The DOI matches its Crossref record; 378 of the 379 references it cites were found in a registry or an index.
Reactive Oxygen Species in Metabolic and Inflammatory Signaling
Open accessAbstract
Reactive oxygen species (ROS) are well known for their role in mediating both physiological and pathophysiological signal transduction. Enzymes and subcellular compartments that typically produce ROS are associated with metabolic regulation, and diseases associated with metabolic dysfunction may be influenced by changes in redox balance. In this review, we summarize the current literature surrounding ROS and their role in metabolic and inflammatory regulation, focusing on ROS signal transduction and its relationship to disease progression. In particular, we examine ROS production in compartments such as the cytoplasm, mitochondria, peroxisome, and endoplasmic reticulum and discuss how ROS influence metabolic processes such as proteasome function, autophagy, and general inflammatory signaling. We also summarize and highlight the role of ROS in the regulation metabolic/inflammatory diseases including atherosclerosis, diabetes mellitus, and stroke. In order to develop therapies that target oxidative signaling, it is vital to understand the balance ROS signaling plays in both physiology and pathophysiology, and how manipulation of this balance and the identity of the ROS may influence cellular and tissue homeostasis. An increased understanding of specific sources of ROS production and an appreciation for how ROS influence cellular metabolism may help guide us in the effort to treat cardiovascular diseases.
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?
The cited source says what the claim attributes to it.
In the citing paper
“ROS act as one of the key molecules that regulate inflammatory signaling [52].”
From A tailored bioactive 3D porous poly(lactic-acid)-exosome scaffold with osteo-immunomodulatory and osteogenic differentiation properties (2022) · cites this paper as [52]
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
4 retracted
Mitochondrial Autophagy Is an HIF-1-dependent Adaptive Metabolic Response to Hypoxia
Zhang, H., Bosch-Marce, M., Shimoda, L. A., Tan, Y. S., Baek, J. H., Wesley, J. B., Gonzalez, F. J., & Semenza, G. L. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m800102200 · Cited by 1,601
RetractedMartinez, J., Malireddi, R. K. S., Lu, Q., Cunha, L. D., Pelletier, S., Gingras, S., Orchard, R., Guan, J.-L., Tan, H., Peng, J., et al. (2015) · Nature Cell Biology · doi:10.1038/ncb3192 · Cited by 758
RetractedXu, J., Wu, Y., Song, P., Zhang, M., Wang, S., & Zou, M. (2007) · Circulation · doi:10.1161/circulationaha.106.684795 · Cited by 193
RetractedZou, M., Hou, X., Shi, C., Kirkpatick, S., Liu, F., Goldman, M. H., & Cohen, R. A. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m300215200 · Cited by 168
RetractedRepertoires of Autophagy in the Pathogenesis of Ocular Diseases
Li, Y., Jiang, Q. L., Cao, G.-F., Yao, J., & Yan, B. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000373980 · Cited by 16,351
How mitochondria produce reactive oxygen species
Murphy, M. P. (2009) · Biochemical Journal · doi:10.1042/bj20081386 · Cited by 8,207
Autophagy in the Pathogenesis of Disease
Levine, B., & Kroemer, G. (2008) · Cell · doi:10.1016/j.cell.2007.12.018 · Cited by 7,069
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
Ayala, A., Muñoz, M., & Argüelles, S. (2014) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2014/360438 · Cited by 6,837
Xu, H., Barnes, G. T., Yang, Q., Tan, G., Yang, D., Chou, C. J., Sole, J., Nichols, A., Ross, J. S., Tartaglia, L. A., et al. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200319451 · Cited by 6,760
Flagged first, then by citations
1 of the 379 references couldn’t be matched to a known paper.
Research works printed but not linked: 2
- 10.1172/JCI19451 · DOI · Paper page
- 10.1172/JCI11927 · DOI · Paper page
Cited by
Sorted by citations
Items 101–200 of 1,000
Muñoz, M., López‐Oliva, M. E., Rodríguez, C., Martínez, M. P., Medina, J. S., Sánchez, A., Climent, B., Benedito, S., García‐Sacristán, A., Rivera, L., et al. (2019) · Redox Biology · doi:10.1016/j.redox.2019.101330 · Cited by 143
Patil, P., Russo, K. A., McCune, J. T., Pollins, A. C., Cottam, M. A., Dollinger, B. R., DeJulius, C. R., Gupta, M. K., d’Arcy, R., Colazo, J. M., et al. (2022) · Science Translational Medicine · doi:10.1126/scitranslmed.abm6586 · Cited by 144
Mild Hyperthermia-Assisted ROS Scavenging Hydrogels Achieve Diabetic Wound Healing
Qi, X., Tong, X., You, S., Mao, R., Cai, E., Pan, W., Zhang, C., Hu, R., & Shen, J. (2022) · ACS Macro Letters · doi:10.1021/acsmacrolett.2c00290 · Cited by 142
Huang, Q., Yang, Y., Zhu, Y., Chen, Q., Zhao, T., Xiao, Z., Wang, M., Song, X., Jiang, Y., Yang, Y., et al. (2023) · Small · doi:10.1002/smll.202207350 · Cited by 141
Microvascular and lymphatic dysfunction in HFpEF and its associated comorbidities
Cuijpers, I., Simmonds, S. J., van Bilsen, M., Czarnowska, E., González, A., Heymans, S. R. B., Kuhn, A.-R., Mulder, P. G. H., Ratajska, A., Jones, E. A. V., et al. (2020) · Basic Research in Cardiology · doi:10.1007/s00395-020-0798-y · Cited by 144
Activatable NIR-II organic fluorescent probes for bioimaging
Zhang, X., Li, S., Ma, H., Wang, H., Zhang, X., & Zhang, X. (2022) · Theranostics · doi:10.7150/thno.71359 · Cited by 141
Eastman, C. L., D’Ambrosio, R., & Ganesh, T. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.107907 · Cited by 140
Ma, Y., Zhao, J., Cheng, L., Li, C., Yan, X., Deng, Z., Zhang, Y., Liang, J., Liu, C., & Zhang, M. (2023) · Carbon · doi:10.1016/j.carbon.2023.01.006 · Cited by 137
Crosstalk Between the Oxidative Stress and Glia Cells After Stroke: From Mechanism to Therapies
Zhu, G., Wang, X., Chen, L., Lenahan, C., Fu, Z., Fang, Y., & Yu, W. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.852416 · Cited by 138
Microglial metabolic disturbances and neuroinflammation in cerebral infarction
Takeda, H., Yamaguchi, T., Yano, H., & Tanaka, J. (2020) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2020.11.007 · Cited by 133
Metabolic Spectrum of Liver Failure in Type 2 Diabetes and Obesity: From NAFLD to NASH to HCC
Kim, H.-M., Lee, D. S., An, T. H., Park, H., Kim, W. K., Bae, K., & Oh, K. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094495 · Cited by 133
Luna-Marco, C., de Marañon, A. M., Hermo-Argibay, A., Rodriguez-Hernandez, Y., Hermenejildo, J., Fernández-Reyes, M., Apostolova, N., Vila, J. M., Solá, E., Morillas, C., et al. (2023) · Redox Biology · doi:10.1016/j.redox.2023.102849 · Cited by 136
Molecular Interactions Between Reactive Oxygen Species and Autophagy in Kidney Disease
Kaushal, G. P., Chandrashekar, K., & Juncos, L. A. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20153791 · Cited by 130
Malko, P., & Jiang, L. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101755 · Cited by 128
Oxidative Stress and Redox Signaling in the Pathophysiology of Liver Diseases
Mooli, R. G. R., Mukhi, D., & Ramakrishnan, S. K. (2022) · Comprehensive physiology · doi:10.1002/cphy.c200021 · Cited by 134
Cell death and ischemia-reperfusion injury in lung transplantation
Capuzzimati, M., Hough, O., & Liu, M. (2022) · The Journal of Heart and Lung Transplantation · doi:10.1016/j.healun.2022.05.013 · Cited by 135
Canugovi, C., Stevenson, M., Vendrov, A. E., Hayami, T., Robidoux, J., Xiao, H., Zhang, Y., Eitzman, D. T., Runge, M. S., & Madamanchi, N. R. (2019) · Redox Biology · doi:10.1016/j.redox.2019.101288 · Cited by 126
mTOR-Dependent Oxidative Stress Regulates oxLDL-Induced Trained Innate Immunity in Human Monocytes
Sohrabi, Y., Lagache, S. M. M., Schnack, L., Godfrey, R., Kahles, F., Bruemmer, D., Waltenberger, J. L., & Findeisen, H. M. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2018.03155 · Cited by 122
Drosophila macrophages switch to aerobic glycolysis to mount effective antibacterial defense
Krejčová, G., Danielová, A., Nedbalová, P., Kazek, M., Strych, L., Chawla, G., Tennessen, J. M., Lieskovská, J., Jindra, M., Doležal, T., et al. (2019) · eLife · doi:10.7554/elife.50414 · Cited by 124
Molecular Mechanisms of Muscle Fatigue
Constantin‐Teodosiu, D., & Constantin, D. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111587 · Cited by 134
N-acetyl cysteine-loaded graphene oxide-collagen hybrid membrane for scarless wound healing
Li, J., Zhou, C., Luo, C., Qian, B., Liu, S., Zeng, Y., Hou, J., Deng, B., Sun, Y., Yang, J., et al. (2019) · Theranostics · doi:10.7150/thno.34480 · Cited by 117
Vitamin D and Microbiota: Is There a Link with Allergies?
Murdaca, G., Gerosa, A., Paladin, F., Petrocchi, L., Banchero, S., & Gangemi, S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22084288 · Cited by 121
Reactive oxygen species (ROS) in cancer: from mechanism to therapeutic implications
Akter, S., Madhuvilakku, R., Kar, A. K., Nila, I. S., Liu, P., Inuzuka, H., Wei, W., & Hong, Y. (2026) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-026-02583-x · Cited by 135
Immune aging in diabetes and its implications in wound healing
Moura, J., Madureira, P., Leal, E. C., Fonseca, A. C., & Carvalho, E. (2019) · Clinical Immunology · doi:10.1016/j.clim.2019.02.002 · Cited by 122
Cao, P., Wu, S., Wu, T., Deng, Y., Zhang, Q., Wang, K., & Zhang, Y. (2020) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2020.116346 · Cited by 117
Cellular and molecular pathophysiology in the progression of Parkinson’s disease
Zaman, V., Shields, D. C., Shams, R., Drasites, K. P., Matzelle, D. D., Haque, A., & Banik, N. L. (2021) · Metabolic Brain Disease · doi:10.1007/s11011-021-00689-5 · Cited by 119
Oxidative stress: fundamentals and advances in quantification techniques
Krishnamurthy, H. K., Pereira, M., Rajavelu, I., Jayaraman, V., Krishna, K., Wang, T., Bei, K., & Rajasekaran, J. J. (2024) · Frontiers in Chemistry · doi:10.3389/fchem.2024.1470458 · Cited by 127
Zhang, L., Guo, Z., Wang, Y., Geng, J., & Han, S. (2019) · Drug Development Research · doi:10.1002/ddr.21495 · Cited by 114
STING, the Endoplasmic Reticulum, and Mitochondria: Is Three a Crowd or a Conversation?
Smith, J. A. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.611347 · Cited by 116
Type I Interferon Production of Plasmacytoid Dendritic Cells under Control
Bencze, D., Fekete, T., & Pázmándi, K. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22084190 · Cited by 117
Krawczyk, M., Burzyńska-Pędziwiatr, I., Woźniak, L. A., & Bukowiecka‐Matusiak, M. (2023) · Biomolecules · doi:10.3390/biom13091402 · Cited by 120
González, A., Huerta-Salgado, C., Orozco-Aguilar, J., Aguirre, F. S., Tacchi, F., Simón, F., & Cabello‐Verrugio, C. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/1617805 · Cited by 120
Purinergic signaling in the modulation of redox biology
Savio, L. E. B., Leite-Aguiar, R., Alves, V. S., Coutinho‐Silva, R., & Wyse, Â. T. D. S. (2021) · Redox Biology · doi:10.1016/j.redox.2021.102137 · Cited by 115
Mechanisms of obesity-induced metabolic and vascular dysfunctions
Caldwell, R. W. (2019) · Frontiers in bioscience · doi:10.2741/4758 · Cited by 112
Advances in Therapies to Treat Neonatal Hypoxic-Ischemic Encephalopathy
Ranjan, A. K., & Gulati, A. (2023) · Journal of Clinical Medicine · doi:10.3390/jcm12206653 · Cited by 117
Nutraceuticals for the Treatment of Diabetic Retinopathy
Rossino, M. G., & Casini, G. (2019) · Nutrients · doi:10.3390/nu11040771 · Cited by 113
Role of oxidative stress in calcific aortic valve disease and its therapeutic implications
Greenberg, H. Z. E., Zhao, G., Shah, A. M., & Zhang, M. (2021) · Cardiovascular Research · doi:10.1093/cvr/cvab142 · Cited by 115
Natural hydrogel dressings in wound care: Design, advances, and perspectives
Liang, X., Huang, C., Liu, H., Chen, H., Shou, J., Cheng, H., & Liu, G. (2023) · Chinese Chemical Letters · doi:10.1016/j.cclet.2023.109442 · Cited by 110
Diabetic Wound Repair: From Mechanism to Therapeutic Opportunities
Wang, R., Gu, S., Kim, Y. H., Lee, A., Lin, H., & Jiang, D. (2025) · MedComm · doi:10.1002/mco2.70406 · Cited by 118
Knock, G. A. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.09.029 · Cited by 110
Uzhachenko, R. V., Bharti, V., Ouyang, Z., Blevins, A., Mont, S., Saleh, N., Lawrence, H. A., Shen, C., Chen, S., Ayers, G. D., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108944 · Cited by 109
Endogenous/exogenous stimuli‐responsive smart hydrogels for diabetic wound healing
Khattak, S., Ullah, I., Sohail, M. F., Akbar, M. U., Rauf, M. A., Ullah, S., Shen, J., & Xu, H. (2024) · Aggregate · doi:10.1002/agt2.688 · Cited by 110
Role of Oxidative Stress in Liver Disorders
Conde de la Rosa, L., Goicoechea, L., Torres, S., Garcia-Ruiz, C., & Fernandez-Checa, J. C. (2022) · Livers · doi:10.3390/livers2040023 · Cited by 107
Reactive Oxygen Species: A Crosslink between Plant and Human Eukaryotic Cell Systems
Guo, W., Xing, Y., Luo, X., Li, F., Ren, M., & Liang, Y. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241713052 · Cited by 114
Xie, Y., Xiao, S., Huang, L., Guo, J., Bai, M., Gao, Y., Zhou, H., Qiu, L., Cheng, C., & Han, X. (2023) · ACS Nano · doi:10.1021/acsnano.3c04328 · Cited by 107
Cao, B., Qin, J., Pan, B., Qazi, I. H., Ye, J., Fang, Y., & Zhou, G. (2022) · Cells · doi:10.3390/cells11223573 · Cited by 112
Ultrasmall Antioxidant Cerium Oxide Nanoparticles for Regulation of Acute Inflammation
Kim, J., Hong, G., Mazaleuskaya, L., Hsu, J. C., Rosario‐Berríos, D. N., Großer, T., Cho-Park, P. F., & Cormode, D. P. (2021) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.1c16126 · Cited by 105
Baek, S., Park, T., Kang, M.-G., & Park, D. (2020) · Molecules · doi:10.3390/molecules25184089 · Cited by 103
Redox Role of ROS and Inflammation in Pulmonary Diseases
Zuo, L., & Wijegunawardana, D. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-68748-9_11 · Cited by 110
Oxygen-Vacancy Engineering of Cerium-Oxide Nanoparticles for Antioxidant Activity
Gunawan, C., Lord, M. S., Lovell, E. C., Wong, R. J., Jung, M., Oscar, D., Mann, R., & Amal, R. (2019) · ACS Omega · doi:10.1021/acsomega.9b00521 · Cited by 104
Focusing on mitochondria in the brain: from biology to therapeutics
Song, N., Mei, S., Wang, X.-X., Hu, G., & Lu, M. (2024) · Translational Neurodegeneration · doi:10.1186/s40035-024-00409-w · Cited by 111
Oxidative Stress at the Crossroads of Aging, Stroke and Depression
Shao, A., Lin, D., Wang, L., Tu, S., Lenahan, C., & Zhang, J. (2020) · Aging and Disease · doi:10.14336/ad.2020.0225 · Cited by 101
Pharmacological and Therapeutic Applications of Esculetin
Garg, S. S., Gupta, J., Sahu, D., & Liu, C.-J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232012643 · Cited by 101
Understanding Anthracycline Cardiotoxicity From Mitochondrial Aspect
Huang, J., Wu, R., Chen, L., Yang, Z., Yan, D., & Li, M. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.811406 · Cited by 102
Role of reactive oxygen species in atherosclerosis: Lessons from murine genetic models
Nègre‐Salvayre, A., Guerby, P., Gayral, S., Laffargue, M., & Salvayre, R. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.10.011 · Cited by 102
Crosstalk between Oxidative Stress and Exosomes
Zhang, W., Liu, R., Chen, Y., Wang, M., & Du, J. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/3553617 · Cited by 98
Antioxidant Activity in Extracts from Zingiberaceae Family: Cardamom, Turmeric, and Ginger
Ballester, P., Cerdá, B., Arcusa, R., García‐Muñoz, A. M., Marhuenda, J., & Zafrilla, P. (2023) · Molecules · doi:10.3390/molecules28104024 · Cited by 98
Molecular Atlas of Postnatal Mouse Heart Development
Talman, V., Teppo, J., Pöhö, P., Movahedi, P., Vaikkinen, A., Karhu, S. T., Trôst, K., Suvitaival, T., Heikkonen, J., Pahikkala, T., et al. (2018) · Journal of the American Heart Association · doi:10.1161/jaha.118.010378 · Cited by 99
The Role of Oxidative Stress in the Aging Heart
Pagan, L. U., Gomes, M. J., Gatto, M., Mota, G. A. F., Okoshi, K., & Okoshi, M. P. (2022) · Antioxidants · doi:10.3390/antiox11020336 · Cited by 99
Doxorubicin-induced cardiotoxicity: causative factors and possible interventions
Jones, I. C., & Dass, C. R. (2022) · Journal of Pharmacy and Pharmacology · doi:10.1093/jpp/rgac063 · Cited by 91
Wang, D., Jin, M., Zhao, X., Zhao, T., Lin, W., He, Z.-L., Fan, M., Jin, W., Zhou, J., Jin, L., et al. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1696-9 · Cited by 96
Ushio‐Fukai, M., Ash, D., Nagarkoti, S., de Chantemèle, E. J. B., Fulton, D. J., & Fukai, T. (2021) · Antioxidants and Redox Signaling · doi:10.1089/ars.2020.8161 · Cited by 99
Role of pyroptosis in the pathogenesis of various neurological diseases
Oladapo, A., Jackson, T., Menolascino, J., & Periyasamy, P. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.02.001 · Cited by 101
The Importance of Natural Antioxidants in Female Reproduction
Vašková, J., Klepcová, Z., Špaková, I., Urdzík, P., Štofilová, J., Bertková, I., Kľoc, M., & Rabajdová, M. (2023) · Antioxidants · doi:10.3390/antiox12040907 · Cited by 101
Afsharpour, F., Javadi, M., Hashemipour, S., Koushan, Y., & Haghighian, H. K. (2019) · Complementary Therapies in Medicine · doi:10.1016/j.ctim.2019.03.001 · Cited by 100
Interplay between Cellular Metabolism and the DNA Damage Response in Cancer
Moretton, A., & Loizou, J. I. (2020) · Cancers · doi:10.3390/cancers12082051 · Cited by 97
Chen, C., Wang, S., Huang, C., Dong, C., Huang, C.-Y., Chang, C., & Chang, J. (2021) · Journal of Bioscience and Bioengineering · doi:10.1016/j.jbiosc.2021.06.005 · Cited by 93
Silver Nanoparticles for the Therapy of Tuberculosis
Tăbăran, F., MATEA, C. T., Mocan, T., Tăbăran, F., Mihaiu, M., Iancu, C., & MOCAN, L. C. (2020) · International Journal of Nanomedicine · doi:10.2147/ijn.s241183 · Cited by 95
The up‐to‐date pathophysiology of Kawasaki disease
Hara, T., Yamamura, K., & Sakai, Y. (2021) · Clinical & Translational Immunology · doi:10.1002/cti2.1284 · Cited by 92
Mitochondrial Reactive Oxygen Species in Infection and Immunity
Mukherjee, A., Ghosh, K. K., Chakrabortty, S., Gulyás, B. Z., Padmanabhan, P., & Ball, W. B. (2024) · Biomolecules · doi:10.3390/biom14060670 · Cited by 99
Metal-Phenolic Nanomedicines Regulate T-Cell Antitumor Function for Sono-Metabolic Cancer Therapy
Yan, J., Li, W., Tian, H., Li, B., Yu, X., Wang, G., Sang, W., & Dai, Y. (2023) · ACS Nano · doi:10.1021/acsnano.3c02428 · Cited by 92
Oxygen releasing materials: Towards addressing the hypoxia-related issues in tissue engineering
Agarwal, T., Kazemi, S., Costantini, M., Perfeito, F. G., Correia, C. R., Gaspar, V. M., Montazeri, L., Maria, C. D., Mano, J. F., Vosough, M., et al. (2021) · Materials Science and Engineering C · doi:10.1016/j.msec.2021.111896 · Cited by 93
Li, A., Li, L., Zhao, B., Li, X., Liang, W., Lang, M., Cheng, B., & Li, J. (2021) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2021.11.146 · Cited by 90
Tu, Y., Liu, J., Kong, D., Guo, X., Li, J., Long, Z., Peng, J., Wang, Z., Wu, H., Liu, P., et al. (2023) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2023.03.014 · Cited by 89
Żwierełło, W., Maruszewska, A., Skórka-Majewicz, M., Goschorska, M., Baranowska‐Bosiacka, I., Dec, K., Styburski, D., Nowakowska, A., & Gutowska, I. (2019) · Chemosphere · doi:10.1016/j.chemosphere.2019.124901 · Cited by 89
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
Therapeutic Strategies Targeting Oxidative Stress and Inflammation: A Narrative Review
Manful, C. F., Fordjour, E., Ikumoinein, E., Abbey, L., & Thomas, R. (2025) · BioChem · doi:10.3390/biochem5040035 · Cited by 96
Afolabi, O. K., Aderibigbe, F. A., Folarin, D. T., Arinola, A., & Wusu, A. D. (2019) · Heliyon · doi:10.1016/j.heliyon.2019.e02274 · Cited by 88
Gong, L., Lei, Y., Liu, Y., Tan, F., Li, S., Wang, X., Xu, M., Cai, W., Du, B., Xu, F., et al. (2019) · PubMed Central · Cited by 88
Reactive oxygen species-responsive dendritic cell-derived exosomes for rheumatoid arthritis
Lee, E. S., Sul, J. H., Shin, J. M., Shin, S., Lee, J. A., Kim, H. K., Cho, Y. E., Ko, H., Son, S., Lee, J., et al. (2021) · Acta Biomaterialia · doi:10.1016/j.actbio.2021.04.026 · Cited by 88
Jiang, X., Gray, P. J., Patel, M. A., Zheng, J., & Yin, J. (2020) · Journal of Materials Chemistry B · doi:10.1039/c9tb02524c · Cited by 87
Hypoxia and Mitochondrial Dysfunction in Pregnancy Complications
Hu, X., & Zhang, L. (2021) · Antioxidants · doi:10.3390/antiox10030405 · Cited by 93
Metal ions overloading and cell death
Lai, Y., Gao, F. F., Ge, R. T., Liu, R., Ma, S., & Liu, X. (2024) · Cell Biology and Toxicology · doi:10.1007/s10565-024-09910-4 · Cited by 90
Liu, H., Tian, R., Wang, H., Feng, S., Li, H., Xiao, Y., Luan, X., Zhang, Z., Shi, N., Niu, H., et al. (2020) · Journal of Translational Medicine · doi:10.1186/s12967-020-02539-x · Cited by 88
Developmental toxicity of glyphosate on embryo-larval zebrafish (Danio rerio)
Liu, Z., Shangguan, Y., Zhu, P., Sultan, Y. Y., Feng, Y., Li, X., & Ma, J. (2022) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2022.113493 · Cited by 86
Small-Molecule Inhibitors of Reactive Oxygen Species Production
Sassetti, E., Clausen, M. H., & Laraia, L. (2021) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.0c01914 · Cited by 85
Brahma, M. K., Gilglioni, E. H., Zhou, L., Trépo, E., Chen, P., & Gurzov, E. N. (2021) · Oncogene · doi:10.1038/s41388-021-01950-y · Cited by 85
Lin, Z., Xie, R., Zhong, C., Huang, J., Shi, P., & Yao, H. (2021) · Journal of Ginseng Research · doi:10.1016/j.jgr.2021.07.008 · Cited by 84
González-Jiménez, I., Perlin, D. S., & Shor, E. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1276406 · Cited by 88
Zhou, J., Wen, B., Xie, H.-Y., Zhang, C., Bai, Y., Cao, H., Che, Q., Guo, J., & Su, Z. (2020) · Food & Function · doi:10.1039/d0fo02768e · Cited by 82
Kodam, P., Sai Swaroop, R., Pradhan, S. S., Sivaramakrishnan, V., & Vadrevu, R. (2023) · Scientific Reports · doi:10.1038/s41598-023-30892-6 · Cited by 82
Research progress on the mechanism of curcumin anti-oxidative stress based on signaling pathway
Cui, J., Li, H., Zhang, T., Lin, F., Chen, M., Zhang, G., & Feng, Z. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1548073 · Cited by 82
Tryptophan Metabolism, Inflammation, and Oxidative Stress in Patients with Neurovascular Disease
Hajšl, M., Hlaváčková, A., Broulíková, K., Šrámek, M., Malý, M., Dyr, J. E., & Suttnar, J. (2020) · Metabolites · doi:10.3390/metabo10050208 · Cited by 81
Shi, J., Zhang, Y., Zhang, X., Chen, R., Wei, J., Hou, J., Wang, B., Lai, H., & Huang, Y. (2021) · Journal of Nanobiotechnology · doi:10.1186/s12951-021-01175-x · Cited by 81
A Systematic Review on Advances in Management of Oxidative Stress-Associated Cardiovascular Diseases
Jin, S., & Kang, P. M. (2024) · Antioxidants · doi:10.3390/antiox13080923 · Cited by 86
Bonet, M. L., Ribot, J., Galmés, S., Serra, F. A., & Palou, A. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2020.158676 · Cited by 82
Chen, Y., Guan, M., Ren, R., Gao, C., Cheng, H., Li, Y., Gao, B., Wei, Y., Fu, J., Sun, J. S., et al. (2020) · International Journal of Nanomedicine · doi:10.2147/ijn.s242919 · Cited by 84
Deng, C., Zhang, J., Huo, Y., Xue, H., Wang, W., Zhang, J., & Wang, X. (2022) · Journal of Pineal Research · doi:10.1111/jpi.12819 · Cited by 80
Nanoparticles as a Tool for Alleviating Plant Stress: Mechanisms, Implications, and Challenges
Kumari, A., Gupta, A. K., Sharma, S., Jadon, V. S., Sharma, V., Chun, S. C., & Sivanesan, I. (2024) · Plants · doi:10.3390/plants13111528 · Cited by 83
Liu, Y., Yang, H., Luo, N., Fu, Y., Qiu, F., Pan, Z., Li, X., Jian, W., Yang, X., Xue, Q., et al. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-04345-7 · Cited by 79
Metadata
- Authors
- Forrester, S. J., Kikuchi, D. S., Hernandes, M. S., Xu, Q., & Griendling, K. K.
- Affiliations
- Emory University (US)
- Venue
- Circulation Research
- Published
- 2018-03-16
- Volume
- 122
- Issue
- 6
- Pages
- 877-902
- ISSN
- 0009-7330 (ISSN-L)
- 1524-4571
- PMC
- PMC5926825
- OpenAlex
- W2791564057
- Cited by
- 2,081
- References
- 379
- Citations by year
- 2026: 232 · 2025: 300 · 2024: 317 · 2023: 324 · 2022: 316 · 2021: 281 · 2020: 195 · 2019: 97 · 2018: 15
- FWCI
- 14.44
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Circulation Research (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- American Heart Association (17SDG33410777)
- National Heart, Lung, and Blood Institute (T32HL007745, P01HL095070)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Keywords
- reactive oxygen species, redox signaling, metabolic regulation, inflammation, signal transduction, mitochondria, peroxisomes, endoplasmic reticulum, proteasome function, autophagy, atherosclerosis, diabetes mellitus, stroke, cardiovascular disease, oxidative stress
- MeSH terms
- Animals, Cardiovascular Diseases, Humans, Metabolic Diseases, Signal Transduction, Reactive Oxygen Species
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