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Protective effect of isoliquiritigenin in amiodarone‐induced damage of human umbilical vein endothelial cells

OBJECTIVE: Amiodarone (AM) is a drug commonly used in patients with ventricular arrhythmias. It can damage vascular endothelial cells and easily cause phlebitis. At present, the prevention and treatment of phlebitis induced by the use of AM is not clear due to the lack of corresponding primary resea...

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Autores principales: Guo, Jin‐Li, Han, Xiang, Yan, Xian‐Yan, Wang, Juan‐Juan, Chang, Ya‐Qiong, Zhang, Bei‐Lei, Guo, Xiu‐Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10683558/
https://www.ncbi.nlm.nih.gov/pubmed/38018585
http://dx.doi.org/10.1002/iid3.1094
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author Guo, Jin‐Li
Han, Xiang
Yan, Xian‐Yan
Wang, Juan‐Juan
Chang, Ya‐Qiong
Zhang, Bei‐Lei
Guo, Xiu‐Juan
author_facet Guo, Jin‐Li
Han, Xiang
Yan, Xian‐Yan
Wang, Juan‐Juan
Chang, Ya‐Qiong
Zhang, Bei‐Lei
Guo, Xiu‐Juan
author_sort Guo, Jin‐Li
collection PubMed
description OBJECTIVE: Amiodarone (AM) is a drug commonly used in patients with ventricular arrhythmias. It can damage vascular endothelial cells and easily cause phlebitis. At present, the prevention and treatment of phlebitis induced by the use of AM is not clear due to the lack of corresponding primary research. Isoliquiritigenin (ISL) has an anti‐inflammatory effect, but until now, has not been explored much in the field of research in primary care nursing. The purpose of this study is to investigate the efficacy and mechanism of action of ISL in treating phlebitis induced by AM. METHODS: In our study, we used human umbilical vein endothelial cells (HUVECs) that were divided into three groups: the NC group (normal), the AM group (AM 30 μmol/L for 24 h), and the ISL pretreatment group (isoliquiritigenin 10 μmol/L after 1 h of pretreatment with amiodarone for 24 h). We used CCK‐8 to detect cell proliferation, cell scratch assay to detect the migration capability of cells, flow cytometry to measure apoptosis, angiogenesis assay to check the total length and total branches of angiogenesis, and PCR and WB to detect the expression of PCNA, casepase‐3, and VEGFA. WB was used to detect NF‐κBp65 and p‐NF‐κBp65 expression. RESULTS: Compared with the AM group, the ISL pretreatment promoted cell proliferation and migration, inhibited cell apoptosis, increased the total length and total branches of angiogenesis, and downregulated p‐NF‐κBp65 expression. CONCLUSION: ISL shows promise in the prevention and treatment of clinical phlebitis and can be used as a potential therapeutic drug to prevent phlebitis.
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spelling pubmed-106835582023-11-30 Protective effect of isoliquiritigenin in amiodarone‐induced damage of human umbilical vein endothelial cells Guo, Jin‐Li Han, Xiang Yan, Xian‐Yan Wang, Juan‐Juan Chang, Ya‐Qiong Zhang, Bei‐Lei Guo, Xiu‐Juan Immun Inflamm Dis Original Articles OBJECTIVE: Amiodarone (AM) is a drug commonly used in patients with ventricular arrhythmias. It can damage vascular endothelial cells and easily cause phlebitis. At present, the prevention and treatment of phlebitis induced by the use of AM is not clear due to the lack of corresponding primary research. Isoliquiritigenin (ISL) has an anti‐inflammatory effect, but until now, has not been explored much in the field of research in primary care nursing. The purpose of this study is to investigate the efficacy and mechanism of action of ISL in treating phlebitis induced by AM. METHODS: In our study, we used human umbilical vein endothelial cells (HUVECs) that were divided into three groups: the NC group (normal), the AM group (AM 30 μmol/L for 24 h), and the ISL pretreatment group (isoliquiritigenin 10 μmol/L after 1 h of pretreatment with amiodarone for 24 h). We used CCK‐8 to detect cell proliferation, cell scratch assay to detect the migration capability of cells, flow cytometry to measure apoptosis, angiogenesis assay to check the total length and total branches of angiogenesis, and PCR and WB to detect the expression of PCNA, casepase‐3, and VEGFA. WB was used to detect NF‐κBp65 and p‐NF‐κBp65 expression. RESULTS: Compared with the AM group, the ISL pretreatment promoted cell proliferation and migration, inhibited cell apoptosis, increased the total length and total branches of angiogenesis, and downregulated p‐NF‐κBp65 expression. CONCLUSION: ISL shows promise in the prevention and treatment of clinical phlebitis and can be used as a potential therapeutic drug to prevent phlebitis. John Wiley and Sons Inc. 2023-11-28 /pmc/articles/PMC10683558/ /pubmed/38018585 http://dx.doi.org/10.1002/iid3.1094 Text en © 2023 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Guo, Jin‐Li
Han, Xiang
Yan, Xian‐Yan
Wang, Juan‐Juan
Chang, Ya‐Qiong
Zhang, Bei‐Lei
Guo, Xiu‐Juan
Protective effect of isoliquiritigenin in amiodarone‐induced damage of human umbilical vein endothelial cells
title Protective effect of isoliquiritigenin in amiodarone‐induced damage of human umbilical vein endothelial cells
title_full Protective effect of isoliquiritigenin in amiodarone‐induced damage of human umbilical vein endothelial cells
title_fullStr Protective effect of isoliquiritigenin in amiodarone‐induced damage of human umbilical vein endothelial cells
title_full_unstemmed Protective effect of isoliquiritigenin in amiodarone‐induced damage of human umbilical vein endothelial cells
title_short Protective effect of isoliquiritigenin in amiodarone‐induced damage of human umbilical vein endothelial cells
title_sort protective effect of isoliquiritigenin in amiodarone‐induced damage of human umbilical vein endothelial cells
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10683558/
https://www.ncbi.nlm.nih.gov/pubmed/38018585
http://dx.doi.org/10.1002/iid3.1094
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