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重复经颅磁刺激(rTMS)能否促进亚急性人类缺血性卒中后的神经发生和轴突发生?

Can Repetitive Transcranial Magnetic Stimulation (rTMS) Promote Neurogenesis and Axonogenesis in Subacute Human Ischemic Stroke?

作者信息

De Michele Manuela, Piscopo Paola, Costanzo Matteo, Lorenzano Svetlana, Crestini Alessio, Rivabene Roberto, Manzini Valeria, Petraglia Luca, Iacobucci Marta, Berto Irene, Schiavo Oscar Gaetano, Conte Antonella, Belvisi Daniele, Berardelli Alfredo, Toni Danilo

机构信息

Emergency Department, Stroke Unit, Policlinico Umberto I Hospital, Sapienza University, 00161 Rome, Italy.

Department of Neuroscience, Italian National Institute of Health, 00161 Rome, Italy.

出版信息

Biomedicines. 2024 Mar 17;12(3):670. doi: 10.3390/biomedicines12030670.

Abstract

BACKGROUND

Ischemic stroke may trigger neuroplastic changes via proliferation, migration towards the lesion, and differentiation of neuroprogenitor cells into mature neurons. Repetitive Transcranial Magnetic Stimulation (rTMS) may promote brain plasticity. This study aimed to assess rTMS's effect on post-stroke endogenous neuroplasticity by dosing plasma miRs 17~92, Netrin-1, Sema3A, and BDNF.

METHODS

In this case-controlled study, we randomized 19 ischemic stroke patients within five days from symptoms onset (T0) to neuronavigated-rTMS or sham stimulation. Stimulation was applied on the stroke hemisphere daily between the 7th and 14th day from stroke onset. Blood samples were collected at T0, before the first rTMS section (T7), and at the end of the last rTMS session (T14). Five healthy controls were also enrolled in this study.

RESULTS

Of 19 patients, 10 received rTMS and 9 sham stimulation. Compared with the sham group, in the rTMS group, plasma levels of miRs17~92 and Ntn-1 significantly increased whereas Sema3A levels tended to decrease. In multivariate linear regression analyses, rTMS was independently related to Ntn-1 and miR-25 levels at T14.

CONCLUSIONS

We found an association between rTMS and neurogenesis/axonogenesis biomarker enhancement. Our preliminary data suggest that rTMS may positively interfere with natural endogenous plasticity phenomena of the post-ischemic human brain.

摘要

背景

缺血性中风可能通过神经祖细胞的增殖、向病变部位迁移以及分化为成熟神经元来触发神经可塑性变化。重复经颅磁刺激(rTMS)可能促进脑可塑性。本研究旨在通过检测血浆miR 17~92、Netrin-1、Sema3A和脑源性神经营养因子(BDNF)来评估rTMS对中风后内源性神经可塑性的影响。

方法

在这项病例对照研究中,我们将19例症状发作后5天内的缺血性中风患者(T0)随机分为神经导航rTMS组或假刺激组。在中风发作后第7天至第14天,每天对中风半球进行刺激。在T0、第一次rTMS治疗前(T7)和最后一次rTMS治疗结束时(T14)采集血样。本研究还纳入了5名健康对照者。

结果

19例患者中,l0例接受rTMS治疗,9例接受假刺激。与假刺激组相比,rTMS组血浆miR17~92和Ntn-1水平显著升高,而Sema3A水平呈下降趋势。在多变量线性回归分析中,rTMS与T14时的Ntn-1和miR-25水平独立相关。

结论

我们发现rTMS与神经发生/轴突发生生物标志物增强之间存在关联。我们的初步数据表明,rTMS可能对缺血后人脑的自然内源性可塑性现象产生积极影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8f6/10968490/44f4fc418f98/biomedicines-12-00670-g001.jpg

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