Nucleus accumbens deep brain stimulation improves depressive-like behaviors through BDNF-mediated alterations in brain functional connectivity of dopaminergic pathway

IF 4.3 2区 医学 Q1 NEUROSCIENCES Neurobiology of Stress Pub Date : 2023-09-01 DOI:10.1016/j.ynstr.2023.100566
Ssu-Ju Li , Yu-Chun Lo , Hsin-Yi Tseng , Sheng-Huang Lin , Chao-Hung Kuo , Ting-Chieh Chen , Ching-Wen Chang , Yao-Wen Liang , Yi-Chen Lin , Chih-Yu Wang , Tsai-Yu Cho , Mu-Hua Wang , Ching-Te Chen , You-Yin Chen
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Abstract

Major depressive disorder (MDD), a common psychiatric condition, adversely affects patients’ moods and quality of life. Despite the development of various treatments, many patients with MDD remain vulnerable and inadequately controlled. Since anhedonia is a feature of depression and there is evidence of leading to metabolic disorder, deep brain stimulation (DBS) to the nucleus accumbens (NAc) might be promising in modulating the dopaminergic pathway. To determine whether NAc-DBS alters glucose metabolism via mitochondrial alteration and neurogenesis and whether these changes increase neural plasticity that improves behavioral functions in a chronic social defeat stress (CSDS) mouse model. The Lab-designed MR-compatible neural probes were implanted in the bilateral NAc of C57BL/6 mice with and without CSDS, followed by DBS or sham stimulation. All animals underwent open-field and sucrose preference testing, and brain resting-state functional MRI analysis. Meanwhile, we checked the placement of neural probes in each mouse by T2 images. By confirming the placement location, mice with incorrect probe placement (the negative control group) showed no significant therapeutic effects in behavioral performance and functional connectivity (FC) after receiving electrical stimulation and were excluded from further analysis. Western blotting, seahorse metabolic analysis, and electron microscopy were further applied for the investigation of NAc-DBS. We found NAc-DBS restored emotional deficits in CSDS-subjected mice. Concurrent with behavioral amelioration, the CSDS DBS-on group exhibited enhanced FC in the dopaminergic pathway with increased expression of BDNF- and NeuN-positive cells increased dopamine D1 receptor, dopamine D2 receptors, and TH in the medial prefrontal cortex, NAc, ventral hippocampus, ventral tegmental area, and amygdala. Increased pAMPK/total AMPK and PGC-1α levels, functions of oxidative phosphorylation, and mitochondrial biogenesis were also observed after NAc-DBS treatment. Our findings demonstrate that NAc-DBS can promote BDNF expression, which alters FC and metabolic profile in the dopaminergic pathway, suggesting a potential strategy for ameliorating emotional processes in individuals with MDD.

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伏隔核深部脑刺激通过BDNF介导的多巴胺能通路脑功能连接的改变改善抑郁样行为
重性抑郁障碍(MDD)是一种常见的精神疾病,会对患者的情绪和生活质量产生不利影响。尽管有各种治疗方法的发展,许多MDD患者仍然很脆弱,控制不足。由于快感缺乏是抑郁症的一个特征,并且有证据表明它会导致代谢紊乱,因此对伏隔核(NAc)的脑深部刺激(DBS)可能有希望调节多巴胺能通路。在慢性社交失败应激(CSDS)小鼠模型中,确定NAc-DBS是否通过线粒体改变和神经发生改变葡萄糖代谢,以及这些变化是否增加神经可塑性,从而改善行为功能。将实验室设计的MR兼容神经探针植入有和没有CSDS的C57BL/6小鼠的双侧NAc中,然后进行DBS或假刺激。所有动物都接受了开放视野和蔗糖偏好测试,以及大脑静息状态功能MRI分析。同时,我们通过T2图像检查了神经探针在每只小鼠中的位置。通过确认放置位置,探针放置不正确的小鼠(阴性对照组)在接受电刺激后,在行为表现和功能连接(FC)方面没有显示出显著的治疗效果,因此被排除在进一步分析之外。蛋白质印迹、海马代谢分析和电子显微镜进一步应用于NAc-DBS的研究。我们发现NAc-DBS恢复了CSDS小鼠的情绪缺陷。在行为改善的同时,CSDS-DBS组在多巴胺能通路中表现出FC增强,BDNF-和NeuN阳性细胞的表达增加,内侧前额叶皮层、NAc、腹侧海马、腹侧被盖区和杏仁核中的多巴胺D1受体、多巴胺D2受体和TH增加。NAc-DBS治疗后,还观察到pAMPK/总AMPK和PGC-1α水平增加、氧化磷酸化功能和线粒体生物发生。我们的研究结果表明,NAc-DBS可以促进BDNF的表达,从而改变多巴胺能通路中的FC和代谢谱,这表明了改善MDD患者情绪过程的潜在策略。
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来源期刊
Neurobiology of Stress
Neurobiology of Stress Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
9.40
自引率
4.00%
发文量
74
审稿时长
48 days
期刊介绍: Neurobiology of Stress is a multidisciplinary journal for the publication of original research and review articles on basic, translational and clinical research into stress and related disorders. It will focus on the impact of stress on the brain from cellular to behavioral functions and stress-related neuropsychiatric disorders (such as depression, trauma and anxiety). The translation of basic research findings into real-world applications will be a key aim of the journal. Basic, translational and clinical research on the following topics as they relate to stress will be covered: Molecular substrates and cell signaling, Genetics and epigenetics, Stress circuitry, Structural and physiological plasticity, Developmental Aspects, Laboratory models of stress, Neuroinflammation and pathology, Memory and Cognition, Motivational Processes, Fear and Anxiety, Stress-related neuropsychiatric disorders (including depression, PTSD, substance abuse), Neuropsychopharmacology.
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