1. Volume 70, Issue 4, Pages 724-731 (August 2006)
Albumin-bound fatty acids induce mitochondrial oxidant stress and impair antioxidant responses in proximal tubular cells 
D.A. Ishola, J.A. Post, M.M. van Timmeren, S.J.L. Bakker, R. Goldschmeding, H.A. Koomans, B. Braam, J.A. Joles 
Kidney International 
Volume 70, Issue 4, Pages (August 2006)
DOI: /sj.ki
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2. Figure 1
Effects of BSA and OA-BSA on cellular ROS production and viability. (a) ROS production after exposure to albumin (BSA) alone or enriched with oleic acid (OA-BSA) in proximal tubular epithelial cells (PTECs), measured by DCF fluorescence normalized to control values (a.u.). *P<0.05, **P<0.001 vs control (untreated) cells; #P<0.001, OA-BSA vs corresponding BSA concentration. Mean (s.e.m.) of at least three independent experiments is shown. (b) MTT and LDH release assays. Cells exposed to cumene hydroperoxide for the same duration were used as positive control. *P<0.05, **P<0.001 vs all other groups. Mean (s.e.m.) of three independent experiments is shown.
Kidney International  , DOI: ( /sj.ki )
Copyright © 2006 International Society of Nephrology Terms and Conditions

3. Figure 2
Effects of inhibitors of ROS sources on stimulated and basal cellular ROS production. (a) ROS production by HK-2 cells after OA-BSA treatment in the presence or absence of blockers of potential ROS sources. Mitochondrial inhibitors used were CCCP (uncoupling agent), rotenone (ROT) (complex I), and 2-thenoyltrifuoroacetone (complex II). Nω-nitro-L-arginine methyl ester is a nitric oxide synthase inhibitor, APO an NADPH oxidase inhibitor, and allopurinol (ALLO) a xanthine oxidase inhibitor. *P<0.001 vs OA-BSA. Mean (s.e.m.) of at least three independent experiments is shown. (b) Effects of the above-named intervention agents on baseline (control) cellular ROS levels.
Kidney International  , DOI: ( /sj.ki )
Copyright © 2006 International Society of Nephrology Terms and Conditions

4. Figure 3
Illustrative bands from reverse transcription-polymerase chain reaction experiments, normalized to 18S and related to control levels, showing transcriptional changes induced by BSA and OA-BSA. C, control; B, BSA; O, OA-BSA. Densitometric data are shown as median (range) fold difference vs control, 4–5 independent experiments, *P<0.05, BSA vs OA-BSA (Friedman). (a) Expression pattern of pro-oxidant genes: NADPH oxidase components (rac1, rac2, p22phox) and xanthine oxidase. (b) Expression of antioxidant genes: SOD1, SOD2, glutathione peroxidase. (c) Expression of genes of downstream mediators: inflammatory cytokines IL-6 and IL-8, and the antioxidant molecule HO-1.
Kidney International  , DOI: ( /sj.ki )
Copyright © 2006 International Society of Nephrology Terms and Conditions

5. Figure 4
ROS production by HK-2 cells after OA-BSA treatment in the presence or absence of EUK-8, a manganese SOD mimetic. *P<0.001 vs all other groups.
Kidney International  , DOI: ( /sj.ki )
Copyright © 2006 International Society of Nephrology Terms and Conditions

6. Figure 5
Schema of ROS pathways of interest. Abbreviations: •O2−, superoxide anion, H2O2, hydrogen peroxide; GPx, glutathione peroxidase; GSSG, oxidized glutathione; H2O, water; O2, molecular oxygen; •OH, hydroxyl ion.
Kidney International  , DOI: ( /sj.ki )
Copyright © 2006 International Society of Nephrology Terms and Conditions