Cargando…

Tocotrienols Ameliorate Neurodegeneration and Motor Deficits in the 6-OHDA-Induced Rat Model of Parkinsonism: Behavioural and Immunohistochemistry Analysis

Parkinson’s disease (PD) is a debilitating neurodegenerative disease, which progresses over time, causing pathological depigmentation of the substantia nigra (SN) in the midbrain due to loss of dopaminergic neurons. Emerging studies revealed the promising effects of some nutrient compounds in reduci...

Descripción completa

Detalles Bibliográficos
Autores principales: Kumari, Mangala, Ramdas, Premdass, Radhakrishnan, Ammu Kutty, Kutty, Methil Kannan, Haleagrahara, Nagaraja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8150907/
https://www.ncbi.nlm.nih.gov/pubmed/34068460
http://dx.doi.org/10.3390/nu13051583
_version_ 1783698258557665280
author Kumari, Mangala
Ramdas, Premdass
Radhakrishnan, Ammu Kutty
Kutty, Methil Kannan
Haleagrahara, Nagaraja
author_facet Kumari, Mangala
Ramdas, Premdass
Radhakrishnan, Ammu Kutty
Kutty, Methil Kannan
Haleagrahara, Nagaraja
author_sort Kumari, Mangala
collection PubMed
description Parkinson’s disease (PD) is a debilitating neurodegenerative disease, which progresses over time, causing pathological depigmentation of the substantia nigra (SN) in the midbrain due to loss of dopaminergic neurons. Emerging studies revealed the promising effects of some nutrient compounds in reducing the risk of PD. One such nutrient compound that possess neuroprotective effects and prevents neurodegeneration is tocotrienol (T3), a vitamin E family member. In the present study, a single dose intracisternal injection of 250 µg 6-hydroxydopamine (6-OHDA) was used to induce parkinsonism in male Sprague Dawley (SD) rats. Forty-eight hours post injection, the SD rats were orally supplemented with alpha (α)- and gamma (γ)-T3 for 28 days. The neuroprotective effects of α- and γ-T3 were evaluated using behavioural studies and immunohistochemistry (IHC). The findings from this study revealed that supplementation of α- and γ-T3 was able to ameliorate the motor deficits induced by 6-OHDA and improve the neuronal functions by reducing inflammation, reversing the neuronal degradation, and preventing further reduction of dopaminergic neurons in the SN and striatum (STR) fibre density.
format Online
Article
Text
id pubmed-8150907
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-81509072021-05-27 Tocotrienols Ameliorate Neurodegeneration and Motor Deficits in the 6-OHDA-Induced Rat Model of Parkinsonism: Behavioural and Immunohistochemistry Analysis Kumari, Mangala Ramdas, Premdass Radhakrishnan, Ammu Kutty Kutty, Methil Kannan Haleagrahara, Nagaraja Nutrients Article Parkinson’s disease (PD) is a debilitating neurodegenerative disease, which progresses over time, causing pathological depigmentation of the substantia nigra (SN) in the midbrain due to loss of dopaminergic neurons. Emerging studies revealed the promising effects of some nutrient compounds in reducing the risk of PD. One such nutrient compound that possess neuroprotective effects and prevents neurodegeneration is tocotrienol (T3), a vitamin E family member. In the present study, a single dose intracisternal injection of 250 µg 6-hydroxydopamine (6-OHDA) was used to induce parkinsonism in male Sprague Dawley (SD) rats. Forty-eight hours post injection, the SD rats were orally supplemented with alpha (α)- and gamma (γ)-T3 for 28 days. The neuroprotective effects of α- and γ-T3 were evaluated using behavioural studies and immunohistochemistry (IHC). The findings from this study revealed that supplementation of α- and γ-T3 was able to ameliorate the motor deficits induced by 6-OHDA and improve the neuronal functions by reducing inflammation, reversing the neuronal degradation, and preventing further reduction of dopaminergic neurons in the SN and striatum (STR) fibre density. MDPI 2021-05-10 /pmc/articles/PMC8150907/ /pubmed/34068460 http://dx.doi.org/10.3390/nu13051583 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kumari, Mangala
Ramdas, Premdass
Radhakrishnan, Ammu Kutty
Kutty, Methil Kannan
Haleagrahara, Nagaraja
Tocotrienols Ameliorate Neurodegeneration and Motor Deficits in the 6-OHDA-Induced Rat Model of Parkinsonism: Behavioural and Immunohistochemistry Analysis
title Tocotrienols Ameliorate Neurodegeneration and Motor Deficits in the 6-OHDA-Induced Rat Model of Parkinsonism: Behavioural and Immunohistochemistry Analysis
title_full Tocotrienols Ameliorate Neurodegeneration and Motor Deficits in the 6-OHDA-Induced Rat Model of Parkinsonism: Behavioural and Immunohistochemistry Analysis
title_fullStr Tocotrienols Ameliorate Neurodegeneration and Motor Deficits in the 6-OHDA-Induced Rat Model of Parkinsonism: Behavioural and Immunohistochemistry Analysis
title_full_unstemmed Tocotrienols Ameliorate Neurodegeneration and Motor Deficits in the 6-OHDA-Induced Rat Model of Parkinsonism: Behavioural and Immunohistochemistry Analysis
title_short Tocotrienols Ameliorate Neurodegeneration and Motor Deficits in the 6-OHDA-Induced Rat Model of Parkinsonism: Behavioural and Immunohistochemistry Analysis
title_sort tocotrienols ameliorate neurodegeneration and motor deficits in the 6-ohda-induced rat model of parkinsonism: behavioural and immunohistochemistry analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8150907/
https://www.ncbi.nlm.nih.gov/pubmed/34068460
http://dx.doi.org/10.3390/nu13051583
work_keys_str_mv AT kumarimangala tocotrienolsameliorateneurodegenerationandmotordeficitsinthe6ohdainducedratmodelofparkinsonismbehaviouralandimmunohistochemistryanalysis
AT ramdaspremdass tocotrienolsameliorateneurodegenerationandmotordeficitsinthe6ohdainducedratmodelofparkinsonismbehaviouralandimmunohistochemistryanalysis
AT radhakrishnanammukutty tocotrienolsameliorateneurodegenerationandmotordeficitsinthe6ohdainducedratmodelofparkinsonismbehaviouralandimmunohistochemistryanalysis
AT kuttymethilkannan tocotrienolsameliorateneurodegenerationandmotordeficitsinthe6ohdainducedratmodelofparkinsonismbehaviouralandimmunohistochemistryanalysis
AT haleagraharanagaraja tocotrienolsameliorateneurodegenerationandmotordeficitsinthe6ohdainducedratmodelofparkinsonismbehaviouralandimmunohistochemistryanalysis