细胞凋亡
内皮干细胞
生物
氧化应激
血管生成
内分泌学
内科学
生物化学
癌症研究
医学
体外
作者
Yue Zhang,Ruonan Wang,Huiling Tan,Kaili Wu,Yaju Hu,Hongtao Diao,Dongwei Wang,Xinyuan Tang,Mingyang Leng,Liangzhi Xu,Zhenlu Cai,Duosheng Luo,Xiaoqi Shao,Meiling Yan,Yingyu Chen,Xianglu Rong,Jiao Guo
标识
DOI:10.1016/j.jep.2023.116766
摘要
Fufang Zhenzhu TiaoZhi (FTZ), a Chinese medicinal decoction, has continuously been used to treat metabolic syndrome. Atherosclerosis is the main pathological basis of cardiovascular disease. The N6 methyladenosine (m6A) modification is a highly dynamic and reversible process involving a variety of important biological processes.Here, we investigated the therapeutic effects and mechanism of FTZ in diabetes-accelerated atherosclerosis.Doppler ultrasonography was used to examine the carotid intima-media thickness and plaque area in diabetic atherosclerosis patients. HFD mice were injected with streptozotocin to induce diabetes. HE and Oil red O staining were used to assess the effect of FTZ on lipid deposition. HUVECs were induced with HG/ox-LDL as a model of diabetic atherosclerosis. Furthermore, application of m6A methylation level kit, qRT-PCR, Western blot, tunel staining, reactive oxygen species staining and mPTP staining were performed to analyze the detailed mechanism.Clinical trials of FTZ have shown obvious effect of lowering blood glucose and blood lipids. These effects were reversed after FTZ intervention. Compared with the control, lipid deposition decreased significantly after FTZ administration. FTZ reduced endothelial cell apoptosis. At the same time, we found that FTZ reversed the increase of methylation reader YTHDF2 caused by ox-LDL treatment. Subsequently, we discovered that YTHDF2 degraded SIRT3 mRNA, leading to endothelial cell apoptosis and oxidative stress.FTZ attenuated diabetes-accelerated atherosclerosis by decreasing blood glucose and serum lipids levels, and increased endothelial cell antioxidant capacity, inhibited endothelial cell apoptosis via inhibiting YTHDF2-mediated m6A modification of SIRT3 mRNA, which reduced mRNA degradation.
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