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Neuronal circuitry for pain processing in the dorsal horn
Open accessAbstract
Neurons in the spinal dorsal horn process sensory information, which is then transmitted to several brain regions, including those responsible for pain perception. The dorsal horn provides numerous potential targets for the development of novel analgesics and is thought to undergo changes that contribute to the exaggerated pain felt after nerve injury and inflammation. Despite its obvious importance, we still know little about the neuronal circuits that process sensory information, mainly because of the heterogeneity of the various neuronal components that make up these circuits. Recent studies have begun to shed light on the neuronal organization and circuitry of this complex region.
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“Activated microglia released numerous inflammatory mediators (IL-1β, TNF-α, NO, and ROS) that led to changes in protein expression, as well as reached synapse endings, promoted glutamate release, and affected neuronal action potentials, thereby resulting in abnormal neural circuits (Todd, 2010, Ma et al., 2021, Costigan et al., 2009, Inoue and Tsuda, 2018, Chen et al., 2018).”
From Picroside Ⅱ attenuates neuropathic pain by regulating inflammation and spinal excitatory synaptic transmission (2024) · cites this paper as Todd, 2010
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“Nerve injury induces hyperexcitability, thereby causing functional alterations in the neuronal network such as loss of function of inhibitory neurons in the dorsal horn, and results in neuropathic pain (Prescott et al, 2014;Todd, 2010).”
From The endogenous cannabinoid system: a budding source of targets for treating inflammatory and neuropathic pain (2018) · cites this paper as Todd, 2010
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A peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in man
Bennett, G. J., & Xie, Y.-K. (1988) · Pain · doi:10.1016/0304-3959(88)90209-6 · Cited by 5,376
Ho Kim, S., & Mo Chung, J. (1992) · Pain · doi:10.1016/0304-3959(92)90041-9 · Cited by 3,069
Spared nerve injury: an animal model of persistent peripheral neuropathic pain
Décosterd, I., & Woolf, C. J. (2000) · Pain · doi:10.1016/s0304-3959(00)00276-1 · Cited by 2,317
The cytoarchitectonic organization of the spinal cord in the cat
Rexed, B. (1952) · The Journal of Comparative Neurology · doi:10.1002/cne.900960303 · Cited by 1,675
AMPA receptor trafficking at excitatory synapses
Bredt, D. S., & Nicoll, R. A. (2003) · Neuron · doi:10.1016/s0896-6273(03)00640-8 · Cited by 1,150
Models and Mechanisms of Hyperalgesia and Allodynia
Sandkühler, J. (2009) · Physiological Reviews · doi:10.1152/physrev.00025.2008 · Cited by 1,148
Trans-synaptic shift in anion gradient in spinal lamina I neurons as a mechanism of neuropathic pain
Coull, J. A. M., Boudreau, D., Bachand, K., Prescott, S. A., Nault, F., Attila Gabor, S. I. K., Koninck, P. D., & Koninck, Y. D. (2003) · Nature · doi:10.1038/nature01868 · Cited by 1,118
Peripheral nerve injury triggers central sprouting of myelinated afferents
Woolf, C. J., Shortland, P. J., & Coggeshall, R. E. (1992) · Nature · doi:10.1038/355075a0 · Cited by 1,083
Descending control of nociception: Specificity, recruitment and plasticity
Heinricher, M. M., Tavares, I., Leith, J. L., & Lumb, B. M. (2008) · Brain Research Reviews · doi:10.1016/j.brainresrev.2008.12.009 · Cited by 953
PKA phosphorylation of AMPA receptor subunits controls synaptic trafficking underlying plasticity
Esteban, J. A., Shi, S.-H., Wilson, C., Nuriya, M., Huganir, R. L., & Malinow, R. (2003) · Nature Neuroscience · doi:10.1038/nn997 · Cited by 894
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- Todd, A. J. in Handbook of Clinical Neurology 3rd Series, Pain. (Eds Cervero, F. and Jensen, T. S.) 61–76 (Elsevier, Edinburgh, 2006).
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Sorted by citations
Items 101–200 of 998
A functional subdivision within the somatosensory system and its implications for pain research
Ma, Q. (2022) · Neuron · doi:10.1016/j.neuron.2021.12.015 · Cited by 112
Vachon, P., Millecamps, M., Low, L. A., Thompsosn, S. J., Pailleux, F., Beaudry, F., Bushnell, C. M., & Stone, L. S. (2013) · Behavioral and Brain Functions · doi:10.1186/1744-9081-9-22 · Cited by 111
Obara, I., Tochiki, K. K., Géranton, S. M., Carr, F. B., Lumb, B. M., Liu, Q., & Hunt, S. P. (2011) · Pain · doi:10.1016/j.pain.2011.07.025 · Cited by 110
Missig, G., Roman, C. W., Vizzard, M. A., Braas, K. M., Hammack, S. E., & May, V. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.06.022 · Cited by 109
The lateral parabrachial nucleus is actively involved in the acquisition of fear memory in mice
Satô, M., Ito, M., Nagase, M., Sugimura, Y. K., Takahashi, Y., Watabe, A. M., & Kato, F. (2015) · Molecular Brain · doi:10.1186/s13041-015-0108-z · Cited by 111
Fine-Grained Nociceptive Maps in Primary Somatosensory Cortex
Mancini, F., Haggard, P., Iannetti, G. D., Longo, M. R., & Sereno, M. I. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.3059-12.2012 · Cited by 107
Morecraft, R. J., Ge, J., Stilwell‐Morecraft, K. S., McNeal, D. W., Pizzimenti, M. A., & Darling, W. G. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23410 · Cited by 102
The etiological contribution of GABAergic plasticity to the pathogenesis of neuropathic pain
Li, C., Lei, Y., Tian, Y., Xu, S., Shen, X., Wu, H., Bao, S., & Wang, F. (2019) · Molecular Pain · doi:10.1177/1744806919847366 · Cited by 107
Liang, S., Zhao, W., Yin, J.-B., Chen, Y.-B., Li, J., Feng, B., Lu, Y.-C., Wang, J., Dong, Y., & Li, Y.-Q. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2487-19.2020 · Cited by 104
A central role for spinal dorsal horn neurons that express neurokinin-1 receptors in chronic itch
Akiyama, T., Nguyen, T., Curtis, E., Nishida, K., Devireddy, J., Delahanty, J., Carstens, M. I., & Carstens, E. E. (2015) · Pain · doi:10.1097/j.pain.0000000000000172 · Cited by 103
Boakye, P. A., Tang, S.-J., & Smith, P. A. (2021) · Frontiers in Pain Research · doi:10.3389/fpain.2021.698157 · Cited by 102
Pharmacological Regulation of Neuropathic Pain Driven by Inflammatory Macrophages
Kiguchi, N., Kobayashi, D., Saika, F., Matsuzaki, S., & Kishioka, S. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18112296 · Cited by 106
Imaging pain: a potent means for investigating pain mechanisms in patients
Lee, M., & Tracey, I. (2013) · British Journal of Anaesthesia · doi:10.1093/bja/aet174 · Cited by 108
The search for novel analgesics: targets and mechanisms
Yaksh, T. L., Woller, S. A., Ramachandran, R., & Sorkin, L. S. (2015) · F1000Prime Reports · doi:10.12703/p7-56 · Cited by 100
Identification of Early RET+ Deep Dorsal Spinal Cord Interneurons in Gating Pain
Cui, L., Miao, X., Liang, L., Abdus-Saboor, I., Olson, W., Fleming, M. S., Ma, M., Tao, Y.-X., & Luo, W. (2016) · Neuron · doi:10.1016/j.neuron.2016.07.038 · Cited by 100
Jiang, B., He, L., Wu, X., Shi, H. M., Zhang, W., Zhang, Z., Cao, D., Li, C., Gu, J., & Gao, Y. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2262-16.2016 · Cited by 106
Spinal ascending pathways for somatosensory information processing
Wang, L.-H., Ding, W.-Q., & Sun, Y.-G. (2022) · Trends in Neurosciences · doi:10.1016/j.tins.2022.05.005 · Cited by 109
Transient receptor potential ion channels in primary sensory neurons as targets for novel analgesics
Valente, J. D. S., Andreou, A. P., Urbán, L., & Nagy, I. (2013) · British Journal of Pharmacology · doi:10.1111/bph.12532 · Cited by 97
Chen, Z. (2021) · Nature reviews. Neuroscience · doi:10.1038/s41583-021-00526-9 · Cited by 98
The dorsal spinal cord and hindbrain: From developmental mechanisms to functional circuits.
Hernandez-Miranda, L. R., Müller, T., & Birchmeier, C. (2017) · Developmental Biology · doi:10.1016/j.ydbio.2016.10.008 · Cited by 88
Neuroinflammation, Pain and Depression: An Overview of the Main Findings
Campos, A. C. P., Antunes, G. F., Matsumoto, M., Pagano, R. L., & Martinez, R. C. R. (2020) · Frontiers in Psychology · doi:10.3389/fpsyg.2020.01825 · Cited by 107
Bumgarner, J. R., Walker, W. H., & Nelson, R. J. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.08.004 · Cited by 103
Neuroplasticity related to chronic pain and its modulation by microglia
Hiraga, S.-I., Itokazu, T., Nishibe, M., & Yamashita, T. (2022) · Inflammation and Regeneration · doi:10.1186/s41232-022-00199-6 · Cited by 101
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Romano, M. (2024) · doi:10.1002/9781119514183.ch19 · Cited by 95
Why does my shoulder hurt? A review of the neuroanatomical and biochemical basis of shoulder pain
Dean, B. J. F., Gwilym, S. E., & Carr, A. J. (2013) · British Journal of Sports Medicine · doi:10.1136/bjsports-2012-091492 · Cited by 103
A spinoparabrachial circuit defined by Tacr1 expression drives pain
Barik, A., Sathyamurthy, A., Thompson, J., Seltzer, M., Levine, A., & Chesler, A. (2021) · eLife · doi:10.7554/elife.61135 · Cited by 93
Polgár, E., Sardella, T. C. P., Tiong, S. Y. X., Locke, S., Watanabe, M., & Todd, A. J. (2013) · Pain · doi:10.1016/j.pain.2013.05.001 · Cited by 96
Self-citationBoyle, K. A., Gutierrez-Mecinas, M., Polgár, E., Mooney, N., O'Connor, E., Furuta, T., Watanabe, M., & Todd, A. J. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.08.044 · Cited by 92
Self-citationA Functional Topographic Map for Spinal Sensorimotor Reflexes
Gatto, G., Bourane, S., Ren, X., Di Costanzo, S., Fenton, P. K., Halder, P., Seal, R. P., & Goulding, M. D. (2021) · Neuron · doi:10.1016/j.neuron.2020.10.003 · Cited by 92
Inquimbert, P., Bartels, K., Babaniyi, O., Barrett, L. B., Tegeder, I., & Scholz, J. (2012) · Pain · doi:10.1016/j.pain.2012.08.011 · Cited by 92
A new minimally-invasive method for microinjection into the mouse spinal dorsal horn
Kohro, Y., Sakaguchi, E., Tashima, R., Tozaki‐Saitoh, H., Okano, H., Inoue, K., & Tsuda, M. (2015) · Scientific Reports · doi:10.1038/srep14306 · Cited by 95
Idiopathic distal sensory polyneuropathy
Freeman, R. L., Gewandter, J. S., Faber, C. G., Gibbons, C. H., Haroutounian, S., Lauria, G., Levine, T., Malik, R. A., Singleton, J. R., Smith, A. G., et al. (2020) · Neurology · doi:10.1212/wnl.0000000000010988 · Cited by 92
Interactions between central nervous system and peripheral metabolic organs
Zeng, W., Yang, F., Shen, W. L., Zhan, C., Zheng, P., & Hu, J. (2022) · Science China Life Sciences · doi:10.1007/s11427-021-2103-5 · Cited by 103
Sprenger, C., Finsterbusch, J., & Büchel, C. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4897-14.2015 · Cited by 92
Lee, K. Y., Bae, C., Lee, D., KAGAN, Z. B., Bradley, K., Chung, J. M., & La, J. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2019.12.031 · Cited by 91
Anti–PD-1 treatment impairs opioid antinociception in rodents and nonhuman primates
Wang, Z., Jiang, C., He, Q., Matsuda, M., Han, Q., Wang, K., Bang, S., Ding, H., Ko, M., & Ji, R. (2020) · Science Translational Medicine · doi:10.1126/scitranslmed.aaw6471 · Cited by 91
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Cao, T., Matyas, J. J., Renn, C. L., Faden, A. I., Dorsey, S. G., & Wu, J. (2020) · Cells · doi:10.3390/cells9051194 · Cited by 95
Sensory Neurons, Neuroimmunity, and Pain Modulation by Sex Hormones
Lenert, M. E., Avona, A., Garner, K. M., Barron, L. R., & Burton, M. D. (2021) · Endocrinology · doi:10.1210/endocr/bqab109 · Cited by 97
TRPV1: Receptor structure, activation, modulation and role in neuro-immune interactions and pain
Maximiano, T. K. E., Carneiro, J. A., Fattori, V., & Verri, W. A., Jr. (2024) · Cell Calcium · doi:10.1016/j.ceca.2024.102870 · Cited by 93
Smith, K. M., Boyle, K. A., Madden, J. F., Dickinson, S. A., Jobling, P., Callister, R. J., Hughes, D. I., & Graham, B. A. (2015) · The Journal of Physiology · doi:10.1113/jp270855 · Cited by 88
Paul, J., Zeilhofer, H. U., & Fritschy, J. (2012) · The Journal of Comparative Neurology · doi:10.1002/cne.23129 · Cited by 87
Lechner, S. G., & Lewin, G. R. (2013) · Physiology · doi:10.1152/physiol.00059.2012 · Cited by 82
Sdrulla, A. D., Xu, Q., He, S.-Q., Tiwari, V., Yang, F., Zhang, C., Shu, B., Shechter, R., Raja, S. N., Wang, Y., et al. (2015) · Pain · doi:10.1097/01.j.pain.0000460353.15460.a3 · Cited by 86
Koga, K., Chen, T., Li, X., Descalzi, G., Ling, J. J., Gu, J., & Zhuo, M. (2011) · Molecular Pain · doi:10.1186/1744-8069-7-47 · Cited by 85
The hypothalamic-spinal dopaminergic system: a target for pain modulation
Puopolo, M. (2019) · Neural Regeneration Research · doi:10.4103/1673-5374.250567 · Cited by 85
Missig, G., Mei, L., Vizzard, M. A., Braas, K. M., Waschek, J. A., Ressler, K. J., Hammack, S. E., & May, V. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.08.025 · Cited by 86
Astrocytes contribute to pain gating in the spinal cord
Xu, Q., Ford, N. C., He, S., Huang, Q., Anderson, M., Chen, Z., Yang, F., Crawford, L. K., Caterina, M. J., Guan, Y., et al. (2021) · Science Advances · doi:10.1126/sciadv.abi6287 · Cited by 84
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Megat, S., Shiers, S. I., Moy, J. K., Barragán‐Iglesias, P., Pradhan, G., Seal, R. P., Dussor, G. O., & Price, T. J. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2110-17.2017 · Cited by 89
Spinal cord projection neurons: a superficial, and also deep analysis
Wercberger, R., & Basbaum, A. I. (2019) · Current Opinion in Physiology · doi:10.1016/j.cophys.2019.10.002 · Cited by 82
Xie, R., Gao, Y., Park, C., Lü, N., Luo, C., Wang, W., Wu, S., & Ji, R. (2017) · Neuroscience Bulletin · doi:10.1007/s12264-017-0106-5 · Cited by 82
Gutierrez-Mecinas, M., Furuta, T., Watanabe, M., & Todd, A. J. (2016) · Molecular Pain · doi:10.1177/1744806916629065 · Cited by 81
Self-citationLuz, L. L., Fernandes, E. C., Sivadó, M., Kókai, É., Szűcs, P., & Safronov, B. V. (2015) · Pain · doi:10.1097/j.pain.0000000000000267 · Cited by 81
Okada, T., Kato, D., Nomura, Y., Obata, N., Quan, X., Morinaga, A., Yano, H., Guo, Z., Aoyama, Y., Tachibana, Y., et al. (2021) · Science Advances · doi:10.1126/sciadv.abd8261 · Cited by 84
Berta, T., Qadri, Y. J., Chen, G., & Ji, R. (2016) · Journal of Dental Research · doi:10.1177/0022034516653604 · Cited by 81
The neurobiology of acute pain
Bell, A. M. (2018) · The Veterinary Journal · doi:10.1016/j.tvjl.2018.05.004 · Cited by 102
Howell, B. L., Lad, S. P., & Grill, W. M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0114938 · Cited by 80
Identification of oxytocin receptor in the dorsal horn and nociceptive dorsal root ganglion neurons
Moreno-López, Y., Martı́nez-Lorenzana, G., Condés‐Lara, M., & Rojas‐Piloni, G. (2012) · Neuropeptides · doi:10.1016/j.npep.2012.09.008 · Cited by 80
Zussy, C., Gómez‐Santacana, X., Rovira, X., Bundel, D. D., Ferrazzo, S., Bosch, D., Asede, D., Malhaire, F., Acher, F., Giraldo, J., et al. (2016) · Molecular Psychiatry · doi:10.1038/mp.2016.223 · Cited by 84
Jang, K., & Garraway, S. M. (2024) · Neurobiology of Pain · doi:10.1016/j.ynpai.2024.100151 · Cited by 83
Zhang, T. C., Janik, J. J., & Grill, W. M. (2014) · Journal of Neurophysiology · doi:10.1152/jn.00254.2014 · Cited by 81
Tashima, R., Koga, K., Sekine, M., Kanehisa, K., Kohro, Y., Tominaga, K., Matsushita, K., Tozaki‐Saitoh, H., Fukazawa, Y., Inoue, K., et al. (2018) · eNeuro · doi:10.1523/eneuro.0450-17.2018 · Cited by 80
Microglia-Mediated Regulation of Neuropathic Pain: Molecular and Cellular Mechanisms
Tsuda, M. (2019) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b19-00715 · Cited by 79
GluN2B and GluN2D NMDARs dominate synaptic responses in the adult spinal cord
Hildebrand, M. E., Pitcher, G. M., Harding, E. K., Li, H., Beggs, S., & Salter, M. W. (2014) · Scientific Reports · doi:10.1038/srep04094 · Cited by 78
Heijmans, L., Mons, M. R., & Joosten, E. A. J. (2021) · Molecular Pain · doi:10.1177/17448069211043965 · Cited by 77
GPR177 in A-fiber sensory neurons drives diabetic neuropathic pain via WNT-mediated TRPV1 activation
Xie, Y., Luo, H., Zhang, S.-X., Chen, X., Guo, R., Liu, S., Liu, S., Wu, H. B. K., Zhen, X., Zhen, X., et al. (2022) · Science Translational Medicine · doi:10.1126/scitranslmed.abh2557 · Cited by 84
Matak, I., Rossetto, O., & Lacković, Z. (2014) · Pain · doi:10.1016/j.pain.2014.04.027 · Cited by 77
Imlach, W. L., Bhola, R. F., Mohammadi, S. A., & Christie, M. J. (2016) · Scientific Reports · doi:10.1038/srep37104 · Cited by 81
Dickie, A. C., Bell, A. M., Iwagaki, N., Polgár, E., Gutièrrez‐Mecinas, M., Kelly, R., Lyon, H., Turnbull, K., West, S. J., Etlin, A., et al. (2018) · Pain · doi:10.1097/j.pain.0000000000001406 · Cited by 79
Self-citationDynorphin is Expressed Primarily by GABAergic Neurons That Contain Galanin in the Rat Dorsal Horn
Sardella, T. C. P., Polgár, E., Garzo, F., Furuta, T., Kaneko, T., Watanabe, M., & Todd, A. J. (2011) · Molecular Pain · doi:10.1186/1744-8069-7-76 · Cited by 80
Self-citationLiu, C., Gao, Y., Luo, H., Berta, T., Xu, Z., Ji, R., & Tan, P.-H. (2016) · Scientific Reports · doi:10.1038/srep34356 · Cited by 76
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Lee, I., Cheon, S., & Park, J.-Y. (2019) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2019/1304152 · Cited by 76
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Tsuda, M., Masuda, T., & Kohno, K. (2023) · Trends in Neurosciences · doi:10.1016/j.tins.2023.05.001 · Cited by 81
Neuronal diversity in the somatosensory system: bridging the gap between cell type and function
Gatto, G., Smith, K. M., Ross, S. E., & Goulding, M. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.03.002 · Cited by 74
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Uttam, S., Wong, C., Price, T. J., & Khoutorsky, A. (2018) · Frontiers in Genetics · doi:10.3389/fgene.2018.00470 · Cited by 79
Dedek, A., Xu, J., Lorenzo, L.-É., Godin, A. G., Kandegedara, C. M., Glavina, G., Landrigan, J., Lombroso, P. J., Koninck, Y. D., Tsai, E. C., et al. (2021) · Brain · doi:10.1093/brain/awab408 · Cited by 84
Zic2-Dependent Axon Midline Avoidance Controls the Formation of Major Ipsilateral Tracts in the CNS
Escalante, A., Murillo, B. R., Morenilla‐Palao, C., Klar, A., & Herrera, E. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.007 · Cited by 74
Pagadala, P., Park, C., Bang, S., Xu, Z., Xie, R., Liu, T., Han, B.-X., Tracey, W. D., Wang, F., & Ji, R. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0454-13.2013 · Cited by 74
Chen, Q., Roeder, Z., Li, M., Zhang, Y., Ingram, S., & Heinricher, M. M. (2017) · eNeuro · doi:10.1523/eneuro.0202-17.2017 · Cited by 73
Bittar, A., Jun, J., La, J., Wang, J., Leem, J. W., & Chung, J. M. (2017) · Pain · doi:10.1097/j.pain.0000000000001014 · Cited by 73
Gutièrrez‐Mecinas, M., Bell, A. M., Marin, A., Taylor, R., Boyle, K. A., Furuta, T., Watanabe, M., Polgár, E., & Todd, A. J. (2016) · Pain · doi:10.1097/j.pain.0000000000000778 · Cited by 72
Self-citationA spinal analog of memory reconsolidation enables reversal of hyperalgesia
Bonin, R. P., & Koninck, Y. D. (2014) · Nature Neuroscience · doi:10.1038/nn.3758 · Cited by 72
Peláez, F. J. R., & Taniguchi, S. (2015) · Neural Plasticity · doi:10.1155/2016/4131395 · Cited by 71
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Zhu, X., Zhou, W., Jin, Y., Tang, H.-D., Cao, P., Mao, Y., Xie, W., Zhang, X., Zhao, F., Luo, M.-H., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.11.003 · Cited by 74
Quantitative study of NPY‐expressing GABAergic neurons and axons in rat spinal dorsal horn
Polgár, E., Sardella, T. C. P., Watanabe, M., & Todd, A. J. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22570 · Cited by 69
Self-citationSensory axon regeneration: rebuilding functional connections in the spinal cord
Smith, G. M., Falone, A. E., & Frank, E. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.10.006 · Cited by 72
Premenstrual dysphoric disorder and prefrontal reactivity during anticipation of emotional stimuli
Gingnell, M., Bannbers, E., Wikström, J., Fredrikson, M., & Poromaa, I. S. (2013) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2013.08.002 · Cited by 69
Sugimura, Y. K., Takahashi, Y., Watabe, A. M., & Kato, F. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00946.2015 · Cited by 69
Semi-intact ex vivo approach to investigate spinal somatosensory circuits
Hachisuka, J., Baumbauer, K. M., Omori, Y., Snyder, L. M., Koerber, H. R., & Ross, S. E. (2016) · eLife · doi:10.7554/elife.22866 · Cited by 68
Ion channels and neuronal hyperexcitability in chemotherapy-induced peripheral neuropathy
Aromolaran, K. A., & Goldstein, P. A. (2017) · Molecular Pain · doi:10.1177/1744806917714693 · Cited by 68
Shinohara, K., Watabe, A. M., Nagase, M., Okutsu, Y., Takahashi, Y., Kurihara, H., & Kato, F. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13662 · Cited by 68
Benson, C. A., Paylor, J. W., Tenorio, G., Winship, I. R., Baker, G. B., & Kerr, B. J. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.05.017 · Cited by 68
Nees, T. A., Tappe‐Theodor, A., Sliwinski, C., Motsch, M., Rupp, R., Kuner, R., Weidner, N., & Blesch, A. (2015) · Pain · doi:10.1097/j.pain.0000000000000422 · Cited by 68
Sugimoto, M., Takahashi, Y., Sugimura, Y. K., Tokunaga, R., Yajima, M., & Kato, F. (2021) · Pain · doi:10.1097/j.pain.0000000000002224 · Cited by 66
Nakao, A., Takahashi, Y., Nagase, M., Ikeda, R., & Kato, F. (2012) · Molecular Pain · doi:10.1186/1744-8069-8-51 · Cited by 70
Takazawa, T., Choudhury, P., Tong, C., Conway, C. M., Scherrer, G., Flood, P. D., Mukai, J., & MacDermott, A. B. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2354-16.2017 · Cited by 66
Dedek, A., Xu, J., Kandegedara, C. M., Lorenzo, L.-É., Godin, A. G., Koninck, Y. D., Lombroso, P. J., Tsai, E. C., & Hildebrand, M. E. (2019) · Brain · doi:10.1093/brain/awz105 · Cited by 70
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Burston, J. J., & Woodhams, S. G. (2013) · Proceedings of The Nutrition Society · doi:10.1017/s0029665113003650 · Cited by 67
Barrio, M. G. D., Bourane, S., Grossmann, K. S., Schüle, R., Britsch, S., O’Leary, D. D. M., & Goulding, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0077928 · Cited by 65
Metadata
- Authors
- Todd, A. J.
- Affiliations
- University of Glasgow (GB)
- Corresponding author
- Todd, Andrew J.
- ORCID
- Todd, Andrew J.
- Venue
- Nature Reviews Neuroscience
- Published
- 2010-11-11
- Volume
- 11
- Issue
- 12
- Pages
- 823-836
- ISSN
- 1471-003X (ISSN-L)
- 1471-0048
- PMC
- PMC3277941
- OpenAlex
- W2059635921
- Cited by
- 1,475
- References
- 162
- Citations by year
- 2026: 100 · 2025: 114 · 2024: 95 · 2023: 108 · 2022: 122 · 2021: 137 · 2020: 106 · 2019: 125 · 2018: 85 · 2017: 85 · 2016: 90 · 2015: 86 · 2014: 75 · 2013: 76 · 2012: 39
- FWCI
- 4.69
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) (acceptedVersion)
- Funders
- Wellcome Trust (076976)
- 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
- dorsal horn, spinal cord, pain processing, neural circuits, hyperalgesia, allodynia, sensory neurons, analgesic targets, nerve injury, inflammation, pain perception
- MeSH terms
- Afferent Pathways, Animals, Brain, Disease Models, Animal, Humans, Nerve Net, Nociceptors, Pain, Posterior Horn Cells
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