Document Type
Article
Publication Date
6-19-2023
Department
Department of Biomedical Engineering; Department of Materials Science and Engineering
Abstract
Platinum-containing stents are commonly used in humans with hypercholesterolemia, whereas preclinical stent evaluation has commonly been performed in healthy animal models, providing inadequate information about stent performance under hypercholesterolemic conditions. In this investigation, we used an ApoE−/− mouse model to test the impact of hypercholesterolemia on neointima formation on platinum-containing implants. We implanted 125 μm diameter platinum wires into the abdominal aortas of ApoE−/− and ApoE+/+ mice for 6 months, followed by histological and immunofluorescence examination of neointimal size and composition. It was found that ApoE−/− mice developed neointimas with four times larger area and ten times greater thickness than ApoE+/+ counterparts. Neointimas developed in the ApoE−/− mice also contained higher amounts of lipids quantified as having 370 times more coverage compared to ApoE+/+, a 3-fold increase in SMCs, and a 22-fold increase in macrophages. A confluent endothelium had regenerated in both mouse strains. The ApoE−/− mice experienced luminal reductions more closely resembling clinically relevant restenosis in humans. Overall, the response to platinum arterial implants was highly dependent upon the atherogenic environment.
Publication Title
Sci
Recommended Citation
Morath, L. M.,
Guillory II, R. J.,
Oliver, A. A.,
Liu, S. Q.,
Bocks, M. L.,
Levy, G. K.,
Drelich, J.,
&
Goldman, J.
(2023).
Conventional Platinum Metal Implants Provoke Restenosis Responses in Atherogenic but Not Healthy Arteries.
Sci,
5(2).
http://doi.org/10.3390/sci5020025
Retrieved from: https://digitalcommons.mtu.edu/michigantech-p/17341
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.
Version
Publisher's PDF
Included in
Biomedical Engineering and Bioengineering Commons, Materials Science and Engineering Commons
Publisher's Statement
Copyright: © 2023 by the authors. Licensee MDPI, Basel, Switzerland. Publisher’s version of record: https://doi.org/10.3390/sci5020025