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Central Sensitization: A Generator of Pain Hypersensitivity by Central Neural Plasticity
Open accessAbstract
Unlabelled Central sensitization represents an enhancement in the function of neurons and circuits in nociceptive pathways caused by increases in membrane excitability and synaptic efficacy as well as to reduced inhibition and is a manifestation of the remarkable plasticity of the somatosensory nervous system in response to activity, inflammation, and neural injury. The net effect of central sensitization is to recruit previously subthreshold synaptic inputs to nociceptive neurons, generating an increased or augmented action potential output: a state of facilitation, potentiation, augmentation, or amplification. Central sensitization is responsible for many of the temporal, spatial, and threshold changes in pain sensibility in acute and chronic clinical pain settings and exemplifies the fundamental contribution of the central nervous system to the generation of pain hypersensitivity. Because central sensitization results from changes in the properties of neurons in the central nervous system, the pain is no longer coupled, as acute nociceptive pain is, to the presence, intensity, or duration of noxious peripheral stimuli. Instead, central sensitization produces pain hypersensitivity by changing the sensory response elicited by normal inputs, including those that usually evoke innocuous sensations.Perspective In this article, we review the major triggers that initiate and maintain central sensitization in healthy individuals in response to nociceptor input and in patients with inflammatory and neuropathic pain, emphasizing the fundamental contribution and multiple mechanisms of synaptic plasticity caused by changes in the density, nature, and properties of ionotropic and metabotropic glutamate receptors.
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“Undergirding the chronicity is that chronic pain and attendant psychosocial distress can change the structure of the brain's widespread cognitive and affective structures in ways that perpetuate pain perception (Latremoliere and Woolf, 2009).”
From Physiological feelings (2019) · cites this paper as Latremoliere and Woolf, 2009
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“Changes in central synaptic plasticity, which are involved in regulating the development and maintenance of chronic pain, are considered a primary cause of central sensitization in NPP (10).”
From Nociplastic pain: the prominent role of non-neuronal cells in central and peripheral sensitization (2026) · cites this paper as [10]
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Cites
A synaptic model of memory: long-term potentiation in the hippocampus
Bliss, T. V. P., & Collingridge, G. L. (1993) · Nature · doi:10.1038/361031a0 · Cited by 11,566
Resting microglial cells are highly dynamic surveillants of brain parenchyma in vivo
Nimmerjahn, A., Kirchhoff, F., & Helmchen, F. (2005) · Science · doi:10.1126/science.1110647 · Cited by 5,827
Malenka, R. C., & Bear, M. F. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.012 · Cited by 3,968
ATP mediates rapid microglial response to local brain injury in vivo
Davalos, D., Grutzendler, J., Yang, G., Kim, J. V., Zuo, Y., Jung, S., Littman, D. R., Dustin, M. L., & Gan, W.-B. (2005) · Nature Neuroscience · doi:10.1038/nn1472 · Cited by 3,913
Neuronal plasticity: Increasing the gain in pain
Woolf, C. J., & Salter, M. W. (2000) · Science · doi:10.1126/science.288.5472.1765 · Cited by 3,781 · cited 5×
“as large low-threshold mechanoreceptor myelinated fibers to produce Ab fiber–mediated pain.(376) It also produces pain hypersensitivity in noninflamed tissue by changing the sensory response elicited by normal inputs”
InfluentialSelf-citationPHARMACOLOGY AND FUNCTIONS OF METABOTROPIC GLUTAMATE RECEPTORS
Conn, P. J., & Pin, J. (1997) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.37.1.205 · Cited by 3,083
Voltage-dependent block by Mg2+ of NMDA responses in spinal cord neurones
Mayer, M. L., Westbrook, G. L., & Guthrie, P. B. (1984) · Nature · doi:10.1038/309261a0 · Cited by 2,941
Functional imaging of brain responses to pain. A review and meta-analysis (2000)
Peyron, R., Laurent, B., & García-Larrea, L. (2000) · Neurophysiologie Clinique/Clinical Neurophysiology · doi:10.1016/s0987-7053(00)00227-6 · Cited by 2,171
Evidence for a central component of post-injury pain hypersensitivity
Woolf, C. J. (1983) · Nature · doi:10.1038/306686a0 · Cited by 2,157
Self-citationInduction of c-fos-like protein in spinal cord neurons following sensory stimulation
Hunt, S. P., Pini, A., & Evan, G. I. (1987) · Nature · doi:10.1038/328632a0 · Cited by 1,986
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- Young, 1997, Behavioural and electrophysiological evidence supporting a role for group I metabotropic glutamate receptors in the mediation of nociceptive inputs to the rat spinal cord, Brain Res, 777, 161
Cited by
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Items 801–900 of 1,020
Role of Anoctamin-1 and Bestrophin-1 in Spinal Nerve Ligation-Induced Neuropathic Pain in Rats
Pineda-Farías, J. B., Barragán‐Iglesias, P., Loeza‐Alcocer, E., Torres‐López, J. E., Rocha-González, H. I., Pérez‐Severiano, F., Delgado‐Lezama, R., & Granados‐Soto, V. (2015) · Molecular Pain · doi:10.1186/s12990-015-0042-1 · Cited by 42
Serra, J., Solà, R., Aleu, J., Quiles, C., Navarro, X., & Bostock, H. (2010) · Pain · doi:10.1016/j.pain.2010.10.039 · Cited by 42
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Dancey, E., Murphy, B. A., Srbely, J. Z., & Yielder, P. C. (2014) · Experimental Brain Research · doi:10.1007/s00221-014-3966-1 · Cited by 42
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Kraychete, D. C., Sakata, R. K., Lannes, L. D. O. C., Bandeira, I. D., & Sadatsune, E. J. (2016) · Brazilian Journal of Anesthesiology (English Edition) · doi:10.1016/j.bjane.2014.12.005 · Cited by 45
Xu, B., Cao, J., Zhang, J., Jia, S., Wu, S., Mo, K., Wei, G., Liang, L., Miao, X., Bekker, A., et al. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00350 · Cited by 42
Juškys, R., & Šustickas, G. (2018) · Acta medica Lituanica · doi:10.6001/actamedica.v25i2.3757 · Cited by 42
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Pan, F., & Jones, G. (2018) · Current Rheumatology Reports · doi:10.1007/s11926-018-0796-3 · Cited by 42
van Laarhoven, A. I. M., Marker, J. B., Elberling, J., Yosipovitch, G., Arendt‐Nielsen, L., & Andersen, H. H. (2019) · Pain · doi:10.1097/j.pain.0000000000001678 · Cited by 42
Ocular pain response to treatment in dry eye patients
Siedlecki, A. N., Smith, S. D. G., Siedlecki, A., Hayek, S. M., & Sayegh, R. R. (2020) · The Ocular Surface · doi:10.1016/j.jtos.2019.12.004 · Cited by 44
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O’Reilly, M. L., & Tom, V. J. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00187 · Cited by 44
Current Considerations for the Treatment of Severe Chronic Pain: The Potential for Tapentadol
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Zhang, W., Lei, M., Wen, Q., Zhang, D., Qin, G., Zhou, J., & Chen, L. (2022) · The Journal of Headache and Pain · doi:10.1186/s10194-022-01469-x · Cited by 41
Ciechanowska, A., & Mika, J. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25073788 · Cited by 46
Zhao, T., Liu, X., Zhen, X., & Guo, S. (2010) · Reproductive Sciences · doi:10.1177/1933719110381928 · Cited by 41
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Dworkin, R. H., Turk, D. C., Basch, E., Berger, A. M., Cleeland, C. S., Farrar, J. T., Haythornthwaite, J. A., Jensen, M. P., Kerns, R. D., Markman, J. D., et al. (2011) · Pain · doi:10.1016/j.pain.2011.02.026 · Cited by 41
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Wei, M., Li, L., Zhang, Y., Zhang, Z., Liu, H., & Bao, H. (2018) · Journal of Cellular Biochemistry · doi:10.1002/jcb.27088 · Cited by 41
Galán-Martín, M. Á., Montero-Cuadrado, F., Lluch‐Girbés, E., Coca-López, M. C., Mayo-Íscar, A., & Vargas, A. I. C. (2019) · BMC Musculoskeletal Disorders · doi:10.1186/s12891-019-2889-1 · Cited by 45
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Karki, P., Kurihara, T., Nakamachi, T., Watanabe, J., Asada, T., Oyoshi, T., Shioda, S., Yoshimura, M., Arita, K., & Miyata, A. (2015) · Molecular Pain · doi:10.1186/s12990-015-0003-8 · Cited by 43
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Kussman, B. D., Aasted, C. M., Yücel, M. A., Steele, S., Alexander, M. E., Boas, D. A., Borsook, D., & Becerra, L. R. (2016) · PLoS ONE · doi:10.1371/journal.pone.0158975 · Cited by 41
Wigerblad, G., Huie, J. R., Yin, H. Z., Leinders, M., Pritchard, R. A., Koehrn, F. J., Xiao, W. H., Bennett, G. J., Huganir, R. L., Ferguson, A. R., et al. (2017) · Experimental Neurology · doi:10.1016/j.expneurol.2017.04.004 · Cited by 40
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Perrotta, A., Serrao, M., Tassorelli, C., Arce‐Leal, N., Guaschinol, E., Sances, G., Rossil, P., Bartolol, M., Pierelli, F., Sandrinil, G., et al. (2010) · European Journal of Pain · doi:10.1016/j.ejpain.2010.09.010 · Cited by 40
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Andrade, P., Hoogland, G., Rosario, J. S. D., Steinbusch, H. W. M., Visser-Vandewalle, V. E. R. M., & Daemen, M. A. R. C. (2014) · Journal of Neuroscience Research · doi:10.1002/jnr.23432 · Cited by 39
Berube, M., Choinière, M., Laflamme, Y. G., & Gélinas, C. (2016) · International Journal of Orthopaedic and Trauma Nursing · doi:10.1016/j.ijotn.2016.04.002 · Cited by 39
Huang, C.-P., Lin, Y., Lee, D.-Y., & Hsieh, C. (2019) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2019/6784735 · Cited by 39
Willett, M., Siebertz, M. W., Petzke, F. W., Erlenwein, J., Rushton, A. B., Soldini, E., Barbero, M., & Falla, D. (2019) · Pain Practice · doi:10.1111/papr.12851 · Cited by 39
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Yousuf, M. S., Samtleben, S., Lamothe, S. M., Friedman, T. N., Catuneanu, A., Thorburn, K. C., Desai, M., Tenorio, G., Schenk, G. J., Ballanyi, K., et al. (2020) · The FASEB Journal · doi:10.1096/fj.202001163r · Cited by 39
Suzuki, K., Haruyama, Y., Kobashi, G., Sairenchi, T., Uchiyama, K., Yamaguchi, S., & Hirata, K. (2021) · Pain Research and Management · doi:10.1155/2021/6656917 · Cited by 39
Muller, P. A., Pascual‐Leone, Á., & Rotenberg, A. (2011) · Brain stimulation · doi:10.1016/j.brs.2011.05.003 · Cited by 39
Wang, W., Petralia, R., Takamiya, K., Xia, J., Li, Y.-Q., Huganir, R., Tao, Y.-X., & Yaster, M. (2011) · Molecular Pain · doi:10.1186/1744-8069-7-11 · Cited by 42
Crespo, M. Á. D. L. C., Donegan, T., Amestoy, B., Just, A., Combalía, A., & Sanchez-Vives, M. V. (2023) · Journal of Orthopaedic Surgery and Research · doi:10.1186/s13018-023-04158-w · Cited by 44
Ballas, S. K. (2014) · European Journal Of Haematology · doi:10.1111/ejh.12460 · Cited by 39
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Wildgaard, K., Ringsted, T. K., Aasvang, E. K., Ravn, J. B., Werner, M. U., & Kehlet, H. (2011) · Clinical Journal of Pain · doi:10.1097/ajp.0b013e3182261650 · Cited by 38
Obara, I., Goulding, S. P., Hu, J.-H., Klugmann, M., Worley, P. F., & Szumlinski, K. K. (2013) · Pain · doi:10.1016/j.pain.2013.03.035 · Cited by 38
Clarke, H. A., Woodhouse, L. J., Kennedy, D. M., Stratford, P. W., & Katz, J. D. (2011) · Physiotherapy Canada · doi:10.3138/ptc.2009-49p · Cited by 38
Kayaoğlu, G., Gürel, M., Sarıçam, E., ILHAN, M. N., & İlk, Ö. (2015) · Journal of Endodontics · doi:10.1016/j.joen.2015.09.021 · Cited by 38
Michels, L., Christidi, F., Steiger, V. R., Sándor, P. S., Gantenbein, A. R., Landmann, G., Schreglmann, S. R., Kollias, S., & Riederer, F. (2016) · Cephalalgia · doi:10.1177/0333102416652625 · Cited by 38
Weber, K. A., II, Chen, Y. J., Wang, X., Kahnt, T., & Parrish, T. B. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.09.015 · Cited by 36
Hu, X., Zhang, H., Xu, H., Zhang, H., Chen, L., Cui, W., Yang, W., & Shen, W. (2017) · Scientific Reports · doi:10.1038/s41598-017-04198-3 · Cited by 39
Chen, W., Chi, Y.-N., Kang, X.-J., Liu, Q.-Y., Zhang, H., Li, Z., Zhao, Z., Yang, Y., Su, L., Cai, J., et al. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00024 · Cited by 42
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Bilika, P., Neblett, R., Georgoudis, G., Dimitriadis, Z., Fandridis, E. M., Στριμπάκος, Ν., & Kapreli, E. (2019) · Pain Practice · doi:10.1111/papr.12843 · Cited by 38
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Qiao, L. Y., & Tiwari, N. (2020) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00323.2020 · Cited by 38
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Bazzari, A. H., & Bazzari, F. H. (2022) · The Egyptian Journal of Neurology Psychiatry and Neurosurgery · doi:10.1186/s41983-022-00472-y · Cited by 40
Trouvin, A., Attal, N., & Perrot, S. (2022) · Joint Bone Spine · doi:10.1016/j.jbspin.2022.105399 · Cited by 38
Szabó, E., Chang, Y.-H., Shulman, J., Sieberg, C. B., Sethna, N. F., Borsook, D., Holmes, S. A., & Lebel, A. (2022) · Headache The Journal of Head and Face Pain · doi:10.1111/head.14360 · Cited by 38
Wåhlén, K., Olausson, P., Carlsson, A. K., Ghafouri, N., Gerdle, B. U. C., & Ghafouri, B. (2017) · Journal of Pain Research · doi:10.2147/jpr.s128597 · Cited by 38
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Metadata
- Authors
- Latremoliere, A., & Woolf, C. J.
- Affiliations
- Harvard University (US)
- Corresponding author
- Woolf, Clifford J.
- ORCID
- Woolf, Clifford J.
- Venue
- The Journal of Pain
- Publisher
- Elsevier BV
- Published
- 2009-09
- Volume
- 10
- Issue
- 9
- Pages
- 895-926
- ISSN
- 1526-5900 (ISSN-L)
- PMC
- PMC2750819
- OpenAlex
- W2155524482
- Cited by
- 3,913
- References
- 416
- Citations by year
- 2026: 318 · 2025: 343 · 2024: 295 · 2023: 330 · 2022: 284 · 2021: 306 · 2020: 275 · 2019: 230 · 2018: 217 · 2017: 219 · 2016: 198 · 2015: 189 · 2014: 176 · 2013: 162 · 2012: 141
- FWCI
- 13.46
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Journal of Pain (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (R01NS058870, R01NS038253, R01NS039518)
- National Institute of Dental and Craniofacial Research (R01DE017821)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Pain Mechanisms and Treatments
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Health Sciences › Medicine › Anesthesiology and Pain Medicine › Pain Management and Treatment
- Keywords
- central sensitization, hyperalgesia, synaptic plasticity, nociceptive pathways, glutamate receptors, metabotropic glutamate receptors, ionotropic glutamate receptors, inflammatory pain, neuropathic pain, chronic pain, membrane excitability
- MeSH terms
- Afferent Pathways, Animals, Central Nervous System, Humans, Hyperalgesia, Synaptic Transmission, Neuronal Plasticity, Nociceptors, Pain, Sensory Receptor Cells, Pain Threshold
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