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Depth-targeted intracortical microstroke by two-photon photothrombosis in rodent brain

SIGNIFICANCE: Photothrombosis is a widely used model of ischemic stroke in rodent experiments. In the photothrombosis model, the photosensitizer rose bengal (RB) is systemically introduced into the blood stream and activated by green light to induce aggregation of platelets that eventually cause ves...

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Autores principales: Fukuda, Masahiro, Matsumura, Takayoshi, Suda, Toshio, Hirase, Hajime
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Photo-Optical Instrumentation Engineers 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8929553/
https://www.ncbi.nlm.nih.gov/pubmed/35311215
http://dx.doi.org/10.1117/1.NPh.9.2.021910
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author Fukuda, Masahiro
Matsumura, Takayoshi
Suda, Toshio
Hirase, Hajime
author_facet Fukuda, Masahiro
Matsumura, Takayoshi
Suda, Toshio
Hirase, Hajime
author_sort Fukuda, Masahiro
collection PubMed
description SIGNIFICANCE: Photothrombosis is a widely used model of ischemic stroke in rodent experiments. In the photothrombosis model, the photosensitizer rose bengal (RB) is systemically introduced into the blood stream and activated by green light to induce aggregation of platelets that eventually cause vessel occlusion. Since the activation of RB is a one-photon phenomenon and the molecules in the illuminated area (light path) are subject to excitation, targeting of thrombosis is unspecific, especially in the depth dimension. We developed a photothrombosis protocol that can target a single vessel in the cortical parenchyma by two-photon excitation. AIM: We aim to induce a thrombotic stroke in the cortical parenchyma by two-photon activation of RB to confine photothrombosis within a vessel of a target depth. APPROACH: FITC-dextran is injected into the blood stream to visualize the cerebral blood flow in anesthetized adult mice with a cranial window. After a target vessel is chosen by two-photon imaging (950 nm), RB is injected into the blood stream. The scanning wavelength is changed to 720 nm, and photothrombosis is induced by scanning the target vessel. RESULTS: Two-photon depth-targeted single-vessel photothrombosis was achieved with a success rate of [Formula: see text] and an irradiation duration of [Formula: see text]. Attempts without RB (i.e., only with FITC) did not result in photothrombosis at the excitation wavelength of 720 nm. CONCLUSIONS: We described a protocol that achieves depth-targeted single-vessel photothrombosis by two-photon excitation. Simultaneous imaging of blood flow in the targeted vessel using FITC dextran enabled the confirmation of vessel occlusion and prevention of excess irradiation that possibly induces unintended photodamage.
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spelling pubmed-89295532022-03-18 Depth-targeted intracortical microstroke by two-photon photothrombosis in rodent brain Fukuda, Masahiro Matsumura, Takayoshi Suda, Toshio Hirase, Hajime Neurophotonics Special Section on Imaging Neuroimmune, Neuroglial, and Neurovascular Interfaces (Part I) SIGNIFICANCE: Photothrombosis is a widely used model of ischemic stroke in rodent experiments. In the photothrombosis model, the photosensitizer rose bengal (RB) is systemically introduced into the blood stream and activated by green light to induce aggregation of platelets that eventually cause vessel occlusion. Since the activation of RB is a one-photon phenomenon and the molecules in the illuminated area (light path) are subject to excitation, targeting of thrombosis is unspecific, especially in the depth dimension. We developed a photothrombosis protocol that can target a single vessel in the cortical parenchyma by two-photon excitation. AIM: We aim to induce a thrombotic stroke in the cortical parenchyma by two-photon activation of RB to confine photothrombosis within a vessel of a target depth. APPROACH: FITC-dextran is injected into the blood stream to visualize the cerebral blood flow in anesthetized adult mice with a cranial window. After a target vessel is chosen by two-photon imaging (950 nm), RB is injected into the blood stream. The scanning wavelength is changed to 720 nm, and photothrombosis is induced by scanning the target vessel. RESULTS: Two-photon depth-targeted single-vessel photothrombosis was achieved with a success rate of [Formula: see text] and an irradiation duration of [Formula: see text]. Attempts without RB (i.e., only with FITC) did not result in photothrombosis at the excitation wavelength of 720 nm. CONCLUSIONS: We described a protocol that achieves depth-targeted single-vessel photothrombosis by two-photon excitation. Simultaneous imaging of blood flow in the targeted vessel using FITC dextran enabled the confirmation of vessel occlusion and prevention of excess irradiation that possibly induces unintended photodamage. Society of Photo-Optical Instrumentation Engineers 2022-03-16 2022-04 /pmc/articles/PMC8929553/ /pubmed/35311215 http://dx.doi.org/10.1117/1.NPh.9.2.021910 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/Published by SPIE under a Creative Commons Attribution 4.0 International License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI.
spellingShingle Special Section on Imaging Neuroimmune, Neuroglial, and Neurovascular Interfaces (Part I)
Fukuda, Masahiro
Matsumura, Takayoshi
Suda, Toshio
Hirase, Hajime
Depth-targeted intracortical microstroke by two-photon photothrombosis in rodent brain
title Depth-targeted intracortical microstroke by two-photon photothrombosis in rodent brain
title_full Depth-targeted intracortical microstroke by two-photon photothrombosis in rodent brain
title_fullStr Depth-targeted intracortical microstroke by two-photon photothrombosis in rodent brain
title_full_unstemmed Depth-targeted intracortical microstroke by two-photon photothrombosis in rodent brain
title_short Depth-targeted intracortical microstroke by two-photon photothrombosis in rodent brain
title_sort depth-targeted intracortical microstroke by two-photon photothrombosis in rodent brain
topic Special Section on Imaging Neuroimmune, Neuroglial, and Neurovascular Interfaces (Part I)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8929553/
https://www.ncbi.nlm.nih.gov/pubmed/35311215
http://dx.doi.org/10.1117/1.NPh.9.2.021910
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