Pharmacological adjuncts and transcranial magnetic stimulation-induced synaptic plasticity: a systematic review.

IF 4.1 2区 医学 Q2 NEUROSCIENCES
Journal of Psychiatry & Neuroscience Pub Date : 2024-02-15 Print Date: 2024-01-01 DOI:10.1503/jpn.230090
Myren N Sohn, Joshua C Brown, Prayushi Sharma, Ulf Ziemann, Alexander McGirr
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引用次数: 0

Abstract

Background: Transcranial magnetic stimulation (TMS) is a noninvasive neurostimulation modality that has been used to study human synaptic plasticity. Leveraging work in ex vivo preparations, mechanistically informed pharmacological adjuncts to TMS have been used to improve our fundamental understanding of TMS-induced synaptic plasticity.

Methods: We systematically reviewed the literature pairing pharmacological adjuncts with TMS plasticity-induction protocols in humans. We searched MEDLINE, PsycINFO, and Embase from 2013 to Mar. 10, 2023. Studies published before 2013 were extracted from a previous systematic review. We included studies using repetitive TMS, theta-burst stimulation, paired associative stimulation, and quadripulse stimulation paradigms in healthy and clinical populations.

Results: Thirty-six studies met our inclusion criteria (28 in healthy and 8 in clinical populations). Most pharmacological agents have targeted the glutamatergic N-methyl-d-aspartate (NMDA; 15 studies) or dopamine receptors (13 studies). The NMDA receptor is necessary for TMS-induced plasticity; however, sufficiency has not been shown across protocols. Dopaminergic modulation of TMS-induced plasticity appears to be dose-dependent. The GABAergic, cholinergic, noradrenergic, and serotonergic neurotransmitter systems have small evidence bases supporting modulation of TMS-induced plasticity, as do voltage-gated calcium and sodium channels. Studies in clinical populations suggest that pharmacological adjuncts to TMS may rescue motor cortex plasticity, with implications for therapeutic applications of TMS and a promising clinical trial in depression.

Limitations: This review is limited by the predominance in the literature of studies with small sample sizes and crossover designs.

Conclusion: Pharmacologically enhanced TMS largely parallels findings from ex vivo preparations. As this area expands and novel targets are tested, adequately powered samples in healthy and clinical populations will inform the mechanisms of TMS-induced plasticity in health and disease.

药理辅助药物和经颅磁刺激诱导的突触可塑性:系统综述。
背景:经颅磁刺激(TMS经颅磁刺激(TMS)是一种非侵入性神经刺激方式,已被用于研究人类突触可塑性。借助体外制备工作,TMS 的机理药理辅助药物已被用于提高我们对 TMS 诱导的突触可塑性的基本认识:我们系统地回顾了将药理学辅助疗法与 TMS 可塑性诱导方案配对使用的人类文献。我们检索了 2013 年至 2023 年 3 月 10 日期间的 MEDLINE、PsycINFO 和 Embase。2013年之前发表的研究摘自之前的系统综述。我们纳入了在健康和临床人群中使用重复 TMS、θ-脉冲刺激、配对联想刺激和四脉冲刺激范式的研究:有 36 项研究符合我们的纳入标准(28 项针对健康人群,8 项针对临床人群)。大多数药理药剂都针对谷氨酸能 N-甲基-d-天冬氨酸受体(NMDA;15 项研究)或多巴胺受体(13 项研究)。NMDA 受体是 TMS 诱导可塑性的必要条件,但尚未在各种方案中显示出充分性。多巴胺能对 TMS 诱导的可塑性的调节似乎与剂量有关。GABA能、胆碱能、去甲肾上腺素能和5-羟色胺能神经递质系统以及电压门控钙通道和钠通道对TMS诱导的可塑性调节的支持证据较少。对临床人群的研究表明,TMS 的药理辅助治疗可挽救运动皮层的可塑性,这对 TMS 的治疗应用和抑郁症的临床试验具有重要意义:本综述受限于文献中样本量较小的研究和交叉设计:结论:药理增强型 TMS 与体内外制剂的研究结果基本一致。随着这一领域的不断扩大和新靶点的测试,在健康和临床人群中采集充分有效的样本将有助于了解 TMS 在健康和疾病中诱导可塑性的机制。
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来源期刊
CiteScore
6.80
自引率
2.30%
发文量
51
审稿时长
2 months
期刊介绍: The Journal of Psychiatry & Neuroscience publishes papers at the intersection of psychiatry and neuroscience that advance our understanding of the neural mechanisms involved in the etiology and treatment of psychiatric disorders. This includes studies on patients with psychiatric disorders, healthy humans, and experimental animals as well as studies in vitro. Original research articles, including clinical trials with a mechanistic component, and review papers will be considered.
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