TY - JOUR
T1 - Rapid inhibition of atherosclerotic plaque progression by sonodynamic therapy
AU - Sun, Xin
AU - Guo, Shuyuan
AU - Yao, Jianting
AU - Wang, Huan
AU - Peng, Chenghai
AU - Li, Bicheng
AU - Wang, Yu
AU - Jiang, Yongxing
AU - Wang, Tengyu
AU - Yang, Yang
AU - Cheng, Jiali
AU - Wang, Wei
AU - Cao, Zhengyu
AU - Zhao, Xuezhu
AU - Li, Xiang
AU - Sun, Jing
AU - Yang, Jiemei
AU - Tian, Fang
AU - Chen, Xi
AU - Li, Qiannan
AU - Gao, Weiwei
AU - Shen, Jing
AU - Zhou, Qi
AU - Wang, Peng
AU - Li, Zhitao
AU - Tian, Zhen
AU - Zhang, Zhiguo
AU - Cao, Wenwu
AU - Li, Min
AU - Tian, Ye
N1 - Publisher Copyright:
© The Author(s) 2018.
PY - 2019/1/1
Y1 - 2019/1/1
N2 - Aims 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. Methods and results 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. Conclusion SDT is a non-invasive and efficacious regimen to inhibit atherosclerotic plaque progression.
AB - Aims 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. Methods and results 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. Conclusion SDT is a non-invasive and efficacious regimen to inhibit atherosclerotic plaque progression.
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U2 - 10.1093/cvr/cvy139
DO - 10.1093/cvr/cvy139
M3 - Article
C2 - 29878150
AN - SCOPUS:85058915706
SN - 0008-6363
VL - 115
SP - 190
EP - 203
JO - Cardiovascular Research
JF - Cardiovascular Research
IS - 1
ER -