Alterations in large-scale resting-state network nodes following transcranial focused ultrasound of deep brain structures.

IF 2.4 3区 医学 Q3 NEUROSCIENCES Frontiers in Human Neuroscience Pub Date : 2024-12-04 eCollection Date: 2024-01-01 DOI:10.3389/fnhum.2024.1486770
Stephanie M Gorka, Jagan Jimmy, Katherine Koning, K Luan Phan, Natalie Rotstein, Bianca Hoang-Dang, Sabrina Halavi, Norman Spivak, Martin M Monti, Nicco Reggente, Susan Y Bookheimer, Taylor P Kuhn
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Abstract

Background: Low-intensity transcranial focused ultrasound (tFUS) is a brain stimulation approach that holds promise for the treatment of brain-based disorders. Studies in humans have shown that tFUS can successfully modulate perfusion in focal sonication targets, including the amygdala; however, limited research has explored how tFUS impacts large-scale neural networks.

Objective: The aim of the current study was to address this gap and examine changes in resting-state connectivity between large-scale network nodes using a randomized, double-blind, within-subjects crossover study design.

Methods: Healthy adults (n = 18) completed two tFUS sessions, 14 days apart. Each session included tFUS of either the right amygdala or the left entorhinal cortex (ErC). The inclusion of two active targets allowed for within-subjects comparisons as a function of the locus of sonication. Resting-state functional magnetic resonance imaging was collected before and after each tFUS session.

Results: tFUS altered resting-state functional connectivity (rsFC) within and between rs-network nodes. Pre-to-post sonication of the right amygdala modulated connectivity within nodes of the salience network (SAN) and between nodes of the SAN and the default mode network (DMN) and frontoparietal network (FRP). A decrease in SAN to FPN connectivity was specific to the amygdala target. Pre-to-post sonication of the left ErC modulated connectivity between the dorsal attention network (DAN) and FPN and DMN. An increase in DAN to DMN connectivity was specific to the ErC target.

Conclusion: These preliminary findings may suggest that tFUS induces neuroplastic changes beyond the immediate sonication target. Additional studies are needed to determine the long-term stability of these effects.

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经颅聚焦超声脑深部结构后大尺度静息状态网络节点的改变。
背景:低强度经颅聚焦超声(tFUS)是一种脑刺激方法,有望治疗脑基础疾病。对人类的研究表明,tFUS可以成功地调节局灶超声靶点的灌注,包括杏仁核;然而,有限的研究探讨了tFUS如何影响大规模神经网络。目的:本研究的目的是通过随机、双盲、受试者内交叉研究设计来解决这一差距,并检查大规模网络节点之间静息状态连通性的变化。方法:健康成人(n = 18)完成两次tFUS疗程,间隔14天。每次都包括右杏仁核或左内嗅皮层(ErC)的tFUS。两个活动目标的包含允许在主体内比较作为超声轨迹的功能。静息状态功能磁共振成像在每次tFUS之前和之后采集。结果:tFUS改变了rs网络节点内和节点间的静息状态功能连接(rsFC)。右杏仁核的前后超声调节了突出网络(SAN)节点内以及SAN与默认模式网络(DMN)和额顶叶网络(FRP)节点之间的连通性。SAN到FPN连通性的减少是杏仁核目标所特有的。左ErC的前后超声调制了背侧注意网络(DAN)与FPN和DMN之间的连接。DAN到DMN连通性的增加是ErC目标所特有的。结论:这些初步发现可能提示tFUS诱导的神经可塑性改变超出了直接超声目标。需要进一步的研究来确定这些影响的长期稳定性。
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来源期刊
Frontiers in Human Neuroscience
Frontiers in Human Neuroscience 医学-神经科学
CiteScore
4.70
自引率
6.90%
发文量
830
审稿时长
2-4 weeks
期刊介绍: Frontiers in Human Neuroscience is a first-tier electronic journal devoted to understanding the brain mechanisms supporting cognitive and social behavior in humans, and how these mechanisms might be altered in disease states. The last 25 years have seen an explosive growth in both the methods and the theoretical constructs available to study the human brain. Advances in electrophysiological, neuroimaging, neuropsychological, psychophysical, neuropharmacological and computational approaches have provided key insights into the mechanisms of a broad range of human behaviors in both health and disease. Work in human neuroscience ranges from the cognitive domain, including areas such as memory, attention, language and perception to the social domain, with this last subject addressing topics, such as interpersonal interactions, social discourse and emotional regulation. How these processes unfold during development, mature in adulthood and often decline in aging, and how they are altered in a host of developmental, neurological and psychiatric disorders, has become increasingly amenable to human neuroscience research approaches. Work in human neuroscience has influenced many areas of inquiry ranging from social and cognitive psychology to economics, law and public policy. Accordingly, our journal will provide a forum for human research spanning all areas of human cognitive, social, developmental and translational neuroscience using any research approach.
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