The development and maintenance of paclitaxel-induced neuropathic pain require activation of the sphingosine 1-phosphate receptor subtype 1
| Autor: | Joshua W. Little, Kali Janes, Ashley J. Snider, Irina Petrache, Daniela Salvemini, William L. Neumann, Lina M. Obeid, Leesa Bryant, Emanuela Esposito, Erhard Bieberich, Chao Li, Zhoumou Chen, Grant D. Nicol, Collin L. Chen, Krzysztof Kamocki, Salvatore Cuzzocrea, Timothy M. Doyle |
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| Rok vydání: | 2014 |
| Předmět: |
MAPK/ERK pathway
Male Ceramide Paclitaxel Sphingosine-1-phosphate receptor Organophosphonates Thiophenes Pharmacology Biochemistry Neuroprotection Rats Sprague-Dawley chemistry.chemical_compound Sphingosine medicine Animals Humans Anilides Molecular Biology Sphingosine-1-Phosphate Receptors S1PR1 Oxadiazoles Fingolimod Hydrochloride Chronic pain Molecular Bases of Disease Cell Biology medicine.disease Antineoplastic Agents Phytogenic Rats Enzyme Activation Receptors Lysosphingolipid Thiazoles chemistry Propylene Glycols Neuropathic pain Indans Cytokines Neuralgia Lysophospholipids Immunosuppressive Agents Signal Transduction |
| Zdroj: | The Journal of biological chemistry. 289(30) |
| ISSN: | 1083-351X |
| Popis: | The ceramide-sphingosine 1-phosphate (S1P) rheostat is important in regulating cell fate. Several chemotherapeutic agents, including paclitaxel (Taxol), involve pro-apoptotic ceramide in their anticancer effects. The ceramide-to-S1P pathway is also implicated in the development of pain, raising the intriguing possibility that these sphingolipids may contribute to chemotherapy- induced painful peripheral neuropathy, which can be a critical dose-limiting side effect of many widely used chemotherapeutic agents.We demonstrate that the development of paclitaxel-induced neuropathic pain was associated with ceramide and S1P formation in the spinal dorsal horn that corresponded with the engagement of S1P receptor subtype 1 (S1PR(1))- dependent neuroinflammatory processes as follows: activation of redox-sensitive transcription factors (NFκB) and MAPKs (ERK and p38) as well as enhanced formation of pro-inflammatory and neuroexcitatory cytokines (TNF-α and IL-1β). Intrathecal delivery of the S1PR1 antagonist W146 reduced these neuroinflammatory processes but increased IL-10 and IL-4, potent anti-inflammatory/ neuroprotective cytokines. Additionally, spinal W146 reversed established neuropathic pain. Noteworthy, systemic administration of the S1PR1 modulator FTY720 (Food and Drug Administration- approved for multiple sclerosis) attenuated the activation of these neuroinflammatory processes and abrogated neuropathic pain without altering anticancer properties of paclitaxel and with beneficial effects extended to oxaliplatin. Similar effects were observed with other structurally and chemically unrelated S1PR1 modulators (ponesimod and CYM-5442) and S1PR1 antagonists (NIBR-14/15) but not S1PR1 agonists (SEW2871). Our findings identify for the first time the S1P/S1PR1 axis as a promising molecular and therapeutic target in chemotherapy-induced painful peripheral neuropathy, establish a mechanistic insight into the biomolecular signaling pathways, and provide the rationale for the clinical evaluation of FTY720 in chronic pain patients. |
| Databáze: | OpenAIRE |
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