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Oxidative Stress: A Key Modulator in Neurodegenerative Diseases.
Molecules. 2019 Apr 22; 24(8)M

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.

Authors+Show Affiliations

Nucleic Acids Research Lab, Department of Chemistry, University of Delhi (North Campus), Delhi 110007, India. anju11278@gmail.com. Department of Chemistry, Ramjas College, University of Delhi, Delhi 110007, India. anju11278@gmail.com.Academy of Scientific and Innovative Research (AcSIR), CSIR-Institute of Genomics and Integrative Biology (CSIR-IGIB) Campus, Delhi 110007, India. ritus@igib.res.in. Genomics and Molecular Medicine Unit, Institute of Genomics and Integrative Biology (IGIB), Council of Scientific and Industrial Research (CSIR), Mall Road, Delhi 110007, India. ritus@igib.res.in.Department of Physiology and Pharmacology "Vittorio Erspamer", Sapienza University of Rome, P. le Aldo Moro 5, 00185 Rome, Italy. luciano.saso@uniroma1.it.Nucleic Acids Research Lab, Department of Chemistry, University of Delhi (North Campus), Delhi 110007, India. shrikant.kukreti6@gmail.com.

Pub Type(s)

Journal Article
Review

Language

eng

PubMed ID

31013638

Citation

Singh, Anju, et al. "Oxidative Stress: a Key Modulator in Neurodegenerative Diseases." Molecules (Basel, Switzerland), vol. 24, no. 8, 2019.
Singh A, Kukreti R, Saso L, et al. Oxidative Stress: A Key Modulator in Neurodegenerative Diseases. Molecules. 2019;24(8).
Singh, A., Kukreti, R., Saso, L., & Kukreti, S. (2019). Oxidative Stress: A Key Modulator in Neurodegenerative Diseases. Molecules (Basel, Switzerland), 24(8). https://doi.org/10.3390/molecules24081583
Singh A, et al. Oxidative Stress: a Key Modulator in Neurodegenerative Diseases. Molecules. 2019 Apr 22;24(8) PubMed PMID: 31013638.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Oxidative Stress: A Key Modulator in Neurodegenerative Diseases. AU - Singh,Anju, AU - Kukreti,Ritushree, AU - Saso,Luciano, AU - Kukreti,Shrikant, Y1 - 2019/04/22/ PY - 2019/02/28/received PY - 2019/04/02/revised PY - 2019/04/16/accepted PY - 2019/4/25/entrez PY - 2019/4/25/pubmed PY - 2019/8/14/medline KW - Alzheimer’s disease (AD) KW - Parkinson’s disease (PD) KW - mitochondria KW - neurodegenerative disease KW - oxidative stress (OS) KW - reactive oxygen species (ROS) JF - Molecules (Basel, Switzerland) JO - Molecules VL - 24 IS - 8 N2 - 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. SN - 1420-3049 UR - https://www.unboundmedicine.com/medline/citation/31013638/Oxidative_Stress:_A_Key_Modulator_in_Neurodegenerative_Diseases_ DB - PRIME DP - Unbound Medicine ER -