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. 1986 Aug;377:267–282. doi: 10.1113/jphysiol.1986.sp016186

Intracellular tetraethylammonium ions enhance group Ia excitatory post-synaptic potentials evoked in cat motoneurones.

J D Clements, P G Nelson, S J Redman
PMCID: PMC1182832  PMID: 2432243

Abstract

Single fibre group Ia excitatory post-synaptic potentials (e.p.s.p.s) were recorded in cat spinal motoneurones after the neurones were injected with tetraethylammonium (TEA) ions. TEA injection increased the peak amplitude of most e.p.s.p.s. The time course of e.p.s.p.s generated at the soma was unaffected, but the time course of e.p.s.p.s generated in the dendrites was prolonged. The membrane time constant did not change after TEA injection. Somatic e.p.s.p.s were voltage clamped after TEA was injected. The reversal potential for these e.p.s.p.s was more positive than for e.p.s.p.s unaffected by TEA. Composite e.p.s.p.s added linearly, or greater than linearly, whereas in motoneurones without TEA they added linearly or less than linearly. The enhanced amplitude and prolonged time course observed in dendritic e.p.s.p.s after TEA injection was reduced by small hyperpolarizing currents. Greater than linear summation of composite e.p.s.p.s was converted to linear summation by small hyperpolarizing currents. The increase in somatic e.p.s.p.s was attributed to a more positive reversal potential for the e.p.s.p.s. We suggest that TEA decreases the relative permeability of K+ in the subsynaptic channels. We propose that in the presence of TEA, dendritic depolarization activates an inward current which amplifies and prolongs synaptic potentials spreading towards the soma.

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Selected References

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  1. Armstrong C. M., Hille B. The inner quaternary ammonium ion receptor in potassium channels of the node of Ranvier. J Gen Physiol. 1972 Apr;59(4):388–400. doi: 10.1085/jgp.59.4.388. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bak M. J., Schmidt E. M. An improved time-amplitude window discriminator. IEEE Trans Biomed Eng. 1977 Sep;24(5):486–489. doi: 10.1109/TBME.1977.326198. [DOI] [PubMed] [Google Scholar]
  3. Burke R. E. Composite nature of the monosynaptic excitatory postsynaptic potential. J Neurophysiol. 1967 Sep;30(5):1114–1137. doi: 10.1152/jn.1967.30.5.1114. [DOI] [PubMed] [Google Scholar]
  4. Finkel A. S., Redman S. J. The synaptic current evoked in cat spinal motoneurones by impulses in single group 1a axons. J Physiol. 1983 Sep;342:615–632. doi: 10.1113/jphysiol.1983.sp014872. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Finkel A. S., Redman S. A shielded microelectrode suitable for single-electrode voltage clamping of neurones in the CNS. J Neurosci Methods. 1983 Sep;9(1):23–29. doi: 10.1016/0165-0270(83)90105-x. [DOI] [PubMed] [Google Scholar]
  6. Henneman E., Lüscher H. R., Mathis J. Simultaneously active and inactive synapses of single Ia fibres on cat spinal motoneurones. J Physiol. 1984 Jul;352:147–161. doi: 10.1113/jphysiol.1984.sp015283. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Honig M. G., Collins W. F., 3rd, Mendell L. M. Alpha-motoneuron EPSPs exhibit different frequency sensitivities to single Ia-afferent fiber stimulation. J Neurophysiol. 1983 Apr;49(4):886–901. doi: 10.1152/jn.1983.49.4.886. [DOI] [PubMed] [Google Scholar]
  8. Huang L. Y., Catterall W. A., Ehrenstein G. Comparison of ionic selectivity of batrachotoxin-activated channels with different tetrodotoxin dissociation constants. J Gen Physiol. 1979 Jun;73(6):839–854. doi: 10.1085/jgp.73.6.839. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. 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]
  10. Jack J. J., Miller S., Porter R., Redman S. J. The time course of minimal excitory post-synaptic potentials evoked in spinal motoneurones by group Ia afferent fibres. J Physiol. 1971 Jun;215(2):353–380. doi: 10.1113/jphysiol.1971.sp009474. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. 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]
  12. Kehoe J. Three acetylcholine receptors in Aplysia neurones. J Physiol. 1972 Aug;225(1):115–146. doi: 10.1113/jphysiol.1972.sp009931. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Llinás R., Sugimori M. Electrophysiological properties of in vitro Purkinje cell dendrites in mammalian cerebellar slices. J Physiol. 1980 Aug;305:197–213. doi: 10.1113/jphysiol.1980.sp013358. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Llinás R., Yarom Y. Electrophysiology of mammalian inferior olivary neurones in vitro. Different types of voltage-dependent ionic conductances. J Physiol. 1981 Jun;315:549–567. doi: 10.1113/jphysiol.1981.sp013763. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Llinás R., Yarom Y. Properties and distribution of ionic conductances generating electroresponsiveness of mammalian inferior olivary neurones in vitro. J Physiol. 1981 Jun;315:569–584. doi: 10.1113/jphysiol.1981.sp013764. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Mayer M. L., Westbrook G. L. Mixed-agonist action of excitatory amino acids on mouse spinal cord neurones under voltage clamp. J Physiol. 1984 Sep;354:29–53. doi: 10.1113/jphysiol.1984.sp015360. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Mayer M. L., Westbrook G. L. The action of N-methyl-D-aspartic acid on mouse spinal neurones in culture. J Physiol. 1985 Apr;361:65–90. doi: 10.1113/jphysiol.1985.sp015633. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Neher E., Lux H. D. Differential action of TEA + on two K + -current componentss of a molluscan neurone. Pflugers Arch. 1972;336(2):87–100. doi: 10.1007/BF00592924. [DOI] [PubMed] [Google Scholar]
  19. Nowak L., Bregestovski P., Ascher P., Herbet A., Prochiantz A. Magnesium gates glutamate-activated channels in mouse central neurones. Nature. 1984 Feb 2;307(5950):462–465. doi: 10.1038/307462a0. [DOI] [PubMed] [Google Scholar]
  20. Nó R. L., Condouris G. A. DECREMENTAL CONDUCTION IN PERIPHERAL NERVE. INTEGRATION OF STIMULI IN THE NEURON. Proc Natl Acad Sci U S A. 1959 Apr;45(4):592–617. doi: 10.1073/pnas.45.4.592. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Redman S., Walmsley B. The time course of synaptic potentials evoked in cat spinal motoneurones at identified group Ia synapses. J Physiol. 1983 Oct;343:117–133. doi: 10.1113/jphysiol.1983.sp014884. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Schwartzkroin P. A., Prince D. A. Effects of TEA on hippocampal neurons. Brain Res. 1980 Mar 3;185(1):169–181. doi: 10.1016/0006-8993(80)90680-0. [DOI] [PubMed] [Google Scholar]
  23. Schwartzkroin P. A., Slawsky M. Probable calcium spikes in hippocampal neurons. Brain Res. 1977 Oct 21;135(1):157–161. doi: 10.1016/0006-8993(77)91060-5. [DOI] [PubMed] [Google Scholar]
  24. Schwindt P. C., Crill W. E. Differential effects of TEA and cations on outward ionic currents of cat motoneurons. J Neurophysiol. 1981 Jul;46(1):1–16. doi: 10.1152/jn.1981.46.1.1. [DOI] [PubMed] [Google Scholar]
  25. Schwindt P. C., Crill W. E. Effects of barium on cat spinal motoneurons studied by voltage clamp. J Neurophysiol. 1980 Oct;44(4):827–846. doi: 10.1152/jn.1980.44.4.827. [DOI] [PubMed] [Google Scholar]
  26. Schwindt P. C., Crill W. E. Properties of a persistent inward current in normal and TEA-injected motoneurons. J Neurophysiol. 1980 Jun;43(6):1700–1724. doi: 10.1152/jn.1980.43.6.1700. [DOI] [PubMed] [Google Scholar]
  27. Shapovalov A. I., Kurchavyi G. G. Effects of trans-membrane polarization and TEA injection on monosynaptic actions from motor cortex, red nucleus and group Ia afferents on lumbar motoneurons in the monkey. Brain Res. 1974 Dec 20;82(1):49–67. doi: 10.1016/0006-8993(74)90892-0. [DOI] [PubMed] [Google Scholar]

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