首页> 外文期刊>Canadian Journal of Physiology and Pharmacology >Effect of resveratrol derivative BTM-0512 on high glucose-induced dysfunction of endothelial cells: role of SIRT1.
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Effect of resveratrol derivative BTM-0512 on high glucose-induced dysfunction of endothelial cells: role of SIRT1.

机译:白藜芦醇衍生物BTM-0512对高糖诱导的内皮细胞功能障碍的影响:SIRT1的作用。

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摘要

Hyperglycemia impairs the function of endothelial cells. Sirtuin 1 (SIRT1) is involved in regulating the function of endothelial cells. Resveratrol, a polyphenol found in many plant species, exerts protective effects on endothelial cells through activation of SIRT1. The aims of this work were to explore whether BTM-0512, a novel derivative of resveratrol, is able to exert beneficial effects on high glucose-induced dysfunction of endothelial cells through regulation of SIRT1. We found that high glucose significantly impaired the function of endothelial cells as shown by reduced tube formation, cell migration, and cell adhesion concomitantly with downregulation of mRNA expression of SIRT1 and vascular endothelial growth factor as well as increased tumor necrosis factor-alpha release and reactive oxygen species production. These effects of high glucose were inhibited by pretreatment with BTM-0512. The beneficial effects of BTM-0512 on high glucose-induced cell dysfunction were abolished by splitomicin, a specific inhibitor of SIRT1. The regulatory effects of BTM-0512 on high glucose-induced changes in vascular endothelial growth factor mRNA expression and tumor necrosis factor-alpha release were also abolished by splitomicin. The results suggest that BTM-0512 exerts beneficial effects on high glucose-induced endothelial cell dysfunction through regulation of the SIRT1 - reactive oxygen species - vascular endothelial growth factor - tumor necrosis factor-alpha pathway.
机译:高血糖损害内皮细胞的功能。 Sirtuin 1(SIRT1)参与调节内皮细胞的功能。白藜芦醇是多种植物中发现的一种多酚,可通过激活SIRT1对内皮细胞发挥保护作用。这项工作的目的是探讨白藜芦醇的新型衍生物BTM-0512是否能够通过调节SIRT1对高糖诱导的内皮细胞功能障碍发挥有益作用。我们发现高糖显着损害内皮细胞的功能,如管形成减少,细胞迁移和细胞粘附减少,同时SIRT1和血管内皮生长因子的mRNA表达下调,以及肿瘤坏死因子-α释放和反应性升高氧气种类的产生。 BTM-0512预处理抑制了高血糖的这些作用。 BTM-0512对高糖诱导的细胞功能障碍的有益作用被SIRT1的特异性抑制剂Splitomicin取消。 Splitomicin还取消了BTM-0512对高葡萄糖诱导的血管内皮生长因子mRNA表达和肿瘤坏死因子-α释放变化的调节作用。结果表明,BTM-0512通过调节SIRT1-活性氧-血管内皮生长因子-肿瘤坏死因子-α途径对高糖诱导的内皮细胞功能障碍产生有益作用。

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