血管生成
药理学
缺血性中风
医学
信号转导
新生血管
背景(考古学)
治疗性血管生成
冲程(发动机)
缺血
化学
癌症研究
缺血性损伤
缺氧诱导因子1
作者
Chao Zhao,Xiaodan Bai,Yi Ding,Aiguo Zeng,Aidong Wen,Qiang Fu,Jingwen Wang
标识
DOI:10.1080/13880209.2025.2605571
摘要
CONTEXT: Andrews, respectively. OBJECTIVE: We investigated whether SAB combined with BP alleviated IS by promoting micrangium angiogenesis and determined the potential molecular mechanisms. MATERIALS AND METHODS: The impact of SAB-BP on angiogenesis after IS was investigated in middle cerebral artery occlusion (MCAO) rat model, ponatinib-induced ischemic stroke in zebrafish, and human umbilical vein endothelial cells (HUVECs). The neuroprotective effect of SAB-BP in rats was assessed using behavior tests and histopathological staining. The cerebral thrombosis assessment and angiogenesis assay were performed in the zebrafish model. Cell proliferation and angiogenesis in oxygen-glucose deprivation and reperfusion (OGD/R) HUVECs were assessed through cell viability, tube formation, migration, and invasion assays. Western blot analysis and immunofluorescence staining were used to determine the protein expression levels of Nrf2, HO-1, and VEGFA. RESULTS: The findings indicated that SAB-BP significantly reduced neurological impairment following IS and promoted the formation of functional vessels in the cerebral ischemic penumbra. Furthermore, SAB-BP up-regulated the protein expression of Nrf2, HO-1, HIF-1α, and VEGFA. Intriguingly, the pro-angiogenic effect of SAB-BP markedly restrained by adding the inhibitor of Nrf2 (ML385). DISCUSSION AND CONCLUSION: . SAB-BP could serve as a promising therapeutic agent for IS recovery.
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