Enhancing neuronal chloride extrusion rescues α2/α3 GABA


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
13 02 2020
Historique:
received: 09 05 2018
accepted: 16 12 2019
entrez: 15 2 2020
pubmed: 15 2 2020
medline: 28 4 2020
Statut: epublish

Résumé

Spinal disinhibition has been hypothesized to underlie pain hypersensitivity in neuropathic pain. Apparently contradictory mechanisms have been reported, raising questions on the best target to produce analgesia. Here, we show that nerve injury is associated with a reduction in the number of inhibitory synapses in the spinal dorsal horn. Paradoxically, this is accompanied by a BDNF-TrkB-mediated upregulation of synaptic GABA

Identifiants

pubmed: 32054836
doi: 10.1038/s41467-019-14154-6
pii: 10.1038/s41467-019-14154-6
pmc: PMC7018745
doi:

Substances chimiques

Analgesics 0
Bdnf protein, rat 0
Brain-Derived Neurotrophic Factor 0
Chlorides 0
Fluorobenzenes 0
GABA-A Receptor Agonists 0
Ligands 0
Receptors, GABA-A 0
Symporters 0
Triazoles 0
L 838,417 8CZO0970G3
Ntrk2 protein, rat EC 2.7.10.1
Receptor, trkB EC 2.7.10.1

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

869

Références

Labrakakis,C., Ferrini,F., & De Koninck,Y. Mechanisms of plasticity of inhibition in chronic pain conditions in Inhibitory Synaptic Plasticity 91-105 (Springer, 2011).
Yaksh, T. L. Behavioral and autonomic correlates of the tactile evoked allodynia produced by spinal glycine inhibition: effects of modulatory receptor systems and excitatory amino acid antagonists. Pain 37, 111–123 (1989).
pubmed: 2542867 doi: 10.1016/0304-3959(89)90160-7 pmcid: 2542867
Coull, J. A. et al. Trans-synaptic shift in anion gradient in spinal lamina I neurons as a mechanism of neuropathic pain. Nature 424, 938–942 (2003).
pubmed: 12931188 doi: 10.1038/nature01868 pmcid: 12931188
Eto, K. 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. 32, 16552–16559 (2012).
pubmed: 23175811 pmcid: 6621771 doi: 10.1523/JNEUROSCI.2104-12.2012
Janssen, S. P. et al. Decreased intracellular GABA levels contribute to spinal cord stimulation-induced analgesia in rats suffering from painful peripheral neuropathy: the role of KCC2 and GABA(A) receptor-mediated inhibition. Neurochem. Int. 60, 21–30 (2012).
pubmed: 22107704 doi: 10.1016/j.neuint.2011.11.006 pmcid: 22107704
Miletic, G. & Miletic, V. Loose ligation of the sciatic nerve is associated with TrkB receptor-dependent decreases in KCC2 protein levels in the ipsilateral spinal dorsal horn. Pain 137, 532–539 (2008).
pubmed: 18063479 doi: 10.1016/j.pain.2007.10.016 pmcid: 18063479
Okada-Ogawa, A. et al. Involvement of medullary GABAergic system in extraterritorial neuropathic pain mechanisms associated with inferior alveolar nerve transection. Exp. Neurol. 267, 42–52 (2015).
pubmed: 25736265 doi: 10.1016/j.expneurol.2015.02.030 pmcid: 25736265
Scholz, J. et al. Blocking caspase activity prevents transsynaptic neuronal apoptosis and the loss of inhibition in lamina II of the dorsal horn after peripheral nerve injury. J. Neurosci. 25, 7317–7323 (2005).
pubmed: 16093381 pmcid: 6725303 doi: 10.1523/JNEUROSCI.1526-05.2005
Polgar, E., Hughes, D. I., Arham, A. Z. & Todd, A. J. Loss of neurons from laminas I-III of the spinal dorsal horn is not required for development of tactile allodynia in the spared nerve injury model of neuropathic pain. J. Neurosci. 25, 6658–6666 (2005).
pubmed: 16014727 pmcid: 6725431 doi: 10.1523/JNEUROSCI.1490-05.2005
Braz, J. M. et al. Forebrain GABAergic neuron precursors integrate into adult spinal cord and reduce injury-induced neuropathic pain. Neuron 74, 663–675 (2012).
pubmed: 22632725 pmcid: 3361692 doi: 10.1016/j.neuron.2012.02.033
Castro-Lopes, J. M., Tavares, I. & Coimbra, A. GABA decreases in the spinal cord dorsal horn after peripheral neurectomy. Brain Res. 620, 287–291 (1993).
pubmed: 8369960 doi: 10.1016/0006-8993(93)90167-L pmcid: 8369960
Ibuki, T., Hama, A. T., Wang, X. T., Pappas, G. D. & Sagen, J. Loss of GABA-immunoreactivity in the spinal dorsal horn of rats with peripheral nerve injury and promotion of recovery by adrenal medullary grafts. Neuroscience 76, 845–858 (1997).
pubmed: 9135056 doi: 10.1016/S0306-4522(96)00341-7 pmcid: 9135056
Moore, K. A. et al. Partial peripheral nerve injury promotes a selective loss of GABAergic inhibition in the superficial dorsal horn of the spinal cord. J. Neurosci. 22, 6724–6731 (2002).
pubmed: 12151551 pmcid: 6758148 doi: 10.1523/JNEUROSCI.22-15-06724.2002
Eaton, M. J., Plunkett, J. A., Karmally, S., Martinez, M. A. & Montanez, K. Changes in GAD- and GABA- immunoreactivity in the spinal dorsal horn after peripheral nerve injury and promotion of recovery by lumbar transplant of immortalized serotonergic precursors. J. Chem. Neuroanat. 16, 57–72 (1998).
pubmed: 9924973 doi: 10.1016/S0891-0618(98)00062-3 pmcid: 9924973
Lorenzo, L. E. et al. Spatial and temporal pattern of changes in the number of GAD65-immunoreactive inhibitory terminals in the rat superficial dorsal horn following peripheral nerve injury. Mol. Pain. 10, 57 (2014).
pubmed: 25189404 pmcid: 4164746 doi: 10.1186/1744-8069-10-57
Polgar, E. & Todd, A. J. Tactile allodynia can occur in the spared nerve injury model in the rat without selective loss of GABA or GABA(A) receptors from synapses in laminae I-II of the ipsilateral spinal dorsal horn. Neuroscience 156, 193–202 (2008).
pubmed: 18675320 pmcid: 2553186 doi: 10.1016/j.neuroscience.2008.07.009
Satoh, O. & Omote, K. Roles of monoaminergic, glycinergic and GABAergic inhibitory systems in the spinal cord in rats with peripheral mononeuropathy. Brain Res. 728, 27–36 (1996).
pubmed: 8864294 doi: 10.1016/0006-8993(96)00371-X pmcid: 8864294
Castro-Lopes, J. M., Malcangio, M., Pan, B. H. & Bowery, N. G. Complex changes of GABAA and GABAB receptor binding in the spinal cord dorsal horn following peripheral inflammation or neurectomy. Brain Res. 679, 289–297 (1995).
pubmed: 7633890 doi: 10.1016/0006-8993(95)00262-O pmcid: 7633890
Kaila, K., Price, T. J., Payne, J. A., Puskarjov, M. & Voipio, J. Cation-chloride cotransporters in neuronal development, plasticity and disease. Nat. Rev. Neurosci. 15, 637–654 (2014).
pubmed: 25234263 pmcid: 4294553 doi: 10.1038/nrn3819
Lorenzo, L. E. et al. Gephyrin clusters are absent from small diameter primary afferent terminals despite the presence of GABAA receptors. J. Neurosci. 34, 8300–8317 (2014).
pubmed: 24920633 pmcid: 6608243 doi: 10.1523/JNEUROSCI.0159-14.2014
Abraira, V. E. et al. The cellular and synaptic architecture of the mechanosensory dorsal horn. Cell 168, 295–310 (2017).
pubmed: 28041852 pmcid: 5236062 doi: 10.1016/j.cell.2016.12.010
McClellan, A. M. & Twyman, R. E. Receptor system response kinetics reveal functional subtypes of native murine and recombinant human GABAA receptors. J. Physiol. 515(Pt 3), 711–727 (1999).
pubmed: 10066899 pmcid: 2269184 doi: 10.1111/j.1469-7793.1999.711ab.x
Gingrich, K. J., Roberts, W. A. & Kass, R. S. Dependence of the GABAA receptor gating kinetics on the alpha-subunit isoform: implications for structure-function relations and synaptic transmission. J. Physiol. 489(Pt 2), 529–543 (1995).
pubmed: 8847645 pmcid: 1156777 doi: 10.1113/jphysiol.1995.sp021070
McKernan,R. M. et al. Sedative but not anxiolytic properties of benzodiazepines are mediated by the GABA(A) receptor alpha1 subtype. Nat. Neurosci. 3, 587-592 (2000).
Knabl, J. et al. Reversal of pathological pain through specific spinal GABAA receptor subtypes. Nature 451, 330–334 (2008).
pubmed: 18202657 doi: 10.1038/nature06493 pmcid: 18202657
Doyon, N. et al. Efficacy of synaptic inhibition depends on multiple, dynamically interacting mechanisms implicated in chloride homeostasis. PLoS Comput. Biol. 7, e1002149 (2011).
pubmed: 21931544 pmcid: 3169517 doi: 10.1371/journal.pcbi.1002149
Doyon, N., Vinay, L., Prescott, S. A. & De Koninck, Y. Chloride regulation: a dynamic equilibrium crucial for synaptic inhibition. Neuron 89, 1157–1172 (2016).
pubmed: 26985723 doi: 10.1016/j.neuron.2016.02.030 pmcid: 26985723
M.Gagnon, et al. Chloride extrusion enhancers as novel therapeutics for neurological diseases. Nat. Med. 19, 1524–1528 (2013).
pubmed: 24097188 pmcid: 4005788 doi: 10.1038/nm.3356
Beggs, S. & Salter, M. W. Stereological and somatotopic analysis of the spinal microglial response to peripheral nerve injury. Brain Behav. Immun. 21, 624–633 (2007).
pubmed: 17267172 doi: 10.1016/j.bbi.2006.10.017 pmcid: 17267172
Paul, J., Zeilhofer, H. U. & Fritschy, J. M. Selective distribution of GABA(A) receptor subtypes in mouse spinal dorsal horn neurons and primary afferents. J. Comp. Neurol. 520, 3895–3911 (2012).
pubmed: 22522945 doi: 10.1002/cne.23129 pmcid: 22522945
Witschi, R. et al. Presynaptic {alpha}2-GABAA receptors in primary afferent depolarization and spinal pain control. J. Neurosci. 31, 8134–8142 (2011).
pubmed: 21632935 pmcid: 3567284 doi: 10.1523/JNEUROSCI.6328-10.2011
Schneider Gasser, E. M. et al. Immunofluorescence in brain sections: simultaneous detection of presynaptic and postsynaptic proteins in identified neurons. Nat. Protoc. 1, 1887–1897 (2006).
pubmed: 17487173 doi: 10.1038/nprot.2006.265 pmcid: 17487173
Otis, T. S., De Koninck, Y. & Mody, I. Lasting potentiation of inhibition is associated with an increased number of GABA
pubmed: 8052645 doi: 10.1073/pnas.91.16.7698 pmcid: 8052645
Nusser, Z., Hajos, N., Somogyi, P. & Mody, I. Increased number of synaptic GABA(A) receptors underlies potentiation at hippocampal inhibitory synapses. Nature 395, 172–177 (1998).
pubmed: 9744275 doi: 10.1038/25999
Piller, N., Decosterd, I. & Suter, M. R. Reverse transcription quantitative real-time polymerase chain reaction reference genes in the spared nerve injury model of neuropathic pain: validation and literature search. BMC Res. Notes 6, 266 (2013).
pubmed: 23841944 pmcid: 3717014 doi: 10.1186/1756-0500-6-266
Godin, A. G. et al. Revealing protein oligomerization and densities in situ using spatial intensity distribution analysis. Proc. Natl Acad. Sci. USA 108, 7010–7015 (2011).
pubmed: 21482753 doi: 10.1073/pnas.1018658108
Godin, A. G. et al. Spatial intensity distribution analysis reveals abnormal oligomerization of proteins in single cells. Biophys. J. 109, 710–721 (2015).
pubmed: 26287623 pmcid: 4547338 doi: 10.1016/j.bpj.2015.06.068
Okada, M., Onodera, K., Van, R. C., Sieghart, W. & Takahashi, T. Functional correlation of GABA(A) receptor alpha subunits expression with the properties of IPSCs in the developing thalamus. J. Neurosci. 20, 2202–2208 (2000).
pubmed: 10704495 pmcid: 6772493 doi: 10.1523/JNEUROSCI.20-06-02202.2000
Mortensen, M., Patel, B. & Smart, T. G. GABA potency at GABA(A) receptors found in synaptic and extrasynaptic zones. Front. Cell Neurosci. 6, 1 (2011).
pubmed: 22319471 pmcid: 22319471
Imlach, W. L., Bhola, R. F., Mohammadi, S. A. & Christie, M. J. Glycinergic dysfunction in a subpopulation of dorsal horn interneurons in a rat model of neuropathic pain. Sci. Rep. 6, 37104 (2016).
pubmed: 27841371 pmcid: 5107903 doi: 10.1038/srep37104
Kletke, O., Gisselmann, G., May, A., Hatt, H. & Sergeeva, A. Partial agonism of taurine at gamma-containing native and recombinant GABAA receptors. PLoS ONE 8, e61733 (2013).
pubmed: 23637894 pmcid: 3640040 doi: 10.1371/journal.pone.0061733
Succol, F., Fiumelli, H., Benfenati, F., Cancedda, L. & Barberis, A. Intracellular chloride concentration influences the GABA(A) receptor subunit composition. Nat. Commun. 3, 738 (2012).
pubmed: 22415829 pmcid: 3316884 doi: 10.1038/ncomms1744
Heubl, M. et al. GABAA receptor dependent synaptic inhibition rapidly tunes KCC2 activity via the Cl(-)-sensitive WNK1 kinase. Nat. Commun. 8, 1776 (2017).
pubmed: 29176664 pmcid: 5701213 doi: 10.1038/s41467-017-01749-0
Delpire, E. et al. Small-molecule screen identifies inhibitors of the neuronal K-Cl cotransporter KCC2. Proc. Natl Acad. Sci. USA 106, 5383–5388 (2009).
pubmed: 19279215 doi: 10.1073/pnas.0812756106
Lavertu, G., Cote, S. L. & De Koninck, Y. Enhancing K-Cl co-transport restores normal spinothalamic sensory coding in a neuropathic pain model. Brain 137, 724–738 (2014).
pubmed: 24369380 doi: 10.1093/brain/awt334
Bos, R. et al. Activation of 5-HT2A receptors upregulates the function of the neuronal K-Cl cotransporter KCC2. Proc. Natl Acad. Sci. USA 110, 348–353 (2013).
pubmed: 23248270 doi: 10.1073/pnas.1213680110
Ferrini, F. et al. Morphine hyperalgesia gated through microglia-mediated disruption of neuronal Cl(-) homeostasis. Nat. Neurosci. 16, 183–192 (2013).
pubmed: 23292683 pmcid: 4974077 doi: 10.1038/nn.3295
Thompson, S. W. N., Bennett, D. L. H., Kerr, B. J., Bradbury, E. J. & McMahon, S. B. Brain-derived neurotrophic factor is an endogenous modulator of nociceptive responses in the spinal cord. Proc. Natl Acad. Sci. USA 96, 7714–7718 (1999).
pubmed: 10393886 doi: 10.1073/pnas.96.14.7714
Coull, J. A. et al. BDNF from microglia causes the shift in neuronal anion gradient underlying neuropathic pain. Nature 438, 1017–1021 (2005).
doi: 10.1038/nature04223
De Koninck, Y. Altered chloride homeostasis in neurological disorders: a new target. Curr. Opin. Pharmacol. 7, 93–99 (2007).
pubmed: 17182282 doi: 10.1016/j.coph.2006.11.005
Dedek, A. et al. Loss of STEP61 couples disinhibition to N-methyl-d-aspartate receptor potentiation in rodent and human spinal pain processing. Brain 142, 1535–1546 (2019).
pubmed: 31135041 pmcid: 6536915 doi: 10.1093/brain/awz105
Mapplebeck, J. C. S. et al. Chloride dysregulation through downregulation of KCC2 mediates neuropathic pain in both sexes. Cell Rep. 28, 590–596 (2019).
pubmed: 31315039 doi: 10.1016/j.celrep.2019.06.059
Richner, M. et al. Sortilin gates neurotensin and BDNF signaling to control peripheral neuropathic pain. Sci. Adv. 5, eaav9946 (2019).
pubmed: 31223654 pmcid: 6584543 doi: 10.1126/sciadv.aav9946
Rivera, C. et al. BDNF-induced TrkB activation down-regulates the K+-Cl- cotransporter KCC2 and impairs neuronal Cl- extrusion. J. Cell Biol. 159, 747–752 (2002).
pubmed: 12473684 pmcid: 2173387 doi: 10.1083/jcb.200209011
Labrakakis, C., Rudolph, U. & De Koninck, Y. The heterogeneity in GABA receptor-mediated IPSC kinetics reflects heterogeneity of subunit composition among inhibitory and excitatory interneurons in spinal lamina II. Front. Cell Neurosci. 8, 424 (2014).
pubmed: 25565959 pmcid: 4263102 doi: 10.3389/fncel.2014.00424
Browne, S. H. et al. Kinetic and pharmacological properties of GABA(A) receptors in single thalamic neurons and GABA(A) subunit expression. J. Neurophysiol. 86, 2312–2322 (2001).
pubmed: 11698521 doi: 10.1152/jn.2001.86.5.2312
Balkowiec, A. & Katz, D. M. Activity-dependent release of endogenous brain-derived neurotrophic factor from primary sensory neurons detected by ELISA in situ. J. Neurosci. 20, 7417–7423 (2000).
pubmed: 11007900 pmcid: 6772775 doi: 10.1523/JNEUROSCI.20-19-07417.2000
De Koninck, Y. & Mody, I. The effects of raising intracellular calcium on synaptic GABA
pubmed: 9014153 doi: 10.1016/S0028-3908(96)00063-9
Kuczewski, N. et al. Mechanism of GABAB receptor-induced BDNF secretion and promotion of GABAA receptor membrane expression. J. Neurochem. 118, 533–545 (2011).
pubmed: 21255015 doi: 10.1111/j.1471-4159.2011.07192.x
Leinekugel, X. et al. GABA is the principal fast-acting excitatory transmitter in the neonatal brain. Adv. Neurol. 79, 189–201 (1999).
pubmed: 10514814
Kano, M. Calcium-induced long-lasting potentiation of GABAergic currents in cerebellar Purkinje cells. Jpn. J. Physiol. 44(Suppl 2), S131–S136 (1994).
pubmed: 7752516
Ellis-Davies, G. C. & Kaplan, J. H. Nitrophenyl-EGTA, a photolabile chelator that selectively binds Ca2+ with high affinity and releases it rapidly upon photolysis. Proc. Natl Acad. Sci. USA 91, 187–191 (1994).
pubmed: 8278362 doi: 10.1073/pnas.91.1.187
Tsien, R. Y. New calcium indicators and buffers with high selectivity against magnesium and protons: design, synthesis, and properties of prototype structures. Biochemistry 19, 2396–2404 (1980).
pubmed: 6770893 doi: 10.1021/bi00552a018
Wang, Y. T., Pak, Y. S. & Salter, M. W. Rundown of NMDA-receptor mediated currents is resistant to lowering intracellular [Ca
pubmed: 8233050 doi: 10.1016/0304-3940(93)90732-Z pmcid: 8233050
Paul, J. et al. Antihyperalgesia by alpha2-GABA receptors occurs via a genuine spinal action and does not involve supraspinal sites. Neuropsychopharmacology 39, 477–487 (2013).
pubmed: 24045508 pmcid: 3870792 doi: 10.1038/npp.2013.221
Nickolls, S. et al. A comparison of the alpha2/3/5 selective positive allosteric modulators L-838,417 and TPA023 in preclinical models of inflammatory and neuropathic. Pain. Adv. Pharmacol. Sci. 2011, 608912 (2011).
pubmed: 22162674 pmcid: 22162674
Toyoda, H. et al. Induction of NMDA and GABAA receptor-mediated Ca2+ oscillations with KCC2 mRNA downregulation in injured facial motoneurons. J. Neurophysiol. 89, 1353–1362 (2003).
pubmed: 12612004 doi: 10.1152/jn.00721.2002 pmcid: 12612004
Cordero-Erausquin, M., Coull, J. A., Boudreau, D., Rolland, M. & De Koninck, Y. Differential maturation of GABA action and anion reversal potential in spinal lamina I neurons: impact of chloride extrusion capacity. J. Neurosci. 25, 9613–9623 (2005).
pubmed: 16237166 pmcid: 6725724 doi: 10.1523/JNEUROSCI.1488-05.2005
Asiedu, M., Ossipov, M. H., Kaila, K. & Price, T. J. Acetazolamide and midazolam act synergistically to inhibit neuropathic pain. Pain 148, 302–308 (2010).
pubmed: 20007010 doi: 10.1016/j.pain.2009.11.015 pmcid: 20007010
Chen, M. et al. APP modulates KCC2 expression and function in hippocampal GABAergic inhibition. Elife. 6, 1–26 (2017).
Ferrini, F., Lorenzo, L. E., Godin, A. G., Quang, M. L. & De Koninck, Y. Enhancing KCC2 function counteracts morphine-induced hyperalgesia. Sci. Rep. 7, 3870 (2017).
pubmed: 28634406 pmcid: 5478677 doi: 10.1038/s41598-017-04209-3
Tallarida, R. J. An overview of drug combination analysis with isobolograms. J. Pharmacol. Exp. Ther. 319, 1–7 (2006).
pubmed: 16670349 doi: 10.1124/jpet.106.104117 pmcid: 16670349
Tallarida, R. J. Revisiting the isobole and related quantitative methods for assessing drug synergism. J. Pharmacol. Exp. Ther. 342, 2–8 (2012).
pubmed: 22511201 pmcid: 3383036 doi: 10.1124/jpet.112.193474
Chou, T. C. Theoretical basis, experimental design, and computerized simulation of synergism and antagonism in drug combination studies. Pharmacol. Rev. 58, 621–681 (2006).
pubmed: 16968952 doi: 10.1124/pr.58.3.10 pmcid: 16968952
Colburn, R. W. et al. Attenuated cold sensitivity in TRPM8 null mice. Neuron 54, 379–386 (2007).
pubmed: 17481392 doi: 10.1016/j.neuron.2007.04.017 pmcid: 17481392
Ostroumov, A. et al. Stress increases ethanol self-administration via a shift toward excitatory GABA signaling in the ventral tegmental area. Neuron 92, 493–504 (2016).
pubmed: 27720487 pmcid: 5091663 doi: 10.1016/j.neuron.2016.09.029
Hewitt, S. A., Wamsteeker, J. I., Kurz, E. U. & Bains, J. S. Altered chloride homeostasis removes synaptic inhibitory constraint of the stress axis. Nat. Neurosci. 12, 438–443 (2009).
pubmed: 19252497 doi: 10.1038/nn.2274
Kaila, K. Ionic basis of GABAA receptor channel function in the nervous system. Prog. Neurobiol. 42, 489–537 (1994).
pubmed: 7522334 doi: 10.1016/0301-0082(94)90049-3
Staley, K. J., Soldo, B. L. & Proctor, W. R. Ionic mechanisms of neuronal excitation by inhibitory GABAA receptors. Science 269, 977–981 (1995).
pubmed: 7638623 doi: 10.1126/science.7638623
Ribeiro-da-Silva, A. Substantia gelatinosa of the spinal cord in The Rat Nervous System (ed. Paxinos,G.) 129-148 (Elsevier Academic Press, San Diego, 2004).
doi: 10.1016/B978-012547638-6/50007-9
Villa, K. L. et al. Inhibitory synapses are repeatedly assembled and removed at persistent sites in vivo. Neuron 89, 756–769 (2016).
pubmed: 26853302 pmcid: 4760889 doi: 10.1016/j.neuron.2016.01.010
Kontinen, V. K., Stanfa, L. C., Basu, A. & Dickenson, A. H. Electrophysiologic evidence for increased endogenous gabaergic but not glycinergic inhibitory tone in the rat spinal nerve ligation model of neuropathy. Anesthesiology 94, 333–339 (2001).
pubmed: 11176099 doi: 10.1097/00000542-200102000-00024 pmcid: 11176099
Duggan, M. J., Pollard, S. & Stephenson, F. A. Immunoaffinity purification of GABAA receptor alpha-subunit iso-oligomers. Demonstration of receptor populations containing alpha 1 alpha 2, alpha 1 alpha 3, and alpha 2 alpha 3 subunit pairs. J. Biol. Chem. 266, 24778–24784 (1991).
pubmed: 1662216 pmcid: 1662216
Schoffnegger, D., Heinke, B., Sommer, C. & Sandkuhler, J. Physiological properties of spinal lamina II GABAergic neurons in mice following peripheral nerve injury. J. Physiol. 577, 869–878 (2006).
pubmed: 17053034 pmcid: 1890379 doi: 10.1113/jphysiol.2006.118034
Fritschy, J. M., Paysan, J., Enna, A. & Mohler, H. Switch in the expression of rat GABAA-receptor subtypes during postnatal development: an immunohistochemical study. J. Neurosci. 14, 5302–5324 (1994).
pubmed: 8083738 pmcid: 6577100 doi: 10.1523/JNEUROSCI.14-09-05302.1994
Ma, W., Saunders, P. A., Somogyi, R., Poulter, M. O. & Barker, J. L. Ontogeny of GABAA receptor subunit mRNAs in rat spinal cord and dorsal root ganglia. J. Comp. Neurol. 338, 337–359 (1993).
pubmed: 7509352 doi: 10.1002/cne.903380303 pmcid: 7509352
Young, G. T. et al. Characterizing human stem cell-derived sensory neurons at the single-cell level reveals their ion channel expression and utility in pain research. Mol. Ther. 22, 1530–1543 (2014).
pubmed: 24832007 pmcid: 4435594 doi: 10.1038/mt.2014.86
Hammond, D. L., Ackerman, L., Holdsworth, R. & Elzey, B. Effects of spinal nerve ligation on immunohistochemically identified neurons in the L4 and L5 dorsal root ganglia of the rat. J. Comp. Neurol. 475, 575–589 (2004).
pubmed: 15236238 doi: 10.1002/cne.20209 pmcid: 15236238
Echeverry, S. et al. Spinal microglia are required for long-term maintenance of neuropathic pain. Pain 158, 1792–1801 (2017).
pubmed: 28746078 doi: 10.1097/j.pain.0000000000000982 pmcid: 28746078
Mosconi, T. & Kruger, L. Fixed-diameter polyethylene cuffs applied to the rat sciatic nerve induce a painful neuropathy: ultrastructural morphometric analysis of axonal alterations. Pain 64, 37–57 (1996).
pubmed: 8867246 doi: 10.1016/0304-3959(95)00077-1 pmcid: 8867246
Chaplan, S. R., Bach, F. W., Pogrel, J. W., Chung, J. M. & Yaksh, T. L. Quantitative assessment of tactile allodynia in the rat paw. J. Neurosci. Methods 53, 55–63 (1994).
pubmed: 7990513 doi: 10.1016/0165-0270(94)90144-9 pmcid: 7990513
Sorge, R. E. et al. Olfactory exposure to males, including men, causes stress and related analgesia in rodents. Nat. Methods 11, 629–632 (2014).
pubmed: 24776635 doi: 10.1038/nmeth.2935 pmcid: 24776635
Fritschy, J. M. & Mohler, H. GABAA-receptor heterogeneity in the adult rat brain: differential regional and cellular distribution of seven major subunits. J. Comp. Neurol. 359, 154–194 (1995).
pubmed: 8557845 doi: 10.1002/cne.903590111 pmcid: 8557845
Perez-Sanchez, J. et al. alpha5GABAA Receptors Mediate Tonic Inhibition in the Spinal Cord Dorsal Horn and Contribute to the Resolution Of Hyperalgesia. J. Neurosci. Res. 95, 1307–1318 (2017).
pubmed: 27792253 doi: 10.1002/jnr.23981 pmcid: 27792253
Benke, D., Cicin-Sain, A., Mertens, S. & Mohler, H. Immunochemical identification of the alpha 1- and alpha 3-subunits of the GABAA-receptor in rat brain. J. Recept. Res. 11, 407–424 (1991).
pubmed: 1653345 doi: 10.3109/10799899109066418 pmcid: 1653345
Benke, D., Honer, M., Michel, C. & Mohler, H. GABAA receptor subtypes differentiated by their gamma-subunit variants: prevalence, pharmacology and subunit architecture. Neuropharmacology 35, 1413–1423 (1996).
pubmed: 9014158 doi: 10.1016/S0028-3908(96)00068-8 pmcid: 9014158
Fritschy, J. M., Panzanelli, P., Kralic, J. E., Vogt, K. E. & Sassoe-Pognetto, M. Differential dependence of axo-dendritic and axo-somatic GABAergic synapses on GABAA receptors containing the alpha1 subunit in Purkinje cells. J. Neurosci. 26, 3245–3255 (2006).
pubmed: 16554475 pmcid: 6674111 doi: 10.1523/JNEUROSCI.5118-05.2006
Kralic,J. E. et al. Compensatory alteration of inhibitory synaptic circuits in cerebellum and thalamus of gamma-aminobutyric acid type A receptor alpha1 subunit knockout mice. J Comp Neurol. 495, 408-421 (2006).
Bohlhalter, S., Mohler, H. & Fritschy, J. M. Inhibitory neurotransmission in rat spinal cord: co-localization of glycine- and GABAA-receptors at GABAergic synaptic contacts demonstrated by triple immunofluorescence staining. Brain Res. 642, 59–69 (1994).
pubmed: 8032902 doi: 10.1016/0006-8993(94)90905-9 pmcid: 8032902
Bohlhalter, S., Weinmann, O., Mohler, H. & Fritschy, J. M. Laminar compartmentalization of GABAA-receptor subtypes in the spinal cord: an immunohistochemical study. J. Neurosci. 16, 283–297 (1996).
pubmed: 8613794 pmcid: 6578721 doi: 10.1523/JNEUROSCI.16-01-00283.1996
Waldvogel, H. J. et al. Differential localization of gamma-aminobutyric acid type A and glycine receptor subunits and gephyrin in the human pons, medulla oblongata and uppermost cervical segment of the spinal cord: an immunohistochemical study. J. Comp. Neurol. 518, 305–328 (2010).
pubmed: 19950251 doi: 10.1002/cne.22212 pmcid: 19950251
Slany, A., Zezula, J., Tretter, V. & Sieghart, W. Rat beta 3 subunits expressed in human embryonic kidney 293 cells form high affinity [35S]t-butylbicyclophosphorothionate binding sites modulated by several allosteric ligands of gamma-aminobutyric acid type A receptors. Mol. Pharmacol. 48, 385–391 (1995).
pubmed: 7565617 pmcid: 7565617
Todd, A. J., Watt, C., Spike, R. C. & Sieghart, W. Colocalization of GABA, glycine, and their receptors at synapses in the rat spinal cord. J. Neurosci. 16, 974–982 (1996).
pubmed: 8558266 pmcid: 6578783 doi: 10.1523/JNEUROSCI.16-03-00974.1996
Togel, M., Mossier, B., Fuchs, K. & Sieghart, W. gamma-Aminobutyric acidA receptors displaying association of gamma 3-subunits with beta 2/3 and different alpha-subunits exhibit unique pharmacological properties. J. Biol. Chem. 269, 12993–12998 (1994).
pubmed: 8175718 pmcid: 8175718
Kasugai, Y. et al. Quantitative localisation of synaptic and extrasynaptic GABAA receptor subunits on hippocampal pyramidal cells by freeze-fracture replica immunolabelling. Eur. J. Neurosci. 32, 1868–1888 (2010).
pubmed: 21073549 pmcid: 4487817 doi: 10.1111/j.1460-9568.2010.07473.x
Baer, K. et al. Association of gephyrin and glycine receptors in the human brainstem and spinal cord: an immunohistochemical analysis. Neuroscience 122, 773–784 (2003).
pubmed: 14622920 doi: 10.1016/S0306-4522(03)00543-8 pmcid: 14622920
Pfeiffer, F., Graham, D. & Betz, H. Purification by affinity chromatography of the glycine receptor of rat spinal cord. J. Biol. Chem. 257, 9389–9393 (1982).
pubmed: 6286620 pmcid: 6286620
Pfeiffer, F., Simler, R., Grenningloh, G. & Betz, H. Monoclonal antibodies and peptide mapping reveal structural similarities between the subunits of the glycine receptor of rat spinal cord. Proc. Natl Acad. Sci. USA 81, 7224–7227 (1984).
pubmed: 6095276 doi: 10.1073/pnas.81.22.7224 pmcid: 6095276
Schroder, S., Hoch, W., Becker, C. M., Grenningloh, G. & Betz, H. Mapping of antigenic epitopes on the alpha 1 subunit of the inhibitory glycine receptor. Biochemistry 30, 42–47 (1991).
pubmed: 1703015 doi: 10.1021/bi00215a007 pmcid: 1703015
Durisic, N. et al. Stoichiometry of the human glycine receptor revealed by direct subunit counting. J. Neurosci. 32, 12915–12920 (2012).
pubmed: 22973015 pmcid: 3475605 doi: 10.1523/JNEUROSCI.2050-12.2012
Kirsch, J. & Betz, H. Glycine-receptor activation is required for receptor clustering in spinal neurons. Nature 392, 717–720 (1998).
pubmed: 9565032 doi: 10.1038/33694 pmcid: 9565032
Fischer, F. et al. Reduced synaptic clustering of GABA and glycine receptors in the retina of the gephyrin null mutant mouse. J. Comp. Neurol. 427, 634–648 (2000).
pubmed: 11056469 doi: 10.1002/1096-9861(20001127)427:4<634::AID-CNE10>3.0.CO;2-X pmcid: 11056469
Kneussel, M. et al. Loss of postsynaptic GABA(A) receptor clustering in gephyrin-deficient mice. J. Neurosci. 19, 9289–9297 (1999).
pubmed: 10531433 pmcid: 6782938 doi: 10.1523/JNEUROSCI.19-21-09289.1999
Lardi-Studler, B. et al. Vertebrate-specific sequences in the gephyrin E-domain regulate cytosolic aggregation and postsynaptic clustering. J. Cell Sci. 120, 1371–1382 (2007).
pubmed: 17374639 doi: 10.1242/jcs.003905 pmcid: 17374639
Lorenzo, L. E., Barbe, A. & Bras, H. Mapping and quantitative analysis of gephyrin cytoplasmic trafficking pathways in motoneurons, using an optimized Transmission Electron Microscopy Color Imaging (TEMCI) procedure. J. Neurocytol. 33, 241–249 (2004).
pubmed: 15322382 doi: 10.1023/B:NEUR.0000030699.74642.7d
Gibson, S. J. et al. Calcitonin gene-related peptide immunoreactivity in the spinal cord of man and of eight other species. J. Neurosci. 4, 3101–3111 (1984).
pubmed: 6209366 pmcid: 6564846 doi: 10.1523/JNEUROSCI.04-12-03101.1984
Hunt, S. P. & Rossi, J. Peptide- and non-peptide-containing unmyelinated primary sensory afferents: the parallel processing of nociceptive information. Philos. Trans. R. Soc. Lond. 308, 283–289 (1985).
Ju, G. et al. Primary sensory neurons of the rat showing calcitonin gene-related peptide immunoreactivity and their relation to substance P-, somatostatin-, galanin-, vasoactive intestinal polypeptide- and cholecystokinin-immunoreactive ganglion cells. Cell Tissue Res. 247, 417–431 (1987).
pubmed: 2434236 doi: 10.1007/BF00218323 pmcid: 2434236
Rosenfeld, M. G. et al. Production of a novel neuropeptide encoded by the calcitonin gene via tissue-specific RNA processing. Nature 304, 129–135 (1983).
pubmed: 6346105 doi: 10.1038/304129a0 pmcid: 6346105
Sugiura,Y. Distribution of unmyelinated primary afferent fibers in the dorsal horn in Processing of sensory information in the superficial dorsal horn of the spinal cord (eds. Cervero, F., Bennett, G. J. & Headley, P. M.) 15-23 (Plenum Press, New York, 1989).
Rice, F. L. Structure, vascularization, and innervation of the mystacial pad of the rat as revealed by the lectin Griffonia simplicifolia. J. Comp. Neurol. 337, 386–399 (1993).
pubmed: 8282849 doi: 10.1002/cne.903370304 pmcid: 8282849
Alvarez, F. J. & Fyffe, R. E. Nociceptors for the 21st century. Curr. Rev. Pain. 4, 451–458 (2000).
pubmed: 11060591 doi: 10.1007/s11916-000-0069-4 pmcid: 11060591
Fang, X. et al. Intense isolectin-B4 binding in rat dorsal root ganglion neurons distinguishes C-fiber nociceptors with broad action potentials and high Nav1.9 expression. J. Neurosci. 26, 7281–7292 (2006).
pubmed: 16822986 pmcid: 6673936 doi: 10.1523/JNEUROSCI.1072-06.2006
Mercado, A., Broumand, V., Zandi-Nejad, K., Enck, A. H. & Mount, D. B. A C-terminal domain in KCC2 confers constitutive K+-Cl- cotransport. J. Biol. Chem. 281, 1016–1026 (2006).
pubmed: 16291749 doi: 10.1074/jbc.M509972200 pmcid: 16291749
Williams, J. R., Sharp, J. W., Kumari, V. G., Wilson, M. & Payne, J. A. The neuron-specific K-Cl cotransporter, KCC2. Antibody development and initial characterization of the protein. J. Biol. Chem. 274, 12656–12664 (1999).
pubmed: 10212246 doi: 10.1074/jbc.274.18.12656 pmcid: 10212246
Otsu, N. Threshold selection method from gray-level histograms. IEEE Trans. Syst. Man Cybern. 9, 62–66 (1979).
doi: 10.1109/TSMC.1979.4310076
Mesnage,B. et al. Morphological and functional characterization of cholinergic interneurons in the dorsal horn of the mouse spinal cord. J. Comp. Neurol. 519, 3139–3158 (2011).
pubmed: 21618225 doi: 10.1002/cne.22668 pmcid: 21618225
Lorenzo, L. E., Ramien, M., St.Louis, M., De Koninck, Y. & Ribeiro-da-Silva, A. Postnatal changes in the Rexed lamination and markers of nociceptive afferents in the superficial dorsal horn of the rat. J. Comp. Neurol. 508, 592–604 (2008).
pubmed: 18383051 doi: 10.1002/cne.21691 pmcid: 18383051
Godin, A. G., Lounis, B. & Cognet, L. Super-resolution microscopy approaches for live cell imaging. Biophys. J. 107, 1777–1784 (2014).
pubmed: 25418158 pmcid: 4213717 doi: 10.1016/j.bpj.2014.08.028
Dani, A., Huang, B., Bergan, J., Dulac, C. & Zhuang, X. Superresolution imaging of chemical synapses in the brain. Neuron 68, 843–856 (2010).
pubmed: 21144999 pmcid: 3057101 doi: 10.1016/j.neuron.2010.11.021
Durand, A. et al. A machine learning approach for online automated optimization of super-resolution optical microscopy. Nat. Commun. 9, 5247 (2018).
pubmed: 30531817 pmcid: 6286316 doi: 10.1038/s41467-018-07668-y
Huang, B., Babcock, H. & Zhuang, X. Breaking the diffraction barrier: super-resolution imaging of cells. Cell 143, 1047–1058 (2010).
pubmed: 21168201 pmcid: 3272504 doi: 10.1016/j.cell.2010.12.002
Barbeau, A. et al. Spatial intensity distribution analysis (SpIDA): a new tool for receptor tyrosine kinase activation and transactivation quantification. Methods Cell Biol. 117, 1–19 (2013).
pubmed: 24143969 doi: 10.1016/B978-0-12-408143-7.00001-3
Barbeau, A. et al. Quantification of receptor tyrosine kinase activation and transactivation by G-protein-coupled receptors using spatial intensity distribution analysis (SpIDA). Methods Enzymol. 522, 109–131 (2013).
pubmed: 23374183 doi: 10.1016/B978-0-12-407865-9.00007-8
Kolin, D. L. & Wiseman, P. W. Advances in image correlation spectroscopy: measuring number densities, aggregation states, and dynamics of fluorescently labeled macromolecules in cells. Cell Biochem. Biophys. 49, 141–164 (2007).
pubmed: 17952641 doi: 10.1007/s12013-007-9000-5
Patrizio, A. & Specht, C. G. Counting numbers of synaptic proteins: absolute quantification and single molecule imaging techniques. Neurophotonics 3, 041805 (2016).
pubmed: 27335891 pmcid: 4891561 doi: 10.1117/1.NPh.3.4.041805
Sugiyama, Y., Kawabata, I., Sobue, K. & Okabe, S. Determination of absolute protein numbers in single synapses by a GFP-based calibration technique. Nat. Methods 2, 677–684 (2005).
pubmed: 16118638 doi: 10.1038/nmeth783
Verdaasdonk, J. S., Lawrimore, J. & Bloom, K. Determining absolute protein numbers by quantitative fluorescence microscopy. Methods Cell Biol. 123, 347–365 (2014).
pubmed: 24974037 pmcid: 4221264 doi: 10.1016/B978-0-12-420138-5.00019-7
Korobchevskaya,K., Lagerholm,C. B., Colin-York,H., & Fritzsche,M. Exploring the potential of airyscan microscopy for live cell imaging. Photonics 4, 1–19 (2017).
Haring, M. et al. Neuronal atlas of the dorsal horn defines its architecture and links sensory input to transcriptional cell types. Nat. Neurosci. 21, 869–880 (2018).
pubmed: 29686262 doi: 10.1038/s41593-018-0141-1
Foust, D. J., Godin, A. G., Ustione, A., Wiseman, P. W. & Piston, D. W. Two-color spatial cumulant analysis detects heteromeric interactions between membrane proteins. Biophys. J. 117, 1764–1777 (2019).
pubmed: 31606123 doi: 10.1016/j.bpj.2019.09.028
Sigel, E. & Steinmann, M. E. Structure, function, and modulation of GABA(A) receptors. J. Biol. Chem. 287, 40224–40231 (2012).
pubmed: 23038269 pmcid: 3504738 doi: 10.1074/jbc.R112.386664
Ribeiro-da-Silva,A., Priestley,J. V., & Cuello,A. C. Pre-embedding ultrastructural immunocytochemistry in Immunohistochemistry II (ed. Cuello,A. C.) 181-227 (John Wiley & Sons, Chichester, 1993).
Chery, N. & De Koninck, Y. Junctional versus extrajunctional glycine and GABA(A) receptor-mediated IPSCs in identified lamina I neurons of the adult rat spinal cord. J. Neurosci. 19, 7342–7355 (1999).
pubmed: 10460241 pmcid: 6782499 doi: 10.1523/JNEUROSCI.19-17-07342.1999
Tallarida, R. J. Quantitative methods for assessing drug synergism. Genes Cancer 2, 1003–1008 (2011).
pubmed: 22737266 pmcid: 3379564 doi: 10.1177/1947601912440575
Perrais, D. & Ropert, N. Altering the concentration of GABA in the synaptic cleft potentiates miniature IPSCs in rat occipital cortex. Eur. J. Neurosci. 12, 400–404 (2000).
pubmed: 10651898 doi: 10.1046/j.1460-9568.2000.00957.x pmcid: 10651898
Legendre, P. A reluctant gating mode of glycine receptor channels determines the time course of inhibitory miniature synaptic events in zebrafish hindbrain neurons. J. Neurosci. 18, 2856–2870 (1998).
pubmed: 9526003 pmcid: 6792586 doi: 10.1523/JNEUROSCI.18-08-02856.1998
Barberis, A., Petrini, E. M. & Mozrzymas, J. W. Impact of synaptic neurotransmitter concentration time course on the kinetics and pharmacological modulation of inhibitory synaptic currents. Front. Cell Neurosci. 5, 6 (2011).
pubmed: 21734864 pmcid: 3123770 doi: 10.3389/fncel.2011.00006
Hill, M. W., Reddy, P. A., Covey, D. F. & Rothman, S. M. Contribution of subsaturating GABA concentrations to IPSCs in cultured hippocampal neurons. J. Neurosci. 18, 5103–5111 (1998).
pubmed: 9651194 pmcid: 6793480 doi: 10.1523/JNEUROSCI.18-14-05103.1998
Clements, J. D. Transmitter timecourse in the synaptic cleft: its role in central synaptic function. Trends Neurosci. 19, 163–171 (1996).
pubmed: 8723198 doi: 10.1016/S0166-2236(96)10024-2 pmcid: 8723198
De Koninck, Y. & Mody, I. Noise analysis of miniature IPSCs in adult rat brain slices: Properties and modulation of synaptic GABA
pubmed: 8035217 doi: 10.1152/jn.1994.71.4.1318 pmcid: 8035217
Kaila, K. & Voipio, J. Postsynaptic fall in intracellular pH induced by GABA-activated bicarbonate conductance. Nature 330, 163–165 (1987).
pubmed: 3670401 doi: 10.1038/330163a0 pmcid: 3670401
Dijkstra, K., Hofmeijer, J. & van Gils, S. A. & van Putten, M.J. A biophysical model for cytotoxic cell swelling. J. Neurosci. 36, 11881–11890 (2016).
pubmed: 27881775 pmcid: 6604918 doi: 10.1523/JNEUROSCI.1934-16.2016
Prescott, S. A., Sejnowski, T. J. & De Koninck, Y. Reduction of anion reversal potential subverts the inhibitory control of firing rate in spinal lamina I neurons: towards a biophysical basis for neuropathic pain. Mol. Pain. 2, 32 (2006).
pubmed: 17040565 pmcid: 1624821 doi: 10.1186/1744-8069-2-32
Keller, A. F., Beggs, S., Salter, M. W. & De Koninck, Y. Transformation of the output of spinal lamina I neurons after nerve injury and microglia stimulation underlying neuropathic pain. Mol. Pain. 3, 27 (2007).
pubmed: 17900333 pmcid: 2093929 doi: 10.1186/1744-8069-3-27

Auteurs

Louis-Etienne Lorenzo (LE)

CERVO Brain Research Centre, Quebec Mental Health Institute, Québec, QC, Canada.
Department of Pharmacology & Therapeutics, McGill University, Montreal, QC, Canada.

Antoine G Godin (AG)

CERVO Brain Research Centre, Quebec Mental Health Institute, Québec, QC, Canada.
Department of Psychiatry & Neuroscience, Université Laval, Québec, QC, Canada.
Graduate program in Neuroscience, Université Laval, Québec, QC, Canada.

Francesco Ferrini (F)

CERVO Brain Research Centre, Quebec Mental Health Institute, Québec, QC, Canada.
Department of Psychiatry & Neuroscience, Université Laval, Québec, QC, Canada.
Graduate program in Neuroscience, Université Laval, Québec, QC, Canada.
Department of Veterinary Sciences, University of Turin, Turin, Italy.

Karine Bachand (K)

CERVO Brain Research Centre, Quebec Mental Health Institute, Québec, QC, Canada.

Isabel Plasencia-Fernandez (I)

CERVO Brain Research Centre, Quebec Mental Health Institute, Québec, QC, Canada.
Graduate program in Neuroscience, Université Laval, Québec, QC, Canada.

Simon Labrecque (S)

CERVO Brain Research Centre, Quebec Mental Health Institute, Québec, QC, Canada.

Alexandre A Girard (AA)

CERVO Brain Research Centre, Quebec Mental Health Institute, Québec, QC, Canada.
Ecole Polytechnique, IP Paris, Palaiseau, France.

Dominic Boudreau (D)

CERVO Brain Research Centre, Quebec Mental Health Institute, Québec, QC, Canada.
Graduate program in Neuroscience, Université Laval, Québec, QC, Canada.

Irenej Kianicka (I)

Chlorion Pharma, Laval, Québec, QC, Canada.
Laurent Pharmaceuticals Inc., Montreal, QC, Canada.

Martin Gagnon (M)

CERVO Brain Research Centre, Quebec Mental Health Institute, Québec, QC, Canada.
Centre for Innovation, University of Otago, Dunedin, New Zealand.

Nicolas Doyon (N)

CERVO Brain Research Centre, Quebec Mental Health Institute, Québec, QC, Canada.
Finite Element Interdisciplinary Research Group (GIREF), Université Laval, Québec, QC, Canada.

Alfredo Ribeiro-da-Silva (A)

Department of Pharmacology & Therapeutics, McGill University, Montreal, QC, Canada.
Department of Anatomy & Cell Biology, McGill University, Montreal, QC, Canada.
Alan Edwards Centre for Research on Pain, McGill University, Montreal, QC, Canada.

Yves De Koninck (Y)

CERVO Brain Research Centre, Quebec Mental Health Institute, Québec, QC, Canada. yves.dekoninck@neuro.ulaval.ca.
Department of Pharmacology & Therapeutics, McGill University, Montreal, QC, Canada. yves.dekoninck@neuro.ulaval.ca.
Department of Psychiatry & Neuroscience, Université Laval, Québec, QC, Canada. yves.dekoninck@neuro.ulaval.ca.
Graduate program in Neuroscience, Université Laval, Québec, QC, Canada. yves.dekoninck@neuro.ulaval.ca.
Alan Edwards Centre for Research on Pain, McGill University, Montreal, QC, Canada. yves.dekoninck@neuro.ulaval.ca.

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