The DOI matches its Crossref record; 220 of the 220 references it cites were found in a registry or an index.
The Role of Free Radicals in the Aging Brain and Parkinson’s Disease: Convergence and Parallelism
Open accessAbstract
Free radical production and their targeted action on biomolecules have roles in aging and age-related disorders such as Parkinson's disease (PD). There is an age-associated increase in oxidative damage to the brain, and aging is considered a risk factor for PD. Dopaminergic neurons show linear fallout of 5-10% per decade with aging; however, the rate and intensity of neuronal loss in patients with PD is more marked than that of aging. Here, we enumerate the common link between aging and PD at the cellular level with special reference to oxidative damage caused by free radicals. Oxidative damage includes mitochondrial dysfunction, dopamine auto-oxidation, α-synuclein aggregation, glial cell activation, alterations in calcium signaling, and excess free iron. Moreover, neurons encounter more oxidative stress as a counteracting mechanism with advancing age does not function properly. Alterations in transcriptional activity of various pathways, including nuclear factor erythroid 2-related factor 2, glycogen synthase kinase 3β, mitogen activated protein kinase, nuclear factor kappa B, and reduced activity of superoxide dismutase, catalase and glutathione with aging might be correlated with the increased incidence of PD.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Altered glial cell activity is a major source of free radicals under altered neurological conditions [78],”
From Beneficial Effects of Spirulina Consumption on Brain Health (2022) · cites this paper as [78]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
1 retracted
RETRACTED: Glycogen synthase kinase 3β (GSK3β) mediates 6‐ hydroxydopamine‐induced neuronal death
Chen, G., Bower, K. A., Ma, C., Fang, S., Thiele, C. J., & Luo, J. (2004) · The FASEB Journal · doi:10.1096/fj.04-1551fje · Cited by 311
RetractedStaging of brain pathology related to sporadic Parkinson’s disease
Braak, H., Tredici, K. D., Rüb, U., de Vos, R. A. I., Jansen Steur, E. N. H., & Braak, E. (2003) · Neurobiology of Aging · doi:10.1016/s0197-4580(02)00065-9 · Cited by 10,777
Sequence and organization of the human mitochondrial genome
Anderson, S., Bankier, A. T., Barrell, B. G., de Bruijn, M. H. L., Coulson, A. R., Drouin, J., Eperon, I. C., Nierlich, D. P., Roe, B. A., Sanger, F., et al. (1981) · Nature · doi:10.1038/290457a0 · Cited by 9,740
Aging: a theory based on free radical and radiation chemistry
Harman, D. (1956) · Journal of Gerontology · doi:10.1093/geronj/11.3.298 · Cited by 8,567
The NOX Family of ROS-Generating NADPH Oxidases: Physiology and Pathophysiology
Bedard, K., & Krause, K.-H. (2007) · Physiological Reviews · doi:10.1152/physrev.00044.2005 · Cited by 6,989
Free radicals, metals and antioxidants in oxidative stress-induced cancer
Valko, M., Rhodes, C. J., Moncol, J., Izakovic, M., & Mazur, M. (2006) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2005.12.009 · Cited by 6,680
Oxygen toxicity, oxygen radicals, transition metals and disease
Halliwell, B., & Gutteridge, J. M. C. (1984) · Biochemical Journal · doi:10.1042/bj2190001 · Cited by 5,330
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
Kitada, T., Asakawa, S., Hattori, N., Matsumine, H., Yamamura, Y., Minoshima, S., Yokochi, M., Mizuno, Y., & Shimizu, N. (1998) · Nature · doi:10.1038/33416 · Cited by 5,227
Mitochondrial formation of reactive oxygen species
Turrens, J. F. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.049478 · Cited by 5,084
Hayden, M. S., & Ghosh, S. (2004) · Genes & Development · doi:10.1101/gad.1228704 · Cited by 3,842
Flagged first, then by citations
Cited by
Sorted by citations
Zielonka, J., Joseph, J., Sikora, A., Hardy, M., Ouari, O., Vasquez-Vivar, J., Cheng, G., Lopez, M., & Kalyanaraman, B. (2017) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00042 · Cited by 1,683
Oxidative stress, mitochondrial damage and neurodegenerative diseases.
Guo, C., Sun, L., Chen, X., & Zhang, D. (2013) · PubMed Central · doi:10.3969/j.issn.1673-5374.2013.21.009 · Cited by 1,367
Metals, oxidative stress and neurodegeneration: A focus on iron, manganese and mercury
Farina, M., Ávila, D. S., da Rocha, J. B. T., & Aschner, M. (2012) · Neurochemistry International · doi:10.1016/j.neuint.2012.12.006 · Cited by 578
Physicochemical Properties of Cells and Their Effects on Intrinsically Disordered Proteins (IDPs)
Theillet, F., Binolfi, A., Frembgen-Kesner, T., Hingorani, K. S., Sarkar, M., Kyne, C., Li, C., Crowley, P. B., Gierasch, L. M., Pielak, G. J., et al. (2014) · Chemical Reviews · doi:10.1021/cr400695p · Cited by 521
The Role of Dopamine and Its Dysfunction as a Consequence of Oxidative Stress
Olguı́n, H. J., Guzmán, D. C., García, E. H., & Mejía, G. B. (2015) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/9730467 · Cited by 514
Glutathione metabolism and Parkinson's disease
Smeyne, M., & Smeyne, R. J. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.05.001 · Cited by 436
The role of Nrf2 signaling in counteracting neurodegenerative diseases
Dinkova‐Kostova, A. T., Kostov, R. V., & Kazantsev, A. G. (2018) · The FEBS Journal · doi:10.1111/febs.14379 · Cited by 342
Natural product-derived pharmacological modulators of Nrf2/ARE pathway for chronic diseases
Kumar, H., Kim, I., More, S. V., Kim, B.-W., & Choi, D. (2013) · Natural Product Reports · doi:10.1039/c3np70065h · Cited by 338
Self-citationA Review on Free Radicals and Antioxidants
Alkadi, H. (2018) · Infectious Disorders - Drug Targets · doi:10.2174/1871526518666180628124323 · Cited by 392
Role of Nrf2 and Its Activators in Respiratory Diseases
Liu, Q., Gao, Y., & Ci, X. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/7090534 · Cited by 280
Pinto, A., Bonucci, A., Maggi, E., Corsi, M., & Businaro, R. (2018) · Antioxidants · doi:10.3390/antiox7050063 · Cited by 269
Clemente‐Suárez, V. J., Redondo-Flórez, L., Beltrán-Velasco, A. I., Ramos‐Campo, D. J., Belinchón-deMiguel, P., Martínez‐Guardado, I., Dalamitros, A. A., Sepulveda, R. A. Y., Martín-Rodríguez, A., & Tornero-Aguilera, J. F. (2023) · Biomedicines · doi:10.3390/biomedicines11092488 · Cited by 251
The impact of reactive oxygen species and genetic mitochondrial mutations in Parkinson's disease
Zuo, L., & Motherwell, M. S. (2013) · Gene · doi:10.1016/j.gene.2013.07.085 · Cited by 200
Hypoxia Inducible Factor Pathway and Physiological Adaptation: A Cell Survival Pathway?
Kumar, H., & Choi, D. (2015) · Mediators of Inflammation · doi:10.1155/2015/584758 · Cited by 192
Self-citationOxidative stress and neurodegeneration: the involvement of iron
Carocci, A., Catalano, A. A., Sinicropi, M. S., & Genchi, G. (2018) · BioMetals · doi:10.1007/s10534-018-0126-2 · Cited by 188
Neuroprotective Activities of Curcumin in Parkinson’s Disease: A Review of the Literature
Nebrisi, E. E. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222011248 · Cited by 165
Mitochondrial Oxidative Stress and “Mito-Inflammation”: Actors in the Diseases
Patergnani, S., Bouhamida, E., Leo, S., Pinton, P., & Rimessi, A. (2021) · Biomedicines · doi:10.3390/biomedicines9020216 · Cited by 178
Hernández‐Aguilera, A., Rull, A., Rodríguez‐Gallego, E., Riera-Borrull, M., Luciano‐Mateo, F., Camps, J., Menéndez, J. A., & Joven, J. (2013) · Mediators of Inflammation · doi:10.1155/2013/135698 · Cited by 167
Tan, S. H., Karri, V., Tay, N. W. R., Chang, K. H., Ah, H. Y., Ng, P. Q., Ho, H. S., Keh, H. W., & Candasamy, M. (2019) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.12.101 · Cited by 151
Protective Mechanisms of Flavonoids in Parkinson’s Disease
Magalingam, K. B., Radhakrishnan, A. K., & Haleagrahara, N. (2015) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2015/314560 · Cited by 144
Brain Renin–Angiotensin System at the Intersect of Physical and Cognitive Frailty
Cosarderelioglu, C., Nidadavolu, L. S., George, C. J., Oh, E. S., Bennett, D. A., Walston, J. D., & Abadir, P. M. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.586314 · Cited by 134
Thioredoxin-1 Rescues MPP+/MPTP-Induced Ferroptosis by Increasing Glutathione Peroxidase 4
Bai, L., Yan, F., Deng, R., Gu, R., Zhang, X., & Bai, J. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02320-1 · Cited by 130
Gastrodin Protects Apoptotic Dopaminergic Neurons in a Toxin-Induced Parkinson’s Disease Model
Kumar, H., Kim, I., More, S. V., Kim, B.-W., Bahk, Y.-Y., & Choi, D. (2013) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2013/514095 · Cited by 129
Self-citationMilani, P., Ambrosi, G., Gammoh, O. S., Blandini, F., & Cereda, C. (2013) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2013/836760 · Cited by 128
Ganesan, P., Ko, H.-M., Kim, I., & Choi, D. (2015) · International Journal of Nanomedicine · doi:10.2147/ijn.s93918 · Cited by 119
Self-citationBehavioral Tests in Neurotoxin-Induced Animal Models of Parkinson’s Disease
Prasad, E. M., & Hung, S. (2020) · Antioxidants · doi:10.3390/antiox9101007 · Cited by 125
Current Therapies in Clinical Trials of Parkinson’s Disease: A 2021 Update
Prasad, E. M., & Hung, S. (2021) · Pharmaceuticals · doi:10.3390/ph14080717 · Cited by 118
Balakrishnan, R., Azam, S., Cho, D.-Y., Su-Kim, I., & Choi, D. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/6680935 · Cited by 117
Self-citationKumar, H., Ropper, A. E., Lee, S., & Han, I. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-9910-6 · Cited by 104
Self-citationAhmad, S., Ullah, F., Sadiq, A., Ayaz, M., Imran, M., Ali, I., Zeb, A., Ullah, F., & Shah, M. R. (2016) · BMC Complementary and Alternative Medicine · doi:10.1186/s12906-016-0998-z · Cited by 100
Beneficial Effects of Spirulina Consumption on Brain Health
Trotta, T., Porro, C., Cianciulli, A., & Panaro, M. A. (2022) · Nutrients · doi:10.3390/nu14030676 · Cited by 98
Introduction: Oxidation and Inflammation, A Molecular Link Between Non-communicable Diseases
Camps, J., & García‐Heredia, A. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-07320-0_1 · Cited by 92
Glutathione as a Biomarker in Parkinson’s Disease: Associations with Aging and Disease Severity
Mischley, L. K., Standish, L. J., Weiss, N. S., Padowski, J. M., Kavanagh, T. J., White, C. C., & Rosenfeld, M. E. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/9409363 · Cited by 91
Denzer, I., Münch, G. W., & Friedland, K. (2015) · Pharmacological Research · doi:10.1016/j.phrs.2015.11.019 · Cited by 91
Karvandi, M. S., Hesari, F. S., Aref, A. R., & Mahdavi, M. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1105247 · Cited by 97
Singh, A.-K., Yadav, D., Sharma, N., & Jin, J. (2021) · Pharmaceuticals · doi:10.3390/ph14060586 · Cited by 97
Karthivashan, G., Fard, M. T., Arulselvan, P., Abas, F., & Fakurazi, S. (2013) · Journal of Food Science · doi:10.1111/1750-3841.12233 · Cited by 83
Reactive oxygen species (ROS): sources, generation, disease pathophysiology, and antioxidants
Ansari, W. A., Srivastava, K., Nasibullah, M., & Khan, M. F. (2025) · Discover Chemistry. · doi:10.1007/s44371-025-00275-z · Cited by 97
Alhakmani, F., Khan, S. A., & Ahmad, A. (2014) · Asian Pacific Journal of Tropical Biomedicine · doi:10.12980/apjtb.4.2014apjtb-2014-0273 · Cited by 76
Ventral posterior substantia nigra iron increases over 3 years in Parkinson's disease
Bergsland, N., Zivadinov, R., Schweser, F., Hagemeier, J., Lichter, D. G., & Guttuso, T. J. (2019) · Movement Disorders · doi:10.1002/mds.27730 · Cited by 75
Neuroprotective effect of naringenin against MPTP-induced oxidative stress
Sugumar, M., Sevanan, M., & Sekar, S. (2018) · International Journal of Neuroscience · doi:10.1080/00207454.2018.1545772 · Cited by 56
Riederer, P. F., Nagatsu, T., Youdim, M. B. H., Wulf, M., Dijkstra, J. M., & Sian‐Hülsmann, J. (2023) · Journal of Neural Transmission · doi:10.1007/s00702-023-02630-9 · Cited by 71
Adedeji, H. A., Ishola, I. O., & Adeyemi, O. O. (2013) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2013.10.014 · Cited by 68
Kim, Y.-S., Hwang, J.-W., Sung, S.-H., Jeon, Y., Jeong, J.-H., Jeon, B.-T., Moon, S.-H., & Park, P. (2014) · Food Chemistry · doi:10.1016/j.foodchem.2014.07.106 · Cited by 67
Epigenetic Changes and Its Intervention in Age-Related Neurodegenerative Diseases
Murshid, N. M., Lubis, F. A., & Makpol, S. (2020) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-00979-z · Cited by 69
A Brief Review on the Neuroprotective Mechanisms of Vitexin
Lima, L. K. F., Pereira, S. K. S., Sousa, R. D. S., Santos, F. P. D. S., Nascimento, A. D. S., Feitosa, C. M., Figuerêdo, J. D. S., Cavalcante, A. D. N., Araújo, E. C. D. C., & Rai, M. (2018) · BioMed Research International · doi:10.1155/2018/4785089 · Cited by 61
The anti-aging mechanism of ginsenosides with medicine and food homology
Tian, T., Ko, C.-N., Luo, W., Li, D., & Yang, C. (2023) · Food & Function · doi:10.1039/d3fo02580b · Cited by 62
Venuprasad, M. P., Kandikattu, H. K., & Khanum, F. (2013) · Neurochemical Research · doi:10.1007/s11064-013-1128-7 · Cited by 59
Bi, Y., Qu, P.-C., Wang, Q., Li, Z., Liu, H., Luo, R., Chen, X.-Q., Ba, Y., Wu, X., & Yang, H. (2015) · Pharmaceutical Biology · doi:10.3109/13880209.2014.991835 · Cited by 54
Redox Homeostasis and Prospects for Therapeutic Targeting in Neurodegenerative Disorders
Akanji, M. A., Rotimi, D. E., Elebiyo, T. C., Awakan, O. J., & Adeyemı, O. S. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/9971885 · Cited by 55
Chobot, V., Hadaček, F., Weckwerth, W., & Kubicová, L. (2015) · Journal of Organometallic Chemistry · doi:10.1016/j.jorganchem.2015.01.005 · Cited by 51
González‐Burgos, E., Fernández‐Moriano, C., Lozano, R., Iglesias, I., & Gómez-Serranillos, M. P. (2017) · Food and Chemical Toxicology · doi:10.1016/j.fct.2017.08.013 · Cited by 51
Dong, Y., Zeng, C., Okyere, S. K., Chen, Z., & Hu, Y. (2020) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2020.126680 · Cited by 50
Mitochondrial dynamics in aging and disease
Bereiter-Hahn, J. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-394625-6.00004-0 · Cited by 48
Uranga, R. M., & Salvador, G. A. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/2850341 · Cited by 48
Inhibitory activities of grape bioactive compounds against enzymes linked with human diseases
Dwibedi, V., Jain, S., Singhal, D., Mittal, A., Rath, S. K., & Saxena, S. (2022) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-022-11801-9 · Cited by 50
Muscle Weakness in Rheumatoid Arthritis: The Role of Ca 2+ and Free Radical Signaling
Yamada, T., Steinz, M. M., Kenne, E. M., & Lanner, J. T. (2017) · EBioMedicine · doi:10.1016/j.ebiom.2017.07.023 · Cited by 47
Free radical biology in neurological manifestations: mechanisms to therapeutics interventions
Tripathi, R. S., Gupta, R. V., Sahu, M., Srivastava, D., Das, A., Ambasta, R. K., & Kumar, P. (2021) · Environmental Science and Pollution Research · doi:10.1007/s11356-021-16693-2 · Cited by 54
Zhong, J., Xie, J., Xiao, J., Li, D., Xu, B., Wang, X., Wen, H., Zhou, Z., Cheng, Y., Xu, J., et al. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.02.027 · Cited by 46
Lim, H.-W., Kumar, H., Kim, B.-W., More, S. V., Kim, I.-W., Park, J.-I., Park, S., Kim, S., & Choi, D. (2014) · Food and Chemical Toxicology · doi:10.1016/j.fct.2014.07.018 · Cited by 45
Self-citationThe need to incorporate aged animals into the preclinical modeling of neurological conditions
Sun, M., McDonald, S. J., Brady, R. D., Collins‐Praino, L. E., Yamakawa, G. R., Monif, M., O'Brien, T. J., CLOUD, G. C., Sobey, C. G., Mychasiuk, R., et al. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.12.027 · Cited by 44
The Body, the Brain, the Environment, and Parkinson’s Disease
Dorsey, E. R., Miranda, B. R. D., Horsager, J., & Borghammer, P. (2024) · Journal of Parkinson s Disease · doi:10.3233/jpd-240019 · Cited by 48
Selective Neuronal Death in Neurodegenerative Diseases: The Ongoing Mystery.
Subramaniam, S. (2019) · Europe PMC (PubMed Central) · Cited by 40
Morales, L. G. F., Correa‐Basurto, J., & Rosales‐Hernández, M. C. (2021) · Antioxidants · doi:10.3390/antiox10020218 · Cited by 39
Ianniello, R. G., Ricciardi, A., Parente, E., Tramutola, A., Reale, A., & Zotta, T. (2014) · LWT · doi:10.1016/j.lwt.2014.10.020 · Cited by 37
Wang, Z., Zhang, Y.-H., Guo, C., Gao, H., Zhong, M., Huang, T., Liu, N., Guo, R.-F., Lan, T., Zhang, W., et al. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00009 · Cited by 37
Bar‐Am, O., Amit, T., Youdim, M. B. H., & Weinreb, O. (2015) · Journal of Neural Transmission · doi:10.1007/s00702-015-1395-3 · Cited by 37
El-Sayed, E. K., Ahmed, A., Morsy, E. M. E., & Nofal, S. (2018) · Human & Experimental Toxicology · doi:10.1177/0960327118788139 · Cited by 36
Liu, C., Zhang, C., Lo, S. Q., Ang, S. T., Chew, K. C. M., Yu, D., Chai, B. H., Tan, B. C. Y., Tsang, F., Tai, Y. K., et al. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.3262-17.2018 · Cited by 34
Li, L., Jiang, Y., Liu, Y., Li, H., Bari, A., Ullah, R., & Xue, J. (2019) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2019.111657 · Cited by 33
Antioxidant activity and total phenolic compound content of certain medicinal plants
(2014) · International Journal of Biosciences (IJB) · doi:10.12692/ijb/5.9.213-222 · Cited by 33
Li, K.-R., Wu, A., Tang, Y., He, X., Yu, C., Wu, J., Hu, G., & Yu, L. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02944-x · Cited by 34
Zhang, X., Chu, X., Gong, X., Zhou, H., & Cai, C. (2019) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.14808 · Cited by 32
Kalyanaraman, B. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101665 · Cited by 31
Kaur, M., & Aran, K. R. (2025) · Metabolic Brain Disease · doi:10.1007/s11011-025-01552-7 · Cited by 31
Perindopril May Improve the Hippocampal Reduced Glutathione Content in Rats
Mashhoody, T., Rastegar, K., & Zal, F. (2013) · Europe PMC (PubMed Central) · doi:10.5681/apb.2014.023 · Cited by 30
Rajendran, R., Raghavan, R. P., Al-Sehemi, A. G., Uddin, M. S., Aleya, L., & Mathew, B. (2022) · Environmental Science and Pollution Research · doi:10.1007/s11356-021-17931-3 · Cited by 29
Sridharan, S., Mohankumar, K., Jeepipalli, S. P. K., Sankaramourthy, D., Ronsard, L., Kavimani, S., Manivasagam, T., Raja, K., Chandra, V. K., & Sadras, S. R. (2015) · NeuroToxicology · doi:10.1016/j.neuro.2015.10.012 · Cited by 29
Wu, Q., Wang, M., Chen, W., Wang, K., & Wang, Y. (2021) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.22949 · Cited by 28
Gage, M., Putra, M. R. E., Wachter, L., Dishman, K., Gard, M., Gomez-Estrada, C., & Thippeswamy, T. (2021) · Antioxidants · doi:10.3390/antiox11010061 · Cited by 28
Garcia, I. J. P., Kinoshita, P. F., Silva, L. N. D. E., Busch, M., Atella, G. C., Scavone, C., Cortes, V. F., Barbosa, L. A., & Santos, H. D. L. (2018) · Journal of Cellular Biochemistry · doi:10.1002/jcb.27693 · Cited by 28
Chen, J., Singh, N. N., Tay, H., & Walczyk, T. (2014) · Metallomics · doi:10.1039/c4mt00054d · Cited by 27
Age-Dependent Effects of ELF-MF on Oxidative Stress in the Brain of Mongolian Gerbils
Selaković, V., Balind, S. R., Radenović, L., Prolić, Z., & Petković, B. B. (2013) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-012-9498-z · Cited by 25
Do we age because we have mitochondria?
Bereiter‐Hahn, J. (2013) · PROTOPLASMA · doi:10.1007/s00709-013-0515-x · Cited by 25
Implication of Paraprobiotics in Age-Associated Gut Dysbiosis and Neurodegenerative Diseases
Rahman, Z., & Dandekar, M. P. (2022) · NeuroMolecular Medicine · doi:10.1007/s12017-022-08722-1 · Cited by 25
Ouabain attenuates the oxidative stress induced by lipopolysaccharides in the cerebellum of rats
Garcia, I. J. P., Kinoshita, P. F., Braga, Í. D. O., Parreira, G. M., Mignaco, J. A., Scavone, C., Barbosa, L. A., & Santos, H. D. L. (2017) · Journal of Cellular Biochemistry · doi:10.1002/jcb.26377 · Cited by 24
Chen, N.-Y., Liu, C., Wei, L., Ding, Y., Bian, Z., Huang, L., Huang, H., Yu, K., Chen, S., Sun, Y., et al. (2017) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2017/4757520 · Cited by 24
Selective GSK3β Inhibition Mediates an Nrf2-Independent Anti-inflammatory Microglial Response
Yousef, M. H., Salama, M., El‐Fawal, H. A. N., & Abdelnaser, A. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02923-2 · Cited by 23
Kaur, S., Sehrawat, A., Mastana, S. S., Kandimalla, R. J. L., Sharma, P. K., Bhatti, G. K., & Bhatti, J. S. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.121995 · Cited by 23
Tang, Y., Su, G., Li, N., Li, W., Chen, G., Chen, R., Zhou, D., & Hou, Y. (2018) · Journal of Natural Medicines · doi:10.1007/s11418-018-1266-y · Cited by 23
Chowdhury, S., & Kumar, S. (2020) · Journal of Food Biochemistry · doi:10.1111/jfbc.13571 · Cited by 22
Yang, L., Cheng, Y. Z., Sun, Y., Xuan, Y., Niu, J., Guan, J., Rong, Y., Jia, Y., Zhuang, Z., Yan, G., et al. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.792778 · Cited by 24
Wang, S., Song, H., Yin, C., & Huo, F. (2025) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2025.216940 · Cited by 21
Wang, Y., Zhang, T., Zhao, H., Qi, C., Ji, X., Yan, H., Cui, R., Zhang, G., Kang, Y., & Shi, G. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/6695613 · Cited by 20
Marchetti, B., Giachino, C., Tirolo, C., & Serapide, M. F. (2022) · Aging Cell · doi:10.1111/acel.13575 · Cited by 22
Cui, R., Kang, Y., Wang, L., Li, S., Ji, X., Yan, W., Zhang, G., Cui, H., & Shi, G. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00172 · Cited by 22
Bhatia, G., Dhuna, V., Dhuna, K., Kaur, M., & Singh, J. V. (2017) · Chinese Journal of Natural Medicines · doi:10.1016/s1875-5364(18)30017-7 · Cited by 21
Wang, S., Li, N., Zou, H.-X., & Wu, M. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.12.021 · Cited by 21
Singh, S., Mishra, A., Tiwari, V., & Shukla, S. (2019) · Behavioural Pharmacology · doi:10.1097/fbp.0000000000000516 · Cited by 21
Wang, Y., Kang, Y., Qi, C., Zhang, T., Zhao, H., Ji, X., Yan, W., Huang, Y., Cui, R., Zhang, G., et al. (2020) · Aging · doi:10.18632/aging.104155 · Cited by 23
Metadata
- Authors
- Kumar, H., Lim, H.-W., More, S. V., Kim, B.-W., Koppula, S., Kim, I. S., & Choi, D.-K.
- Affiliations
- Konkuk University (KR)
- Corresponding author
- Choi, Dong-Kug
- Venue
- International Journal of Molecular Sciences
- Publisher
- MDPI AG
- Published
- 2012-08-21
- Volume
- 13
- Issue
- 8
- Pages
- 10478-10504
- ISSN
- 1422-0067 (ISSN-L)
- PMC
- PMC3431873
- OpenAlex
- W2138898590
- Cited by
- 212
- References
- 220
- Citations by year
- 2026: 4 · 2025: 15 · 2024: 9 · 2023: 16 · 2022: 29 · 2021: 18 · 2020: 18 · 2019: 15 · 2018: 17 · 2017: 14 · 2016: 8 · 2015: 16 · 2014: 11 · 2013: 21 · 2012: 1
- FWCI
- 2.25
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- International Journal of Molecular Sciences (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Funders
- Konkuk University
- Ministry of Knowledge Economy
- Topics
- Health Sciences › Medicine › Clinical Neurology › Parkinson's Disease Mechanisms and Treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Receptors and Signaling
- Keywords
- free radicals, Parkinson's disease, brain aging, oxidative stress, oxidative damage, dopaminergic neurons, mitochondrial dysfunction, alpha-synuclein aggregation, glial activation, calcium signaling, free iron, NF-κB, Nrf2, glycogen synthase kinase-3β, mitogen-activated protein kinase, superoxide dismutase, catalase, glutathione
- MeSH terms
- Aging, Animals, Brain, Free Radicals, Humans, Oxidation-Reduction, Parkinson Disease, Oxidative Stress
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review