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Erythropoietin-derived Peptide ARA290 Mediates Brain Tissue Protection Through the Β-Common Receptor in Mice with Cerebral Ischemic Stroke

Communications and Network Security (CNS)(2024)

Capital Med Univ

Cited 0|Views28
Abstract
Aim: To explore the neuroprotective effects of ARA290 and the role of beta-common receptor (beta CR) in a mouse model of middle cerebral artery occlusion (MCAO). Methods: This study included male C57BL/6J mice that underwent MCAO and reperfusion. The neuroprotective effect of ARA290 on MCAO-induced brain injury was investigated using neurological function tests (Longa and modified neurological severity score). Cerebral infarction was examined by 2, 3, 5-triphenyl tetrazolium chloride staining, neuronal apoptosis was assessed by immunofluorescence staining, blood parameters were measured using a flow cytometry-based automated hematology analyzer, liquid chromatography with tandem mass spectrometry was used to identify the serum metabolomics signature, inflammatory cytokines and liver index were detected by commercially available kits, and the protein levels of the erythropoietin (EPO) receptor and beta CR were measured by western blot. Results: ARA290 exerted a qualitatively similar neuroprotective effect after MCAO as EPO. ARA290 significantly reduced neuronal apoptosis and the level of inflammatory cytokines in the brain tissue. However, ARA290's neuroprotective effect was significantly suppressed following the injection of siRNA against beta CR. Conclusion: ARA290 provided a neuroprotective effect via beta CR in cerebral ischemic mice without causing erythropoiesis. This study provides novel insights into the role of ARA290 in ischemic stroke intervention.
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ARA290,cerebral ischemia,neuroprotection,beta-Common receptor
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要点】:研究揭示了来源于促红细胞生成素(EPO)的肽段ARA290通过β-共同受体(βCR)在小鼠大脑中动脉闭塞(MCAO)模型中发挥神经保护作用,并不引起红细胞生成,为缺血性中风干预提供了新见解。

方法】:通过Longa神经功能测试和改良神经严重性评分来评估ARA290对MCAO引起的大脑损伤的神经保护效果,使用2,3,5-三苯基四氮唑氯盐染色检测脑梗死,通过免疫荧光染色评估神经细胞凋亡,运用流式细胞术自动血液分析仪测量血液参数,液相色谱-串联质谱法鉴定血清代谢组特征,使用商业试剂盒检测炎症细胞因子和肝指数,并通过西方印迹法测量促红细胞生成素受体(EPO)和βCR的蛋白水平。

实验】:在C57BL/6J雄性小鼠中建立MCAO和再灌注模型,ARA290显著降低了大脑组织的神经细胞凋亡和炎症细胞因子水平,且其神经保护效果可被针对βCR的siRNA注射显著抑制。