The DOI matches its Crossref record; 12 of the 12 references it cites were found in a registry or an index.
Motor cortex stimulation for neuropathic pain: From phenomenology to mechanisms
Abstract
Motor cortex stimulation (MCS) is relatively recent neurosurgical technique for pain control, the use of which is growing steadily since its description in the last decade. While clinical series show that at least 50% of patients with chronic, pharmacoresistant neuropathic pain may benefit from this technique, the mechanisms of action of MCS remain elusive. In this review, we synthesise a number of studies that, combining electrophysiology and functional imaging, have permitted to proceed from phenomenology to models that may account for part of such mechanisms. MCS appears to trigger rapid and phasic activation in the lateral thalamus, which leads to a cascade of events of longer time-course in medial thalamus, anterior cingulate/orbitofrontal cortices and periaqueductal grey matter. Activity in these latter structures is delayed relative to actual cortical neurostimulation and becomes maximal during the hours that follow MCS arrest. Current hypotheses suggest that MCS may act through at least two mechanisms: activation of perigenual cingulate and orbitofrontal areas may modulate the emotional appraisal of pain, rather than its intensity, while top down activation of brainstem PAG may lead to descending inhibition toward the spinal cord. Recent evidence also points to a possible secretion of endogenous opioids triggered by chronic MCS. This, along with the delayed and long-lasting activation of several brain structures, is consistent with the clinical effects of MCS, which m…
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“Several viral infections, including HIV [19], HCV [20], and HSV [21] increase activation of the KP, which interestingly is implicated in the neurological and cognitive impairments of patients with HIV, HCV, and HSV [21,22].”
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“Several mechanisms have been reported to explain the analgesic effects of rTMS, including local changes at the motor cortex level itself (in particular, restoration of intracortical inhibition)(16) as well as distant effects such as the following: (1) activation of perigenual cingulate and orbitofrontal areas modulati…”
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“Prefrontal TMS may engage similar circuits as MCS thus attenuating pain experience by possibly blunting the affective dimension of pain (pACC) while engaging descending pain inhibitory control circuits that involve the prefrontal cortex, orbitofrontal cortex, pACC, basal ganglia, thalamus, and PAG.16 It is not clear w…”
BackgroundRole of the primary motor cortex in the maintenance and treatment of pain in fibromyalgia
Saavedra, L. C., de Mendonça, M. E., & Fregni, F. (2014) · Medical Hypotheses · doi:10.1016/j.mehy.2014.06.007 · Cited by 82
“These alterations could be secondary to maladaptive neuroplasticity as a result of either persistent nociceptive input or to a baseline alteration in neuronal circuits implicated in pain modulation, leading to potentiation or disinhibition of anatomical areas that participate in processing of pain perception [2,24,25].”
BackgroundNguyen, J., Velasco, F., Brugières, P., Velasco, M., Kéravel, Y., Boleaga, B., Brito, F., & Lefaucheur, J. (2008) · Brain Stimulation · doi:10.1016/j.brs.2008.03.007 · Cited by 86
“However, functional imaging showed that MCS could also act on neural structures involved in the emotional appraisal of pain (perigenual cingulate and orbitofrontal cortical areas).(20) In conclusion, this controlled study showed that MCS was an effective method to improve various types of drugresistant chronic neuropa…”
MethodVaseghi, B., Zoghi, M., & Jaberzadeh, S. (2015) · PLoS ONE · doi:10.1371/journal.pone.0118340 · Cited by 84
O'Connell, N., Cossar, J., Marston, L., Wand, B., Bunce, D., Souza, L. H. D., Maskill, D. W., Sharp, A. S. P., & Moseley, G. (2013) · The Clinical Journal of Pain · doi:10.1097/ajp.0b013e318247ec09 · Cited by 78
Mercier, C., & Léonard, G. (2011) · Physiotherapy Canada. Physiothérapie Canada · doi:10.3138/ptc.2010-08p · Cited by 77
Yılmaz, B., Kesikburun, S., Yaşar, E., & Tan, A. K. (2014) · Journal of Spinal Cord Medicine (JSCM) · doi:10.1179/2045772313y.0000000172 · Cited by 75
Lamusuo, S., Hirvonen, J., Lindholm, P., Martikainen, I. K., Hagelberg, N. M., Parkkola, R. K., Taiminen, T. J., Hietala, J. A., Helin, S., Virtanen, A., et al. (2017) · European Journal of Pain · doi:10.1002/ejp.1052 · Cited by 81
“A plausible explanation for this finding is that rTMS of M1/S1 induced changes in the topdown mechanisms related to appraisal of pain rather than in the intensity of the ascending afferent barrage (Garcia-Larrea and Peyron, 2007; Bradley et al., 2016).”
BackgroundViisanen, H., & Pertovaara, A. (2010) · Neuroscience Letters · doi:10.1016/j.neulet.2010.04.014 · Cited by 74
Putative physiological mechanisms underlying tDCS analgesic effects
Knotková, H., Nitsche, M. A., & Cruciani, R. A. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00628 · Cited by 75
“Indeed, changes in regional cerebral blood flow following epidural motor cortex stimulation (Peyron et al., 1995; Garcia-Larrea et al., 1999; Garcia-Larrea and Peyron, 2007) indicated that stimulation of the motor cortex may trigger rapid and phasic activation in the lateral thalamus (which…”
BackgroundThe rubber hand illusion and its application to clinical neuroscience
Ramakonar, H., Franz, E. A., & Lind, C. R. P. (2011) · Journal of Clinical Neuroscience · doi:10.1016/j.jocn.2011.05.008 · Cited by 51
Ahn, H., Zhong, C., Miao, H.-Y., Chaoul, A., Park, L., Yen, I. H., Vila, M. A., Sorkpor, S., & Abdi, S. (2019) · Journal of clinical neuroscience · doi:10.1016/j.jocn.2019.08.047 · Cited by 68
Transcranial Direct Current Stimulation to Lessen Neuropathic Pain After Spinal Cord Injury
Yoon, E. J., Kim, Y. K., Kim, H., Kim, S. E., Lee, Y., & Shin, H. (2013) · Neurorehabilitation and neural repair · doi:10.1177/1545968313507632 · Cited by 109
Non-invasive Brain Stimulation for Chronic Pain: State of the Art and Future Directions
Xiong, H.-Y., Zheng, J., & Wang, X. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.888716 · Cited by 75
“ACC, anterior cingulate cortex; PFC, prefrontal cortex; AMY, amygdala; PAG, periaqueductal gray; RVM, rostroventral medulla; DH, dorsal horn; INS, insula; S1, primary somatosensory cortex; S2, secondary somatosensory cortex; MCC, medial cingulate cortex; PCC, posterior cingulate cortex; PB, parabrachial nucleus.”
BackgroundLefaucheur, J., Holsheimer, J., Goujon, C., Kéravel, Y., & Nguyen, J. (2010) · Experimental Neurology · doi:10.1016/j.expneurol.2010.02.008 · Cited by 65
Lenoir, C., Algoet, M., & Mouraux, A. (2018) · The Journal of Physiology · doi:10.1113/jp276359 · Cited by 63
Ahn, H. B., Suchting, R., Woods, A. J., Miao, H., Green, C., Cho, R., Choi, E., & Fillingim, R. B. (2018) · Journal of Pain Research · doi:10.2147/jpr.s173080 · Cited by 70
“57,58 In addition, Garcia-Larrea and Peyron 59 reported that motor cortex stimulation might facilitate descending pain inhibitory mechanisms.”
Al-Wardat, M. S., Pisani, A., Etoom, M., Carpenedo, R., Chinè, E., Dauri, M., Leonardis, F., & Natoli, S. (2020) · Journal of Neural Transmission · doi:10.1007/s00702-020-02223-w · Cited by 63
Focused Ultrasound (FUS) for Chronic Pain Management: Approved and Potential Applications
di Biase, L., Falato, E., Caminiti, M. L., Pecoraro, P. M., Narducci, F., & Lazzaro, V. D. (2021) · Neurology Research International · doi:10.1155/2021/8438498 · Cited by 59
“M1 stimulation reduces the thalamic and brainstem nuclei hyperactivity underlying pain [48], while DLPFC stimulation probably mediates analgesic effects by modulating affective-emotional networks related to pain [45].”
BackgroundMotor cortex stimulation for facial chronic neuropathic pain: A review of the literature
Monsalve, G. (2012) · Surgical neurology international · doi:10.4103/2152-7806.103023 · Cited by 54
Neurophysiology of Cortical Stimulation
Lefaucheur, J. (2012) · International review of neurobiology · doi:10.1016/b978-0-12-404706-8.00005-x · Cited by 63
Ahn, H., Sorkpor, S., Miao, H.-Y., Zhong, C., Jorge, R., Park, L., Abdi, S., & Cho, R. Y. (2019) · Journal of clinical neuroscience · doi:10.1016/j.jocn.2019.05.023 · Cited by 51
Zhao, C.-G., Sun, W., Ju, F., Wang, H., Sun, X.-L., Mou, X., & Yuan, H. (2019) · Pain medicine (Malden, Mass.) · doi:10.1093/pm/pnz290 · Cited by 49
A pilot functional MRI study of the effects of prefrontal rTMS on pain perception.
Martin, L., Borckardt, J., Reeves, S., Frohman, H. A., Beam, W., Nahas, Z., Johnson, K., Younger, J., Madan, A., Patterson, D., et al. (2013) · Pain medicine (Malden, Mass.) · doi:10.1111/pme.12129 · Cited by 49
Jürgens, T. P., Schulte, A., Klein, T., & May, A. (2012) · European Journal of Pain · doi:10.1002/j.1532-2149.2012.00135.x · Cited by 50
“…projections by MCS, which then initiates a cascade of events involving the activation of medial thalamus, anterior cingulate/orbitofrontal cortex and brainstem structures like the periaqueductal grey matter (PAG; Garcia-Larrea et al., 1999; Garcia-Larrea and Peyron, 2007; Peyron et al., 2007).”
BackgroundKupers, R., Frokjaer, V., Naert, A., Christensen, R., Budtz-Joergensen, E., Kehlet, H., & Knudsen, G. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2008.10.011 · Cited by 47
“Interestingly, motor cortex stimulation is successfully used in the treatment of neuropathic pain (Garcia-Larrea and Peyron, 2007).”
Vaseghi, B., Zoghi, M., & Jaberzadeh, S. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.13043 · Cited by 53
“Recent studies have shown that the primary motor cortex (M1) is also involved in pain modulation (Talbot et al., 1991; Casey, 1999; Vogt & Sikes, 2000; Ploner & Schnitzler, 2004; Garcia-Larrea & Peyron, 2007; Tang et al., 2009).”
BackgroundViisanen, H., Ansah, O., & Pertovaara, A. (2012) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2012.08.002 · Cited by 46
Shokur, S., Donati, A., Campos, D., Gitti, C. M., Bao, G., Fischer, D., Almeida, S., Braga, V. A. S., Augusto, P., Petty, C., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0206464 · Cited by 44
Wei, S., Chao, H., Tu, C., Lin, M., Li, W., Low, I., Shen, H.-D., Chen, L., & Hsieh, J. (2016) · Scientific Reports · doi:10.1038/srep23639 · Cited by 46
tDCS modulates cortical nociceptive processing but has little to no impact on pain perception
Ihle, K., Rodriguez‐Raecke, R., Luedtke, K., & May, A. (2014) · Pain · doi:10.1016/j.pain.2014.07.018 · Cited by 51
“The aim of this study was to explore the underpinnings of the previously suggested antinociceptive effects of tDCS over the motor cortex [21,22,50].”
BackgroundLefaucheur, J., Jarry, G., Drouot, X., Ménard-Lefaucheur, I., Kéravel, Y., & Nguyen, J. (2010) · Clinical Neurophysiology · doi:10.1016/j.clinph.2009.12.028 · Cited by 43
“81 Positron emission tomography studies showed metabolic changes in both SII/insular and ACC/orbitofrontal regions in patients with chronic neuropathic pain treated by motor cortex stimulation (García-Larrea and Peyron, 2007).”
BackgroundAnalgesic Effects Evoked by Real and Imagined Acupuncture: A Neuroimaging Study
Cao, J., Tu, Y., Orr, S. P., Lang, C., Park, J., Vangel, M. G., Chen, L. L., Gollub, R. L., & Kong, J. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy190 · Cited by 46
Kolodziej, M., Hellwig, D., Nimsky, C., & Benes, L. (2015) · Journal of Neurological Surgery—Part A · doi:10.1055/s-0035-1558419 · Cited by 41
França, N. R. M., Toniolo, E. F., Franciosi, A. C., Alves, A. S., de Andrade, D. C., Fonoff, E. T., Britto, L. R. G., & Dale, C. S. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.05.019 · Cited by 45
Viisanen, H., & Pertovaara, A. (2010) · Experimental Brain Research · doi:10.1007/s00221-009-2038-4 · Cited by 41
“It should be noted that in clinical studies, pain alleviation by M1 stimulation may be based not only on spinal but also on supraspinal actions that influence higher processing of nociceptive signals such as emotional appraisal of pain ( Garcia-Larrea and Peyron 2007; Ohara et al. 2005).”
BackgroundEffects of Exercise-induced Hypoalgesia and Its Neural Mechanisms
Wu, B., Zhou, L.-L., Chen, C.-C., Wang, J., Hu, L., & Wang, X.-Q. (2021) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000002781 · Cited by 39
de Assis, E. B., Martins, W. K. N., de Carvalho, C. D., Ferreira, C. M., Gomes, R., Rodrigues, E. T. D. A., Meira, U., de Holanda, L. J., Lindquist, A. R. R., Morya, E., et al. (2021) · Scientific Reports · doi:10.1038/s41598-022-05254-3 · Cited by 39
Lopes, P. S. S., Campos, A. C. P., Fonoff, E. T., de Britto, L. R. G., & Pagano, R. L. (2019) · Behavioral and Brain Functions · doi:10.1186/s12993-019-0156-0 · Cited by 44
Validation of Computational Studies for Electrical Brain Stimulation With Phantom Head Experiments.
Kim, D., Jeong, J., Jeong, S., Kim, S., Jun, S., & Chung, E. (2015) · Brain Stimulation · doi:10.1016/j.brs.2015.06.009 · Cited by 39
“However, despite these animal [11–13] and human studies [14,15], a thorough understanding of the fundamental mechanisms of EBS is still lacking; thus, the stimulation parameters for the best medical practices (electrode position, amplitude, waveform, and duration) remain unclear.”
Deep Brain Stimulation and Motor Cortical Stimulation for Neuropathic Pain
Stadler, J. A. I., Ellens, D. J., & Rosenow, J. (2011) · Current pain and headache reports · doi:10.1007/s11916-010-0161-3 · Cited by 39
“PET and electrophysiological studies demonstrate regional activity differences during stimulation [ 28 ].”
BackgroundInfluentialEffects of transcranial theta-burst stimulation on acute pain perception
Antal, A., & Paulus, W. (2010) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-2010-0555 · Cited by 39
“…of M1 appears to trigger activation in the lateral thalamus, which leads to a flow of events in the medial thalamus, anterior cingulate and orbitofrontal cortices and periaqueductal grey matter (for a review with regard the possible mechanisms of M1 stimulation see Garcia-Larrea and Peyron, 2007).”
Mutual interaction between motor cortex activation and pain in fibromyalgia: EEG-fNIRS study
Gentile, E., Brunetti, A., Ricci, K., Delussi, M. D., Bevilacqua, V., & de Tommaso, M. (2020) · PLoS ONE · doi:10.1371/journal.pone.0228158 · Cited by 43
Mo, J.-J., Hu, W.-H., Zhang, C., Wang, X., Liu, C., Zhao, B.-T., Zhou, J., & Zhang, K. (2019) · BMC Neurology · doi:10.1186/s12883-019-1273-y · Cited by 36
Bolognini, N., Spandri, V., Olgiati, E., Fregni, F., Ferraro, F., & Maravita, A. (2013) · Journal of Pain and Symptom Management · doi:10.1016/j.jpainsymman.2013.06.014 · Cited by 36
Motor corticospinal excitability: a novel facet of pain modulation?
Granovsky, Y., Sprecher, E., & Sinai, A. (2019) · PAIN Reports · doi:10.1097/pr9.0000000000000725 · Cited by 33
“synaptic events influencing activity in the medial thalamus and in the brain structures involved in descending pain inhibition such as perigenual anterior cingulate cortex, orbitofrontal cortex, and periaqueductal gray.(21,22,46) In addition to the established in-”
BackgroundO'Brien, A. T., Amorim, R., Rushmore, R., Eden, U., Afifi, L., Pietro, L. D., Wagner, T., & Valero-Cabré, A. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00545 · Cited by 33
Epoxy fatty acids mediate analgesia in murine diabetic neuropathy
Wagner, K. M., Lee, K. S. S., Yang, J., & Hammock, B. D. (2016) · European Journal of Pain · doi:10.1002/ejp.939 · Cited by 37
“GABA interneurons in the PAG or raphe magnus modulate the enkephalin sensitive neurons in these areas which may be subject to opioid receptor antagonism (Garcia-Larrea and Peyron, 2007).”
BackgroundSpatial and Temporal Brain Responses to Noxious Heat Thermal Stimuli in Burning Mouth Syndrome
Shinozaki, T., Imamura, Y., Kohashi, R., Dezawa, K., Nakaya, Y., Sato, Y., Watanabe, K., Morimoto, Y., Shizukuishi, T., Abe, O., et al. (2016) · Journal of dentistry research · doi:10.1177/0022034516653580 · Cited by 33
“ACC and PCC are reported to be the key structures in pain processing and modulation (Garcia-Larrea and Peyron 2007; Staud et al. 2007; Bogdanov et al. 2014).”
BackgroundHouzé, B., Bradley, C., Magnin, M., & Garcı́a-Larrea, L. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs255 · Cited by 33
“…induces greater metabolic and BOLD changes in the lateral thalamus than in sensorimotor cortex, and this whether the stimulation is epidural (Garcia-Larrea and Peyron 2007) or transcranial (Bestmann et al. 2004), lending support to the hypothesis of significant cortico-thalamo-cortical…”
BackgroundResultInfluentialSelf-citationPeyron, R. (2016) · Pain · doi:10.1097/j.pain.0000000000000387 · Cited by 31
Self-citationZheng, Y., Liu, C. W., Chan, D. X. H., Ong, D., Ker, J., Ng, W. H., & Wan, K. R. (2023) · Neuromodulation Technology at the Neural Interface · doi:10.1016/j.neurom.2023.05.003 · Cited by 37
Brietzke, A. P., Rozisky, J. R., Dussán‐Sarria, J. A., Deitos, A., Laste, G., Hoppe, P. F. T., Müller, S., Torres, I. L. D. S., Álvares‐da‐Silva, M. R., de Amorim, R. F. B., et al. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00498 · Cited by 32
Bai, Y., Pacheco‐Barrios, K., Pacheco-Barrios, N. V., Liang, G., & Fregni, F. (2024) · Nature Mental Health · doi:10.1038/s44220-024-00235-z · Cited by 34
“There is a wealth of imaging literature underscoring functional activation of PAG in patients with NP during EMCS 22,23,47 , which was corroborated by preclinical data showing enhanced neuronal firing rates and FOS expression in ipsilateral PAG induced by EMCS 29,48,49 .”
InfluentialCortical Regulation of Nociception of the Trigeminal Nucleus Caudalis
Castro, A., Raver, C., Li, Y., Uddin, O., Rubin, D. C., Ji, Y., Masri, R. M., & Keller, A. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3897-16.2017 · Cited by 34
“Although motor cortex stimulation provides relief to some patients, the efficacy of this approach remains relatively low and inconsistent (Canavero and Bonicalzi, 2002; Garcia-Larrea and Peyron, 2007; Lima and Fregni, 2008).”
BackgroundHuman primary somatosensory cortex is differentially involved in vibrotaction and nociception.
Lenoir, C., Huang, G., Vandermeeren, Y., Hatem, S., & Mouraux, A. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00615.2016 · Cited by 28
“This has led some authors to propose that the rTMS or tDCS delivered over the sensorimotor cortex may activate descending inhibitory control mechanisms acting on the spinal transmission of ascending nociceptive inputs (Garcia-Larrea and Peyron 2007).”
Devoize, L., Alvarezl, P., Monconduit, L., & Dallel, R. (2011) · European Journal of Pain · doi:10.1016/j.ejpain.2010.11.017 · Cited by 29
“However, the ventral mPFC may also be more directly involved in the perception of pain, notably through the modulation of diencephalon and/or brainstem structures modulating pain (Lorenz et al., 2003; Garcia-Larrea and Peyron, 2007).”
BackgroundMeeker, T. J., Schmid, A., Keaser, M. L., Khan, S. A., Gullapalli, R. P., Dorsey, S. G., Greenspan, J. D., & Seminowicz, D. A. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119278 · Cited by 34
“Demonstrating the potential clinical importance of the DPMN, enhanced FC within the DPMN during placebo analgesia and motor cortex stimulation is positively related to magnitude of analgesia experienced (Bingel et al., 2006; Eippert et al., 2009; Garcia-Larrea and Peyron, 2007; Meeker et al., 2019); additionally, ther…”
Zhao, C., Sun, W., Ju, F., Jiang, S., Wang, H., Sun, X., Mou, X., & Yuan, H. M. (2021) · Pain and Therapy · doi:10.1007/s40122-021-00261-0 · Cited by 32
“First, rTMS may improve the excitability of the cerebral cortex, leading to top-down activation of the brainstem and descending inhibition [38].”
BackgroundLi, J., Ji, Y., Voulalas, P. J., Keaser, M. L., Xu, S., Gullapalli, R. P., Greenspan, J. D., & Masri, R. M. (2014) · Brain stimulation · doi:10.1016/j.brs.2013.12.013 · Cited by 35
“Previous studies investigating brain activation using PET showed no significant changes in S1 after MCS (17, 28).”
BackgroundPain influences hedonic assessment of visual inputs
Godinho, F. L. F., Frot, M., Perchet, C., Magnin, M., & Garcı́a-Larrea, L. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06196.x · Cited by 30
“Similar conclusions have been recently reached in the context of pain and analgesia, where increased activity in perigenual ACC was associated with the relief of neuropathic pain (Willoch et al., 2003; Garcia-Larrea & Peyron, 2007).”
ResultSelf-citationGarcı́a-Larrea, L., & Magnin, M. (2008) · La Presse Médicale · doi:10.1016/j.lpm.2007.07.025 · Cited by 39
Waris, A., Siraj, M., Khan, A. A., Lin, J., Asim, M., & Alhumaydhi, F. A. (2024) · ACS Pharmacology & Translational Science · doi:10.1021/acsptsci.4c00494 · Cited by 30
Cho, Y. U., Kim, K., Dutta, A., Park, S., Lee, J. Y., Kim, H. W., Park, J., Kim, J., Min, W. K., Won, C., et al. (2023) · Advanced Functional Materials · doi:10.1002/adfm.202310908 · Cited by 30
Li, L.-L., Huang, H.-L., Yu, Y., Jia, Y.-Q., Liu, Z.-Y., Shi, X., Wang, F., & Zhang, T. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.800560 · Cited by 25
Martucci, K. T., & Mackey, S. (2016) · Anesthesiology Clinics · doi:10.1016/j.anclin.2016.01.001 · Cited by 35
“Current techniques use adaptive models(97) and target brain regions that have the potential to activate multiple downstream effects.(98)”
Background
Metadata
- Authors
- Garcia-Larrea, L., & Peyron, R.
- Affiliations
- Inserm (FR)
- ORCID
- Peyron, Roland
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 2007
- Volume
- 37
- Pages
- S71-S79
- ISSN
- 1053-8119 (ISSN-L)
- OpenAlex
- W2029045410
- Cited by
- 259
- References
- 75
- Citations by year
- 2026: 8 · 2025: 4 · 2024: 12 · 2023: 13 · 2022: 15 · 2021: 20 · 2020: 14 · 2019: 18 · 2018: 11 · 2017: 11 · 2016: 17 · 2015: 21 · 2014: 16 · 2013: 13 · 2012: 15
- FWCI
- 2.15
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- NeuroImage (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Fondation pour la Recherche Médicale
- Topics
- Health Sciences › Medicine › Anesthesiology and Pain Medicine › Pain Management and Treatment
- Health Sciences › Medicine › Clinical Neurology › Deep Brain Stimulation and Movement Disorders
- Health Sciences › Medicine › Physiology (medical) › Pain Mechanisms and Treatments
- Keywords
- motor cortex stimulation, neuropathic pain, chronic pain, mechanism of action, lateral thalamus, medial thalamus, periaqueductal gray, anterior cingulate cortex, orbitofrontal cortex, descending pain inhibition, endogenous opioids, pain management
- MeSH terms
- Animals, Cerebrovascular Circulation, Chronic Disease, Endorphins, Humans, Magnetic Resonance Imaging, Motor Cortex, Pain, Peripheral Nervous System Diseases, Neurosurgical Procedures, Positron-Emission Tomography, Pain Management
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