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In vitro study on the feasibility of magnetic stent hyperthermia for the treatment of cardiovascular restenosis

Thermal treatment or hyperthermia has received considerable attention in recent years due to its high efficiency, safety and relatively few side-effects. In this study, we investigated whether it was possible to utilize targeted thermal or instent thermal treatments for the treatment of restenosis f...

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Autores principales: LI, LI, WANG, RUI, SHI, HUAN-HUAN, XIE, LE, LI, JING-DING-SHA, KONG, WEI-CHAO, TANG, JIN-TIAN, KE, DA-NIAN, ZHAO, LING-YUN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3786833/
https://www.ncbi.nlm.nih.gov/pubmed/24137187
http://dx.doi.org/10.3892/etm.2013.1177
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author LI, LI
WANG, RUI
SHI, HUAN-HUAN
XIE, LE
LI, JING-DING-SHA
KONG, WEI-CHAO
TANG, JIN-TIAN
KE, DA-NIAN
ZHAO, LING-YUN
author_facet LI, LI
WANG, RUI
SHI, HUAN-HUAN
XIE, LE
LI, JING-DING-SHA
KONG, WEI-CHAO
TANG, JIN-TIAN
KE, DA-NIAN
ZHAO, LING-YUN
author_sort LI, LI
collection PubMed
description Thermal treatment or hyperthermia has received considerable attention in recent years due to its high efficiency, safety and relatively few side-effects. In this study, we investigated whether it was possible to utilize targeted thermal or instent thermal treatments for the treatment of restenosis following percutaneous transluminal coronary angioplasty (PTCA) through magnetic stent hyperthermia (MSH). A 316L stainless steel stent and rabbit vascular smooth muscle cells (VSMCs) were used in the present study, in which the inductive heating characteristics of the stent under alternative magnetic field (AMF) exposure, as well as the effect of MSH on the proliferation, apoptosis, cell cycle and proliferating cell nuclear antigen (PCNA) expression of the rabbit VSMCs, were evaluated. The results demonstrated that 316L stainless steel coronary stents possess ideal inductive heating characteristics under 300 kHz AMF exposure. The heating properties were shown to be affected by the field intensity of the AMF, as well as the orientation the stent axis. MSH had a significant effect on the proliferation and apoptosis of VSMCs, and the effect was temperature-dependent. While a mild temperature of 43°C demonstrated negligible effects on the growth of VSMCs, MSH treatment above 47°C effectively inhibited the VSMC proliferation and induced apoptosis. Furthermore, a 47°C treatment exhibited a significant and long-term inhibitory effect on VSMC migration. The results strongly suggested that MSH may be potentially applied in the clinic as an alternative approach for the prevention and treatment of restenosis.
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spelling pubmed-37868332013-10-17 In vitro study on the feasibility of magnetic stent hyperthermia for the treatment of cardiovascular restenosis LI, LI WANG, RUI SHI, HUAN-HUAN XIE, LE LI, JING-DING-SHA KONG, WEI-CHAO TANG, JIN-TIAN KE, DA-NIAN ZHAO, LING-YUN Exp Ther Med Articles Thermal treatment or hyperthermia has received considerable attention in recent years due to its high efficiency, safety and relatively few side-effects. In this study, we investigated whether it was possible to utilize targeted thermal or instent thermal treatments for the treatment of restenosis following percutaneous transluminal coronary angioplasty (PTCA) through magnetic stent hyperthermia (MSH). A 316L stainless steel stent and rabbit vascular smooth muscle cells (VSMCs) were used in the present study, in which the inductive heating characteristics of the stent under alternative magnetic field (AMF) exposure, as well as the effect of MSH on the proliferation, apoptosis, cell cycle and proliferating cell nuclear antigen (PCNA) expression of the rabbit VSMCs, were evaluated. The results demonstrated that 316L stainless steel coronary stents possess ideal inductive heating characteristics under 300 kHz AMF exposure. The heating properties were shown to be affected by the field intensity of the AMF, as well as the orientation the stent axis. MSH had a significant effect on the proliferation and apoptosis of VSMCs, and the effect was temperature-dependent. While a mild temperature of 43°C demonstrated negligible effects on the growth of VSMCs, MSH treatment above 47°C effectively inhibited the VSMC proliferation and induced apoptosis. Furthermore, a 47°C treatment exhibited a significant and long-term inhibitory effect on VSMC migration. The results strongly suggested that MSH may be potentially applied in the clinic as an alternative approach for the prevention and treatment of restenosis. D.A. Spandidos 2013-08 2013-06-21 /pmc/articles/PMC3786833/ /pubmed/24137187 http://dx.doi.org/10.3892/etm.2013.1177 Text en Copyright © 2013, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
LI, LI
WANG, RUI
SHI, HUAN-HUAN
XIE, LE
LI, JING-DING-SHA
KONG, WEI-CHAO
TANG, JIN-TIAN
KE, DA-NIAN
ZHAO, LING-YUN
In vitro study on the feasibility of magnetic stent hyperthermia for the treatment of cardiovascular restenosis
title In vitro study on the feasibility of magnetic stent hyperthermia for the treatment of cardiovascular restenosis
title_full In vitro study on the feasibility of magnetic stent hyperthermia for the treatment of cardiovascular restenosis
title_fullStr In vitro study on the feasibility of magnetic stent hyperthermia for the treatment of cardiovascular restenosis
title_full_unstemmed In vitro study on the feasibility of magnetic stent hyperthermia for the treatment of cardiovascular restenosis
title_short In vitro study on the feasibility of magnetic stent hyperthermia for the treatment of cardiovascular restenosis
title_sort in vitro study on the feasibility of magnetic stent hyperthermia for the treatment of cardiovascular restenosis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3786833/
https://www.ncbi.nlm.nih.gov/pubmed/24137187
http://dx.doi.org/10.3892/etm.2013.1177
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