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Topical moringin-cream relieves neuropathic pain by suppression of inflammatory pathway and voltage-gated ion channels in murine model of multiple sclerosis.

AbstractBackground:
Neuropathic pain represents the major public health burden with a strong impact on quality life in multiple sclerosis patients. Although some advances have been obtained in the last years, the conventional therapies remain poorly effective. Thus, the discovery of innovative approaches to improve the outcomes for multiple sclerosis patients is a goal of primary importance. With this aim, we investigated the efficacy of the 4-(α−L-rhamnopyranosyloxy)benzyl isothiocyanate (moringin), purified from Moringa oleifera seeds and ready-to-use as topical treatment in experimental autoimmune encephalomyelitis, murine model of multiple sclerosis. Female C57BL/6 mice immunized with myelin oligodendrocyte glycoprotein (MOG35–55) were topically treated with 2% moringin cream twice daily from the onset of the symptoms until the sacrifice occurred about 21 days after experimental autoimmune encephalomyelitis induction.
Results:
Our observations showed the efficacy of 2% moringin cream treatment in reducing clinical and histological disease score, as well as in alleviating neuropathic pain with consequent recovering of the hind limbs and response to mechanical stimuli. In particular, Western blot analysis and immunohistochemical evaluations revealed that 2% moringin cream was able to counteract the inflammatory cascade by reducing the production of pro-inflammatory cytokines (interleukin-17 and interferon-γ) and in parallel by increasing the expression of anti-inflammatory cytokine (interleukin-10). Interestingly, 2% moringin cream treatment was found to modulate the expression of voltage-gated ion channels (results focused on P2X7, Nav 1.7, Nav 1.8 KV4.2, and α2δ-1) as well as metabotropic glutamate receptors (mGluR5 and xCT) involved in neuropathic pain initiation and maintenance.
Conclusions:
Finally, our evidences suggest 2% moringin cream as a new pharmacological trend in the management of multiple sclerosis-induced neuropathic pain.
AuthorsSabrina Giacoppo, Renato Iori, Placido Bramanti, Emanuela Mazzon
JournalMolecular pain (Mol Pain) 2017 Jan-Dec Vol. 13 Pg. 1744806917724318 ISSN: 1744-8069 [Electronic] United States
PMID28741431 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Anti-Inflammatory Agents
  • Cytokines
  • Ion Channels
  • Isothiocyanates
  • Plant Extracts
  • moringin
  • benzyl isothiocyanate
Topics
  • Animals
  • Anti-Inflammatory Agents (therapeutic use)
  • Cytokines (metabolism)
  • Disease Models, Animal
  • Encephalomyelitis, Autoimmune, Experimental (drug therapy)
  • Female
  • Ion Channels (drug effects)
  • Isothiocyanates (pharmacology)
  • Mice, Inbred C57BL
  • Multiple Sclerosis (drug therapy)
  • Neuralgia (drug therapy)
  • Plant Extracts (pharmacology)

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