Hyperalgesic and hypoalgesic mechanisms evoked by the acute administration of CCL5 in mice
| Autor: | Agustín Hidalgo, Ana Lastra, Miguel G. Álvarez, María Teresa Fernández-García, Alicia R. Folgueras, Rafael Cernuda-Cernuda, Sara González-Rodríguez, Mario García-Domínguez, Luis Menéndez, Ana Baamonde |
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| Rok vydání: | 2016 |
| Předmět: |
0301 basic medicine
Male Pain Threshold Diclofenac Receptors CCR5 Immunology TRPV1 Receptors CCR1 Pharmacology κ-opioid receptor 03 medical and health sciences Behavioral Neuroscience chemistry.chemical_compound Mice 0302 clinical medicine medicine Animals Chemokine CCL5 Endogenous opioid Pain Measurement Cyclooxygenase 2 Inhibitors Endocrine and Autonomic Systems Anti-Inflammatory Agents Non-Steroidal Antagonist Dynorphin A 030104 developmental biology Nociception chemistry Celecoxib Hyperalgesia medicine.symptom Capsazepine 030217 neurology & neurosurgery |
| Zdroj: | Brain, behavior, and immunity. 62 |
| ISSN: | 1090-2139 |
| Popis: | We show here that the intraplantar administration of CCL5 in mice produces hyperalgesia at low doses but activates compensatory antinociceptive mechanisms at doses slightly higher. Thus, the injection of 3–10 ng of CCL5 evoked thermal hyperalgesia through the activation of CCR1 and CCR5 receptors, as demonstrated by the inhibitory effect exerted by the selective antagonists J113863 (0.01–0.1 μg) and DAPTA (0.3–3 μg), respectively. The prevention of this hyperalgesia by diclofenac (1–10 μg), the inhibitors of COX-1 SC-560 (0.1–1 μg) or COX-2 celecoxib (1–5 μg), the TRPV1 antagonist capsazepine (0.03–0.3 μg) or the TRPA1 antagonist HC030031 (10–50 μg) demonstrates the involvement of prostaglandin synthesis and TRP sensitization in CCL5-evoked hyperalgesia. Doses of CCL5 higher than 17 μg did not evoke hyperalgesia. However, this effect was restored by the administration of naloxone-methiodide (5 μg), nor-binaltorphimine (10 mg/kg) or an anti-dynorphin A antibody (0.62–2.5 ng). The administration of 30 ng of CCL5 also induced hyperalgesia in mice with reduced number of circulating white blood cells in response to cyclophosphamide or with selective neutrophil depletion induced by an anti-Ly6G antibody. In fact, the number of neutrophils present in paws treated with 30 ng of CCL5 was greater than in paws receiving the administration of the hyperalgesic dose of 10 ng. Finally, the expression of the endogenous opioid peptide dynorphin A was demonstrated by double immunofluorescence assays in these neutrophils attracted by CCL5. These results support previous data describing the hyperalgesic properties of CCL5 and constitute the first indication that a chemokine of the CC group can activate endogenous analgesic mechanisms. |
| Databáze: | OpenAIRE |
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