W. C. Abraham, Metaplasticity: tuning synapses and networks for plasticity, Nat Rev Neurosci, vol.9, pp.387-399, 2008.

W. C. Abraham and M. F. Bear, Metaplasticity: the plasticity of synaptic plasticity, Trends Neurosci, vol.19, pp.126-130, 1996.

W. C. Abraham, B. Gustafsson, and H. Wigstrom, Long-term potentiation involves enhanced synaptic excitation relative to synaptic inhibition in guinea-pig hippocampus, J Physiol, vol.394, pp.367-380, 1987.

W. C. Abraham and A. Huggett, Induction and reversal of long-term potentiation by repeated high-frequency stimulation in rat hippocampal slices, Hippocampus, vol.7, pp.137-145, 1997.

W. C. Abraham and W. P. Tate, Metaplasticity: a new vista across the field of synaptic plasticity, Prog Neurobiol, vol.52, pp.303-323, 1997.

A. Agmon and B. W. Connors, Thalamocortical responses of mouse somatosensory (barrel) cortex in vitro, Neuroscience, vol.41, pp.365-380, 1991.

C. D. Aizenman and D. J. Linden, Rapid, synaptically driven increases in the intrinsic excitability of cerebellar deep nuclear neurons, Nat Neurosci, vol.3, pp.109-111, 2000.

S. Armano, P. Rossi, V. Taglietti, D. Angelo, and E. , Long-term potentiation of intrinsic excitability at the mossy fiber-granule cell synapse of rat cerebellum, J Neurosci, vol.20, pp.5208-5216, 2000.

V. Aroniadou-anderjaska and A. Keller, LTP in the barrel cortex of adult rats, Neuroreport, vol.6, pp.2297-2300, 1995.

A. Artola and W. Singer, Long-term depression of excitatory synaptic transmission and its relationship to long-term potentiation, Trends Neurosci, vol.16, pp.480-487, 1993.

A. Artola, S. Bröcher, and W. Singer, Different voltage-dependent thresholds for inducing long-term depression and long-term potentiation in slices of rat visual cortex, Nature, vol.347, pp.69-72, 1990.

A. Artola, A. Kamal, G. M. Ramakers, G. J. Biessels, and W. H. Gispen, Diabetes mellitus concomitantly facilitates the induction of long-term depression and inhibits that of long-term potentiation in hippocampus, Eur J Neurosci, vol.22, pp.169-178, 2005.

G. Barrionuevo, F. Schottler, and G. Lynch, The effects of repetitive low frequency stimulation on control and "potentiated" synaptic responses in the hippocampus, Life Sci, vol.27, pp.2385-2391, 1980.

E. L. Bienenstock, L. N. Cooper, and P. W. Munro, Theory for the development of neuron selectivity: orientation specificity and binocular interaction in visual cortex, J Neurosci, vol.2, pp.32-48, 1982.

A. Belmeguenai, E. Hosy, F. Bengtsson, C. Pedroarena, C. Piochon et al., Intrinsic plasticity complements long-term potentiation in parallel fiber input gain control in cerebellar Purkinje cells, J Neurosci, vol.30, pp.13630-13643, 2010.

J. Benda and A. V. Herz, A universal model for spike-frequency adaptation, Neural Comput, vol.15, pp.2523-2564, 2003.

G. Q. Bi and M. M. Poo, Synaptic modifications in cultured hippocampal neurons: dependence on spike timing, synaptic strength, and postsynaptic cell type, J Neurosci, vol.18, pp.10464-10472, 1998.

Z. A. Bortolotto, Z. I. Bashir, C. H. Davies, and G. L. Collingridge, A molecular switch activated by metabotropic glutamate receptors regulates induction of long-term potentiation, Nature, vol.368, pp.740-743, 1994.

D. H. Brager and D. Johnston, Plasticity of intrinsic excitability during long-term depression is mediated through mGluR-dependent changes in I(h) in hippocampal CA1 pyramidal neurons, J Neurosci, vol.27, pp.13926-13937, 2007.

S. Bröcher, A. Artola, and W. Singer, Intracellular injection of Ca2+ chelators blocks induction of long-term depression in rat visual cortex, Proc Natl Acad Sci, vol.89, pp.123-127, 1992.

E. Campanac, G. Daoudal, N. Ankri, and D. Debanne, Downregulation of dendritic I(h) in CA1 pyramidal neurons after LTP, J Neurosci, vol.28, pp.8635-8643, 2008.

E. Campanac and D. Debanne, Spike timing-dependent plasticity: a learning rule for dendritic integration in rat CA1 pyramidal neurons, J Physiol, vol.586, pp.779-793, 2008.
URL : https://hal.archives-ouvertes.fr/hal-01766849

E. Campanac, C. Gasselin, A. Baude, S. Rama, N. Ankri et al., Enhanced intrinsic excitability in basket cells maintains excitatory-inhibitory balance in hippocampal circuits, Neuron, vol.77, pp.712-722, 2013.
URL : https://hal.archives-ouvertes.fr/hal-01774392

M. A. Castro-alamancos, J. P. Donoghue, and B. W. Connors, Different forms of synaptic plasticity in somatosensory and motor areas of the neocortex, J. Neurosci, vol.15, pp.5324-5433, 1995.

B. R. Christie and W. C. Abraham, Priming of associative long-term depression in the dentate gyrus by theta frequency synaptic activity, Neuron, vol.8, pp.79-84, 1992.

B. R. Christie, D. Stellwagen, and W. C. Abraham, Evidence for common expression mechanisms underlying heterosynaptic and associative long-term depression in the dentate gyrus, J Neurophysiol, vol.74, pp.1244-1247, 1995.

E. J. Coan, A. J. Irving, and G. L. Collingridge, Low frequency activation of the NMDA receptor system can prevent the induction of LTP, Neurosci Lett, vol.105, pp.205-210, 1989.

R. H. Cudmore and G. G. Turrigiano, Long-term potentiation of intrinsic excitability in LV visual cortical neurons, J Neurophysiol, vol.92, pp.341-348, 2004.

J. A. Cummings, R. M. Mulkey, R. A. Nicoll, and R. C. Malenka, Ca 2+ signaling requirements for long-term depression in the hippocampus, Neuron, vol.16, pp.825-833, 1996.

C. Gasselin, Y. Inglebert, N. Ankri, and D. Debanne, Plasticity of intrinsic excitability during LTD is mediated by bidirectional changes in h-channel activity, Sci Rep, vol.7, issue.1, p.14418, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01766825

S. Griffiths, H. Scott, C. Glover, A. Bienemann, M. T. Ghorbel et al., Expression of long-term depression underlies visual recognition memory, Neuron, vol.58, issue.2, pp.186-194, 2008.

C. Hansel, A. Artola, and W. Singer, Relation between dendritic Ca 2+ levels and the polarity of synaptic long-term modifications in rat visual cortex neurons, Eur J Neurosci, vol.9, pp.2309-2322, 1997.

Y. Huang, A. Colino, D. K. Selig, and R. C. Malenka, The influence of prior synaptic activity on the induction of long-term potentiation, Science, vol.255, pp.730-733, 1992.

P. T. Huerta and J. E. Lisman, Bidirectional synaptic plasticity induced by a single burst during cholinergic theta oscillation in CA1 in vitro, Neuron, vol.15, pp.1053-1063, 1995.

C. Hölscher, R. Anwyl, and M. J. Rowan, Stimulation on the positive phase of hippocampal theta rhythm induces long-term potentiation that can Be depotentiated by stimulation on the negative phase in area CA1 in vivo, J Neurosci, vol.17, pp.6470-6477, 1997.

J. M. Hyman, B. P. Wyble, V. Goyal, C. A. Rossi, and M. E. Hasselmo, Stimulation in hippocampal region CA1 in behaving rats yields long-term potentiation when delivered to the peak of theta and long-term depression when delivered to the trough, J. Neurosci, vol.23, pp.11725-11731, 2003.

H. Kitagawa, Y. Nishimura, K. Yoshioka, M. Lin, and T. Yamamoto, Long-term potentiation and depression in layer III and V pyramidal neurons in the cat sensorimotor cortex in vitro, Brain Res, vol.751, pp.339-343, 1997.

A. Kirkwood and M. F. Bear, Homosynaptic long-term depression in the visual cortex, J Neurosci, vol.14, pp.3404-3412, 1994.

A. Kirkwood, S. M. Dudek, J. T. Gold, C. D. Aizenman, and M. F. Bear, Common forms of synaptic plasticity in the hippocampus and neocortex in vitro, Science, vol.260, pp.1518-1521, 1993.

M. F. Nolan, G. Malleret, K. H. Lee, E. Gibbs, J. T. Dudman et al., The hyperpolarization-activated HCN1 channel is important for motor learning and neuronal integration by cerebellar Purkinje cells, Cell, vol.115, pp.551-564, 2003.

C. M. Norris, D. L. Korol, and T. C. Foster, Increased susceptibility to induction of long-term depression and long-term potentiation reversal during aging, J Neurosci, vol.16, pp.5382-5392, 1996.

T. J. O'dell and E. R. Kandel, Low-frequency stimulation erases LTP through an NMDA receptor-mediated activation of protein phosphatases, Learn Mem, vol.1, pp.129-139, 1994.

G. Ohtsuki, C. Piochon, J. P. Adelman, and C. Hansel, SK2 channel modulation contributes to compartment-specific dendritic plasticity in cerebellar Purkinje cells, Neuron, vol.75, pp.108-120, 2012.

J. T. Paz, S. Mahon, P. Tiret, S. Genet, B. Delord et al., Multiple forms of activitydependent intrinsic plasticity in layer V cortical neurones in vivo, J Physiol, vol.587, pp.3189-205, 2009.

C. Pozzorini, R. Naud, S. Mensi, and W. Gerstner, Temporal whitening by power-law adaptation in neocortical neurons, Nat Neurosci, vol.16, pp.942-948, 2013.

M. Sessolo, I. Marcon, S. Bovetti, G. Losi, M. Cammarota et al., Parvalbumin-Positive Inhibitory Interneurons Oppose Propagation But Favor Generation of Focal Epileptiform Activity, J Neurosci, vol.35, pp.9544-9557, 2015.

A. P. Rizwan, X. Zhan, G. W. Zamponi, and R. W. Turner, Long-Term Potentiation at the Mossy Fiber-Granule Cell Relay Invokes Postsynaptic Second-Messenger Regulation of Kv4 Channels, J Neurosci, vol.36, pp.11196-11207, 2016.

P. Sah and J. M. Bekkers, Apical dendritic location of slow afterhyperpolarization current in hippocampal pyramidal neurons: implications for the integration of long-term potentiation, J Neurosci, vol.16, pp.4537-4542, 1996.

H. G. Shim, D. C. Jang, J. Lee, G. Chung, S. Lee et al., Long-Term Depression of Intrinsic Excitability Accompanied by Synaptic Depression in Cerebellar Purkinje Cells, J Neurosci, vol.37, pp.5659-5669, 2017.

P. J. Sjöström, G. G. Turrigiano, and S. B. Nelson, Endocannabinoid-dependent neocortical layer-5 LTD in the absence of postsynaptic spiking, J Neurophysiol, vol.92, pp.3338-3343, 2004.

V. Sourdet, M. Russier, G. Daoudal, N. Ankri, and D. Debanne, Long-term enhancement of neuronal excitability and temporal fidelity mediated by metabotropic glutamate receptor subtype 5, J Neurosci, vol.23, pp.10238-10248, 2003.

U. Staubli and G. Lynch, Stable depression of potentiated synaptic responses in the hippocampus with 1-5 Hz stimulation, Brain Res, vol.513, pp.113-118, 1990.

C. F. Stevens and Y. Wang, Changes in reliability of synaptic function as a mechanism for plasticity, Nature, vol.371, pp.704-707, 1994.

H. Toyoda, M. G. Zhao, and M. Zhuo, Roles of NMDA receptor NR2A and NR2B subtypes for long-term depression in the anterior cingulate cortex, Eur J Neurosci, vol.22, pp.485-494, 2005.

J. J. Wagner and B. E. Alger, GABAergic and developmental influences on homosynaptic LTD and depotentiation in rat hippocampus, J Neurosci, vol.15, pp.1577-1586, 1995.

Y. Wang, J. Wu, M. J. Rowan, and R. Anwyl, Role of the protein kinase C in the induction of homosynaptic long-term depression by brief low frequency stimulation in the dentate gyrus in the rat hippocampus in vitro, J Physiol, vol.513, pp.467-475, 1998.

Z. Wang, N. L. Xu, C. P. Wu, S. Duan, and M. M. Poo, Bidirectional changes in spatial dendritic integration accompanying long-term synaptic modifications, Neuron, vol.37, pp.463-472, 2003.

V. Wespatat, F. Tennigkeit, and . Singer, Phase sensitivity of synaptic modifications in oscillating cells of rat visual cortex, J. Neurosci, vol.24, pp.9067-9075, 2004.

E. M. Wexler and P. K. Stanton, Priming of homosynaptic long-term depression in hippocampus by previous synaptic activity, NeuroReport, vol.4, pp.591-594, 1993.

J. Xu, N. Kang, L. Jiang, M. Nedergaard, and J. Kang, Activity-dependent long-term potentiation of intrinsic excitability in hippocampal CA1 pyramidal neurons, J Neurosci, vol.25, pp.1750-1760, 2005.

X. Yang and D. S. Faber, Initial synaptic efficacy influences induction and expression of long-term changes in transmission, Proc Natl Acad Sci, vol.88, pp.4299-4303, 1991.

Z. Yang and F. Santamaria, Purkinje cell intrinsic excitability increases after synaptic longterm depression, J Neurophysiol, vol.116, issue.3, pp.1208-1217, 2016.

W. C. Abraham, Metaplasticity: tuning synapses and networks for plasticity, Nat Rev Neurosci, vol.9, pp.387-399, 2008.

W. C. Abraham and A. Huggett, Induction and reversal of long-term potentiation by repeated high-frequency stimulation in rat hippocampal slices, Hippocampus, vol.7, pp.137-145, 1997.

A. Agmon and B. W. Connors, Thalamocortical responses of mouse somatosensory (barrel) cortex in vitro, Neuroscience, vol.41, pp.365-380, 1991.

C. D. Aizenman and D. J. Linden, Rapid, synaptically driven increases in the intrinsic excitability of cerebellar deep nuclear neurons, Nat Neurosci, vol.3, pp.109-111, 2000.

S. Armano, P. Rossi, V. Taglietti, D. Angelo, and E. , Long-term potentiation of intrinsic excitability at the mossy fiber-granule cell synapse of rat cerebellum, J Neurosci, vol.20, pp.5208-5216, 2000.

A. Artola, S. Bröcher, and W. Singer, Different voltage-dependent thresholds for inducing long-term depression and long-term potentiation in slices of rat visual cortex, Nature, vol.347, pp.69-72, 1990.

G. Barrionuevo, F. Schottler, and G. Lynch, The effects of repetitive low frequency stimulation on control and "potentiated" synaptic responses in the hippocampus, Life Sci, vol.27, pp.2385-2391, 1980.

A. I. Basbaum, D. M. Bautista, G. Scherrer, and J. D. , Cellular and molecular mechanisms of pain, Cell, vol.139, pp.267-284, 2009.

A. Belmeguenai, E. Hosy, F. Bengtsson, C. Pedroarena, C. Piochon et al., Intrinsic plasticity complements long-term potentiation in parallel fiber input gain control in cerebellar Purkinje cells, J Neurosci, vol.30, pp.13630-13643, 2010.

J. Benda and A. V. Herz, A universal model for spike-frequency adaptation, Neural Comput, vol.15, pp.2523-2564, 2003.

B. Bie, D. L. Brown, and M. Naguib, Increased synaptic GluR1 subunits in the anterior cingulate cortex of rats with peripheral inflammation, Eur J Pharmacol, vol.653, issue.1-3, pp.26-31, 2011.

Z. A. Bortolotto, Z. I. Bashir, C. H. Davies, and G. L. Collingridge, A molecular switch activated by metabotropic glutamate receptors regulates induction of long-term potentiation, Nature, vol.368, pp.740-743, 1994.

N. Boyer, R. Dallel, A. Artola, and L. Monconduit, General trigeminospinal central sensitization and impaired descending pain inhibitory controls contribute to migraine progression, Pain, vol.155, issue.7, pp.1196-205, 2014.

M. C. Bushnell, M. Ceko, and L. A. Low, Cognitive and emotional control of pain and its disruption in chronic pain, Nat. Rev. Neurosci, vol.14, pp.502-511, 2013.

M. C. Bushnell, G. H. Duncan, R. K. Hofbauer, B. Ha, J. I. Chen et al., Pain perception: is there a role for primary somatosensory cortex?, Proc. Natl. Acad. Sci, vol.96, pp.7705-7709, 1999.

E. Campanac, G. Daoudal, N. Ankri, and D. Debanne, Downregulation of dendritic I(h) in CA1 pyramidal neurons after LTP, J Neurosci, vol.28, pp.8635-8643, 2008.

E. Campanac and D. Debanne, Spike timing-dependent plasticity: a learning rule for dendritic integration in rat CA1 pyramidal neurons, J Physiol, vol.586, pp.779-793, 2008.
URL : https://hal.archives-ouvertes.fr/hal-01766849

Z. Y. Chen, F. Y. Shen, L. Jiang, X. Zhao, X. L. Shen et al., Attenuation of Neuropathic Pain by Inhibiting Electrical Synapses in the Anterior Cingulate Cortex, Anesthesiology, vol.124, issue.1, pp.169-183, 2016.

T. Chen, K. Koga, G. Descalzi, S. Qiu, J. Wang et al., Postsynaptic potentiation of corticospinal projecting neurons in the anterior cingulate cortex after nerve injury, Mol Pain, vol.10, 2014.

C. S. Chiou, C. C. Chen, T. C. Tsai, C. C. Huang, D. Chou et al., Alleviating Bone Cancerinduced Mechanical Hypersensitivity by Inhibiting Neuronal Activity in the Anterior Cingulate Cortex, Anesthesiology, vol.125, issue.4, pp.779-792, 2016.

B. R. Christie and W. C. Abraham, Priming of associative long-term depression in the dentate gyrus by e` frequency synaptic activity, Neuron, vol.8, pp.79-84, 1992.

J. Cichon, T. Blanck, W. B. Gan, and G. Yang, Activation of cortical somatostatin interneurons prevents the development of neuropathic pain, Nat Neurosci, vol.20, issue.8, pp.1122-1132, 2017.

J. A. Coull, S. Beggs, D. Boudreau, D. Boivin, M. Tsuda et al., BDNF from microglia causes the shift in neuronal anion gradient underlying neuropathic pain, Nature, vol.438, issue.7070, pp.1017-1021, 2005.

J. A. Coull, D. Boudreau, K. Bachand, S. A. Prescott, F. Nault et al., Trans-synaptic shift in anion gradient in spinal lamina I neurons as a mechanism of neuropathic pain, Nature, vol.424, issue.6951, pp.938-942, 2003.

G. Daoudal, Y. Hanada, and D. (. Debanne, Bidirectional plasticity of excitatory postsynaptic potential (EPSP)-spike coupling in CA1 hippocampal pyramidal neurons, Proc Natl Acad Sci, vol.99, pp.14512-14517, 2002.
URL : https://hal.archives-ouvertes.fr/hal-01766854

D. De-ridder, D. Mulder, G. Menovsky, T. Sunaert, S. Kovacs et al., Electrical stimulation of auditory and somatosensory cortices for treatment of tinnitus and pain, Prog. Brain Res, vol.166, pp.377-388, 2007.

J. F. Disterhoft, D. A. Coulter, and D. L. Alkon, Conditioning-specific membrane changes of rabbit hippocampal neurons measured in vitro, Proc. Natl. Acad. Sci. USA, vol.83, pp.2733-2737, 1986.

G. P. Dugué, A. Dumoulin, A. Triller, and S. Dieudonné, Target-dependent use of co-released inhibitory transmitters at central synapses, J Neurosci, vol.25, pp.6490-6498, 2005.

K. Eto, H. Wake, M. Watanabe, H. Ishibashi, M. Noda et al., Interregional contribution of enhanced activity of the primary somatosensory cortex to the anterior cingulate cortex accelerates chronic pain behavior, J Neurosci, vol.31, issue.21, pp.7631-7636, 2011.

K. Eto, H. Ishibashi, T. Yoshimura, M. Watanabe, A. Miyamoto et al., Enhanced GABAergic activity in the mouse primary somatosensory cortex is insufficient to alleviate chronic pain behavior with reduced expression of neuronal potassium-chloride cotransporter, J Neurosci, vol.32, issue.47, pp.16552-16559, 2012.

Y. Fan, D. Fricker, D. H. Brager, X. Chen, H. C. Lu et al., Activitydependent decrease of excitability in rat hippocampal neurons through increases in I(h), 2005.

, Nat Neurosci, vol.8, pp.1542-1551

H. Flor, C. Denke, M. Schaefer, and S. Grüsser, Effect of sensory discrimination training on cortical reorganisation and phantom limb pain, Lancet, vol.357, pp.1763-1764, 2001.

U. Frey, K. Schollmeier, K. G. Reymann, and T. Seidenbecher, Asymptotic hippocampal longterm potentiation in rats does not preclude additional potentiation at later phases, Neuroscience, vol.67, pp.799-807, 1995.

S. Fujii, K. Saito, H. Miyakawa, K. Ito, and H. Kato, Reversal of longterm potentiation (depotentiation) induced by tetanus stimulation of the input to CA1 neurons of guinea pig hippocampal slices, Brain Res, vol.555, pp.112-122, 1991.

C. Gasselin, Y. Inglebert, N. Ankri, and D. Debanne, Plasticity of intrinsic excitability during LTD is mediated by bidirectional changes in h-channel activity, Sci Rep, vol.7, issue.1, p.14418, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01766825

J. Gross, A. Schnitzler, L. Timmermann, and M. (. Ploner, Gamma oscillations in human primary somatosensory cortex reflect pain perception, PLoS Biol, vol.5, p.133, 2007.

L. Gu, M. L. Uhelski, S. Anand, M. Romero-ortega, Y. T. Kim et al., Pain inhibition by optogenetic activation of specific anterior cingulate cortical neurons, PLoS One, vol.10, issue.2, p.117746, 2015.

Y. Huang, A. Colino, D. K. Selig, and R. C. Malenka, The influence of prior synaptic activity on the induction of long-term potentiation, Science, vol.255, pp.730-733, 1992.

L. L. Holland and J. J. Wagner, Primed facilitation of homosynaptic long-term depression and depotentiation in rat hippocampus, J Neurosci, vol.18, pp.887-894, 1998.

K. Koga, G. Descalzi, T. Chen, H. G. Ko, J. Lu et al., Coexistence of two forms of LTP in ACC provides a synaptic mechanism for the interactions between anxiety and chronic pain, Neuron, vol.85, issue.2, pp.377-389, 2015.

S. Kourrich, D. J. Calu, and A. Bonci, Intrinsic plasticity: an emerging player in addiction, Nat Rev Neurosci, vol.16, issue.3, pp.173-184, 2015.

R. Kuner, Central mechanisms of pathological pain, Nat. Med, vol.16, pp.1258-1266, 2010.

J. Larson, J. P. Xiao, and G. Lynch, Reversal of LTP by theta frequency stimulation, Brain Res, vol.600, pp.97-102, 1993.

A. Latremoliere and C. J. Woolf, Central sensitization: a generator of pain hypersensitivity by central neural plasticity, J Pain, vol.10, issue.9, pp.895-926, 2009.

X. Y. Li, H. G. Ko, T. Chen, G. Descalzi, K. Koga et al., Alleviating neuropathic pain hypersensitivity by inhibiting PKMzeta in the anterior cingulate cortex, Science, vol.330, issue.6009, pp.1400-1404, 2010.

M. Lotze, W. Grodd, N. Birbaumer, M. Erb, E. Huse et al., Does use of a myoelectric prosthesis prevent cortical reorganization and phantom limb pain?, Nat. Neurosci, vol.2, pp.501-502, 1999.

W. Magerl, N. Hansen, R. D. Treede, and T. Klein, The human pain system exhibits higher-order plasticity (metaplasticity), Neurobiol Learn Mem, vol.154, pp.112-120, 2018.

J. R. Moyer, L. T. Thompson, and J. F. Disterhoft, Trace eyeblink conditioning increases CA1 excitability in a transient and learning-specific manner, J. Neurosci, vol.16, pp.5536-5546, 1996.

R. Narayanan and D. Johnston, Long-term potentiation in rat hippocampal neurons is accompanied by spatially widespread changes in intrinsic oscillatory dynamics and excitability, Neuron, vol.56, pp.1061-1075, 2007.

A. Ngezahayo, M. Schachner, and A. Artola, Synaptic activity modulates the induction of bidirectional synaptic changes in adult mouse hippocampus, J. Neurosci, vol.20, pp.2451-2458, 2000.

L. Ning, L. Q. Ma, Z. R. Wang, and Y. W. Wang, Chronic constriction injury induced long-term changes in spontaneous membrane-potential oscillations in anterior cingulate cortical neurons in vivo, Pain Physician, vol.16, issue.5, pp.577-89, 2013.

C. M. Norris, D. L. Korol, and T. C. Foster, Increased susceptibility to induction of long-term depression and long-term potentiation reversal during aging, J Neurosci, vol.16, pp.5382-5392, 1996.

T. J. O'dell and E. R. Kandel, Low-frequency stimulation erases LTP through an NMDA receptor-mediated activation of protein phosphatases, Learn Mem, vol.1, pp.129-139, 1994.

G. Ohtsuki, C. Piochon, J. P. Adelman, and C. Hansel, SK2 channel modulation contributes to compartment-specific dendritic plasticity in cerebellar Purkinje cells, Neuron, vol.75, pp.108-120, 2012.

R. Peyron, F. Schneider, I. Faillenot, P. Convers, F. G. Barral et al., An fMRI study of cortical representation of mechanical allodynia in patients with neuropathic pain, Neurology, vol.63, pp.1838-1846, 2004.

C. Pozzorini, R. Naud, S. Mensi, and W. Gerstner, Temporal whitening by power-law adaptation in neocortical neurons, Nat Neurosci, vol.16, pp.942-948, 2013.

B. G. Schreurs, P. A. Gusev, D. Tomsic, D. L. Alkon, and T. Shi, Intracellular correlates of acquisition and long-term memory of classical conditioning in Purkinje cell dendrites in slices of rabbit cerebellar lobule HVI, J. Neurosci, vol.18, pp.5498-5507, 1998.

M. Sessolo, I. Marcon, S. Bovetti, G. Losi, M. Cammarota et al., Parvalbumin-Positive Inhibitory Interneurons Oppose Propagation But Favor Generation of Focal Epileptiform Activity, J Neurosci, vol.35, pp.9544-9557, 2015.

A. P. Rizwan, X. Zhan, G. W. Zamponi, and R. W. Turner, Long-Term Potentiation at the Mossy Fiber-Granule Cell Relay Invokes Postsynaptic Second-Messenger Regulation of Kv4 Channels, J Neurosci, vol.36, pp.11196-11207, 2016.

C. Y. Saab, Pain-related changes in the brain: diagnostic and therapeutic potentials. rends Neurosci, vol.35, pp.629-637, 2012.

F. Seifert and C. Maihöfner, Central mechanisms of experimental and chronic neuropathic pain: findings from functional imaging studies, Cell. Mol. Life Sci, vol.66, pp.375-390, 2009.

D. Seminowicz, A. L. Laferriere, M. Millecamps, J. S. Yu, T. J. Coderre et al., MRI structural brain changes associated with sensory and emotional function in a rat model of long-term neuropathic pain, Neuroimage, vol.47, pp.1007-1014, 2009.

A. Shackman, T. V. Salomons, H. A. Slagter, A. S. Fox, J. J. Winter et al., The integration of negative affect, pain and cognitive control in the cingulate cortex, Nat. Rev. Neurosci, vol.12, pp.154-167, 2011.

F. Y. Shen, Z. Y. Chen, W. Zhong, L. Q. Ma, C. Chen et al., Alleviation of neuropathic pain by regulating T-type calcium channels in rat anterior cingulate cortex, 2015.

, Mol Pain, vol.11, p.7

H. G. Shim, D. C. Jang, J. Lee, G. Chung, S. Lee et al., Long-Term Depression of Intrinsic Excitability Accompanied by Synaptic Depression in Cerebellar Purkinje Cells, J Neurosci, vol.37, pp.5659-5669, 2017.

U. Staubli and G. Lynch, Stable depression of potentiated synaptic responses in the hippocampus with 1-5 Hz stimulation, Brain Res, vol.513, pp.113-118, 1990.

L. L. Tan, P. Pelzer, C. Heinl, W. Tang, V. Gangadharan et al., A pathway from midcingulate cortex to posterior insula gates nociceptive hypersensitivity, Nat Neurosci, vol.20, issue.11, pp.1591-1601, 2017.

K. Thibault, W. K. Lin, A. Rancillac, M. Fan, T. Snollaerts et al., BDNF-dependent plasticity induced by peripheral inflammation in the primary sensory and the cingulate cortex triggers cold allodynia and reveals a major role for endogenous BDNF as a tuner of the affective aspect of pain, J Neurosci, vol.34, issue.44, pp.14739-51, 2014.
URL : https://hal.archives-ouvertes.fr/inserm-02119514

H. K. Titley, N. Brunel, and C. Hansel, Toward a Neurocentric View of Learning, Neuron, vol.95, issue.1, pp.19-32, 2017.

B. A. Vogt, G. R. Berger, and S. Derbyshire, Structural and functional dichotomy of human midcingulate cortex, Eur. J. Neurosci, vol.18, pp.3134-3144, 2003.

B. A. Vogt, Pain and emotion interactions in subregions of the cingulate gyrus, Nat. Rev. Neurosci, vol.6, pp.533-544, 2005.

T. D. Wager, L. Y. Atlas, M. A. Lindquist, M. Roy, C. W. Woo et al., An fMRI-based neurologic signature of physical pain, N. Engl. J. Med, vol.368, pp.1388-1397, 2013.

J. J. Wagner and B. E. Alger, GABAergic and developmental influences on homosynaptic LTD and depotentiation in rat hippocampus, J Neurosci, vol.15, pp.1577-1586, 1995.

G. Q. Wang, C. Cen, C. Li, S. Cao, N. Wang et al., Deactivation of excitatory neurons in the prelimbic cortex via Cdk5 promotes pain sensation and anxiety, Nat Commun, vol.6, p.7660, 2015.

Y. Wang, J. Wu, M. J. Rowan, and R. Anwyl, Role of the protein kinase C in the induction of homosynaptic long-term depression by brief low frequency stimulation in the dentate gyrus in the rat hippocampus in vitro, J Physiol, vol.513, pp.467-475, 1998.

Z. Wang, N. L. Xu, C. P. Wu, S. Duan, and M. M. Poo, Bidirectional changes in spatial dendritic integration accompanying long-term synaptic modifications, Neuron, vol.37, pp.463-472, 2003.

F. Wei, C. S. Qiu, S. J. Kim, L. Muglia, J. W. Maas et al., Genetic elimination of behavioral sensitization in mice lacking calmodulin-stimulated adenylyl cyclases, Neuron, vol.36, issue.4, pp.713-739, 2002.

F. Wei, G. D. Wang, G. A. Kerchner, S. J. Kim, H. M. Xu et al., Genetic enhancement of inflammatory pain by forebrain NR2B overexpression, Nat Neurosci, vol.4, issue.2, pp.164-169, 2001.

E. M. Wexler and P. K. Stanton, Priming of homosynaptic long-term depression in hippocampus by previous synaptic activity, NeuroReport, vol.4, pp.591-594, 1993.

L. J. Wu, H. Toyoda, M. G. Zhao, Y. S. Lee, J. Tang et al., , 2005.

, Upregulation of forebrain NMDA NR2B receptors contributes to behavioral sensitization after inflammation, J Neurosci, vol.25, issue.48, pp.11107-11116

H. Xu, L. J. Wu, H. Wang, X. Zhang, K. I. Vadakkan et al., Presynaptic and postsynaptic amplifications of neuropathic pain in the anterior cingulate cortex, J Neurosci, vol.28, issue.29, pp.7445-7453, 2008.

J. Xu, N. Kang, L. Jiang, M. Nedergaard, and J. Kang, Activity-dependent long-term potentiation of intrinsic excitability in hippocampal CA1 pyramidal neurons, J Neurosci, vol.25, pp.1750-1760, 2005.

X. Yang and D. S. Faber, Initial synaptic efficacy influences induction and expression of long-term changes in transmission, Proc Natl Acad Sci, vol.88, pp.4299-4303, 1991.

Z. Yang and F. Santamaria, Purkinje cell intrinsic excitability increases after synaptic long term depression, J Neurophysiol, vol.116, issue.3, pp.1208-1217, 2016.

W. Zhang and D. J. Linden, The other side of the engram: experience-driven changes in neuronal intrinsic excitability, Nat Rev Neurosci, vol.4, issue.11, pp.885-900, 2003.

M. G. Zhao, S. W. Ko, L. J. Wu, H. Toyoda, H. Xu et al., Enhanced presynaptic neurotransmitter release in the anterior cingulate cortex of mice with chronic pain, J Neurosci, vol.26, issue.35, pp.8923-8930, 2006.

M. Zhuo, Neural Mechanisms Underlying Anxiety-Chronic Pain Interactions, Trends Neurosci, vol.39, issue.3, pp.136-145, 2016.

C. Alba-delgado, E. Khoueiry, C. Peirs, C. Dallel, R. Artola et al., Subpopulations of PKCgamma interneurons within the medullary dorsal horn revealed by electrophysiologic and morphologic approach, CrossRef Medline Cutting JE, Garvin JJ (1987) Fractal curves and complexity, vol.156, pp.365-370, 2015.

T. A. Ferreira, L. L. Iacono, C. Gross, M. Jacob, J. C. Sarria et al., Serotonin receptor 1A modulates actin dynamics and restricts dendritic growth in hippocampal neurons, CrossRef Medline Meijering E, vol.32, pp.18-26, 2004.

, Cytometry A, vol.58, pp.167-176

T. G. Smith, G. D. Lange, W. Marks, G. Kato, H. Furue et al., Cell-type-specific excitatory and inhibitory circuits involving primary afferents in the substantia gelatinosa of the rat spinal dorsal horn in vitro, CrossRef Medline Yasaka, vol.69, pp.603-618, 1996.

, Une grande attention s'est portée sur l'ACC. Or, le cortex S1 est aussi impliqué dans la douleur chronique. Il est le siège d'une hyperactivité chez le patient comme chez l'animal douloureux chronique. Mais cette hyperactivité est-elle soutenue par une plasticité ? Et si oui, laquelle ? En effet, il est maintenant clairement établi que l'activité synaptique peut déclencher simultanément de nombreux phénomènes de plasticité, incluant notamment (i) des changements bidirectionnels durables de la transmission synaptique (LTP ou LTD), (ii) des changements dans la capacité même qu'a cette transmission synaptique d'exprimer une future plasticité synaptique (métaplasticité), (iii) des changements bidirectionnels durables de l'excitabilité neuronale (LTP-IE et LTD-IE) et (iv) une réorganisation morphologique, De nombreuses données expérimentales suggèrent que la chronicisation d'une douleur met en jeu une plasticité des voies de la douleur parmi lesquelles le cortex

. Dans-une-première-Étape, En effet, il est crucial de connaitre à la fois (i) les relations entre activité synaptique et chaque type de plasticité ou règles de plasticité (synaptique, intrinsèque) et (ii) les relations entre ces différentes plasticités -i.e. les différentes règles de plasticité -pour déterminer le rôle de chaque plasticité dans l'engram, ici la mémoire douloureuse. Nous montrons qu'en règle générale, dans les couches 2/3 du cortex S1, changements synaptiques et changements neuronaux sont synergiques : LTP synaptique avec LTP-IE et LTD synaptique avec LTD-IE. Ainsi les changements d'excitabilité intrinsèque tendent à amplifier les changements synaptiques. De plus, nous révélons que les deux règles de plasticité, synaptique et intrinsèque, sont (i) superposables et (ii) varient parallèlement en fonction de l, nous avons recherché, en conditions contrôles, quels sont les phénomènes de plasticité déclenchés par l'activation synaptique dans les couches superficielles

. Voir-ngezahayo, Nous avons montré que s'il y a par exemple induction d'une LTP synaptique, l'induction ultérieure de la LTD est facilitée et celle de la LTP au contraire inhibée. Or cette métaplasticité, homéostatique, est spécifique des synapses qui ont été activées ; l'induction des LTD/LTP synaptiques dans les autres synapses n'est pas modifiée, Il est intéressant de comparer ici le rôle respectif des plasticités synaptique et neuronale dans le contrôle de l'induction ultérieure d'une plasticité synaptique, 2000.

. La-ltp-synaptique-s'accompagne-d'une-ltp-ie, Cette hyperexcitabilité, elle, facilite l'induction d'une plasticité synaptique -elle est donc synergique -dans l'ensemble des synapses sur ce neurone

W. C. Abraham, Metaplasticity: tuning synapses and networks for plasticity, Nat Rev Neurosci, vol.9, issue.5, p.387, 2008.

M. Aigner, R. Lukas, J. Denk, M. Ziya-ghazvini, F. Kaider et al., Somatotopic organization of primary afferent perikarya of the guinea-pig extraocular muscles in the trigeminal ganglion:a post-mortem DiI-tracing study, Exp Eye Res, vol.70, issue.4, pp.411-418, 2000.

C. Alba-delgado, S. Mountadem, M. , N. Monconduit, L. Dallel et al., 5-HT2A receptor-induced morphological reorganization of PKC?-expressing interneurons gates inflammatory mechanical allodynia in rat, J Neurosci, vol.pii, pp.1294-1312, 2018.

T. F. Almeida, S. Roizenblatt, and S. Tufik, Afferent pain pathways:a neuroanatomical review, Brain Rese, vol.1000, issue.1, pp.40-56, 2004.

P. Alvarez, W. Dieb, A. Hafidi, D. L. Voisin, and R. Dallel, Insular cortex representation of dynamic mechanical allodynia in trigeminal neuropathic rats, Neurobiol Dis, vol.33, issue.1, pp.89-95, 2008.

D. Andrew and A. D. Craig, Spinothalamic lamina I neurons selectively sensitive to histamine:a central neural pathway for itch, Nat Neurosci, vol.4, issue.1, pp.72-77, 2001.

J. Arvidsson, K. Pfaller, and S. Gmeiner, The ganglionic origins and central projections of primary sensory neurons innervating the upper and lower lips in the rat, Somatosensory Motor Res, vol.9, issue.3, pp.199-209, 1992.

A. V. Apkarian, M. C. Bushnell, R. D. Treede, and J. K. Zubieta, Human brain mechanisms of pain perception and regulation in health and disease, Eur J Pain, vol.9, pp.463-84, 2005.

N. Attal, S. Perrot, J. Fermanian, and D. Bouhassira, The neuropathic components of chronic low back pain:a prospective multicenter study using the DN4 Questionnaire, J Pain Off J Am Pain Soc, vol.12, issue.10, pp.1080-1087, 2011.

J. R. Augustine, The insular lobe in primates including humans, Neurol Res, vol.7, issue.1, pp.2-10, 1985.

J. R. Augustine, Circuitry and functional aspects of the insular lobe in primates including humans, Brain Res Rev, vol.22, issue.3, pp.229-244, 1996.

R. Baron, A. Binder, and G. Wasner, Neuropathic pain:diagnosis, pathophysiological mechanisms, and treatment, Lancet Neurol, vol.9, issue.8, pp.807-819, 2010.

D. L. Bennett, G. J. Michael, N. Ramachandran, J. B. Munson, S. Averill et al., A distinct subgroup of small DRG cells express GDNF receptor components and GDNF is protective for these neurons after nerve injury, J Neurosci, vol.18, issue.8, pp.3059-3072, 1998.

M. Berthier, S. Starkstein, and R. Leiguarda, Asymbolia for pain:A sensory-limbic disconnection syndrome, Ann Neurol, vol.24, issue.1, pp.41-49, 1988.

J. M. Besson and A. Chaouc, Peripheral and spinal mechanisms of nociception, Physiologi Rev, vol.67, issue.1, pp.67-186, 1987.

R. W. Beuerman and D. L. Tanelian, Corneal pain evoked by thermal stimulation, Pain, vol.7, issue.1, pp.1-14, 1979.

B. Bie, D. L. Brown, and M. Naguib, Increased synaptic GluR1 subunits in the anterior cingulate cortex of rats with peripheral inflammation, Eur J Pharmacol, vol.653, issue.1-3, pp.26-31, 2011.

A. Biemond, The conduction of pain above the level of the thalamus opticus, Arch Neurol Psychiatry, vol.75, pp.231-275, 1956.

T. V. Bliss and G. L. Collingridge, A synaptic model of memory: long-term potentiation in the hippocampus, Nature, vol.6407, issue.361, pp.31-40, 1993.

T. V. Bliss, G. L. Collingridge, B. Kaang, and M. Zhuo, Synaptic plasticity in the anterior cingulate cortex in acute and chronic pain, Nat Rev Neurosci, vol.17, issue.8, pp.485-96, 2016.

D. Borsook, Pain and motor system plasticity, Pain, vol.132, issue.1-2, p.8, 2007.

D. Bouhassira and N. Attal, Douleurs Neuropathiques. Edition Arnette Groupe Liaison S.A, 2007.

E. O. Bragin, Z. V. Yeliseeva, G. F. Vasilenko, E. E. Meizerov, B. T. Chuvin et al., Cortical projections to the periaqueductal grey in the cat:a retrograde horseradish peroxidase study, Neurosci Lett, vol.51, pp.271-275, 1984.

B. Bromm, E. Scharein, and C. Vahle-hinz, Cortex areas involved in the processing of normal and altered pain, Progr Brain Resc, vol.129, pp.289-302, 2000.

R. Burstein, Y. Hiroyoshi, A. M. Strassman, and M. , Chemical stimulation of the intracranial dura induces enhanced responses to facial stimulation in brain stem trigeminal neurons, J Neurophysiol, vol.79, issue.2, pp.964-982, 1998.

R. Burstein, M. F. Cutrer, and D. Yarnitsky, The development of cutaneous allodynia during a migraine attack clinical evidence for the sequential recruitment of spinal and supraspinal nociceptive neurons in migraine, Brain, vol.123, pp.1703-1709, 2000.

M. C. Bushnell, M. Ceko, and L. A. Low, Cognitive and emotional control of pain and its disruption in chronic pain, Nat Rev Neurosci, vol.14, issue.7, pp.502-513, 2013.

M. C. Bushnell, G. H. Duncan, R. K. Hofbauer, B. Ha, J. I. Chen et al., Pain perception:is there a role for primary somatosensory cortex?, Proc. Natl. Acad. Sci, vol.96, pp.7705-7709, 1999.

N. F. Capra and T. D. Wax, Distribution and central projections of primary afferent neurons that innervate the masseter muscle and mandibular periodontium:a double-label study, J Comp Neurol, vol.279, issue.3, pp.341-352, 1989.

F. Caruana, A. Jezzini, B. Sbriscia-fioretti, G. Rizzolatti, and V. Gallese, Emotional and social behaviors elicited by electrical stimulation of the insula in the macaque monkey, Curr Biol, vol.21, pp.195-204, 2011.

K. L. Casey, Forebrain mechanisms of nociception and pain:analysis through imaging, Proc Natl Acad Sci U S A, vol.96, issue.14, pp.7668-7674, 1999.

K. L. Casey, S. Minoshima, T. J. Morrow, and R. A. Koeppe, Comparison of human cerebral activation patterns during cutaneous warmth, heat pain, and deep cold pain, J Neurophysiol, vol.76, issue.1, pp.571-581, 1996.

M. J. Caterina, M. A. Schumacher, M. Tominaga, T. A. Rosen, J. D. Levine et al., The capsaicin receptor:a heat-activated ion channel in the pain pathway, Nature, vol.389, issue.6653, pp.816-824, 1997.

F. Cervero, Sensory innervation of the viscera:peripheral basis of visceral pain, Physiol Rev, vol.74, issue.1, pp.95-138, 1994.

T. Chen, K. Koga, G. Descalzi, S. Qiu, J. Wang et al., Postsynaptic potentiation of corticospinal projecting neurons in the anterior cingulate cortex after nerve injury, Mol Pain, vol.10, p.33, 2014.

Z. Y. Chen, F. Y. Shen, L. Jiang, X. Zhao, X. L. Shen et al., Attenuation of Neuropathic Pain by Inhibiting Electrical Synapses in the Anterior Cingulate Cortex, Anesthesiology, vol.124, issue.1, pp.169-183, 2016.

C. S. Chiou, C. C. Chen, T. C. Tsai, C. C. Huang, D. Chou et al., Alleviating Bone Cancerinduced Mechanical Hypersensitivity by Inhibiting Neuronal Activity in the Anterior Cingulate Cortex, Anesthesiology, vol.125, issue.4, pp.779-792, 2016.

P. Chua, M. Krams, T. I. Passingham, R. Dolan, and R. , A functional anatomy of anticipatory anxiety, Neuroimage, vol.9, issue.6, pp.563-571, 1999.

J. Cichon, T. Blanck, W. B. Gan, and G. Yang, Activation of cortical somatostatin interneurons prevents the development of neuropathic pain, Nat Neurosci, vol.20, issue.8, pp.1122-1132, 2017.

R. C. Coghill, C. N. Sang, J. M. Maisog, and M. J. Iadarola, Pain intensity processing within the human brain:a bilateral, distributed mechanism, J Neurophysiol, vol.82, issue.4, pp.1934-1943, 1999.

J. E. Cometto-muñiz and W. S. Cain, Relative sensitivity of the ocular trigeminal, nasal trigeminal and olfactory systems to airborne chemicals, Chemical Senses, vol.20, issue.2, pp.191-198, 1995.

G. L. Collingridge, S. Peineau, J. G. Howland, and Y. T. Wang, Long-term depression in the CNS, Nat Rev Neurosci, vol.11, issue.7, pp.459-73, 2010.

J. Coste, D. L. Voisin, L. S. Miraucourt, R. Dallel, and P. Luccarini, Dorsal horn NK1-expressing neurons control windup of downstream trigeminal nociceptive neurons, Pain, vol.137, issue.2, pp.340-351, 2008.
URL : https://hal.archives-ouvertes.fr/hal-01543208

M. Costigan, J. Scholz, and C. J. Woolf, Neuropathic pain: a maladaptive response of the nervous system to damage, Annu Rev Neurosci, vol.32, pp.1-32, 2009.

A. D. Craig, How do you feel-now? The anterior insula and human awareness, Nat Rev Neurosci, vol.10, pp.59-70, 2009.

A. D. Craig and K. D. Kniffki, Spinothalamic lumbosacral lamina I cells responsive to skin and muscle stimulation in the cat, J Physiol, vol.365, pp.197-221, 1985.

G. Cruccu, M. J. Aminoff, G. Curio, J. M. Guerit, R. Kakigi et al., Recommendations for the clinical use of somatosensoryevoked potentials, Clin Neurophysiol, vol.119, issue.8, pp.1705-1719, 2008.

R. Curtis, Self-organizing processes, anxiety, and change, J Psychot Integr, vol.2, issue.4, pp.295-319, 1992.

R. Dallel, P. Clavelou, and A. Woda, Effects of tractotomy on nociceptive reactions induced by tooth pulp stimulation in the rat, Exp Neurol, vol.106, issue.1, pp.78-84, 1989.

R. Dallel, C. Dualé, and J. L. Molat, Morphine administered in the substantia gelatinosa of the spinal trigeminal nucleus caudalis inhibits nociceptive activities in the spinal trigeminal nucleus oralis, J Neurosci, vol.18, issue.10, pp.3529-3536, 1998.

R. Dallel, C. Duale, P. Luccarini, and J. L. Molat, Stimulus-function, wind-up and modulation by diffuse noxious inhibitory controls of responses of convergent neurons of the spinal trigeminal nucleus oralis, Eur J Neuroscie, vol.11, issue.1, pp.31-40, 1999.

A. R. Damasio, T. J. Grabowski, A. Bechara, H. Damasio, L. L. Ponto et al., Subcortical and cortical brain activity during the feeling of self-generated emotions, Nat Neurosci, vol.3, issue.10, pp.1049-1056, 2000.

D. De-ridder, D. Mulder, G. Menovsky, T. Sunaert, S. Kovacs et al., Electrical stimulation of auditory and somatosensory cortices for treatment of tinnitus and pain, Prog. Brain Res, vol.166, pp.377-388, 2007.

S. W. Derbyshire, A. K. Jones, F. Gyulai, S. Clark, D. Townsend et al., Pain processing during three levels of noxious stimulation produces differential patterns of central activity, Pain, vol.73, issue.3, pp.431-445, 1997.

S. W. Derbyshire, A. K. Jones, F. Creed, T. Starz, C. C. Meltzer et al., Cerebral responses to noxious thermal stimulation in chronic low back pain patients and normal controls, Neuroimage, vol.16, issue.1, pp.158-168, 2002.

R. Dias, T. Robbins, and A. Roberts, Dissociation in prefrontal cortex of affective and attentional shifts, Nature, vol.380, issue.6569, pp.69-72, 1996.

A. Diogenes, A. M. Patwardhan, N. A. Jeske, N. B. Ruparel, V. Goffin et al., Prolactin modulates TRPV1 in female rat trigeminal sensory neurons, J Neurosci, vol.26, issue.31, pp.8126-8136, 2006.

W. K. Dong, E. H. Chudler, K. Sugiyama, V. J. Roberts, and T. Hayashi, Somatosensory, multisensory, and task-related neurons in cortical area 7b (PF) of unanesthetized monkeys, J Neurophysiol, vol.72, issue.2, pp.542-564, 1994.

R. P. Dum, D. J. Levinthal, and P. L. Strick, The spinothalamic system targets motor and sensory areas in the cerebral cortex of monkeys, J Neurosci, vol.29, pp.14223-14235, 2009.

R. H. Dworkin, Advances in neuropathic pain:diagnosis, mechanisms, and treatment recommendations, Arch Neurol, vol.60, issue.11, pp.1524-1534, 2003.

N. I. Eisenberger, M. D. Lieberman, and K. D. Williams, Does rejection hurt? An fMRI study of social exclusion, Science, vol.302, pp.290-292, 2003.

K. Eto, H. Wake, M. Watanabe, H. Ishibashi, M. Noda et al., Interregional contribution of enhanced activity of the primary somatosensory cortex to the anterior cingulate cortex accelerates chronic pain behavior, J Neurosci, vol.31, issue.21, pp.7631-7636, 2011.

K. Eto, H. Ishibashi, T. Yoshimura, M. Watanabe, A. Miyamoto et al., Enhanced GABAergic activity in the mouse primary somatosensory cortex is insufficient to alleviate chronic pain behavior with reduced expression of neuronal potassium-chloride cotransporter, J Neurosci, vol.32, issue.47, pp.555-563, 1960.

J. Feng, Z. Zhang, W. Li, X. Shen, W. Song et al., Missense mutation in the MEFV gene are associated with fibromyalgia syndrome and correlate with elevated IL-1beta plasma level, PLoS One, vol.4, issue.12, p.8480, 2009.

H. Flor, T. Elbert, S. Knecht, C. Wienbruch, C. Pantev et al., Phantom-limb pain as a perceptual correlate of cortical reorganization following arm amputation, Nature, vol.375, issue.6531, pp.482-484, 1995.

H. Flor, C. Denke, M. Schaefer, and S. Grüsser, Effect of sensory discrimination training on cortical reorganisation and phantom limb pain, Lancet, vol.357, pp.1763-1764, 2001.

E. L. Foltz and L. E. White, Pain "Relief" by Frontal Cingulumotomy, J Neurosurgery, vol.19, issue.2, pp.89-100, 1962.

M. Frot, L. Rambaud, M. Guenot, and F. Mauguiere, Intracortical recordings of early painrelated CO2-laser evoked potentials in the human second somatosensory (SII) area, Clin Neurophysiol, vol.110, pp.133-178, 1999.

M. Frot, M. Magnin, F. Mauguière, and L. Garcia-larrea, Cortical representation of pain in primary sensory-motor areas (S1/M1)-a study using intracortical recordings in humans, Hum Brain Mapp, vol.34, pp.2655-68, 2013.
URL : https://hal.archives-ouvertes.fr/hal-02472440

L. Garcia-larrea, The posterior insular-opercular region and the search of a primary cortex for pain, Neurophysiol Clin, vol.42, pp.299-313, 2012.
URL : https://hal.archives-ouvertes.fr/inserm-00744512

L. Garcia-larrea, C. Perchet, C. Creac'h, P. Convers, R. Peyron et al., Operculo-insular pain (parasylvian pain):a distinct central pain syndrome, Brain, vol.133, pp.2528-2567, 2010.

L. Garcia-larrea and R. Peyron, Pain matrices and neuropathic pain matrices:a review, 2013.
URL : https://hal.archives-ouvertes.fr/inserm-00877368

M. W. Gerard, Afferent impulses of the trigeminal nerve. The intramedullary course of the painful thermal and tactile impulses, Arch Neurol Psychiatr, vol.9, pp.306-338, 1923.

D. A. Gonçalves, A. L. Dal-fabbro, J. A. Campos, M. E. Bigal, and J. G. Speciali, Symptoms of temporomandibular disorders in the population:an epidemiological study, J Orofac Pain, vol.24, issue.3, pp.270-278, 2010.

M. Gorsky, S. Silverman, and H. Jr-&-chinn, Clinical characteristics and management outcome in the burning mouth syndrome. An open study of 130 patients. Oral Sur, Oral Med Oral Pathol, vol.72, issue.2, pp.192-195, 1991.

S. H. Graham, F. R. Sharp, and W. Dillon, Intraoral sensation in patients with brainstem lesions:role of the rostral spinal trigeminal nuclei in pons, Neurology, vol.38, issue.10, pp.1529-1533, 1988.

J. D. Greenspan, R. R. Lee, and F. A. Lenz, Pain sensitivity alterations as a function of lesion location in the parasylvian cortex, PAIN, vol.81, pp.273-82, 1999.

J. Gross, A. Schnitzler, L. Timmermann, and M. Ploner, Gamma oscillations in human primary somatosensory cortex reflect pain perception, PLoS Biol, vol.5, p.133, 2007.

L. Gu, M. L. Uhelski, S. Anand, M. Romero-ortega, Y. T. Kim et al., Pain inhibition by optogenetic activation of specific anterior cingulate cortical neurons, PLoS ONE, vol.10, p.117746, 2015.

G. Guilbaud, V. Kayser, J. M. Benoist, and M. Gautron, Modifications in the responsiveness of rat ventrobasal thalamic neurons at different stages of carrageeninproduced inflammation, Brain Res, vol.385, pp.86-98, 1986.

G. Guilbaud, J. M. Benoist, F. Jazat, and M. Gautron, Neuronal responsiveness in the ventrobasal thalamic complex of rats with an experimental peripheral mononeuropathy, J. Neurophysiol, vol.64, pp.1537-1554, 1990.

A. Guo, L. Vulchanova, J. Wang, X. Li, and R. Elde, Immunocytochemical localization of the vanilloid receptor 1 (VR1):relationship to neuropeptides, the P2X3 purinoceptor and IB4 binding sites, Eur J Neurosci, vol.11, issue.3, pp.946-958, 1999.

C. E. Hagains, A. K. Senapati, P. J. Huntington, J. W. He, and Y. B. Peng, Inhibition of spinal cord dorsal horn neuronal activity by electrical stimulation of the cerebellar cortex, J Neurophysiol, vol.106, issue.5, pp.2515-2522, 2011.

S. Han, M. T. Soleiman, M. E. Soden, L. S. Zweifel, and R. D. Palmiter, Elucidating an affective pain circuit that creates a threat memory, Cell, vol.162, pp.363-374, 2015.

R. Hari, K. Portin, B. Kettenmann, V. Jousmäki, and G. Kobal, Right-hemisphere preponderance of responses to painful CO2 stimulation of the human nasal mucosa, Pain, vol.72, issue.1, pp.145-151, 1997.

B. G. Hiester, M. I. Becker, A. B. Bowen, S. L. Schwartz, and M. J. Kennedy, Mechanisms and Role of Dendritic Membrane Trafficking for Long-Term Potentiation, Front. Cell. Neurosci, vol.12, p.391, 2018.

K. D. Hoffmann and M. A. Matthews, Comparison of sympathetic neurons in orofacial and upper extremity nerves:implications for causalgia, J Oral Maxillofacial Surg, vol.48, issue.7, pp.720-726, 1990.

E. W. Howland, R. T. Wakai, B. A. Mjaanes, J. P. Balog, and C. S. Cleeland, Whole head mapping of magnetic fields following painful electric finger shock, Brain Res Cogn Brain Res, vol.2, issue.3, pp.165-172, 1995.

J. W. Hu, B. J. Sessle, P. Raboisson, R. Dallel, and A. Woda, Stimulation of craniofacial muscle afferents induces prolonged facilitatory effects in trigeminal nociceptive brain-stem neurones, Pain, vol.48, issue.1, pp.53-60, 1992.

J. W. Hu, A. Woda, and B. J. Sessle, Effects of pre-emptive local anaesthesia on tooth pulp deafferentation-induced neuroplastic changes in cat trigeminal brainstem neurones, Arch Oral Biol, vol.44, issue.3, pp.287-293, 1999.

D. I. Hughes, D. T. Scott, A. J. Todd, and J. S. Riddell, Lack of evidence for sprouting of Abeta afferents into the superficial laminas of the spinal cord dorsal horn after nerve section, J Neurosci, vol.23, issue.29, pp.9491-9499, 2003.

S. P. Hunt and J. Rossi, Peptide-and non-peptide-containing unmyelinated primary afferents:the parallel processing of nociceptive information, PhilosTransactions of the R Soc Lond B Biol Sci, vol.308, pp.283-289, 1136.

S. P. Hunt and P. W. Mantyh, The molecular dynamics of pain control, Nat Rev Neurosci, vol.2, issue.2, pp.83-91, 2001.

R. Hurt and H. T. Ballantine, Stereotactic anterior cingulate lesions for persistent pain:a report on 68 cases, Clin Neurosurg, vol.21, pp.334-351, 1973.

A. Iggo and K. H. Andres, Morphology of Cutaneous Receptors, Ann Rev Neurosci, vol.5, issue.1, pp.1-31, 1982.

H. Ikeda, B. Heinke, R. Ruscheweyh, and J. Sandkühler, Synaptic plasticity in spinal lamina I projection neurons that mediate hyperalgesia, Science, vol.299, issue.5610, pp.1237-1240, 2003.

H. Ikeda, J. Stark, H. Fischer, M. Wagner, R. Drdla et al., Synaptic amplifier of inflammatory pain in the spinal dorsal horn, Science, vol.312, pp.1659-1662, 2006.

R. Ikeda, Y. Takahashi, K. Inoue, and F. Kato, NMDA receptor-independent synaptic plasticity in the central amygdala in the rat model of neuropathic pain, Pain, vol.127, pp.161-172, 2007.

J. Isnard, M. Magnin, J. Jung, F. Mauguière, and L. Garcia-larrea, Does the insula tell our brain that we are in pain?, PAIN, vol.152, pp.946-51, 2011.

K. B. Jensen, C. Berna, M. L. Loggia, A. D. Wasan, R. R. Edwards et al., The use of functional neuroimaging to evaluate psychological and other non-pharmacological treatments for clinical pain, Neuroscience letters, vol.520, issue.2, pp.156-164, 2012.

M. P. Jensen, A neuropsychological model of pain:research and clinical implications, The J Pain, vol.11, issue.1, pp.2-12, 2010.

E. G. Jones, The thalamus, 2012.

G. I. Juhl, T. S. Jensen, S. E. Norholt, and P. Svensson, Central Sensitization Phenomena after Third Molar Surgery:A Quantitative Sensory Testing Study, Eur J Pain, vol.12, issue.1, pp.116-127, 2008.

D. Julius and A. Basbaum, Molecular mechanisms of nociception, Nature, vol.413, issue.6852, pp.203-210, 2001.

E. Kandel, J. Schwartz, and T. Jessell, Principles of Neural Science, 1414.

S. J. Kang, C. Kwak, J. Lee, S. E. Sim, J. Shim et al., Bidirectional modulation of hyperalgesia via the specific control of excitatory and inhibitory neuronal activity in the ACC, Mol. Brain, vol.8, p.81, 2015.

D. R. Kenshalo, Comparison of thermal sensitivity of the forehead, lip, conjunctiva and cornea, J Appl Physiol, vol.15, pp.987-991, 1960.

G. F. Khayyat, U. J. Yu, and R. B. King, Response patterns to noxious and non-noxious stimuli in rostral trigeminal relay nuclei, Brain Res, vol.97, issue.1, pp.47-60, 1975.

S. K. Kim and J. Nabekura, Rapid synaptic remodeling in the adult somatosensory cortex following peripheral nerve injury and its association with neuropathic pain, J Neurosci, vol.31, issue.14, pp.5477-82, 2011.

K. Koga, G. Descalzi, T. Chen, H. G. Ko, J. Lu et al., Coexistence of two forms of LTP in ACC provides a synaptic mechanism for the interactions between anxiety and chronic pain, Neuron, vol.85, issue.2, pp.377-389, 2015.

M. Koltzenburg and . Scadding, Neuropathic pain, Cur Opin Neurol, vol.14, issue.5, pp.641-647, 2001.

R. Kwiatek, L. Barnden, T. R. Jarrett, R. Chew, J. Rowe et al., Regional cerebral blood flow in fibromyalgia:Single-photon-emission computed tomography evidence of reduction in the pontine tegmentum and thalami, Arthritis Rheum, vol.43, issue.12, pp.2823-2833, 2000.

M. C. Lagerström, K. Rogoz, B. Abrahamsen, E. Persson, B. Reinius et al., VGLUT2-dependent sensory neurons in the TRPV1 population regulate pain and itch, Neuron, vol.68, issue.3, pp.529-542, 2010.

P. J. Lamey and M. A. Lewis, Oral medicine in practice:burning mouth syndrome, Brit Dent J, vol.167, issue.6, pp.197-200, 1989.

R. D. Lane, E. M. Reiman, M. M. Bradley, P. J. Lang, G. L. Ahern et al., Neuroanatomical correlates of pleasant and unpleasant emotion, Neuropsychologia, vol.35, issue.11, pp.1437-1444, 1997.

A. Latremoliere and C. J. Woolf, Central sensitization: a generator of pain hypersensitivity by central neural plasticity, J Pain, vol.10, issue.9, pp.895-926, 2009.

N. E. Lazarov, Comparative analysis of the chemical neuroanatomy of the mammalian trigeminal ganglion and mesencephalic trigeminal nucleus, Pro Neurobiol, vol.66, issue.1, pp.19-59, 2002.

E. M. Leise, Modular construction of nervous systems:a basic principle of design for invertebrates and vertebrates, Brain Res, vol.15, issue.1, pp.1-23, 1990.

F. A. Lenz, R. H. Gracely, A. J. Romanoski, E. J. Hope, L. H. Rowaland et al., Stimulation in the human somatosensory thalamus can reproduce both the affective and sensory dimensions of previously experienced pain, Nat Med, vol.1, pp.910-913, 1995.

F. A. Lenz, M. Rios, A. Zirh, D. Chau, G. Krauss et al., Painful stimuli evoke potentials recorded over the human anterior cingulate gyrus, J Neurophysiol, vol.79, pp.2231-2235, 1998.

F. A. Lenz, M. Rios, D. Chau, G. L. Krauss, T. A. Zirh et al., Painful stimuli evoke potentials recorded from the parasylvian cortex in humans, J Neurophysiol, vol.80, pp.2077-88, 1998.

D. Levy, S. Andrew, and M. , Mechanical response properties of A and C primary afferent neurons innervating the rat intracranial dura, J Neurophysiol, vol.88, issue.6, pp.3021-3031, 2002.

J. Lévesque, F. Eugène, Y. Joanette, V. Paquette, B. Mensour et al., Neural circuitry underlying voluntary suppression of sadness, Biol Psychiatry, vol.53, issue.6, pp.502-510, 2003.

X. Y. Li, H. G. Ko, T. Chen, G. Descalzi, K. Koga et al., Alleviating neuropathic pain hypersensitivity by inhibiting PKMzeta in the anterior cingulate cortex, Science, vol.330, issue.6009, pp.1400-1404, 2010.

Y. Li, V. Esain, L. Teng, J. Xu, W. Kwan et al., Inflammatory signaling regulates embryonic hematopoietic stem and progenitor cell production, Genes Dev, vol.28, issue.23, pp.2597-612, 2014.

A. R. Light and E. Perl, Spinal termination of functionally identified primary afferent neurons with slowly conducting myelinated fibers, J Comp Neurol, vol.186, issue.2, pp.133-150, 1979.

M. G. Liu, K. Koga, Y. Y. Guo, S. J. Kang, G. L. Collingridge et al., Long-term depression of synaptic transmission in the adult mouse insular cortex in vitro, Eur. J. Neurosci, vol.38, pp.3128-3145, 2013.

M. G. Liu, S. J. Kang, T. Y. Shi, K. Koga, M. M. Zhang et al., Long-term potentiation of synaptic transmission in the adult mouse insular cortex: multielectrode array recordings, J. Neurophysiol, vol.110, pp.505-521, 2013.

Y. Liu, A. Samad, O. Zhang, L. Duan, B. Tong et al., VGLUT2-dependent glutamate release from nociceptors is required to sense pain and suppress itch, Neuron, vol.68, issue.3, pp.543-556, 2010.

L. De-no and R. , Cerebral cortex:architecture, intracortical connexions, motor projections, Physiology of the nervous system (Fulton JF, pp.291-339, 1938.

J. Lorenz and K. Casey, Imaging of acute versus pathological pain in humans, Eur J Pain, vol.9, issue.2, pp.163-165, 2005.

M. Lotze, W. Grodd, N. Birbaumer, M. Erb, E. Huse et al., Does use of a myoelectric prosthesis prevent cortical reorganization and phantom limb pain?, Nat. Neurosci, vol.2, pp.501-502, 1999.

Y. Lu, P. Edward, and R. , Modular organization of excitatory circuits between neurons of the spinal superficial dorsal horn (laminae I and II), J Neurosci, vol.25, issue.15, pp.3900-3907, 2005.

L. Lundy-ekman, Neuroscience:Fundamentals for Rehabilitation, vol.575, 2007.

B. Lynn, Silent' nociceptors in the skin, Trends Neurosci, vol.14, issue.3, p.95, 1991.

L. S. Löken, J. Wessberg, I. Morrison, F. Mcglone, and H. Olausson, Coding of pleasant touch by unmyelinated afferents in humans, Nat Neurosc, vol.12, issue.5, pp.547-548, 2009.

W. Ma and M. Peschanski, Spinal and trigeminal projections to the parabrachial nucleus in the rat:electron-microscopic evidence of a spino-pontoamygdalian somatosensory pathway, Somatosens. Res, vol.5, pp.247-257, 1998.

A. B. Malmberg, E. P. Brandon, R. L. Idzerda, H. Liu, G. S. Mcknight et al., Diminished inflammation and nociceptive pain with preservation of neuropathic pain in mice with a targeted mutation of the type I regulatory subunit of cAMP-dependent protein kinase, J Neurosci, vol.17, pp.7462-7470, 1997.

C. F. Marfurt, The somatotopic organization of the cat trigeminal ganglion as determined by the horseradish peroxidase technique, Anat Record, vol.201, issue.1, pp.105-118, 1981.

C. F. Marfurt and D. M. Rajchert, Trigeminal primary afferent projections to "non-trigeminal" areas of the rat central nervous system, J Compara Neurol, vol.303, issue.3, pp.489-511, 1991.

B. Matthews, Autonomic mechanisms in oral sensations, Proc Fin Dent So, vol.85, issue.4-5, pp.365-373, 1989.

L. Mazzola, J. Isnard, and F. Mauguiere, Somatosensory and pain responses to stimulation of the second somatosensory area (SII) in humans:a comparison with SI and insular responses, Cereb Cortex, vol.16, pp.960-968, 2006.

L. Mazzola, J. Isnard, R. Peyron, and F. Mauguière, Stimulation of the human cortex and the experience of pain:Wilder Penfield's observations revisited, Brain, vol.135, pp.631-671, 2012.

F. Mcglone, A. B. Vallbo, H. Olausson, L. Loken, and J. Wessberg, Discriminative touch and emotional touch, Can J ExpPsychol, vol.61, issue.3, pp.173-183, 2007.

G. Mcmahon, Phantom limb pain following amputation, Paediatric Nurs, vol.10, issue.6, pp.22-25, 1998.

R. Melzack, From the gate to the neuromatrix, Pain, vol.82, pp.121-126, 1999.

R. Melzack, T. J. Coderre, J. Katz, and A. L. Vaccarino, Central neuroplasticity and pathological pain, Annals of the New York Aca Sci, vol.933, issue.1, pp.157-174, 2001.

H. Merskey and N. Bogduk, Classification of Chronic Pain. IASP Task Force on Taxonomy. Classification of Chronic Pain:Description of Chronic Pain Syndromes and Definitions of Pain Terms Seattle, 1994.

A. E. Metz, H. J. Yau, M. V. Centeno, A. V. Apkarian, and M. Martina, Morphological and functional reorganization of rat medial prefrontal cortex in neuropathic pain, Proc. Natl Acad. Sci. USA, vol.106, pp.2423-2428, 2009.

K. Michaud and F. Wolfe, Comorbidities in Rheumatoid Arthritis, Best Pract Res Clin Rheumatol, vol.21, issue.5, pp.885-906, 2007.

. Millan, The induction of pain:an integrative review, Prog Neurobiol, vol.57, issue.1, pp.1-164, 1999.

T. Mima, T. Nagamine, K. Nakamura, and H. Shibasaki, Attention modulates both primary and second somatosensory cortical activities in humans:a magnetoencephalographic study, J Neurophysiol, vol.80, issue.4, pp.2215-2221, 1998.

L. S. Miraucourt, R. Dallel, and D. L. Voisin, Glycine inhibitory dysfunction turns touch into pain through PKCgamma interneurons, PloS One, vol.2, issue.11, p.1116, 2007.

L. S. Miraucourt, X. Moisset, R. Dallel, and D. L. Voisin, Glycine inhibitory dysfunction induces a selectively dynamic, morphine-resistant, and neurokinin 1 receptor-independent mechanical allodynia, J Neurosci, vol.29, issue.8, pp.2519-2527, 2009.

J. M. Mountz, L. A. Bradley, J. G. Modell, R. W. Alexander, M. Triana-alexander et al., Fibromyalgia in women. Abnormalities of regional cerebral blood flow in the thalamus and the caudate nucleus are associated with low pain threshold levels, Arthritis Rheum, vol.38, issue.7, pp.926-938, 1995.

V. B. Mountcastle, Modality and topographic properties of single neurons of cat's somatic sensory cortex, J Neurophysiol, vol.20, issue.4, pp.408-434, 1957.

L. J. Müller, L. Pels, and G. F. Vrensen, Ultrastructural organization of human corneal nerves, Invest Ophthalmol Vis Sci, vol.37, issue.4, pp.476-488, 1996.

J. I. Nagy and S. P. Hunt, Fluoride-resistant acid phosphatase-containing neurones in dorsal root ganglia are separate from those containing substance P or somatostatin, Neurosci, vol.7, issue.1, pp.89-97, 1982.

A. Nakao, Y. Takahashi, M. Nagase, R. Ikeda, and F. Kato, Role of capsaicin-sensitive C-fiber afferents in neuropathic pain-induced synaptic potentiation in the nociceptive amygdala, Mol. Pain, vol.8, p.51, 2012.

V. Neugebauer and W. Li, Differential sensitization of amygdala neurons to afferent inputs in a model of arthritic pain, J Neurophysiol, vol.89, issue.2, pp.716-727, 2003.

S. Neumann, J. M. Braz, K. Skinner, I. J. Llewellyn-smith, and A. I. Basbaum, Innocuous, not noxious, input activates PKCgamma interneurons of the spinal dorsal horn via myelinated afferent fibers, J Neurosci, vol.28, issue.32, pp.7936-7944, 2008.

A. Ngezahayo, M. Schachner, and A. Artola, Synaptic activity modulates the induction of bidirectional synaptic changes in adult mouse hippocampus, J Neurosci, vol.20, issue.7, pp.2451-2459, 2010.

L. Ning, L. Q. Ma, Z. R. Wang, and Y. W. Wang, Chronic constriction injury induced long-term changes in spontaneous membrane-potential oscillations in anterior cingulate cortical neurons in vivo, Pain Physician, vol.16, issue.5, pp.577-89, 2013.

T. Nishimori, M. Sera, S. Suemune, A. Yoshida, K. Tsuru et al., The distribution of muscle primary afferents from the masseter nerve to the trigeminal sensory nuclei, Brain Res, vol.372, issue.2, pp.375-381, 1986.

S. Ohara, W. S. Anderson, H. C. Lawson, H. T. Lee, and F. A. Lenz, Endogenous and exogenous modulators of potentials evoked by a painful cutaneous laser (LEPs), Acta Neurochir Suppl, vol.99, pp.77-86, 2006.

P. Olausson, J. D. Jentsch, and J. R. Taylor, Repeated nicotine exposure enhances reward-related learning in the rat, Neuropsychopharmacology, vol.28, issue.7, pp.1264-1271, 2003.

J. Pajot, T. Pelissier, F. Sierralta, P. Raboisson, and R. Dallel, Differential effects of trigeminal tractotomy on Adelta-and C-fiber-mediated nociceptive responses, Brain Res, vol.863, issue.1-2, pp.289-292, 2000.

S. Panteleev, A. Y. Sokolov, K. V. Amelinn, and Y. D. Ignatov, Responses of neurons in the spinal nucleus of the trigeminal nerve to electrical stimulation of the dura mater of the rat brain, Neurosc Behav Physiol, vol.35, issue.5, pp.555-559, 2005.

A. A. Pearson, Role of gelatinous substance of spinal cord in conduction of pain, A.M.A, vol.68, issue.4, pp.515-529, 1952.

L. C. Pereira, A. M. Modesto, R. Sugai, and L. A. Da-mota, Pain sensitive cerebral areas and intracranial structures revealed at fully awake craniotomies for primary intracranial tumor resection. Communication to the 11th World Congress of the IASP, Pain Program, 2005.

C. Peirs, S. P. Williams, X. Zhao, C. E. Walsh, J. Y. Gedeon et al., Dorsal Horn Circuits for Persistent Mechanical Pain, Neuron, vol.87, issue.4, pp.797-812, 2015.

E. R. Perl, Pain and nociception, Handbook of physiology. The nervous system, vol.3, pp.915-975, 1984.

P. Petrovic, K. M. Petersson, P. H. Ghatan, S. Stone-elander, and M. Ingvar, Pain-related cerebral activation is altered by a distracting cognitive task, Pain, vol.85, issue.1, pp.19-30, 2000.

R. Peyron, B. Laurent, and L. Garcia-larrea, Functional imaging of brain responses to pain:a review and meta-analysis, Neurophysiol Clin, vol.30, pp.263-88, 2000.

R. Peyron, L. Garcia-larrea, M. C. Gregoire, P. Convers, F. Lavenne et al., Parietal and cingulate processing in central pain:a positron emission tomography study, PAIN, vol.84, pp.77-87, 2000.

R. Peyron, F. Schneider, I. Faillenot, P. Convers, F. G. Barral et al., An fMRI study of cortical representation of mechanical allodynia in patients with neuropathic pain, Neurology, vol.63, pp.1838-1846, 2004.

N. Pham-dang, A. Descheemaeker, R. Dallel, and A. Artola, Activation of medullary dorsal horn ? isoform of protein kinase C interneurons is essential to the development of both static and dynamic facial mechanical allodynia, Eur J Neurosci, vol.43, issue.6, pp.802-810, 2016.

A. Ploghaus, I. Tracey, J. S. Gati, C. S. Menon, R. S. Matthews et al., Dissociating pain from its anticipation in the human brain, Science, vol.284, issue.5422, pp.1979-1981, 1999.

M. Ploner, F. Schmitz, H. J. Freund, and A. Schnitzler, Differential organization of touch and pain in human primary somatosensory cortex, J Neurophysiol, vol.83, issue.3, pp.1770-1776, 2000.

F. B. Pomares, I. Faillenot, F. G. Barral, and R. Peyron, The where and the when of the BOLD response to pain in the insular cortex:discussion on amplitudes and latencies, Neuroimage, vol.64, pp.466-75, 2013.
URL : https://hal.archives-ouvertes.fr/hal-00793562

C. A. Porro, P. Baraldi, G. Pagnoni, M. Serafini, P. Facchin et al., Does anticipation of pain affect cortical nociceptive systems?, J Neurosci, vol.22, issue.8, pp.3206-3214, 2002.

D. D. Price, Psychological and neural mechanisms of the affective dimension of pain, Science, vol.288, pp.1769-1772, 2000.

S. Qiu, T. Chen, K. Koga, Y. Y. Guo, H. Xu et al., An increase in synaptic NMDA receptors in the insular cortex contributes to neuropathic pain, Sci. Signal, vol.6, p.34, 2013.

S. Qiu, M. Zhang, Y. Liu, Y. Guo, H. Zhao et al., GluA1 phosphorylation contributes to postsynaptic amplification of neuropathic pain in the insular cortex, J. Neurosci, vol.34, pp.13505-13515, 2014.

P. Raboisson, R. Dallel, and A. Woda, Responses of neurones in the ventrobasal complex of the thalamus to orofacial noxious stimulation after large trigeminal tractotomy, Ex Brain Res, vol.77, issue.3, pp.569-576, 1989.

P. Rainville, G. H. Duncan, D. D. Price, B. Carrier, and M. C. Bushnell, Pain affect encoded in human anterior cingulate but not somatosensory cortex, Science, vol.277, issue.5328, pp.968-971, 1997.

E. M. Reiman, R. D. Lane, G. L. Ahern, G. E. Schwartz, R. J. Davidson et al., Neuroanatomical correlates of externally and internally generated human emotion, Am J Psychiatry, vol.154, issue.7, pp.918-925, 1997.

B. Rexed, The cytoarchitectonic organization of the spinal cord in the cat, J Comp Neurol, vol.96, issue.3, pp.414-495, 1952.

A. Ribeiro-da-silva, J. M. Castro-lopes, and A. Coimbra, Distribution of glomeruli with fluoride-resistant acid phosphatase (FRAP)-containing terminals in the substantia gelatinosa of the rat, Brain Res, vol.377, issue.2, pp.323-329, 1986.

R. Romo, A. Hernández, A. Zainos, L. Lemus, and C. D. Brody, Neuronal correlates of decisionmaking in secondary somatosensory cortex, Nat Neurosci, vol.5, issue.11, pp.1217-1225, 2002.

A. J. Rózsa and R. W. Beuerman, Density and organization of free nerve endings in the corneal epithelium of the rabbit, Pain, vol.14, issue.2, pp.105-120, 1982.

R. Ruscheweyh, O. Wilder-smith, R. Drdla, X. G. Liu, and J. Sandkuhler, Long-term potentiation in spinal nociceptive pathways as a novel target for pain therapy, Mol. Pain, vol.7, p.20, 2011.

C. Saab and W. Willis, Nociceptive visceral stimulation modulates the activity of cerebellar Purkinje cells, Exp Brain Res, vol.140, issue.1, pp.122-126, 2001.

J. Sandkuhler, Understanding LTP in pain pathways, Mol. Pain, vol.3, p.9, 2007.

J. Sandkuhler and X. Liu, Induction of long-term potentiation at spinal synapses by noxious stimulation or nerve injury, Eur. J. Neurosci, vol.10, pp.2476-2480, 1998.

K. Schepelmann, A. Ebersberger, M. Pawlak, M. Oppmann, and K. Messlinger, Response properties of trigeminal brain stem neurons with input from dura mater encephali in the rat, Neurosci, vol.90, issue.2, pp.543-554, 1999.

M. Schmelz, A neural pathway for itch, Nat Neurosci, vol.4, issue.1, pp.9-10, 2001.

M. Schmelz, R. Schmidt, A. Bickel, H. O. Handwerker, and H. E. Torebjörk, Specific C-receptors for itch in human skin, J Neurosci, vol.17, issue.20, pp.8003-8008, 1997.

R. Schmidt, M. Schmelz, C. Forster, M. Ringkamp, E. Torebjörk et al., Novel classes of responsive and unresponsive C nociceptors in human skin, J Neurosci, issue.1, pp.333-341, 1995.

R. P. Seal, X. Wang, Y. Guan, S. N. Raja, C. J. Woodbury et al., Injuryinduced mechanical hypersensitivity requires C-low threshold mechanoreceptors, Nature, vol.462, issue.7273, pp.651-655, 2009.

F. Seifert and C. Maihöfner, Central mechanisms of experimental and chronic neuropathic pain:findings from functional imaging studies, Cell Mol Life Sci, vol.66, pp.375-390, 2009.

J. Sellmeijer, V. Mathis, S. Hugel, X. H. Li, Q. Song et al., Hyperactivity of Anterior Cingulate Cortex Areas 24a/24b Drives Chronic Pain-Induced Anxiodepressive-like Consequences, J Neurosci, vol.38, issue.12, pp.3102-3115, 2018.
URL : https://hal.archives-ouvertes.fr/hal-02437472

D. A. Seminowicz, A. L. Laferriere, M. Millecamps, J. S. Yu, T. J. Coderre et al., MRI structural brain changes associated with sensory and emotional function in a rat model of long-term neuropathic pain, Neuroimage, vol.47, pp.1007-1014, 2009.

B. J. Sessle and L. F. Greenwood, Inputs to trigeminal brain stem neurones from facial, oral, tooth pulp and pharyngolaryngeal tissues:I. Responses to innocuous and noxious stimuli, Brain Res, vol.117, issue.2, pp.211-226, 1976.

B. J. Sessle, J. W. Hu, and X. M. Yu, Brainstem. Mechanisms of referred pain and hyperalgesia in the orofacial and temporomandibular region, New trends in referred pain and hyperalgesia, pp.59-71, 1993.

B. J. Sessle, D. Yao, H. Nishiura, K. Yoshino, J. C. Lee et al., Properties and plasticity of the primate somatosensory and motor cortex related to orofacial sensorimotor function, Clin Exp Pharmacol Physiol, vol.32, issue.1-2, pp.109-114, 2005.

F. Y. Shen, Z. Y. Chen, W. Zhong, L. Q. Ma, C. Chen et al., Alleviation of neuropathic pain by regulating T-type calcium channels in rat anterior cingulate cortex, Mol Pain, vol.11, p.7, 2015.

C. S. Sherrington, The integrative action of the nervous system, 1906.

Y. Shigenaga, M. Sera, T. Nishimori, S. Suemune, M. Nishimura et al., The central projection of masticatory afferent fibers to the trigeminal sensory nuclear complex and upper cervical spinal cord, J Comp Neurol, vol.268, issue.4, pp.489-507, 1988.

B. C. Shyu and B. A. Vogt, Short-term synaptic plasticity in the nociceptive thalamic-anterior cingulate pathway, Mol. Pain, vol.5, p.51, 2009.

P. Siegel and J. G. Wepsic, Alteration of nociception by stimulation of cerebellar structures in the monkey, Physiol Behav, vol.13, issue.2, pp.189-194, 1974.

R. W. Sikes and B. A. Vogt, Nociceptive neurons in area 24 of rabbit cingulate cortex, J Neurophysiol, vol.68, pp.1720-1720, 1992.

J. D. Silverman and L. Kruger, Lectin and neuropeptide labeling of separate populations of dorsal root ganglion neurons and associated « nociceptor » thin axons in rat testis and cornea whole-mount preparations, Somatos Res, vol.5, issue.3, pp.259-267, 1988.

T. Singer, B. Seymour, J. O'doherty, H. Kaube, R. J. Dolan et al., Empathy for pain involves the affective but not sensory components of pain, Science, vol.303, issue.5661, pp.1157-1162, 2004.

W. D. Snider and S. B. Mcmahon, Tackling pain at the source:new ideas about nociceptors, Neuron, vol.20, issue.4, pp.629-632, 1998.

T. J. Steiner, A. I. Scher, W. F. Stewart, K. Kolodner, J. Liberman et al., The prevalence and disability burden of adult migraine in England and their relationships to age, gender and ethnicity, Cephalalgia, vol.23, issue.7, pp.519-527, 2003.

W. F. Stewart, R. B. Lipton, D. D. Celentano, and M. L. Reed, Prevalence of migraine headache in the United States. Relation to age, income, race, and other sociodemographic factors, JAMA, vol.267, issue.1, pp.64-69, 1992.

A. Strassman, S. A. Raymond, and R. Burstein, Sensitization of meningeal sensory neurons and the origin of headaches, Nature, vol.384, issue.6609, pp.560-564, 1996.

A. M. Strassman, W. Weissner, M. Williams, S. Ali, and D. Levy, Axon diameters and intradural trajectories of the dural innervation in the rat, J Comp Neurol, vol.473, issue.3, pp.364-376, 2004.

P. Svensson, S. Minoshima, A. Beydoun, T. J. Morrow, and K. L. Casey, Cerebral processing of acute skin and muscle pain in humans, J Neurophysiol, vol.78, issue.1, pp.450-460, 1997.

J. D. Talbot, S. Marrett, A. C. Evans, E. Meyer, M. C. Bushnell et al., Multiple representations of pain in human cerebral cortex, Science, vol.251, pp.1355-1363, 1991.

T. Tammiala-salonen, T. Hiidenkari, and T. Parvinen, Burning mouth in a Finnish adult population, Community Dent Oral Epidemiol, vol.21, issue.2, pp.67-71, 1993.

L. L. Tan, P. Pelzer, C. Heinl, W. Tang, V. Gangadharan et al., A pathway from midcingulate cortex to posterior insula gates nociceptive hypersensitivity, Nat Neurosci, vol.20, issue.11, pp.1591-1601, 2017.

I. Tracey and P. W. Mantyh, The cerebral signature for pain perception and its modulation, Neuron, vol.55, pp.377-91, 2007.

H. O. Trowbridge, M. Franks, E. Korostoff, and R. Emling, Sensory response to thermal stimulation in human teeth, J Endodontics, vol.6, issue.1, pp.405-412, 1980.

D. Vardeh, D. Wang, M. Costigan, M. Lazarus, C. B. Saper et al., COX2 in CNS Neural Cells mediates Mechanical Inflammatory Pain Hypersensitivity in Mice, J Clin Invest, vol.119, issue.2, pp.287-294, 2009.

V. Korff, M. Dunn, and K. M. , Chronic pain reconsidered, Pain, vol.138, issue.2, pp.267-276, 2008.

G. Q. Wang, C. Cen, C. Li, S. Cao, N. Wang et al., Deactivation of excitatory neurons in the prelimbic cortex via Cdk5 promotes pain sensation and anxiety, Nat Commun, vol.6, p.7660, 2015.

F. Wei, P. Li, and M. Zhuo, Loss of synaptic depression in mammalian anterior cingulate cortex after amputation, J Neurosci, vol.19, pp.9346-9354, 1999.

F. Wei, G. D. Wang, G. A. Kerchner, S. J. Kim, H. M. Xu et al., Genetic enhancement of inflammatory pain by forebrain NR2B overexpression, Nat Neurosci, vol.4, issue.2, pp.164-169, 2001.

F. Wei, C. S. Qiu, S. J. Kim, L. Muglia, J. W. Maas et al., Genetic elimination of behavioral sensitization in mice lacking calmodulin-stimulated adenylyl cyclases, Neuron, vol.36, issue.4, pp.713-739, 2002.

J. Wessberg, H. Olausson, K. W. Fernström, and A. B. Vallbo, Receptive field properties of unmyelinated tactile afferents in the human skin, J Neurophy, vol.89, issue.3, pp.1567-1575, 2003.

B. Wicker, C. Keysers, J. Plailly, J. P. Royet, V. Gallese et al., Both of us disgusted in My insula:the common neural basis of seeing and feeling disgust, Neuron, vol.40, pp.655-64, 2003.

G. Wik, H. Fischer, B. Bragée, B. Finer, and M. Fredrikson, Functional anatomy of hypnotic analgesia:a PET study of patients with fibromyalgia, Eur J Pain, vol.3, issue.1, pp.7-12, 1999.

A. Woda, O. Blanc, D. L. Voisin, J. Coste, J. L. Molat et al., Bidirectional modulation of windup by NMDA receptors in the rat spinal trigeminal nucleus, Eur J Neurosci, vol.19, issue.8, pp.2009-2016, 2004.
URL : https://hal.archives-ouvertes.fr/hal-01543022

C. J. Woolf and Q. Ma, Nociceptors--Noxious Stimulus Detectors, Neuron, vol.55, issue.3, pp.353-364, 2007.

L. J. Wu, H. Toyoda, M. G. Zhao, Y. S. Lee, J. Tang et al., Upregulation of forebrain NMDA NR2B receptors contributes to behavioral sensitization after inflammation, J Neurosci, vol.25, issue.48, pp.11107-11116, 2005.

H. Xu, L. J. Wu, H. Wang, X. Zhang, K. I. Vadakkan et al., Presynaptic and postsynaptic amplifications of neuropathic pain in the anterior cingulate cortex, J Neurosci, vol.28, issue.29, pp.7445-7453, 2008.

J. M. Yang, S. N. Wu, and I. J. Chen, Spinal adenosine modulates capsaicin-induced depressor reflex:Involvement of adenosine A2 receptor, Gen Pharmacol, vol.24, issue.4, pp.961-970, 1993.

A. Yoshino, Y. Okamoto, K. Onoda, S. Yoshimura, Y. Kunisato et al., Sadness enhances the experience of pain via neural activation in the anterior cingulate cortex and amygdala:an fMRI study, Neuroimage, vol.50, pp.1194-1201, 2010.

M. G. Zhao, S. W. Ko, L. J. Wu, H. Toyoda, H. Xu et al., Enhanced presynaptic neurotransmitter release in the anterior cingulate cortex of mice with chronic pain, J Neurosci, vol.26, issue.35, pp.8923-8930, 2006.

M. Zhuo, Cortical excitation and chronic pain, Trends Neurosci, vol.31, pp.199-207, 2008.

M. Zhuo, Long-term potentiation in the anterior cingulate cortex and chronic pain, Philos Trans R Soc Lond B Biol Sci, vol.369, p.20130146, 1633.

M. Zhuo, Contribution of synaptic plasticity in the insular cortex to chronic pain, Neuroscience, vol.338, pp.220-229, 2016.

, Abstract Chronic neuropathic or inflammatory pain is believed to result from long-lasting synaptic and neuronal changes in pain pathways, including the primary somatosensory cortex (S1) which codes for pain intensity and location. Using ex vivo electrophysiological recordings from S1

, We first establish the relation in basal conditions between synaptic activity and (i) bidirectional synaptic plasticity (long-term depression/potentiation

, LTD/LTP), (ii) changes in the ability to express synaptic plasticity (metaplasticity), (iii) bidirectional changes in intrinsic neuronal excitability (LTP/LTD-IE)

, the rules for synaptic and intrinsic plasticity in S1 layer 2/3 pyramidal neurons

, At 1-hour, mechanical allodynia is associated with (i) LTP of excitatory synaptic transmission, together with (ii) an inhibition to generate further LTP but a facilitation to generate LTD (metaplasticity), consistent with LTP of synaptic transmission, (iii) LTP-IE and (iv) reduced dendritic arbor complexity of S1 layer 2/3 pyramidal neurons. At 3 days, LTP and LTP-IE were still present but metaplasticity and dendritic arbor complexity

, Utilisant des enregistrements électrophysiologiques ex vivo de neurones pyramidaux des couches 2/3 de S1, nous avons étudié la plasticité induite dans un modèle de douleur inflammatoire chronique de la face chez le rat

, entre activité synaptique et (i) plasticité synaptique bidirectionnelle (long-term depression/potentiation ; LTD/LTP), (ii) changements dans la capacité d'exprimer une plasticité synaptique (métaplasticité), (iii) changements bidirectionnels de l, Nous établissons d'abord la relation, dans les conditions normales

, Nous étudions alors ces plasticités chez des rats exprimant une allodynie mécanique faciale, p.1

, heure et 3 jours après l'injection de CFA. A 1 heure, l'allodynie mécanique est associée à (i)

, une LTP de la transmission synaptique excitatrice, combinée à (ii) une inhibition de l'induction de la LTP/facilitation de l'induction de la LTD (métaplasticité), consistants avec la LTP

L. Et, A 3 jours, LTP and LTP-IE sont toujours présentes mais métaplasticité et complexité de l'arbre dendritique sont retournées à l