Université de La Réunion, INSERM, UMR 1188 Diabète athérothrombose, Thérapies Réunion Océan Indien (DéTROI), Saint-Denis, La Réunion, 97490, France.
CHU de La Réunion, Saint-Pierre, La Réunion, 97410, France.
Mol Nutr Food Res. 2020 Jul;64(13):e1900779. doi: 10.1002/mnfr.201900779. Epub 2020 Jun 16.
Hyperglycemia alters cerebral endothelial cell and blood-brain barrier functions, aggravating cerebrovascular complications such as stroke during diabetes. Redox and inflammatory changes play a causal role. This study evaluates polyphenol protective effects in cerebral endothelial cells and a mouse stroke model during hyperglycemia.
Murine bEnd.3 cerebral endothelial cells and a mouse stroke model are exposed to a characterized, polyphenol-rich extract of Antirhea borbonica or its predominant constituent caffeic acid, during hyperglycemia. Polyphenol effects on redox, inflammatory and vasoactive markers, infarct volume, and hemorrhagic transformation are determined. In vitro, polyphenols improve reactive oxygen species levels, Cu/Zn superoxide dismutase activity, and both NAPDH oxidase 4 and nuclear factor erythroid 2-related factor 2 (Nrf2) gene expression deregulated by high glucose. Polyphenols reduce Nrf2 nuclear translocation and counteract nuclear factor-ĸappa B activation, interleukin-6 secretion, and the altered production of vasoactive markers mediated by high glucose. In vivo, polyphenols reduce cerebral infarct volume and hemorrhagic transformation aggravated by hyperglycemia. Polyphenols attenuate redox changes, increase vascular endothelial-Cadherin production, and decrease neuro-inflammation in the infarcted hemisphere.
Polyphenols protect against hyperglycemia-mediated alterations in cerebral endothelial cells and a mouse stroke model. It is relevant to assess polyphenol benefits to improve cerebrovascular damages during diabetes.
高血糖会改变脑内皮细胞和血脑屏障的功能,加重糖尿病期间的脑血管并发症,如中风。氧化还原和炎症变化起着因果关系。本研究评估了多酚在高血糖期间对脑内皮细胞和小鼠中风模型的保护作用。
在高血糖条件下,将小鼠 bEnd.3 脑内皮细胞和小鼠中风模型暴露于富含多酚的 Antirhea borbonica 提取物或其主要成分咖啡酸。测定多酚对氧化还原、炎症和血管活性标志物、梗死体积和出血转化的影响。在体外,多酚可改善由高葡萄糖引起的活性氧水平、Cu/Zn 超氧化物歧化酶活性、以及 NADPH 氧化酶 4 和核因子红细胞 2 相关因子 2(Nrf2)基因表达的失调。多酚可减少 Nrf2 的核易位,并拮抗核因子-κB 的激活、白细胞介素-6 的分泌以及由高葡萄糖介导的血管活性标志物的改变产生。在体内,多酚可减少高血糖加重的脑梗死体积和出血转化。多酚可减轻氧化还原变化,增加血管内皮钙粘蛋白的产生,并减少梗死半球的神经炎症。
多酚可防止高血糖引起的脑内皮细胞和小鼠中风模型的改变。评估多酚对改善糖尿病期间脑血管损伤的益处是很重要的。