Dorsal root ganglion (DRG) neurons are involved in the transmission of nociceptive information from peripheral tissues to the central nervous system. A class of these sense organs differ from all others in that they display a property called """"""""sensitization"""""""" wherein the response to successive noxious stimuli increases and the threshold is lowered - the opposite of """"""""adaptation"""""""". Recently several neuropeptides known as tachykinins (substance P, substance K, and neuromedin K) have been shown to be synthesized by mammalian DRG neurons. Recent data has strongly implicated these neuropeptides in the afferent transmission of nociceptive information and in the efferent regulation of inflammation and sensitization in peripheral tissues. In addition another powerful vasodilator, calcitonin gene related peptide (CGRP), has been shown to co- exist with substance P containing DRG neurons and appears to potentiate the nociceptive actions of substance P in the rat spinal cord. The hypothesis we will test in the present proposal is whether tachykinin and CGRP-containing DRG neurons change biochemically and pharmacologically in response to an inflammatory pain state, and if so, to what extent these changes are associated with the phenomena of sensitization. The model system we will use to investigate this will be a standard experimental arthritis in the rat which will serve as a simple, reproducible and humane animal model of a chronic pain syndrome of high incidence in man. The goal of the present proposal is clear; to understand how peripheral tachykinin and CGRP containing neurons are involved in the genesis of chronic pain and inflammation in arthritis and to determine the effectiveness of the 30 known putative tachykinin antagonists in ameliorating the pain or inflammation associated with the arthritic condition. We feel the proposed work is the most tangible, direct and quantitative approach for studying those factors which might activate nociceptors in ordinary innocuous joint movement; obviously a problem of practical importance.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
1R01NS023970-01A1
Application #
3408133
Study Section
Neurological Sciences Subcommittee 1 (NLS)
Project Start
1987-04-01
Project End
1990-03-31
Budget Start
1987-04-01
Budget End
1988-03-31
Support Year
1
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
Schools of Medicine
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Chartier, Stephane R; Mitchell, Stefanie A T; Majuta, Lisa A et al. (2018) The Changing Sensory and Sympathetic Innervation of the Young, Adult and Aging Mouse Femur. Neuroscience 387:178-190
Majuta, Lisa A; Mitchell, Stefanie A T; Kuskowski, Michael A et al. (2018) Anti-nerve growth factor does not change physical activity in normal young or aging mice but does increase activity in mice with skeletal pain. Pain 159:2285-2295
Chartier, Stephane R; Mitchell, Stefanie At; Majuta, Lisa A et al. (2017) Immunohistochemical localization of nerve growth factor, tropomyosin receptor kinase A, and p75 in the bone and articular cartilage of the mouse femur. Mol Pain 13:1744806917745465
Majuta, Lisa A; Guedon, Jean-Marc G; Mitchell, Stefanie A T et al. (2017) Anti-nerve growth factor therapy increases spontaneous day/night activity in mice with orthopedic surgery-induced pain. Pain 158:605-617
Majuta, Lisa A; Guedon, Jean-Marc G; Mitchell, Stefanie A T et al. (2017) Mice with cancer-induced bone pain show a marked decline in day/night activity. Pain Rep 2:e614
Majuta, Lisa A; Guedon, Jean-Marc G; Mitchell, Stefanie A T et al. (2016) Anti-nerve growth factor therapy increases spontaneous day/night activity in mice with orthopedic surgery induced pain. Pain :
Thompson, Michelle L; Chartier, Stephane R; Mitchell, Stefanie A et al. (2016) Preventing painful age-related bone fractures: Anti-sclerostin therapy builds cortical bone and increases the proliferation of osteogenic cells in the periosteum of the geriatric mouse femur. Mol Pain 12:
Guedon, Jean-Marc G; Longo, Geraldine; Majuta, Lisa A et al. (2016) Dissociation between the relief of skeletal pain behaviors and skin hypersensitivity in a model of bone cancer pain. Pain 157:1239-47
Thompson, Michelle L; Jimenez-Andrade, Juan Miguel; Mantyh, Patrick W (2016) Sclerostin Immunoreactivity Increases in Cortical Bone Osteocytes and Decreases in Articular Cartilage Chondrocytes in Aging Mice. J Histochem Cytochem 64:179-89
Thompson, Michelle L; Jimenez-Andrade, Juan M; Chartier, Stephane et al. (2015) Targeting cells of the myeloid lineage attenuates pain and disease progression in a prostate model of bone cancer. Pain 156:1692-702

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