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An electron microscopic study of the nodose (inferior vagal) ganglion cells in the monkey

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Journal of Neurocytology

Summary

The present study described the normal ultrastructure of the monkey nodose ganglion cells. Furthermore, experimental monkeys were subjected to supranodose vagotomy in order to ascertain if the parent cell bodies would undergo degeneration following severance of their central processes. In the normal materials, most of the ganglion cells possessed a single neurite. However, occasional cells bearing more than one process in a sectioned profile were observed. The neurites, ranging between 2–4 μm in diameter, displayed a relatively regular contour. Their cytoplasm contained parallel arrays of microtubules, ribosomes, endoplasmic reticulum and slender mitochondria. The electron density of some of these neurites was abnormally high. Embedded in these darkened neurites were a variable number of swollen mitochondria characterized by disrupted cristae. Axon terminals containing round agranular and a few large dense cored vesicles formed synaptic contacts primarily with the neurites of some of the ganglion cells. Three days after supranodose vagotomy, darkened neurites were more commonly observed but their incidence was comparable to that of the normal ganglion in longer survival animals. Another reactive change was the appearance of axon terminals undergoing various degrees of degeneration. There was no evidence of cell death in the duration studied.

It was concluded from this study that the occasional darkened neurites from the normal ganglion cells was probably undergoing ‘spontaneous degeneration’ which appeared to be accentuated when their central process was severed by supranodose vagotomy. The degeneration of axon terminals associated with some of the ganglion cells following the vagotomy suggested that they were derived from vagal descending fibres which were undergoing anterograde degeneration. The presence of synapses on some of the ganglion cells was also discussed and the possibility considered that the latter may represent ‘aberrant’ or displaced autonomic neurons.

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References

  • Abdel-Magied, E. M. (1984) Degeneration of the distal vagal ganglion cells of the domestic fowl after section of their central processes.Journal of Anatomy 139, 667–75.

    Google Scholar 

  • Aldskogius, H. (1978) Fine structural changes in nerve cell bodies of the adult rabbit dorsal motor vagal nucleus during axon reaction.Neuropathology and Applied Neurobiology 4, 323–41.

    Google Scholar 

  • Aldskogius, H. &Arvidsson, J. (1978) Nerve cell degeneration and death in the trigeminal ganglion of the adult rat following peripheral nerve transection.Journal of Neurocytology 7, 229–50.

    Google Scholar 

  • Beckstead, R. M. &Norgren, R. (1979) An autoradiographic examination of the central distribution of the trigeminal, facial, glossopharyngeal and vagal nerves in the monkey.Journal of Comparative Neurology 184, 455–72.

    Google Scholar 

  • Böck, P. (1982)The Paraganglia Springer-Verlag, Berlin, Heidelberg, New York.

    Google Scholar 

  • Cajal, S. R. Y. (1928) Degeneration and Regeneration of the Nervous System. Vol. II. editor and translater R. M. May (1959). Hafner Publishing Co., New York.

    Google Scholar 

  • Cammermeyer, J. (1962) An evaluation of the significance of the ‘dark’ neuron.Ergebnisse der Anatomie und Entwick-lungsgeschicht 36, 1–61.

    Google Scholar 

  • Grillo, M. A., Jacobs, L. &Comroe, J. H. (1974) A combined fluorescence histochemical and electron microscopic method for studying special monoaminecontaining cells (SIF cells).Journal of Comparative Neurology 153, 1–14.

    Google Scholar 

  • Hamilton, R. B., Pritchard, T. C. &Norgren, R. (1987) Central distribution of the cervical vagus nerve in Old and New World primates.Journal of the Autonomic Nervous System 19, 153–69.

    Google Scholar 

  • Hedlund, K. O. &Ebendal, T. (1980) The chick embryo nodose ganglion: effects of nerve growth factor in culture.Journal of Neurocytology 9, 665–82.

    Google Scholar 

  • Kalia, M. &Mesulam, M. M. (1980a) Brain stem projections of sensory and motor components of the vagus complex in the cat. I. The Cervical vagus and nodose ganglion.Journal of Comparative Neurology 193, 436–65.

    Google Scholar 

  • Kalia, M. &Mesulam, M. M. (1980b) Brain stem projections of sensory and motor components of the vagus complex in the cat. II. Laryngeal, tracheobronchial, pulmonary, cardiac and gastrointestinal branches.Journal of Comparative Neurology 193, 467–508.

    Google Scholar 

  • Katz, D. M. &Karten, H. J. (1980) Substance P in the vagal sensory ganglia: localization in cell bodies and pericellular arborization.Journal of Comparative Neurology 193, 549–64.

    Google Scholar 

  • Kayahara, T. (1986) Synaptic connections between motorneurons and dorsal root ganglion cells in the cat.Brain Research 376, 299–309.

    Google Scholar 

  • Kayahara, T., Takimoto, T. &Sakashita, S. (1981) Synaptic junctions in the cat spinal ganglion.Brain Research 216, 277–90.

    Google Scholar 

  • Kayahara, T., Sakashita, S. &Takimoto, T. (1984) Evidence of spinal origin of neurons synapsing with dorsal root ganglion cells of the cat.Brain Research 293, 225–30.

    Google Scholar 

  • Kiss, F. (1932) Sympathetic elements in the cranial and spinal ganglia.Journal of Anatomy 66, 488–98.

    Google Scholar 

  • Lewis, P. R., Blundell, J. P., Breathnach, S. M. &Navaratnam, V. (1972) Regenerative capacity of visceral preganglionic neurons.Nature, New Biology 236, 181–82.

    Google Scholar 

  • Lieberman, A. R. (1969a) Absence of ultrastructural changes in ganglionic neurons after supranodose vagotomy.Journal of Anatomy 104, 49–54.

    Google Scholar 

  • Lieberman, A. R. (1969b) Light- and electron-microscope observations on the Golgi apparatus of normal and axotomized sensory neurons.Journal of Anatomy 104, 309–25.

    Google Scholar 

  • Lieberman, A. R. (1971) The axon reaction: a review of the principal features of perikaryal to axon injury.International Review of Neurobiology 14, 49–124.

    Google Scholar 

  • Lieberman, A. R. (1976) Sensory Ganglia. InThe Peripheral Nerve (edited byD. N. Landon) pp. 188–278. Chapman and Hall Ltd., London.

    Google Scholar 

  • Ling, E. A. &Leong, S. K. (1987) Effects of intraneural injection of Ricinus communis agglutinin-60 into the rat vagus nerve.Journal of Neurocytology 16, 373–87.

    Google Scholar 

  • Ling, E. A., Wong, W. C., Yick, T. Y. &Leong, S. K. (1986) Ultrastructural changes in the dorsal motor nucleus of monkey following bilateral cervical vagotomy.Journal of Neurocytology 15, 1–15.

    Google Scholar 

  • Ling, E. A., Shieh, J. Y., Wen, C. Y., Yick, T. Y. &Wong, W. C. (1987) The dorsal motor nucleus of the vagus nerve of the hamster: ultrastructure of vagal neurons and their responses to vagotomy.Journal of Anatomy 152, 161–72.

    Google Scholar 

  • Majumdur, S., Mills, E. &Smith, P. G. (1983) Degenerative and regenerative changes in central projections of glossopharyngeal and vagal sensory neurons after peripheral axotomy in cats: a structural basis for central reorganization of arterial chemoreflex pathways.Neuroscience 10, 841–49.

    Google Scholar 

  • McLean, J. H. &Hopkins, D. A. (1982) Ultrastructural identification of labelled neurons in the dorsal motor nucleus of the vagus nerve following injections of horseradish peroxidase into the vagus nerve and brainstem.Journal of Comparative Neurology 206, 243–52.

    Google Scholar 

  • McLean, J. H. &Hopkins, D. A. (1985) Ultrastructure of the dorsal motor nucleus of the vagus nerve in the monkey with a comparison of synaptology in monkey and cat.Journal of Comparative Neurology 231, 162–74.

    Google Scholar 

  • Miller, R. V., Kruger, S., Coates, P. W. &Orkand, P. M. (1970) Formation of synaptic contacts on dissociated chick embryo sensory ganglion cellsin vitro.Brain Research 24, 356–58.

    Google Scholar 

  • Mitchell, G. A. G. &Warwick, R. (1955) The dorsal vagal nucleus.Acta Anatomica 25, 371–95.

    Google Scholar 

  • Mugnaini, E. (1965) Dark cells in electron micrographs from the central nervous system of vertebrates.Journal of Ultrastructure Research 121, 235–36.

    Google Scholar 

  • Navaratnam, V. &Lewis, P. R. (1975) Effects of vagotomy on the distribution of cholinesterase in the cat medulla oblongata.Brain Research 100, 599–613.

    Google Scholar 

  • Peters, A., Palay, S. &Webster, H. deF (1976)The Fine Structure of the Nervous System: The Neurons and Supporting Cells, W. B. Saunders, Philadelphia — London — Toronto.

    Google Scholar 

  • Pineda, A., Maxwell, D. S. &Kruger, L. (1967) The fine structure of neurons and satellite cells in the trigeminal ganglion of cat and monkey.American Journal of Anatomy 121, 461–88.

    Google Scholar 

  • Szereda-Przestaszewska, M. (1985) Retrograde degeneration within the dorsal motor vagal nucleus following bilateral vagotomy in rabbits.Acta Anatomica 121, 133–39.

    Google Scholar 

  • Tay, S. S. W., Wong, W. C. &Ling, E. A. (1984) An ultrastructural study of the neuronal changes in the cardiac ganglia of the monkey (Macaca fascicularis) following unilateral vagotomy.Journal of Anatomy 138, 67–80.

    Google Scholar 

  • Vaithilingham, U. D., Wong, W. C. &Ling, E. A. (1986) Transneuronal changes in the myenteric ganglia of the monkey following vagotomy.Neuroscience 17, 829–36.

    Google Scholar 

  • Wakley, G. K. &Bower, A. J. (1981) The dorsal vagal ganglion of the hen (Gallus domesticus). A histological and physiological study.Journal of Anatomy 132, 95–105.

    Google Scholar 

  • Zalewski, A. A. (1970) Continuous trophic influence of chromatolysed gustatory neurons on taste buds.Anatomical Record 167, 165–174.

    Google Scholar 

  • Zalewski, A. A. (1980) Survival, regeneration and trophic function of neurons in 1-year transplants of sensory ganglia.Experimental Neurology 68, 390–94.

    Google Scholar 

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Ling, EA., Wong, WC. An electron microscopic study of the nodose (inferior vagal) ganglion cells in the monkey. J Neurocytol 17, 845–857 (1988). https://doi.org/10.1007/BF01216711

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  • DOI: https://doi.org/10.1007/BF01216711

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