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The chemokine CCL5 induces CCR1-mediated hyperalgesia in mice inoculated with NCTC 2472 tumoral cells.
- Source :
-
Neuroscience [Neuroscience] 2014 Feb 14; Vol. 259, pp. 113-25. Date of Electronic Publication: 2013 Dec 04. - Publication Year :
- 2014
-
Abstract
- Although the expression of the chemokine receptor CCR1 has been demonstrated in several structures related to nociception, supporting the nociceptive role of chemokines able to activate it, the involvement of CCR1 in neoplastic pain has not been previously assessed. We have assayed the effects of a CCR1 antagonist, J113863, in two murine models of neoplastic hyperalgesia based on the intratibial injection of either NCTC 2472 fibrosarcoma cells, able to induce osteolytic bone injury, or B16-F10 melanoma cells, associated to mixed osteolytic/osteoblastic bone pathological features. The systemic administration of J113863 inhibited thermal and mechanical hyperalgesia but not mechanical allodynia in mice inoculated with NCTC 2472 cells. Moreover, in these mice, thermal hyperalgesia was counteracted following the peritumoral (10-30μg) but not spinal (3-5μg) administration of J113863. In contrast, hyperalgesia and allodynia measured in mice inoculated with B16-F10 cells remained unaffected after the administration of J113863. The inoculation of tumoral cells did not modify the levels of CCL3 at tumor or spinal cord. In contrast, although the concentration of CCL5 remained unmodified in mice inoculated with B16-F10 cells, increased levels of this chemokine were measured in tumor-bearing limbs, but not the spinal cord, of mice inoculated with NCTC 2472 cells. Increased levels of CCL5 were also found following the incubation of NCTC 2472, but not B16-F10, cells in the corresponding culture medium. The intraplantar injection of CCL5 (0.5ng) to naïve mice evoked thermal hyperalgesia prevented by the coadministration of J113863 or the CCR5 antagonist, d-Ala-peptide T-amide (DAPTA), demonstrating that CCL5 can induce thermal hyperalgesia in mice through the activation of CCR1 or CCR5. However, contrasting with the inhibitory effect evoked by J113863, the systemic administration of DAPTA did not prevent tumoral hyperalgesia. Finally, the peritumoral administration of an anti-CCL5 antibody completely inhibited thermal hyperalgesia evoked by the inoculation of NCTC 2472 cells.<br /> (Copyright © 2013 IBRO. Published by Elsevier Ltd. All rights reserved.)
- Subjects :
- Analysis of Variance
Animals
Cell Line, Tumor
Chemokine CCL5 antagonists & inhibitors
Disease Models, Animal
Dose-Response Relationship, Drug
Enzyme-Linked Immunosorbent Assay
Functional Laterality
Hyperalgesia blood
Hyperalgesia metabolism
Male
Mice
Mice, Inbred C3H
Mice, Inbred C57BL
Neoplasm Transplantation adverse effects
Pain Measurement drug effects
Pain Threshold drug effects
Pain Threshold physiology
Peptide T therapeutic use
Receptors, CCR1 antagonists & inhibitors
Xanthenes therapeutic use
Bone Neoplasms complications
Chemokine CCL5 metabolism
Gene Expression Regulation, Neoplastic physiology
Hyperalgesia etiology
Receptors, CCR1 metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1873-7544
- Volume :
- 259
- Database :
- MEDLINE
- Journal :
- Neuroscience
- Publication Type :
- Academic Journal
- Accession number :
- 24316469
- Full Text :
- https://doi.org/10.1016/j.neuroscience.2013.11.055