Long-term potentiation of neuronal excitation in the central nucleus of the rat amygdala revealed by imaging with a voltage-sensitive dye

Brain Research

Volumn 1349, Issue , 2010, Pages 32-40

  Kiritoshi, Takaki ^a   Ikeda, Hiroshi ^a   Murase, Kazuyuki ^a  

^a UNIVERSITY OF FUKUI   (Japan)

Author keywords

Optical imaging; Pain; PKA; Plasticity

Indexed keywords

CALCIUM ION; CYCLIC AMP; CYCLIC AMP DEPENDENT PROTEIN KINASE; DYE; FORSKOLIN; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; UNCLASSIFIED DRUG; VOLTAGE SENSITIVE DYE;

AMYGDALOID NUCLEUS; ANIMAL TISSUE; ARTICLE; BRAIN SLICE; CONTROLLED STUDY; ENZYME ACTIVATION; IMAGING; INTRACELLULAR SIGNALING; LONG TERM POTENTIATION; NERVE CELL EXCITABILITY; NERVE CELL STIMULATION; NONHUMAN; PRIORITY JOURNAL; RAT;

6-CYANO-7-NITROQUINOXALINE-2,3-DIONE; AMYGDALA; ANIMALS; ANIMALS, NEWBORN; ANISOMYCIN; BIOPHYSICS; CALCIUM; CARBAZOLES; ELECTRIC STIMULATION; ENZYME INHIBITORS; EXCITATORY AMINO ACID ANTAGONISTS; FORSKOLIN; LONG-TERM POTENTIATION; NEURONS; PATCH-CLAMP TECHNIQUES; PROTEIN SYNTHESIS INHIBITORS; PYRROLES; RATS; RATS, WISTAR; TIME FACTORS; VALINE; VOLTAGE-SENSITIVE DYE IMAGING;

RATTUS;

EID: 77955655113     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2010.06.039     Document Type: Article

References (47)

1. V. Aroniadou-Anderjaska, R.M. Post, M.A. Rogawski, and H. Li Input-specific LTP and depotentiation in the basolateral amygdala Neuroreport 12 2001 635 640
2. J.F. Bernard, G.F. Huang, and J.M. Besson Nucleus centralis of the amygdala and the globus pallidus ventralis: electrophysiological evidence for an involvement in pain processes J. Neurophysiol. 68 1992 551 569
3. J.F. Bernard, M. Alden, and J.M. Besson The organization of the efferent projections from the pontine parabrachial area to the amygdaloid complex: a Phaseolus vulgaris leucoagglutinin (PHA-L) study in the rat J. Comp. Neurol. 329 1993 201 229
4. G.C. Bird, L.L. Lash, J.S. Han, X. Zou, W.D. Willis, and V. Neugebauer Protein kinase A-dependent enhanced NMDA receptor function in pain-related synaptic plasticity in rat amygdala neurones J. Physiol. 564 2005 907 921
5. L. Bourgeais, C. Gauriau, and J.F. Bernard Projections from the nociceptive area of the central nucleus of the amygdala to the forebrain: a PHA-L study in the rat Eur. J. Neurosci. 14 2001 229 255
6. J. Buritova, J.M. Besson, and J.F. Bernard Involvement of the spinoparabrachial pathway in inflammatory nociceptive processes: a c-Fos protein study in the awake rat J. Comp. Neurol. 397 1998 10 28
7. R.C. Carroll, E.C. Beattie, M. von Zastrow, and R.C. Malenka Role of AMPA receptor endocytosis in synaptic plasticity Nat. Rev. Neurosci. 2 2001 315 324
8. P.F. Chapman, M.F. Ramsay, W. Krezel, and S.G. Knevett Synaptic plasticity in the amygdala: comparisons with hippocampus Ann. N. Y. Acad. Sci. 985 2003 114 124
9. 2+ channel activity in area CA1 of hippocampus Proc. Natl. Acad. Sci. U. S. A. 88 1991 6467 6471
10. A receptor subtypes to somatic and dendritic synapses in the central amygdala J. Neurophysiol. 86 2001 717 723
11. V. Doyère, G.E. Schafe, T. Sigurdsson, and J.E. LeDoux Long-term potentiation in freely moving rats reveals asymmetries in thalamic and cortical inputs to the lateral amygdala Eur. J. Neurosci. 17 2003 2703 2715
12. T.J. Ebner, and G. Chen Use of voltage-sensitive dyes and optical recordings in the central nervous system Prog. Neurobiol. 46 1995 463 506
13. 2+/ calmodulin sensitivity may be common to all forms of neural adenylate cyclase Proc. Natl. Acad. Sci. U. S. A. 86 1989 9564 9568
14. Y. Fu, and V. Neugebauer Differential mechanisms of CRF1 and CRF2 receptor functions in the amygdala in pain-related synaptic facilitation and behavior J. Neurosci. 28 2008 3861 3876
15. Y. Fu, and P. Shinnick-Gallagher Two intra-amygdaloid pathways to the central amygdala exhibit different mechanisms of long-term potentiation J. Neurophysiol. 93 2005 3012 3015
16. Y. Fu, J. Han, T. Ishola, M. Scerbo, H. Adwanikar, C. Ramsey, and V. Neugebauer PKA and ERK, but not PKC, in the amygdala contribute to pain-related synaptic plasticity and behavior Mol. Pain 4 2008 26
17. J.S. Han, and V. Neugebauer Synaptic plasticity in the amygdala in a visceral pain model in rats Neurosci. Lett. 361 2004 254 257
18. J.S. Han, and V. Neugebauer mGluR1 and mGluR5 antagonists in the amygdala inhibit different components of audible and ultrasonic vocalizations in a model of arthritic pain Pain 113 2005 211 222
19. J.S. Han, G.C. Bird, and V. Neugebauer Enhanced group III mGluR-mediated inhibition of pain-related synaptic plasticity in the amygdala Neuropharmacology 46 2004 918 926
20. J.S. Han, W. Li, and V. Neugebauer Critical role of calcitonin gene-related peptide 1 receptors in the amygdala in synaptic plasticity and pain behavior J. Neurosci. 25 2005 10717 10728
21. J.S. Han, Y. Fu, G.C. Bird, and V. Neugebauer Enhanced group II mGluR-mediated inhibition of pain-related synaptic plasticity in the amygdala Mol. Pain 2 2006 18
22. M.T. Harnett, B.E. Bernier, K.C. Ahn, and H. Morikawa Burst-timing-dependent plasticity of NMDA receptor-mediated transmission in midbrain dopamine neurons Neuron 62 2009 826 838
23. H. Ikeda, and K. Murase Glial nitric oxide-mediated long-term presynaptic facilitation revealed by optical imaging in rat spinal dorsal horn J. Neurosci. 24 2004 9888 9896
24. H. Ikeda, M. Tsuda, K. Inoue, and K. Murase Long-term potentiation of neuronal excitation by neuron-glia interactions in the rat spinal dorsal horn Eur. J. Neurosci. 25 2007 1297 1306
25. 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 127 2007 161 172
26. L. Jasmin, A.R. Burkey, J.P. Card, and A.I. Basbaum Transneuronal labeling of a nociceptive pathway, the spino-(trigemino-)parabrachio-amygdaloid, in the rat J. Neurosci. 17 1997 3751 3765
27. G. Ji, and V. Neugebauer Pro- and anti-nociceptive effects of corticotropin-releasing factor (CRF) in central amygdala neurons are mediated through different receptors J. Neurophysiol. 99 2008 1201 1212
28. G. Ji, C. Horváth, and V. Neugebauer NR2B receptor blockade inhibits pain-related sensitization of amygdala neurons Mol. Pain 5 2009 21
29. R. Kajiwara, I. Takashima, Y. Mimura, M.P. Witter, and T. Iijima Amygdala input promotes spread of excitatory neural activity from perirhinal cortex to the entorhinal-hippocampal circuit J. Neurophysiol. 89 2003 2176 2184
30. R. Kajiwara, T. Tominaga, and I. Takashima Olfactory information converges in the amygdaloid cortex via the piriform and entorhinal cortices: observations in the guinea pig isolated whole-brain preparation Eur. J. Neurosci. 25 2007 3648 3658
31. W. Li, and V. Neugebauer Differential changes of group II and group III mGluR function in central amygdala neurons in a model of arthritic pain J. Neurophysiol. 96 2006 1803 1815
32. M. López de Armentia, and P. Sah Bidirectional synaptic plasticity at nociceptive afferents in the rat central amygdala J. Physiol. 581 2007 961 970
33. A receptor subtypes in the amygdala Eur. J. Neurosci. 20 2004 1281 1289
34. F.J. Monsma Jr., L.C. Mahan, L.D. McVittie, C.R. Gerfen, and D.R. Sibley Molecular cloning and expression of a D1 dopamine receptor linked to adenylyl cyclase activation Proc. Natl. Acad. Sci. U. S. A. 87 1990 6723 6727
35. A. Morozov, I.A. Muzzio, R. Bourtchouladze, N. Van-Strien, K. Lapidus, D. Yin, D.G. Winder, J.P. Adams, J.D. Sweatt, and E.R. Kandel Rap1 couples cAMP signaling to a distinct pool of p42/44MAPK regulating excitability, synaptic plasticity, learning, and memory Neuron 39 2003 309 325
36. V. Neugebauer, and W. Li Processing of nociceptive mechanical and thermal information in central amygdala neurons with knee-joint input J. Neurophysiol. 87 2002 103 112
37. V. Neugebauer, W. Li, G.C. Bird, G. Bhave, and R.W. Gereau IV 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
38. P.V. Nguyen, and N.H. Woo Regulation of hippocampal synaptic plasticity by cyclic AMP-dependent protein kinases Prog. Neurobiol. 71 2003 401 437
39. H. Onimaru, and I. Homma Spontaneous oscillatory burst activity in the piriform-amygdala region and its relation to in vitro respiratory activity in newborn rats Neuroscience 144 2007 387 394
40. E. Palazzo, Y. Fu, G. Ji, S. Maione, and V. Neugebauer Group III mGluR7 and mGluR8 in the amygdala differentially modulate nocifensive and affective pain behaviors Neuropharmacology 55 2008 537 545
41. A. Pitkänen, V. Savander, and J.E. LeDoux Organization of intra-amygdaloid circuitries in the rat: an emerging framework for understanding functions of the amygdala Trends Neurosci. 20 1997 517 523
42. P.A. Rodríguez Manzanares, N.A. Isoardi, H.F. Carrer, and V.A. Molina Previous stress facilitates fear memory, attenuates GABAergic inhibition, and increases synaptic plasticity in the rat basolateral amygdala J. Neurosci. 25 2005 8725 8734
43. K.B. Seamon, and J.W. Daly Forskolin: its biological and chemical properties Adv. Cyclic Nucleotide Protein Phosphor. Res. 20 1986 1 150
44. T. Sigurdsson, V. Doyère, C.K. Cain, and J.E. LeDoux Long-term potentiation in the amygdala: a cellular mechanism of fear learning and memory Neuropharmacology 52 2007 215 227
45. I. Song, and R.L. Huganir Regulation of AMPA receptors during synaptic plasticity Trends Neurosci. 25 2002 578 588
46. W.J. Tang, and A.G. Gilman Type-specific regulation of adenylyl cyclase by G protein beta gamma subunits Science 254 1991 1500 1503
47. C. Wang, W.A. Wilson, and S.D. Moore Role of NMDA, non-NMDA, and GABA receptors in signal propagation in the amygdala formation J. Neurophysiol. 86 2001 1422 1429