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Focal induction of ROS-release to trigger local vascular degeneration

Reactive oxygen species (ROS) play an important role in the process of cardiovascular degeneration. We evaluated the potential of a controlled, local induction of ROS-release by application of rose bengal (RB) and photo energy to induce atherosclerosis-like focal vascular degeneration in vivo. After...

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Autores principales: Minol, Jan-Philipp, Reinsch, Isabella, Luik, Maximilian, Leferink, Anne, Barth, Mareike, Assmann, Alexander, Lichtenberg, Artur, Akhyari, Payam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470706/
https://www.ncbi.nlm.nih.gov/pubmed/28614411
http://dx.doi.org/10.1371/journal.pone.0179342
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author Minol, Jan-Philipp
Reinsch, Isabella
Luik, Maximilian
Leferink, Anne
Barth, Mareike
Assmann, Alexander
Lichtenberg, Artur
Akhyari, Payam
author_facet Minol, Jan-Philipp
Reinsch, Isabella
Luik, Maximilian
Leferink, Anne
Barth, Mareike
Assmann, Alexander
Lichtenberg, Artur
Akhyari, Payam
author_sort Minol, Jan-Philipp
collection PubMed
description Reactive oxygen species (ROS) play an important role in the process of cardiovascular degeneration. We evaluated the potential of a controlled, local induction of ROS-release by application of rose bengal (RB) and photo energy to induce atherosclerosis-like focal vascular degeneration in vivo. After injection of RB, rats fed with a pro-degenerative diet underwent focal irradiation of the abdominal aorta by a green laser (ROS group), while the controls received irradiation without RB. Aortic tissue was analyzed by histology and immunohistochemistry at 0, 2, 4, 8, 28 and 56 days (n = 5). The intimal surface topography was analyzed by scanning electron microscopy. In the ROS group, an initial thrombus formation had disappeared by day 8. Similarly, ROS-derived products displayed the highest concentrations at day 0. Relative matrix metalloproteinase (MMP) activity achieved a maximum after 8 days (ROS group vs. control group: 1.60 ± 0.11 vs. 0.98 ± 0.01; p < 0.001). After 28 days, no significant differences in any aspect were found between the ROS group and the controls. However, after 56 days, the aortic tissue of ROS animals exhibited relative media-pronounced thickening (ROS vs. control: 2.15 ± 0.19 vs. 0.87 ± 0.10; p < 0.001) with focal calcification and reduced expression of alpha smooth muscle actin (aSMA). The ROS-releasing application of RB and photo energy allowed for the induction of vascular degeneration in a rodent model. This protocol may be used for the focal induction of vascular disease without systemic side effects and can thereby elucidate the role of ROS in the multifactorial processes of vessel degeneration and atherogenesis.
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spelling pubmed-54707062017-07-03 Focal induction of ROS-release to trigger local vascular degeneration Minol, Jan-Philipp Reinsch, Isabella Luik, Maximilian Leferink, Anne Barth, Mareike Assmann, Alexander Lichtenberg, Artur Akhyari, Payam PLoS One Research Article Reactive oxygen species (ROS) play an important role in the process of cardiovascular degeneration. We evaluated the potential of a controlled, local induction of ROS-release by application of rose bengal (RB) and photo energy to induce atherosclerosis-like focal vascular degeneration in vivo. After injection of RB, rats fed with a pro-degenerative diet underwent focal irradiation of the abdominal aorta by a green laser (ROS group), while the controls received irradiation without RB. Aortic tissue was analyzed by histology and immunohistochemistry at 0, 2, 4, 8, 28 and 56 days (n = 5). The intimal surface topography was analyzed by scanning electron microscopy. In the ROS group, an initial thrombus formation had disappeared by day 8. Similarly, ROS-derived products displayed the highest concentrations at day 0. Relative matrix metalloproteinase (MMP) activity achieved a maximum after 8 days (ROS group vs. control group: 1.60 ± 0.11 vs. 0.98 ± 0.01; p < 0.001). After 28 days, no significant differences in any aspect were found between the ROS group and the controls. However, after 56 days, the aortic tissue of ROS animals exhibited relative media-pronounced thickening (ROS vs. control: 2.15 ± 0.19 vs. 0.87 ± 0.10; p < 0.001) with focal calcification and reduced expression of alpha smooth muscle actin (aSMA). The ROS-releasing application of RB and photo energy allowed for the induction of vascular degeneration in a rodent model. This protocol may be used for the focal induction of vascular disease without systemic side effects and can thereby elucidate the role of ROS in the multifactorial processes of vessel degeneration and atherogenesis. Public Library of Science 2017-06-14 /pmc/articles/PMC5470706/ /pubmed/28614411 http://dx.doi.org/10.1371/journal.pone.0179342 Text en © 2017 Minol et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Minol, Jan-Philipp
Reinsch, Isabella
Luik, Maximilian
Leferink, Anne
Barth, Mareike
Assmann, Alexander
Lichtenberg, Artur
Akhyari, Payam
Focal induction of ROS-release to trigger local vascular degeneration
title Focal induction of ROS-release to trigger local vascular degeneration
title_full Focal induction of ROS-release to trigger local vascular degeneration
title_fullStr Focal induction of ROS-release to trigger local vascular degeneration
title_full_unstemmed Focal induction of ROS-release to trigger local vascular degeneration
title_short Focal induction of ROS-release to trigger local vascular degeneration
title_sort focal induction of ros-release to trigger local vascular degeneration
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470706/
https://www.ncbi.nlm.nih.gov/pubmed/28614411
http://dx.doi.org/10.1371/journal.pone.0179342
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