N-oleoylethanolamide suppresses intimal hyperplasia after balloon injury in rats through AMPK/PPARα pathway

作者：Zhao, Yun; Liu, Yijun; Jing, Zuo; Peng, Lu; Jin, Peng; Lin, Yangbin; Zhou, Yu; Yang, Lichao; Ren, Jie; Xie, Qiang^*; Jin, Xin^*

来源：Biochemical and Biophysical Research Communications, 2018, 496(2): 415-421.

DOI：10.1016/j.bbrc.2018.01.015

• Vascular smooth muscle cells
• Proliferation
• Migration
• N-oleoylethanolamide
• Intimal hyperplasia

Vascular smooth muscle cell (VSMC) proliferation and migration are crucial events in the pathological course of restenosis after percutaneous coronary intervention (PCI). N-oleoylethanolamide (OEA) is a bioactive lipid amide released upon dietary fat digestion with many reported actions. However, the effect of OEA on restenosis after vascular injury remains unknown. Here, we investigated the effects of OEA on intimal hyperplasia after balloon injury in vivo, its effect on VSMC proliferation and migration induced by platelet-derived growth factor (PDGF) stimulation in vitro, and the underlying mechanism underlying these effects. The results showed that OEA-treated rats displayed a significant reduction in neointima formation after balloon injury. In cultured VSMCs, treatment with OEA decreased cell proliferation and migration induced by PDGF. OEA treatment both in vivo and in vitro led to an increase in adenosine monophosphate-activated protein kinase (AMPK) phosphorylation and peroxisome proliferator-activated receptor alpha (PPAR alpha), and a decrease in proliferating cell nuclear antigen (PCNA) and cyclinD1 expression. Pharmacological inhibition of AMPK and PPAR alpha reversed the suppressive effects of OEA on VSMC proliferation and migration, suggesting that the suppressive effect of OEA on VSMC proliferation and migration is mediated through the activation of AMPK and PPAR alpha. In conclusion, our present study demonstrated that OEA attenuated neointima formation in response to balloon injury by suppressing SMC proliferation and migration through an AMPK and PPAR alpha-dependent mechanism. Our data suggests that OEA may be a potential therapeutic agent for restenosis after PCI.

• 出版日期2018-2-5
• 单位厦门大学