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L-carnosine (beta-alanyl-L-histidine) and carcinine (beta-alanylhistamine) act as natural antioxidants with hydroxyl-radical-scavenging and lipid-peroxidase activities.

ABSTRACT: Carnosine (beta-alanyl-L-histidine) and carcinine (beta-alanylhistamine) are natural imidazole-containing compounds found in the non-protein fraction of mammalian tissues. Carcinine was synthesized by an original procedure and characterized. Both carnosine and carcinine (10-25 mM) are capable of inhibiting the catalysis of linoleic acid and phosphatidylcholine liposomal peroxidation (LPO) by the O2(-.)-dependent iron-ascorbate and lipid-peroxyl-radical-generating linoleic acid 13-monohydroperoxide (LOOH)-activated haemoglobin systems, as measured by thiobarbituric-acid-reactive substance. Carcinine and carnosine are good scavengers of OH. radicals, as detected by iron-dependent radical damage to the sugar deoxyribose. This suggests that carnosine and carcinine are able to scavenge free radicals or donate hydrogen ions. The iodometric, conjugated diene and t.l.c. assessments of lipid hydroperoxides (13-monohydroperoxide linoleic acid and phosphatidylcholine hydroperoxide) showed their efficient reduction and deactivation by carnosine and carcinine (10-25 mM) in the liberated and bound-to-artificial-bilayer states. This suggests that the peroxidase activity exceeded that susceptible to direct reduction with glutathione peroxidase. Imidazole, solutions of beta-alanine, or their mixtures with peptide moieties did not show antioxidant potential. Free L-histidine and especially histamine stimulated iron (II) salt-dependent LPO. Due to the combination of weak metal chelating (abolished by EDTA), OH. and lipid peroxyl radicals scavenging, reducing activities to liberated fatty acid and phospholipid hydroperoxides, carnosine and carcinine appear to be physiological antioxidants able to efficiently protect the lipid phase of biological membranes and aqueous environments.

SUBMITTER: Babizhayev MA

PROVIDER: S-EPMC1137521 | biostudies-other | 1994 Dec

REPOSITORIES: biostudies-other

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Project description:Advanced oxidation treatment processes used in various applications to treat contaminated soil, water, and groundwater involve powerful radical intermediates, including hydroxyl radicals (•OH). Inefficiency in •OH-driven treatment systems involves scavenging reactions where •OH react with non-target species in the aqueous and solid phases. Here, •OH were generated in iron (Fe)- and UV-activated hydrogen peroxide (Fe-AHP, UV-AHP) systems where the loss of rhodamine B served as a quantitative metric for •OH activity. Kinetic analysis methods were developed to estimate the specific •OH surface scavenging rate constant (k≡S). In the Fe-AHP system, k≡S for silica (2.85 × 106 1/m2 × s) and alumina (3.92 × 106 1/m2 × s) were similar. In the UV-AHP system, estimates of k≡S for silica (4.50 × 106 1/m2 × s) and alumina (7.45 × 106 1/m2 × s) were higher. k≡S for montmorillonite (MMT) in the UV-AHP system was ≤4.22 × 105 1/m2 × s. Overall, k≡S,silica ∼ k≡S, alumina > k≡S,MMT indicating k≡S is mineral specific. Radical scavenging was dominated by surface scavenging at 10-50 g/L silica, alumina, or MMT, in both Fe-AHP and UV-AHP systems. The experimentally-derived surface •OH scavenging rate constants were extended to in-situ chemical oxidation (ISCO) treatment conditions to contrast •OH reaction rates with contaminant and aqueous phase reactants found in aquifer systems. •OH reaction was dominated by solid surfaces comprised of silica, alumina, and montmorillonite minerals relative to •OH reaction with trichloroethylene, the target compound, and H2O2, a well-documented radical scavenger. These results indicate that solid mineral surfaces play a key role in limiting the degradation rate of contaminants found in soil and groundwater, and the overall treatment efficiency in ISCO systems. The aggressive •OH scavenging measured was partially attributed to the relative abundance of scavenging sites on mineral surfaces.

Project description:Inhalation of ambient particulate matter causes morbidity and mortality in humans. One hypothesized mechanism of toxicity is the particle-induced formation of reactive oxygen species (ROS) - including the highly damaging hydroxyl radical ((·)OH) - followed by inflammation and a variety of diseases. While past studies have found correlations between ROS formation and a variety of metals, there are no quantitative measurements of (·)OH formation from transition metals at concentrations relevant to 24-hour ambient particulate exposure. This research reports specific and quantitative measurements of (·)OH formation from 10 individual transition metals (and several mixtures) in a cell-free surrogate lung fluid (SLF) with four antioxidants: ascorbate, citrate, glutathione, and uric acid. We find that Fe and Cu can produce (·)OH under all antioxidant conditions as long as ascorbate is present and that mixtures of the two metals synergistically increase (·)OH production. Manganese and vanadium can also produce (·)OH under some conditions, but given that their ambient levels are typically very low, these metals are not likely to chemically produce significant levels of (·)OH in the lung fluid. Cobalt, chromium, nickel, zinc, lead, and cadmium do not produce (·)OH under any of our experimental conditions. The antioxidant composition of our SLF significantly affects (·)OH production from Fe and Cu: ascorbate is required for (·)OH formation, citrate increases (·)OH production from Fe, and both citrate and glutathione suppress (·)OH production from Cu. MINTEQ ligand speciation modeling indicates that citrate and glutathione affect (·)OH production by changing metal speciation, altering the reactivity of the metals. In the most realistic SLF (i.e., with all four antioxidants), Fe generates approximately six times more (·)OH than does the equivalent amount of Cu. Since levels of soluble Fe in PM are typically higher than those of Cu, our results suggest that Fe dominates the chemical generation of (·)OH from deposited particles in the lungs.

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L-carnosine (beta-alanyl-L-histidine) and carcinine (beta-alanylhistamine) act as natural antioxidants with hydroxyl-radical-scavenging and lipid-peroxidase activities.

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