Baek Ahreum, Kim Ji Hyun, Pyo Soonil, Jung Joon-Ho, Park Eun Jee, Kim Sung Hoon, Cho Sung-Rae
Department and Rehabilitation Medicine, Yonsei University Wonju College of Medicine, Wonju, South Korea.
Department and Research Institute of Rehabilitation Medicine, Yonsei University College of Medicine, Seoul, South Korea.
Front Neurol. 2018 Feb 13;9:50. doi: 10.3389/fneur.2018.00050. eCollection 2018.
Repetitive transcranial magnetic stimulation (rTMS) is a non-invasive therapy that has been implicated in treatment of serious neurological disorders. However, the neurobiological mechanisms underlying the effects of rTMS remain unclear. Therefore, this study examined the differential effects of repetitive magnetic stimulation (rMS) in an neuronal model of ischemia/reperfusion (I/R) injury, depending on low and high frequency. Neuro-2a cells were differentiated with retinoic acid and established for neuronal model of I/R injury under a subsequent 3 h of oxygen and glucose deprivation/reoxygenation (OGD/R) condition. After the I/R injury, the differentiated neuronal cells were stimulated with rMS on day 1 and randomly divided into three groups: OGD/R+sham, OGD/R+low-frequency, and OGD/R+high-frequency groups. High-frequency rMS increases cell proliferation through activation of extracellular signal-regulated kinases and AKT-signaling pathway and inhibits apoptosis in OGD/R-injured cells. Furthermore, high-frequency rMS increases Ca-calmodulin-dependent protein kinase II (CaMKII)-cAMP-response element binding protein (CREB) signaling pathway, further leading to alternation of brain-derived neurotrophic factor expression and synaptic plasticity in OGD/R injured cells. These results verified the neurobiological mechanisms of frequency-dependent rMS in I/R injury-treated neuronal cells. These mechanisms will help develop more powerful and credible rTMS stimulation treatment protocols.
重复经颅磁刺激(rTMS)是一种非侵入性治疗方法,已被用于治疗严重的神经疾病。然而,rTMS作用的神经生物学机制仍不清楚。因此,本研究在缺血/再灌注(I/R)损伤的神经元模型中,研究了低频和高频重复磁刺激(rMS)的不同作用。用视黄酸诱导Neuro-2a细胞分化,并在随后3小时的氧糖剥夺/复氧(OGD/R)条件下建立I/R损伤的神经元模型。I/R损伤后,在第1天用rMS刺激分化的神经元细胞,并随机分为三组:OGD/R+假刺激组、OGD/R+低频组和OGD/R+高频组。高频rMS通过激活细胞外信号调节激酶和AKT信号通路增加细胞增殖,并抑制OGD/R损伤细胞的凋亡。此外,高频rMS增加钙/钙调蛋白依赖性蛋白激酶II(CaMKII)-环磷酸腺苷反应元件结合蛋白(CREB)信号通路,进一步导致OGD/R损伤细胞中脑源性神经营养因子表达和突触可塑性的改变。这些结果证实了频率依赖性rMS在I/R损伤神经元细胞中的神经生物学机制。这些机制将有助于制定更有效、更可靠的rTMS刺激治疗方案。