Neuronal circuitry for pain processing in the dorsal horn

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

An experimental model for peripheral neuropathy produced by segmental spinal nerve ligation in the rat

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

Investigating dynamic pain sensitivity in the context of the fear‐avoidance model

Gay, C. W., Horn, M. E., Bishop, M. D., Robinson, M. E., & Bialosky, J. E. (2014) · European Journal of Pain · doi:10.1002/ejp.519 · Cited by 24

Downregulation of connexin36 in mouse spinal dorsal horn neurons leads to mechanical allodynia

Nakamura, Y., Morioka, N., Zhang, F. F., Hisaoka‐Nakashima, K., & Nakata, Y. (2014) · Journal of Neuroscience Research · doi:10.1002/jnr.23515 · Cited by 24

Interoception, body awareness and chronic pain: Results from a case–control study

d'Alcalà, C. R., Webster, D. G., & Esteves, J. E. (2014) · International journal of osteopathic medicine · doi:10.1016/j.ijosm.2014.08.003 · Cited by 26

Neuroanatomy of the Spinal Cord

Darby, S. A., & Frysztak, R. J. (2013) · Elsevier eBooks · doi:10.1016/b978-0-323-07954-9.00009-8 · Cited by 24

Spatiotemporal trajectories of reactivation of somatosensory cortex by direct and secondary pathways after dorsal column lesions in squirrel monkeys

Qi, H., Wang, F., Liao, C., Friedman, R. M., Tang, C., Kaas, J. H., & Avison, M. J. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.08.015 · Cited by 24

Noradrenergic inhibition of spinal hyperexcitation elicited by cutaneous cold stimuli in rats with oxaliplatin-induced allodynia: electrophysiological and behavioral assessments

Choi, S., Yamada, A., Kim, W., Kim, S. K., & Furue, H. (2016) · The Journal of Physiological Sciences · doi:10.1007/s12576-016-0505-9 · Cited by 24

Functional Organization of Cutaneous and Muscle Afferent Synapses onto Immature Spinal Lamina I Projection Neurons

Li, J., & Baccei, M. L. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3164-16.2016 · Cited by 24

Imaging Acute and Chronic Pain in the Human Brainstem and Spinal Cord

Henderson, L. A., & Keay, K. A. (2017) · The Neuroscientist · doi:10.1177/1073858417703911 · Cited by 24

Heteromeric α/β glycine receptors regulate excitability in parvalbumin‐expressing dorsal horn neurons through phasic and tonic glycinergic inhibition

Gradwell, M. A., Boyle, K. A., Callister, R. J., Hughes, D. I., & Graham, B. A. (2017) · The Journal of Physiology · doi:10.1113/jp274926 · Cited by 23

Diverse spinal commissural neuron populations revealed by fate mapping and molecular profiling using a novel Robo3Cre mouse

Tulloch, A. J., Teo, S., Carvajal, B. V., Tessier‐Lavigne, M., & Jaworski, A. (2019) · The Journal of Comparative Neurology · doi:10.1002/cne.24720 · Cited by 24

Diverse firing properties and Aβ-, Aδ-, and C-afferent inputs of small local circuit neurons in spinal lamina I

Fernandes, E. C., Luz, L. L., Mytakhir, O., Lukoyanov, N., Szűcs, P., & Safronov, B. V. (2016) · Pain · doi:10.1097/j.pain.0000000000000394 · Cited by 24

Glutamatergic neuronal populations in the brainstem of the sea lamprey, Petromyzon marinus: An in situ hybridization and immunocytochemical study

Villar‐Cerviño, V., Barreiro‐Iglesias, A., Fernández‐López, B., Mazan, S., Rodicio, M. C., & Anadón, R. (2012) · The Journal of Comparative Neurology · doi:10.1002/cne.23189 · Cited by 24

Neonatal Injury Evokes Persistent Deficits in Dynorphin Inhibitory Circuits within the Adult Mouse Superficial Dorsal Horn

Brewer, C. L., Li, J., O'Conor, K., Serafin, E. K., & Baccei, M. L. (2020) · The Journal of Neuroscience · doi:10.1523/jneurosci.0029-20.2020 · Cited by 23

An atlas of neuropathic pain-associated molecular pathological characteristics in the mouse spinal cord

Dong, F., Yu, L., Feng, P.-D., Ren, J., Bai, X., Lin, J., Cao, D., Deng, Y.-T., Zhang, Y., Shen, H., et al. (2025) · Communications Biology · doi:10.1038/s42003-025-07506-0 · Cited by 27

Electroacupuncture-Induced Muscular Inflammatory Pain Relief Was Associated With Activation of Low-Threshold Mechanoreceptor Neurons and Inhibition of Wide Dynamic Range Neurons in Spinal Dorsal Horn

Duanmu, C.-L., Zhang, X.-N., Shi, H., Su, Y., Wan, Y., Wang, Y., Qu, Z., He, W., Wang, X., & Jing, X. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.687173 · Cited by 23

Characterisation of lamina I anterolateral system neurons that express Cre in a Phox2a-Cre mouse line

Alsulaiman, W. A. A., Quillet, R., Bell, A. M., Dickie, A. C., Polgár, E., Boyle, K. A., Watanabe, M., Roome, R. B., Kania, A., Todd, A. J., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-97105-w · Cited by 28

2-Bromopalmitate decreases spinal inflammation and attenuates oxaliplatin-induced neuropathic pain via reducing Drp1-mediated mitochondrial dysfunction

Dong, Z.-B., Wang, Y.-J., Cheng, M.-L., Wang, B., Lu, H., Zhu, H.-L., Liu, L., & Xie, M. (2022) · PLoS ONE · doi:10.1371/journal.pone.0275428 · Cited by 24

C-LTMRs evoke wet dog shakes via the spinoparabrachial pathway

Zhang, D., Turecek, J., Choi, S., DeLisle, M. M., Pamplona, C. L., Meltzer, S., & Ginty, D. D. (2024) · Science · doi:10.1126/science.adq8834 · Cited by 23

Effects of baclofen on mechanical noxious and innocuous transmission in the spinal dorsal horn of the adult rat: in vivo patch‐clamp analysis

Fukuhara, K., Katafuchi, T., & Yoshimura, M. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12345 · Cited by 23

Whole-body Vibration at Thoracic Resonance Induces Sustained Pain and Widespread Cervical Neuroinflammation in the Rat

Zeeman, M. E., Kartha, S., Jaumard, N. V., Baig, H. A., Stablow, A. M., Lee, J., Guarino, B. B., & Winkelstein, B. A. (2015) · Clinical Orthopaedics and Related Research · doi:10.1007/s11999-015-4315-9 · Cited by 23

Peripheral and spinal circuits involved in mechanical allodynia

Arcourt, A., & Lechner, S. G. (2015) · Pain · doi:10.1097/01.j.pain.0000460818.62406.38 · Cited by 23

Selective impact of Tau loss on nociceptive primary afferents and pain sensation

Sotiropoulos, I., Lopes, A. T., Pinto, V., Lopes, S., Carlos, S., Duarte-Silva, S., Neves-Carvalho, A., Pinto-Ribeiro, F., Pinheiro, S., Fernandes, R., et al. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2014.07.008 · Cited by 23

Are all spinal segments equal: intrinsic membrane properties of superficial dorsal horn neurons in the developing and mature mouse spinal cord

Tadros, M. A., Harris, B. M., Anderson, W. B., Brichta, A. M., Graham, B. A., & Callister, R. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.227389 · Cited by 23

Dorsal horn circuitry

Benarroch, E. E. (2016) · Neurology · doi:10.1212/wnl.0000000000002478 · Cited by 23

Long‐term, dynamic synaptic reorganization after GABAergic precursor cell transplantation into adult mouse spinal cord

Llewellyn‐Smith, I. J., Basbaum, A. I., & Braz, J. M. (2017) · The Journal of Comparative Neurology · doi:10.1002/cne.24346 · Cited by 22

Long-term effects of direct current are reproduced by intermittent depolarization of myelinated nerve fibers

Bączyk, M., & Jankowska, E. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00236.2018 · Cited by 23

PKCγ interneurons, a gateway to pathological pain in the dorsal horn

Artola, A., Voisin, D. L., & Dallel, R. (2020) · Journal of Neural Transmission · doi:10.1007/s00702-020-02162-6 · Cited by 24

GABAB Receptors and Pain

Benke, D. (2020) · Current topics in behavioral neurosciences · doi:10.1007/7854_2020_130 · Cited by 23

Dendritic Spine Dynamics after Peripheral Nerve Injury: An Intravital Structural Study

Benson, C. A., Fenrich, K. K., Olson, K.-L., Patwa, S., Bangalore, L., Waxman, S. G., & Tan, A. M. (2020) · The Journal of Neuroscience · doi:10.1523/jneurosci.2858-19.2020 · Cited by 22

Current Concepts of Pain Pathways: A Brief Review of Anatomy, Physiology, and Medical Imaging

Gonzalez-Hermosillo, D.-C., González-Hermosillo, L.-M., Villaseñor-Almaraz, M., Herrera, D. B., Moreno‐Jiménez, S., Corona-Cedillo, R., Velasco‐Campos, F., Carrillo-Ruiz, J. D., & Roldán-Valadéz, E. (2023) · Current Medical Imaging Formerly Current Medical Imaging Reviews · doi:10.2174/1573405620666230519144112 · Cited by 22

Morphological and Physiological Plasticity of Spinal Lamina II GABA Neurons Is Induced by Sciatic Nerve Chronic Constriction Injury in Mice

Zhang, H., Li, Y., Yang, Q. K., Liu, X., & Dougherty, P. M. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00143 · Cited by 22

Lamina‐specific population encoding of cutaneous signals in the spinal dorsal horn using multi‐electrode arrays

Greenspon, C. M., Battell, E. E., Devonshire, I. M., Donaldson, L. F., Chapman, V., & Hathway, G. J. (2018) · The Journal of Physiology · doi:10.1113/jp277036 · Cited by 26

Persistent Rheb-induced mTORC1 activation in spinal cord neurons induces hypersensitivity in neuropathic pain

Ma, X., Du, W., Wang, W., Luo, L., Huang, M., Wang, H., Lin, R., Li, Z., Shi, H., Yuan, T., et al. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-02966-0 · Cited by 21

Projections from the lateral parabrachial nucleus to the lateral and ventral lateral periaqueductal gray subregions mediate the itching sensation

Li, J., Ren, J.-H., He, C.-B., Zhao, W., Li, H., Dong, Y., & Li, Y.-Q. (2021) · Pain · doi:10.1097/j.pain.0000000000002193 · Cited by 22

Differential expression of GluN2 NMDA receptor subunits in the dorsal horn of male and female rats

Temi, S., Rudyk, C., Armstrong, J., Landrigan, J., Dedek, C., Salmaso, N., & Hildebrand, M. E. (2021) · Channels · doi:10.1080/19336950.2020.1871205 · Cited by 22

Real-World Outcomes Using a Spinal Cord Stimulation Device Capable of Combination Therapy for Chronic Pain: A European, Multicenter Experience

Kallewaard, J. W., Paz-Solis, J. F., Negri, P. D., Canos-Verdecho, M. A., Belaïd, H., Thomson, S., Abejón, D., Vesper, J., Mehta, V., Rigoard, P., et al. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10184085 · Cited by 22

Small molecule targeting NaV1.7 via inhibition of the CRMP2-Ubc9 interaction reduces pain in chronic constriction injury (CCI) rats

Li, J., Stratton, H. J., Lorca, S. A., Grace, P. M., & Khanna, R. (2022) · Channels · doi:10.1080/19336950.2021.2023383 · Cited by 22

Inhibition of itch by neurokinin 1 receptor (Tacr1) -expressing ON cells in the rostral ventromedial medulla in mice

Follansbee, T., Domocos, D. T., Nguyen, E. K., Nguyen, A., Bountouvas, A., Velasquez, L., Carstens, M. I., Takanami, K., Ross, S. E., & Carstens, E. E. (2022) · eLife · doi:10.7554/elife.69626 · Cited by 21

A developmental shift in habituation to pain in human neonates

Rupawala, M., Bucsea, O., Laudiano‐Dray, M. P., Whitehead, K., Meek, J. H., Fitzgerald, M., Olhede, S. C., Jones, L., & Lorenzo Fabrizi, D. (2023) · Current Biology · doi:10.1016/j.cub.2023.02.071 · Cited by 26

Mechanism of GABA involvement in post‐traumatic trigeminal neuropathic pain: Activation of neuronal circuitry composed of PKCγ interneurons and pERK 1/2 expressing neurons

Dieb, W., & Hafidi, A. (2014) · European Journal of Pain · doi:10.1002/ejp.525 · Cited by 22

Segmental disinhibition suppresses C‐fiber inputs to the rat superficial medullary dorsal horn via the activation of GABA Breceptors

Melin, C., Jacquot, F., Dallel, R., & Artola, A. (2012) · European Journal of Neuroscience · doi:10.1111/ejn.12048 · Cited by 22

Therapeutic potential of group III metabotropic glutamate receptor ligands in pain

Acher, F., & Goudet, C. (2014) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2014.11.007 · Cited by 22

Inhibition of the mammalian target of rapamycin complex 1 signaling pathway reduces itch behaviour in mice

Obara, I., Medrano, M., Signoret-Genest, J., Jiménez‐Díaz, L., Géranton, S. M., & Hunt, S. P. (2015) · Pain · doi:10.1097/j.pain.0000000000000197 · Cited by 22

Phosphorylated Histone 3 at Serine 10 Identifies Activated Spinal Neurons and Contributes to the Development of Tissue Injury-Associated Pain

Torres-Pérez, J. V., Sántha, P., Varga, A., Szűcs, P., Valente, J. D. S., Gaál, B., Sivadó, M., Andreou, A. P., Beattie, S., Nagy, B. M., et al. (2017) · Scientific Reports · doi:10.1038/srep41221 · Cited by 22

Role of RGS12 in the differential regulation of kappa opioid receptor-dependent signaling and behavior

Gross, J., Kaski, S. W., Schmidt, K. T., Cogan, E. S., Boyt, K. M., Wix, K., Schroer, A. B., McElligott, Z. A., Siderovski, D. P., & Setola, V. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0423-7 · Cited by 22

The anti-inflammatory and analgesic effects of intraperitoneal melatonin after spinal nerve ligation are mediated by inhibition of the NF-κB/NLRP3 inflammasome signaling pathway

Wang, Y., Tang, Y., Gao, X. W., Liu, J., Zhang, N., Liang, Z., Li, Y., & Pan, L.-X. (2021) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2021.01.015 · Cited by 22

Involvement of the Spinal Cord in Parkinson's Disease

Raudino, F., & Leva, S. (2011) · International Journal of Neuroscience · doi:10.3109/00207454.2011.613551 · Cited by 22

Spatial transcriptomics combined with single-nucleus RNA sequencing reveals glial cell heterogeneity in the human spinal cord

Chen, Y., Wei, Y., Liu, J., Zhu, T., Zhou, C., & Zhang, D. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-23-01876 · Cited by 22

Optogenetics and photopharmacology in pain research and therapeutics

Iseppon, F., & Arcangeletti, M. (2020) · STEMedicine · doi:10.37175/stemedicine.v1i3.43 · Cited by 22

Pharmacological Evidence on Augmented Antiallodynia Following Systemic Co-Treatment with GlyT-1 and GlyT-2 Inhibitors in Rat Neuropathic Pain Model

Mohammadzadeh, A., Lakatos, P. P., Balogh, M., Zádor, F., Karádi, D. Á., Zádori, Z., Király, K. P., Galambos, A. R., Barsi, S., Riba, P., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052479 · Cited by 21

Drosophila Fezf functions as a transcriptional repressor to direct layer-specific synaptic connectivity in the fly visual system

Santiago, I. J., Zhang, D., Saras, A., Pontillo, N., Xu, C., Chen, X., Weirauch, M. T., Mistry, M., Ginty, D. D., Pecot, M. Y., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2025530118 · Cited by 17

Inhibition of Spinal 5-HT3 Receptor and Spinal Dorsal Horn Neuronal Excitability Alleviates Hyperalgesia in a Rat Model of Parkinson’s Disease

Li, C.-J., Zhang, L.-G., Liu, L.-B., An, M.-Q., Dong, L.-G., Gu, H., Dai, Y.-P., Wang, F., Mao, C., & Liu, C. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-03034-8 · Cited by 21

Voltage-gated calcium channel subunit α2δ-1 in spinal dorsal horn neurons contributes to aberrant excitatory synaptic transmission and mechanical hypersensitivity after peripheral nerve injury

Koga, K., Kobayashi, K., Tsuda, M., Kubota, K., Kitano, Y., & Furue, H. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1099925 · Cited by 21

Alleviation of neuropathic pain with neuropeptide Y requires spinal Npy1r interneurons that coexpress Grp

Nelson, T. S., Allen, H. N., Basu, P., Prasoon, P., Nguyen, E. K., Arokiaraj, C. M., dos Santos, D. F. D. S., Seal, R. P., Ross, S. E., Todd, A. J., et al. (2023) · JCI Insight · doi:10.1172/jci.insight.169554 · Cited by 21

A Novel Flp Reporter Mouse Shows That TRPA1 Expression Is Largely Limited to Sensory Neuron Subsets

Patil, M. J., Kim, S.-H., Bahia, P. K., Nair, S. S., Darcey, T. S., Fiallo, J., Zhu, X. X., Frisina, R. D., Hadley, S. H., & Taylor‐Clark, T. E. (2023) · eNeuro · doi:10.1523/eneuro.0350-23.2023 · Cited by 23

Subpopulation‐specific patterns of intrinsic connectivity in mouse superficial dorsal horn as revealed by laser scanning photostimulation

Kosugi, M., Kato, G., Lukashov, S., Pendse, G., Puskár, Z., Kozsurek, M., & Strassman, A. M. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2012.244210 · Cited by 21

The Glutamatergic Neurons in the Spinal Cord of the Sea Lamprey: An In Situ Hybridization and Immunohistochemical Study

Fernández‐López, B., Villar‐Cerviño, V., Valle-Maroto, S. M., Barreiro‐Iglesias, A., Anadón, R., & Rodicio, M. C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0047898 · Cited by 21

Role of the potassium chloride cotransporter isoform 2-mediated spinal chloride homeostasis in a rat model of visceral hypersensitivity

Tang, D., Qian, A., Song, D., Ben, Q., Yao, W., Sun, J. P., Li, W., Xu, T., & Yuan, Y. (2015) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00313.2014 · Cited by 21

Transient, Activity Dependent Inhibition of Transmitter Release from Low Threshold Afferents Mediated by GABAA Receptors in Spinal Cord Lamina III/IV

Betelli, C., MacDermott, A. B., & Bardoni, R. (2015) · Molecular Pain · doi:10.1186/s12990-015-0067-5 · Cited by 23

RNA control in pain: Blame it on the messenger

de la Peña, J. B., Song, J. J., & Campbell, Z. T. (2019) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1546 · Cited by 21

Differential modulation of excitatory and inhibitory populations of superficial dorsal horn neurons in lumbar spinal cord by Aβ-fiber electrical stimulation

Fan, W., & Sdrulla, A. D. (2020) · Pain · doi:10.1097/j.pain.0000000000001836 · Cited by 21

New insights into the mechanisms behind mechanical itch

Sakai, K., & Akiyama, T. (2020) · Experimental Dermatology · doi:10.1111/exd.14143 · Cited by 21

Interactions between superficial and deep dorsal horn spinal cord neurons in the processing of nociceptive information

Petitjean, H., Rodeau, J., & Schlichter, R. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08273.x · Cited by 21

Activation of medullary dorsal horn γ isoform of protein kinase C interneurons is essential to the development of both static and dynamic facial mechanical allodynia

Pham‐Dang, N., Descheemaeker, A., Dallel, R., & Artola, A. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13165 · Cited by 21

Differential Activation of TRP Channels in the Adult Rat Spinal Substantia Gelatinosa by Stereoisomers of Plant-Derived Chemicals

Kumamoto, E., & Fujita, T. (2016) · Pharmaceuticals · doi:10.3390/ph9030046 · Cited by 21

Analysis of spontaneous activity of superficial dorsal horn neurons in vitro: neuropathy-induced changes

Roza, C., Mazo, I., Rivera‐Arconada, I., Cisneros, E., Alayón, I., & Lopez-Garcia, J. A. (2016) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-016-1886-6 · Cited by 21

5-HT1Dreceptors inhibit the monosynaptic stretch reflex by modulating C-fiber activity

Lucas‐Osma, A. M., Li, Y., Murray, K., Lin, S., Black, S., Stephens, M. J., Ahn, A. H., Heckman, C. J., Fenrich, K. K., Fouad, K., et al. (2019) · Journal of Neurophysiology · doi:10.1152/jn.00805.2018 · Cited by 21

Spinal Cord Stimulation

Guan, Y., Bradley, K., Parker, J. L., Krames, E. S., & Linderoth, B. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-805353-9.00015-2 · Cited by 21

Review of Treatment for Central Spinal Neuropathic Pain and Its Effect on Quality of Life: Implications for Neuromyelitis Optica Spectrum Disorder

Mealy, M. A., Kozachik, S. L., & Levy, M. (2019) · Pain Management Nursing · doi:10.1016/j.pmn.2019.03.003 · Cited by 20

Transition from Acute to Chronic Pain: Where Cells, Systems and Society Meet

Glare, P., Overton, S., & Aubrey, K. (2020) · Pain Management · doi:10.2217/pmt-2019-0039 · Cited by 20

Behavioral and neural correlates of diverse conditioned fear responses in male and female rats

Mitchell, J. R., Vincelette, L. K., Tuberman, S., Sheppard, V., Bergeron, E., Calitri, R., Clark, R., Cody, C. R., Kannan, A., Keith, J., et al. (2024) · Neurobiology of Stress · doi:10.1016/j.ynstr.2024.100675 · Cited by 22

A pontine center in descending pain control

Li, T., Zhou, W., Jin, K., Chen, M., Wang, Z., Hayashi, L., Su, X., Jia, W., Huang, W., Wang, C.-S., et al. (2025) · Neuron · doi:10.1016/j.neuron.2025.02.028 · Cited by 22

Characterization of the Gbx1−/− Mouse Mutant: A Requirement for Gbx1 in Normal Locomotion and Sensorimotor Circuit Development

Buckley, D. M., Burroughs-Garcìa, J., Lewandoski, M. B., & Waters, S. T. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056214 · Cited by 20

Conserved contributions of NMDA receptor subtypes to synaptic responses in lamina II spinal neurons across early postnatal development

Mahmoud, H., Martin, N., & Hildebrand, M. E. (2020) · Molecular Brain · doi:10.1186/s13041-020-00566-9 · Cited by 20

Independent evolution of pain insensitivity in African mole-rats: origins and mechanisms

Smith, E. S. J., Park, T. J., & Lewin, G. R. (2020) · Journal of Comparative Physiology A · doi:10.1007/s00359-020-01414-w · Cited by 21

NMDA Receptor Modulates Spinal Iron Accumulation Via Activating DMT1(-)IRE in Remifentanil-Induced Hyperalgesia

Shu, R., Zhang, L., Zhang, H., Li, Y., Wang, C., Su, L., Zhao, H., & Wang, G. (2020) · Journal of Pain · doi:10.1016/j.jpain.2020.03.007 · Cited by 20

Activation of microglial GPR109A alleviates thermal hyperalgesia in female lupus mice by suppressing IL ‐18 and glutamatergic synaptic activity

Viatchenko‐Karpinski, V., Kong, L., & Weng, H. (2021) · Glia · doi:10.1002/glia.24130 · Cited by 20

In vitro atlas of dorsal spinal interneurons reveals Wnt signaling as a critical regulator of progenitor expansion

Gupta, S. K., Kawaguchi, R., Heinrichs, E., Gallardo, S., Castellanos, S., Mandric, I., Novitch, B. G., & Butler, S. J. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111119 · Cited by 21

Long-term actions of BDNF on inhibitory synaptic transmission in identified neurons of the rat substantia gelatinosa

Lu, V. B., Colmers, W. F., & Smith, P. A. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00457.2011 · Cited by 20

A MusD Retrotransposon Insertion in the Mouse Slc6a5 Gene Causes Alterations in Neuromuscular Junction Maturation and Behavioral Phenotypes

Bogdanik, L. P., Chapman, H. D., Miers, K. E., SERREZE, D. V., & Burgess, R. W. (2012) · PLoS ONE · doi:10.1371/journal.pone.0030217 · Cited by 20

Herpes simplex virus-based nerve targeting gene therapy in pain management

Wolfe, D. P., Goss, J. R., Krisky, D. M., & Wechuck, J. (2014) · Journal of Pain Research · doi:10.2147/jpr.s36619 · Cited by 20

Identifying spinal sensory pathways activated by noxious esophageal acid

Harrington, A. M., Brierley, S. M., Isaacs, N. J., Young, R. L., & Blackshaw, L. A. (2013) · Neurogastroenterology & Motility · doi:10.1111/nmo.12180 · Cited by 20

The Development of Translational Biomarkers as a Tool for Improving the Understanding, Diagnosis and Treatment of Chronic Neuropathic Pain

Buckley, D. A., Jennings, E. M., Burke, N. N., Roche, M., McInerney, V., Wren, J. D., Finn, D. P., & McHugh, P. (2017) · Molecular Neurobiology · doi:10.1007/s12035-017-0492-8 · Cited by 20

Astrocytes in the spinal dorsal horn and chronic itch

Tsuda, M. (2017) · Neuroscience Research · doi:10.1016/j.neures.2017.08.010 · Cited by 20

Prostaglandin Signaling Governs Spike Timing-Dependent Plasticity at Sensory Synapses onto Mouse Spinal Projection Neurons

Li, J., Serafin, E. K., & Baccei, M. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2152-17.2018 · Cited by 15

Central expression of synaptophysin and synaptoporin in nociceptive afferent subtypes in the dorsal horn

Chung, J., Franklin, J. F., & Lee, H. J. (2019) · Scientific Reports · doi:10.1038/s41598-019-40967-y · Cited by 20

L-bupivacaine Inhibition of Nociceptive Transmission in Rat Peripheral and Dorsal Horn Neurons

Uta, D., Koga, K., Furue, H., Imoto, K., & Yoshimura, M. (2020) · Anesthesiology · doi:10.1097/aln.0000000000003596 · Cited by 20

Mechanisms Underlying the Anti-Suicidal Treatment Potential of Buprenorphine

Cameron, C. M., Nieto, S. J., Bosler, L., Wong, M. H., Bishop, I., Mooney, L. J., & Cahill, C. M. (2021) · Advances in Drug and Alcohol Research · doi:10.3389/adar.2021.10009 · Cited by 20

Relationship of membrane properties, spike burst responses, laminar location, and functional class of dorsal horn neurons recorded in vitro

Dougherty, P. M., & Chen, J. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00187.2016 · Cited by 20

Substance P-expressing Neurons in the Superficial Dorsal Horn of the Mouse Spinal Cord: Insights into Their Functions and their Roles in Synaptic Circuits

Polgár, E., Bell, A. M., Gutierrez-Mecinas, M., Dickie, A. C., Akar, O., Costreie, M., Watanabe, M., & Todd, A. J. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.06.038 · Cited by 19

Characterization and pharmacological modulation of noci-responsive deep dorsal horn neurons across diverse rat models of pathological pain

McGaraughty, S., Chu, K. L., & Xu, J. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00325.2018 · Cited by 19

Increased Expression of Fibronectin Leucine-Rich Transmembrane Protein 3 in the Dorsal Root Ganglion Induces Neuropathic Pain in Rats

Yamada, M., Fujita, Y., Hayano, Y., Hayakawa, H., Baba, K., Mochizuki, H., & Yamashita, T. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.0295-19.2019 · Cited by 19

Analysis of ALS-related proteins during herpes simplex virus-2 latent infection

Cabrera, J. R., Rodríguez‐Izquierdo, I., Jiménez, J. L., & Muñoz‐Fernández, M. Á. (2020) · Journal of Neuroinflammation · doi:10.1186/s12974-020-02044-4 · Cited by 19

The structure of sensory afferent compartments in health and disease

Middleton, S. J., Pérez-Sánchez, J., & Dawes, J. M. (2021) · Journal of Anatomy · doi:10.1111/joa.13544 · Cited by 23

Calretinin-expressing islet cells are a source of pre- and post-synaptic inhibition of non-peptidergic nociceptor input to the mouse spinal cord

Davis, O., Dickie, A. C., Mustapa, M., Boyle, K. A., Browne, T. J., Gradwell, M. A., Smith, K. M., Polgár, E., Bell, A. M., Kókai, É., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-38605-9 · Cited by 21

Striatal-enriched protein tyrosine phosphatase modulates nociception

Azkona, G., Saavedra, A., Aira, Z., Aluja, D., Xifró, X., Baguley, T. D., Alberch, J., Ellman, J. A., Lombroso, P. J., Azkue, J. J., et al. (2015) · Pain · doi:10.1097/j.pain.0000000000000329 · Cited by 19

Therapeutic potential of Pak1 inhibition for pain associated with cutaneous burn injury

Guo, Y., Benson, C. A., Hill, M., Henry, S. S., Effraim, P. R., Waxman, S. G., Dib‐Hajj, S. D., & Tan, A. M. (2018) · Molecular Pain · doi:10.1177/1744806918788648 · Cited by 19

Cell-Type Specific Distribution of T-Type Calcium Currents in Lamina II Neurons of the Rat Spinal Cord

Wu, J., Peng, S., Xiao, L., Cheng, X., Kuang, H., Zhu, M., Zhang, D., Jiang, C., & Liu, T. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00370 · Cited by 19

Supraspinal neuroimmune crosstalk in chronic pain states

Austin, P. J., & Fiore, N. T. (2019) · Current Opinion in Physiology · doi:10.1016/j.cophys.2019.03.008 · Cited by 19

Distinct mechanisms of signal processing by lamina I spino-parabrachial neurons

Agashkov, K., Krotov, V., Krasniakova, M., Shevchuk, D. P., Andrianov, Y., Zabenko, Y. Y., Safronov, B. V., Voitenko, N. V., & Belan, P. V. (2019) · Scientific Reports · doi:10.1038/s41598-019-55462-7 · Cited by 23

An update on the spinal and peripheral pathways of pain signalling

Lechner, S. G. (2017) · e-Neuroforum · doi:10.1515/nf-2017-a020 · Cited by 8

Neuronal networks and nociceptive processing in the dorsal horn of the spinal cord

Cordero‐Erausquin, M., Inquimbert, P., Schlichter, R., & Hugel, S. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.08.048 · Cited by 59

Dorsal Horn Pain Mechanisms

Zeilhofer, H. U., & Ganley, R. P. (2019) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780190860509.013.23 · Cited by 6

Synaptic Transmission of Pain in the Dorsal Horn

McDowell, T. S. (2019) · Springer eBooks · doi:10.1007/978-3-319-99124-5_10 · Cited by 1

Sensory plasticity of dorsal horn silent neurons as a critical mechanism for neuropathic pain

Negm, A., Gabrielli, F., Zbili, M., Poncet‐Megemont, L., Hérault, K., Makhoul, J., Legrand, A., Luccarini, P., Artola, A., Dallel, R., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-76982-7