Suppr超能文献

抑制Wnt/Ca信号通路的基因可减轻脑缺血/再灌注损伤。

Gen inhibiting the Wnt/Ca signaling pathway alleviates cerebral ischemia/reperfusion injury.

作者信息

Li Li, Liu Saisai, Wang Mengzhe, Li Mengjia, Liu Yi, Chen Haili, Chen Jie, Tao Weiting, Huang Li, Zhao Shidi

机构信息

Department of Pathophysiology, Bengbu Medical University, Bengbu, 233030, Anhui, China.

Department of Pathology, Anqing 116 Hospital, Anqing, 246000, Anhui, China.

出版信息

Sci Rep. 2025 Feb 7;15(1):4661. doi: 10.1038/s41598-025-88136-8.

Abstract

Cerebral ischemia/reperfusion injury (CIRI) is a major complication of acute ischemic stroke (AIS), characterized by calcium overload, oxidative stress, and cell apoptosis. In this study, we investigated the therapeutic potential of Genistein (Gen) in alleviating CIRI by focusing on its effects on the Wnt/Ca signaling pathway. Using a rat model of cerebral ischemia/reperfusion and in vitro experiments on PC12 cells, we observed that Gen treatment reduced infarct size, improved neurological function, and mitigated calcium overload, oxidative stress, and apoptosis. Further analysis revealed that Gen regulates key proteins in the Wnt/Ca signaling pathway, including Wnt5a and Frizzled-2, effectively preventing intracellular calcium accumulation and subsequent damage. The knockdown of Frizzled-2 confirmed the pathway's role in mediating calcium overload and subsequent damage. Our findings suggest that Gen alleviates CIRI by inhibiting the Wnt/Ca signaling pathway, positioning it as a promising candidate for therapeutic intervention in stroke treatment.

摘要

脑缺血/再灌注损伤(CIRI)是急性缺血性中风(AIS)的主要并发症,其特征为钙超载、氧化应激和细胞凋亡。在本研究中,我们通过聚焦染料木黄酮(Gen)对Wnt/Ca信号通路的影响,研究了其在减轻CIRI方面的治疗潜力。使用脑缺血/再灌注大鼠模型和对PC12细胞进行的体外实验,我们观察到Gen治疗可减小梗死体积、改善神经功能,并减轻钙超载、氧化应激和细胞凋亡。进一步分析表明,Gen调节Wnt/Ca信号通路中的关键蛋白,包括Wnt5a和卷曲蛋白-2,有效防止细胞内钙积累及随后的损伤。卷曲蛋白-2的敲低证实了该通路在介导钙超载及随后损伤中的作用。我们的研究结果表明,Gen通过抑制Wnt/Ca信号通路减轻CIRI,使其成为中风治疗中治疗干预的有希望的候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1068/11805899/df830ce463f9/41598_2025_88136_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验