Quantifying progression and regression of thrombotic risk in experimental atherosclerosis Article Swipe
Rohun U Palekar
,
Andrew Jallouk
,
Matthew Goette
,
Junjie Chen
,
Jacob W. Myerson
,
John S. Allen
,
Antonina Akk
,
Lihua Yang
,
Yizheng Tu
,
Mark J. Miller
,
Christine T. N. Pham
,
Samuel A. Wickline
,
Hua Pan
·
YOU?
·
· 2015
· Open Access
·
· DOI: https://doi.org/10.1096/fj.14-269084
YOU?
·
· 2015
· Open Access
·
· DOI: https://doi.org/10.1096/fj.14-269084
Currently, there are no generally applicable noninvasive methods for defining the relationship between atherosclerotic vascular damage and risk of focal thrombosis. Herein, we demonstrate methods to delineate the progression and regression of vascular damage in response to an atherogenic diet by quantifying the in vivo accumulation of semipermeable 200‐300 nm per‐fluorocarbon core nanoparticles (PFC‐NP) in ApoE null mouse plaques with [ 19 F] magnetic resonance spectroscopy (MRS). Permeability to PFC‐NP remained minimal until 12 weeks on diet, then increased rapidly following 12 weeks, but regressed to baseline within 8 weeks after diet normalization. Markedly accelerated clotting (53.3% decrease in clotting time) was observed in carotid artery preparations of fat‐fed mice subjected to photochemical injury as defined by the time to flow cessation. For all mice on and off diet, an inverse linear relationship was observed between the permeability to PFC‐NP and accelerated thrombosis ( P = 0.02). Translational feasibility for quantifying plaque permeability and vascular damage in vivo was demonstrated with clinical 3 T MRI of PFC‐NP accumulating in plaques of atherosclerotic rabbits. These observations suggest that excessive permeability to PFC‐NP may indicate prothrombotic risk in damaged atherosclerotic vasculature, which resolves within weeks after dietary therapy.—Palekar, R. U., Jallouk, A. P., Goette, M. J., Chen, J., Myerson, J. W., Allen, J. S., Akk, A., Yang, L., Tu, Y., Miller, M. J., Pham, C. T. N., Wickline, S. A., Pan, H. Quantifying progression and regression of thrombotic risk in experimental atherosclerosis. FASEB J . 29, 3100‐3109 (2015). www.fasebj.org
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Metadata
- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.1096/fj.14-269084
- OA Status
- green
- Cited By
- 15
- References
- 38
- Related Works
- 10
- OpenAlex ID
- https://openalex.org/W2063706136
All OpenAlex metadata
Raw OpenAlex JSON
- OpenAlex ID
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https://openalex.org/W2063706136Canonical identifier for this work in OpenAlex
- DOI
-
https://doi.org/10.1096/fj.14-269084Digital Object Identifier
- Title
-
Quantifying progression and regression of thrombotic risk in experimental atherosclerosisWork title
- Type
-
articleOpenAlex work type
- Language
-
enPrimary language
- Publication year
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2015Year of publication
- Publication date
-
2015-04-09Full publication date if available
- Authors
-
Rohun U Palekar, Andrew Jallouk, Matthew Goette, Junjie Chen, Jacob W. Myerson, John S. Allen, Antonina Akk, Lihua Yang, Yizheng Tu, Mark J. Miller, Christine T. N. Pham, Samuel A. Wickline, Hua PanList of authors in order
- Landing page
-
https://doi.org/10.1096/fj.14-269084Publisher landing page
- Open access
-
YesWhether a free full text is available
- OA status
-
greenOpen access status per OpenAlex
- OA URL
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https://www.ncbi.nlm.nih.gov/pmc/articles/4478795Direct OA link when available
- Concepts
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Fibrous cap, In vivo, Internal medicine, Vascular permeability, Thrombosis, Cardiology, Magnetic resonance imaging, Pathology, Medicine, Endocrinology, Chemistry, Biology, Radiology, BiotechnologyTop concepts (fields/topics) attached by OpenAlex
- Cited by
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15Total citation count in OpenAlex
- Citations by year (recent)
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2023: 2, 2022: 1, 2021: 1, 2020: 3, 2019: 1Per-year citation counts (last 5 years)
- References (count)
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38Number of works referenced by this work
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10Other works algorithmically related by OpenAlex
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