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Combined proteomic and metabolomic analyses of cerebrospinal fluid from mice with ischemic stroke reveals the effects of a Buyang Huanwu decoction in neurodegenerative disease

机译:缺血性中风小鼠脑脊髓液的蛋白质组学和代谢组学分析相结合,揭示了补阳还五汤对神经退行性疾病的作用

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摘要

Ischemic stroke is one of the most common causes of death worldwide and is a major cause of acquired disability in adults. However, there is still a need for an effective drug for its treatment. Buyang Huanwu decoction (BHD), a traditional Chinese medicine (TCM) prescription, has long been used clinically to aid neurological recovery after stroke. To establish potential clinical indicators of BHD efficacy in stroke treatment and prognosis, we conducted a combined proteomic and metabolomic analysis of cerebrospinal fluid (CSF) samples in a mouse stroke model. CSF samples were obtained from male mice with acute ischemic stroke induced by middle cerebral ischemic/reperfusion (CI/R) injury, some of which were then treated with BHD. Label-free quantitative proteomics was conducted using nano-LC-MS/MS on an LTQ Orbitrap mass and metabolomic analysis was performed using nanoprobe NMR and UHPLC-QTOF-MS. The results showed that several proteins and metabolites were present at significantly different concentrations in the CSF samples from mice with CI/R alone and those treated with BHD. These belonged to pathways related to energy demand, inflammatory signaling, cytoskeletal regulation, Wnt signaling, and neuroprotection against neurodegenerative diseases. In conclusion, our in silico data suggest that BHD treatment is not only protective but can also ameliorate defects in pathways affected by neurological disorders. These data shed light on the mechanism whereby BHD may be effective in the treatment and prevention of stroke-related neurodegenerative disease.
机译:缺血性中风是全世界最常见的死亡原因之一,并且是成年人后天致残的主要原因。然而,仍然需要用于其治疗的有效药物。补阳还五汤(BHD)是一种中药(TCM)处方,长期以来一直在临床上用于中风后的神经恢复。为了建立BHD在中风治疗和预后中潜在的临床指标,我们在小鼠中风模型中对脑脊液(CSF)样品进行了蛋白质组学和代谢组学分析。从中脑缺血/再灌注(CI / R)损伤诱发的具有急性缺血性中风的雄性小鼠中获取CSF样品,然后用BHD处理其中一些。使用纳米LC-MS / MS对LTQ Orbitrap质量进行无标记的定量蛋白质组学,并使用纳米探针NMR和UHPLC-QTOF-MS进行代谢组学分析。结果表明,单独使用CI / R的小鼠和用BHD处理的小鼠的CSF样品中,几种蛋白质和代谢物的浓度存在明显不同。这些属于与能量需求,炎性信号传导,细胞骨架调节,Wnt信号传导以及针对神经退行性疾病的神经保护相关的途径。总之,我们的计算机模拟数据表明,BHD治疗不仅具有保护作用,而且还可以改善受神经系统疾病影响的途径中的缺陷。这些数据阐明了BHD可能有效治疗和预防中风相关性神经退行性疾病的机制。

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