Skip to main content
Log in

Primary afferent terminals in the nucleus of the solitary tract of the frog: An electron microscopic study

  • Published:
Experimental Brain Research Aims and scope Submit manuscript

Summary

In the frog solitarius nucleus, primary afferent terminals of the facial and glossopharyngealvagal nerves were identified with cobalt labelling and electron microscopy. The labelled terminals were grouped in two main categories, one with small (1–2 μm) and pale terminals, and another with large (3–5 μm) and dark terminals. The small terminals greatly outnumbered the large ones. In addition many terminals intermediate in size and staining reactions were found. All kinds of labelled boutons contained medium-size clear synaptic vesicles, among which dense-core vesicles of the smaller type frequently occurred. The labelled primary afferent terminals established axo-dendritic contacts of the asymmetric type. Close to these contact sites they were themselves very frequently contacted by a profile interpreted as presynaptic in relation to them. Such profiles contained spherical, pleomorphic (including dense-core) or flattened vesicles; a fourth kind was interpreted as presynaptic dendrites. It is concluded that viscerosensory fibres, as opposed to somatosensory fibres, predominantly generate small and lightly stained terminals. It is likely that the effect of synaptic transmission at the solitarius tract terminals is modulated in a very versatile manner by the various presynaptic profiles converging on these terminals.

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

  • Beckstead RM, Norgren R (1979) An autoradiographic examination of the central distribution of the trigeminal, facial, glossopharyngeal, and vagal nerves in the monkey. J Comp Neurol 184: 455–472

    Google Scholar 

  • Chiba T, Doba N (1975) The synaptic structure of catecholaminergic axon varicosities in the dorso-medial portion of the nucleus tractus solitarius of the cat: possible roles in the regulation of cardiovascular reflexes. Brain Res 84: 31–46

    Google Scholar 

  • Chiba T, Doba N (1976) Catecholaminergic axo-axonic synapses in the nucleus of the tractus solitarius (pars commissuralis) of the cat: possible relation to presynaptic regulation of baroreceptor reflexes. Brain Res 102: 255–265

    Google Scholar 

  • Chiba T, Kato M (1978) Synaptic structures and quantification of Catecholaminergic axons in the nucleus tractus solitarius of the rat: possible modulatory roles of catecholamines in baroreceptor reflexes. Brain Res 151: 323–338

    Google Scholar 

  • Ciriello J, Hrycyshyn AW, Calaresu FR (1981) Glossopharyngeal and vagal efferent projections to the brain stem of the cat: a horseradish peroxidase study. J Auton Nerv Syst 4: 63–79

    Google Scholar 

  • Conradi S (1969) On motoneuron synaptology in adult cat. Acta Physiol Scand (Suppl) 332: 1–115

    Google Scholar 

  • Finger TE (1981) Enkephalin-like immunoreactivity in the gustatory lobes and visceral nuclei in the brains of goldfish and catfish. Neuroscience 6: 2747–2758

    Google Scholar 

  • Gobel S (1974) Synaptic organization of the substantia gelatinosa glomeruli in the spinal trigeminal nucleus of the adult cat. J Neurocytol 3: 219–243

    Google Scholar 

  • Gwyn DG, Leslie RA (1979) A projection of vagus nerve to the area subpostrema in the cat. Brain Res 161: 335–341

    Google Scholar 

  • !wyn DG, Leslie RA, Hopkins DA (1979) Gastric afferents to the nucleus of the solitary tract in the cat. Neurosci Lett 14: 13–17

    Google Scholar 

  • Gwyn DG, Wilkinson PH, Leslie RA (1982) The ultrastructural identification of vagal terminals in the solitary nucleus of the cat after anterograde labelling with horseradish peroxidase. Neurosci Lett 28: 139–143

    Google Scholar 

  • Inagaki S, Shiosaka S, Takatsuki K, Sakanaka M, Takagi H, Senba E, Matsuzaki T, Tohyama M (1981) Distribution of somatostatin in the frog brain, Rana catesbiana, in relation to location of catecholamine-containing neuron system. J Comp Neurol 202: 89–101

    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. J Comp Neurol 193: 435–465

    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. J Comp Neurol 193: 467–508

    Google Scholar 

  • Katz DM, Karten HJ (1979) The discrete anatomical localization of vagal aortic afferents within a catecholamine-containing cell group in the nucleus solitarius. Brain Res 171: 187–195

    Google Scholar 

  • Leslie RA, Gwyn DG, Hopkins DA (1982) The ultrastructure of the subnucleus gelatinosus of the nucleus of the tractus solitarius in the cat. J Comp Neurol 206: 109–118

    Google Scholar 

  • Lévai G, Matesz C, Székely G (1982) Fine structure of dorsal root terminals in the dorsal horn of the frog spinal cord. Acta Biol Acad Sci Hung 33: 231–246

    Google Scholar 

  • Loewy AD, McKellar S (1980) The neuroanatomical basis of central cardiovascular control. Fed Proc 39: 2495–2503

    Google Scholar 

  • Matesz C, Székely G (1978) The motor column and sensory projections of the branchial cranial nerves in the frog. J Comp Neurol 178: 157–176

    Google Scholar 

  • Nieuwenhuys R, Opdam P (1976) Structure of the brain stem. In: Llinás R, Precht W (eds) Frog neurobiology. Springer, Berlin Heidelberg New York, pp 811–855

    Google Scholar 

  • Ralston HJ III, Ralston DD (1979) The distribution of dorsal root axons in laminae I, II and III of the macaque spinal cord: a quantitative electron microscope study. J Comp Neurol 184: 643–684

    Google Scholar 

  • Reis DJ (1981) The nucleus tractus solitarius and experimental neurogenic hypertension: evidence for a central neural imbalance hypothesis of hypertensive disease. In: Martin JB, Reichlin S, Bick KL (eds) Neurosecretion and brain peptides. Raven Press, New York, pp 409–420

    Google Scholar 

  • Réthelyi M, Szentágothai J (1969) The large synaptic complexes of the substantia gelatinosa. Exp Brain Res 7: 258–274

    Google Scholar 

  • Straussfeld NJ, Obermayer M (1976) Resolution of intraneuronal and transsynaptic migration of cobalt in the insect visual and central nervous systems. J Comp Physiol 110: 1–12

    Google Scholar 

  • Székely G, Kosaras B (1976) Dendro-dendritic contacts between frog motoneurons shown with the cobalt labeling technique. Brain Res 108: 194–198

    Google Scholar 

  • Székely G, Kosaras B (1977) Electron microscopic identification of postsynaptic dorsal root terminals: a possible substrate of dorsal root potentials in the frog spinal cord. Exp Brain Res 29: 531–539

    Google Scholar 

  • Yamamoto T, Satomi H, Hiromi I, Takahashi Y (1977) Evidence of the dual innervation of the cat stomach by the vagal dorsal motor and medial solitary nuclei as demonstrated by the horseradish peroxidase method. Brain Res 122: 125–131

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Supported by the Scientific Research Council, Ministry of Health, Hungary (06/2-10/111)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Székely, G., Lévai, G. & Matesz, K. Primary afferent terminals in the nucleus of the solitary tract of the frog: An electron microscopic study. Exp Brain Res 53, 109–117 (1983). https://doi.org/10.1007/BF00239403

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00239403

Key words

Navigation