Long-term potentiation phenomena in the rat limbic forebrain

Long-term potentiation (LTP) phenomena were investigated in several limbic forebrain pathways. With the possible exception of the lateral olfactory tract, LTP could be produced in all pathways tested. LTP effects tended to increase as the stimulation site moved caudally along the pyriform lobe. The largest effects were produced by stimulation of pathways into and out of the hippocampus. Target sites also differed, with the hippocampal sites showing the strongest and longest lasting LTP effects. The time course of LTP appeared to be best fitted by the sum of two exponential curves with time constants of about 1.5 h and 5 days respectively. We also looked at the potentiation effects produced by repeated epileptogenic (kindling) stimulations, and the effect of this potentiation on subsequent tests of short-term and long-term potentiation. In most cases, the short-term effects, and the first component of the LTP effect, were still intact after kindling. The longest lasting component, however, could no longer be produced with either amygdala or perforant path stimulation. This result indicates that the potentiation produced by kindling may be based upon the same mechanism as the LTP effect.

[1]  R. Racine,et al.  Post-activation potentiation and the kindling phenomenon. , 1975, Electroencephalography and clinical neurophysiology.

[2]  B. McNaughton,et al.  Synaptic enhancement in fascia dentata: Cooperativity among coactive afferents , 1978, Brain Research.

[3]  A Mallart,et al.  An analysis of facilitation of transmitter release at the neuromuscular junction of the frog , 1967, The Journal of physiology.

[4]  Michel Baudry,et al.  Hypothesis regarding the cellular mechanisms responsible for long-term synaptic potentiation in the hippocampus , 1980, Experimental Neurology.

[5]  R. Miledi,et al.  Delayed effects of peripheral severance of afferent nerve fibres on the efficacy of their central synapses , 1959, The Journal of physiology.

[6]  D. P. Lloyd The origin and nature of ganglion after‐potentials , 1939, The Journal of physiology.

[7]  C. Stevens,et al.  The kinetics of transmitter release at the frog neuromuscular junction , 1972, The Journal of physiology.

[8]  P. Schwartzkroin,et al.  Long-lasting facilitation of a synaptic potential following tetanization in thein vitro hippocampal slice , 1975, Brain Research.

[9]  J. Cooke,et al.  Cumulative and persistent effects of nerve terminal depolarization on transmitter release , 1973, The Journal of physiology.

[10]  J. Eccles,et al.  The effects of disuse and of activity on mammalian spinal reflexes , 1953, The Journal of physiology.

[11]  T. E. Boyd RECOVERY OF THE TONGUE FROM CURARE PARALYSIS, FOLLOWING PROLONGED STIMULATION OF THE HYPOGLOSSAL NERVE , 1932 .

[12]  R. Racine Kindling: the first decade. , 1978, Neurosurgery.

[13]  B. Katz,et al.  Quantal components of the end‐plate potential , 1954, The Journal of physiology.

[14]  K. Magleby The effect of tetanic and post‐tetanic potentiation on facilitation of transmitter release at the frog neuromuscular junction , 1973, The Journal of physiology.

[15]  G. Buzsáki,et al.  Commissural projection to the dentate gyrus of the rat: evidence for feed-forward inhibition , 1981, Brain Research.

[16]  K L Magleby,et al.  The effect of repetitive stimulation on facilitation of transmitter release at the frog neuromuscular junction , 1973, The Journal of physiology.

[17]  L. Pellegrino,et al.  stereotaxic atlas of the rat brain , 1967 .

[18]  K. Magleby,et al.  A dual effect of repetitive stimulation on post‐tetanic potentiation of transmitter release at the frog neuromuscular junction. , 1975, The Journal of physiology.

[19]  D. Hebb,et al.  The Nature of Thought : Essays in Honor of D.o. Hebb , 1980 .

[20]  J. Zengel,et al.  Stimulation‐induced factors which affect augmentation and potentiation of trasmitter release at the neuromuscular junction. , 1976, The Journal of physiology.

[21]  S. Siegel,et al.  Nonparametric Statistics for the Behavioral Sciences , 2022, The SAGE Encyclopedia of Research Design.

[22]  B. L. McNaughton,et al.  Evidence for two physiologically distinct perforant pathways to the fascia dentata , 1980, Brain Research.

[23]  G. Lynch,et al.  Synaptic phosphoproteins: specific changes after repetitive stimulation of the hippocampal slice. , 1979, Science.

[24]  R. Racine,et al.  A Further Investigation into the Mechanisms Underlying the Kindling Phenomenon , 1978 .

[25]  G. Lynch,et al.  Trifluoperazine inhibits hippocampal long-term potentiation and the phosphorylation of a 40,000 dalton protein , 1980, Neuroscience Letters.

[26]  R. Douglas,et al.  Long-term potentiation of the perforant path-granule cell synapse in the rat hippocampus , 1975, Brain Research.

[27]  B. Meldrum,et al.  Systemic factors and epileptic brain damage. Prolonged seizures in paralyzed, artificially ventilated baboons. , 1973, Archives of neurology.

[28]  T. H. Brown,et al.  Electrotonic structure and specific membrane properties of mouse dorsal root ganglion neurons. , 1981, Journal of neurophysiology.

[29]  C. Yamamoto,et al.  Long-term potentiation in thin hippocampal sections studied by intracellular and extracellular recordings , 1978, Experimental Neurology.

[30]  K L Magleby,et al.  Long term changes in augmentation, potentiation, and depression of transmitter release as a function of repeated synaptic activity at the frog neuromuscular junction. , 1976, The Journal of physiology.

[31]  A. Mauro,et al.  Effects of calcium and magnesium on the frequency of miniature end‐plate potentials during prolonged tetanization , 1971, The Journal of physiology.

[32]  K L Magleby,et al.  A quantitative description of tetanic and post‐tetanic potentiation of transmitter release at the frog neuromuscular junction. , 1975, The Journal of physiology.

[33]  S. Younkin,et al.  An analysis of the role of calcium in facilitation at the frog neuromuscular junction , 1974, The Journal of physiology.

[34]  P. Andersen,et al.  Specific long-lasting potentiation of synaptic transmission in hippocampal slices , 1977, Nature.

[35]  A. W. Liley,et al.  The quantal components of the mammalian end‐plate potential , 1956, The Journal of physiology.

[36]  R. Racine,et al.  Modification of seizure activity by electrical stimulation. II. Motor seizure. , 1972, Electroencephalography and clinical neurophysiology.

[37]  K. Magleby,et al.  Augmentation: A process that acts to increase transmitter release at the frog neuromuscular junction. , 1976, The Journal of physiology.

[38]  C. Sherrington,et al.  Studies on the flexor reflex.—I. Latent period , 1931 .

[39]  J. Eccles,et al.  Plasticity of Mammalian Monosynaptic Reflexes , 1951, Nature.

[40]  B. McNaughton,et al.  Effects of Diazepam on Hippocampal Excitability in the Rat: Action in the Dentate Area , 1981, Epilepsia.

[41]  T. A. Ryan,et al.  Significance tests for multiple comparison of proportions, variances, and other statistics. , 1960, Psychological bulletin.

[42]  D. P. Lloyd POST-TETANIC POTENTIATION OF RESPONSE IN MONOSYNAPTIC REFLEX PATHWAYS OF THE SPINAL CORD , 1949, The Journal of general physiology.

[43]  G. V. Goddard,et al.  A permanent change in brain function resulting from daily electrical stimulation. , 1969, Experimental neurology.

[44]  R. Racine,et al.  Epileptiform activity and neural plasticity in limbic structures. , 1972, Brain research.

[45]  Short-term retention of location within a homogeneous behavior sequence in rats. , 1973 .

[46]  W. Rall Time constants and electrotonic length of membrane cylinders and neurons. , 1969, Biophysical journal.

[47]  R. Miledi,et al.  Tetanic and post‐tetanic rise in frequency of miniature end‐plate potentials in low‐calcium solutions , 1971, The Journal of physiology.

[48]  C. Barnes Memory deficits associated with senescence: a neurophysiological and behavioral study in the rat. , 1979, Journal of comparative and physiological psychology.

[49]  R. Racine,et al.  Kindling, Unit Discharge Patterns and Neural Plasticity , 1975, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

[50]  T. Bliss,et al.  Long‐lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path , 1973, The Journal of physiology.

[51]  T. H. Brown,et al.  Long-term synaptic potentiation in the superior cervical ganglion. , 1982, Science.