Literature DB >> 6155172

Axonal transport of substance P in the vagus and sciatic nerves of the guinea pig.

S Brimijoin, J M Lundberg, E Brodin, T Hökfelt, G Nilsson.   

Abstract

The axonal transport and apparent subcellular distribution of substance P-like immunoreactive material (SPLI) were examined in nerves of guinea pigs by means of a sensitive radioimmunoassay and by immunohistofluorescence. Crushes or ligations were made at various levels above and below the nodose ganglion of the vagus, on the sciatic nerve, and on the central process of the S1 spinal ganglion. From the relative rates of accumulation of SPLI in the adjacent segments, it was concluded that the bulk of the substance P produced in the sensory ganglion cells was being exported toward the terminal regions of their peripheral branches. The average velocity of transport of SPLI in the peripheral direction was calculated to be 1 mm/h in the sciatic nerve and 1.25 mm/h in the vagus. The removal of SPLI from regions of nerve distal to a ligature indicated that only 26% of the peptide in vagus nerve and 17% of the peptide in sciatic nerve was available for rapid transport. It was therefore estimated that the mean velocity of the moving fraction was 5-6 mm/h. Stop-flow experiments with local cooling and rewarming in vivo suggested that some SPLI may have been transported as rapidly as 10 mm/h. The behavior of SPLI during ultracentrifugation of nerve and ganglion extracts indicated that this peptide was normally present both in a soluble form and in association with particles but was transported primarily in the latter form.

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Year:  1980        PMID: 6155172     DOI: 10.1016/0006-8993(80)91293-7

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  23 in total

1.  Substance P presynaptically depresses the transmission of sensory input to bronchopulmonary neurons in the guinea pig nucleus tractus solitarii.

Authors:  Shin-ichi Sekizawa; Jesse P Joad; Ann C Bonham
Journal:  J Physiol       Date:  2003-10-15       Impact factor: 5.182

Review 2.  Relationships between the rapid axonal transport of newly synthesized proteins and membranous organelles.

Authors:  R S Smith; R E Snyder
Journal:  Mol Neurobiol       Date:  1992 Summer-Fall       Impact factor: 5.590

3.  Correlation of neuronal size and peptide immunoreactivity in the guinea-pig trigeminal ganglion.

Authors:  W Kummer; C Heym
Journal:  Cell Tissue Res       Date:  1986       Impact factor: 5.249

4.  Substance P-like immunoreactive trigeminal ganglion cells supplying the cornea.

Authors:  J I Lehtosalo
Journal:  Histochemistry       Date:  1984

5.  Differential effects of capsaicin on the content of somatostatin, substance P, and neurotensin in the nervous system of the rat.

Authors:  R Gamse; S E Leeman; P Holzer; F Lembeck
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1981-09       Impact factor: 3.000

6.  Reinnervation of striated muscle by peripheral vagal fibres cut above or below the nodose ganglion in the cat and rabbit.

Authors:  J Coget; J P Rousseau
Journal:  J Physiol       Date:  1983-02       Impact factor: 5.182

7.  Peptide-containing neurons intrinsic to the gut wall. An experimental study in the pig.

Authors:  G Malmfors; S Leander; E Brodin; R Håkanson; T Holmin; F Sundler
Journal:  Cell Tissue Res       Date:  1981       Impact factor: 5.249

8.  Substance P-immunoreactive neurons in the brainstem of the cat related to cardiovascular centers.

Authors:  J Triepel; A Weindl; I Kiemle; J Mader; H P Volz; M Reinecke; W G Forssmann
Journal:  Cell Tissue Res       Date:  1985       Impact factor: 5.249

9.  Cannabinoid1 receptor in the dorsal vagal complex modulates lower oesophageal sphincter relaxation in ferrets.

Authors:  E R Partosoedarso; T P Abrahams; R T Scullion; J M Moerschbaecher; P J Hornby
Journal:  J Physiol       Date:  2003-07-01       Impact factor: 5.182

10.  Neonatal capsaicin pretreatment suppresses intramedullary inflammation in adjuvant-induced spondylitis.

Authors:  S Imai; S Hukuda; T Maeda
Journal:  Clin Exp Immunol       Date:  1994-01       Impact factor: 4.330

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