胰岛素抵抗
伊诺斯
内分泌学
内科学
氧化应激
内皮功能障碍
川地31
胰岛素
内皮
血管舒张
一氧化氮
2型糖尿病
医学
糖尿病
脐静脉
一氧化氮合酶
化学
血管生成
体外
生物化学
作者
An He,Huilin Yu,Yu Hu,Huiling Chen,Xiang Li,Jian Shen,Rongjuan Zhuang,Yi Chen,Bryan Richard Sasmita,Minghao Luo,Dingyi Lv
标识
DOI:10.1016/j.bbrc.2022.02.057
摘要
We aimed to examine the effect of Honokiol (HKL) on endothelial dysfunction in type 2 diabetic rats and its possible mechanism. A high-fat diet and streptozotocin (STZ) were used to establish the type 2 diabetic model in rats. Part of these rats were intraperitoneally injected with HKL 10 mg/kg daily. Then the expression of Ser1177 phosphorylation of endothelial nitric oxide synthase (p-eNOS), eNOS, and CD31, vasodilation function, insulin signaling, indicators of oxidative stress and relative signaling pathway were measured. Human umbilical vein endothelial cells (HUVECs) were used to explore the underlying mechanism of the effect of HKL on high glucose-related endothelial injury in vitro. The data showed that HKL could reverse the decline of the expression of p-eNOS and CD31, endothelium-related vasodilation dysfunction, insulin resistance and activation of oxidative stress induced by type 2 diabetes in vivo. The similar results were obtained in vitro. In summary, our study demonstrates that HKL improves endothelial function and diminishes insulin resistance and oxidative stress, suggesting that HKL could be used as a treatment option for diabetes in the future.
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