Increased dipeptidyl peptidase-4 accelerates chronic stress-related thrombosis in a mouse carotid artery model

医学 氧化应激 血管性血友病因子 血小板活化 内科学 ADAMTS13号 内分泌学 内皮功能障碍 血小板 免疫学
作者
Xianglan Jin,Chunzi Jin,Kae Nakamura,Tiefeng Jin,Minglong Xin,Ying Wan,Xueling Yue,Sheng‐Yu Jin,Hailong Wang,Aiko Inoue,Yongshan Nan,Zhenhua Lin,Masafumi Kuzuya,Xian Wu Cheng
出处
期刊:Journal of Hypertension [Ovid Technologies (Wolters Kluwer)]
卷期号:38 (8): 1504-1513 被引量:22
标识
DOI:10.1097/hjh.0000000000002418
摘要

Objective: Exposure to chronic psychosocial stress is a risk factor for metabolic cardiovascular disorders. Given that dipeptidyl peptidase-4 (DPP-4) has an important role in human pathobiology, we investigated the role of DPP-4 in stress-related thrombosis in mice, focusing on oxidative stress and the von Willebrand factor (vWF)-cleaving protease ADAMTS13 (a disintegrin and metalloproteinase with thrombospondin type 1 motif, member 13). Methods and results: Male mice randomly assigned to nonstress and 2-week immobilized-stress groups underwent iron chloride3 (FeCl 3 )-induced carotid artery thrombosis surgery for morphological and biochemical studies at specific times. On day 14 post-stress/surgery, stress had enhanced the lengths and weights of arterial thrombi, with alterations of plasma DPP-4, plasminogen activation inhibitor-1 and ADAMTS13. The stressed mice had increased levels of vascular cell adhesion molecule-1, intracellular adhesion molecule-1, monocyte chemoattractant protein-1, gp91phox, p22phox, matrix metalloproteinase-2 (MMP-2), MMP-9, cathepsins S and K mRNAs and/or proteins, and reduced levels of endothelial nitric oxide synthase, catalase and superoxide dismutase-1 mRNAs and/or proteins. Stress also accelerated arterial endothelial cell damage. The DPP-4 inhibitor anagliptin ameliorated the stress-induced targeted molecular and morphological changes and thrombosis. In vitro , DPP-4 inhibition also mitigated the alterations in the targeted ADAMTS13 and other oxidative and inflammatory molecules in human umbilical vein endothelial cells in response to H 2 O 2 . Conclusion: DPP-4 inhibition appeared to improve the FeCl 3 -induced thrombosis in mice that received stress, possibly via the improvement of ADAMTS13 and oxidative stress, suggesting that DPP-4 could become a novel therapeutic target for chronic psychological stress-related thrombotic events in metabolic cardiovascular disorders.
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