Polycyclic aromatic hydrocarbon coated onto Fe2O3 particles: assessment ofcellular membrane damage and antioxidant system disruption in human epithelial lung cells (L132) in culture
G. Garcon et al., Polycyclic aromatic hydrocarbon coated onto Fe2O3 particles: assessment ofcellular membrane damage and antioxidant system disruption in human epithelial lung cells (L132) in culture, TOX LETT, 117(1-2), 2000, pp. 25-35
The aim of this study was to investigate the oxidative effects of Fe2O3, be
nzo(a)pyrene (B(a)P) and pyrene, alone or in association (B(a)P or pyrene c
oated onto Fe2O3 particles), in normal human embryonic lung epithelial cell
s (L132) in culture. We evaluated: (i) membrane integrity, through fatty ac
id release (stearic acid, oleic acid, linoleic and linolenic acids, homolin
olenic acid, arachidonic acid) and malondialdehyde (MDA) production; and (i
i) antioxidant status, through enzymatic and non-enzymatic antioxidant defe
nses (superoxide dismutase (SOD), glutathione peroxidase (GPx), glutathione
reductase (GR), glutathione status, beta-carotene). Fe2O3 did not induce a
ny change in L132 cells. In pyrene-treated cells, SOD induction (P < 0.05),
glutathione oxidation (P < 0.05) and beta-carotene consumption (P < 0.001)
may counteract free radicals (FR)-induced damage. However, in B(a)P-incuba
ted cells, SOD inactivation (P ( 0.05), GR increases (P ( 0.05), glutathion
e oxidation (P ( 0.05) and beta-carotene decreases (P < 0.001) showed high
disruption of antioxidants, thereby allowing FR-induced damage (i.e. arachi
donic acid release, P < 0.01; MDA production, P(0.01). Our main finding was
that both associations caused higher FR-induced damage (i.e. MDA productio
n. P < 0.001; SOD inactivation, P(0.01) than either chemical alone, Several
mechanisms could account for this result: enhanced uptake of Fe2O3 particl
es and/or greater availability of polycyclic aromatic hydrocarbons (PAHs).
Wt hypothesized also that Fe2O3 and polycyclic aromatic hydrocarbons are mo
re deleterious by virtue of their associations being able to produce higher
oxidative effects than either chemical alone. (C) 2000 Elsevier Science Ir
eland Ltd. All rights reserved.