Abstract
Retrograde tracing with Fluoro-Gold was used to identify the complete population of knee joint afferents in the lumbar dorsal root ganglia of adult female Wistar rats. There was an average of 581±31 (mean± S.D.) afferents supplying each joint. These were found distributed from L1 to L5 with the great majority localised in the L3 and L4 ganglia. Electron microscopy of the posterior articular nerve of the knee revealed an average of 103±15 (mean± S.D.) myelinated and 513±39 unmyelinated axonal profiles. Since about 50–60% of the unmyelinated profiles would be expected to be sympathetic efferents, these numbers are consistent with the numbers of afferents found by Fluoro-Gold retrograde tracing and suggest that the posterior articular nerve contains about 50% of the total number of knee joint afferents in the rat. Immunohistochemistry revealed that an average of 10% of identified joint afferents expressed substance P-like immunoreactivity and that 33% expressed calcitonin gene-related peptide-like immunoreactivity.
Keywords: Sensory ganglia, substance P, calcitonin gene-related peptide, Fluoro-Gold
Full Text
The Full Text of this article is available as a PDF (577.7 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Coggeshall R. E., Hong K. A., Langford L. A., Schaible H. G., Schmidt R. F. Discharge characteristics of fine medial articular afferents at rest and during passive movements of inflamed knee joints. Brain Res. 1983 Aug 1;272(1):185–188. doi: 10.1016/0006-8993(83)90379-7. [DOI] [PubMed] [Google Scholar]
- Coggeshall R. E., La Forte R., Klein C. M. Calibration of methods for determining numbers of dorsal root ganglion cells. J Neurosci Methods. 1990 Dec;35(3):187–194. doi: 10.1016/0165-0270(90)90123-w. [DOI] [PubMed] [Google Scholar]
- Cooke T. D. Pathogenetic mechanisms in polyarticular osteoarthritis. Clin Rheum Dis. 1985 Aug;11(2):203–238. [PubMed] [Google Scholar]
- Ferrell W. R., Baxendale R. H., Carnachan C., Hart I. K. The influence of joint afferent discharge on locomotion, proprioception and activity in conscious cats. Brain Res. 1985 Nov 11;347(1):41–48. doi: 10.1016/0006-8993(85)90887-x. [DOI] [PubMed] [Google Scholar]
- Freeman M. A., Wyke B. The innervation of the knee joint. An anatomical and histological study in the cat. J Anat. 1967 Jun;101(Pt 3):505–532. [PMC free article] [PubMed] [Google Scholar]
- Hanesch U., Heppelmann B., Schmidt R. F. Substance P- and calcitonin gene-related peptide immunoreactivity in primary afferent neurons of the cat's knee joint. Neuroscience. 1991;45(1):185–193. doi: 10.1016/0306-4522(91)90114-4. [DOI] [PubMed] [Google Scholar]
- Hildebrand C., Oqvist G., Brax L., Tuisku F. Anatomy of the rat knee joint and fibre composition of a major articular nerve. Anat Rec. 1991 Apr;229(4):545–555. doi: 10.1002/ar.1092290415. [DOI] [PubMed] [Google Scholar]
- Johansson H., Sjölander P., Sojka P. Actions on gamma-motoneurones elicited by electrical stimulation of joint afferent fibres in the hind limb of the cat. J Physiol. 1986 Jun;375:137–152. doi: 10.1113/jphysiol.1986.sp016110. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kidd B. L., Mapp P. I., Blake D. R., Gibson S. J., Polak J. M. Neurogenic influences in arthritis. Ann Rheum Dis. 1990 Aug;49(8):649–652. doi: 10.1136/ard.49.8.649. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Levine J. D., Clark R., Devor M., Helms C., Moskowitz M. A., Basbaum A. I. Intraneuronal substance P contributes to the severity of experimental arthritis. Science. 1984 Nov 2;226(4674):547–549. doi: 10.1126/science.6208609. [DOI] [PubMed] [Google Scholar]
- Mapp P. I., Kidd B. L., Gibson S. J., Terry J. M., Revell P. A., Ibrahim N. B., Blake D. R., Polak J. M. Substance P-, calcitonin gene-related peptide- and C-flanking peptide of neuropeptide Y-immunoreactive fibres are present in normal synovium but depleted in patients with rheumatoid arthritis. Neuroscience. 1990;37(1):143–153. doi: 10.1016/0306-4522(90)90199-e. [DOI] [PubMed] [Google Scholar]
- Mapp P. I., Walsh D. A., Garrett N. E., Kidd B. L., Cruwys S. C., Polak J. M., Blake D. R. Effect of three animal models of inflammation on nerve fibres in the synovium. Ann Rheum Dis. 1994 Apr;53(4):240–246. doi: 10.1136/ard.53.4.240. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Neugebauer V., Lücke T., Schaible H. G. Requirement of metabotropic glutamate receptors for the generation of inflammation-evoked hyperexcitability in rat spinal cord neurons. Eur J Neurosci. 1994 Jul 1;6(7):1179–1186. doi: 10.1111/j.1460-9568.1994.tb00616.x. [DOI] [PubMed] [Google Scholar]
- Salo P. T., Tatton W. G. Age-related loss of knee joint afferents in mice. J Neurosci Res. 1993 Aug 15;35(6):664–677. doi: 10.1002/jnr.490350609. [DOI] [PubMed] [Google Scholar]
- Schaible H. G., Grubb B. D. Afferent and spinal mechanisms of joint pain. Pain. 1993 Oct;55(1):5–54. doi: 10.1016/0304-3959(93)90183-P. [DOI] [PubMed] [Google Scholar]
- Schaible H. G., Schmidt R. F. Activation of groups III and IV sensory units in medial articular nerve by local mechanical stimulation of knee joint. J Neurophysiol. 1983 Jan;49(1):35–44. doi: 10.1152/jn.1983.49.1.35. [DOI] [PubMed] [Google Scholar]
- Schaible H. G., Schmidt R. F. Effects of an experimental arthritis on the sensory properties of fine articular afferent units. J Neurophysiol. 1985 Nov;54(5):1109–1122. doi: 10.1152/jn.1985.54.5.1109. [DOI] [PubMed] [Google Scholar]
- Schaible H. G., Schmidt R. F. Time course of mechanosensitivity changes in articular afferents during a developing experimental arthritis. J Neurophysiol. 1988 Dec;60(6):2180–2195. doi: 10.1152/jn.1988.60.6.2180. [DOI] [PubMed] [Google Scholar]
- Schmued L. C., Fallon J. H. Fluoro-Gold: a new fluorescent retrograde axonal tracer with numerous unique properties. Brain Res. 1986 Jul 2;377(1):147–154. doi: 10.1016/0006-8993(86)91199-6. [DOI] [PubMed] [Google Scholar]
- Sluka K. A., Dougherty P. M., Sorkin L. S., Willis W. D., Westlund K. N. Neural changes in acute arthritis in monkeys. III. Changes in substance P, calcitonin gene-related peptide and glutamate in the dorsal horn of the spinal cord. Brain Res Brain Res Rev. 1992 Jan-Apr;17(1):29–38. doi: 10.1016/0165-0173(92)90004-6. [DOI] [PubMed] [Google Scholar]
- Sluka K. A., Lawand N. B., Westlund K. N. Joint inflammation is reduced by dorsal rhizotomy and not by sympathectomy or spinal cord transection. Ann Rheum Dis. 1994 May;53(5):309–314. doi: 10.1136/ard.53.5.309. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smith G. D., Harmar A. J., McQueen D. S., Seckl J. R. Increase in substance P and CGRP, but not somatostatin content of innervating dorsal root ganglia in adjuvant monoarthritis in the rat. Neurosci Lett. 1992 Mar 30;137(2):257–260. doi: 10.1016/0304-3940(92)90417-6. [DOI] [PubMed] [Google Scholar]
- Theriault E., Marshall K. W., Homonko D. A. Maintained peptidergic innervation of the knee joint in an animal model of antigen-induced arthritis. Regul Pept. 1993 Jul 2;46(1-2):204–207. doi: 10.1016/0167-0115(93)90034-6. [DOI] [PubMed] [Google Scholar]
- Theriault E., Tator C. H. Persistence of rubrospinal projections following spinal cord injury in the rat. J Comp Neurol. 1994 Apr 8;342(2):249–258. doi: 10.1002/cne.903420208. [DOI] [PubMed] [Google Scholar]
- Widenfalk B., Wiberg M. Origin of sympathetic and sensory innervation of the knee joint. A retrograde axonal tracing study in the rat. Anat Embryol (Berl) 1989;180(4):317–323. doi: 10.1007/BF00311164. [DOI] [PubMed] [Google Scholar]
- Yaksh T. L. Substance P release from knee joint afferent terminals: modulation by opioids. Brain Res. 1988 Aug 23;458(2):319–324. doi: 10.1016/0006-8993(88)90474-x. [DOI] [PubMed] [Google Scholar]
- el-Bohy A., Cavanaugh J. M., Getchell M. L., Bulas T., Getchell T. V., King A. I. Localization of substance P and neurofilament immunoreactive fibers in the lumbar facet joint capsule and supraspinous ligament of the rabbit. Brain Res. 1988 Sep 20;460(2):379–382. doi: 10.1016/0006-8993(88)90386-1. [DOI] [PubMed] [Google Scholar]