Huacong Liu , Weijia Huang , Qian Ding , Yumeng Huang , Zhenyi Lai , Zhaoxing Liu , Shaoxiong Li , Xinyi Peng , Zhenhong Wu , Liangbin Deng , Yong Huang , Junqi Chen
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Moreover, 74 upregulated and 50 downregulated proteins were identified in the MCAO group compared to the sham group, whilst 52 up-regulated and 50 down-regulated proteins were identified in the SA group compared to the MCAO group. Bioinformatics analysis indicated that SA may exert neuroprotective effects by modulating the acute inflammatory response and microglial activation. Additionally, SA down-regulated the expression levels of Iba-1, TNF-α, IL-1β, and IL-6, while up-regulating those of IL-4 and IL-10. Likewise, it downregulated the expression levels of three key proteins identified via proteomics analysis (Kng1, Brd9, and Magl) that may mediate the anti-inflammatory effects of SA. Overall, these results indicate that SA attenuates neuronal damage in the hippocampus and ischemic penumbra and ameliorates neurological deficits. Proteomic analysis suggested that this effect is related to the modulation of the acute inflammatory response. 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引用次数: 0
摘要
越来越多的证据表明,头皮针灸(SA)可有效缓解急性缺血性脑卒中(IS)患者的神经功能缺损,但它对急性IS患者海马远端损伤的影响及其潜在机制仍难以捉摸。因此,我们进行了蛋白质组学分析,以确定 SA 治疗急性 IS 的潜在靶点。在大脑中动脉闭塞(MCAO)大鼠中,SA能明显缩小脑梗死体积,减轻缺血半影和海马的神经元损伤,并缓解神经功能缺损。此外,与假体组相比,MCAO 组发现了 74 个上调蛋白和 50 个下调蛋白,而与 MCAO 组相比,SA 组发现了 52 个上调蛋白和 50 个下调蛋白。生物信息学分析表明,SA 可通过调节急性炎症反应和小胶质细胞活化发挥神经保护作用。此外,SA 下调了 Iba-1、TNF-α、IL-1β 和 IL-6 的表达水平,同时上调了 IL-4 和 IL-10 的表达水平。同样,它还下调了通过蛋白质组学分析确定的三种关键蛋白(Kng1、Brd9 和 Magl)的表达水平,这三种蛋白可能介导了 SA 的抗炎作用。总之,这些结果表明南澳大利亚能减轻海马和缺血半影区的神经元损伤,改善神经功能缺损。蛋白质组分析表明,这种效应与急性炎症反应的调节有关。SA通过抑制小胶质细胞活化和神经炎症减轻了IS后的远端海马损伤。最后,Kng1、Brd9 和 Magl 被确定为介导 SA 抗炎作用的潜在靶点。
Scalp acupuncture alleviates remote hippocampal damage in MCAO rats by inhibiting neuroinflammation: A TMT-based proteomics analysis
While mounting evidence suggests that scalp acupuncture (SA) may be effective in alleviating neurological deficits in patients with acute ischemic stroke (IS), its effect on remote hippocampal damage in acute IS and the underlying mechanisms remain elusive. Thus, proteomics analysis was conducted to identify potential targets of SA therapy in acute IS. SA significantly reduced cerebral infarct volume and attenuated neuronal damage in the ischemic penumbra and hippocampus, as well as alleviated neurological deficits in rats with middle cerebral artery occlusion (MCAO). Moreover, 74 upregulated and 50 downregulated proteins were identified in the MCAO group compared to the sham group, whilst 52 up-regulated and 50 down-regulated proteins were identified in the SA group compared to the MCAO group. Bioinformatics analysis indicated that SA may exert neuroprotective effects by modulating the acute inflammatory response and microglial activation. Additionally, SA down-regulated the expression levels of Iba-1, TNF-α, IL-1β, and IL-6, while up-regulating those of IL-4 and IL-10. Likewise, it downregulated the expression levels of three key proteins identified via proteomics analysis (Kng1, Brd9, and Magl) that may mediate the anti-inflammatory effects of SA. Overall, these results indicate that SA attenuates neuronal damage in the hippocampus and ischemic penumbra and ameliorates neurological deficits. Proteomic analysis suggested that this effect is related to the modulation of the acute inflammatory response. SA attenuated remote hippocampal damage after IS by inhibiting microglia activation and neuroinflammation. Lastly, Kng1, Brd9, and Magl were identified as potential targets that mediate the anti-inflammatory effects of SA.
期刊介绍:
Neuroscience publishes papers describing the results of original research on any aspect of the scientific study of the nervous system. Any paper, however short, will be considered for publication provided that it reports significant, new and carefully confirmed findings with full experimental details.