Effects of aniracetam after LTP induction are suggestive of interactions on the kinetics of the AMPA receptor channel

Brain Research

Volumn 788, Issue 1-2, 1998, Pages 269-286

  Kolta, Arlette ^a   Lynch, Gary ^a   Ambros Ingerson, José ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Channel kinetics; Decay time constant; Glutamate receptor model; Hippocampus

Indexed keywords

2 HYDROXYSACLOFEN; 4 AMINOBUTYRIC ACID RECEPTOR BLOCKING AGENT; AMPA RECEPTOR; ANIRACETAM; PICROTOXIN; TETRODOTOXIN;

ANIMAL TISSUE; ARTICLE; BRAIN SLICE; CONTROLLED STUDY; EXCITATORY POSTSYNAPTIC POTENTIAL; HIPPOCAMPUS; LONG TERM POTENTIATION; NONHUMAN; PRIORITY JOURNAL; RAT; WAVEFORM;

EID: 0032579794     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-8993(97)01444-3     Document Type: Article

References (69)

1. Ambros-Ingerson J., Larson J., Xiao P., Lynch G. LTP changes the waveform of synaptic responses. Synapse. 9:1991;314-316.
2. Ambros-Ingerson J., Lynch G. Channel gating kinetics and synaptic efficacy: a hypothesis for the expression of long-term potentiation. Proc. Natl. Acad. Sci. U.S.A. 90:1993;7903-7907.
3. Ambros-Ingerson J., Xiao P., Larson J., Lynch G. Waveform analysis suggests that LTP alters the kinetics of synaptic receptor channels. Brain Res. 620:1993;237-244.
4. Arai A., Kessler M., Rogers G., Lynch G. Effects of a memory-enhancing drug on DL-α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor currents and synaptic transmission in hippocampus. J. Pharmacol. Exp. Ther. 278:1996;627-638.
5. Arai A., Larson J., Lynch G. Anoxia reveals a vulnerable period in the development of long-term potentiation. Brain Res. 511:1990;353-357.
6. Arai A., Silberg J., Kessler M., Lynch G. Effect of thiocyanate on AMPA receptor mediated responses in excised patches and hippocampal slices. Neurosci. 66:1995;815-827.
7. Asztely F., Gustafsson B. Dissociation between long-term potentiation and associated changes in field EPSP waveform in the hippocampal CA1 region - an in vitro study in guinea pig brain slices. Hippocampus. 4:1994;148-156.
8. Asztely F., Hanse E., Wigstrom H., Gustafsson B. Aniracetam-evoked potentiation does not interact with long-term potentiation in the CA1 region of the hippocampus. Synapse. 11:1992;342-345.
9. Barrionuevo G., Schottler F., Lynch G. The effects of repetitive low frequency stimulation on control and 'potentiated' synaptic responses in the hippocampus. Life Sci. 27:1980;2385-2391.
10. Baskys A., Carlen P.L., Wojtowicz J.M. Long-term potentiation of synaptic responses in the rat dentate gyrus is due to increased quantal content. Neurosci. Lett. 127:1992;169-172.
11. Bekkers J.M., Stevens C.F. NMDA and non-NMDA receptors are co-localized at individual excitatory synapses in cultured rat hippocampus. Nature. 341:1989;230-233.
12. Bekkers J.M., Stevens C.F. Presynaptic mechanisms for long-term potentiation in the hippocampus. Nature. 346:1990;724-729.
13. Bliss T.V.P., Collingridge G.L. A synaptic model of memory: long-term potentiation in the hippocampus. Nature. 361:1993;31-39.
14. Bliss T.V.P., Lømo T. Long lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path. J. Physiol. (London). 332:1973;331-356.
15. T.V.P. Bliss, M.A. Lynch, Long-term potentiation of synaptic transmission in the hippocampus: Properties and mechanisms, in: P.W. Landfield, S.A. Deadwyler (Eds.), Long-Term Potentiation: from Biophysics to Behavior, Alan R. Liss, New York, 1988, pp. 3-72.
16. Clements J.D., Lester R.A., Tong G., Jahr C.E., Westbrook G.L. The time course of glutamate in the synaptic cleft. Science. 258:1992;1498-1501.
17. Colquhoun D., Jonas P., Sakmann B. Action of brief pulses of glutamate on AMPA/kainate receptors in patches from different neurones of rat hippocampal slices. J. Physiol. 458:1992;261-287.
18. Davies S., Lester R., Reymann K., Collingridge G. Temporally distinct pre- and postsynaptic mechanisms maintain long-term potentiation. Nature. 338:1989;500-503.
19. Diamond J.S., Jahr C.E. Asynchronous release of synaptic vesicles determines the time course of the AMPA receptor-mediated EPSC. Neuron. 15:1995;1097-1107.
20. Foster T.C., McNaughton B.L. Long-term synaptic enhancement in CA1 is due to increased quantal size, not quantal content. Hippocampus. 1:1991;79-91.
21. Hemart N., Daniel H., Jaillard D., Crepel F. Properties of glutamate receptors are modified during long-term depression in rat cerebellar Purkinje cells. Neurosci. Res. 19:1994;213-221.
22. Hollmann M., O'Shea-Greenfield A., Rogers S.W., Heinemann S. Cloning by functional expression of a member of the glutamate receptor family. Nature. 342:1989;643-648.
23. Honoré T., Drejer J., Nielsen E.O., Nielsen M. Non-NMDA glutamate receptor antagonist 3H-CNQX binds with equal affinity to two agonist states of quisqualate receptors. Biochem. Pharmacol. 38:1989;3207-3212.
24. Isaac J.T., Hjelmstad G.O., Nicoll R.A., Malenka R.C. Long-term potentiation at single fiber inputs to hippocampal CA1 pyramidal cells. Proc. Natl. Acad. Sci. U.S.A. 93:1996;8710-8715.
25. Isaacson J.S., Nicoll R.A. Aniracetam reduces glutamate receptor desensitization and slows the decay of fast excitatory synaptic currents in the hippocampus. Proc. Natl. Acad. Sci. U.S.A. 88:1991;10936-10940.
26. Isaacson J.S., Nicoll R.A. The uptake inhibitor L-trans-PDC enhances responses to glutamate but fails to alter the kinetics of excitatory synaptic currents in the hippocampus. J. Neurophysiol. 70:1993;2187-2191.
27. Ito I., Tanabe S., Khoda A., Sugiyama H. Allosteric potentiation of quisqualate receptors by a nootropic drug aniracetam. J. Physiol. (London). 424:1990;533-543.
28. Jonas P., Sakmann B. Glutamate receptor channels in isolated patches from CA1 and CA3 pyramidal cells or rat hippocampal slices. J. Physiol. 455:1992;143-171.
29. Jung M.W., Larson J., Lynch G. Evidence that changes in spine neck resistance are not responsible for expression of LTP. Synapse. 7:1991;216-220.
30. Katz B., Thesleff S. A study of the desensitization produced by acetylcholine at the motor end-plate. J. Physiol. 138:1957;63-80.
31. Kauer J.A., Malenka R.C., Nicoll R.A. A persistent postsynaptic modification mediates long-term potentiation in the hippocampus. Neuron. 1:1988;911-917.
32. Keinänen K., Wisden W., Sommer B., Werner P., Herb A., Verdoorn T.A., Sakmann B., Seeburg P.H. A family of AMPA-selective glutamate receptors. Science. 249:1990;556-560.
33. Kolta A., Ambros-Ingerson J., Larson J., Lynch G. Interaction between aniracetam and LTP in 'disinhibited' slices. Soc. Neurosci. Abstr. 19:1993;374.6.
34. Kolta A., Ambros-Ingerson J., Lynch G. Early and late components of AMPA-receptor mediated field potentials in hippocampal slices. Brain Res. 737:1996;133-145.
35. Kolta A., Larson J., Lynch G. Comparison of long-term potentiation in the proximal versus distal stratum radiatum of hippocampal field CA1. Neuroscience. 66:1995;277-289.
36. Kuhnt U., Hess G., Voronin L.L. Statistical analysis of long-term potentiation of large excitatory postsynaptic potentials recorded in guinea pig hippocampal slices: binomial model. Exp. Brain Res. 89:1992;265-274.
37. Kullmann D.M., Nicoll R.A. Long-term potentiation is associated with increases in quantal content and quantal amplitude. Nature. 347:1992;240-244.
38. Larkman A., Hannay T., Stratford K., Jack J. Presynaptic release probability influences the locus of long-term potentiation. Nature. 360:1992;70-73.
39. Larson J., Le L.T., Hall R., Lynch G. Effects of cyclothiazide on synaptic responses in slices of adult and neonatal rat hippocampus. NeuroReport. 5:1994;389-392.
40. Larson J., Lynch G. A test of the spine resistance hypothesis of LTP expression. Brain Res. 538:1991;347-350.
41. Larson J., Wong D., Lynch G. Patterned stimulation at the theta frequency is optimal for induction of long-term potentiation. Brain Res. 368:1986;347-350.
42. Larson J., Xiao P., Lynch G. Reversal of LTP by theta frequency stimulation. Brain Res. 600:1993;97-102.
43. Liao D., Jones A., Malinow R. Direct measurement of quantal changes underlying long-term potentiation in CA1 hippocampus. Neuron. 9:1992;1089-1097.
44. Lynch G., Baudry M. The biochemistry of memory: a new and specific hypothesis. Science. 224:1984;1057-1063.
45. Magleby K.L., Stevens C.F. A quantitative description of end-plate currents. J. Physiol. 223:1972;173-197.
46. Malinow R. Transmission between pairs of hippocampal slice neurons: Quantal levels, oscillations, and LTP. Nature. 252:1991;722-724.
47. Malinow R., Tsien R.W. Presynaptic enhancement shown by whole cell recordings of long-term potentiation in hippocampal slices. Nature. 346:1990;177-180.
48. Manabe T., Renner P., Nicoll R.A. Postsynaptic contribution to long-term potentiation revealed by the analysis of miniature synaptic currents. Nature. 355:1992;50-55.
49. Marquardt D.W. An algorithm for least-squares estimation of nonlinear parameters. J. Soc. Indust. Appl. Math. 11:1963;431-441.
50. Muller D., Joly M., Lynch G. Contributions of quisqualate and NMDA receptors to the induction and expression of LTP. Science. 242:1988;1694-1697.
51. Muller D., Lynch G. Long-term potentiation differentially affects two components of synaptic receptors in hippocampus. Proc. Natl. Acad. Sci. U.S.A. 85:1988;9346-9350.
52. Oliet S.H., Malenka R.C., Nicoll R.A. Bidirectional control of quantal size by synaptic activity in the hippocampus. Science. 271:1996;1294-1297.
53. Partin K.M., Fleck M.W., Mayer M.L. AMPA receptor flip/flop mutants affecting deactivation, desensitization, and modulation by cyclothiazide, aniracetam, and thiocyanate. J. Neurosci. 16:1996;6634-6647.
54. Patneau D.K., Mayer M.L. Kinetic analysis of interactions between kainate and AMPA: Evidence for activation of a single receptor in mouse hippocampal neurons. Neuron. 6:1991;785-798.
55. W.H. Press, B.P. Flannery, S.A. Teukolsky, W.T. Vetterling, Numerical Recipes, Cambridge Univ. Press, New York, 1989.
56. W. Rall, Dendritic spines and synaptic potency, in: R. Porter (Ed.), Studies in Neurophysiology, Cambridge Univ. Press, Cambridge, MA, 1978, pp. 203-209.
57. Sarantis M., Ballerini L., Miller B., Silver R.A., Edwards M., Attwell D. Glutamate uptake from the synaptic cleft does not shape the decay of the non-NMDA component of the synaptic current. Neuron. 11:1993;541-549.
58. Staubli U., Ambros-Ingerson J., Lynch G. Receptor changes and LTP: an analysis using aniracetam, a drug that modifies glutamate (AMPA) receptors. Hippocampus. 2:1992;49-58.
59. Staubli U., Chun D. Factors regulating the reversibility of long-term potentiation. J. Neurosci. 16:1996;853-860.
60. Staubli U., Kessler M., Lynch G. Aniracetam has proportionately smaller effects on synapses expressing long-term potentiation: evidence that receptor changes subserve LTP. Psychobiology. 18:1990;377-381.
61. Staubli U., Lynch G. Stable depression of potentiated synaptic responses in the hippocampus with 1-5 Hz stimulation. Brain Res. 513:1990;113-118.
62. Stricker C., Field A.C., Redman S.J. Changes in quantal parameters of EPSCs in rat CA1 neurones in vitro after the induction of long-term potentiation. J. Physiol. (London). 490:1996;443-454.
63. Tang C.-M., Shi Q.-Y., Katchman A., Lynch G. Aniracetam modulates the time course of fast excitatory synaptic currents and glutamate channel kinetics. Science. 254:1991;288-290.
64. Tsuzuki K., Takeuchi T., Ozawa S. Agonist- and subunit-dependent potentiation of glutamate receptors by a nootropic drug aniracetam. Mol. Brain Res. 16:1992;105-110.
65. Vanderklish P., Neve R., Bahr B.A., Arai A., Hennegriff M., Larson J., Lynch G. Translational suppression of a glutamate receptor subunit impairs long-term potentiation. Synapse. 12:1992;333-337.
66. Vyklicky L. Jr., Patneau D.K., Mayer M.L. Modulation of excitatory synaptic transmission by drugs that reduce desensitization at AMPA/kainate receptors. Neuron. 7:1991;971-984.
67. Xiao P., Staubli U., Kessler M., Lynch G. Selective effects of aniracetam across receptor types and forms of synaptic facilitation in hippocampus. Hippocampus. 1:1991;373-390.
68. Xie X., Liaw J.-S., Baudry M., Berger T. Novel expression mechanism for synaptic potentiation: Alignment of presynaptic release site and postsynaptic receptor. Proc. Natl. Acad. Sci. U.S.A. 94:1997;6983-6988.
69. Zucker R.S. Changes in the statistics of transmitter release during facilitation. J. Physiol. 229:1973;787-810.