首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Mesencephalic Electrical Stimulation Reduces Neuroinflammation after Photothrombotic Stroke in Rats by Targeting the Cholinergic Anti-Inflammatory Pathway
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Mesencephalic Electrical Stimulation Reduces Neuroinflammation after Photothrombotic Stroke in Rats by Targeting the Cholinergic Anti-Inflammatory Pathway

机译:通过靶向胆碱能抗炎途径在大鼠中中脑电气刺激减少了在大鼠中的血栓脑卒中后的神经炎症

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摘要

Inflammation is crucial in the pathophysiology of stroke and thus a promising therapeutic target. High-frequency stimulation (HFS) of the mesencephalic locomotor region (MLR) reduces perilesional inflammation after photothrombotic stroke (PTS). However, the underlying mechanism is not completely understood. Since distinct neural and immune cells respond to electrical stimulation by releasing acetylcholine, we hypothesize that HFS might trigger the cholinergic anti-inflammatory pathway via activation of the α7 nicotinic acetylcholine receptor (α7nAchR). To test this hypothesis, rats underwent PTS and implantation of a microelectrode into the MLR. Three hours after intervention, either HFS or sham-stimulation of the MLR was applied for 24 h. IFN-γ, TNF-α, and IL-1α were quantified by cytometric bead array. Choline acetyltransferase (ChAT)+ CD4+-cells and α7nAchR+-cells were quantified visually using immunohistochemistry. Phosphorylation of NFĸB, ERK1/2, Akt, and Stat3 was determined by Western blot analyses. IFN-γ, TNF-α, and IL-1α were decreased in the perilesional area of stimulated rats compared to controls. The number of ChAT+ CD4+-cells increased after MLR-HFS, whereas the amount of α7nAchR+-cells was similar in both groups. Phospho-ERK1/2 was reduced significantly in stimulated rats. The present study suggests that MLR-HFS may trigger anti-inflammatory processes within the perilesional area by modulating the cholinergic system, probably via activation of the α7nAchR.
机译:炎症在中风的病理生理学中是至关重要的,因此是有前途的治疗目标。中脑运动区域(MLR)的高频刺激(HFS)减少了光癌中风(PTS)后的血管炎症。然而,潜在的机制并不完全理解。由于不同的神经和免疫细胞通过释放乙酰胆碱反应电刺激,因此我们假设HFS可以通过激活α7烟碱乙酰胆碱受体(α7nAChr)来引发胆碱能抗炎途径。为了测试该假设,大鼠接受PTS并将微电极植入MLR。干预三小时后,将MLR的HFS或假刺激施用24小时。通过细胞计数珠阵列量化IFN-γ,TNF-α和IL-1α。使用免疫组织化学在视觉上量化胆碱乙酰转移酶(聊天)+ CD4 + -Cells和α7NACHR+ -Cells。 NF 1b,ERK1 / 2,AKT和STAT3的磷酸化通过Western印迹分析测定。与对照相比,IFN-γ,TNF-α和IL-1α降低了受刺激的大鼠的细胞区域。 MLR-HFS后聊天+ CD4 + -Cells的数量增加,而两组α7nAChr+ -Cell的量相似。受刺激的大鼠的磷酸-ERK1 / 2显着降低。本研究表明,MLR-HF可以通过调节胆碱能系统来触发血管区域内的抗炎方法,可能通过α7NACHR的激活来触发胆碱能系统。

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