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Blood, Vol. 95 No. 11 (June 1), 2000:
pp. 3442-3450
Ferriporphyrins and endothelium: a 2-edged sword promotion of
oxidation and induction of cytoprotectants
József Balla,
György Balla,
Viktoria Jeney,
György Kakuk,
Harry S. Jacob, and
Gregory M. Vercellotti
From the Department of Medicine and Department of Pediatrics,
University Medical School of Debrecen, Debrecen, Hungary, and the
Division of Hematology, University of Minnesota, Minneapolis, MN.
Heme arginate infusions blunt the symptoms of patients with acute
intermittent porphyria without evidence of the vascular or thrombotic
side effects reported for hematin. To provide a rationale for
heme arginate's safety, the present study examined the effects of
various ferriporphyrins to sensitize human endothelial cells to free
radical injury and to induce heme oxygenase and ferritin expression.
Heme arginate, unlike hematin, did not amplify oxidant-induced
cytotoxicity mediated by hydrogen peroxide (5.3 ± 2.4 versus 62.3 ± 5.3% 51Cr release,
P < .0001) or by activated neutrophils
(14.4 ± 2.9 versus 41.1 ± 6.0%, P < .0001).
Nevertheless, heme arginate efficiently entered endothelial cells
similarly to hematin, since both markedly induced heme oxygenase mRNA
(more than 20-fold increase) and enzyme activity. Even with efficient
permeation, endothelial cell ferritin content was only minimally
increased by heme arginate compared with a 10-fold induction by
hematin; presumably less free iron was derived from heme arginate
despite up-regulation of heme oxygenase. Hematin is potentially
vasculopathic by its marked catalysis of oxidation of low-density
lipoprotein (LDL) to endothelial-toxic moieties.
Heme arginate was significantly less catalytic. Heme arginate-conditioned LDL was less than half as cytotoxic to
endothelial cells as hematin-conditioned LDL (P < .004). It
is concluded that heme arginate may be less vasculotoxic than hematin
since it is an effective heme oxygenase gene regulator but a less
efficient free-radical catalyst.

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