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The Association of Iron and the Pathologies of Parkinson’s Diseases in MPTP/MPP(+)-Induced Neuronal Degeneration in Non-human Primates and in Cell Culture

Despite much efforts in the last few decades, the mechanism of degeneration of dopamine (DA) neurons in the substantia nigra (SN) in Parkinson’s disease (PD) remains unclear. This represents a major knowledge gap in idiopathic and genetic forms of PD. Among various possible key factors postulated, i...

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Autores principales: Shi, Liangqin, Huang, Chao, Luo, Qihui, Rogers, Edmond, Xia, Yu, Liu, Wentao, Ma, Wenjing, Zeng, Wen, Gong, Li, Fang, Jing, Tang, Li, Cheng, Anchun, Shi, Riyi, Chen, Zhengli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6729105/
https://www.ncbi.nlm.nih.gov/pubmed/31543809
http://dx.doi.org/10.3389/fnagi.2019.00215
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author Shi, Liangqin
Huang, Chao
Luo, Qihui
Rogers, Edmond
Xia, Yu
Liu, Wentao
Ma, Wenjing
Zeng, Wen
Gong, Li
Fang, Jing
Tang, Li
Cheng, Anchun
Shi, Riyi
Chen, Zhengli
author_facet Shi, Liangqin
Huang, Chao
Luo, Qihui
Rogers, Edmond
Xia, Yu
Liu, Wentao
Ma, Wenjing
Zeng, Wen
Gong, Li
Fang, Jing
Tang, Li
Cheng, Anchun
Shi, Riyi
Chen, Zhengli
author_sort Shi, Liangqin
collection PubMed
description Despite much efforts in the last few decades, the mechanism of degeneration of dopamine (DA) neurons in the substantia nigra (SN) in Parkinson’s disease (PD) remains unclear. This represents a major knowledge gap in idiopathic and genetic forms of PD. Among various possible key factors postulated, iron metabolism has been widely suggested to be involved with fueling oxidative stress, a known factor in the pathogenesis of PD. However, the correlation between iron and DA neuron loss, specifically in the SN, has not been described in experimental animal models with great detail, with most studies utilizing rodents and, rarely, non-human primates. In the present study, aiming to gain further evidence of a pathological role of iron in PD, we have examined the correlation of iron with DA neuron loss in a non-human primate model of PD induced by MPTP. We report a significant iron accumulation accompanied by both DA degeneration in the SN and motor deficits in the monkey that displayed the most severe PD pathology and behavioral deficits. The other two monkeys subjected to MPTP displayed less severe PD pathologies and motor deficits, however, their SN iron levels were significantly lower than controls. These findings suggest that high iron may indicate and contribute to heightened MPP(+)-induced PD pathology in late or severe stages of PD, while depressed levels of iron may signal an early stage of disease. Similarly, using a cell culture preparation, we have found that high doses of ferric ammonium citrate (FAC), a factor known to enhance iron accumulation, increased MPP(+)-induced cell death in U251 and SH-SY5Y cells, and even in control cells. However, at low dose FAC restored or increased the viability of U251 and SH-SY5Y cells in the absence or presence of MPP(+). These observations imply that high levels of iron likely contribute to or heighten MPP(+) toxicity in the later stages of PD. While we report reduced iron levels in the earlier stages of MPTP induced PD, the significance of these changes remains to be determined.
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spelling pubmed-67291052019-09-20 The Association of Iron and the Pathologies of Parkinson’s Diseases in MPTP/MPP(+)-Induced Neuronal Degeneration in Non-human Primates and in Cell Culture Shi, Liangqin Huang, Chao Luo, Qihui Rogers, Edmond Xia, Yu Liu, Wentao Ma, Wenjing Zeng, Wen Gong, Li Fang, Jing Tang, Li Cheng, Anchun Shi, Riyi Chen, Zhengli Front Aging Neurosci Neuroscience Despite much efforts in the last few decades, the mechanism of degeneration of dopamine (DA) neurons in the substantia nigra (SN) in Parkinson’s disease (PD) remains unclear. This represents a major knowledge gap in idiopathic and genetic forms of PD. Among various possible key factors postulated, iron metabolism has been widely suggested to be involved with fueling oxidative stress, a known factor in the pathogenesis of PD. However, the correlation between iron and DA neuron loss, specifically in the SN, has not been described in experimental animal models with great detail, with most studies utilizing rodents and, rarely, non-human primates. In the present study, aiming to gain further evidence of a pathological role of iron in PD, we have examined the correlation of iron with DA neuron loss in a non-human primate model of PD induced by MPTP. We report a significant iron accumulation accompanied by both DA degeneration in the SN and motor deficits in the monkey that displayed the most severe PD pathology and behavioral deficits. The other two monkeys subjected to MPTP displayed less severe PD pathologies and motor deficits, however, their SN iron levels were significantly lower than controls. These findings suggest that high iron may indicate and contribute to heightened MPP(+)-induced PD pathology in late or severe stages of PD, while depressed levels of iron may signal an early stage of disease. Similarly, using a cell culture preparation, we have found that high doses of ferric ammonium citrate (FAC), a factor known to enhance iron accumulation, increased MPP(+)-induced cell death in U251 and SH-SY5Y cells, and even in control cells. However, at low dose FAC restored or increased the viability of U251 and SH-SY5Y cells in the absence or presence of MPP(+). These observations imply that high levels of iron likely contribute to or heighten MPP(+) toxicity in the later stages of PD. While we report reduced iron levels in the earlier stages of MPTP induced PD, the significance of these changes remains to be determined. Frontiers Media S.A. 2019-08-30 /pmc/articles/PMC6729105/ /pubmed/31543809 http://dx.doi.org/10.3389/fnagi.2019.00215 Text en Copyright © 2019 Shi, Huang, Luo, Rogers, Xia, Liu, Ma, Zeng, Gong, Fang, Tang, Cheng, Shi and Chen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Shi, Liangqin
Huang, Chao
Luo, Qihui
Rogers, Edmond
Xia, Yu
Liu, Wentao
Ma, Wenjing
Zeng, Wen
Gong, Li
Fang, Jing
Tang, Li
Cheng, Anchun
Shi, Riyi
Chen, Zhengli
The Association of Iron and the Pathologies of Parkinson’s Diseases in MPTP/MPP(+)-Induced Neuronal Degeneration in Non-human Primates and in Cell Culture
title The Association of Iron and the Pathologies of Parkinson’s Diseases in MPTP/MPP(+)-Induced Neuronal Degeneration in Non-human Primates and in Cell Culture
title_full The Association of Iron and the Pathologies of Parkinson’s Diseases in MPTP/MPP(+)-Induced Neuronal Degeneration in Non-human Primates and in Cell Culture
title_fullStr The Association of Iron and the Pathologies of Parkinson’s Diseases in MPTP/MPP(+)-Induced Neuronal Degeneration in Non-human Primates and in Cell Culture
title_full_unstemmed The Association of Iron and the Pathologies of Parkinson’s Diseases in MPTP/MPP(+)-Induced Neuronal Degeneration in Non-human Primates and in Cell Culture
title_short The Association of Iron and the Pathologies of Parkinson’s Diseases in MPTP/MPP(+)-Induced Neuronal Degeneration in Non-human Primates and in Cell Culture
title_sort association of iron and the pathologies of parkinson’s diseases in mptp/mpp(+)-induced neuronal degeneration in non-human primates and in cell culture
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6729105/
https://www.ncbi.nlm.nih.gov/pubmed/31543809
http://dx.doi.org/10.3389/fnagi.2019.00215
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