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The effect of titanium dioxide nanoparticles on mice midbrain substantia nigra
OBJECTIVE(S): Widely used Titanium dioxide nanoparticles (TiO(2)) enter into the body and cause various organ damages. Therefore, we aimed to study the effect of TiO(2) on the substantia nigra of midbrain. MATERIALS AND METHODS: 40 male BALB/c mice were randomly divided into five groups: three group...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Mashhad University of Medical Sciences
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196354/ https://www.ncbi.nlm.nih.gov/pubmed/32373295 http://dx.doi.org/10.22038/ijbms.2019.33611.8018 |
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author | Heidari, Zahra Mohammadipour, Abbas Haeri, Parisa Ebrahimzadeh-bideskan, Alireza |
author_facet | Heidari, Zahra Mohammadipour, Abbas Haeri, Parisa Ebrahimzadeh-bideskan, Alireza |
author_sort | Heidari, Zahra |
collection | PubMed |
description | OBJECTIVE(S): Widely used Titanium dioxide nanoparticles (TiO(2)) enter into the body and cause various organ damages. Therefore, we aimed to study the effect of TiO(2) on the substantia nigra of midbrain. MATERIALS AND METHODS: 40 male BALB/c mice were randomly divided into five groups: three groups received TiO(2) at doses of 10, 25, and 50 mg/kg, the fourth group received normal saline for 45 days by gavage, and control group (without intervention). Then, Motor tests including pole and hanging tests were done to investigate motor disorders. The animal brain was removed for histological purposes. Accordingly, immunohistochemistry was performed to detect tyrosine hydroxylase positive cells, and then toluidine blue staining was done to identify dark neurons in the substantia nigra. Eventually, the total number of these neurons were counted using stereological methods in different groups. RESULTS: The results showed that the time recorded for mice to turn completely downward on the pole in the TiO(2)-50 group increased and also the time recorded for animals to hang on the wire in the hanging test significantly decreased (P<0.05) in comparison with other groups. Also, the average number of tyrosine hydroxylase positive neurons in TiO(2)-25 and TiO(2)-50 groups significantly decreased as compared to the TiO(2)-10 and control groups (P<0.05). The total number of dark neurons in the TiO(2)-25 and TiO(2)-50 groups was substantially higher than the TiO(2)-10, control and normal saline groups (P<0.05). CONCLUSION: Our findings indicated that TiO(2), depending on dose, can cause the destruction of dopaminergic neurons and consequently increase the risk of Parkinson’s disease. |
format | Online Article Text |
id | pubmed-7196354 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-71963542020-05-05 The effect of titanium dioxide nanoparticles on mice midbrain substantia nigra Heidari, Zahra Mohammadipour, Abbas Haeri, Parisa Ebrahimzadeh-bideskan, Alireza Iran J Basic Med Sci Original Article OBJECTIVE(S): Widely used Titanium dioxide nanoparticles (TiO(2)) enter into the body and cause various organ damages. Therefore, we aimed to study the effect of TiO(2) on the substantia nigra of midbrain. MATERIALS AND METHODS: 40 male BALB/c mice were randomly divided into five groups: three groups received TiO(2) at doses of 10, 25, and 50 mg/kg, the fourth group received normal saline for 45 days by gavage, and control group (without intervention). Then, Motor tests including pole and hanging tests were done to investigate motor disorders. The animal brain was removed for histological purposes. Accordingly, immunohistochemistry was performed to detect tyrosine hydroxylase positive cells, and then toluidine blue staining was done to identify dark neurons in the substantia nigra. Eventually, the total number of these neurons were counted using stereological methods in different groups. RESULTS: The results showed that the time recorded for mice to turn completely downward on the pole in the TiO(2)-50 group increased and also the time recorded for animals to hang on the wire in the hanging test significantly decreased (P<0.05) in comparison with other groups. Also, the average number of tyrosine hydroxylase positive neurons in TiO(2)-25 and TiO(2)-50 groups significantly decreased as compared to the TiO(2)-10 and control groups (P<0.05). The total number of dark neurons in the TiO(2)-25 and TiO(2)-50 groups was substantially higher than the TiO(2)-10, control and normal saline groups (P<0.05). CONCLUSION: Our findings indicated that TiO(2), depending on dose, can cause the destruction of dopaminergic neurons and consequently increase the risk of Parkinson’s disease. Mashhad University of Medical Sciences 2019-07 /pmc/articles/PMC7196354/ /pubmed/32373295 http://dx.doi.org/10.22038/ijbms.2019.33611.8018 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Heidari, Zahra Mohammadipour, Abbas Haeri, Parisa Ebrahimzadeh-bideskan, Alireza The effect of titanium dioxide nanoparticles on mice midbrain substantia nigra |
title | The effect of titanium dioxide nanoparticles on mice midbrain substantia nigra |
title_full | The effect of titanium dioxide nanoparticles on mice midbrain substantia nigra |
title_fullStr | The effect of titanium dioxide nanoparticles on mice midbrain substantia nigra |
title_full_unstemmed | The effect of titanium dioxide nanoparticles on mice midbrain substantia nigra |
title_short | The effect of titanium dioxide nanoparticles on mice midbrain substantia nigra |
title_sort | effect of titanium dioxide nanoparticles on mice midbrain substantia nigra |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196354/ https://www.ncbi.nlm.nih.gov/pubmed/32373295 http://dx.doi.org/10.22038/ijbms.2019.33611.8018 |
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