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The effect of lead, restraint stress or their co-exposure on the movement disorders incidence in male mice
Lead is known as an environmental contaminant with neurotoxic properties. In addition, people experience different types of chronic stress, especially in developing countries. It has been established that lead or stress causes structural and physiological damages to the neural pathway like dopaminer...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6714115/ https://www.ncbi.nlm.nih.gov/pubmed/31516511 http://dx.doi.org/10.4103/1735-5362.263558 |
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author | Hosseini-Sharifabad, Ali Naghibzadeh, Sara Hajhashemi, Valiollah |
author_facet | Hosseini-Sharifabad, Ali Naghibzadeh, Sara Hajhashemi, Valiollah |
author_sort | Hosseini-Sharifabad, Ali |
collection | PubMed |
description | Lead is known as an environmental contaminant with neurotoxic properties. In addition, people experience different types of chronic stress, especially in developing countries. It has been established that lead or stress causes structural and physiological damages to the neural pathway like dopaminergic connections. Nevertheless, the effect of lead and restraint stress on movement behaviors when are experienced together has not been studied yet. In this study, male albino mice were randomly divided into different groups (n = 6). Lead acetate was daily injected at 15 mg/kg intraperitoneally for 2, 4, or 6 weeks. Restraint stress (6 h in a day) was applied alone or in combination with lead acetate for 2, 4, or 6 weeks. The catalepsy, akinesia, and the balance of animals were measured by bar test, elevated beam device, and rotarod to evaluate the movement disorders. 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine, a known neurotoxin causes movement disorders, was used as positive control group. The results showed that exposure to the lead or stress or their combination for 6 weeks caused catalepsy, akinesia, and imbalance in the animals, while exposure for 2 or 4 weeks didn’t affect the movement items indices. The combination of lead and stress did not show any significant difference compared to the exposure to each of them individually. From the findings, Lead, stress, and their combination caused movement disorders in a time dependent manner. Short time exposure did not change movement behavior. The co-exposure to the lead and stress did not show additive or synergistic effects. |
format | Online Article Text |
id | pubmed-6714115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-67141152019-09-12 The effect of lead, restraint stress or their co-exposure on the movement disorders incidence in male mice Hosseini-Sharifabad, Ali Naghibzadeh, Sara Hajhashemi, Valiollah Res Pharm Sci Original Article Lead is known as an environmental contaminant with neurotoxic properties. In addition, people experience different types of chronic stress, especially in developing countries. It has been established that lead or stress causes structural and physiological damages to the neural pathway like dopaminergic connections. Nevertheless, the effect of lead and restraint stress on movement behaviors when are experienced together has not been studied yet. In this study, male albino mice were randomly divided into different groups (n = 6). Lead acetate was daily injected at 15 mg/kg intraperitoneally for 2, 4, or 6 weeks. Restraint stress (6 h in a day) was applied alone or in combination with lead acetate for 2, 4, or 6 weeks. The catalepsy, akinesia, and the balance of animals were measured by bar test, elevated beam device, and rotarod to evaluate the movement disorders. 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine, a known neurotoxin causes movement disorders, was used as positive control group. The results showed that exposure to the lead or stress or their combination for 6 weeks caused catalepsy, akinesia, and imbalance in the animals, while exposure for 2 or 4 weeks didn’t affect the movement items indices. The combination of lead and stress did not show any significant difference compared to the exposure to each of them individually. From the findings, Lead, stress, and their combination caused movement disorders in a time dependent manner. Short time exposure did not change movement behavior. The co-exposure to the lead and stress did not show additive or synergistic effects. Wolters Kluwer - Medknow 2019-08 /pmc/articles/PMC6714115/ /pubmed/31516511 http://dx.doi.org/10.4103/1735-5362.263558 Text en Copyright: © 2019 Research in Pharmaceutical Sciences http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Hosseini-Sharifabad, Ali Naghibzadeh, Sara Hajhashemi, Valiollah The effect of lead, restraint stress or their co-exposure on the movement disorders incidence in male mice |
title | The effect of lead, restraint stress or their co-exposure on the movement disorders incidence in male mice |
title_full | The effect of lead, restraint stress or their co-exposure on the movement disorders incidence in male mice |
title_fullStr | The effect of lead, restraint stress or their co-exposure on the movement disorders incidence in male mice |
title_full_unstemmed | The effect of lead, restraint stress or their co-exposure on the movement disorders incidence in male mice |
title_short | The effect of lead, restraint stress or their co-exposure on the movement disorders incidence in male mice |
title_sort | effect of lead, restraint stress or their co-exposure on the movement disorders incidence in male mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6714115/ https://www.ncbi.nlm.nih.gov/pubmed/31516511 http://dx.doi.org/10.4103/1735-5362.263558 |
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