Open Access
Oxidative Stress: A Key Modulator in Neurodegenerative Diseases
Publication type: Journal Article
Publication date: 2019-04-22
PubMed ID:
31013638
Organic Chemistry
Drug Discovery
Physical and Theoretical Chemistry
Pharmaceutical Science
Molecular Medicine
Analytical Chemistry
Chemistry (miscellaneous)
Abstract
Oxidative stress is proposed as a regulatory element in ageing and various neurological disorders. The excess of oxidants causes a reduction of antioxidants, which in turn produce an oxidation–reduction imbalance in organisms. Paucity of the antioxidant system generates oxidative-stress, characterized by elevated levels of reactive species (oxygen, hydroxyl free radical, and so on). Mitochondria play a key role in ATP supply to cells via oxidative phosphorylation, as well as synthesis of essential biological molecules. Various redox reactions catalyzed by enzymes take place in the oxidative phosphorylation process. An inefficient oxidative phosphorylation may generate reactive oxygen species (ROS), leading to mitochondrial dysfunction. Mitochondrial redox metabolism, phospholipid metabolism, and proteolytic pathways are found to be the major and potential source of free radicals. A lower concentration of ROS is essential for normal cellular signaling, whereas the higher concentration and long-time exposure of ROS cause damage to cellular macromolecules such as DNA, lipids and proteins, ultimately resulting in necrosis and apoptotic cell death. Normal and proper functioning of the central nervous system (CNS) is entirely dependent on the chemical integrity of brain. It is well established that the brain consumes a large amount of oxygen and is highly rich in lipid content, becoming prone to oxidative stress. A high consumption of oxygen leads to excessive production of ROS. Apart from this, the neuronal membranes are found to be rich in polyunsaturated fatty acids, which are highly susceptible to ROS. Various neurodegenerative diseases such as Parkinson’s disease (PD), Alzheimer’s disease (AD), Huntington’s disease (HD), and amyotrophic lateral sclerosis (ALS), among others, can be the result of biochemical alteration (due to oxidative stress) in bimolecular components. There is a need to understand the processes and role of oxidative stress in neurodegenerative diseases. This review is an effort towards improving our understanding of the pivotal role played by OS in neurodegenerative disorders.
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GOST
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Singh A. et al. Oxidative Stress: A Key Modulator in Neurodegenerative Diseases // Molecules. 2019. Vol. 24. No. 8. p. 1583.
GOST all authors (up to 50)
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Singh A., Kukreti R., Saso L., Kukreti S. Oxidative Stress: A Key Modulator in Neurodegenerative Diseases // Molecules. 2019. Vol. 24. No. 8. p. 1583.
Cite this
RIS
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TY - JOUR
DO - 10.3390/molecules24081583
UR - https://doi.org/10.3390/molecules24081583
TI - Oxidative Stress: A Key Modulator in Neurodegenerative Diseases
T2 - Molecules
AU - Singh, Anju
AU - Kukreti, Ritushree
AU - Saso, Luciano
AU - Kukreti, Shrikant
PY - 2019
DA - 2019/04/22
PB - MDPI
SP - 1583
IS - 8
VL - 24
PMID - 31013638
SN - 1420-3049
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2019_Singh,
author = {Anju Singh and Ritushree Kukreti and Luciano Saso and Shrikant Kukreti},
title = {Oxidative Stress: A Key Modulator in Neurodegenerative Diseases},
journal = {Molecules},
year = {2019},
volume = {24},
publisher = {MDPI},
month = {apr},
url = {https://doi.org/10.3390/molecules24081583},
number = {8},
pages = {1583},
doi = {10.3390/molecules24081583}
}
Cite this
MLA
Copy
Singh, Anju, et al. “Oxidative Stress: A Key Modulator in Neurodegenerative Diseases.” Molecules, vol. 24, no. 8, Apr. 2019, p. 1583. https://doi.org/10.3390/molecules24081583.