Literature DB >> 15694688

Low dose naltrexone therapy in multiple sclerosis.

Y P Agrawal1.   

Abstract

The use of low doses of naltrexone for the treatment of multiple sclerosis (MS) enjoys a worldwide following amongst MS patients. There is overwhelming anecdotal evidence, that in low doses naltrexone not only prevents relapses in MS but also reduces the progression of the disease. It is proposed that naltrexone acts by reducing apoptosis of oligodendrocytes. It does this by reducing inducible nitric oxide synthase activity. This results in a decrease in the formation of peroxynitrites, which in turn prevent the inhibition of the glutamate transporters. Thus, the excitatory neurotoxicity of glutamate on neuronal cells and oligodendrocytes via activation of the alpha-amino-3-hydroxy-5-methyl-isoxazole-4-propionic acid class of glutamate receptor is prevented. It is crucial that the medical community respond to patient needs and investigate this drug in a clinical trial.

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Year:  2005        PMID: 15694688     DOI: 10.1016/j.mehy.2004.09.024

Source DB:  PubMed          Journal:  Med Hypotheses        ISSN: 0306-9877            Impact factor:   1.538


  4 in total

Review 1.  Multiple sclerosis: molecular mechanisms and therapeutic opportunities.

Authors:  Djordje Miljković; Ivan Spasojević
Journal:  Antioxid Redox Signal       Date:  2013-04-22       Impact factor: 8.401

2.  Low dose naltrexone in multiple sclerosis: Effects on medication use. A quasi-experimental study.

Authors:  Guttorm Raknes; Lars Småbrekke
Journal:  PLoS One       Date:  2017-11-03       Impact factor: 3.240

3.  Maternally administered sustained-release naltrexone in rats affects offspring neurochemistry and behaviour in adulthood.

Authors:  Waleed O Farid; Andrew J Lawrence; Elena V Krstew; Robert J Tait; Gary K Hulse; Sarah A Dunlop
Journal:  PLoS One       Date:  2012-12-26       Impact factor: 3.240

4.  Naltrexone reverses ethanol-induced rat hippocampal and serum oxidative damage.

Authors:  Inmaculada Almansa; Jorge M Barcia; Rosa López-Pedrajas; María Muriach; María Miranda; Francisco Javier Romero
Journal:  Oxid Med Cell Longev       Date:  2013-12-01       Impact factor: 6.543

  4 in total

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