TY - JOUR
T1 - Anthraquinone derivative O,O′-bis-(3′-iodopropyl)-1,4- dihidroxyanthraquinone modulates immune response and improves experimental autoimmune encephalomyelitis
AU - Alves, Caio C.S.
AU - Castro, Sandra B.R.
AU - Costa, Cristiane F.
AU - Dias, Alyria T.
AU - Alves, Chrystian J.
AU - Rodrigues, Michele F.
AU - Teixeira, Henrique C.
AU - Almeida, Mauro V.
AU - Ferreira, Ana Paula
PY - 2012/10
Y1 - 2012/10
N2 - 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.
AB - 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.
KW - Chemokines
KW - Cytokines
KW - EAE
KW - Mitoxantrone analog
KW - Multiple sclerosis
UR - http://www.scopus.com/inward/record.url?scp=84864055206&partnerID=8YFLogxK
U2 - 10.1016/j.intimp.2012.06.013
DO - 10.1016/j.intimp.2012.06.013
M3 - Article
C2 - 22749732
AN - SCOPUS:84864055206
SN - 1567-5769
VL - 14
SP - 127
EP - 132
JO - International Immunopharmacology
JF - International Immunopharmacology
IS - 2
ER -