Cargando…

Effects of a Matrix Metalloproteinase Inhibitor-Eluting Stent on In-Stent Restenosis

BACKGROUND: The aim of this study was to compare changes in the extracellular matrix after implantation of a stent that elutes a matrix metalloproteinase (MMP) inhibitor (GM6001); and to determine the effects of the GM6001-eluting stent upon prevention of in-stent restenosis (ISR). MATERIAL/METHODS:...

Descripción completa

Detalles Bibliográficos
Autores principales: Song, Jian-bo, Shen, Jing, Fan, Jun, Zhang, Zhe, Yi, Zheng-jia, Bai, Shuo, Mu, Xiao-lin, Xiao, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119448/
https://www.ncbi.nlm.nih.gov/pubmed/32214058
http://dx.doi.org/10.12659/MSM.922556
_version_ 1783514768676487168
author Song, Jian-bo
Shen, Jing
Fan, Jun
Zhang, Zhe
Yi, Zheng-jia
Bai, Shuo
Mu, Xiao-lin
Xiao, Liang
author_facet Song, Jian-bo
Shen, Jing
Fan, Jun
Zhang, Zhe
Yi, Zheng-jia
Bai, Shuo
Mu, Xiao-lin
Xiao, Liang
author_sort Song, Jian-bo
collection PubMed
description BACKGROUND: The aim of this study was to compare changes in the extracellular matrix after implantation of a stent that elutes a matrix metalloproteinase (MMP) inhibitor (GM6001); and to determine the effects of the GM6001-eluting stent upon prevention of in-stent restenosis (ISR). MATERIAL/METHODS: We included 48 Guangxi Bama mini-pigs in this study. A GM6001-eluting stent was placed in one iliac artery and a stent that did not elute GM6001 was placed in the contralateral iliac artery. The iliac arteries were removed at 6 hours as well as 1, 7, 14, 56, 84, and 336 days after stent placement. Arteries were analyzed for morphometry, gelatinase content, different phenotypes of vascular smooth muscle cells (VSMCs), collagen content, apoptotic rate, and cell density. RESULTS: The vascular lumen areas of the GM6001 group were significantly increased and the neointimal areas were significantly reduced compared with the control group from the 7 days to the 336 days. In the 2 groups, expression of MMP-2 and MMP-9 peaked simultaneously, but GM6001-eluting stents inhibited expression of MMP-2 and MMP-9 in the vascular media and neointima (especially around the struts) significantly. In the GM6001 group, expression of tissue inhibitor of matrix metalloproteinase (TIMP)-1, TIMP-2, myosin heavy chain 10 (MYH-10, marker of the proliferative phenotype of VSMCs), collagen content, percentage of apoptotic cells, and cell density were also decreased significantly compared with those in the control group. CONCLUSION: Use of GM6001-eluting stents resulted in persistent and potent inhibition of intimal hyperplasia, an increase in luminal area, and no obvious thrombosis in the arteries of the mini-pigs.
format Online
Article
Text
id pubmed-7119448
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher International Scientific Literature, Inc.
record_format MEDLINE/PubMed
spelling pubmed-71194482020-04-21 Effects of a Matrix Metalloproteinase Inhibitor-Eluting Stent on In-Stent Restenosis Song, Jian-bo Shen, Jing Fan, Jun Zhang, Zhe Yi, Zheng-jia Bai, Shuo Mu, Xiao-lin Xiao, Liang Med Sci Monit Animal Study BACKGROUND: The aim of this study was to compare changes in the extracellular matrix after implantation of a stent that elutes a matrix metalloproteinase (MMP) inhibitor (GM6001); and to determine the effects of the GM6001-eluting stent upon prevention of in-stent restenosis (ISR). MATERIAL/METHODS: We included 48 Guangxi Bama mini-pigs in this study. A GM6001-eluting stent was placed in one iliac artery and a stent that did not elute GM6001 was placed in the contralateral iliac artery. The iliac arteries were removed at 6 hours as well as 1, 7, 14, 56, 84, and 336 days after stent placement. Arteries were analyzed for morphometry, gelatinase content, different phenotypes of vascular smooth muscle cells (VSMCs), collagen content, apoptotic rate, and cell density. RESULTS: The vascular lumen areas of the GM6001 group were significantly increased and the neointimal areas were significantly reduced compared with the control group from the 7 days to the 336 days. In the 2 groups, expression of MMP-2 and MMP-9 peaked simultaneously, but GM6001-eluting stents inhibited expression of MMP-2 and MMP-9 in the vascular media and neointima (especially around the struts) significantly. In the GM6001 group, expression of tissue inhibitor of matrix metalloproteinase (TIMP)-1, TIMP-2, myosin heavy chain 10 (MYH-10, marker of the proliferative phenotype of VSMCs), collagen content, percentage of apoptotic cells, and cell density were also decreased significantly compared with those in the control group. CONCLUSION: Use of GM6001-eluting stents resulted in persistent and potent inhibition of intimal hyperplasia, an increase in luminal area, and no obvious thrombosis in the arteries of the mini-pigs. International Scientific Literature, Inc. 2020-03-26 /pmc/articles/PMC7119448/ /pubmed/32214058 http://dx.doi.org/10.12659/MSM.922556 Text en © Med Sci Monit, 2020 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Animal Study
Song, Jian-bo
Shen, Jing
Fan, Jun
Zhang, Zhe
Yi, Zheng-jia
Bai, Shuo
Mu, Xiao-lin
Xiao, Liang
Effects of a Matrix Metalloproteinase Inhibitor-Eluting Stent on In-Stent Restenosis
title Effects of a Matrix Metalloproteinase Inhibitor-Eluting Stent on In-Stent Restenosis
title_full Effects of a Matrix Metalloproteinase Inhibitor-Eluting Stent on In-Stent Restenosis
title_fullStr Effects of a Matrix Metalloproteinase Inhibitor-Eluting Stent on In-Stent Restenosis
title_full_unstemmed Effects of a Matrix Metalloproteinase Inhibitor-Eluting Stent on In-Stent Restenosis
title_short Effects of a Matrix Metalloproteinase Inhibitor-Eluting Stent on In-Stent Restenosis
title_sort effects of a matrix metalloproteinase inhibitor-eluting stent on in-stent restenosis
topic Animal Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119448/
https://www.ncbi.nlm.nih.gov/pubmed/32214058
http://dx.doi.org/10.12659/MSM.922556
work_keys_str_mv AT songjianbo effectsofamatrixmetalloproteinaseinhibitorelutingstentoninstentrestenosis
AT shenjing effectsofamatrixmetalloproteinaseinhibitorelutingstentoninstentrestenosis
AT fanjun effectsofamatrixmetalloproteinaseinhibitorelutingstentoninstentrestenosis
AT zhangzhe effectsofamatrixmetalloproteinaseinhibitorelutingstentoninstentrestenosis
AT yizhengjia effectsofamatrixmetalloproteinaseinhibitorelutingstentoninstentrestenosis
AT baishuo effectsofamatrixmetalloproteinaseinhibitorelutingstentoninstentrestenosis
AT muxiaolin effectsofamatrixmetalloproteinaseinhibitorelutingstentoninstentrestenosis
AT xiaoliang effectsofamatrixmetalloproteinaseinhibitorelutingstentoninstentrestenosis