Skip to main content
Log in

Origin and peptide content of nerve fibers in the nasal mucosa of rats

  • Original Articles
  • Published:
Anatomy and Embryology Aims and scope Submit manuscript

Abstract

Injection of the retrograde neuronal tracer True blue into the anterior-lateral part of the nasal mucosa of rats labeled nerve cell bodies in the superior cervical ganglion, the sphenopalatine ganglion, the otic ganglion and the trigeminal ganglion on the ipsilateral side. In the superior cervical ganglion, the sphenopalatine ganglion and the trigeminal ganglion on the contralateral side, very few nerve cell bodies were labeled, indicating that these ganglia provide minor contributions only. The number of labeled cell bodies indicates that the superior cervical ganglion, the sphenopalatine ganglion and the trigeminal ganglion contribute most to the innervation of the nose, while the contribution from the otic ganglion is minor. Cell bodies in the superior cervical ganglion harbored noradrenaline (NA) or NA/neuropeptide Y (NPY); in the sphenopalatine ganglion vasoactive intestinal peptide (VIP) or VIP/NPY; in the otic ganglion VIP, VIP/NPY or VIP/substance P (SP) and in the trigeminal ganglion calcitonin gene-related peptide (CGRP) or CGRP/SP. The results from denervations and tracer experiments suggest that all NA-containing and the majority of NPY-containing fibers in the nasal mucosa are derived from the superior cervical ganglion (sympathetic nerve supply). VIP- and VIP/NPY-containing fibers originate from the sphenopalatine and otic ganglia (parasympathetic nerve supply). Nerve fibers containing CGRP and CGRP/SP emanate from the trigeminal ganglion (sensory nerve supply).

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

  • Änggård A (1974) The effect of parasympathetic nerve stimulation on the microcirculation and secretion in the nasal mucosa of the cat. Acta Otolaryngol 78:98–105

    Google Scholar 

  • Anton F, Peppel P (1991) Central projections of trigeminal primary afferents innervating the nasal mucosa: a horseradish study in the rat. Neuroscience 41:617–628

    Google Scholar 

  • Azuma E, Asakura K, Kataura A (1982) Histochemical demonstration of peripheral autonomic innervation in canine nasal mucosa by retrograde axonal transport of horseradish peroxidase. Acta Otolaryngol 93:139–146

    Google Scholar 

  • Coons AH, Leduc EH, Connolly JM (1955) Studies on antibody production. 1. A method for the histochemical demonstration of specific antibody and its application to a study of the hyper-immune rabbit. J Exp Med 102:49–60

    Google Scholar 

  • Dahlström A, Fuxe K (1965) The adrenergic innervation of the nasal mucosa of certain mammals. Acta Otolaryngol (Stockh) 59:65–72

    Google Scholar 

  • Eccles R, Wilson H (1973) The parasympathetic secretory nerves of the nose of the cat. J Physiol 230:213–220

    Google Scholar 

  • Furness JB, Costa M, Keast JR (1984) Choline acetyltransferase- and peptide immunoreactivity of submucous neurons in the small intestine of the guinea pig. Cell Tissue Res 237:329–336

    Google Scholar 

  • Grunditz T, Håkanson R, Rerup C, Sundler F, Uddman R (1984) Neuropeptide Y in the thyroid gland: neuronal localization and enhancement of stimulated thyroid hormone secretion. Endocrinology 115:1537–1542

    Google Scholar 

  • Grunditz T, Håkanson R, Hedge G, Rerup C, Sundler F, Uddman R (1986) Peptide histidine isoleucine amide stimulates thyroid hormone secretion and coexists with vasoactive intestinal polypeptide in intrathyroid nerve fibers from laryngeal ganglia. Endocrinology 118:783–790

    Google Scholar 

  • Grunditz T, Håkanson R, Sundler F, Uddman R (1988a) Neuronal pathways to the rat thyroid revealed by retrograde tracing and immunocytochemistry. Neuroscience 24:321–335

    Google Scholar 

  • Grunditz T, Ekman R, Håkanson R, Sundler F, Uddman R (1988b) Neuropeptide Y and vasoactive intestinal peptide coexist in rat thyroid nerve fibers emanating from the thyroid ganglion. Regul Pept 23:193–208

    Google Scholar 

  • Ishii T (1970) The cholinergic innervation of the human nasal mucosa. Pract Otol Rhinol Laryngol 32:153–158

    Google Scholar 

  • Lacroix JS, Änggård A, Hökfelt T, O'Hare MMT, Fahrenkrug J, Lundberg JM (1990) Neuropeptide Y: presence in sympathetic and parasympathetic innervation of the nasal mucosa. Cell Tissue Res 259:119–128

    Google Scholar 

  • Leblanc G, Landis S (1988) Target specificity of neuropeptide Y-immunoreactive cranial parasympathetic neurons. J Neurosci 8(1): 146–155

    Google Scholar 

  • Lundblad L, Änggård A, Lundberg JM (1983) Effects of antidromic trigeminal nerve stimulation in relation to parasympathetic vasodilation in cat nasal mucosa. Acta Physiol Scand119:7–13

    Google Scholar 

  • Luts A, Sundler F (1989) Peptide-containing nerve fibers in the respiratory tract of the ferret. Cell Tissue Res 258:259–267

    Google Scholar 

  • Malm L (1973) Stimulation of sympathetic nerve fibers to the nose in cats. Acta Otolaryngol 75:519–526

    Google Scholar 

  • Rush RA, Geffen LB (1981) Dopamine-beta-hydroxylase in health and disease. CRC Crit Rev Clin Lab Sci 12:241–277

    Google Scholar 

  • Shipley MT (1985) Transport of molecules from nose to brain: Transneuronal anterograde and retrograde labeling in the rat olfactory system by wheat germ agglutinin-horseradish peroxidase applied to the nasal epithelium. Brain Res Bull 15:129–142

    Google Scholar 

  • Skagerberg G, Björklund A, Lundvall O (1985) Further studies on the use of True Blue as a retrograde fluorescent tracer in combination with monoamine histochemistry. J Neurosci Methods 14:25–40

    Google Scholar 

  • Stewart W (1985) Labelling of olfactory bulb glomeruli following horseradish peroxidase lavage of the nasal cavity. Brain Res 347:200–203

    Google Scholar 

  • Stjärne P, Lundblad L, Änggård A, Hökfelt T, Lundberg JM (1989) Tachykinins and calcitonin gene-related peptide: coexistence in sensory nerves of the nasal mucosa and effects on blood flow. Cell Tissue Res 256:439–446

    Google Scholar 

  • Sundler F, Brodin E, Ekblad E, Håkanson R, Uddman R (1985) Sensory nerve fibers: distribution of substance P, neurokinin A and calcitonin gene-related peptide. In: Håkanson R, Sundler F (eds) Tachykinin antagonists. Elsevier, Amsterdam, pp 3–14

    Google Scholar 

  • Sundler F, Ekblad E, Grunditz T, Håkanson R Luts A, Uddman R (1989) NPY in peripheral non-adrenergic neurons. In: Mutt V et al. (ed) Neuropeptide Y. Raven Press, New York, pp 93–102

    Google Scholar 

  • Uddman R, Alumets J, Densert O, Håkanson R, Sundler F (1978) Occurrence and distribution of VIP nerves in the nasal mucosa and tracheobronchial wall. Acta Otolaryngol (Stockh) 86:443–448

    Google Scholar 

  • Uddman R, Malm L, Sundler F (1981) Peptide-containing nerves in the nasal mucosa. Rhinology 19:75–79

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Grunditz, T., Uddman, R. & Sundler, F. Origin and peptide content of nerve fibers in the nasal mucosa of rats. Anat Embryol 189, 327–337 (1994). https://doi.org/10.1007/BF00190589

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00190589

Key words

Navigation