Altered hippocampal long-term potentiation after peripheral nerve injury in mice

European Journal of Pharmacology

Volumn 574, Issue 2-3, 2007, Pages 127-132

  Kodama, Daisuke ^a   Ono, Hideki ^a   Tanabe, Mitsuo ^a  

^a NAGOYA CITY UNIVERSITY   (Japan)

Author keywords

Adrenoceptor; Hippocampus; Long term potentiation; Neuropathic pain; Synaptic transmission

Indexed keywords

BETA ADRENERGIC RECEPTOR BLOCKING AGENT; BETA ADRENERGIC RECEPTOR STIMULATING AGENT; ISOPRENALINE; PROPRANOLOL;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BRAIN SLICE; CHRONIC PAIN; COGNITIVE DEFECT; CONTROLLED STUDY; HIPPOCAMPUS; LEARNING; LONG TERM DEPRESSION; LONG TERM POTENTIATION; MALE; MEMORY; MOUSE; NERVE CELL PLASTICITY; NEUROPATHIC PAIN; NONHUMAN; PERIPHERAL NERVE INJURY; PRIORITY JOURNAL; SCIATIC NERVE; SCIATIC NEUROPATHY; SYNAPTIC TRANSMISSION; TETANUS;

ANIMALS; CHRONIC DISEASE; HIPPOCAMPUS; LONG-TERM POTENTIATION; MALE; MICE; NEURONAL PLASTICITY; PAIN; RECEPTORS, ADRENERGIC, BETA; SCIATIC NEUROPATHY; SYNAPTIC TRANSMISSION;

EID: 35348812500     PISSN: 00142999     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejphar.2007.07.054     Document Type: Article

References (40)

1. Argoff C.E. The existence of neuropathic pain, sleep, and psychiatric disorders: a novel treatment approach. Clin. J. Pain 23 (2007) 15-22
2. Blackburn-Munro G., and Blackburn-Munro R.E. Chronic pain, chronic stress and depression: coincidence or consequence?. J. Neuroendocrinol. 13 (2001) 1009-1023
3. Brankack J., and Buzsaki G. Hippocampal responses evoked by tooth pulp and acoustic stimulation: depth profiles and effect of behavior. Brain Res. 378 (1986) 303-314
4. Carrasco G.A., and Van de Kar L.D. Neuroendocrine pharmacology of stress. Eur. J. Pharmacol. 463 (2003) 235-272
5. 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
6. Covey W.C., Ignatowski T.A., Knight P.R., and Spengler R.N. Brain-derived TNFα: involvement in neuropathic changes implicated in the conscious perception of persistent pain. Brain Res. 859 (2000) 113-122
7. Dixon W.J. Efficient analysis of experimental observation. Annu. Rev. Pharmacol. Toxicol. 20 (1980) 441-462
8. Duric V., and McCarson K.E. Hippocampal neurokinin-1 receptor and brain-derived neurotrophic factor gene expression is decreased in rat models of pain and stress. Neuroscience 133 (2005) 999-1006
9. 3H] cyclic AMP binding to protein kinase (PKA), cyclic AMP-dependent PKA activity, and protein levels of selective regulatory and catalytic subunit isoforms of PKA in rat brain. J. Pharmacol. Exp. Ther. 294 (2000) 103-116
10. Eccleston C. Chronic pain and attention: a cognitive approach. Br. J. Clin. Psychol. 33 (1994) 535-547
11. Gelinas J.N., and Nguyen P.V. β-adrenergic receptor activation facilitates induction of a protein synthesis-dependent late phase of long-term potentiation. J. Neurosci. 25 (2005) 3294-3303
12. Guo N.N., and Li B.M. Cellular and subcellular distributions of β1- and β2-adrenoceptors in the CA1 and CA3 regions of the rat hippocampus. Neuroscience 146 (2007) 298-305
13. Hillman K.L., Knudson C.A., Carr P.A., Doze V.A., and Porter J.E. Adrenergic receptor characterization of CA1 hippocampal neurons using real time single cell RT-PCR. Mol. Brain Res. 139 (2005) 267-276
14. Holden J.E., and Pizzi J.A. The challenge of chronic pain. Adv. Drug Deliv. Rev. 55 (2003) 935-948
15. Jamison R.N., Sbrocco T., and Parris W.C. The influence of problems with concentration and memory on emotional distress and daily activities in chronic pain patients. Int. J. Psychiatry Med. 18 (1988) 183-191
16. Khanna S., and Sinclair J.G. Noxious stimuli produce prolonged changes in the CA1 region of the rat hippocampus. Pain 39 (1989) 337-343
17. Khanna S., Chang L.S., Jiang F., and Koh H.C. Nociception-driven decreased induction of Fos protein in ventral hippocampus field CA1 of the rat. Brain Res. 1004 (2004) 167-176
18. Kloet E.R., Vreugdenhil E., Oitzl M.S., and Joëls M. Brain corticosteroid receptor balance in health and disease. Endocr. Rev. 19 (1998) 269-301
19. Livengood J.M., Schnurr R.F., and Porzelius J. Effects of memory impairment on treatment of chronic pain. American Pain Society, 14th Annual Scientific Meeting. Los Angeles, CA (1995)
20. Luine V., Villegas M., Martinez C., and McEwen B.S. Repeated stress causes reversible impairments of spatial memory performance. Brain Res. 639 (1994) 167-170
21. Martin S.J., Grimwood P.D., and Morris R.G.M. Synaptic plasticity and memory: an evaluation of the hypothesis. Annu. Rev. Neurosci. 23 (2000) 649-711
22. Nakao K., Ikegaya Y., Yamada M.K., Nishiyama N., and Matsuki N. Hippocampal long-term depression as an index of spatial working memory. Eur. J. Neurosci. 16 (2002) 970-974
23. Pacak K., Armando I., Fukuhara K., Kvetnansky R., Palkovits M., Kopin I.J., and Goldstein D.S. Noradrenergic activation in the paraventricular nucleus during acute and chronic immobilization stress in rats: an in vivo microdialysis study. Brain Res. 589 (1992) 91-96
24. Pavlides C., Ogawa S., Kimura A., and McEwen B.S. Role of adrenal steroid mineralocorticoid receptors in long-term potentiation in the CA1 field of hippocampal slices. Brain Res. 738 (1996) 229-235
25. Pearse D., Mirza A., and Leah J. Jun, Fos and Krox in the hippocampus after noxious stimulation: simultaneous-input-dependent expression and nuclear speckling. Brain Res. 894 (2001) 193-208
26. 2-adrenoceptor sensitivity in the rat brain. Stress 6 (2003) 281-287
27. 2-adrenergic receptors in rat brain. Proc. Natl. Acad. Sci. U. S. A. 81 (1984) 1585-1589
28. Ramos B.P., Colgan L., Nou E., Ovadia S., Wilson S.R., and Arnsten A.F.T. The beta-1 adrenergic antagonist, betaxolol, improves working memory performance in rats and monkeys. Biol. Psychiatry 58 (2005) 894-900
29. Schimanski L.A., Ali D.W., Baker G.B., and Nguyen P.V. Impaired hippocampal LTP in inbred mouse strains can be rescued by β-adrenergic receptor activation. Eur. J. Neurosci. 25 (2007) 1589-1598
30. Schnurr R.F., and MacDonald M.R. Memory complaints in chronic pain. Clin. J. Pain 11 (1995) 103-111
31. Seltzer Z., Dubner R., and Shir Y. A novel behavioral model of neuropathic pain disorders produced in rats by partial sciatic nerve injury. Pain 43 (1990) 205-218
32. Shors T.J., Seib T.B., Levine S., and Thompson R.F. Inescapable versus escapable shock modulates long-term potentiation in the rat hippocampus. Science 244 (1989) 224-226
33. Sinclair J.G., and Lo G.F. Morphine, but not atropine, blocks nociceptor-driven activity in rat dorsal hippocampal neurons. Neurosci. Lett. 68 (1986) 47-50
34. Thomas M.J., Moody T.D., Makhinson M., and O'Dell T.J. Activity-dependent beta-adrenergic modulation of low frequency stimulation induced LTP in the hippocampal CA1 region. Neuron 17 (1996) 475-482
35. Ulrich-Lai Y.M., Xie W., Meij J.T.A., Dolgas C.M., Yu L., and Herman J.P. Limbic and HPA axis function in an animal model of chronic neuropathic pain. Physiol. Behav. 88 (2006) 67-76
36. Winder D.G., Martin K.C., Muzzio I.A., Rohrer D., Chruscinski A., Kobilka B., and Kandel E.R. ERK plays a regulatory role in induction of LTP by theta frequency stimulation and its modulation by β-adrenergic receptors. Neuron 24 (1999) 715-726
37. Wright R.L., Lightner E.N., Harman J.S., Meijer O.C., and Conrad C.D. Attenuating corticosterone levels on the day of memory assessment prevents chronic stress-induced impairments in spatial memory. Eur. J. Neurosci. 24 (2006) 595-605
38. Yang H.W., Lin Y.W., Yen C.D., and Min M.Y. Change in bi-directional plasticity at CA1 synapses in hippocampal slices taken from 6-hydroxydopamine-treated rats: the role of endogenous norepinephrine. Eur. J. Neurosci. 16 (2002) 1117-1128
39. Yang C.H., Huang C.C., and Hsu K.S. Behavioral stress modifies hippocampal synaptic plasticity through corticosterone-induced sustained extracellular signal-regulated kinase/mitogen-activated protein kinase activation. J. Neurosci. 24 (2004) 11029-11034
40. Zheng H., Yang Q., and Xu C.T. Effects of chronic stress and phenytoin on the long-term potentiation (LTP) in rat hippocampal CA1 region. Acta Biochim. Biophys. Sin. 36 (2004) 375-378