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Neuroprotective Effects and Related Mechanisms of Echinacoside in MPTP-Induced PD Mice

OBJECTIVE: To explore the neuroprotective effect and the related mechanisms of echinacoside (ECH) in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced Parkinson’s disease (PD) mice. METHODS: Parkinson’s disease is induced in mice by MPTP and the neurobehaviors of mice in different groups a...

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Autores principales: Zhang, Zhen-Nian, Hui, Zhen, Chen, Chang, Liang, Yan, Tang, Li-Li, Wang, Su-Lei, Xu, Cheng-Cheng, Yang, Hui, Zhang, Jing-Si, Zhao, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8184243/
https://www.ncbi.nlm.nih.gov/pubmed/34113108
http://dx.doi.org/10.2147/NDT.S299685
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author Zhang, Zhen-Nian
Hui, Zhen
Chen, Chang
Liang, Yan
Tang, Li-Li
Wang, Su-Lei
Xu, Cheng-Cheng
Yang, Hui
Zhang, Jing-Si
Zhao, Yang
author_facet Zhang, Zhen-Nian
Hui, Zhen
Chen, Chang
Liang, Yan
Tang, Li-Li
Wang, Su-Lei
Xu, Cheng-Cheng
Yang, Hui
Zhang, Jing-Si
Zhao, Yang
author_sort Zhang, Zhen-Nian
collection PubMed
description OBJECTIVE: To explore the neuroprotective effect and the related mechanisms of echinacoside (ECH) in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced Parkinson’s disease (PD) mice. METHODS: Parkinson’s disease is induced in mice by MPTP and the neurobehaviors of mice in different groups are observed. Then, immunohistochemistry and Western blot analysis are adopted to measure the expression of tyrosine hydroxylase (TH) and α-synuclein in the substantia nigra (SN). The content of dopamine (DA) and other neurotransmitters in the brain is detected by high-performance liquid chromatography. The expression of nerve growth factors and inflammatory factors in SN in mice in each group is measured by quantitative polymerase chain reaction. Finally, the expression of oxidative stress-related parameters in each group is measured. RESULTS: Compared with the model group, the pole-climbing time among mice in the moderate and high-dose ECH groups is significantly reduced (P < 0.01). The rotarod staying time, as well as fore and hind-limb strides, shows a significant increase (P < 0.01), as does spontaneous activity (P < 0.01). Moreover, the expression levels of TH, DA, glial cell line-derived neurotrophic factor, and brain-derived neurotrophic factor in SN in mice show significant increases in these two groups (P < 0.01). The content of superoxide dismutase, catalase, and glutathione peroxidase indicates significant increases in the low, moderate, and high-dose ECH groups (P < 0.01), and the content of MDA was reduced (P < 0.01). In the high-dose ECH group, the expression of interleukin (IL) 6 and tumor necrosis factor-α is significantly reduced (P < 0.01), while the expression of IL-10 shows a marked increase (P < 0.01) alongside a decrease in the expression of α-synuclein (P < 0.01). CONCLUSION: Echinacoside improves neurobehavioral symptoms in PD mice and significantly increases the expression of TH and DA. The neuroprotective effect potentially correlates with anti-inflammation and anti-oxidation actions, promotes the expression of nerve growth factor, and reduces the accumulation of α-synuclein.
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spelling pubmed-81842432021-06-09 Neuroprotective Effects and Related Mechanisms of Echinacoside in MPTP-Induced PD Mice Zhang, Zhen-Nian Hui, Zhen Chen, Chang Liang, Yan Tang, Li-Li Wang, Su-Lei Xu, Cheng-Cheng Yang, Hui Zhang, Jing-Si Zhao, Yang Neuropsychiatr Dis Treat Original Research OBJECTIVE: To explore the neuroprotective effect and the related mechanisms of echinacoside (ECH) in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced Parkinson’s disease (PD) mice. METHODS: Parkinson’s disease is induced in mice by MPTP and the neurobehaviors of mice in different groups are observed. Then, immunohistochemistry and Western blot analysis are adopted to measure the expression of tyrosine hydroxylase (TH) and α-synuclein in the substantia nigra (SN). The content of dopamine (DA) and other neurotransmitters in the brain is detected by high-performance liquid chromatography. The expression of nerve growth factors and inflammatory factors in SN in mice in each group is measured by quantitative polymerase chain reaction. Finally, the expression of oxidative stress-related parameters in each group is measured. RESULTS: Compared with the model group, the pole-climbing time among mice in the moderate and high-dose ECH groups is significantly reduced (P < 0.01). The rotarod staying time, as well as fore and hind-limb strides, shows a significant increase (P < 0.01), as does spontaneous activity (P < 0.01). Moreover, the expression levels of TH, DA, glial cell line-derived neurotrophic factor, and brain-derived neurotrophic factor in SN in mice show significant increases in these two groups (P < 0.01). The content of superoxide dismutase, catalase, and glutathione peroxidase indicates significant increases in the low, moderate, and high-dose ECH groups (P < 0.01), and the content of MDA was reduced (P < 0.01). In the high-dose ECH group, the expression of interleukin (IL) 6 and tumor necrosis factor-α is significantly reduced (P < 0.01), while the expression of IL-10 shows a marked increase (P < 0.01) alongside a decrease in the expression of α-synuclein (P < 0.01). CONCLUSION: Echinacoside improves neurobehavioral symptoms in PD mice and significantly increases the expression of TH and DA. The neuroprotective effect potentially correlates with anti-inflammation and anti-oxidation actions, promotes the expression of nerve growth factor, and reduces the accumulation of α-synuclein. Dove 2021-06-03 /pmc/articles/PMC8184243/ /pubmed/34113108 http://dx.doi.org/10.2147/NDT.S299685 Text en © 2021 Zhang et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Zhang, Zhen-Nian
Hui, Zhen
Chen, Chang
Liang, Yan
Tang, Li-Li
Wang, Su-Lei
Xu, Cheng-Cheng
Yang, Hui
Zhang, Jing-Si
Zhao, Yang
Neuroprotective Effects and Related Mechanisms of Echinacoside in MPTP-Induced PD Mice
title Neuroprotective Effects and Related Mechanisms of Echinacoside in MPTP-Induced PD Mice
title_full Neuroprotective Effects and Related Mechanisms of Echinacoside in MPTP-Induced PD Mice
title_fullStr Neuroprotective Effects and Related Mechanisms of Echinacoside in MPTP-Induced PD Mice
title_full_unstemmed Neuroprotective Effects and Related Mechanisms of Echinacoside in MPTP-Induced PD Mice
title_short Neuroprotective Effects and Related Mechanisms of Echinacoside in MPTP-Induced PD Mice
title_sort neuroprotective effects and related mechanisms of echinacoside in mptp-induced pd mice
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8184243/
https://www.ncbi.nlm.nih.gov/pubmed/34113108
http://dx.doi.org/10.2147/NDT.S299685
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