Zinc differentially acts on components of long-term potentiation at hippocampal CA1 synapses

Brain Research

Volumn 1323, Issue , 2010, Pages 59-64

  Takeda, Atsushi ^a   Iwaki, Haruka ^a   Ando, Masaki ^a   Itagaki, Kosuke ^a   Suzuki, Miki ^a   Oku, Naoto ^a  

^a UNIVERSITY OF SHIZUOKA   (Japan)

Author keywords

Antagonist; Heavy metal; Hippocampal CA1; LTP; NMDA receptor; Zinc

Indexed keywords

2 AMINO 5 PHOSPHONOVALERIC ACID; HEAVY METAL; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; N METHYL DEXTRO ASPARTIC ACID RECEPTOR BLOCKING AGENT; ZINC; ZINC CHLORIDE;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; HIPPOCAMPUS; HIPPOCAMPUS POTENTIAL; LONG TERM POTENTIATION; MALE; NERVE STIMULATION; NONHUMAN; PRIORITY JOURNAL; RAT; SYNAPSE; SYNAPTIC INHIBITION;

ANALYSIS OF VARIANCE; ANIMALS; CA1 REGION, HIPPOCAMPAL; CHLORIDES; ELECTRIC STIMULATION; ELECTROPHYSIOLOGY; EXCITATORY POSTSYNAPTIC POTENTIALS; LONG-TERM POTENTIATION; MALE; RATS; RATS, WISTAR; RECEPTORS, N-METHYL-D-ASPARTATE; SYNAPSES; ZINC COMPOUNDS;

EID: 77953135668     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2010.01.085     Document Type: Article

References (52)

1. Aedo F., Delgado R., Wolff D., and Vergara C. Copper and zinc as modulators of neuronal excitability in a physiologically significant concentration range. Neurochem. Int. 50 (2007) 591-600
2. Artola A., von Frijtag J.C., Fermont P.C.J., Gispen W.H., Schrama L.H., Kamal A., and Spruijt B.M. Long-lasting modulation of the induction of LTD and LTP in rat hippocampal CA1 by behavioural stress and environmental enrichment. Eur. J. Neurosci. 23 (2006) 261-272
3. Ballabh P., Braun A., and Nedergaard M. The blood-brain barrier: an overview: structure, regulation, and clinical implications. Neurobiol. Dis. 16 (2004) 1-13
4. Bliss T.V.P., and Collingridge G.L. A synaptic model of memory: long-term potentiation in the hippocampus. Nature 361 (1993) 31-39
5. Bliss T.V.P., and Lomo T. Long-lasting potentiation of synaptic transmission in the dentate area of the anesthetized rabbit following stimulatin of the perforant path. J. Physiol. (Lond) 232 (1973) 331-356
6. Castelli L., Tanzi F., and Magistretti T.J. Cu2+, Co2+, and Mn2+ modify the gating kinetics of high-voltage-activated Ca2+ channels in rat palaeocortical neurons. J. Membrane Biol. 195 (2003) 121-136
7. Cavuş I., and Teyler T. Two forms of long-term potentiation in area CA1 activate different signal transduction cascades. J. Neurophysiol. 76 (1996) 3038-3047
8. Donaldson J. The physiopathologic significance of manganese in brain: its relation to schizophrenia and neurodegenerative disorders. NeuroToxicology 8 (1987) 451-462
9. Donaldson J., Cloutier T., Minnich J.L., and Barbeau A. Trace metals and biogenic amines in rat brain. Adv. Neurol. 5 (1974) 245-252
10. Doreulee N., Yanovsky Y., and Haas H.L. Suppresion of long-term potentiation in hippocampal slices by copper. Hippocampus 7 (1997) 666-669
11. Frederickson C.J. Neurobiology of zinc and zinc-containing neurons. Int. Rev. Neurobiol. 31 (1989) 145-238
12. Genuis S.J. Toxic causes of mental illness are overlooked. Neurotoxicology 29 (2008) 1147-1149
13. Grover L.M., and Teyler T.J. Two components of long-term potentiation induced by different patterns of afferent activation. Nature 347 (1990) 477-479
14. Guilarte T.R., and Chen M.K. Manganese inhibits NMDA receptor channel function: implications to psychiatric and cognitive effects. NeuroToxicology 28 (2007) 1147-1152
15. Hanig R.C., and Aprison M.H. Determination of calcium, copper, iron, magnesium, manganese, potassium, sodium, zinc, and chloride concentrations in several brain areas. Anal. Biochem. 21 (1967) 169-177
16. Harris E.W., and Cotman C.W. Long-term potentiation of guinea pig mossy fiber responses is not blocked by N-methyl d-aspartate antagonists. Neurosci. Lett. 70 (1986) 132-137
17. Hopt A., Korte S., Fink H., Panne U., Niessner R., Jahn R., Kretzschmar H., and Herms J. Methods for studying synaptosomal copper release. J. Neurosci. Methods 128 (2003) 159-172
18. Horning M.S., and Trombley P.O. Zinc and copper influence excitability of rat olfactory bulb neurons by multiple mechanisms. J. Neurophysiol. 86 (2001) 1652-1660
19. Itoh K., Sakata M., Watanabe M., Aikawa Y., and Fujii H. The entry of manganese ions into the brain is accelerated by the activation of N-methyl-d-aspartate receptors. Neuroscience 154 (2008) 732-740
20. Izumi Y., Auberson Y.P., and Zorumski C.F. Zinc modulates bidirectional hippocampal plasticity by effects on NMDA receptors. J. Neurosci. 26 (2006) 7181-7188
21. Jia Y., Jeng J.M., Sensi S.L., and Weiss J.H. Zn2+ currents are mediated by calcium-permeable AMPA/kainate channels in cultured murine hippocampal neurones. J. Physiol. 543 (2002) 35-48
22. Kostyuk P.G. Calcium channels in the cell membrane. Neurosci. Behav. Physiol. 16 (1986) 401-410
23. Li X.M., Gu Y., She J.Q., Zhu D.M., Niu Z.D., Wang M., Chen J.T., Sun L.G., and Ruan D.Y. Lead inhibited N-methyl-d-aspartate receptor-independent long-term potentiation involved ryanodine-sensitive calcium stores in rat hippocampal area CA1. Neuroscience 139 (2006) 463-473
24. Luscher C., Nicoll R.A., Malenka R.C., and Muller D. Synaptic plasticity and dynamic modulation of the postsynaptic membrane. Nat. Neurosci. 3 (2000) 545-550
25. Malenka R.C., and Bear M.F. LTP and LTD: an embarrassment of riches. Neuron 44 (2004) 5-21
26. Malenka R.C., and Nicoll R.A. Long-term potentiation-a decade of progress?. Science 285 (1999) 1870-1874
27. Marchi N., Cavaglia M., Fazio V., Bhudia S., Hallene K., and Janigro D. Peripheral markers of blood-brain barrier damage. Clin. Chim. Acta 342 (2004) 1-12
28. Mathie A., Sutton G.L., Clarke C.E., and Veale E.L. Zinc and copper: pharmacological probes and endogenous modulators of neuronal excitability. Pharmacol. Ther. 111 (2006) 567-583
29. Mayer M.I., and Armstrong N. Structure and function of glutamate receptor ion channels. Annu. Rev. Physiol. 66 (2004) 161-181
30. Mayer M.L., Vyklicky Jr. L., and Westbrook G.L. Modulation of excitatory amino acid receptors for group IIB metal cations in cultured mouse hippocampal neurons. J. Physiol. 415 (1989) 329-350
31. Minami A., Takeda A., Nishibaba N., Takefuta S., and Oku N. Cadmium toxicity in synaptic neurotransmission in the brain. Brain Res. 894 (2001) 336-339
32. Morgan S.L., and Teyler T.J. VDCCs and NMDARs underlie two forms of LTP in CA1 hippocampus in vivo. J. Neurophysiol. 82 (1999) 736-740
33. Nicoll R.A., and Malenka R.C. Expression mechanisms underlying NMDA receptor-dependent long-term potentiation. Ann. N. Y. Acad. Sci. 868 (1999) 515-525
34. Paoletti P., Vergnano A.M., Barbour B., and Casado M. Zinc at glutamatergic synapses. Neuroscience 158 (2009) 126-136
35. Prohaska J.R. Functions of trace elements in brain metabolism. Physiol. Rev. 67 (1987) 858-901
36. Sensi S.L., Canzoniero L.M.T., Yu S.P., Ying H.S., Koh J.Y., Kerchner G.A., and Choi D.W. Measurement of intracellular free zinc in living cortical neurons: routes of entry. J. Neurosci. 15 (1997) 9554-9564
37. Shankar S., Teyler T.J., and Robbins N. Aging differentially alters forms of long-term potentiation in rat hippocampal area CA1. J. Neurophysiol. 79 (1998) 334-341
38. Takeda A. Manganese action in brain function. Brain Res Rev 41 (2003) 79-87
39. Takeda A., and Tamano H. Insight into zinc signaling from dietary zinc deficiency. Brain Res. Rev. 62 (2009) 33-44
40. Takeda A., Ishiwatari S., and Okada S. In vivo stimulation-induced release of manganese in rat amygdala. Brain Res. 811 (1998) 147-151
41. Takeda A., Hirate M., Tamano H., Nishibaba D., and Oku N. Susceptibility to kainate-induced seizures under dietary zinc deficiency. J. Neurochem. 85 (2003) 1575-1580
42. Takeda A., Fuke S., Tsutsumi W., and Oku N. Negative modulation of presynaptic activity by zinc released from Schaffer collaterals. J. Neurosci. Res. 85 (2007) 3666-3672
43. Takeda A., Kanno S., Sakurada N., Ando M., and Oku N. Attenuation of hippocampal mossy fiber long-term potentiation by low micromolar concentrations of zinc. J. Neurosci. Res. 86 (2008) 2909-2911
44. Takeda A., Fuke S., Ando M., and Oku N. Positive modulation of long-term potentiation at hippocampal CA1 synapses by low micromolar concentrations of zinc. Neuroscience 158 (2009) 585-591
45. Takeda A., Sakurada N., Ando M., Kanno S., and Oku N. Facilitation of zinc influx via AMPA/kainate receptor activation in the hippocampus. Neurochem. Int. 55 (2009) 376-382
46. Tarohda T., Yamamoto M., and Amamo R. Regional distribution of manganese, iron, copper, and zinc in the rat brain during development. Anal. Bioanal. Chem. 380 (2004) 240-246
47. Vallee B.L., and Falchuk K.H. The biological basis of zinc physiology. Physiol. Rev. 73 (1993) 79-118
48. Vlachova V., Zemkova H., and Vyklicky Jr. L. Copper moduation of NMDA responses in mouse and rat cultured hippocampal neurons. Eur. J. Neurosci. 8 (1996) 2257-2264
49. Vogt K., Mellor J., Tong G., and Nicoll R. The actions of synaptically released zinc at hippocampal mossy fiber synapses. Neuron 26 (2000) 187-196
50. Weiser T., and Wienrich M. The effects of copper ions on glutamate receptors in cultured rat cortical neurons. Brain Res. 742 (1996) 211-218
51. Weiss J.H., Sensi S.L., and Koh J.Y. Zn(2+): a novel ionic mediator of neural injury in brain disease. Trends Pharmacol. Sci. 21 (2000) 395-401
52. Yokel R.A. Blood-brain barrier flux of aluminum, manganese, iron and other metals suspected to contribute to metal-induced neurodegeneration. J. Alzheimers Dis. 10 (2006) 223-253