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腔内高切变应力区域的电化学阻抗升高:评估富含脂质的动脉粥样硬化病变的意义。

Elevated electrochemical impedance in the endoluminal regions with high shear stress: implication for assessing lipid-rich atherosclerotic lesions.

机构信息

Department of Biomedical Engineering and Cardiovascular Medicine, University of Southern California, Los Angeles, CA 90089, USA.

出版信息

Biosens Bioelectron. 2013 May 15;43:237-44. doi: 10.1016/j.bios.2012.12.024. Epub 2012 Dec 20.

DOI:10.1016/j.bios.2012.12.024
PMID:23318546
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3594425/
Abstract

BACKGROUND

Identifying metabolically active atherosclerotic lesions remains an unmet clinical challenge during coronary intervention. Electrochemical impedance (EIS) increased in response to oxidized low density lipoprotein (oxLDL)-laden lesions. We hereby assessed whether integrating EIS with intravascular ultrasound (IVUS) and shear stress (ISS) provided a new strategy to assess oxLDL-laden lesions in the fat-fed New Zealand White (NZW) rabbits.

METHODS AND RESULTS

A micro-heat transfer sensor was deployed to acquire the ISS profiles at baseline and post high-fat diet (HD) in the NZW rabbits (n=8). After 9 weeks of HD, serum oxLDL levels (mg/dL) increased by 140 fold, accompanied by a 1.5-fold increase in kinematic viscosity (cP) in the HD group. Time-averaged ISS (ISSave) in the thoracic aorta also increased in the HD group (baseline: 17.61±0.24 vs. 9 weeks: 25.22±0.95dyne/cm(2), n=4), but remained unchanged in the normal diet group (baseline: 22.85±0.53dyn/cm(2) vs. 9 weeks: 22.37±0.57dyne/cm(2), n=4). High-frequency intravascular ultrasound (IVUS) revealed atherosclerotic lesions in the regions with augmented ISSave, and concentric bipolar microelectrodes demonstrated elevated EIS signals, which were correlated with prominent anti-oxLDL immuno-staining (oxLDL-free regions: 497±55Ω, n=8 vs. oxLDL-rich lesions: 679±125Ω, n=12, P<0.05). The equivalent circuit model for tissue resistance between the lesion-free and ox-LDL-rich lesions further validated the experimental EIS signals.

CONCLUSIONS

By applying electrochemical impedance in conjunction with shear stress and high-frequency ultrasound sensors, we provided a new strategy to identify oxLDL-laden lesions. The study demonstrated the feasibility of integrating EIS, ISS, and IVUS for a catheter-based approach to assess mechanically unstable plaque.

摘要

背景

在冠状动脉介入治疗过程中,识别代谢活跃的动脉粥样硬化斑块仍然是一个未满足的临床挑战。电化学阻抗(EIS)对氧化型低密度脂蛋白(oxLDL)负荷的病变有反应性增加。因此,我们评估了将 EIS 与血管内超声(IVUS)和剪切力(ISS)相结合是否为评估新西兰白兔脂肪喂养模型中 oxLDL 负荷病变提供了一种新策略。

方法和结果

微热传递传感器用于获取新西兰白兔基线和高脂肪饮食(HD)后(n=8)的 ISS 谱。在 HD 后 9 周,血清 oxLDL 水平(mg/dL)增加了 140 倍,同时 HD 组的运动粘度(cP)增加了 1.5 倍。HD 组胸主动脉的平均 ISS(ISSave)也增加(基线:17.61±0.24 vs. 9 周:25.22±0.95dyne/cm(2),n=4),但在正常饮食组无变化(基线:22.85±0.53dyn/cm(2) vs. 9 周:22.37±0.57dyne/cm(2),n=4)。高频血管内超声(IVUS)显示 ISSave 增加的区域有动脉粥样硬化斑块,双极微电极显示出升高的 EIS 信号,与明显的抗 oxLDL 免疫染色相关(oxLDL 无斑块区域:497±55Ω,n=8 vs. oxLDL 丰富病变:679±125Ω,n=12,P<0.05)。病变无斑块区和 ox-LDL 丰富病变之间的组织电阻等效电路模型进一步验证了实验 EIS 信号。

结论

通过应用电化学阻抗与剪切力和高频超声传感器相结合,我们提供了一种识别 oxLDL 负荷病变的新策略。该研究证明了将 EIS、ISS 和 IVUS 集成用于基于导管的评估机械不稳定斑块的可行性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb70/3594425/4d8f17dad0eb/nihms-430571-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb70/3594425/89184a034ad1/nihms-430571-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb70/3594425/f303b535df8f/nihms-430571-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb70/3594425/2162aa9614da/nihms-430571-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb70/3594425/cf10b5540611/nihms-430571-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb70/3594425/ca3df5428337/nihms-430571-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb70/3594425/4d8f17dad0eb/nihms-430571-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb70/3594425/89184a034ad1/nihms-430571-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb70/3594425/f303b535df8f/nihms-430571-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb70/3594425/2162aa9614da/nihms-430571-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb70/3594425/cf10b5540611/nihms-430571-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb70/3594425/ca3df5428337/nihms-430571-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb70/3594425/4d8f17dad0eb/nihms-430571-f0006.jpg

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