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检测和光动力疗法兔颈动脉粥样硬化斑块炎症。

Detection and photodynamic therapy of inflamed atherosclerotic plaques in the carotid artery of rabbits.

机构信息

Department of Cardiology, The Second Affiliated Hospital, Harbin Medical University, Harbin 150086, PR China.

出版信息

J Photochem Photobiol B. 2011 Jan 10;102(1):26-31. doi: 10.1016/j.jphotobiol.2010.09.001. Epub 2010 Sep 15.

Abstract

Photodynamic therapy (PDT) has been applied in the treatment of artery restenosis following balloon injury. This study aimed to detect the accumulation of 5-aminolevulinic acid (ALA)-derived protoporphyrin IX (PpIX) in inflamed atherosclerotic plaque in rabbit model and evaluate the efficacy of PDT. The inflamed atherosclerotic plaque in the common carotid artery was produced by combination of balloon denudation injury and high cholesterol diet. After intravenous administration of ALA, the fluorescence of PpIX in plaque was detected. At the peak time, the correlation between the fluorescence intensity of PpIX and the macrophage infiltration extent in plaque was analyzed. Subsequently, PDT (635nm at 50J/cm(2)) on the atherosclerotic plaques (n=48) was performed and its effect was evaluated by histopathology and immunohistochemistry. The fluorescence intensity of PpIX in the plaque reached the peak 2h after injection and was 12 times stronger than that of adjacent normal vessel segment, and has a positive correlation with the macrophage content (r=0.794, P<0.001). Compared with the control group, the plaque area was reduced by 59% (P<0.001) at 4week after PDT, the plaque macrophage content decreased by 56% at 1week and 64% at 4week respectively, the smooth muscle cells (SMCs) was depleted by 24% at 1week (P<0.05) and collagen content increased by 44% at 4week (P<0.05). It should be pointed out that the SMC content increased by 18% after PDT at 4week compared with that at 1week (P<0.05). Our study demonstrated that the ALA-derived PpIX can be detected to reflect the macrophage content in the plaque. ALA mediated PDT could reduce macrophage content and inhibit plaque progression, indicating a promising approach to treat inflamed atherosclerotic plaques.

摘要

光动力疗法(PDT)已应用于球囊损伤后动脉再狭窄的治疗。本研究旨在检测兔模型中炎症性动脉粥样硬化斑块中 5-氨基酮戊酸(ALA)衍生原卟啉 IX(PpIX)的积累,并评估 PDT 的疗效。通过球囊剥脱损伤和高胆固醇饮食联合作用制备炎症性动脉粥样硬化斑块。静脉注射 ALA 后,检测斑块中 PpIX 的荧光。在峰值时间,分析 PpIX 荧光强度与斑块中巨噬细胞浸润程度的相关性。随后,对动脉粥样硬化斑块(n=48)进行 PDT(635nm 50J/cm²),并通过组织病理学和免疫组织化学评估其疗效。斑块中 PpIX 的荧光强度在注射后 2 小时达到峰值,比相邻正常血管段强 12 倍,与巨噬细胞含量呈正相关(r=0.794,P<0.001)。与对照组相比,PDT 后 4 周斑块面积减少 59%(P<0.001),斑块巨噬细胞含量在 1 周和 4 周时分别减少 56%和 64%,平滑肌细胞(SMCs)在 1 周时减少 24%(P<0.05),胶原含量在 4 周时增加 44%(P<0.05)。值得注意的是,与 1 周时相比,PDT 后 4 周时 SMC 含量增加了 18%(P<0.05)。本研究表明,ALA 衍生的 PpIX 可被检测以反映斑块中的巨噬细胞含量。ALA 介导的 PDT 可减少巨噬细胞含量并抑制斑块进展,表明其可能是治疗炎症性动脉粥样硬化斑块的一种有前途的方法。

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