Abstract
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 ( approximately 100 ms) facilitation superimposed on a depression, possibly due to depletion of available transmitter, which recovered more slowly ( approximately 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 degrees 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.
MeSH Terms
Animals
Electric Stimulation
Hippocampus/physiology
Kinetics
Male
Membrane Potentials
Rats
Rats, Inbred Strains
Regression Analysis
Synapses/physiology
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
McNaughton B L
References (25)
25 references, click to expand
-
Depression of transmitter release at the neuromuscular junction of the frog.
J Physiol. 1970 Mar;206(3):629-44
PMID: 5498509
-
The effect of tetanic and post-tetanic potentiation on facilitation of transmitter release at the frog neuromuscular junction.
J Physiol. 1973 Oct;234(2):353-71
PMID: 4358352
-
Physiological identification and analysis of dentate granule cell responses to stimulation of the medial and lateral perforant pathways in the rat.
J Comp Neurol. 1977 Oct 15;175(4):439-54
PMID: 915033
-
Long-term potentiation of the perforant path-granule cell synapse in the rat hippocampus.
Brain Res. 1975 Mar 21;86(2):205-15
PMID: 163667
-
Ionic mechanism of post-tetanic potentiation at the neuromuscular junction of the frog.
J Physiol. 1971 Jan;212(2):431-46
PMID: 4323307
-
Post-tetanic potentiation at the neuromuscular junction of the frog.
J Physiol. 1969 Jul;203(1):121-33
PMID: 5821861
-
Statistical factors involved in neuromuscular facilitation and depression.
J Physiol. 1954 Jun 28;124(3):574-85
PMID: 13175200
-
ELECTROPHYSIOLOGICAL STUDIES OF HIPPOCAMPAL NEURONS. 3. RESPONSES OF HIPPOCAMPAL NEURONS TO REPETITIVE PERFORANT PATH VOLLEYS.
Electroencephalogr Clin Neurophysiol. 1964 Oct;17:353-70
PMID: 14236817
-
Estimates of probability of transmitter release at the mammalian neuromuscular junction.
J Physiol. 1970 Nov;210(4):933-45
PMID: 4395959
-
Synaptic enhancement in fascia dentata: cooperativity among coactive afferents.
Brain Res. 1978 Nov 24;157(2):277-93
PMID: 719524
-
An electrical investigation of effects of repetitive stimulation on mammalian neuromuscular junction.
J Neurophysiol. 1953 Sep;16(5):509-27
PMID: 13097199
-
Long term changes in augmentation, potentiation, and depression of transmitter release as a function of repeated synaptic activity at the frog neuromuscular junction.
J Physiol. 1976 May;257(2):471-94
PMID: 820855
-
An investigation of spontaneous activity at the neuromuscular junction of the rat.
J Physiol. 1956 Jun 28;132(3):650-66
PMID: 13332600
-
Presynaptic nature of neuromuscular depression.
Jpn J Physiol. 1962 Dec 15;12:573-84
PMID: 13940675
-
Long-lasting potentiation of synaptic transmission in the dentate area of the unanaestetized rabbit following stimulation of the perforant path.
J Physiol. 1973 Jul;232(2):357-74
PMID: 4727085
-
Entorhinal activation of dentate granule cells.
Acta Physiol Scand. 1966 Apr;66(4):448-60
PMID: 5927271
-
Long-lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path.
J Physiol. 1973 Jul;232(2):331-56
PMID: 4727084
-
The long-lasting depression in neuromuscular transmission of frog.
Jpn J Physiol. 1958 Jun 15;8(2):102-13
PMID: 13563005
-
Evidence for two physiologically distinct perforant pathways to the fascia dentata.
Brain Res. 1980 Oct 13;199(1):1-19
PMID: 7407615
-
A quantitative description of tetanic and post-tetanic potentiation of transmitter release at the frog neuromuscular junction.
J Physiol. 1975 Feb;245(1):183-208
PMID: 165286
-
Augmentation: A process that acts to increase transmitter release at the frog neuromuscular junction.
J Physiol. 1976 May;257(2):449-70
PMID: 820854
-
Post-tetanic potentiation of response in monosynaptic reflex pathways of the spinal cord.
J Gen Physiol. 1949 Nov;33(2):147-70
PMID: 15406744
-
PRESYNAPTIC AND POST-SYNAPTIC EVENTS DURING POST-TETANIC POTENTIATION AND FACILITATION IN THE AVIAN CILIARY GANGLION.
J Physiol. 1964 Dec;175:17-30
PMID: 14241155
-
Potentiation of monosynaptic EPSPs in the perforant path-dentate granule cell synapse.
Exp Brain Res. 1971;12(1):46-63
PMID: 5543201
-
Post-tetanic potentiation and facilitation do not share a common calcium-dependent mechanism.
Nat New Biol. 1973 Aug 1;244(135):155-7
PMID: 4353293