1992
DOI: 10.1016/0014-5793(92)80455-p
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Evidence of cytosolic iron release during post‐ischaemic reperfusion of isolated rat hearts Influence on spin‐trapping experiments with DMPO

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Cited by 30 publications
(7 citation statements)
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“…Release and redistribution of redox-active iron during IR in the liver as well as other organs has been observed by several research laboratories [162][163][164][165][166][167]. Increased levels of mobilized iron indicate a state of increased sensitivity for the cells and may represent the connecting link between H 2 O 2 production and tissue damage during reperfusion.…”
Section: Redox-active Iron In Hepatic Ir Injurymentioning
confidence: 95%
“…Release and redistribution of redox-active iron during IR in the liver as well as other organs has been observed by several research laboratories [162][163][164][165][166][167]. Increased levels of mobilized iron indicate a state of increased sensitivity for the cells and may represent the connecting link between H 2 O 2 production and tissue damage during reperfusion.…”
Section: Redox-active Iron In Hepatic Ir Injurymentioning
confidence: 95%
“…Among several nitrones used as spin traps, 5,5-dimethyl-1-pyrroline N-oxide (DMPO) has received the most attention. Reaction of this spin trap with superoxide and hydroxyl radicals or radicals of a lipid nature derived from hydroxyl radicals produces spin-trapped adducts with characteristic EPR spectra (5,6). Moreover, spin trapping using DMPO has been used to detect and distinguish between carbon-centered, alkoxyl, and peroxyl radicals produced during metal ion-and lipoxygenase-catalyzed breakdown (7), as well as photolytic breakdown of peroxidized fatty acids (8).…”
mentioning
confidence: 99%
“…Iron metabolism is normally thought to be tightly controlled ; nevertheless, the chemical nature and subcellular distribution of free iron within cells are completely unknown, except that this pool seems to be normally kept very small (Crichton and Charloteaux-Wauters, 1987 ;Halliwell, 1992) . In addition, certain pathological conditions are known to increase free iron concentrations by releasing this ion from ferritin (Thomas and Aust, 1986;Boucher et al, 1992) . It should be noted that even the lowest concentration of iron (11) or (111) (30 pM) used in our studies was found to increase significantly the production of TOPA compounds over baseline autoxidation .…”
Section: Discussionmentioning
confidence: 99%