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5-Hydroxymethylfurfural: A Particularly Harmful Molecule Inducing Toxic Lipids and Proteins?

ORCID
0000-0001-6676-0908
Affiliation
Division of Medicinal Chemistry, Otto Loewi Research Center, Medical University of Graz, 8036 Graz, Austria
Greilberger, Joachim;
Affiliation
Institute of Anatomy and Clinical Morphology, Witten University, 58448 Witten, Germany;
Feigl, Georg;
Affiliation
Institut fuer Laborwissenschaften Dr. Greilberger, Schwarzl Klinik, 8301 Lassnitzhoehe, Austria;(M.G.);(M.G.)
Greilberger, Matthias;
Affiliation
Zentrum für Regenerative Medizin des Bewegungsapparates, 4040 Linz, Austria;
Bystrianska, Simona;
Affiliation
Institut fuer Laborwissenschaften Dr. Greilberger, Schwarzl Klinik, 8301 Lassnitzhoehe, Austria;(M.G.);(M.G.)
Greilberger, Michaela

Introduction: 5-HMF is a molecule found in carbohydrate-rich foods that is associated not only with cancer and anaphylactic reactions, but also with anti-oxidant properties. Questions arose as to whether 5-HMF exhibited a catalytic effect in relation to lipid peroxidation and lipoprotein oxidation in presence of metals and/or radicals. Methods: Peroxynitrite (ONOO − )-induced chemiluminescence and ONOO − nitration of tyrosine residues on BSA using anti-nitro-tyrosine-antibodies were used to measure the protection of 5-HMF against peroxides or nitration compared to vitamin C (VitC). The reductive potential of 5-HMF or VitC on Cu 2+ or Fe 3 was estimated using the bicinchoninic acid (BCA) or Fenton-complex method. Human plasma was used to measure the generation of malondialdehyde (MDA), 4-hydroxynonenal (HNE), and total thiols after Fe 2+ /H 2 O 2 oxidation in the presence of different concentrations of 5-HMF or VitC. Finally, Cu 2+ oxidation of LDL after 4 h was carried out with 5-HMF or VitC, measuring the concentration of MDA in LDL with the thiobarbituric assay (TBARS). Results: VitC was 4-fold more effective than 5-HMF in scavenging ONOO − to nearly 91.5% at 4 mM, with the exception of 0.16 mM, where the reduction of ONOO − by VitC was 3.3-fold weaker compared to 0.16 mM 5-HMF. VitC or 5-HMF at a concentration of 6 mM inhibited the nitration of tyrosine residues on BSA to nearly 90% with a similar course. While 5-HMF reduced free Fe 3+ in presence of phenanthroline, forming Fe 2+ (phenantroleine) 3 [Fe 2+ (phe) 3 ] or complexed Cu 2+ (BCA) 4 to Cu + (BCA) 4 weakly, VitC was 7- to 19-fold effective in doing so over all the used concentrations (0–25 mM). A Fe 2+ —H 2 O 2 solution mixed with human plasma showed a 6–10 times higher optical density (OD) of MDA or HNE in the presence of 5-HMF compared to VitC. The level of thiols was significantly decreased in the presence of higher VitC levels (1 mM: 198.4 ± 7.7 µM; 2 mM: 160.0 ± 13.4 µM) compared to equal 5-HMF amounts (2562 ± 7.8 µM or 242.4 ± 2.5 µM), whereas the usage of lower levels at 0.25 µM 5-HMF resulted in a significant decrease in thiols (272.4 ± 4.0 µM) compared to VitC (312.3 ± 19.7 µM). Both VitC and 5-HMF accelerated copper-mediated oxidation of LDL equally: while the TBARS levels from 4 h oxidized LDL reached 137.7 ± 12.3 nmol/mg, it was 1.7-fold higher using 6 mM VitC (259.9 ± 10.4 nmol/mg) or 6 mM 5-HMF (239.3 ± 10.2 nmol/mg). Conclusions: 5-HMF appeared to have more pro-oxidative potential compared to VitC by causing lipid peroxidation as well as protein oxidation.

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