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Archived Comments for: Metformin overdose, but not lactic acidosis per se, inhibits oxygen consumption in pigs

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  1. Metformin-induced effects in oxygen consumption

    Heikki Savolainen, Ministry of Social Affairs and Health

    14 May 2012

    Dear Editor,

    The authors of this study have to be congratulated for their elegant experiments and reaching the correct conclusions.

    The drug is, in fact, an inhibitor of the complex I in the mitochondrial respiratory chain. This seems to be the main reason for the deleterious effects. Two other circumstances may, however, contribute and aggravate it. D-lactate produced excessively from glucose is slowly metabolized by the D-lactic acid oxidase prolonging the metabolic acidosis, and acidotic excessive protons impair the the terminal cytochrome oxidase which is essentially a proton pump to molecular oxygen.

    Thus, metformin interferes with the oxidative phosphorylation at several stages.

    Competing interests

    None

  2. excellent paper

    H M, Other

    28 May 2012

    metformin is a uncoupling agent causes uncoupling of oxidative phosphorylation; due to an increase in permeability of the inner mitochondrial membrane, protons heat is generated without atp, (not using ATP synthase ligated channels) reactions involving NADH, FADH increase, H+'s used, generating heat. other uncoupling agents include Salicyates, Alcohol, Dinitrophenol, and of course Metformin. , "SAD-M". Perhaps induced hypothermia would be of benefit in cases with malignant hyperthermia.

    Competing interests

    None declared

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