Acute Intermittent Theta-Burst Stimulation Produces Antidepressant-Like Effects by Modulating Neuronal Oscillations and Serotonin Levels of the Medial Prefrontal Cortex in Experimental Parkinson's Disease

IF 3.4 3区 医学 Q2 NEUROSCIENCES Journal of Neuroscience Research Pub Date : 2025-02-04 DOI:10.1002/jnr.70022
Yixuan Wang, Jian Liu, Yanping Hui, Zhongheng Wu, Xiang Wu, Yihua Bai, Jing Li, Lei Zhang, Kuncheng Liu, Qiaojun Zhang, Libo Li
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Abstract

Parkinson's disease (PD)-related depression is associated with aberrant neuronal oscillations and 5-hydroxytryptamine (5-HT) neurotransmission in the medial prefrontal cortex (mPFC). Intermittent theta-burst stimulation (iTBS), an updated pattern of high-frequency repetitive transcranial magnetic stimulation, has possible efficacy in PD-related depression. However, whether iTBS alleviates PD-related depression through modulating neuronal oscillations and 5-HT levels in the mPFC has not been determined. In this study, male Sprague–Dawley rats were used to establish a unilateral 6-hydroxydopamine-induced PD model. Then, acute iTBS was applied to the parkinsonian rats, and behavioral, neurochemical, and electrophysiological experiments were performed. We found that the parkinsonian rats exhibited increased immobility time and decreased sucrose preference accompanied by an increase of δ power and a decrease of θ power in the mPFC compared to sham-operated rats. One block of iTBS (1 block-iTBS, 300 stimuli) alleviated depressive-like behaviors in parkinsonian rats and elevated 5-HT levels in the mPFC compared to sham-iTBS. Additionally, it altered neuronal oscillations in the mPFC in the opposite fashion by suppressing the δ rhythm and enhancing the θ and β rhythms compared to sham-iTBS, suggesting that acute iTBS induces hyperactivity in the mPFC. With this iTBS paradigm, we also observed decreased parvalbumin expression in the mPFC, reflecting reduced cortical inhibition. Finally, correlation analyses showed strong correlation between immobility time and θ power after 1 block-iTBS. These findings suggest that the application of acute iTBS in parkinsonian rats produces antidepressant-like effects, which may be associated with elevated 5-HT levels and normalized neuronal oscillations in the mPFC.

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实验性帕金森氏症患者急性间歇性θ - burst刺激通过调节神经元振荡和内侧前额叶皮层血清素水平产生抗抑郁样作用
帕金森病(PD)相关抑郁与内侧前额叶皮层(mPFC)的异常神经元振荡和5-羟色胺(5-HT)神经传递有关。间歇性脉冲刺激(iTBS)是一种更新的高频重复经颅磁刺激模式,可能对pd相关抑郁症有疗效。然而,iTBS是否通过调节神经元振荡和mPFC中的5-HT水平来缓解pd相关抑郁尚未确定。本研究采用雄性Sprague-Dawley大鼠建立单侧6-羟多巴胺诱导的PD模型。然后将急性iTBS应用于帕金森大鼠,进行行为学、神经化学和电生理实验。我们发现,与假手术大鼠相比,帕金森病大鼠mPFC的δ功率增加,θ功率降低,且固定时间增加,蔗糖偏好降低。与假iTBS相比,1块iTBS(1块iTBS, 300个刺激)减轻了帕金森大鼠的抑郁样行为,并提高了mPFC中的5-羟色胺水平。此外,与假iTBS相比,它通过抑制δ节律和增强θ和β节律,以相反的方式改变了mPFC中的神经元振荡,这表明急性iTBS诱导mPFC过度活跃。在这种iTBS模式下,我们还观察到mPFC中的小白蛋白表达减少,反映了皮质抑制的减少。最后,相关分析显示,1块- itbs后,静止时间与θ功率有较强的相关性。这些发现表明,在帕金森大鼠中应用急性iTBS可产生抗抑郁样作用,这可能与5-羟色胺水平升高和mPFC中正常化的神经元振荡有关。
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来源期刊
Journal of Neuroscience Research
Journal of Neuroscience Research 医学-神经科学
CiteScore
9.50
自引率
2.40%
发文量
145
审稿时长
1 months
期刊介绍: The Journal of Neuroscience Research (JNR) publishes novel research results that will advance our understanding of the development, function and pathophysiology of the nervous system, using molecular, cellular, systems, and translational approaches. JNR covers both basic research and clinical aspects of neurology, neuropathology, psychiatry or psychology. The journal focuses on uncovering the intricacies of brain structure and function. Research published in JNR covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of the nervous system, with emphasis on how disease modifies the function and organization.
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