Anthraquinone derivative O,O′-bis-(3′-iodopropyl)-1,4- dihidroxyanthraquinone modulates immune response and improves experimental autoimmune encephalomyelitis

Caio C.S. Alves, Sandra B.R. Castro, Cristiane F. Costa, Alyria T. Dias, Chrystian J. Alves, Michele F. Rodrigues, Henrique C. Teixeira, Mauro V. Almeida, Ana Paula Ferreira

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14 Scopus citations

Abstract

The present study investigated the effects of the anthraquinone derivative (O,O′-bis-(3′-iodopropyl)-1,4-dihidroxyanthraquinone - DIPDHAQ), mitoxantrone analog, in an experimental autoimmune encephalomyelitis (EAE) model. The results showed that DIPDHAQ treatment improved the clinical signs of the disease (n = 10; vehicle: 3.8 ± 0.3; DIPDHAQ: 1.4 ± 0.9). The improvement was associated with a decrease of inflammatory cells, demyelination, IL-17, IFN-γ, IL-12p40, IL-6, TGF-β, CCL5 and CCL20 levels in the spinal cord. DIPDHAQ presented a low cytotoxicity when in vitro assays were performed. Therefore, the findings suggest a major role for DIPDHAQ in multiple sclerosis, disease characterized as an autoimmune inflammatory disorder against myelin proteins of the brain and spinal cord. The attenuation of inflammation and consequently improvement of clinical signs, involving a decrease of pro-inflammatory cytokines and the low cytotoxicity of DIPDHAQ, suggest that this compound could be used as an alternative treatment for autoimmune diseases in the central nervous system.

Original languageEnglish
Pages (from-to)127-132
Number of pages6
JournalInternational Immunopharmacology
Volume14
Issue number2
DOIs
StatePublished - Oct 2012
Externally publishedYes

Keywords

  • Chemokines
  • Cytokines
  • EAE
  • Mitoxantrone analog
  • Multiple sclerosis

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