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

Aneurysms Endovascular treatment Flow-Diverter Multiphoton microscopy Second harmonic generation Stenting

Journal

Journal of neuroradiology = Journal de neuroradiologie
ISSN: 0150-9861
Titre abrégé: J Neuroradiol
Pays: France
ID NLM: 7705086

Informations de publication

Date de publication:
May 2021
Historique:
received: 13 12 2019
revised: 09 03 2020
accepted: 10 03 2020
pubmed: 25 3 2020
medline: 26 11 2021
entrez: 25 3 2020
Statut: ppublish

Résumé

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. 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. 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. 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.

Sections du résumé

BACKGROUND 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 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 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 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.

Identifiants

pubmed: 32205257
pii: S0150-9861(20)30133-4
doi: 10.1016/j.neurad.2020.03.005
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

200-206

Informations de copyright

Copyright © 2020 Elsevier Masson SAS. All rights reserved.

Auteurs

Sylvia M Bardet (SM)

University of Limoges, 123, avenue Albert-Thomas, XLIM UMR CNRS 7252, 87060 Limoges, France. Electronic address: sylvia.bardetcoste@unilim.fr.

Jonathan Cortese (J)

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

Raphaël Blanc (R)

Department of Interventional Neuroradiology, Fondation Ophtalmologique Adolphe-de-Rothschild, Paris, France.

Charbel Mounayer (C)

University of Limoges, 123, avenue Albert-Thomas, XLIM UMR CNRS 7252, 87060 Limoges, France; University Hospital, Department of Interventional Neuroradiology, Limoges, France.

Aymeric Rouchaud (A)

University of Limoges, 123, avenue Albert-Thomas, XLIM UMR CNRS 7252, 87060 Limoges, France; University Hospital, Department of Interventional Neuroradiology, Limoges, France. Electronic address: aymeric.rouchaud@unilim.fr.

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Classifications MeSH