|
|
||||||||
Department of Psychology, Dalhousie University, Halifax, Nova Scotia, Canada B3H 4J1
Cerebral Functions Group, Department of Anatomy and Embryology, University College London, Gower Street, London WC1E 6BT*
1. The component processes contributing to post-activation change in synaptic efficacy in the perforant pathway to the fascia dentata were studied in rats under sodium pentobarbitone anaesthesia.
2. With low stimulus strength, which activated only a relatively small number of perforant path fibres, repetitive stimulation led to effects which had very similar characteristics to those observed at neuromuscular synapses under similar conditions. Paired shocks resulted in a short (
100 ms) facilitation superimposed on a depression, possibly due to depletion of available transmitter, which recovered more slowly (
4 s). Short trains of stimuli at 125-250 Hz led to a longer lasting increase in synaptic strength which decayed to control levels with a double exponential time course. The two exponential components behaved like augmentation and potentiation at neuromuscular synapses, with time constants at 33 °C of about 5 s and about 90 s respectively.
3. High-intensity stimulus trains of identical frequency and duration led to an enhancement of synaptic strength which lasted for longer than 30 min.
4. The paired shock depletion effect was increased in direct proportion to the amount of augmentation and potentiation present following low-intensity stimulus trains. Following high-intensity trains the paired shock depletion effect was increased by the same amount, and recovered with the same time course as following low-intensity stimulus trains, even though there remained a significant enhancement of the synaptic response.
5. The results are interpreted as indicating that augmentation and potentiation are due to an increase in the probability of transmitter release whereas long-term enhancement acts through some other, as yet undetermined, mechanism. Following high-intensity stimulation all three processes are activated.
This article has been cited by other articles:
![]() |
E. Garcia-Perez and J. F. Wesseling Augmentation Controls the Fast Rebound From Depression at Excitatory Hippocampal Synapses J Neurophysiol, April 1, 2008; 99(4): 1770 - 1786. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Crepel and H. Daniel Developmental Changes in Agonist-Induced Retrograde Signaling at Parallel Fiber Purkinje Cell Synapses: Role of Calcium-Induced Calcium Release J Neurophysiol, November 1, 2007; 98(5): 2550 - 2565. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Korogod, X. Lou, and R. Schneggenburger Posttetanic potentiation critically depends on an enhanced Ca2+ sensitivity of vesicle fusion mediated by presynaptic PKC PNAS, October 2, 2007; 104(40): 15923 - 15928. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Ris, B. Capron, C. Sclavons, J.-F. Liegeois, V. Seutin, and E. Godaux Metaplastic effect of apamin on LTP and paired-pulse facilitation Learn. Mem., June 5, 2007; 14(6): 390 - 399. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Crepel Developmental Changes in Retrograde Messengers Involved in Depolarization-Induced Suppression of Excitation at Parallel Fiber-Purkinje Cell Synapses in Rodents J Neurophysiol, January 1, 2007; 97(1): 824 - 836. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. F. Cooke and T. V. P. Bliss Plasticity in the human central nervous system Brain, July 1, 2006; 129(7): 1659 - 1673. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Korogod, X. Lou, and R. Schneggenburger Presynaptic Ca2+ Requirements and Developmental Regulation of Posttetanic Potentiation at the Calyx of Held J. Neurosci., May 25, 2005; 25(21): 5127 - 5137. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. M. Kalkstein and K. L. Magleby Augmentation Increases Vesicular Release Probability in the Presence of Masking Depression at the Frog Neuromuscular Junction J. Neurosci., December 15, 2004; 24(50): 11391 - 11403. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. J. Palmer, J. T. R. Isaac, and G. L. Collingridge Multiple, Developmentally Regulated Expression Mechanisms of Long-Term Potentiation at CA1 Synapses J. Neurosci., May 26, 2004; 24(21): 4903 - 4911. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Granseth and S. Lindstrom Augmentation of corticogeniculate EPSCs in principal cells of the dorsal lateral geniculate nucleus of the rat investigated in vitro J. Physiol., April 1, 2004; 556(1): 147 - 157. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. P. O'Boyle, V. Do, B. E. Derrick, and B. J. Claiborne In Vivo Recordings of Long-Term Potentiation and Long-Term Depression in the Dentate Gyrus of the Neonatal Rat J Neurophysiol, February 1, 2004; 91(2): 613 - 622. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. M. L. IV, B. Wroblewska, J. M. Sarvey, and J. H. Neale {beta}-NAAG Rescues LTP From Blockade by NAAG in Rat Dentate Gyrus via the Type 3 Metabotropic Glutamate Receptor J Neurophysiol, March 1, 2001; 85(3): 1097 - 1106. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Thiels, N. N. Urban, G. R. Gonzalez-Burgos, B. I. Kanterewicz, G. Barrionuevo, C. T. Chu, T. D. Oury, and E. Klann Impairment of Long-term Potentiation and Associative Memory in Mice That Overexpress Extracellular Superoxide Dismutase J. Neurosci., October 15, 2000; 20(20): 7631 - 7639. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. A. Xu-Friedman and W. G. Regehr Probing Fundamental Aspects of Synaptic Transmission with Strontium J. Neurosci., June 15, 2000; 20(12): 4414 - 4422. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. S. Kumar and D. S. Faber Plasticity of First-Order Sensory Synapses: Interactions between Homosynaptic Long-Term Potentiation and Heterosynaptically Evoked Dopaminergic Potentiation J. Neurosci., March 1, 1999; 19(5): 1620 - 1635. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. K. Selig, R. A. Nicoll, and R. C. Malenka Hippocampal Long-Term Potentiation Preserves the Fidelity of Postsynaptic Responses to Presynaptic Bursts J. Neurosci., February 15, 1999; 19(4): 1236 - 1246. [Abstract] [Full Text] [PDF] |
||||
![]() |
X.-Y. Jiang and T. W. Abrams Use-Dependent Decline of Paired-Pulse Facilitation at Aplysia Sensory Neuron Synapses Suggests a Distinct Vesicle Pool or Release Mechanism J. Neurosci., December 15, 1998; 18(24): 10310 - 10319. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Canepari and E. Cherubini Dynamics of Excitatory Transmitter Release: Analysis of Synaptic Responses in CA3 Hippocampal Neurons After Repetitive Stimulation of Afferent Fibers J Neurophysiol, April 1, 1998; 79(4): 1977 - 1988. [Abstract] [Full Text] [PDF] |
||||
![]() |
J.-H. Wang and P. T. Kelly Attenuation of Paired-Pulse Facilitation Associated With Synaptic Potentiation Mediated by Postsynaptic Mechanisms J Neurophysiol, November 1, 1997; 78(5): 2707 - 2716. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. E. Schulz and J. C. Fitzgibbons Differing Mechanisms of Expression for Short- and Long-Term Potentiation J Neurophysiol, July 1, 1997; 78(1): 321 - 334. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. E. Schulz Long-term potentiation involves increases in the probability of neurotransmitter release PNAS, May 27, 1997; 94(11): 5888 - 5893. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. P. Atluri and W. G. Regehr Determinants of the Time Course of Facilitation at the Granule Cell to Purkinje Cell Synapse J. Neurosci., September 15, 1996; 16(18): 5661 - 5671. [Abstract] [Full Text] [PDF] |
||||
![]() |
E I Moser, M B Moser, and P Andersen Potentiation of dentate synapses initiated by exploratory learning in rats: dissociation from brain temperature, motor activity, and arousal. Learn. Mem., January 1, 1994; 1(1): 55 - 73. [Abstract] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |