The DOI matches its Crossref record; 75 of the 75 references it cites were found in a registry or an index.
Reactive Sulfur Species: An Emerging Concept in Oxidative Stress
Abstract
The ingredients of oxidative stress include a variety of reactive species such as reactive oxygen and reactive nitrogen species (ROS, RNS). While sulfur is usually considered as part of cellular antioxidant systems there is mounting evidence that reactive sulfur species (RSS) with stressor properties similar to the ones found in ROS are formed under conditions of oxidative stress. Thiols as well as disulfides are easily oxidised to sulfur species with sulfur in higher oxidation states. Such agents include thiyl radicals, disulfides, sulfenic acids and disulfide-S-oxides. They rapidly oxidise and subsequently inhibit thiol-proteins and enzymes and can be considered as a separate class of oxidative stressors providing new antioxidant drug targets.
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Cites
Oxidants, oxidative stress and the biology of ageing
Finkel, T., & Holbrook, N. J. (2000) · Nature · doi:10.1038/35041687 · Cited by 9,413
Physiological actions of taurine
Huxtable, R. J. (1992) · Physiological Reviews · doi:10.1152/physrev.1992.72.1.101 · Cited by 2,595
Peroxynitrite oxidation of sulfhydryls.
Radi, R., Beckman, J. S., Bush, K. M., & Freeman, B. A. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(20)64313-7 · Cited by 2,490
Strategies of antioxidant defense
SIES, H. (1993) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1993.tb18025.x · Cited by 1,976
Biochemistry of Oxidative Stress
Sies, H. (1986) · Angewandte Chemie International Edition in English · doi:10.1002/anie.198610581 · Cited by 1,306
Antimicrobial properties of allicin from garlic
Ankri, S., & Mirelman, D. (1999) · Microbes and Infection · doi:10.1016/s1286-4579(99)80003-3 · Cited by 1,177
Synthetic organoselenium compounds as antioxidants: glutathione peroxidase activity
Mugesh, G., & Singh, H. B. (2000) · Chemical Society Reviews · doi:10.1039/a908114c · Cited by 666
Therapeutic actions of garlic constituents
Agarwal, K. C. (1996) · Medicinal Research Reviews · doi:10.1002/(sici)1098-1128(199601)16:1<111::aid-med4>3.0.co;2-5 · Cited by 657
Redox‐dependent signal transduction
Finkel, T. (2000) · FEBS Letters · doi:10.1016/s0014-5793(00)01669-0 · Cited by 563
Claiborne, A., Yeh, J. I., Mallett, T. C., Luba, J., Crane, E. J., Charrier, V., & Parsonage, D. (1999) · Biochemistry · doi:10.1021/bi992025k · Cited by 500
Cited by
Graves, D. B. (2012) · Journal of Physics D: Applied Physics · doi:10.1088/0022-3727/45/26/263001 · Cited by 1,518
Chemical and molecular mechanisms of antioxidants: experimental approaches and model systems
Lü, J., Lin, P. H., Yao, Q., & Chen, C. (2010) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2009.00897.x · Cited by 1,308
Oxidative Stress: Relationship with Exercise and Training
Finaud, J., Lac, G., & Filaire, E. (2006) · Sports Medicine · doi:10.2165/00007256-200636040-00004 · Cited by 771
Free Radical Properties, Source and Targets, Antioxidant Consumption and Health
Martemucci, G., Costagliola, C., Mariano, M., D’andrea, L., Napolitano, P., & D’Alessandro, A. G. (2022) · Oxygen · doi:10.3390/oxygen2020006 · Cited by 708
Biogenesis of reactive sulfur species for signaling by hydrogen sulfide oxidation pathways
Mishanina, T. V., Libiad, M., & Banerjee, R. (2015) · Nature Chemical Biology · doi:10.1038/nchembio.1834 · Cited by 615
ABTS/PP Decolorization Assay of Antioxidant Capacity Reaction Pathways
Ilyasov, I. R., Beloborodov, V. L., Selivanova, I. A., & Terekhov, R. P. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21031131 · Cited by 543
Kostova, I., Bhatia, S., Grigorov, P., Balkansky, S., S. Parmar, V., K. Prasad, A., & Saso, L. (2011) · Current Medicinal Chemistry · doi:10.2174/092986711803414395 · Cited by 435
Molecular Probes for Autofluorescence-Free Optical Imaging
Jiang, Y., & Pu, K. (2021) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00506 · Cited by 426
Manevich, Y., & Fisher, A. B. (2005) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2005.02.011 · Cited by 382
Jacob, C. (2006) · Natural Product Reports · doi:10.1039/b609523m · Cited by 373
Self-citationRedox signaling and cancer: The role of “labile” iron
Galaris, D., Skiada, V., & Barbouti, A. (2008) · Cancer Letters · doi:10.1016/j.canlet.2008.02.038 · Cited by 284
Antioxidants from Plants Protect against Skin Photoaging
Petruk, G., Del Giudice, R., Rigano, M. M., & Monti, D. M. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/1454936 · Cited by 283
The biology of reactive sulfur species (RSS)
Gruhlke, M. C. H., & Slusarenko, A. J. (2012) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2012.03.016 · Cited by 274
Lipid oxidation and its implications to meat quality and human health
Huang, X., & Ahn, D. U. (2019) · Food Science and Biotechnology · doi:10.1007/s10068-019-00631-7 · Cited by 258
Oxidative activation of antioxidant defence
Winyard, P. G., Moody, C. J., & Jacob, C. (2005) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2005.06.001 · Cited by 254
Self-citationNikolaienko, R., Bovo, E., & Zima, A. V. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01775 · Cited by 89
Fenoglio, I., Fonsato, S., & Fubini, B. (2003) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(03)00398-8 · Cited by 38
Adaptation of Candida albicans to Reactive Sulfur Species
Chebaro, Y., Lorenz, M., Fa, A., Zheng, R., & Gustin, M. (2017) · Genetics · doi:10.1534/genetics.116.199679 · Cited by 11
Metadata
- Authors
- Giles, G. I., & Jacob, C.
- Venue
- Biological Chemistry
- Publisher
- Walter de Gruyter GmbH
- Published
- 2002-01-12
- Volume
- 383
- Issue
- 3-4
- Pages
- 375-88
- ISSN
- 1431-6730 (ISSN-L)
- OpenAlex
- W2016947117
- Cited by
- 314
- References
- 75
- FWCI
- 2.92
- Type
- journal article
- Language
- en
- Open access
- closed
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