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. 1996 Feb 15;491(Pt 1):163–176. doi: 10.1113/jphysiol.1996.sp021204

Paired-pulse facilitation and depression at unitary synapses in rat hippocampus: quantal fluctuation affects subsequent release.

D Debanne 1, N C Guérineau 1, B H Gähwiler 1, S M Thompson 1
PMCID: PMC1158767  PMID: 9011608

Abstract

1. Excitatory synaptic transmission between pairs of monosynaptically coupled pyramidal cells was examined in rat hippocampal slice cultures. Action potentials were elicited in single CA3 pyramidal cells impaled with microelectrodes and unitary excitatory postsynaptic currents (EPSCs) were recorded in whole-cell voltage-clamped CA1 or CA3 cells. 2. The amplitude of successive unitary EPSCs in response to single action potentials varied. The amplitude of EPSCs was altered by adenosine or changes in the [Mg2+]/[CA2+] ratio. We conclude that single action potentials triggered the release of multiple quanta of glutamate. 3. When two action potentials were elicited in the presynaptic cell, the amplitude of the second EPSC was inversely related to the amplitude of the first. Paired-pulse facilitation (PPF) was observed when the first EPSC was small, i.e. the second EPSC was larger than the first, whereas paired-pulse depression (PPD) was observed when the first EPSC was large. 4. The number of trials displaying PPD was greater when release probability was increased, and smaller when release probability was decreased. 5. PPD was not postsynaptically mediated because it was unaffected by decreasing ionic flux with 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) or receptor desensitization with aniracetam. 6. PPF was maximal at an interstimulus interval of 70 ms and recovered within 500 ms. Recovery from PPD occurred within 5 s. 7. We propose that multiple release sites are formed by the axon of a CA3 pyramidal cell and a single postsynaptic CA1 or CA3 cell. PPF is observed if the first action potential fails to release transmitter at most release sites. PPD is observed if the first action potential successfully triggers release at most release sites. 8. Our observations of PPF are consistent with the residual calcium hypothesis. We conclude that PPD results from a decrease in quantal content, perhaps due to short-term depletion of readily releasable vesicles.

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Selected References

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  1. Arancio O., Korn H., Gulyas A., Freund T., Miles R. Excitatory synaptic connections onto rat hippocampal inhibitory cells may involve a single transmitter release site. J Physiol. 1994 Dec 1;481(Pt 2):395–405. doi: 10.1113/jphysiol.1994.sp020448. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Barrett E. F., Stevens C. F. Quantal independence and uniformity of presynaptic release kinetics at the frog neuromuscular junction. J Physiol. 1972 Dec;227(3):665–689. doi: 10.1113/jphysiol.1972.sp010053. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Betz W. J. Depression of transmitter release at the neuromuscular junction of the frog. J Physiol. 1970 Mar;206(3):629–644. doi: 10.1113/jphysiol.1970.sp009034. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bittner M. A., Holz R. W. Kinetic analysis of secretion from permeabilized adrenal chromaffin cells reveals distinct components. J Biol Chem. 1992 Aug 15;267(23):16219–16225. [PubMed] [Google Scholar]
  5. Chapman P. F., Frenguelli B. G., Smith A., Chen C. M., Silva A. J. The alpha-Ca2+/calmodulin kinase II: a bidirectional modulator of presynaptic plasticity. Neuron. 1995 Mar;14(3):591–597. doi: 10.1016/0896-6273(95)90315-1. [DOI] [PubMed] [Google Scholar]
  6. Creager R., Dunwiddie T., Lynch G. Paired-pulse and frequency facilitation in the CA1 region of the in vitro rat hippocampus. J Physiol. 1980 Feb;299:409–424. doi: 10.1113/jphysiol.1980.sp013133. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. DEL CASTILLO J., KATZ B. Quantal components of the end-plate potential. J Physiol. 1954 Jun 28;124(3):560–573. doi: 10.1113/jphysiol.1954.sp005129. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. DEL CASTILLO J., KATZ B. Statistical factors involved in neuromuscular facilitation and depression. J Physiol. 1954 Jun 28;124(3):574–585. doi: 10.1113/jphysiol.1954.sp005130. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Debanne D., Guérineau N. C., Gähwiler B. H., Thompson S. M. Physiology and pharmacology of unitary synaptic connections between pairs of cells in areas CA3 and CA1 of rat hippocampal slice cultures. J Neurophysiol. 1995 Mar;73(3):1282–1294. doi: 10.1152/jn.1995.73.3.1282. [DOI] [PubMed] [Google Scholar]
  10. Dunwiddie T. V., Haas H. L. Adenosine increases synaptic facilitation in the in vitro rat hippocampus: evidence for a presynaptic site of action. J Physiol. 1985 Dec;369:365–377. doi: 10.1113/jphysiol.1985.sp015907. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. FATT P., KATZ B. Spontaneous subthreshold activity at motor nerve endings. J Physiol. 1952 May;117(1):109–128. [PMC free article] [PubMed] [Google Scholar]
  12. Faber D. S., Korn H. Applicability of the coefficient of variation method for analyzing synaptic plasticity. Biophys J. 1991 Nov;60(5):1288–1294. doi: 10.1016/S0006-3495(91)82162-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. 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]
  14. Gulyás A. I., Miles R., Sík A., Tóth K., Tamamaki N., Freund T. F. Hippocampal pyramidal cells excite inhibitory neurons through a single release site. Nature. 1993 Dec 16;366(6456):683–687. doi: 10.1038/366683a0. [DOI] [PubMed] [Google Scholar]
  15. Gähwiler B. H. Organotypic monolayer cultures of nervous tissue. J Neurosci Methods. 1981 Dec;4(4):329–342. doi: 10.1016/0165-0270(81)90003-0. [DOI] [PubMed] [Google Scholar]
  16. Hess G., Kuhnt U. Presynaptic calcium transients evoked by paired-pulse stimulation in the hippocampal slice. Neuroreport. 1992 Apr;3(4):361–364. doi: 10.1097/00001756-199204000-00018. [DOI] [PubMed] [Google Scholar]
  17. Hess G., Kuhnt U., Voronin L. L. Quantal analysis of paired-pulse facilitation in guinea pig hippocampal slices. Neurosci Lett. 1987 Jun 15;77(2):187–192. doi: 10.1016/0304-3940(87)90584-2. [DOI] [PubMed] [Google Scholar]
  18. Heuser J. E., Reese T. S., Dennis M. J., Jan Y., Jan L., Evans L. Synaptic vesicle exocytosis captured by quick freezing and correlated with quantal transmitter release. J Cell Biol. 1979 May;81(2):275–300. doi: 10.1083/jcb.81.2.275. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Horrigan F. T., Bookman R. J. Releasable pools and the kinetics of exocytosis in adrenal chromaffin cells. Neuron. 1994 Nov;13(5):1119–1129. doi: 10.1016/0896-6273(94)90050-7. [DOI] [PubMed] [Google Scholar]
  20. Ito I., Tanabe S., Kohda A., Sugiyama H. Allosteric potentiation of quisqualate receptors by a nootropic drug aniracetam. J Physiol. 1990 May;424:533–543. doi: 10.1113/jphysiol.1990.sp018081. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Katz B., Miledi R. The role of calcium in neuromuscular facilitation. J Physiol. 1968 Mar;195(2):481–492. doi: 10.1113/jphysiol.1968.sp008469. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Korn H., Mallet A., Triller A., Faber D. S. Transmission at a central inhibitory synapse. II. Quantal description of release, with a physical correlate for binomial n. J Neurophysiol. 1982 Sep;48(3):679–707. doi: 10.1152/jn.1982.48.3.679. [DOI] [PubMed] [Google Scholar]
  23. Liu G., Tsien R. W. Properties of synaptic transmission at single hippocampal synaptic boutons. Nature. 1995 Jun 1;375(6530):404–408. doi: 10.1038/375404a0. [DOI] [PubMed] [Google Scholar]
  24. Lupica C. R., Proctor W. R., Dunwiddie T. V. Presynaptic inhibition of excitatory synaptic transmission by adenosine in rat hippocampus: analysis of unitary EPSP variance measured by whole-cell recording. J Neurosci. 1992 Oct;12(10):3753–3764. doi: 10.1523/JNEUROSCI.12-10-03753.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Malinow R. Transmission between pairs of hippocampal slice neurons: quantal levels, oscillations, and LTP. Science. 1991 May 3;252(5006):722–724. doi: 10.1126/science.1850871. [DOI] [PubMed] [Google Scholar]
  26. Mallart A., Martin A. R. The relation between quantum content and facilitation at the neuromuscular junction of the frog. J Physiol. 1968 Jun;196(3):593–604. doi: 10.1113/jphysiol.1968.sp008525. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Manabe T., Wyllie D. J., Perkel D. J., Nicoll R. A. Modulation of synaptic transmission and long-term potentiation: effects on paired pulse facilitation and EPSC variance in the CA1 region of the hippocampus. J Neurophysiol. 1993 Oct;70(4):1451–1459. doi: 10.1152/jn.1993.70.4.1451. [DOI] [PubMed] [Google Scholar]
  28. OTSUKA M., ENDO M., NONOMURA Y. Presynaptic nature of neuromuscular depression. Jpn J Physiol. 1962 Dec 15;12:573–584. doi: 10.2170/jjphysiol.12.573. [DOI] [PubMed] [Google Scholar]
  29. 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]
  30. Redman R. S., Silinsky E. M. ATP released together with acetylcholine as the mediator of neuromuscular depression at frog motor nerve endings. J Physiol. 1994 May 15;477(Pt 1):117–127. doi: 10.1113/jphysiol.1994.sp020176. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Redman S. Quantal analysis of synaptic potentials in neurons of the central nervous system. Physiol Rev. 1990 Jan;70(1):165–198. doi: 10.1152/physrev.1990.70.1.165. [DOI] [PubMed] [Google Scholar]
  32. Rosahl T. W., Geppert M., Spillane D., Herz J., Hammer R. E., Malenka R. C., Südhof T. C. Short-term synaptic plasticity is altered in mice lacking synapsin I. Cell. 1993 Nov 19;75(4):661–670. doi: 10.1016/0092-8674(93)90487-b. [DOI] [PubMed] [Google Scholar]
  33. Stevens C. F., Tsujimoto T. Estimates for the pool size of releasable quanta at a single central synapse and for the time required to refill the pool. Proc Natl Acad Sci U S A. 1995 Jan 31;92(3):846–849. doi: 10.1073/pnas.92.3.846. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. THIES R. E. NEUROMUSCULAR DEPRESSION AND THE APPARENT DEPLETION OF TRANSMITTER IN MAMMALIAN MUSCLE. J Neurophysiol. 1965 May;28:428–442. doi: 10.1152/jn.1965.28.3.427. [DOI] [PubMed] [Google Scholar]
  35. Thompson S. M., Gähwiler B. H. Activity-dependent disinhibition. I. Repetitive stimulation reduces IPSP driving force and conductance in the hippocampus in vitro. J Neurophysiol. 1989 Mar;61(3):501–511. doi: 10.1152/jn.1989.61.3.501. [DOI] [PubMed] [Google Scholar]
  36. Wilcox K. S., Dichter M. A. Paired pulse depression in cultured hippocampal neurons is due to a presynaptic mechanism independent of GABAB autoreceptor activation. J Neurosci. 1994 Mar;14(3 Pt 2):1775–1788. doi: 10.1523/JNEUROSCI.14-03-01775.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Zengel J. E., Magleby K. L. Differential effects of Ba2+, Sr2+, and Ca2+ on stimulation-induced changes in transmitter release at the frog neuromuscular junction. J Gen Physiol. 1980 Aug;76(2):175–211. doi: 10.1085/jgp.76.2.175. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Zucker R. S. Changes in the statistics of transmitter release during facilitation. J Physiol. 1973 Mar;229(3):787–810. doi: 10.1113/jphysiol.1973.sp010167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Zucker R. S. Short-term synaptic plasticity. Annu Rev Neurosci. 1989;12:13–31. doi: 10.1146/annurev.ne.12.030189.000305. [DOI] [PubMed] [Google Scholar]

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