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Prevention of clinical and histological signs of proteolipid protein (PLP)-induced experimental allergic encephalomyelitis (EAE) in mice by the water-soluble carbon monoxide-releasing molecule (CORM)-A1.

Abstract
We have evaluated the effects of the carbon monoxide-releasing molecule CORM-A1 [Na(2) (BH(3) CO(2) ); ALF421] on the development of relapsing-remitting experimental allergic encephalomyelitis (EAE) in SJL mice, an established model of multiple sclerosis (MS). The data show that the prolonged prophylactic administration of CORM-A1 improves the clinical and histopathological signs of EAE, as shown by a reduced cumulative score, shorter duration and a lower cumulative incidence of the disease as well as milder inflammatory infiltrations of the spinal cords. This study suggests that the use of CORM-A1 might represent a novel therapeutic strategy for the treatment of multiple sclerosis.
AuthorsP Fagone, K Mangano, C Quattrocchi, R Motterlini, R Di Marco, G Magro, N Penacho, C C Romao, F Nicoletti
JournalClinical and experimental immunology (Clin Exp Immunol) Vol. 163 Issue 3 Pg. 368-74 (Mar 2011) ISSN: 1365-2249 [Electronic] England
PMID21235533 (Publication Type: Journal Article)
Copyright© 2011 The Authors. Clinical and Experimental Immunology © 2011 British Society for Immunology.
Chemical References
  • Anti-Inflammatory Agents, Non-Steroidal
  • Boranes
  • Carbonates
  • Myelin Proteolipid Protein
  • Peptide Fragments
  • myelin proteolipid protein (139-151)
  • sodium boranocarbonate
  • Dexamethasone
  • Carbon Monoxide
Topics
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal (administration & dosage, blood, pharmacology, therapeutic use)
  • Body Weight (drug effects)
  • Boranes (pharmacokinetics, therapeutic use)
  • Carbon Monoxide (administration & dosage, blood, pharmacology, therapeutic use)
  • Carbonates (pharmacokinetics, therapeutic use)
  • Dexamethasone (pharmacology, therapeutic use)
  • Encephalomyelitis, Autoimmune, Experimental (diagnosis, immunology, pathology, prevention & control)
  • Female
  • Mice
  • Myelin Proteolipid Protein (immunology)
  • Neutrophils (pathology)
  • Peptide Fragments (immunology)
  • Spinal Cord (drug effects, pathology)

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