Skip to main content
Log in

Spike conduction properties of T-shaped C neurons in the rabbit nodose ganglion

  • Published:
Pflügers Archiv Aims and scope Submit manuscript

Abstract

The electrical activity of C-type neurons was recorded intracellularly in the rabbit nodose ganglion maintained in vitro. The initial segment of their axon is spirally wound close to the cell body and a primary branching point divides it into a central process (CP) projecting to the nucleus of solitary tract in the medulla oblongata and a peripheral process (PP) which conveys sensory inputs from the viscera. Stimulation of the CP induced either somatic (“S”) spikes or low-amplitude axonal (“A”) spikes (“A1” or “A2”). In some cases abrupt changes in the latency of “S” or “A” spikes (jumps) were observed by gradually increasing the stimulus intensity. They are discussed in relation to a secondary branching on the central axon located inside or near the ganglion. Collision experiments showed that antidromic “A” spikes are blocked at the primary bifurcation of the axon (T-shaped neuron). Stimulation of the PP induced either “S” spikes or high amplitude “A” spikes (“A3” or “A4”). Orthodromic spikes could be blocked either before or after the primary bifurcation. When blocking occurs after the bifurcation on the stem axon, the spike can invade the central axon without invading the soma. The study of the refractory periods of the two processes and the application of high frequency stimulation showed that the PP allows higher frequencies than the soma and the CP, and thus that branching and the CP act as low-pass filters. These data support the view that the primary branching point and the CP of these T-shaped cells represent a strategic area to modulate visceral afferent messages.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Aldskogius H, Risling M (1981) Effect of sciatic neurectomy on neuronal number and size distribution in the L7 ganglion of kittens. Exp Neurol 74:597–604

    Google Scholar 

  2. Baccaglini PI, Cooper E (1982) Electrophysiological studies of newborn rat nodose neurons in cell culture. J Physiol (Lond) 324:429–439

    Google Scholar 

  3. Baccaglini PI, Cooper E (1982) Influences on the expression of functional acetylcholine receptors of rat nodose neurons in cell cultures. J Physiol (Lond) 324:441–451

    Google Scholar 

  4. Bahr R, Blumberg H, Jänig W (1981) Do dichotomizing afferent fibers exist which supply visceral organs as well as somatic structures? A contribution to the problem of referred pain. Neurosci Lett 24:25–28

    Article  Google Scholar 

  5. Chung K, Coggeshall RE (1984) The ratio of dorsal root ganglion cells to dorsal root axons in sacral segments of the cat. J Comp Neurol 225:24–30

    PubMed  Google Scholar 

  6. Cooper E (1984) Synapse formation among developing sensory neurons from rat nodose ganglia grown in tissue culture. J Physiol (Lond) 351:263–274

    Google Scholar 

  7. Cooper E, Shrier A (1985) Single-channel analysis of fast transient potassium currents from rat nodose neurons. J Physiol (Lond) 369:199–208

    Google Scholar 

  8. Ducreux C, Reynaud JC, Puizillout JJ (1992) Spike properties of amyelinic neurons in rabbit nodose ganglia. Serotonin effects. In: Bianchi AL, Grélot L, Miller AD, King GL (eds) Mechanisms and control of emesis. INSERM John Libbey, London, pp 91–92

    Google Scholar 

  9. Dudel J (1989) Information transfer by electrical excitation. In: Schmidt RF, Thews G (eds) Springer, Berlin Heidelberg New York, pp 19–42

    Google Scholar 

  10. Fowler JC, Greene R, Weinreich D (1985) Two calcium-sensitive spike after-hyperpolarizations in visceral sensory neurones of the rabbit. J Physiol (Lond) 365:59–75

    Google Scholar 

  11. Gallego R, Eyzaguirre C (1978) Membrane and action potential characteristics of A and C nodose ganglion cells studied in whole ganglia and in tissue slices. J Neurophysiol 41:1217–1232

    Google Scholar 

  12. Gasser HS (1955) Properties of dorsal root unmedullated fibers on the two sides of the ganglion. J Gen Physiol 38:709–728

    Google Scholar 

  13. Gross RA, Uhler MD, McDonald RL (1990) The cyclic AMP-dependent protein kinase catalytic subunit selectively enhances calcium currents in rat nodose neurons. J Physiol (Lond) 429:483–496

    Google Scholar 

  14. Gu X (1991) Effect of conduction block at axon bifurcations on synaptic transmission to different postsynaptic neurons in the leech. J Physiol (Lond) 441:755–778

    Google Scholar 

  15. Ha H (1970) Axonal bifurcation in the dorsal root ganglion of the cat: a light and electron microscopy study. J Comp Neurol 140:227–240

    Google Scholar 

  16. Higashi H, Ueda N, Nishi S, Gallagher JP, Shinnick-Gallagher P (1982) Chemoreceptors for serotonin (5-HT), acetylcholine (ACh), bradykinin (BK), histamine (H) and g-aminobutyric acid (GABA) on rabbit visceral afferent neurons. Brain Res Bull 8:23–32

    Google Scholar 

  17. Hoheisel U, Mense S (1987) Observations on the morphology of axons and somata of slowly conducting dorsal root ganglion cells in the cat. Brain Res 423:269–278

    Google Scholar 

  18. Ikeda SR, Schofield GG, Weight FF (1986) Na+ and Ca2+ currents of acutely isolated adult rat nodose ganglion cells. J Neurophysiol 155:527–539

    Google Scholar 

  19. Ito M (1957) The electrical activity of spinal ganglion cells investigated with intracellular microelectrodes. Jpn J Physiol 7:297–323

    Google Scholar 

  20. Jaffe RA, Sampson SR (1976) Analysis of passive and active electrophysiologic properties of neurons in mammalian nodose ganglia maintained in vitro. J Neurophysiol 39:802–815

    Google Scholar 

  21. Kalia M, Mesulam MM (1980) Brainstem projections of sensory and motor components of the vagus nerve complex in the cat. I: the cervical vagus and nodose ganglion. J Comp Neurol 193:435–465

    Google Scholar 

  22. Kalia M, Mesulam MM (1980) Brainstem projections of sensory and motor components of the vagus complex in the cat. II: Laryngeal, tracheobronchial, pulmonary, cardiac and gastrointestinal branches. J Comp Neurol 193:467–508

    Google Scholar 

  23. Kubin L, Rogers R, Davies RO (1991) Morphology of vagal afferent neurons in the nodose ganglion of the cat. 21st Annual Meeting Society for Neuroscience, New Orleans, Louisiana, November, pp 10–15

  24. Langford LA, Coggeshall RE (1981) Branching of sensory axons in the peripheral nerve of the rat. J Comp Neurol 203:745–750

    Google Scholar 

  25. Lee KH, Chung K, Chung JM, Coggeshall RE (1986) Correlation of cell body size, axon size and signal conduction velocity for individually labelled dorsal root ganglion cells in the cat. J Comp Neurol 243:335–346

    Google Scholar 

  26. Mei N (1970) Disposition anatomique et propriétés électrophysiologiques des neurones sensitifs vagaux chez le chat. Exp Brain Res 11:465–479

    Google Scholar 

  27. Pierau FK, Taylor DCM, Abel W, Friedrich B (1982) Dichotomizing peripheral fibres revealed by intracellular recording from rat sensory neurons. Neurosci Lett 31:123–128

    Google Scholar 

  28. Puizillout JJ, Gambarelli F (1989) Electrophysiological and morphological properties of type C vagal neurons in the nodose ganglion of the cat. J Auton Nerv Syst 29:49–58

    Google Scholar 

  29. Ramon Cajal S (1952) Histologie du système nerveux de l'homme et des vertébrés. Consejo Superior de Investigaciones Científicas (CSIC) Instituto. Ramon Y Cajal (ed.) Madrid, tome 1, pp 427–430

    Google Scholar 

  30. Stansfeld CE, Wallis DI (1985) Properties of visceral primary afferent neurons in the nodose ganglion of the rabbit. J Neurophysiol 54:245–260

    Google Scholar 

  31. Suh YS, Chung K, Coggeshall RE (1984) A study of axonal diameters and areas in lumbosacral roots and nerves in the rat. J Comp Neurol 222:473–481

    Google Scholar 

  32. Tauc L (1962) Site of origin and propagation of spike in the giant neuron of Aplysia. J Gen Physiol 45:1077–1097

    Google Scholar 

  33. Taylor DCM, Pierau FK (1982) Double fluorescence labelling supports electrophysiological evidence for dichotomizing peripheral sensory nerve fibres in rats. Neurosci Lett 33:1–6

    Google Scholar 

  34. Yoshida S, Matsuda Y (1979) Studies on sensory neurons of the mouse with intracellular and horseradish peroxidase injection techniques. J Neurophysiol 42:1134–1145

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ducreux, C., Reynaud, J.C. & Puizillout, J.J. Spike conduction properties of T-shaped C neurons in the rabbit nodose ganglion. Pflügers Arch. 424, 238–244 (1993). https://doi.org/10.1007/BF00384348

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00384348

Key words

Navigation