General fitness, health and nutrition · Public discussion

iron chelators / malaria

Started by doe · · Last activity · 2 posts · 343 views

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General fitness, health and nutrition
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13 August 2003
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  1. Med Trop (Mars). 2003;63(2):119-30. Related Articles, Links

    [In Process Citation]

    [Article in French]

    Pradines B, Millet J, Henry M.

    L'Unite de Parasitologie, Institut de Medecine Tropicale du Service de Sante
    des Armees, Marseille, France. [email hidden]

    Rapid development of significant resistance to antimalarial drugs has been a
    major force driving research to identify and develop new compounds. A number of
    iron(III)-chelating compounds designed for purposes other than treating malaria
    have in vitro antimalarial activity stemming from iron deprivation or toxic
    effects related to free radical release. Several of the iron(III) chelators
    have been effective in animal models of plasmodial infection. Desferrioxamine
    has been used successfully against both uncomplicated and severe malaria in
    humans. Iron-chelating agents seem to be promising therapeutic adjuvants for
    treatment of severe Plasmodium falciparum malaria infection.

    PMID: 12910648 [PubMed - in process]

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  2. (doe) said:

    Med Trop (Mars). 2003;63(2):119-30. Related Articles, Links

    Note that the chelating agents are clearly specified ... EDTA
    would not work where Desferrioxamine is needed. And it's been
    knownm since the late 1980s or early 1990s that this effect
    happens. What is still at issue is whether it is reliable and
    safe.

    http://www.mediscope.ch/cochrane-abstracts/ab001474.htm
    Main results: No evidence of benefit or harm were shown in
    relation to mortality, but studies were small, and one trial was
    tending towards more deaths with the intervention when it was
    stopped. The risk of experiencing persistent seizures was
    significantly lower with desferrioxamine compared to placebo
    treatment (RR 0.80, 95% CI 0.67 to 0.95). Many adverse effects
    were more common in participants treated with desferrioxamine.

    Quoted message said:

    Rapid development of significant resistance to antimalarial drugs has been a
    major force driving research to identify and develop new compounds. A number of
    iron(III)-chelating compounds designed for purposes other than treating malaria
    have in vitro antimalarial activity stemming from iron deprivation or toxic
    effects related to free radical release.


    In vitro: works in the test tube by depriving theparasites of
    iron or releasing free radicals. Not yet tested in animals.

    Quoted message said:

    Several of the iron(III) chelators
    have been effective in animal models of plasmodial infection. Desferrioxamine
    has been used successfully against both uncomplicated and severe malaria in
    humans.

    Quoted message said:

    Iron-chelating agents seem to be promising therapeutic *adjuvants* for
    treatment of severe Plasmodium falciparum malaria infection.

    Translation: it appears to help (adjuvant = helper)

    http://www.mahidol.ac.th/abstracts/annual2000/0261.htm
    "Desferrioxamine, however, reduced oxidative damage during the
    infection without compromising the therapeutic effect of
    artemisinin. These findings suggested that the infected
    erythrocytes were prone to the effect of artemisinin. Addition of
    a chelator such as desferrioxamine is beneficial and can improve
    the treatment of severe malarial."

    Tsu

    --
    To doubt everything or to believe everything
    are two equally convenient solutions; both
    dispense with the necessity of reflection.
    - Jules Henri Poincaré

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