Department of Cardiothoracic Surgery, Affiliated Hospital and Medical School of Nantong University, Nantong, 226001, China.
Research Center of Clinical Medicine, Affiliated Hospital of Nantong University, Nantong, 226001, Jiangsu, China.
Sci Rep. 2024 Sep 2;14(1):20368. doi: 10.1038/s41598-024-71473-5.
Local inflammatory microenvironment in the early stage of myocardial infarction (MI) severely impaired cardiac recovery post-MI. Macrophages play a pivotal role in this process. A classical glycolytic inhibitor, 2-Deoxy-Glucose (2-DG), has been found to regulate the excessive pro-inflammatory macrophage polarization in the infarcted myocardium. This study investigated the effect of 2-DG-loaded chitosan/gelatin composite patch on the infarct microenvironment post-MI and its impact on cardiac repair. The results showed that the 2-DG patch significantly inhibited the expression of inflammatory cytokines, alleviated reactive oxygen species (ROS) accumulation, repressed the proinflammatory polarization of macrophages, attenuated local inflammatory microenvironment in the ischemic hearts, as well as improved cardiac function, reduced scar size, and promoted angiogenesis post-MI. In terms of mechanism, 2-DG exerts anti-inflammatory effects through inhibiting the NF-κB signaling pathway and reducing the assembly and activation of the NLRP3 inflammasome. These findings suggest that 2-DG composite patch may represent a promising therapeutic strategy for cardiac repair after MI.
在心肌梗死(MI)的早期阶段,局部炎症微环境严重损害了 MI 后的心脏恢复。巨噬细胞在这个过程中起着关键作用。一种经典的糖酵解抑制剂,2-脱氧葡萄糖(2-DG),已被发现可调节梗死心肌中过度的促炎型巨噬细胞极化。本研究探讨了载 2-DG 的壳聚糖/明胶复合贴片对 MI 后梗死微环境的影响及其对心脏修复的作用。结果表明,2-DG 贴片显著抑制了炎症细胞因子的表达,减轻了活性氧(ROS)的积累,抑制了巨噬细胞的促炎极化,减轻了缺血心脏的局部炎症微环境,改善了心脏功能,减少了梗死面积,并促进了 MI 后的血管生成。在机制方面,2-DG 通过抑制 NF-κB 信号通路和减少 NLRP3 炎性小体的组装和激活发挥抗炎作用。这些发现表明,2-DG 复合贴片可能代表 MI 后心脏修复的一种有前途的治疗策略。