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The Systemic Administration of the Chemokine CCL1 Evokes Thermal Analgesia in Mice Through the Activation of the Endocannabinoid System

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Abstract

Apart from its involvement in immune functions, the chemokine CCL1 can participate in the modulation of nociceptive processing. Previous studies have demonstrated the hypernociceptive effect produced by CCL1 in the spinal cord, but its possible action on peripheral nociception has not yet been characterized. We describe here that the subcutaneous administration of CCL1 (1–10 µg/kg) produces dose-dependent and long-lasting increases in thermal withdrawal latencies measured by the unilateral hot plate test in mice. The antinociceptive nature of this effect is further supported by the reduction of spinal neurons expressing Fos protein in response to a noxious thermal stimulus observed after the administration of 10 µg/kg of CCL1. CCL1-induced antinociception was inhibited after systemic, but not spinal administration of the selective antagonist R243 (0.1–1 mg/kg), demonstrating the participation of peripheral CCR8 receptors. The absence of this analgesic effect in mice treated with a dose of cyclophosphamide that produces a drastic depletion of leukocytes suggests its dependency on white blood cells. Furthermore, whereas the antinociceptive effect of CCL1 was unaffected after the treatment with either the antagonist of opioid receptors naloxone or the cannabinoid type 1 receptor blocker AM251, it was dose-dependently inhibited after the administration of the CB2 receptor antagonist SR144528 (0.1-1 mg/kg). The detection by ELISA of an increased presence of the endocannabinoid 2-arachidonoylglycerol after the administration of an analgesic dose of CCL1 supports the notion that CCL1 can evoke thermal analgesia through the release of this endocannabinoid from circulating leukocytes.

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Acknowledgements

IUOPA is supported by Obra Social Fundación Cajastur-Liberbank (Asturias, Spain).

Funding

The study was supported by grants from the Ministerio de Economía, Industria y Competitividad, Agencia Estatal de Investigación and FEDER (European Union) (SAF2017-86799-R).

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MG-D helped to develop the study rationale, performed experiments, and analyzed the results. AA helped to design and perform the experiments and analyzed the results. AL helped to perform experiments. AH helped to analyze the results and critically revised the manuscript. AB helped to develop the study rationale and design, performed experiments, analyzed the results, and prepared the manuscript. LM helped to develop the study rationale and design, performed experiments, analyzed the results, and prepared the manuscript.

Corresponding author

Correspondence to Luis Menéndez.

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The authors declare no potential conflicts of interest.

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All applicable international, national, and/or institutional guidelines for the care and use of animals were followed and approved by the Comité Ético de Experimentación Animal de la Universidad de Oviedo. The experiments of this manuscript comply with the current laws of the country in which they were performed.

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García-Domínguez, M., Aguirre, A., Lastra, A. et al. The Systemic Administration of the Chemokine CCL1 Evokes Thermal Analgesia in Mice Through the Activation of the Endocannabinoid System. Cell Mol Neurobiol 39, 1115–1124 (2019). https://doi.org/10.1007/s10571-019-00706-3

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  • DOI: https://doi.org/10.1007/s10571-019-00706-3

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