Department of Biomedical Engineering, National Yang Ming University, No.155, Sec.2, Linong St, Taipei, 11221, Taiwan, ROC.
The Ph.D. Program for Neural Regenerative Medicine, College of Medical Science and Technology, Taipei Medical University, No. 250 Wu-Xing St, Taipei, 11031, Taiwan, ROC; Research Center for Brain and Consciousness, Taipei Medical University, Shuang Ho Hospital, No. 291, Zhongzheng Rd, New Taipei City, 23561, Taiwan, ROC.
Brain Stimul. 2019 Nov-Dec;12(6):1410-1420. doi: 10.1016/j.brs.2019.07.004. Epub 2019 Jul 6.
Social deficit is a core symptom in autism spectrum disorder (ASD). Although deep brain stimulation (DBS) has been proposed as a potential treatment for ASD, an ideal target nucleus is yet to be identified. DBS at the central thalamic nucleus (CTN) is known to alter corticostriatal and limbic circuits, and subsequently increase the exploratory motor behaviors, cognitive performance, and skill learning in neuropsychiatric and neurodegenerative disorders.
We first investigated the ability of CTN-DBS to selectively engage distinct brain circuits and compared the spatial distribution of evoked network activity and modulation. Second, we investigated whether CTN-DBS intervention improves social interaction in a valproic acid-exposed ASD rat offspring model.
Brain regions activated through CTN-DBS by using a magnetic resonance (MR)-compatible neural probe, which is capable of inducing site-selective microstimulations during functional MRI (fMRI), were investigated. We then performed functional connectivity MRI, the three-chamber social interaction test, and Western blotting analyses to evaluate the therapeutic efficacy of CTN-DBS in an ASD rat offspring model.
The DBS-evoked fMRI results indicated that the activated brain regions were mainly located in cortical areas, limbic-related areas, and the dorsal striatum. We observed restoration of brain functional connectivity (FC) in corticostriatal and corticolimbic circuits after CTN-DBS, accompanied with increased social interaction and decreased social avoidance in the three-chamber social interaction test. The dopamine D2 receptor decreased significantly after CTN-DBS treatment, suggesting changes in synaptic plasticity and alterations in the brain circuits.
Applying CTN-DBS to ASD rat offspring increased FC and altered the synaptic plasticity in the corticolimbic and the corticostriatal circuits. This suggests that CTN-DBS could be an effective treatment for improving the social behaviors of individuals with ASD.
社会缺陷是自闭症谱系障碍(ASD)的核心症状。虽然深部脑刺激(DBS)已被提议作为 ASD 的一种潜在治疗方法,但尚未确定理想的靶点核。已知中央丘脑核(CTN)的 DBS 可改变皮质纹状体和边缘回路,随后增加神经精神和神经退行性疾病中的探索性运动行为、认知表现和技能学习。
我们首先研究了 CTN-DBS 选择性参与不同大脑回路的能力,并比较了诱发网络活动和调制的空间分布。其次,我们研究了 CTN-DBS 干预是否能改善丙戊酸暴露的 ASD 大鼠后代模型中的社会互动。
通过使用磁共振(MR)兼容的神经探针研究了 CTN-DBS 通过磁刺激诱导的大脑区域激活,该探针能够在功能磁共振成像(fMRI)期间进行部位选择的微刺激。然后,我们进行了功能连接磁共振成像、三腔社交互动测试和 Western blot 分析,以评估 CTN-DBS 在 ASD 大鼠后代模型中的治疗效果。
DBS 诱发的 fMRI 结果表明,激活的大脑区域主要位于皮质区域、边缘相关区域和背侧纹状体。我们观察到 CTN-DBS 后皮质纹状体和皮质边缘回路的脑功能连接(FC)恢复,伴有三腔社交互动测试中社会互动增加和社会回避减少。CTN-DBS 治疗后多巴胺 D2 受体显著降低,表明突触可塑性发生变化,大脑回路发生改变。
将 CTN-DBS 应用于 ASD 大鼠后代可增加 FC,并改变皮质边缘和皮质纹状体回路中的突触可塑性。这表明 CTN-DBS 可能是改善 ASD 个体社会行为的有效治疗方法。