Recruitment of long-lasting and protein kinase A-dependent long-term potentiation in the CA1 region of hippocampus requires repeated tetanization.

To study how the late phase of long-term potentiation (LTP) in hippocampus arises, we examined the resulting LTP for its time course and its dependence on protein synthesis and different second-messenger kinases by applying various conditioning tetani. We find that one high-frequency train (100 Hz) produces a form of LTP that lasts longer than 1 hr but less than 3 hr (the early phase of LTP, or E-LTP). It is blocked by inhibitors of calcium/calmodulin kinase II (Cam kinase II) but is not affected by an inhibitor of cAMP-dependent protein kinase [protein kinase A (PKA) and the protein synthesis inhibitor anisomycin] nor is it occluded by the cAMP activator forskolin. In contrast, when three high-frequency trains are used, the resulting potentiation persists for at least 6-10 hr. The L-LTP induced by three trains differs from the E-LTP in that it requires new protein synthesis, is blocked by an inhibitor of cAMP-dependent protein kinase, and is occluded by forskolin. These results indicate that the two mechanistically distinctive forms of LTP, a transient, early component (E-LTP) and a more enduring form (L-LTP), can be recruited selectively by changing the number of conditioning tetanic trains. Repeated tetani induce a PKA and protein synthesis-dependent late component that adds to the amplitude and duration of the potentiation induced by a single tetanus.

[1]  Charles F. Stevens,et al.  Modulation of synaptic efficacy in field CA1 of the rat hippocampus by forskolin , 1992, Brain Research.

[2]  Robert C. Malenka,et al.  Postsynaptic factors control the duration of synaptic enhancement in area CA1 of the hippocampus , 1991, Neuron.

[3]  B. Gustafsson,et al.  Postsynaptic, but not presynaptic, activity controls the early time course of long-term potentiation in the dentate gyrus , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[4]  C F Stevens,et al.  Increased transmitter release at excitatory synapses produced by direct activation of adenylate cyclase in rat hippocampal slices , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

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

[6]  R. Huganir,et al.  Functional modulation of GABAA receptors by cAMP-dependent protein phosphorylation. , 1992, Science.

[7]  K. Reymann,et al.  Protein kinase A inhibitors prevent the maintenance of hippocampal long-term potentiation. , 1993, Neuroreport.

[8]  E. Kandel,et al.  Serotonin produces long-term changes in the excitability of Aplysia sensory neurons in culture that depend on new protein synthesis , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[9]  E R Kandel,et al.  Inhibitor of protein synthesis blocks long-term behavioral sensitization in the isolated gill-withdrawal reflex of Aplysia. , 1989, Journal of neurobiology.

[10]  G. Audesirk,et al.  Effects of selective inhibition of protein kinase C, cyclic AMP-dependent protein kinase, and Ca2+-calmodulin-dependent protein kinase on neurite development in cultured rat hippocampal neurons , 1993, International Journal of Developmental Neuroscience.

[11]  E R Kandel,et al.  A critical period for macromolecular synthesis in long-term heterosynaptic facilitation in Aplysia. , 1986, Science.

[12]  L. Squire Memory and the hippocampus: a synthesis from findings with rats, monkeys, and humans. , 1992, Psychological review.

[13]  E. Kandel,et al.  Protein synthesis during acquisition of long-term facilitation is needed for the persistent loss of regulatory subunits of the Aplysia cAMP-dependent protein kinase. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[14]  R. Tsien,et al.  Inhibition of postsynaptic PKC or CaMKII blocks induction but not expression of LTP. , 1989, Science.

[15]  D. Johnston,et al.  N-methyl-D-aspartate receptor activation increases cAMP levels and voltage-gated Ca2+ channel activity in area CA1 of hippocampus. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[16]  P. Greengard,et al.  Enhancement of the glutamate response by cAMP-dependent protein kinase in hippocampal neurons , 1991, Science.

[17]  H. Matthies,et al.  In search of cellular mechanisms of memory , 1989, Progress in Neurobiology.

[18]  Graham L. Collingridge,et al.  Temporally distinct pre- and post-synaptic mechanisms maintain long-term potentiation , 1989, Nature.

[19]  E. Kandel,et al.  Long-term potentiation in the hippocampus is blocked by tyrosine kinase inhibitors , 1991, Nature.

[20]  E. Kandel,et al.  Effects of cAMP simulate a late stage of LTP in hippocampal CA1 neurons. , 1993, Science.

[21]  W N Frost,et al.  Monosynaptic connections made by the sensory neurons of the gill- and siphon-withdrawal reflex in Aplysia participate in the storage of long-term memory for sensitization. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[22]  M. Salter,et al.  Regulation of kainate receptors by cAMP-dependent protein kinase and phosphatases , 1991, Science.

[23]  S. Nakanishi,et al.  Potent and preferential inhibition of Ca2+/calmodulin-dependent protein kinase II by K252a and its derivative, KT5926. , 1991, Biochemical and biophysical research communications.

[24]  R. Nicoll,et al.  An essential role for postsynaptic calmodulin and protein kinase activity in long-term potentiation , 1989, Nature.