Department of Cardiology, The First Affiliated Hospital, Cardiovascular Institute, Harbin Medical University, 23 Youzheng Street, Harbin, PR China.
Department of Pathophysiology and Key Laboratory of Cardiovascular Pathophysiology, Harbin Medical University, Key Laboratory of Cardiovascular Medicine Research (Harbin Medical University), Ministry of Education, 157 Baojian Street, Harbin, PR China.
Cardiovasc Res. 2019 Jan 1;115(1):190-203. doi: 10.1093/cvr/cvy139.
Currently, efficient regimens to reverse atherosclerotic plaques are not available in the clinic. Herein, we present sonodynamic therapy (SDT) as a novel methodology to rapidly inhibit progression of atherosclerotic plaques.
In atherosclerotic rabbit and apoE-deficient mouse models, SDT efficiently decreased the atherosclerotic burden within 1 week, revealing a decrease in the size of the atherosclerotic plaque and enlarged lumen. The shrunken atherosclerotic plaques displayed compositional alterations, with a reduction in lesional macrophages and lipids. The rapid efficacy of SDT may be due to its induction of macrophage apoptosis, enhancement of efferocytosis, and amelioration of inflammation in the atherosclerotic plaque. Compared with atorvastatin, the standard of care for atherosclerosis, SDT showed more significant plaque shrinkage and lumen enlargement during 1 week treatment. Furthermore, SDT displayed good safety without obvious side effects. In a pilot clinical trial recruiting the patients suffering atherosclerotic peripheral artery disease, combination therapy of SDT with atorvastatin efficiently reduced progression of atherosclerotic plaque within 4 weeks, and its efficacy was able to last for at least 40 weeks.
SDT is a non-invasive and efficacious regimen to inhibit atherosclerotic plaque progression.
目前临床上尚无有效的逆转动脉粥样硬化斑块的方法。本文提出声动力学疗法(SDT)是一种抑制动脉粥样硬化斑块进展的新方法。
在动脉粥样硬化兔和载脂蛋白 E 缺陷型小鼠模型中,SDT 在 1 周内有效降低了动脉粥样硬化斑块负担,表现为斑块体积缩小和管腔扩大。缩小的动脉粥样硬化斑块显示出组成的改变,病变中的巨噬细胞和脂质减少。SDT 的快速疗效可能是由于其诱导巨噬细胞凋亡、增强噬作用和改善斑块中的炎症。与动脉粥样硬化的标准治疗药物阿托伐他汀相比,SDT 在 1 周的治疗期间显示出更显著的斑块缩小和管腔扩大。此外,SDT 显示出良好的安全性,没有明显的副作用。在一项招募动脉粥样硬化性外周动脉疾病患者的临床试验中,SDT 联合阿托伐他汀治疗能在 4 周内有效抑制动脉粥样硬化斑块的进展,其疗效至少能持续 40 周。
SDT 是一种抑制动脉粥样硬化斑块进展的非侵入性、有效的治疗方法。