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Iron chelation and multiple sclerosis

Authors :
Steven M. LeVine
Sharon G. Lynch
Kelsey J. Weigel
Source :
ASN NEURO, ASN Neuro, Vol 6 (2014)
Publication Year :
2014

Abstract

Histochemical and MRI studies have demonstrated that MS (multiple sclerosis) patients have abnormal deposition of iron in both gray and white matter structures. Data is emerging indicating that this iron could partake in pathogenesis by various mechanisms, e.g., promoting the production of reactive oxygen species and enhancing the production of proinflammatory cytokines. Iron chelation therapy could be a viable strategy to block iron-related pathological events or it can confer cellular protection by stabilizing hypoxia inducible factor 1α, a transcription factor that normally responds to hypoxic conditions. Iron chelation has been shown to protect against disease progression and/or limit iron accumulation in some neurological disorders or their experimental models. Data from studies that administered a chelator to animals with experimental autoimmune encephalomyelitis, a model of MS, support the rationale for examining this treatment approach in MS. Preliminary clinical studies have been performed in MS patients using deferoxamine. Although some side effects were observed, the large majority of patients were able to tolerate the arduous administration regimen, i.e., 6–8 h of subcutaneous infusion, and all side effects resolved upon discontinuation of treatment. Importantly, these preliminary studies did not identify a disqualifying event for this experimental approach. More recently developed chelators, deferasirox and deferiprone, are more desirable for possible use in MS given their oral administration, and importantly, deferiprone can cross the blood–brain barrier. However, experiences from other conditions indicate that the potential for adverse events during chelation therapy necessitates close patient monitoring and a carefully considered administration regimen.<br />Abnormal iron deposition begins early in the disease course of multiple sclerosis, and this iron may facilitate pathogenesis. Iron chelation is an intervention strategy that can ameliorate iron-related pathogenic events, but it has associated risks.

Subjects

Subjects :
MBP, myelin basic protein
PKAN, pantothenate kinase-associated neurodegeneration
experimental autoimmune encephalomyelitis
Review Article
Pharmacology
chemistry.chemical_compound
Oral administration
deferiprone
TBARS, thiobarbituric acid reactive substances
BBB, blood–brain barrier
MOG, myelin oligodendrocyte glycoprotein
TNF-α, tumor necrosis factor α
EAE, experimental autoimmune encephalomyelitis
PS1, presenilin 1
6-OHDA, 6-hydroxydopamine
PPMS, primary progressive MS
General Neuroscience
Experimental autoimmune encephalomyelitis
SPMS, secondary progressive MS
RBC, red blood cell
ICARS, International Cooperative Ataxia Rating Scale
MFC, magnetic field correlation
3. Good health
Deferoxamine
NBIA, neurodegeneration with brain iron accumulation
Deferiprone
CIS, clinically isolated syndrome
deferasirox
medicine.drug
Multiple Sclerosis
Pyridones
Iron
S6
SWI, susceptibility-weighted imaging
Iron Chelating Agents
AD, Alzheimer’s disease
CNS, central nervous system
lcsh:RC321-571
Proinflammatory cytokine
EDSS, Expanded Disability Status Scale
MS, multiple sclerosis
RNS, reactive nitrogen species
MPTP, 1-methyl-4-phenyl-1,2,3,6-tetrapyridine
ROS, reactive oxygen species
APP, amyloid precursor protein
medicine
Animals
Humans
Chelation therapy
lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry
RRMS, relapsing remitting MS
PD, Parkinson’s disease
business.industry
Multiple sclerosis
Deferasirox
iron deposition
medicine.disease
Aβ, amyloid-β
Chelation Therapy
IL, interleukin
chemistry
Immunology
HIF-1α, hypoxia-inducible factor 1α
FSS, functional status scale
Neurology (clinical)
business

Details

ISSN :
17590914
Volume :
6
Issue :
1
Database :
OpenAIRE
Journal :
ASN neuro
Accession number :
edsair.doi.dedup.....79c3104dda228d1e3b4dfd93b4c9d308