二肽基肽酶-4
医学
糖尿病
炎症
内皮功能障碍
祖细胞
内皮祖细胞
血糖性
疾病
内皮干细胞
2型糖尿病
氧化应激
免疫学
内科学
内分泌学
干细胞
生物
细胞生物学
体外
生物化学
作者
Hengdao Liu,Lingli Guo,Junhui Xing,Peicheng Li,Haiqiang Sang,Xiaofang Hu,Yunpeng Du,Liangping Zhao,Ruipeng Song,Heping Gu
标识
DOI:10.1016/j.ejphar.2020.173037
摘要
Diabetes is a chronic non-communicable disease whose incidence continues to grow rapidly, and it is one of the most serious and critical public health problems. Diabetes complications, especially atherosclerosis-related chronic vascular complications, are a serious threat to human life and health. Growing evidence suggests that dipeptidyl peptidase 4 (DPP4) inhibitors, beyond their role in improving glycemic control, are helpful in ameliorating endothelial dysfunction in humans and animal models of T2DM. In fact, DPP4 inhibitors have been shown by successive studies to play a protective effect against vascular complications. On one hand, in addition to their hypoglycemic effects, DPP4 inhibitors participate in the control of atherosclerotic risk factors by regulating blood lipids and lowering blood pressure. On the other hand, DPP4 inhibitors exert anti-atherosclerotic effects directly through multiple mechanisms, including improving endothelial cell dysfunction, increasing circulating endothelial progenitor cell (EPCs) levels, regulating mononuclear macrophages and smooth muscle cells, inhibiting inflammation and oxidative stress and improving plaque instability. Herein, we review the beneficial roles of DPP4 inhibitors in atherosclerosis as detailed.
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