Corrigendum to "Long-term synaptic plasticity in the spinal dorsal horn and its modulation by electroacupuncture in rats with neuropathic pain" [Exp. Neurol. 208(2007) 323-332] (DOI:10.1016/j.expneurol.2007.09.004);Long-term synaptic plasticity in the spinal dorsal horn and its modulation by electroacupuncture in rats with neuropathic pain

Experimental Neurology

Volumn 208, Issue 2, 2007, Pages 323-332

  Xing, Guo Gang ^a   Liu, Feng Yu ^a   Qu, Xiao Xiu ^a   Han, Ji Sheng ^a   Wan, You ^a  

^a PEKING UNIVERSITY   (China)

Author keywords

Electroacupuncture; Electrophysiology; Long term depression; Long term potentiation; Neuropathic pain; NMDA receptor; Opioid; Spinal dorsal horn

Indexed keywords

DIZOCILPINE; N METHYL DEXTRO ASPARTIC ACID RECEPTOR BLOCKING AGENT; NALOXONE; OPIATE ANTAGONIST;

ANALGESIC ACTIVITY; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; ELECTRIC POTENTIAL; ELECTROACUPUNCTURE; ELECTROPHYSIOLOGY; EVOKED RESPONSE; GABAERGIC SYSTEM; LONG TERM DEPRESSION; LONG TERM POTENTIATION; MALE; NERVE CELL PLASTICITY; NERVE INJURY; NERVE LIGATION; NEUROMODULATION; NEUROPATHIC PAIN; NOCICEPTION; NONHUMAN; PRIORITY JOURNAL; RAT; SEROTONINERGIC NERVE CELL; SPINAL CORD; SPINAL CORD DORSAL HORN; SPINAL CORD NERVE CELL; SPINAL NERVE; SYNAPTIC TRANSMISSION;

EID: 36148955786     PISSN: 00144886     EISSN: 10902430     Source Type: Journal    
DOI: 10.1016/j.expneurol.2008.01.007     Document Type: Erratum

References (68)

1. Amantea B., Gemelli A., Militano D., Salatino I., and Caroleo S. Neuronal plasticity and neuropathic pain. Minerva Anestesiol. 66 (2000) 901-911
2. Bliss T.V., and Collingridge G.L. A synaptic model of memory: long-term potentiation in the hippocampus. Nature 361 (1993) 31-39
3. Bliss T.V., and Lomo T. Long-lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path. J. Physiol. 232 (1973) 331-356
4. Bridges D., Thompson S.W., and Rice A.S. Mechanisms of neuropathic pain. Br. J. Anaesth. 87 (2001) 12-26
5. Campbell J.N., and Meyer R.A. Mechanisms of neuropathic pain. Neuron 52 (2006) 77-92
6. Cavenagh J., Good P., and Ravenscroft P. Neuropathic pain: are we out of the woods yet?. Intern. Med. J. 36 (2006) 251-255
7. Chaplan S.R., Bach F.W., Pogrel J.W., Chung J.M., and Yaksh T.L. Quantitative assessment of tactile allodynia in the rat paw. J. Neurosci. Methods 53 (1994) 55-63
8. Dai Y., Kondo E., Fukuoka T., Tokunaga A., Miki K., and Noguchi K. The effect of electroacupuncture on pain behaviors and noxious stimulus-evoked Fos expression in a rat model of neuropathic pain. J. Pain 2 (2001) 151-159
9. Dixon W.J. Efficient analysis of experimental observations. Annu. Rev. Pharmacol. Toxicol. 20 (1980) 441-462
10. Draganic P., Miletic G., and Miletic V. Changes in post-tetanic potentiation of A-fiber dorsal horn field potentials parallel the development and disappearance of neuropathic pain after sciatic nerve ligation in rats. Neurosci. Lett. 301 (2001) 127-130
11. Dubner R. Pain and hyperalgesia following tissue injury: new mechanisms and new treatments. Pain 44 (1991) 213-214
12. Garraway S.M., and Hochman S. Serotonin increases the incidence of primary afferent-evoked long-term depression in rat deep dorsal horn neurons. J. Neurophysiol. 85 (2001) 1864-1872
13. Guo H.F., Tian J., Wang X., Fang Y., Hou Y., and Han J. Brain substrates activated by electroacupuncture (EA) of different frequencies (II): role of Fos/Jun proteins in EA-induced transcription of preproenkephalin and preprodynorphin genes. Brain Res. Mol. Brain Res. 43 (1996) 167-173
14. Guo H.F., Tian J., Wang X., Fang Y., Hou Y., and Han J. Brain substrates activated by electroacupuncture of different frequencies (I): comparative study on the expression of oncogene c-fos and genes coding for three opioid peptides. Brain Res. Mol. Brain Res. 43 (1996) 157-166
15. Gwak Y.S., Tan H.Y., Nam T.S., Paik K.S., Hulsebosch C.E., and Leem J.W. Activation of spinal GABA receptors attenuates chronic central neuropathic pain after spinal cord injury. J. Neurotrauma. 23 (2006) 1111-1124
16. Hains B.C., Fullwood S.D., Eaton M.J., and Hulsebosch C.E. Subdural engraftment of serotonergic neurons following spinal hemisection restores spinal serotonin, downregulates serotonin transporter, and increases BDNF tissue content in rat. Brain Res. 913 (2001) 35-46
17. Hains B.C., Everhart A.W., Fullwood S.D., and Hulsebosch C.E. Changes in serotonin, serotonin transporter expression and serotonin denervation supersensitivity: involvement in chronic central pain after spinal hemisection in the rat. Exp. Neurol. 175 (2002) 347-362
18. Hains B.C., Johnson K.M., Eaton M.J., Willis W.D., and Hulsebosch C.E. Serotonergic neural precursor cell grafts attenuate bilateral hyperexcitability of dorsal horn neurons after spinal hemisection in rat. Neuroscience 116 (2003) 1097-1110
19. Hains B.C., Willis W.D., and Hulsebosch C.E. Serotonin receptors 5-HT1A and 5-HT3 reduce hyperexcitability of dorsal horn neurons after chronic spinal cord hemisection injury in rat. Exp. Brain Res. 149 (2003) 174-186
20. Han J.S. New evidence to substantiate the frequency specificity of acupuncture-induced analgesia. Acupunct. Res. 26 (2001) 224-227
21. Han J.S. Acupuncture: neuropeptide release produced by electrical stimulation of different frequencies. Trends Neurosci. 26 (2003) 17-22
22. Han J.S. Acupuncture and endorphins. Neurosci. Lett. 361 (2004) 258-261
23. Honda M., Uchida K., Tanabe M., and Ono H. Fluvoxamine, a selective serotonin reuptake inhibitor, exerts its antiallodynic effects on neuropathic pain in mice via 5-HT2A/2C receptors. Neuropharmacology 51 (2006) 866-872
24. Huang C., Li H.T., Shi Y.S., Han J.S., and Wan Y. Ketamine potentiates the effect of electroacupuncture on mechanical allodynia in a rat model of neuropathic pain. Neurosci. Lett. 368 (2004) 327-331
25. Hwang B.G., Min B.I., Kim J.H., Na H.S., and Park D.S. Effects of electroacupuncture on the mechanical allodynia in the rat model of neuropathic pain. Neurosci. Lett. 320 (2002) 49-52
26. Ikeda H., Asai T., Randic M., and Murase K. Robust suppression of afferent-induced excitation in the rat spinal dorsal horn after conditioning low-frequency stimulation. J. Neurophysiol. 82 (1999) 1957-1964
27. Ikeda H., Asai T., and Murase K. Robust changes of afferent-induced excitation in the rat spinal dorsal horn after conditioning high-frequency stimulation. J. Neurophysiol. 83 (2000) 2412-2420
28. Kim S.H., and Chung J.M. An experimental model for peripheral neuropathy produced by segmental spinal nerve ligation in the rat. Pain 50 (1992) 355-363
29. Kim J.H., Min B.I., Na H.S., and Park D.S. Relieving effects of electroacupuncture on mechanical allodynia in neuropathic pain model of inferior caudal trunk injury in rat: mediation by spinal opioid receptors. Brain Res. 998 (2004) 230-236
30. Kim S.K., Park J.H., Bae S.J., Kim J.H., Hwang B.G., Min B.I., Park D.S., and Na H.S. Effects of electroacupuncture on cold allodynia in a rat model of neuropathic pain: mediation by spinal adrenergic and serotonergic receptors. Exp. Neurol. 195 (2005) 430-436
31. Liu X.G., and Sandkuhler J. Long-term potentiation of C-fiber-evoked potentials in the rat spinal dorsal horn is prevented by spinal N-methyl-d-aspartic acid receptor blockage. Neurosci. Lett. 191 (1995) 43-46
32. Liu X., and Sandkuhler J. Characterization of long-term potentiation of C-fiber-evoked potentials in spinal dorsal horn of adult rat: essential role of NK1 and NK2 receptors. J. Neurophysiol. 78 (1997) 1973-1982
33. Liu X.G., and Sandkuhler J. Activation of spinal N-methyl-d-aspartate or neurokinin receptors induces long-term potentiation of spinal C-fibre-evoked potentials. Neuroscience 86 (1998) 1209-1216
34. Liu X.G., Morton C.R., Azkue J.J., Zimmermann M., and Sandkuhler J. Long-term depression of C-fibre-evoked spinal field potentials by stimulation of primary afferent A delta-fibres in the adult rat. Eur. J. Neurosci. 10 (1998) 3069-3075
35. Malan T.P., Mata H.P., and Porreca F. Spinal GABA(A) and GABA(B) receptor pharmacology in a rat model of neuropathic pain. Anesthesiology 96 (2002) 1161-1167
36. Miletic G., and Miletic V. Long-term changes in sciatic-evoked A-fiber dorsal horn field potentials accompany loose ligation of the sciatic nerve in rats. Pain 84 (2000) 353-359
37. Miletic G., and Miletic V. Contribution of GABA-A receptors to metaplasticity in the spinal dorsal horn. Pain 90 (2001) 157-162
38. Miletic G., Draganic P., Pankratz M.T., and Miletic V. Muscimol prevents long-lasting potentiation of dorsal horn field potentials in rats with chronic constriction injury exhibiting decreased levels of the GABA transporter GAT-1. Pain 105 (2003) 347-353
39. Moore K.A., Kohno T., Karchewski L.A., Scholz J., Baba H., and Woolf C.J. Partial peripheral nerve injury promotes a selective loss of GABAergic inhibition in the superficial dorsal horn of the spinal cord. J. Neurosci. 22 (2002) 6724-6731
40. Nam T.S., Choi Y., Yeon D.S., Leem J.W., and Paik K.S. Differential antinociceptive effect of transcutaneous electrical stimulation on pain behavior sensitive or insensitive to phentolamine in neuropathic rats. Neurosci. Lett. 301 (2001) 17-20
41. Nitanda A., Yasunami N., Tokumo K., Fujii H., Hirai T., and Nishio H. Contribution of the peripheral 5-HT 2A receptor to mechanical hyperalgesia in a rat model of neuropathic pain. Neurochem. Int. 47 (2005) 394-400
42. Randic M. Plasticity of excitatory synaptic transmission in the spinal cord dorsal horn. Prog. Brain Res. 113 (1996) 463-506
43. Rapson L.M., Wells N., Pepper J., Majid N., and Boon H. Acupuncture as a promising treatment for below-level central neuropathic pain: a retrospective study. J. Spinal Cord Med. 26 (2003) 21-26
44. Rode F., Jensen D.G., Blackburn-Munro G., and Bjerrum O.J. Centrally-mediated antinociceptive actions of GABA(A) receptor agonists in the rat spared nerve injury model of neuropathic pain. Eur. J. Pharmacol. 516 (2005) 131-138
45. Rygh L.J., Svendsen F., Hole K., and Tjolsen A. Natural noxious stimulation can induce long-term increase of spinal nociceptive responses. Pain 82 (1999) 305-310
46. Sandkuhler J. Learning and memory in pain pathways. Pain 88 (2000) 113-118
47. Sandkuhler J., and Liu X. Induction of long-term potentiation at spinal synapses by noxious stimulation or nerve injury. Eur. J. Neurosci. 10 (1998) 2476-2480
48. Sandkuhler J., Chen J.G., Cheng G., and Randic M. Low-frequency stimulation of afferent Adelta-fibers induces long-term depression at primary afferent synapses with substantia gelatinosa neurons in the rat. J. Neurosci. 17 (1997) 6483-6491
49. Schaible H.G., and Richter F. Pathophysiology of pain. Langenbeck's Arch. Surg. 389 (2004) 237-243
50. Scholz J., Broom D.C., Youn D.H., Mills C.D., Kohno T., Suter M.R., Moore K.A., Decosterd I., Coggeshall R.E., and Woolf C.J. 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 (2005) 7317-7323
51. Somers D.L., and Clemente F.R. Transcutaneous electrical nerve stimulation for the management of neuropathic pain: the effects of frequency and electrode position on prevention of allodynia in a rat model of complex regional pain syndrome type II. Phys. Ther. 86 (2006) 698-709
52. Sun R.Q., Wang H.C., Wang Y., Luo F., and Han J.S. Effect of electroacupuncture with different frequencies on neuropathic pain rat model. Chin. J. Appl. Physiol. 18 (2002) 128-131
53. Sun R.Q., Wang H.C., Wan Y., Wan Y., Jing Z., Luo F., Han J.S., and Wang Y. Suppression of neuropathic pain by peripheral electrical stimulation in rats: mu-opioid receptor and NMDA receptor implicated. Exp. Neurol. 187 (2004) 23-29
54. Sun Q., Tu H., Xing G.G., Han J.S., and Wan Y. Ectopic discharges from injured nerve fibers are highly correlated with tactile allodynia only in early, but not late, stage in rats with spinal nerve ligation. Exp. Neurol. 191 (2005) 128-136
55. Sun Q., Xing G.G., Tu H.Y., Han J.S., and Wan Y. Inhibition of hyperpolarization-activated current by ZD7288 suppresses ectopic discharges of injured dorsal root ganglion neurons in a rat model of neuropathic pain. Brain Res. 1032 (2005) 63-69
56. Svendsen F., Tjolsen A., and Hole K. LTP of spinal A beta and C-fibre evoked responses after electrical sciatic nerve stimulation. Neuroreport 8 (1997) 3427-3430
57. Svendsen F., Rygh L.J., Gjerstad J., Fiska A., Hole K., and Tjolsen A. Recording of long-term potentiation in single dorsal horn neurons in vivo in the rat. Brain Res. Brain Res. Protoc. 4 (1999) 165-172
58. Svendsen F., Hole K., and Tjolsen A. Long-term potentiation in single wide dynamic range neurons induced by noxious stimulation in intact and spinalized rats. Prog. Brain Res. 129 (2000) 153-161
59. Terenzi M.G., and Prado W.A. Antinociception elicited by electrical or chemical stimulation of the rat habenular complex and its sensitivity to systemic antagonists. Brain Res. 535 (1990) 18-24
60. Ulugol A., Aslantas A., Ipci Y., Tuncer A., Hakan K.C., and Dokmeci I. Combined systemic administration of morphine and magnesium sulfate attenuates pain-related behavior in mononeuropathic rats. Brain Res. 943 (2002) 101-104
61. Wan Y., Wilson S.G., Han J., and Mogil J.S. The effect of genotype on sensitivity to electroacupuncture analgesia. Pain 91 (2001) 5-13
62. Woolf C.J. Evidence for a central component of post-injury pain hypersensitivity. Nature 306 (1983) 686-688
63. Woolf C.J. Dissecting out mechanisms responsible for peripheral neuropathic pain: implications for diagnosis and therapy. Life Sci. 74 (2004) 2605-2610
64. Woolf C.J., and Salter M.W. Neuronal plasticity: increasing the gain in pain. Science 288 (2000) 1765-1769
65. Xie W., Strong J.A., Meij J.T., Zhang J.M., and Yu L. Neuropathic pain: early spontaneous afferent activity is the trigger. Pain 116 (2005) 243-256
66. Zhang R.X., Lao L., Wang L., Liu B., Wang X., Ren K., and Berman B.M. Involvement of opioid receptors in electroacupuncture-produced anti-hyperalgesia in rats with peripheral inflammation. Brain Res. 1020 (2004) 12-17
67. Zimmermann M. Ethical guidelines for investigations of experimental pain in conscious animals. Pain 16 (1983) 109-110
68. Zimmermann M. Pathobiology of neuropathic pain. Eur. J. Pharmacol. 429 (2001) 23-37