Abstract
1. EPSCs were evoked in CA1 pyramidal neurones of young rats in vitro by extracellular stimulation of axons in a restricted stratum radiatum field, and were recorded using the whole-cell technique. 2. Quantal fluctuations in EPSC amplitude could be demonstrated for nineteen of fifty EPSCs analysed. Quantal currents (at the soma) ranged from 2.6 to 9.5 pA (after correction for the access resistance) with a mean of 4.0 +/- 2.0 pA. 3. Quantal variance was negligible for the majority (13/19) of the EPSCs. However, a large quantal variance (with a coefficient of variation > 0.4) is one possible reason why a large number of the EPSCs (29/50) could not be shown to have quantal fluctuations. 4. The statistical pattern of fluctuations in the amplitude of the majority of the quantal EPSCs (18/19) could not be described by conventional models of transmitter release. 5. The time course of the EPSC and a compartmental model of CA1 pyramidal neurones were used to calculate synaptic location. The quantal current (at the soma) was independent of the electrotonic location of the synapse at which it was evoked. The peak quantal conductance generating each quantal current ranged from 0.5 to 6.8 nS (mean 1.3 +/- 1.4 nS), its magnitude increasing with distance from the soma. The mean peak conductance is likely to be generated by the opening of at least 60-160 AMPA channels.
Full text
PDF






















Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Allen C., Stevens C. F. An evaluation of causes for unreliability of synaptic transmission. Proc Natl Acad Sci U S A. 1994 Oct 25;91(22):10380–10383. doi: 10.1073/pnas.91.22.10380. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Clamann H. P., Rioult-Pedotti M. S., Lüscher H. R. The influence of noise on quantal EPSP size obtained by deconvolution in spinal motoneurons in the cat. J Neurophysiol. 1991 Jan;65(1):67–75. doi: 10.1152/jn.1991.65.1.67. [DOI] [PubMed] [Google Scholar]
- Edwards F. A., Konnerth A., Sakmann B. Quantal analysis of inhibitory synaptic transmission in the dentate gyrus of rat hippocampal slices: a patch-clamp study. J Physiol. 1990 Nov;430:213–249. doi: 10.1113/jphysiol.1990.sp018289. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Faber D. S., Young W. S., Legendre P., Korn H. Intrinsic quantal variability due to stochastic properties of receptor-transmitter interactions. Science. 1992 Nov 27;258(5087):1494–1498. doi: 10.1126/science.1279813. [DOI] [PubMed] [Google Scholar]
- Foster T. C., McNaughton B. L. Long-term enhancement of CA1 synaptic transmission is due to increased quantal size, not quantal content. Hippocampus. 1991 Jan;1(1):79–91. doi: 10.1002/hipo.450010108. [DOI] [PubMed] [Google Scholar]
- Hestrin S. Activation and desensitization of glutamate-activated channels mediating fast excitatory synaptic currents in the visual cortex. Neuron. 1992 Nov;9(5):991–999. doi: 10.1016/0896-6273(92)90250-h. [DOI] [PubMed] [Google Scholar]
- Iansek R., Redman S. J. The amplitude, time course and charge of unitary excitatory post-synaptic potentials evoked in spinal motoneurone dendrites. J Physiol. 1973 Nov;234(3):665–688. doi: 10.1113/jphysiol.1973.sp010366. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jack J. J., Kullmann D. M., Larkman A. U., Major G., Stratford K. J. Quantal analysis of excitatory synaptic mechanisms in the mammalian central nervous system. Cold Spring Harb Symp Quant Biol. 1990;55:57–67. doi: 10.1101/sqb.1990.055.01.008. [DOI] [PubMed] [Google Scholar]
- Jack J. J., Larkman A. U., Major G., Stratford K. J. Quantal analysis of the synaptic excitation of CA1 hippocampal pyramidal cells. Adv Second Messenger Phosphoprotein Res. 1994;29:275–299. doi: 10.1016/s1040-7952(06)80021-2. [DOI] [PubMed] [Google Scholar]
- Jack J. J., Redman S. J., Wong K. The components of synaptic potentials evoked in cat spinal motoneurones by impulses in single group Ia afferents. J Physiol. 1981 Dec;321:65–96. doi: 10.1113/jphysiol.1981.sp013972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jonas P., Major G., Sakmann B. Quantal components of unitary EPSCs at the mossy fibre synapse on CA3 pyramidal cells of rat hippocampus. J Physiol. 1993 Dec;472:615–663. doi: 10.1113/jphysiol.1993.sp019965. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jonas P., Sakmann B. Glutamate receptor channels in isolated patches from CA1 and CA3 pyramidal cells of rat hippocampal slices. J Physiol. 1992 Sep;455:143–171. doi: 10.1113/jphysiol.1992.sp019294. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kullmann D. M. Applications of the expectation-maximization algorithm to quantal analysis of postsynaptic potentials. J Neurosci Methods. 1989 Dec;30(3):231–245. doi: 10.1016/0165-0270(89)90134-9. [DOI] [PubMed] [Google Scholar]
- Kullmann D. M., Nicoll R. A. Long-term potentiation is associated with increases in quantal content and quantal amplitude. Nature. 1992 May 21;357(6375):240–244. doi: 10.1038/357240a0. [DOI] [PubMed] [Google Scholar]
- Kullmann D. M. Quantal variability of excitatory transmission in the hippocampus: implications for the opening probability of fast glutamate-gated channels. Proc Biol Sci. 1993 Jul 22;253(1336):107–116. doi: 10.1098/rspb.1993.0088. [DOI] [PubMed] [Google Scholar]
- Larkman A., Hannay T., Stratford K., Jack J. Presynaptic release probability influences the locus of long-term potentiation. Nature. 1992 Nov 5;360(6399):70–73. doi: 10.1038/360070a0. [DOI] [PubMed] [Google Scholar]
- Larkman A., Stratford K., Jack J. Quantal analysis of excitatory synaptic action and depression in hippocampal slices. Nature. 1991 Mar 28;350(6316):344–347. doi: 10.1038/350344a0. [DOI] [PubMed] [Google Scholar]
- Liao D., Jones A., Malinow R. Direct measurement of quantal changes underlying long-term potentiation in CA1 hippocampus. Neuron. 1992 Dec;9(6):1089–1097. doi: 10.1016/0896-6273(92)90068-o. [DOI] [PubMed] [Google Scholar]
- Melamed N., Helm P. J., Rahamimoff R. Confocal microscopy reveals coordinated calcium fluctuations and oscillations in synaptic boutons. J Neurosci. 1993 Feb;13(2):632–649. doi: 10.1523/JNEUROSCI.13-02-00632.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Paulsen O., Heggelund P. The quantal size at retinogeniculate synapses determined from spontaneous and evoked EPSCs in guinea-pig thalamic slices. J Physiol. 1994 Nov 1;480(Pt 3):505–511. doi: 10.1113/jphysiol.1994.sp020379. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Raastad Morten, Storm Johan F., Andersen Per. Putative Single Quantum and Single Fibre Excitatory Postsynaptic Currents Show Similar Amplitude Range and Variability in Rat Hippocampal Slices. Eur J Neurosci. 1992 Oct;4(1):113–117. doi: 10.1111/j.1460-9568.1992.tb00114.x. [DOI] [PubMed] [Google Scholar]
- Sayer R. J., Friedlander M. J., Redman S. J. The time course and amplitude of EPSPs evoked at synapses between pairs of CA3/CA1 neurons in the hippocampal slice. J Neurosci. 1990 Mar;10(3):826–836. doi: 10.1523/JNEUROSCI.10-03-00826.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sayer R. J., Redman S. J., Andersen P. Amplitude fluctuations in small EPSPs recorded from CA1 pyramidal cells in the guinea pig hippocampal slice. J Neurosci. 1989 Mar;9(3):840–850. doi: 10.1523/JNEUROSCI.09-03-00840.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Silver R. A., Traynelis S. F., Cull-Candy S. G. Rapid-time-course miniature and evoked excitatory currents at cerebellar synapses in situ. Nature. 1992 Jan 9;355(6356):163–166. doi: 10.1038/355163a0. [DOI] [PubMed] [Google Scholar]
- Solodkin M., Jiménez I., Collins W. F., 3rd, Mendell L. M., Rudomin P. Interaction of baseline synaptic noise and Ia EPSPs: evidence for appreciable negative correlation under physiological conditions. J Neurophysiol. 1991 Apr;65(4):927–945. doi: 10.1152/jn.1991.65.4.927. [DOI] [PubMed] [Google Scholar]
- Sorra K. E., Harris K. M. Occurrence and three-dimensional structure of multiple synapses between individual radiatum axons and their target pyramidal cells in hippocampal area CA1. J Neurosci. 1993 Sep;13(9):3736–3748. doi: 10.1523/JNEUROSCI.13-09-03736.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stricker C., Field A. C., Redman S. J. Changes in quantal parameters of EPSCs in rat CA1 neurones in vitro after the induction of long-term potentiation. J Physiol. 1996 Jan 15;490(Pt 2):443–454. doi: 10.1113/jphysiol.1996.sp021156. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stricker C., Redman S., Daley D. Statistical analysis of synaptic transmission: model discrimination and confidence limits. Biophys J. 1994 Aug;67(2):532–547. doi: 10.1016/S0006-3495(94)80513-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stricker C., Redman S. Statistical models of synaptic transmission evaluated using the expectation-maximization algorithm. Biophys J. 1994 Aug;67(2):656–670. doi: 10.1016/S0006-3495(94)80514-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tong G., Jahr C. E. Multivesicular release from excitatory synapses of cultured hippocampal neurons. Neuron. 1994 Jan;12(1):51–59. doi: 10.1016/0896-6273(94)90151-1. [DOI] [PubMed] [Google Scholar]
- Traynelis S. F., Silver R. A., Cull-Candy S. G. Estimated conductance of glutamate receptor channels activated during EPSCs at the cerebellar mossy fiber-granule cell synapse. Neuron. 1993 Aug;11(2):279–289. doi: 10.1016/0896-6273(93)90184-s. [DOI] [PubMed] [Google Scholar]
- Walmsley B., Edwards F. R., Tracey D. J. Nonuniform release probabilities underlie quantal synaptic transmission at a mammalian excitatory central synapse. J Neurophysiol. 1988 Sep;60(3):889–908. doi: 10.1152/jn.1988.60.3.889. [DOI] [PubMed] [Google Scholar]
- Wilson C. J. Passive cable properties of dendritic spines and spiny neurons. J Neurosci. 1984 Jan;4(1):281–297. doi: 10.1523/JNEUROSCI.04-01-00281.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]


