Endothelial dysfunction induced by hydroxyl radicals - the hidden face of biodegradable Fe-based materials for coronary stents.
Animals
Aorta, Thoracic
/ drug effects
Biocompatible Materials
/ chemistry
Carbachol
/ pharmacology
Catalase
/ metabolism
Cattle
Corrosion
Endothelial Cells
/ cytology
Heme Oxygenase-1
/ metabolism
Hydroxyl Radical
/ metabolism
Iron
/ chemistry
Male
Nitric Oxide
/ metabolism
Nitric Oxide Synthase Type III
/ antagonists & inhibitors
Oxidative Stress
/ drug effects
Prostheses and Implants
Rats
Rats, Wistar
Stents
Biocorrosion
Coronary stent
Endothelial dysfunction
Nitric oxide
Oxidative stress
Reactive oxygen species
Journal
Materials science & engineering. C, Materials for biological applications
ISSN: 1873-0191
Titre abrégé: Mater Sci Eng C Mater Biol Appl
Pays: Netherlands
ID NLM: 101484109
Informations de publication
Date de publication:
Jul 2020
Jul 2020
Historique:
received:
27
05
2019
revised:
14
02
2020
accepted:
05
04
2020
entrez:
16
5
2020
pubmed:
16
5
2020
medline:
4
3
2021
Statut:
ppublish
Résumé
Fe-based materials are currently considered for manufacturing biodegradable coronary stents. Here we show that Fe has a strong potential to generate hydroxyl radicals (HO) during corrosion. This HO generation, but not corrosion, can be inhibited by catalase. Oxidative stress was observed (increased HO-1 expression) in aortic rings after direct exposure to Fe, but not in the presence of catalase or after indirect exposure. This oxidative stress response induced an uncoupling of eNOS in, and a consequent reduced NO production by endothelial cells exposed to Fe. In isolated rat aortic rings NO production was also reduced by HO generated during Fe corrosion, as indicated by the protective role of catalase. Finally, all these mechanisms contributed to impaired endothelium-dependent relaxation in aortic rings caused by HO generated during the direct contact with Fe. This deleterious impact of Fe corrosion on the endothelial function should be integrated when considering the use of biodegradable Fe-based alloys for vascular implants.
Identifiants
pubmed: 32409084
pii: S0928-4931(19)31946-0
doi: 10.1016/j.msec.2020.110938
pii:
doi:
Substances chimiques
Biocompatible Materials
0
Nitric Oxide
31C4KY9ESH
Hydroxyl Radical
3352-57-6
Carbachol
8Y164V895Y
Iron
E1UOL152H7
Catalase
EC 1.11.1.6
Nitric Oxide Synthase Type III
EC 1.14.13.39
Heme Oxygenase-1
EC 1.14.14.18
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
110938Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.