环氧化物水解酶2
内膜增生
环氧二十碳三烯酸
血管平滑肌
平滑肌
新生内膜增生
血小板源性生长因子受体
环氧合酶
花生四烯酸
增生
体内
血小板衍生生长因子
化学
药理学
癌症研究
内分泌学
医学
内科学
生长因子
生物
再狭窄
生物化学
酶
受体
生物技术
支架
作者
Hui Wu,Dai Li,Chen-Yu Zhang,Lingli Huang,Youjie Zeng,Tian-Ge Chen,Ke Yu,Jia-Wei Meng,Yuxin Lin,Ren Guo,Yong Zhou,Ge Gao
标识
DOI:10.1016/j.ejphar.2024.176824
摘要
Intimal hyperplasia (IH) is an innegligible issue for patients undergoing interventional therapy. The proliferation and migration of vascular smooth muscle cells (VSMCs) induced by platelet-derived growth factor-BB (PDGF-BB) are critical events in the development of IH. While the exact mechanism and effective target for IH needs further investigation. Metabolic disorders of arachidonic acid (ARA) are involved in the occurrence and progression of various diseases. In this study, we found that the expressions of soluble epoxide hydrolase (sEH) and cyclooxygenase-2 (COX-2) were significantly increased in the VSMCs during balloon injury-induced IH. Then, we employed a COX-2/sEH dual inhibitor PTUPB to increase the concentration of epoxyeicosatrienoic acids (EETs) while prevent the release of pro-inflammatory prostaglandins. Results showed that PTUPB treatment significantly reduced neointimal thickening induced by balloon injury in rats in vivo and inhibited PDGF-BB-induced proliferation and migration of VSMCs in vitro. Our results showed that PTUPB may reverse the phenotypic transition of VSMCs by inhibiting Pttg1 expression. In conclusion, we found that the dysfunction of ARA metabolism in VSMCs contributes to IH, and the COX-2/sEH dual inhibitor PTUPB attenuates IH progression by reversing the phenotypic switch in VSMC through the Sirt1/Pttg1 pathway.
科研通智能强力驱动
Strongly Powered by AbleSci AI