Cellular, Molecular and Biochemical Impacts of Silver Nanoparticles on Rat Cerebellar Cortex

Background: The excessive exposure to silver nanoparticles (Ag-NPs) has raised concerns about their possible risks to the human health. The brain is a highly vulnerable organ to nano-silver harmfulness. The aim of this work was to evaluate the impacts of Ag-NPs exposure on the cerebellar cortex of r...

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Main Authors: Eman M. Mohamed, Asmaa A. A. Kattaia, Rehab S. Abdul-Maksoud, Samia A. Abd El-Baset
Format: Article
Language:English
Published: MDPI AG 2020-12-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/10/1/7
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author Eman M. Mohamed
Asmaa A. A. Kattaia
Rehab S. Abdul-Maksoud
Samia A. Abd El-Baset
author_facet Eman M. Mohamed
Asmaa A. A. Kattaia
Rehab S. Abdul-Maksoud
Samia A. Abd El-Baset
author_sort Eman M. Mohamed
collection DOAJ
description Background: The excessive exposure to silver nanoparticles (Ag-NPs) has raised concerns about their possible risks to the human health. The brain is a highly vulnerable organ to nano-silver harmfulness. The aim of this work was to evaluate the impacts of Ag-NPs exposure on the cerebellar cortex of rats. Methods: Rats were assigned to: Control, vehicle control and Ag-NP-exposed groups (at doses of 10 mg and 30 mg/kg/day). Samples were processed for light and electron microscopy examinations. Immunohistochemical localization of c-Jun N-terminal kinase (JNK), nuclear factor kappa beta (NF-κB) and calbindin D28k (CB) proteins was performed. Analyses of expression of DNA damage inducible transcript 4 (<i>Ddit4</i>), flavin containing monooxygenase 2 (<i>FMO2</i>) and thioredoxin-interacting protein (<i>Txnip</i>) genes were done. Serum levels of inflammatory cytokines were also measured. Results: Ag-NPs enhanced apoptosis as evident by upregulation of <i>Ddit4</i> gene expressions and JNK protein immune expressions. Alterations of redox homeostasis were verified by enhancement of <i>Txnip</i> and <i>FMO2</i> gene expressions, favoring the activation of inflammatory responses by increasing NF-κB protein immune expressions and serum inflammatory mediator levels. Another cytotoxic effect was the reduction of immune expressions of the calcium regulator CB. Conclusion: Ag-NPs exposure provoked biochemical, cellular and molecular changes of rat cerebellar cortex in a dose-dependent manner.
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spelling doaj.art-9813445957d14e65ab7b4126756b66d02023-11-21T02:05:48ZengMDPI AGCells2073-44092020-12-01101710.3390/cells10010007Cellular, Molecular and Biochemical Impacts of Silver Nanoparticles on Rat Cerebellar CortexEman M. Mohamed0Asmaa A. A. Kattaia1Rehab S. Abdul-Maksoud2Samia A. Abd El-Baset3Department of Medical Histology and Cell Biology, Faculty of Human Medicine, Zagazig University, Zagazig 44519, EgyptDepartment of Medical Histology and Cell Biology, Faculty of Human Medicine, Zagazig University, Zagazig 44519, EgyptDepartment of Medical Biochemistry, Faculty of Human Medicine, Zagazig University, Zagazig 44519, EgyptDepartment of Medical Histology and Cell Biology, Faculty of Human Medicine, Zagazig University, Zagazig 44519, EgyptBackground: The excessive exposure to silver nanoparticles (Ag-NPs) has raised concerns about their possible risks to the human health. The brain is a highly vulnerable organ to nano-silver harmfulness. The aim of this work was to evaluate the impacts of Ag-NPs exposure on the cerebellar cortex of rats. Methods: Rats were assigned to: Control, vehicle control and Ag-NP-exposed groups (at doses of 10 mg and 30 mg/kg/day). Samples were processed for light and electron microscopy examinations. Immunohistochemical localization of c-Jun N-terminal kinase (JNK), nuclear factor kappa beta (NF-κB) and calbindin D28k (CB) proteins was performed. Analyses of expression of DNA damage inducible transcript 4 (<i>Ddit4</i>), flavin containing monooxygenase 2 (<i>FMO2</i>) and thioredoxin-interacting protein (<i>Txnip</i>) genes were done. Serum levels of inflammatory cytokines were also measured. Results: Ag-NPs enhanced apoptosis as evident by upregulation of <i>Ddit4</i> gene expressions and JNK protein immune expressions. Alterations of redox homeostasis were verified by enhancement of <i>Txnip</i> and <i>FMO2</i> gene expressions, favoring the activation of inflammatory responses by increasing NF-κB protein immune expressions and serum inflammatory mediator levels. Another cytotoxic effect was the reduction of immune expressions of the calcium regulator CB. Conclusion: Ag-NPs exposure provoked biochemical, cellular and molecular changes of rat cerebellar cortex in a dose-dependent manner.https://www.mdpi.com/2073-4409/10/1/7cerebellar corteximpactsratsilver nanoparticles
spellingShingle Eman M. Mohamed
Asmaa A. A. Kattaia
Rehab S. Abdul-Maksoud
Samia A. Abd El-Baset
Cellular, Molecular and Biochemical Impacts of Silver Nanoparticles on Rat Cerebellar Cortex
Cells
cerebellar cortex
impacts
rat
silver nanoparticles
title Cellular, Molecular and Biochemical Impacts of Silver Nanoparticles on Rat Cerebellar Cortex
title_full Cellular, Molecular and Biochemical Impacts of Silver Nanoparticles on Rat Cerebellar Cortex
title_fullStr Cellular, Molecular and Biochemical Impacts of Silver Nanoparticles on Rat Cerebellar Cortex
title_full_unstemmed Cellular, Molecular and Biochemical Impacts of Silver Nanoparticles on Rat Cerebellar Cortex
title_short Cellular, Molecular and Biochemical Impacts of Silver Nanoparticles on Rat Cerebellar Cortex
title_sort cellular molecular and biochemical impacts of silver nanoparticles on rat cerebellar cortex
topic cerebellar cortex
impacts
rat
silver nanoparticles
url https://www.mdpi.com/2073-4409/10/1/7
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