Postsynaptic induction and presynaptic expression of hippocampal long-term depression.

Long-term depression (LTD) is an activity-dependent decrease in synaptic efficacy that together with its counterpart, long-term potentiation, is thought to be an important cellular mechanism for learning and memory in the mammalian brain. The induction of LTD in hippocampal CA1 pyramidal neurons in neonatal rats is shown to depend on postsynaptic calcium ion entry through L-type voltage-gated calcium channels paired with the activation of metabotropic glutamate receptors. Although induced postsynaptically, LTD is due to a long-term decrease in transmitter release from presynaptic terminals. This suggests that LTD is likely to require the production of a retrograde messenger.

[1]  W. Abraham,et al.  NMDA‐dependent heterosynaptic long‐term depression in the dentate gyrus of anaesthetized rats , 1992, Synapse.

[2]  T. Teyler,et al.  The role of NMDA receptors in long-term potentiation (LTP) and depression (LTD) in rat visual cortex , 1991, Brain Research.

[3]  G. Collingridge,et al.  Induction of LTP in the hippocampus needs synaptic activation of glutamate metabotropic receptors , 1993, Nature.

[4]  Charles F. Stevens,et al.  Reversal of long-term potentiation by inhibitors of haem oxygenase , 1993, Nature.

[5]  E. Kandel,et al.  Imaging terminals of Aplysia sensory neurons demonstrates role of enhanced Ca2+ influx in presynaptic facilitation , 1993, Nature.

[6]  R. Nicoll,et al.  Postsynaptic contribution to long-term potentiation revealed by the analysis of miniature synaptic currents , 1992, Nature.

[7]  G. Böhme,et al.  Possible involvement of nitric oxide in long-term potentiation. , 1991, European journal of pharmacology.

[8]  E. Kandel,et al.  Nitric oxide and carbon monoxide produce activity-dependent long-term synaptic enhancement in hippocampus. , 1993, Science.

[9]  T. Bliss,et al.  A synaptic model of memory: long-term potentiation in the hippocampus , 1993, Nature.

[10]  M. Ito,et al.  Long-term depression. , 1989, Annual review of neuroscience.

[11]  D. Madison,et al.  A requirement for the intercellular messenger nitric oxide in long-term potentiation. , 1991, Science.

[12]  R. Nicoll,et al.  Modulation of synaptic transmission and long-term potentiation: effects on paired pulse facilitation and EPSC variance in the CA1 region of the hippocampus. , 1993, Journal of neurophysiology.

[13]  K. Stratford,et al.  Presynaptic release probability influences the locus of long-term potentiation , 1992, Nature.

[14]  R. Malenka,et al.  Mechanisms underlying induction of homosynaptic long-term depression in area CA1 of the hippocampus , 1992, Neuron.

[15]  SM Dudek,et al.  Bidirectional long-term modification of synaptic effectiveness in the adult and immature hippocampus , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[16]  F. Edwards LTP is a long term problem , 1991, Nature.

[17]  Jeffery R. Wickens,et al.  The involvement of L-type calcium channels in heterosynaptic long-term depression in the hippocampus , 1991, Neuroscience Letters.

[18]  M. Bear,et al.  Homosynaptic long-term depression in area CA1 of hippocampus and effects of N-methyl-D-aspartate receptor blockade. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[19]  T. Bliss,et al.  Arachidonic acid induces a long-term activity-dependent enhancement of synaptic transmission in the hippocampus , 1989, Nature.

[20]  C. Stevens,et al.  Presynaptic mechanism for long-term potentiation in the hippocampus , 1990, Nature.

[21]  Y. Yoshimura,et al.  Long-term depression but not potentiation is induced in Ca(2+)-chelated visual cortex neurons. , 1990, Neuroreport.

[22]  D. Faber,et al.  Quantal analysis and synaptic efficacy in the CNS , 1991, Trends in Neurosciences.

[23]  N. Kato Dependence of long-term depression on postsynaptic metabotropic glutamate receptors in visual cortex. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[24]  R. Malenka,et al.  Long-term depression: not so depressing after all. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[25]  W. Singer,et al.  Different voltage-dependent thresholds for inducing long-term depression and long-term potentiation in slices of rat visual cortex , 1990, Nature.

[26]  B. McNaughton,et al.  Long‐term enhancement of CA1 synaptic transmission is due to increased quantal size, not quantal content , 1991, Hippocampus.

[27]  M. Sakurai Calcium is an intracellular mediator of the climbing fiber in induction of cerebellar long-term depression. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[28]  R. Tsien,et al.  Presynaptic enhancement shown by whole-cell recordings of long-term potentiation in hippocampal slices , 1990, Nature.

[29]  T. Sejnowski,et al.  Associative long-term depression in the hippocampus induced by hebbian covariance , 1989, Nature.

[30]  G. Collingridge,et al.  Metabotropic glutamate receptors contribute to the induction of long-term depression in the CA1 region of the hippocampus. , 1993, European journal of pharmacology.

[31]  T. Sejnowski,et al.  2-Amino-3-phosphonopropionic acid, an inhibitor of glutamate-stimulated phosphoinositide turnover, blocks induction of homosynaptic long-term depression, but not potentiation, in rat hippocampus , 1991, Neuroscience Letters.

[32]  J. Wickens,et al.  Heterosynaptic long-term depression is facilitated by blockade of inhibition in area CA1 of the hippocampus , 1991, Brain Research.

[33]  R. Nicoll,et al.  Long-term potentiation is associated with increases in quantal content and quantal amplitude , 1992, Nature.

[34]  H. Lux,et al.  Inactivation and block of calcium channels by photo-released Ca2+ in dorsal root ganglion neurons. , 1988, Science.