NMDA receptor-independent synaptic plasticity in the central amygdala in the rat model of neuropathic pain

Pain

Volumn 127, Issue 1-2, 2007, Pages 161-172

  Ikeda, Ryo ^a   Takahashi, Yukari ^a   Inoue, Kazuhide ^b   Kato, Fusao ^a  

^a JIKEI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b KYUSHU UNIVERSITY   (Japan)

Author keywords

Amygdala; Emotion; Excitatory postsynaptic currents; Neuropathic pain; NMDA receptor; Nucleus parabrachialis; Tactile allodynia

Indexed keywords

N METHYL DEXTRO ASPARTIC ACID RECEPTOR; N METHYL DEXTRO ASPARTIC ACID RECEPTOR BLOCKING AGENT;

ALLODYNIA; AMPLITUDE MODULATION; AMYGDALOID NUCLEUS; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTHRITIS; ARTICLE; CHRONIC PAIN; CONTROLLED STUDY; FEMALE; MALE; MOLECULAR MECHANICS; NERVE CELL EXCITABILITY; NERVE CELL PLASTICITY; NERVE LIGATION; NEUROPATHIC PAIN; NOCICEPTION; NONHUMAN; PARABRACHIAL NUCLEUS; PRIORITY JOURNAL; RAT; SENSORY NERVE CONDUCTION; SYNAPTIC TRANSMISSION; TACTILE DISCRIMINATION; VISCERAL PAIN;

AMYGDALA; ANIMALS; DISEASE MODELS, ANIMAL; FEMALE; HUMANS; MALE; MODELS, NEUROLOGICAL; NEURONAL PLASTICITY; NEURONS; PAIN; RATS; RATS, WISTAR; SYNAPTIC TRANSMISSION;

EID: 33845681647     PISSN: 03043959     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pain.2006.09.003     Document Type: Article

References (47)

1. Adamec R., Blundel J., and Burton P. Role of NMDA receptors in the lateralized potentiation of amygdala afferent and efferent neural transmission produced by predator stress. Physiol Behav 86 (2005) 75-91
2. Baker K.B., and Kim J.J. Amygdalar lateralization in fear conditioning: evidence for greater involvement of the right amygdala. Behav Neurosci 118 (2004) 15-23
3. Bernard J.F., and Besson J.M. The spino(trigemino)pontoamygdaloid pathway: electrophysiological evidence for an involvement in pain processes. J Neurophysiol 63 (1990) 473-490
4. Bernard J.F., Huang G.F., and Besson J.M. Nucleus centralis of the amygdala and the globus pallidus ventralis: electrophysiological evidence for an involvement in pain processes. J Neurophysiol 68 (1992) 551-569
5. Bird G.C., Lash L.L., Han J.S., Zou X., Willis W.D., and Neugebauer V. Protein kinase A-dependent enhanced NMDA receptor function in pain-related synaptic plasticity in rat amygdala neurones. J Physiol 564 (2005) 907-921
6. 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
7. Chapman V., Suzuki R., and Dickenson A.H. Electrophysiological characterization of spinal neuronal response properties in anaesthetized rats after ligation of spinal nerves L5-L6. J Physiol 507 (1998) 881-894
8. Coull J.A., Beggs S., Boudreau D., Boivin D., Tsuda M., Inoue K., Gravel C., Salter M.W., and De Koninck Y. BDNF from microglia causes the shift in neuronal anion gradient underlying neuropathic pain. Nature 438 (2005) 1017-1021
9. Coull J.A., Boudreau D., Bachand K., Prescott S.A., Nault F., Sik A., et al. Trans-synaptic shift in anion gradient in spinal lamina I neurons as a mechanism of neuropathic pain. Nature 424 (2003) 938-942
10. Davis M. Anatomic and physiologic substrates of emotion in an animal model. J Clin Neurophysiol 15 (1998) 378-387
11. Gauriau C., and Bernard J.F. Pain pathways and parabrachial circuits in the rat. Exp Physiol 87 (2002) 251-258
12. Han J.S., Li W., and Neugebauer V. Critical role of calcitonin gene-related peptide 1 receptors in the amygdala in synaptic plasticity and pain behavior. J Neurosci 25 (2005) 10717-10728
13. Han J.S., and Neugebauer V. Synaptic plasticity in the amygdala in a visceral pain model in rats. Neurosci Lett 361 (2004) 254-257
14. Hatfield T., Han J.S., Conley M., Gallagher M., and Holland P. Neurotoxic lesions of basolateral, but not central, amygdala interfere with Pavlovian second-order conditioning and reinforcer devaluation effects. J Neurosci 16 (1996) 5256-5265
15. Ikeda R., and Kato F. Early and transient increase in spontaneous synaptic inputs to the rat facial motoneurons after axotomy in isolated brainstem slices of rats. Neuroscience 134 (2005) 889-899
16. Ikeda R., Fujii K., and Kato F. Neuropathic pain-related synaptic plasticity in the central amygdala neurons. Neurosci Res 52 Suppl. (2005) S200
17. Inoue M., Rashid M.H., Fujita R., Contos J.J., Chun J., and Ueda H. Initiation of neuropathic pain requires lysophosphatidic acid receptor signaling. Nat Med 10 (2004) 712-718
18. Jasmin L., Burkey A.R., Card J.P., and Basbaum A.I. Transneuronal labeling of a nociceptive pathway, the spino-(trigemino-)parabrachio-amygdaloid, in the rat. J Neurosci 17 (1997) 3751-3765
19. Killcross S., Robbins T.W., and Everitt B.J. Different types of fear-conditioned behaviour mediated by separate nuclei within amygdala. Nature 388 (1997) 377-380
20. 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
21. LaLumiere R.T., and McGaugh J.L. Memory enhancement induced by post-training intrabasolateral amygdala infusions of β-adrenergic or muscarinic agonists requires activation of dopamine receptors: involvement of right, but not left, basolateral amygdala. Learn Mem 12 (2005) 527-532
22. LeDoux J.E. Emotion circuits in the brain. Annu Rev Neurosci 23 (2000) 155-184
23. Maren S. Synaptic mechanisms of associative memory in the amygdala. Neuron 47 (2005) 783-786
24. McKernan M.G., and Shinnick-Gallagher P. Fear conditioning induces a lasting potentiation of synaptic currents in vitro. Nature 390 (1997) 607-611
25. McWilliams L.A., Cox B.J., and Enns M.W. Mood and anxiety disorders associated with chronic pain: an examination in a nationally representative sample. Pain 106 (2003) 127-133
26. Nayak A., Zastrow D.J., Lickteig R., Zahniser N.R., and Browning M.D. Maintenance of late-phase LTP is accompanied by PKA-dependent increase in AMPA receptor synthesis. Nature 394 (1998) 680-683
27. Neugebauer V., Li W., Bird G.C., Bhave G., and Gereau R.W.t. Synaptic plasticity in the amygdala in a model of arthritic pain: differential roles of metabotropic glutamate receptors 1 and 5. J Neurosci 23 (2003) 52-63
28. Neugebauer V., Li W., Bird G.C., and Han J.S. The amygdala and persistent pain. Neuroscientist 10 (2004) 221-234
29. Pare D., Quirk G.J., and Ledoux J.E. New vistas on amygdala networks in conditioned fear. J Neurophysiol 92 (2004) 1-9
30. Parkinson J.A., Willoughby P.J., Robbins T.W., and Everitt B.J. Disconnection of the anterior cingulate cortex and nucleus accumbens core impairs Pavlovian approach behavior: further evidence for limbic cortical-ventral striatopallidal systems. Behav Neurosci 114 (2000) 42-63
31. Phelps E.A., and LeDoux J.E. Contributions of the amygdala to emotion processing: from animal models to human behavior. Neuron 48 (2005) 175-187
32. Price D.D. Central neural mechanisms that interrelate sensory and affective dimensions of pain. Mol Interv 2 (2002) 392-403 339
33. Rhudy J.L., and Meagher M.W. Negative affect: effects on an evaluative measure of human pain. Pain 104 (2003) 617-626
34. Russo C.M., and Brose W.G. Chronic pain. Annu Rev Med 49 (1998) 123-133
35. Sah P., Faber E.S., Lopez DeArmentia M., and Power J. The amygdaloid complex: anatomy and physiolog. Physiol Rev 83 (2003) 803-834
36. Scholz J., and Woolf C.J. Can we conquer pain?. Nat Neurosci 5 Suppl. (2002) 1062-1067
37. Scicli A.P., Petrovich G.D., Swanson L.W., and Thompson R.F. Contextual fear conditioning is associated with lateralized expression of the immediate early gene c-fos in the central and basolateral amygdala nuclei. Behav Neurosci 118 (2004) 5-14
38. Shi C., and Davis M. Pain pathways involved in fear conditioning measured with fear-potentiated startle: lesion studies. J Neurosci 19 (1999) 420-430
39. 2+ entry through presynaptic P2X receptors elicits postsynaptic firing in the brainstem autonomic network. J Neurosci 24 (2004) 3125-3135
40. Soderling T.R., and Derkach V.A. Postsynaptic protein phosphorylation and LTP. Trends Neurosci 23 (2000) 75-80
41. Tanimoto S., Nakagawa T., Yamauchi Y., Minami M., and Satoh M. Differential contributions of the basolateral and central nuclei of the amygdala in the negative affective component of chemical somatic and visceral pains in rats. Eur J Neurosci 18 (2003) 2343-2350
42. Tsuda M., Shigemoto-Mogami Y., Koizumi S., Mizokoshi A., Kohsaka S., Salter M.W., et al. P2X4 receptors induced in spinal microglia gate tactile allodynia after nerve injury. Nature 424 (2003) 778-783
43. Woolf C.J., and Mannion R.J. Neuropathic pain: aetiology, symptoms, mechanisms, and management. Lancet 353 (1999) 1959-1964
44. Woolf C.J., Shortland P., and Coggeshall R.E. Peripheral nerve injury triggers central sprouting of myelinated afferents. Nature 355 (1992) 75-78
45. Yu S., Undem B.J., and Kollarik M. Vagal afferent nerves with nociceptive properties in guinea-pig oesophagus. J Physiol 563 (2005) 831-842
46. Zald D.H. The human amygdala and the emotional evaluation of sensory stimuli. Brain Res Brain Res Rev 41 (2003) 88-123
47. Zimmermann M. Ethical guidelines for investigations of experimental pain in conscious animals. Pain 16 (1983) 109-110