Skip to main content
Log in

Innervation of dog ciliary ganglion

  • Published:
Histochemistry Aims and scope Submit manuscript

    We’re sorry, something doesn't seem to be working properly.

    Please try refreshing the page. If that doesn't work, please contact support so we can address the problem.

Summary

There are species differences with regard to the composition of the ciliary ganglion. For instance, in rabbits and cats it consists solely of oculomotor nerves and has no sympathetic or sensory innervation. The purpose of this study is to clarify the participation of these nerves in the ciliary ganglion of the dog by histochemical methods. Cholinesterase (ChE) activity was studied by Karnovsky's method and catecholamine fluorescence by the glyoxylic acid method. Furthermore, the origins of the respective nerves were investigated by a serial preparation method, involving unilateral cervical sympathectomy and tracer dye injection in the ganglion. The results obtained were: (1) Ciliary ganglion cells showed intense ChE activity. Oculomotor nerve fibers leading to the ganglion showed moderate ChE activity, while the reaction in the short ciliary nerves was strong. (2) Aminergic nerves were present in the intercellular space of the ciliary ganglion, and bilateral or central innervation was suggested by the results of cervical sympathectomy. (3) Connection between the ciliary and trigeminal ganglia was proved by the dye tracer study. The results show that the ciliary ganglion in dogs is composed of oculomotor, trigeminal and sympathetic nerves.

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

  • Akert K, Glicksman MA, Lang W, Grob P, Huber A (1980) The Edinger-Westphal nucleus in the monkey. A retrograde tracer study. Brain Res 184:491–498

    Google Scholar 

  • Bentivoglio M, Kooy D, Kuypers HGJM (1979) The organization of the efferent projections of the substantia nigra in the rat. A retrograde fluorescent double labeling study. Brain Res 174:1–17

    Google Scholar 

  • Ehinger B (1966) Ocular and orbital vegetative nerves. Acta Physiol Scand 69 (Suppl) 286:1–83

    Google Scholar 

  • El-Badawi A, Schenk EA (1967) Histochemical methods for separate, consecutive and simultaneous demonstration of acetylcholinesterase and norepinephrine in cryostat sections. J Histochem Cytochem 15:580–588

    Google Scholar 

  • Eränkö O (1955) Distribution of fluorescing islets, adrenaline in the adrenal medulla of the hamster. Acta Endocrinol (Kbh) 18:174–179

    Google Scholar 

  • Eränkö O, Härkönen M (1964) Noradrenaline and acetylcholinesterase in sympathetic ganglion cells of the rat. Acta Physiol Scand 61:299–300

    Google Scholar 

  • Falck B (1962) Observations on the possibilities of the cellular localization of monoamines by a fluorescence method. Acta Physiol Scand 56 (Suppl) 197:1–25

    Google Scholar 

  • Grimes P, von Sallmann L (1960) Comparative anatomy of the ciliary nerves. Arch Ophthalmol 64:81–91

    Google Scholar 

  • Hamberger B, Norberg K, Ungerstedt U (1965) Adrenergic synaptic terminals in autonomic ganglia. Acta Physiol Scand 64:285–286

    Google Scholar 

  • Huikuri KT (1966) Histochemistry of the ciliary ganglion of the rat and the effect of preand postsynaptic nerve division. Acta Physiol Scand 69 (Suppl) 286:1–83

    Google Scholar 

  • Jacobowitz D, Koelle GB (1965) Histochemical correrations of acetylcholinesterase and catecholamines in postganglionic autonomic nerves of the cat, rabbit, and guinea pig. J Pharmacol Exp Ther 148:225–237

    Google Scholar 

  • Karnovsky MJ, Roots L (1964) A “direct-coloring” thiocholine method for cholinesterase. J Histochem Cytochem 12:219–221

    Google Scholar 

  • Koelle WA, Koelle GB (1959) The localization of external or functional acetylcholinesterase at the synapses of autonomic ganglia. J Pharmacol Exp Ther 126:1–8

    Google Scholar 

  • Marin J, Salaices M, Rivilla F, Burgos J, Marco EJ (1980) Bilateral innervation of the cerebral arteries by the superior cervical ganglion in cats. J Neurosurg 53:88–91

    Google Scholar 

  • Sunderland S, Huges ESR (1946) The pupilloconstrictor pathway and the nerves to the ocular muscles in man. Brain 69:301–309

    Google Scholar 

  • Sawchenko PE, Swanson LW (1981) A method for tracing biochemically defined pathways in the central nervous system using combined fluorescence retrograde transport and immunohistochemical techniques. Brain Res 210:31–51

    Google Scholar 

  • Tervo T (1977) Consecutive demonstration of nerves containing catecholamine and acetylcholinesterase in the rat cornea. Histochemistry 50:291–299

    Google Scholar 

  • Walsh FB, Hoyt WF (1969) Clinical neuro-ophthalmology, 3rd edit. Williams & Wilkins, Baltimore, pp 471–472

    Google Scholar 

  • Waris T, Rechardt L (1977) Histochemically demonstrable cathecholamines and cholinesterases in nerve fibers of rat dorsal skin. Histochemistry 53:203–216

    Google Scholar 

  • Warwick R (1954) The ocular parasympathetic nerve supply and its mesencephalic sourses. J Anat 88:71–93

    Google Scholar 

  • Williams PL, Warwick G (1975) Functioning neuroanatomy of man. WB Saunders, Philadelphia, pp 998–1000

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hara, H., Kobayashi, S., Sugita, K. et al. Innervation of dog ciliary ganglion. Histochemistry 76, 295–301 (1982). https://doi.org/10.1007/BF00543952

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00543952

Keywords

Navigation