The DOI matches its Crossref record; 215 of the 218 references it cites were found in a registry or an index.
Nitroxidative Signaling Mechanisms in Pathological Pain
Open accessAbstract
Tissue injury can initiate bidirectional signaling between neurons, glia, and immune cells that creates and amplifies pain. While the ability for neurotransmitters, neuropeptides, and cytokines to initiate and maintain pain has been extensively studied, recent work has identified a key role for reactive oxygen and nitrogen species (ROS/RNS; nitroxidative species), including superoxide, peroxynitrite, and hydrogen peroxide. In this review we describe how nitroxidative species are generated after tissue injury and the mechanisms by which they enhance neuroexcitability in pain pathways. Finally, we discuss potential therapeutic strategies for normalizing nitroxidative signaling, which may also enhance opioid analgesia, to help to alleviate the enormous burden of pathological pain.
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
“This is because the mechanisms that cause pathological pain and those that cause exercise-induced muscle pain are different from each other [41,42].”
From Acute effects of brief mindfulness intervention coupled with carbohydrate ingestion to re-energize soccer players: a randomized crossover trial. (2020) · cites this paper as [41]
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
Items 201–215 of 215
Sciatic Nerve Transection Modulates Oxidative Parameters in Spinal and Supraspinal Regions
Scheid, T., Bosco, L. D., Guedes, R. P., Pavanato, M. A., Belló‐Klein, A., & Partata, W. A. (2013) · Neurochemical Research · doi:10.1007/s11064-013-1000-9 · Cited by 26
Fabs specific for 8-oxoguanine: control of DNA binding 1 1Edited by I. A. Wilson
Bespalov, I. A., Bond, J. P., Purmal, A. A., Wallace, S. S., & Melamede, R. J. (1999) · Journal of Molecular Biology · doi:10.1006/jmbi.1999.3214 · Cited by 23
Fan, Y., & Ai, H. (2016) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-015-9280-3 · Cited by 22
Hu, P. L., Mei, Q., Ma, L., Cui, W., Zhou, W., Zhou, D., Zhao, Q. C., Xu, D., Zhao, X., Lu, Q., et al. (2015) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2015.10.024 · Cited by 21
Lorenz, J. E., Kallenborn-Gerhardt, W., Lu, R., Syhr, K. M. J., Eaton, P., Geißlinger, G., & Schmidtko, A. (2014) · Antioxidants and Redox Signaling · doi:10.1089/ars.2013.5585 · Cited by 21
Hydrogen peroxide detection with high specificity in living cells and inflamed tissues
Rong, L., Zhang, C., Lei, Q., Hu, M., Feng, J. X., Shu, H., Liu, Y., & Zhang, X. (2016) · Regenerative Biomaterials · doi:10.1093/rb/rbw022 · Cited by 21
Mn Porphyrin-Based Redox-Active Therapeutics
Batinic̈‐Haberle, I., Tovmasyan, A. G., & Spasojević, I. (2016) · Oxidative stress in applied basic research and clinical practice · doi:10.1007/978-3-319-30705-3_8 · Cited by 21
Role of TRPM2 cation channels in dorsal root ganglion of rats after experimental spinal cord injury
Nazıroğlu, M., Uğuz, A. C., İsmailoğlu, Ö., Çiğ, B., Özgül, C., & Borcak, M. (2013) · Muscle & Nerve · doi:10.1002/mus.23844 · Cited by 20
Mitochondrial dependence of nerve growth factor-induced mechanical hyperalgesia
Chu, C. E., Levine, E. H., Gear, R. W., Bogen, O., & Levine, J. D. (2011) · Pain · doi:10.1016/j.pain.2011.03.034 · Cited by 18
Fan, Y., & Ai, H. (2016) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-016-9365-7 · Cited by 16
Time-course of neuropathic pain in mice deficient in neuronal or inducible nitric oxide synthase
Keilhoff, G., Schröder, H., Peters, B., & Becker, A. (2013) · Neuroscience Research · doi:10.1016/j.neures.2013.08.008 · Cited by 15
Endothelial Nitric Oxide Synthase in Dorsal Root Ganglia during Chronic Inflammatory Nociception
Borsani, E., Giovannozzi, S., Cocchi, M. A., Boninsegna, R., Rezzani, R., & Rodella, L. F. (2012) · Cells Tissues Organs · doi:10.1159/000342518 · Cited by 14
Pharmacologic characterization of novel adenosine A2A receptor agonists in equine neutrophils
Sun, W., Moore, J. N., Hurley, D. J., Vandenplas, M. L., Linden, J. M., & Murray, T. F. (2007) · American Journal of Veterinary Research · doi:10.2460/ajvr.68.9.981 · Cited by 10
Heme oxygenase-1 inhibits neuropathic pain in rats with diabetic mellitus.
Kong, Q., Liu, K., Ling-xi, W., & Wang, L. (2012) · Europe PMC (PubMed Central) · doi:10.3969/j.issn.1673-5374.2012.29.010 · Cited by 7
The Contribution of Nitroxidative Stress to Pathophysiological Pain and Opioid Analgesic Failure
Symons-Liguori, A. M., Janes, K., Neumann, W., & Salvemini, D. (2016) · Oxidative stress in applied basic research and clinical practice · doi:10.1007/978-3-319-30705-3_25 · Cited by 2
Flagged first, then by citations
3 of the 218 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- Gozsy, 1934, On the mechanism of primary respiration in pigeon breast muscle, Hoppe. Seylers Z. Physiol. Chem., 224, 1
Cited by
Sorted by citations
Opioid-Induced Tolerance and Hyperalgesia
Mercadante, S., Arcuri, E., & Santoni, A. (2019) · CNS Drugs · doi:10.1007/s40263-019-00660-0 · Cited by 330
Glial Cells Shape Pathology and Repair After Spinal Cord Injury
Gaudet, A. D., & Fonken, L. K. (2018) · Neurotherapeutics · doi:10.1007/s13311-018-0630-7 · Cited by 242
The superoxide radical switch in the biology of nitric oxide and peroxynitrite
Piacenza, L., Zeida, A., Trujillo, M., & Radí, R. (2022) · Physiological Reviews · doi:10.1152/physrev.00005.2022 · Cited by 214
The Neuroimmunology of Chronic Pain: From Rodents to Humans
Grace, P. M., Tawfik, V. L., Svensson, C. I., Burton, M. D., Loggia, M. L., & Hutchinson, M. R. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1650-20.2020 · Cited by 138
Combination of autophagy and NFE2L2/NRF2 activation as a treatment approach for neuropathic pain
Li, J., Tian, M., Hua, T., Wang, H., Yang, M., Li, W., Zhang, X., & Yuan, H. (2021) · Autophagy · doi:10.1080/15548627.2021.1900498 · Cited by 123
Metadata
- Authors
- Grace, P. M., Gaudet, A. D., Staikopoulos, V., Maier, S. F., Hutchinson, M. R., Salvemini, D., & Watkins, L. R.
- Affiliations
- The University of Texas MD Anderson Cancer Center (US)
- University of Colorado Boulder (US)
- Australian Research Council (AU)
- Saint Louis University (US)
- Corresponding author
- Grace, Peter M.
- ORCID
- Venue
- Trends in Neurosciences
- Publisher
- Elsevier BV
- Published
- 2016-12
- Volume
- 39
- Issue
- 12
- Pages
- 862-879
- ISSN
- 0166-2236 (ISSN-L)
- PMC
- PMC5148691
- OpenAlex
- W2551668281
- Cited by
- 128
- References
- 218
- Citations by year
- 2026: 18 · 2025: 6 · 2024: 9 · 2023: 12 · 2022: 14 · 2021: 22 · 2020: 21 · 2019: 10 · 2018: 10 · 2017: 4 · 2016: 1
- FWCI
- 0.97
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Trends in Neurosciences (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Adelaide Research & Scholarship (AR&S) (University of Adelaide) (submittedVersion)
- Funders
- National Institute of Dental and Craniofacial Research (R01DE021966)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Pain Mechanisms and Treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Life Sciences › Neuroscience › Sensory Systems › Ion Channels and Receptors
- Keywords
- pathological pain, reactive oxygen species, reactive nitrogen species, peroxynitrite, superoxide, hydrogen peroxide, tissue damage, neuroinflammation, neuronal excitability, pain pathways, opioid analgesia, treatment options
- MeSH terms
- Animals, Humans, Mitochondria, Neurons, Pain, Signal Transduction, Reactive Oxygen Species, NADPH Oxidases, Reactive Nitrogen 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