Plant Extracts and Phytochemicals Targeting α-Synuclein Aggregation in Parkinson's Disease Models

α-Synuclein (α-syn) is a presynaptic protein that regulates the release of neurotransmitters from synaptic vesicles in the brain. α-Syn aggregates, including Lewy bodies, are features of both sporadic and familial forms of Parkinson's disease (PD). These aggregates undergo several key stages of...

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Published in:Frontiers in Pharmacology
Main Authors: Hayate Javed, Mohamed Fizur Nagoor Meeran, Sheikh Azimullah, Abdu Adem, Bassem Sadek, Shreesh Kumar Ojha
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-03-01
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Online Access:https://www.frontiersin.org/article/10.3389/fphar.2018.01555/full
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author Hayate Javed
Mohamed Fizur Nagoor Meeran
Sheikh Azimullah
Abdu Adem
Bassem Sadek
Shreesh Kumar Ojha
author_facet Hayate Javed
Mohamed Fizur Nagoor Meeran
Sheikh Azimullah
Abdu Adem
Bassem Sadek
Shreesh Kumar Ojha
author_sort Hayate Javed
collection DOAJ
container_title Frontiers in Pharmacology
description α-Synuclein (α-syn) is a presynaptic protein that regulates the release of neurotransmitters from synaptic vesicles in the brain. α-Syn aggregates, including Lewy bodies, are features of both sporadic and familial forms of Parkinson's disease (PD). These aggregates undergo several key stages of fibrillation, oligomerization, and aggregation. Therapeutic benefits of drugs decline with disease progression and offer only symptomatic treatment. Novel therapeutic strategies are required which can either prevent or delay the progression of the disease. The link between α-syn and the etiopathogenesis and progression of PD are well-established in the literature. Studies indicate that α-syn is an important therapeutic target and inhibition of α-syn aggregation, oligomerization, and fibrillation are an important disease modification strategy. However, recent studies have shown that plant extracts and phytochemicals have neuroprotective effects on α-syn oligomerization and fibrillation by targeting different key stages of its formation. Although many reviews on the antioxidant-mediated, neuroprotective effect of plant extracts and phytochemicals on PD symptoms have been well-highlighted, the antioxidant mechanisms show limited success for translation to clinical studies. The identification of specific plant extracts and phytochemicals that target α-syn aggregation will provide selective molecules to develop new drugs for PD. The present review provides an overview of plant extracts and phytochemicals that target α-syn in PD and summarizes the observed effects and the underlying mechanisms. Furthermore, we provide a synopsis of current experimental models and techniques used to evaluate plant extracts and phytochemicals. Plant extracts and phytochemicals were found to inhibit the aggregation or fibril formation of oligomers. These also appear to direct α-syn oligomer formation into its unstructured form or promote non-toxic pathways and suggested to be valuable drug candidates for PD and related synucleinopathy. Current evidences from in vitro studies require confirmation in the in vivo studies. Further studies are needed to ascertain their potential effects and safety in preclinical studies for pharmaceutical/nutritional development of these phytochemicals or dietary inclusion of the plant extracts in PD treatment.
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spelling doaj-art-044706ffa36d4ea3bc0f8a9433395f4e2025-08-19T20:55:07ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122019-03-01910.3389/fphar.2018.01555386706Plant Extracts and Phytochemicals Targeting α-Synuclein Aggregation in Parkinson's Disease ModelsHayate Javed0Mohamed Fizur Nagoor Meeran1Sheikh Azimullah2Abdu Adem3Bassem Sadek4Shreesh Kumar Ojha5Department of Anatomy, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab EmiratesDepartment of Pharmacology and Therapeutics, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab EmiratesDepartment of Pharmacology and Therapeutics, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab EmiratesDepartment of Pharmacology and Therapeutics, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab EmiratesDepartment of Pharmacology and Therapeutics, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab EmiratesDepartment of Pharmacology and Therapeutics, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emiratesα-Synuclein (α-syn) is a presynaptic protein that regulates the release of neurotransmitters from synaptic vesicles in the brain. α-Syn aggregates, including Lewy bodies, are features of both sporadic and familial forms of Parkinson's disease (PD). These aggregates undergo several key stages of fibrillation, oligomerization, and aggregation. Therapeutic benefits of drugs decline with disease progression and offer only symptomatic treatment. Novel therapeutic strategies are required which can either prevent or delay the progression of the disease. The link between α-syn and the etiopathogenesis and progression of PD are well-established in the literature. Studies indicate that α-syn is an important therapeutic target and inhibition of α-syn aggregation, oligomerization, and fibrillation are an important disease modification strategy. However, recent studies have shown that plant extracts and phytochemicals have neuroprotective effects on α-syn oligomerization and fibrillation by targeting different key stages of its formation. Although many reviews on the antioxidant-mediated, neuroprotective effect of plant extracts and phytochemicals on PD symptoms have been well-highlighted, the antioxidant mechanisms show limited success for translation to clinical studies. The identification of specific plant extracts and phytochemicals that target α-syn aggregation will provide selective molecules to develop new drugs for PD. The present review provides an overview of plant extracts and phytochemicals that target α-syn in PD and summarizes the observed effects and the underlying mechanisms. Furthermore, we provide a synopsis of current experimental models and techniques used to evaluate plant extracts and phytochemicals. Plant extracts and phytochemicals were found to inhibit the aggregation or fibril formation of oligomers. These also appear to direct α-syn oligomer formation into its unstructured form or promote non-toxic pathways and suggested to be valuable drug candidates for PD and related synucleinopathy. Current evidences from in vitro studies require confirmation in the in vivo studies. Further studies are needed to ascertain their potential effects and safety in preclinical studies for pharmaceutical/nutritional development of these phytochemicals or dietary inclusion of the plant extracts in PD treatment.https://www.frontiersin.org/article/10.3389/fphar.2018.01555/fullα-synucleinplantsphytochemicalsParkinson's diseaseneuroprotectivenatural products
spellingShingle Hayate Javed
Mohamed Fizur Nagoor Meeran
Sheikh Azimullah
Abdu Adem
Bassem Sadek
Shreesh Kumar Ojha
Plant Extracts and Phytochemicals Targeting α-Synuclein Aggregation in Parkinson's Disease Models
α-synuclein
plants
phytochemicals
Parkinson's disease
neuroprotective
natural products
title Plant Extracts and Phytochemicals Targeting α-Synuclein Aggregation in Parkinson's Disease Models
title_full Plant Extracts and Phytochemicals Targeting α-Synuclein Aggregation in Parkinson's Disease Models
title_fullStr Plant Extracts and Phytochemicals Targeting α-Synuclein Aggregation in Parkinson's Disease Models
title_full_unstemmed Plant Extracts and Phytochemicals Targeting α-Synuclein Aggregation in Parkinson's Disease Models
title_short Plant Extracts and Phytochemicals Targeting α-Synuclein Aggregation in Parkinson's Disease Models
title_sort plant extracts and phytochemicals targeting α synuclein aggregation in parkinson s disease models
topic α-synuclein
plants
phytochemicals
Parkinson's disease
neuroprotective
natural products
url https://www.frontiersin.org/article/10.3389/fphar.2018.01555/full
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