首页> 美国卫生研究院文献>Brain Sciences >Deep Brain Stimulation of the Pedunculopontine Tegmental Nucleus Renders Neuroprotection through the Suppression of Hippocampal Apoptosis: An Experimental Animal Study
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Deep Brain Stimulation of the Pedunculopontine Tegmental Nucleus Renders Neuroprotection through the Suppression of Hippocampal Apoptosis: An Experimental Animal Study

机译:通过抑制海马细胞凋亡对人脑桥脑被膜盖核的深层脑刺激提供了神经保护作用:一项实验动物研究

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摘要

The core objective of this study was to determine the neuroprotective properties of deep brain stimulation of the pedunculopontine tegmental nucleus on the apoptosis of the hippocampus. The pedunculopontine tegmental nucleus is a prime target for Parkinson′s disease and is a crucial component in a feedback loop connected with the hippocampus. Deep brain stimulation was employed as a potential tool to evaluate the neuroprotective properties of hippocampal apoptosis. Deep brain stimulation was applied to the experimental animals for an hour. Henceforth, the activity of Caspase-3, myelin basic protein, Bcl-2, BAX level, lipid peroxidation, interleukin-6 levels, and brain-derived neurotrophic factor levels were evaluated at hours 1, 3 and 6 and compared with the sham group of animals. Herein, decreased levels of caspases activity and elevated levels of Bcl-2 expressions and inhibited BAX expressions were observed in experimental animals at the aforementioned time intervals. Furthermore, the ratio of Bcl-2/BAX was increased, and interleukin -6, lipid peroxidation levels were not affected by deep brain stimulation in the experimental animals. These affirmative results have explained the neuroprotection rendered by hippocampus apoptosis as a result of deep brain stimulation. Deep brain stimulation is widely used to manage neuro-motor disorders. Nevertheless, this novel study will be a revelation for a better understanding of neuromodulatory management and encourage further research with new dimensions in the field of neuroscience.
机译:这项研究的核心目标是确定深部脑刺激的小脑桥骨被盖核对海马细胞凋亡的神经保护作用。足桥骨被盖核是帕金森氏病的主要靶标,并且是与海马相连的反馈回路中的重要组成部分。深部脑刺激被用作评估海马细胞凋亡的神经保护特性的潜在工具。将深脑刺激应用于实验动物一个小时。此后,在第1、3和6小时分别评估Caspase-3,髓鞘碱性蛋白,Bcl-2,BAX水平,脂质过氧化,白介素-6水平和脑源性神经营养因子水平的活性,并与假手术组进行比较。动物。在本文中,在上述时间间隔的实验动物中观察到胱天蛋白酶活性水平降低,Bcl-2表达水平升高和BAX表达抑制。此外,在实验动物中,Bcl-2 / BAX的比例增加,并且白介素-6,脂质过氧化水平不受脑部深层刺激的影响。这些肯定的结果已经解释了由于深部脑刺激而引起的海马细胞凋亡所提供的神经保护作用。深层脑刺激被广泛用于管理神经运动障碍。然而,这项新颖的研究将为更好地理解神经调节管理提供启示,并鼓励在神经科学领域进行新的研究。

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