Ellagic Acid Prevents Dopamine Neuron Degeneration from Oxidative Stress and Neuroinflammation in MPTP Model of Parkinson’s Disease
Parkinson’s disease (PD) is one of the most common neurodegenerative diseases and is characterized by progressive dopaminergic neurodegeneration in the substantia nigra pars compacta area. In the present study, treatment of EA for 1 week at a dose of 10 mg/kg body weight prior to MPTP (25 mg/kg body...
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MDPI AG
2020-11-01
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author | Mustafa T. Ardah Greeshma Bharathan Tohru Kitada M. Emdadul Haque |
author_facet | Mustafa T. Ardah Greeshma Bharathan Tohru Kitada M. Emdadul Haque |
author_sort | Mustafa T. Ardah |
collection | DOAJ |
description | Parkinson’s disease (PD) is one of the most common neurodegenerative diseases and is characterized by progressive dopaminergic neurodegeneration in the substantia nigra pars compacta area. In the present study, treatment of EA for 1 week at a dose of 10 mg/kg body weight prior to MPTP (25 mg/kg body weight) was carried out. MPTP administration caused oxidative stress, as evidenced by decreased activities of superoxide dismutase and catalase, and the depletion of reduced glutathione with a concomitant rise in the lipid peroxidation product, malondialdehyde. It also significantly increased the pro-inflammatory cytokines and elevated the inflammatory mediators like cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) in the striatum. Immunohistochemical analysis revealed a loss of dopamine neurons in the SNc area and a decrease in dopamine transporter in the striatum following MPTP administration. However, treatment with EA prior to MPTP injection significantly rescued the dopaminergic neurons and dopamine transporter. EA treatment further restored antioxidant enzymes, prevented the depletion of glutathione and inhibited lipid peroxidation, in addition to the attenuation of pro-inflammatory cytokines. EA also reduced the levels of COX-2 and iNOS. The findings of the present study demonstrate that EA protects against MPTP-induced PD and the observed neuroprotective effects can be attributed to its potent antioxidant and anti-inflammatory properties. |
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language | English |
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spelling | doaj.art-1baa1a690e3d4efe9e58671f097ba4ad2023-11-20T20:00:53ZengMDPI AGBiomolecules2218-273X2020-11-011011151910.3390/biom10111519Ellagic Acid Prevents Dopamine Neuron Degeneration from Oxidative Stress and Neuroinflammation in MPTP Model of Parkinson’s DiseaseMustafa T. Ardah0Greeshma Bharathan1Tohru Kitada2M. Emdadul Haque3Department of Biochemistry, College of Medicine and Health Sciences, UAEU, Al Ain, UAEDepartment of Biochemistry, College of Medicine and Health Sciences, UAEU, Al Ain, UAEOtawa-Kagaku Service, Parkinson’s Clinic and Research, Kamakura 247-0061, JapanDepartment of Biochemistry, College of Medicine and Health Sciences, UAEU, Al Ain, UAEParkinson’s disease (PD) is one of the most common neurodegenerative diseases and is characterized by progressive dopaminergic neurodegeneration in the substantia nigra pars compacta area. In the present study, treatment of EA for 1 week at a dose of 10 mg/kg body weight prior to MPTP (25 mg/kg body weight) was carried out. MPTP administration caused oxidative stress, as evidenced by decreased activities of superoxide dismutase and catalase, and the depletion of reduced glutathione with a concomitant rise in the lipid peroxidation product, malondialdehyde. It also significantly increased the pro-inflammatory cytokines and elevated the inflammatory mediators like cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) in the striatum. Immunohistochemical analysis revealed a loss of dopamine neurons in the SNc area and a decrease in dopamine transporter in the striatum following MPTP administration. However, treatment with EA prior to MPTP injection significantly rescued the dopaminergic neurons and dopamine transporter. EA treatment further restored antioxidant enzymes, prevented the depletion of glutathione and inhibited lipid peroxidation, in addition to the attenuation of pro-inflammatory cytokines. EA also reduced the levels of COX-2 and iNOS. The findings of the present study demonstrate that EA protects against MPTP-induced PD and the observed neuroprotective effects can be attributed to its potent antioxidant and anti-inflammatory properties.https://www.mdpi.com/2218-273X/10/11/1519ellagic acidneurodegenerationneurotoxicityParkinson’s disease |
spellingShingle | Mustafa T. Ardah Greeshma Bharathan Tohru Kitada M. Emdadul Haque Ellagic Acid Prevents Dopamine Neuron Degeneration from Oxidative Stress and Neuroinflammation in MPTP Model of Parkinson’s Disease Biomolecules ellagic acid neurodegeneration neurotoxicity Parkinson’s disease |
title | Ellagic Acid Prevents Dopamine Neuron Degeneration from Oxidative Stress and Neuroinflammation in MPTP Model of Parkinson’s Disease |
title_full | Ellagic Acid Prevents Dopamine Neuron Degeneration from Oxidative Stress and Neuroinflammation in MPTP Model of Parkinson’s Disease |
title_fullStr | Ellagic Acid Prevents Dopamine Neuron Degeneration from Oxidative Stress and Neuroinflammation in MPTP Model of Parkinson’s Disease |
title_full_unstemmed | Ellagic Acid Prevents Dopamine Neuron Degeneration from Oxidative Stress and Neuroinflammation in MPTP Model of Parkinson’s Disease |
title_short | Ellagic Acid Prevents Dopamine Neuron Degeneration from Oxidative Stress and Neuroinflammation in MPTP Model of Parkinson’s Disease |
title_sort | ellagic acid prevents dopamine neuron degeneration from oxidative stress and neuroinflammation in mptp model of parkinson s disease |
topic | ellagic acid neurodegeneration neurotoxicity Parkinson’s disease |
url | https://www.mdpi.com/2218-273X/10/11/1519 |
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