Ameliorative Effect of Sodium Selenite on Silver Nanoparticles-Induced Myocardiocyte Structural Alterations in Rats.


Journal

International journal of nanomedicine
ISSN: 1178-2013
Titre abrégé: Int J Nanomedicine
Pays: New Zealand
ID NLM: 101263847

Informations de publication

Date de publication:
2020
Historique:
received: 09 07 2020
accepted: 11 09 2020
entrez: 5 11 2020
pubmed: 6 11 2020
medline: 15 12 2020
Statut: epublish

Résumé

The application of silver nanoparticles (AgNPs) is growing exponentially, and its potential damage to the cardiac remains to be elucidated. The purpose of this study was to investigate the ameliorative effect of sodium selenite on silver nanoparticles-induced myocardiocyte structural alterations in rats. Forty male Sprague-Dawley (SD) rats were randomly divided into four groups: control group, AgNPs group, Se control group, and AgNPs + Se group. SD rats were administered AgNPs through a single intratracheal instillation, and sodium selenite was given by intraperitoneal injection for seven days. Cardiac function was determined by echocardiography and hemodynamic, ultrastructural changes by transmission electron microscopy examination. Mitochondrial fission and autophagy markers were measured by Western blotting. AgNPs caused a significant decrease in cardiac contraction, diastolic dysfunction, fragmentation, and lysis of the myofibrils, the formation of stenosis in the capillary, damaging the mitochondria membrane and cristae. AgNPs significantly increased mitochondrial fission markers dynamin-related protein 1 (Drp1), phospho-Drp1 (p-Drp1), and mitochondrial fission protein 1 (Fis1), as well as autophagy marker LC3 II/I ( We conclude that the protection of sodium selenite against silver nanoparticles-induced myocardiocyte structural alterations is associated with stabilizing mitochondrial dynamic balance and mitophagy.

Sections du résumé

BACKGROUND BACKGROUND
The application of silver nanoparticles (AgNPs) is growing exponentially, and its potential damage to the cardiac remains to be elucidated. The purpose of this study was to investigate the ameliorative effect of sodium selenite on silver nanoparticles-induced myocardiocyte structural alterations in rats.
MATERIALS AND METHODS METHODS
Forty male Sprague-Dawley (SD) rats were randomly divided into four groups: control group, AgNPs group, Se control group, and AgNPs + Se group. SD rats were administered AgNPs through a single intratracheal instillation, and sodium selenite was given by intraperitoneal injection for seven days. Cardiac function was determined by echocardiography and hemodynamic, ultrastructural changes by transmission electron microscopy examination. Mitochondrial fission and autophagy markers were measured by Western blotting.
RESULTS RESULTS
AgNPs caused a significant decrease in cardiac contraction, diastolic dysfunction, fragmentation, and lysis of the myofibrils, the formation of stenosis in the capillary, damaging the mitochondria membrane and cristae. AgNPs significantly increased mitochondrial fission markers dynamin-related protein 1 (Drp1), phospho-Drp1 (p-Drp1), and mitochondrial fission protein 1 (Fis1), as well as autophagy marker LC3 II/I (
CONCLUSION CONCLUSIONS
We conclude that the protection of sodium selenite against silver nanoparticles-induced myocardiocyte structural alterations is associated with stabilizing mitochondrial dynamic balance and mitophagy.

Identifiants

pubmed: 33149575
doi: 10.2147/IJN.S271457
pii: 271457
pmc: PMC7603418
doi:

Substances chimiques

Cardiotonic Agents 0
Fis1 protein, rat 0
Mitochondrial Proteins 0
Silver 3M4G523W1G
Dnm1l protein, rat EC 3.6.5.5
Dynamins EC 3.6.5.5
Sodium Selenite HIW548RQ3W

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

8281-8292

Informations de copyright

© 2020 Ma et al.

Déclaration de conflit d'intérêts

The authors report no conflicts of interest in this work.

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Auteurs

Wanrui Ma (W)

Department of General Medicine, General Hospital of Ningxia Medical University, Yinchuan, Ningxia, People's Republic of China.
Department of Pharmaceutical Sciences, Biomanufacturing Research Institute and Technological Enterprise (BRITE), North Carolina Central University, Durham, NC, USA.

Shan He (S)

Ningxia Medical University, Yinchuan, Ningxia, People's Republic of China.

Yanping Xu (Y)

Unit of Echocardiography, Division of Functional Examination in Heart Center, General Hospital of Ningxia Medical University, Yinchuan, Ningxia, People's Republic of China.

Guoxue Qi (G)

Ningxia Medical University, Yinchuan, Ningxia, People's Republic of China.

Huiyan Ma (H)

Ningxia Medical University, Yinchuan, Ningxia, People's Republic of China.

John J Bang (JJ)

Department of Environmental, Earth and Geospatial Sciences, North Carolina Central University, Durham, NC, USA.

P Andy Li (PA)

Department of Pharmaceutical Sciences, Biomanufacturing Research Institute and Technological Enterprise (BRITE), North Carolina Central University, Durham, NC, USA.

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Classifications MeSH