Release of immunoreactive substance P in the spinal cord during development of acute arthritis in the knee joint of the cat: a study with antibody microprobes

In anaesthetized spinal cats, the release of immunoreactive substance P in the spinal cord during development of an acute inflammation in one knee joint was studied with antibody microprobes. The microprobes bore antibodies directed to the C- or N-terminus of substance P. With the normal knee joint, innocuous mechanical stimuli (flexion, pressure) did not result in spinal release of immunoreactive substance P. Following injection of kaolin and carrageenan into a knee, evidence for release of substance P following joint stimulation was found in 7 of 10 cats. Such release did not occur for several hours after joint injection and was detected predominantly in the superficial dorsal horn, the dorsal columns and at the dorsal surface of the spinal cord. In some experiments release was detected in the deep dorsal horn and upper ventral horn. Release of immunoreactive substance P required periods of mechanical stimulation such as flexion of, or pressure to, the inflamed joint. The failure to detect central release of substance P from stimulation of normal joints, and the release of substance P, after a delay, from inflamed joints, suggest that the fibres releasing this compound require sensitization by inflammatory mediators before they are excited by joint stimuli.

[1]  H. Schaible,et al.  Time course of mechanosensitivity changes in articular afferents during a developing experimental arthritis. , 1988, Journal of neurophysiology.

[2]  W. Hutchison,et al.  Peripheral Stimuli Releasing Neuropeptides in the Dorsal Horn of the Cat , 1989 .

[3]  J. Gybels,et al.  Histochemical changes of substance P, FRAP, serotonin and succinic dehydrogenase in the spinal cord of rats with adjuvant arthritis. , 1985, Life sciences.

[4]  U. Ungerstedt,et al.  In vivo release of substance P in cat dorsal horn studied with microdialysis , 1987, Neuroscience Letters.

[5]  G. Battaglia,et al.  Coexistence of glutamate and substance P in dorsal root ganglion neurons of the rat and monkey , 1988, The Journal of comparative neurology.

[6]  F. Lembeck,et al.  Effects of capsaicin on inflammation and on the substance P content of nervous tissues in rats with adjuvant arthritis. , 1983, Life sciences.

[7]  L. Villanueva,et al.  Dorsal horn (convergent) neurones in the intact anaesthetized arthritic rat. I. Segmental excitatory influences , 1987, Pain.

[8]  C. Pearson Experimental joint disease , 1963 .

[9]  W. Hutchison,et al.  The preparation and use of antibody microprobes , 1988, Journal of Neuroscience Methods.

[10]  A. Cameron,et al.  Coexistence of peptide immunoreactivity in sensory neurons of the cat , 1985, Neuroscience.

[11]  H. Schaible,et al.  Discharge characteristics of fine medial articular afferents at rest and during passive movements of inflamed knee joints , 1983, Brain Research.

[12]  I. Hendry,et al.  Laminar localization of the sites of release of immunoreactive substance P in the dorsal horn with antibody-coated microelectrodes , 1986, Neuroscience Letters.

[13]  A. Duggan,et al.  Analysis of antibody microprobe autoradiographs by computerized image processing , 1988, Journal of Neuroscience Methods.

[14]  M. Moskowitz,et al.  Intraneuronal substance P contributes to the severity of experimental arthritis. , 1984, Science.

[15]  A. Harmar,et al.  Methods for the identification of neuropeptide processing products: somatostatin and the tachykinins. , 1986, Methods in enzymology.

[16]  M. Otsuka,et al.  Effect of a tachykinin antagonist on a nociceptive reflex in the isolated spinal cord‐tail preparation of the newborn rat. , 1988, The Journal of physiology.

[17]  H. Schaible,et al.  Effects of an experimental arthritis on the sensory properties of fine articular afferent units. , 1985 .

[18]  J. Mcculloch,et al.  Substance P: immunohistochemical localization and effect upon cat pial arteries in vitro and in situ. , 1981, The Journal of physiology.

[19]  D. Menétrey,et al.  Electrophysiological characteristics of dorsal horn cells in rats with cutaneous inflammation resulting from chronic arthritis , 1982, PAIN®.

[20]  G. Fisone,et al.  Regulation of the release of coexisting neurotransmitters. , 1988, Annual review of pharmacology and toxicology.

[21]  C. Lee,et al.  The development and application of a novel N-terminal directed substance P antiserum. , 1980, Life sciences.

[22]  V. Go,et al.  Release of substance P from the cat spinal cord. , 1987, The Journal of physiology.

[23]  T. Yaksh Substance P release from knee joint afferent terminals: modulation by opioids , 1988, Brain Research.

[24]  K. Murase,et al.  Substance P augments a persistent slow inward calcium-sensitive current in voltage-clamped spinal dorsal horn neurons of the rat , 1986, Brain Research.

[25]  W. D. Hutchinson,et al.  Cutaneous stimuli releasing immunoreactive substance P in the dorsal horn of the cat , 1988, Brain Research.

[26]  H. Takagi,et al.  Stimulus specificity of peripherally evoked substance P release from the rabbit dorsal horn in situ , 1989, Neuroscience.

[27]  M. Randić,et al.  Slow excitatory transmission in rat dorsal horn: possible mediation by peptides , 1984, Brain Research.

[28]  R. Meyer,et al.  A novel electrophysiological technique for locating cutaneous nociceptive and chemospecific receptors , 1988, Brain Research.

[29]  C. Milstein,et al.  Detection of substance P in the central nervous system by a monoclonal antibody. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[30]  H. Schaible,et al.  Mechanical sensitivity of group III and IV afferents from posterior articular nerve in normal and inflamed cat knee. , 1986, Journal of neurophysiology.

[31]  C. Woolf Evidence for a central component of post-injury pain hypersensitivity , 1983, Nature.

[32]  H. Takagi,et al.  Release of substance P from the spinal dorsal horn is enhanced in polyarthritic rats , 1987, Neuroscience Letters.

[33]  H. Schaible,et al.  Release, spread and persistence of immunoreactive neurokinin A in the dorsal horn of the cat following noxious cutaneous stimulation. Studies with antibody microprobes , 1990, Neuroscience.

[34]  B. Göke,et al.  Metabolism of substance P in human plasma and in the rat circulation. , 1984, Journal of chromatography.

[35]  H. Schaible,et al.  The projection of the medial and posterior articular nerves of the cat's knee to the spinal cord , 1988, The Journal of comparative neurology.

[36]  A. Eschalier,et al.  Evidence for central phenomena participating in the changes of responses of ventrobasal thalamic neurons in arthritic rats , 1989, Brain Research.