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Treatment of auditory hallucinations with bilateral theta burst stimulation: A randomized controlled pilot trial

机译:双侧θ爆裂刺激治疗听觉幻觉:随机对照试验

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Neuroinflammation underlies the pathogenesis of various neurodegenerative disorders including Parkinson's disease (PD). Despite intense investigations, no effective therapy is available to stop its onset or halt its progression. RNS60 is a novel therapeutic containing charge-stabilized nanobubbles in saline, generated by subjecting normal saline to Taylor-Couette-Poiseuille flow under elevated oxygen pressure. Recently, we have delineated that RNS60 inhibits the expression of proinflammatory molecules in glial cells via type 1A phosphatidylinositol-3 kinase (PI3K)-mediated upregulation of IκBα. In this study, we demonstrate that RNS60 inhibited the expression of proinflammatory molecules in cultured microglial cells stimulated by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridium ion (MPP+) and in vivo in the nigra of MPTP-intoxicated mice. While investigating the underlying mechanisms, we found that MPTP intoxication rapidly stimulated the activation of type IB PI3K p110γ in the nigra, while suppressing the activation of type IA PI3K p110α/β. Interestingly, RNS60 treatment suppressed the activation of p110γ PI3K, while inducing the activation of p110α/β PI3K in the nigra of MPTP-intoxicated mice. Accordingly, RNS60 treatment increased the level of IκBα and inhibited the activation of NF-κB in the SNpc of MPTP-intoxicated mice. These findings paralleled dopaminergic neuronal protection, normalized striatal neurotransmitters, and improved motor functions in MPTP-intoxicated mice. These results strongly suggest a promising therapeutic role of this simple modified saline in PD and other neuroinflammatory disorders.
机译:神经炎症是包括帕金森氏病(PD)在内的各种神经退行性疾病的发病机制的基础。尽管进行了深入的研究,但尚无有效的疗法可阻止其发作或阻止其进展。 RNS60是一种新型治疗剂,在盐水中包含电荷稳定的纳米气泡,该气泡是通过在升高的氧气压力下使生理盐水经受Taylor-Couette-Poiseuille流动而产生的。最近,我们描述了RNS60通过1A型磷脂酰肌醇3激酶(PI3K)介导的IκBα上调抑制神经胶质细胞中促炎分子的表达。在这项研究中,我们证明RNS60在1-甲基-4-苯基-1,2,3,6-四氢吡啶鎓离子(MPP +)刺激下和在MPTP-黑素体内抑制了促炎性分子在培养的小胶质细胞中的表达。陶醉的老鼠。在研究潜在机制时,我们发现MPTP中毒迅速刺激了黑质中IB PI3Kp110γ型的激活,同时抑制了IA PI3Kp110α/β型的激活。有趣的是,RNS60处理抑制了MPTP中毒小鼠黑质中p110γPI3K的活化,同时诱导了p110α/βPI3K的活化。因此,RNS60处理增加了MPTP中毒小鼠的SNpc中IκBα的水平并抑制了NF-κB的活化。这些发现与MPTP中毒小鼠的多巴胺能神经元保护,纹状体神经递质正常化和运动功能相似。这些结果强烈暗示了这种简单的改良盐水在PD和其他神经炎性疾病中的有希望的治疗作用。

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