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用于治疗动脉瘤的血流导向支架临床前评估的多光子显微镜技术

Multiphoton microscopy for pre-clinical evaluation of flow-diverter stents for treating aneurysms.

作者信息

Bardet Sylvia M, Cortese Jonathan, Blanc Raphaël, Mounayer Charbel, Rouchaud Aymeric

机构信息

University of Limoges, 123, avenue Albert-Thomas, XLIM UMR CNRS 7252, 87060 Limoges, France.

Bichat University Hospital, INSERM U1148-LVTS, Paris, France; Bicetre Hospital, Department of Interventional Neuroradiology, Paris, France.

出版信息

J Neuroradiol. 2021 May;48(3):200-206. doi: 10.1016/j.neurad.2020.03.005. Epub 2020 Mar 20.

Abstract

BACKGROUND

Conventional histological analyses are the gold standard for the study of aneurysms and vascular pathologies in pre-clinical research. Over the past decade, in vivo and ex vivo imaging using multiphoton microscopy have emerged as powerful pre-clinical tools for detailed tissue analyses that can assess morphology, the extracellular matrix (ECM), cell density and vascularisation. Multiphoton microscopy allows for deeper tissue penetration with minor phototoxicity.

OBJECTIVE

The present study aimed to demonstrate the current status of multimodality imaging, including multiphoton microscopy, for detailed analyses of neo-endothelialisation and ECM evolution after flow-diverter stent (FDS) treatment in an experimental rabbit model of aneurysms.

METHODS

Multiphoton microscopy tools for assessing autofluorescence and second harmonic generation (SHG) signals from biological tissues were used to evaluate the endovascular treatment of intracranial aneurysms in an animal model of aneurysms (pig, rabbit). Results from multiphoton microscopy were compared to those from standard histology, electronic and bright field microscopy.

CONCLUSIONS

The present study describes novel evaluation modes based on multiphoton microscopy for visualising tissue morphology (e.g., collagen, elastin, and cells) to qualify and quantify the extent of neo-intimal formation of covered arteries and device integration into the arterial wall using a rabbit model of intracranial aneurysms treated with FDS.

摘要

背景

在临床前研究中,传统组织学分析是研究动脉瘤和血管病变的金标准。在过去十年中,使用多光子显微镜的体内和体外成像已成为强大的临床前工具,可用于详细的组织分析,能够评估形态学、细胞外基质(ECM)、细胞密度和血管形成。多光子显微镜可实现更深的组织穿透,且光毒性较小。

目的

本研究旨在展示多模态成像(包括多光子显微镜)在实验性兔动脉瘤模型中对血流导向支架(FDS)治疗后新生内膜化和ECM演变进行详细分析的现状。

方法

使用用于评估生物组织自发荧光和二次谐波产生(SHG)信号的多光子显微镜工具,在动脉瘤动物模型(猪、兔)中评估颅内动脉瘤的血管内治疗。将多光子显微镜的结果与标准组织学、电子显微镜和明场显微镜的结果进行比较。

结论

本研究描述了基于多光子显微镜的新型评估模式,用于可视化组织形态(如胶原蛋白、弹性蛋白和细胞),以定性和定量使用FDS治疗的颅内动脉瘤兔模型中覆膜动脉新生内膜形成的程度以及装置与动脉壁的整合情况。

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