以下的单个体素用于代谢量化。结果显示,与假手术相比,活跃tDCS下Glx水平有统计学意义上的显著增加,特别是在第二个10分钟窗口期并持续到刺激后阶段。其他代谢物未观察到显著变化,但检测到一致的性别差异。具体而言,与假手术相比,活跃tDCS下女性的NAA和GABA水平较低,而男性没有明显变化。电场模型显示,电场强度在两性之间没有显著差异,并且在第二次间隔或刺激后,电场强度与活动刺激和假刺激之间Glx水平的变化无关。该研究表明,单次前额叶tDCS会显著提高左侧DLPFC的Glx水平,这种影响在刺激后持续存在。然而,观察到的对tDCS的神经化学反应的性别差异与特定的刺激间隔或电场强度的变化无关,这突出了tDCS效应的复杂性和个性化神经调节策略的必要性。
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来源期刊
Human Brain Mapping
Human Brain Mapping 医学-核医学
CiteScore
8.30
自引率
6.20%
发文量
401
审稿时长
3-6 weeks
期刊介绍: Human Brain Mapping publishes peer-reviewed basic, clinical, technical, and theoretical research in the interdisciplinary and rapidly expanding field of human brain mapping. The journal features research derived from non-invasive brain imaging modalities used to explore the spatial and temporal organization of the neural systems supporting human behavior. Imaging modalities of interest include positron emission tomography, event-related potentials, electro-and magnetoencephalography, magnetic resonance imaging, and single-photon emission tomography. Brain mapping research in both normal and clinical populations is encouraged. Article formats include Research Articles, Review Articles, Clinical Case Studies, and Technique, as well as Technological Developments, Theoretical Articles, and Synthetic Reviews. Technical advances, such as novel brain imaging methods, analyses for detecting or localizing neural activity, synergistic uses of multiple imaging modalities, and strategies for the design of behavioral paradigms and neural-systems modeling are of particular interest. The journal endorses the propagation of methodological standards and encourages database development in the field of human brain mapping.
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