Langbahn Team – Weltmeisterschaft

Antioxidant

Structure of the antioxidant glutathione

Antioxidants are compounds that inhibit oxidation (usually occurring as autoxidation), a chemical reaction that can produce free radicals. Autoxidation leads to degradation of organic compounds, including living matter. Antioxidants are frequently added to industrial products, such as polymers, fuels, and lubricants, to extend their usable lifetimes.[1] Foods are also treated with antioxidants to forestall spoilage, in particular the rancidification of oils and fats. In cells, antioxidants such as glutathione, mycothiol, or bacillithiol, and enzyme systems like superoxide dismutase, can prevent damage from oxidative stress.[2]

Known dietary antioxidants are vitamins A, C, and E, but the term antioxidant has also been applied to numerous other dietary compounds that only have antioxidant properties in vitro, with little evidence for antioxidant properties in vivo.[3] Dietary supplements marketed as antioxidants have not been shown to maintain health or prevent disease in humans.[3][4]

History

As part of their adaptation from marine life, terrestrial plants began producing non-marine antioxidants such as ascorbic acid (vitamin C), polyphenols, and tocopherols. The evolution of angiosperm plants between 50 and 200 million years ago resulted in the development of many antioxidant pigments – particularly during the Jurassic period – as chemical defences against reactive oxygen species that are byproducts of photosynthesis.[5] Originally, the term antioxidant specifically referred to a chemical that prevented the consumption of oxygen. In the late 19th and early 20th centuries, extensive study concentrated on the use of antioxidants in important industrial processes, such as the prevention of metal corrosion, the vulcanization of rubber, and the polymerization of fuels in the fouling of internal combustion engines.[6]

Early research on the role of antioxidants in biology focused on their use in preventing the oxidation of unsaturated fats, which is the cause of rancidity.[7] Antioxidant activity could be measured simply by placing the fat in a closed container with oxygen and measuring the rate of oxygen consumption. However, it was the identification of vitamins C and E as antioxidants that revolutionized the field and led to the realization of the importance of antioxidants in the biochemistry of living organisms.[8][9] The possible mechanisms of action of antioxidants were first explored when it was recognized that a substance with anti-oxidative activity is likely to be one that is itself readily oxidized.[10] Research into how vitamin E prevents the process of lipid peroxidation led to the identification of antioxidants as reducing agents that prevent oxidative reactions, often by scavenging reactive oxygen species before they can damage cells.[11]

Uses in technology

Food preservatives

See also: E number § E300–E399 (antioxidants, acidity regulators)

Antioxidants are used as food additives to help guard against food deterioration. Exposure to oxygen and sunlight are the two main factors in the oxidation of food, so food is preserved by keeping in the dark and sealing it in containers or even coating it in wax, as with cucumbers. However, as oxygen is also important for plant respiration, storing plant materials in anaerobic conditions produces unpleasant flavors and unappealing colors.[12] Consequently, packaging of fresh fruits and vegetables contains an ≈8% oxygen atmosphere. Antioxidants are an especially important class of preservatives as, unlike bacterial or fungal spoilage, oxidation reactions still occur relatively rapidly in frozen or refrigerated food.[13] These preservatives include natural antioxidants such as ascorbic acid (AA, E300) and tocopherols (E306), as well as synthetic antioxidants such as propyl gallate (PG, E310), tertiary butylhydroquinone (TBHQ), butylated hydroxyanisole (BHA, E320) and butylated hydroxytoluene (BHT, E321).[14][15]

Unsaturated fats can be highly susceptible to oxidation, causing rancidification.[16] Oxidized lipids are often discolored and can impart unpleasant tastes and flavors. Thus, these foods are rarely preserved by drying; instead, they are preserved by smoking, salting, or fermenting. Even less fatty foods such as fruits are sprayed with sulfurous antioxidants prior to air drying. Metals catalyse oxidation. Some fatty foods such as olive oil are partially protected from oxidation by their natural content of antioxidants. Fatty foods are sensitive to photooxidation,[17] which forms hydroperoxides by oxidizing unsaturated fatty acids and ester.[18] Exposure to ultraviolet (UV) radiation can cause direct photooxidation and decompose peroxides and carbonyl molecules. These molecules undergo free radical chain reactions, but antioxidants inhibit them by preventing the oxidation processes.[18]

Cosmetics preservatives

Antioxidant stabilizers are also added to fat-based cosmetics such as lipstick and moisturizers to prevent rancidity.[19] Antioxidants in cosmetic products prevent oxidation of active ingredients and lipid content. For example, phenolic antioxidants such as stilbenes, flavonoids, and hydroxycinnamic acid strongly absorb UV radiation due to the presence of chromophores. They reduce oxidative stress from sun exposure by absorbing UV light.[20]

Industrial uses

Substituted phenols and derivatives of phenylenediamine are common antioxidants used to inhibit gum formation in gasoline (petrol).

Antioxidants may be added to industrial products, such as stabilizers in fuels and additives in lubricants, to prevent oxidation and polymerization that leads to the formation of engine-fouling residues.[21]

Fuel additive Components[22] Applications[22]
AO-22 N,N'-di-2-butyl-1,4-phenylenediamine Turbine oils, transformer oils, hydraulic fluids, waxes, and greases
AO-24 N,N'-di-2-butyl-1,4-phenylenediamine Low-temperature oils
AO-29 2,6-di-tert-butyl-4-methylphenol (BHT) Turbine oils, transformer oils, hydraulic fluids, waxes, greases, and gasolines
AO-30 2,4-dimethyl-6-tert-butylphenol Jet fuels and gasolines, including aviation gasolines
AO-31 2,4-dimethyl-6-tert-butylphenol Jet fuels and gasolines, including aviation gasolines
AO-32 2,4-dimethyl-6-tert-butylphenol and 2,6-di-tert-butyl-4-methylphenol Jet fuels and gasolines, including aviation gasolines
AO-37 2,6-di-tert-butylphenol Jet fuels and gasolines, widely approved for aviation fuels

Antioxidant polymer stabilizers are widely used to prevent the degradation of polymers, such as rubbers, plastics and adhesives, that causes a loss of strength and flexibility in these materials.[23] Polymers containing double bonds in their main chains, such as natural rubber and polybutadiene, are especially susceptible to oxidation and ozonolysis. They can be protected by antiozonants. Oxidation can be accelerated by UV radiation in natural sunlight to cause photo-oxidation. Various specialised light stabilisers, such as HALS may be added to plastics to prevent this. An overview of some of the most applied antioxidants for polymer materials is shown below:

(Hindered) Phenolic Antioxidants: Act by scavenging free radicals formed during the thermal oxidation process, thus preventing chain reactions that lead to polymer degradation. Examples: butylated hydroxytoluene, 2,4-dimethyl-6-tert-butylphenol, para tertiary butyl phenol, 2,6-di-tert-butylphenol, 1,3,5-Tris(4-(tert-butyl)-3-hydroxy-2,6-dimethylbenzyl)-1,3,5-triazinane-2,4,6-trione

Phosphites: Act by decomposing peroxides into non-radical products, thus preventing further generation of free radicals, and contributing to the overall oxidate stability of the polymer. Phosphites are often used in combination with phenolic antioxidants for syngeristic effects. Example: tris(2,4-di-tert-butylphenyl)phosphite

Thioesters: Act by decomposing peroxides into non-radical products. Thioesters are also used as co-stabilisers with primary antioxidants.

Hindered Amine Light Stabilizers (HALS): HALS act by scavenging free radicals generated during photo-oxidation, thus preventing the polymer material from UV radiation.

Vitamins: Naturally occurring antioxidants like Vitamin C and Vitamin E are used for specific applications.

Blends: Blends of different types of antioxidants are commonly applied, as they can serve various and multiple purposes.

Environmental and health hazards

Synthetic phenolic antioxidants (SPAs)[24] and aminic antioxidants[25] have potential human and environmental health hazards. SPAs are common in indoor dust, small air particles, sediment, sewage, river water and wastewater.[26] They are synthesized from phenolic compounds and include 2,6-di-tert-butyl-4-methylphenol (BHT), 2,6-di-tert-butyl-p-benzoquinone (BHT-Q), 2,4-di-tert-butyl-phenol (DBP) and 3-tert-butyl-4-hydroxyanisole (BHA). BHT can cause hepatotoxicity and damage to the endocrine system and may increase tumor development rates due to 1,1-dimethylhydrazine.[27] BHT-Q can cause DNA damage and mismatches[28] through the cleavage process, generating superoxide radicals.[26] DBP is toxic to marine life if exposed long-term. Phenolic antioxidants have low biodegradability, but they do not have severe toxicity toward aquatic organisms at low concentrations. Another type of antioxidant, diphenylamine (DPA), is commonly used in the production of commercial, industrial lubricants and rubber products and it also acts as a supplement for automotive engine oils.[29]

Oxidative challenge in biology

Further information: Oxidative stress
The structure of the antioxidant vitamin ascorbic acid (vitamin C)

The vast majority of complex life on Earth requires oxygen for its metabolism, but this same oxygen is a highly reactive element that can damage living organisms.[2][30] Organisms contain chemicals and enzymes that minimize this oxidative damage without interfering with the beneficial effect of oxygen.[31][32] In general, antioxidant systems either prevent these reactive species from being formed, or remove them, thus minimizing their damage.[30][31] Reactive oxygen species can have useful cellular functions, such as redox signaling. Thus, ideally, antioxidant systems do not remove oxidants entirely, but maintain them at some optimum concentration.[33]

Reactive oxygen species produced in cells include hydrogen peroxide (H2O2), hypochlorous acid (HClO), and free radicals such as the hydroxyl radical (·OH), and the superoxide anion (O2−).[34] The hydroxyl radical is particularly unstable and will react rapidly and non-specifically with most biological molecules. This species is produced from hydrogen peroxide in metal-catalyzed redox reactions such as the Fenton reaction.[35] These oxidants can damage cells by starting chemical chain reactions such as lipid peroxidation, or by oxidizing DNA or proteins.[31] Damage to DNA can cause mutations and possibly cancer, if not reversed by DNA repair mechanisms,[36][37] while damage to proteins causes enzyme inhibition, denaturation, and protein degradation.[38]

The use of oxygen as part of the process for generating metabolic energy produces reactive oxygen species.[39] In this process, the superoxide anion is produced as a by-product of several steps in the electron transport chain.[40] Particularly important is the reduction of coenzyme Q in complex III, since a highly reactive free radical is formed as an intermediate (Q·−). This unstable intermediate can lead to electron "leakage", when electrons jump directly to oxygen and form the superoxide anion, instead of moving through the normal series of well-controlled reactions of the electron transport chain.[41] Peroxide is also produced from the oxidation of reduced flavoproteins, such as complex I.[42] However, although these enzymes can produce oxidants, the relative importance of the electron transfer chain to other processes that generate peroxide is unclear.[43][44] In plants, algae, and cyanobacteria, reactive oxygen species are also produced during photosynthesis,[45] particularly under conditions of high light intensity.[46] This effect is partly offset by the involvement of carotenoids in photoinhibition, and in algae and cyanobacteria, by large amount of iodide and selenium,[47] which involves these antioxidants reacting with over-reduced forms of the photosynthetic reaction centres to prevent the production of reactive oxygen species.[48][49]

Examples of bioactive antioxidant compounds

Physiological antioxidants are classified into two broad divisions, depending on whether they are soluble in water (hydrophilic) or in lipids (lipophilic). In general, water-soluble antioxidants react with oxidants in the cell cytosol and the blood plasma, while lipid-soluble antioxidants protect cell membranes from lipid peroxidation.[31] These compounds may be synthesized in the body or obtained from the diet.[32] The different antioxidants are present at a wide range of concentrations in body fluids and tissues, with some such as glutathione or ubiquinone mostly present within cells, while others such as uric acid are more systemically distributed (see table below). Some antioxidants are only found in a few organisms, and can be pathogens or virulence factors.[50]

The interactions between these different antioxidants may be synergistic and interdependent.[51][52] The action of one antioxidant may therefore depend on the proper function of other members of the antioxidant system.[32] The amount of protection provided by any one antioxidant will also depend on its concentration, its reactivity towards the particular reactive oxygen species being considered, and the status of the antioxidants with which it interacts.[32]

Some compounds contribute to antioxidant defense by chelating transition metals and preventing them from catalyzing the production of free radicals in the cell. The ability to sequester iron for iron-binding proteins, such as transferrin and ferritin, is one such function.[44] Selenium and zinc are commonly referred to as antioxidant minerals, but these chemical elements have no antioxidant action themselves, but rather are required for the activity of antioxidant enzymes, such as glutathione reductase and superoxide dismutase. (See also selenium in biology and zinc in biology.)

Antioxidant Solubility Concentration in human serum (μM) Concentration in liver tissue (μmol/kg)
Ascorbic acid (vitamin C) Water 50–60[53] 260 (human)[54]
Glutathione Water 4[55] 6,400 (human)[54]
Lipoic acid Water 0.1–0.7[56] 4–5 (rat)[57]
Uric acid Water 200–400[58] 1,600 (human)[54]
Carotenes Lipid β-carotene: 0.5–1[59]

retinol (vitamin A): 1–3[60]

5 (human, total carotenoids)[61]
α-Tocopherol (vitamin E) Lipid 10–40[60] 50 (human)[54]
Ubiquinol (coenzyme Q) Lipid 5[62] 200 (human)[63]

Uric acid

Uric acid has the highest concentration of any blood antioxidant[58] and provides over half of the total antioxidant capacity of human serum.[64] Uric acid's antioxidant activities are also complex, given that it does not react with some oxidants, such as superoxide, but does act against peroxynitrite,[65] peroxides, and hypochlorous acid.[66] Concerns over elevated UA's contribution to gout must be considered one of many risk factors.[67] By itself, UA-related risk of gout at high levels (415–530 μmol/L) is only 0.5% per year with an increase to 4.5% per year at UA supersaturation levels (535+ μmol/L).[68] Many of these aforementioned studies determined UA's antioxidant actions within normal physiological levels,[69][65] and some found antioxidant activity at levels as high as 285 μmol/L.[70]

Vitamin C

Ascorbic acid or vitamin C, an oxidation-reduction (redox) catalyst found in both animals and plants,[71] can reduce, and thereby neutralize, reactive oxygen species such as hydrogen peroxide.[71][72] In addition to its direct antioxidant effects, ascorbic acid is also a substrate for the redox enzyme ascorbate peroxidase, a function that is used in stress resistance in plants.[73] Ascorbic acid is present at high levels in all parts of plants and can reach concentrations of 20 millimolar in chloroplasts.[74]

Glutathione

The free radical mechanism of lipid peroxidation

Glutathione has antioxidant properties since the thiol group in its cysteine moiety is a reducing agent and can be reversibly oxidized and reduced. In cells, glutathione is maintained in the reduced form by the enzyme glutathione reductase and in turn reduces other metabolites and enzyme systems, such as ascorbate in the glutathione-ascorbate cycle, glutathione peroxidases and glutaredoxins, as well as reacting directly with oxidants.[75] Due to its high concentration and its central role in maintaining the cell's redox state, glutathione is one of the most important cellular antioxidants.[76] In some organisms glutathione is replaced by other thiols, such as by mycothiol in the Actinomycetes, bacillithiol in some gram-positive bacteria,[77][78] or by trypanothione in the Kinetoplastids.[79][80]

Vitamin E

Vitamin E is the collective name for a set of eight related tocopherols and tocotrienols, which are fat-soluble vitamins with antioxidant properties.[81][82] Of these, α-tocopherol has been most studied as it has the highest bioavailability, with the body preferentially absorbing and metabolising this form.[83]

It has been claimed[by whom?] that the α-tocopherol form is the most important lipid-soluble antioxidant, and that it protects membranes from oxidation by reacting with lipid radicals produced in the lipid peroxidation chain reaction.[81][84] This removes the free radical intermediates and prevents the propagation reaction from continuing. This reaction produces oxidised α-tocopheroxyl radicals that can be recycled back to the active reduced form through reduction by other antioxidants, such as ascorbate, retinol or ubiquinol.[85] This is in line with findings showing that α-tocopherol, but not water-soluble antioxidants, efficiently protects glutathione peroxidase 4 (GPX4)-deficient cells from cell death.[86] GPx4 is the only known enzyme that efficiently reduces lipid-hydroperoxides within biological membranes.

However, the roles and importance of the various forms of vitamin E are presently unclear,[87][88] and it has even been suggested that the most important function of α-tocopherol is as a signaling molecule, with this molecule having no significant role in antioxidant metabolism.[89][90] The functions of the other forms of vitamin E are even less well understood, although γ-tocopherol is a nucleophile that may react with electrophilic mutagens,[83] and tocotrienols may be important in protecting neurons from damage.[91]

Pro-oxidant activities

Further information: Pro-oxidant

Antioxidants that are reducing agents can also act as pro-oxidants. For example, vitamin C has antioxidant activity when it reduces oxidizing substances such as hydrogen peroxide;[92] however, it will also reduce metal ions such as iron and copper[93] that generate free radicals through the Fenton reaction.[35][94] While ascorbic acid is effective antioxidant, it can also oxidatively change the flavor and color of food. With the presence of transition metals, there are low concentrations of ascorbic acid that can act as a radical scavenger in the Fenton reaction.[93]

2 Fe3+ + Ascorbate → 2 Fe2+ + Dehydroascorbate
2 Fe2+ + 2 H2O2 → 2 Fe3+ + 2 OH· + 2 OH−

The relative importance of the antioxidant and pro-oxidant activities of antioxidants is an area of current research, but vitamin C, which exerts its effects as a vitamin by oxidizing polypeptides, appears to have a mostly antioxidant action in the human body.[94]

Enzyme systems

Enzymatic pathway for detoxification of reactive oxygen species

As with the chemical antioxidants, cells are protected against oxidative stress by an interacting network of antioxidant enzymes.[30][31] Here, the superoxide released by processes such as oxidative phosphorylation is first converted to hydrogen peroxide and then further reduced to give water. This detoxification pathway is the result of multiple enzymes, with superoxide dismutases catalysing the first step and then catalases and various peroxidases removing hydrogen peroxide. As with antioxidant metabolites, the contributions of these enzymes to antioxidant defenses can be hard to separate from one another, but the generation of transgenic mice lacking just one antioxidant enzyme can be informative.[95]

Superoxide dismutase, catalase, and peroxiredoxins

Superoxide dismutases (SODs) are a class of closely related enzymes that catalyze the breakdown of the superoxide anion into oxygen and hydrogen peroxide.[96][97] SOD enzymes are present in almost all aerobic cells and in extracellular fluids.[98] Superoxide dismutase enzymes contain metal ion cofactors that, depending on the isozyme, can be copper, zinc, manganese or iron. In humans, the copper/zinc SOD is present in the cytosol, while manganese SOD is present in the mitochondrion.[97] There also exists a third form of SOD in extracellular fluids, which contains copper and zinc in its active sites.[99] The mitochondrial isozyme seems to be the most biologically important of these three, since mice lacking this enzyme die soon after birth.[100] In contrast, the mice lacking copper/zinc SOD (Sod1) are viable but have numerous pathologies and a reduced lifespan (see article on superoxide), while mice without the extracellular SOD have minimal defects (sensitive to hyperoxia).[95][101] In plants, SOD isozymes are present in the cytosol and mitochondria, with an iron SOD found in chloroplasts that is absent from vertebrates and yeast.[102]

Catalases are enzymes that catalyse the conversion of hydrogen peroxide to water and oxygen, using either an iron or manganese cofactor.[103][104] This protein is localized to peroxisomes in most eukaryotic cells.[105] Catalase is an unusual enzyme since, although hydrogen peroxide is its only substrate, it follows a ping-pong mechanism. Here, its cofactor is oxidised by one molecule of hydrogen peroxide and then regenerated by transferring the bound oxygen to a second molecule of substrate.[106] Despite its apparent importance in hydrogen peroxide removal, humans with genetic deficiency of catalase — "acatalasemia" — or mice genetically engineered to lack catalase completely, experience few ill effects.[107][108]

Decameric structure of AhpC, a bacterial 2-cysteine peroxiredoxin from Salmonella typhimurium[109]

Peroxiredoxins are peroxidases that catalyze the reduction of hydrogen peroxide, organic hydroperoxides, as well as peroxynitrite.[110] They are divided into three classes: typical 2-cysteine peroxiredoxins; atypical 2-cysteine peroxiredoxins; and 1-cysteine peroxiredoxins.[111] These enzymes share the same basic catalytic mechanism, in which a redox-active cysteine (the peroxidatic cysteine) in the active site is oxidized to a sulfenic acid by the peroxide substrate.[112] Over-oxidation of this cysteine residue in peroxiredoxins inactivates these enzymes, but this can be reversed by the action of sulfiredoxin.[113] Peroxiredoxins seem to be important in antioxidant metabolism, as mice lacking peroxiredoxin 1 or 2 have shortened lifespans and develop hemolytic anaemia, while plants use peroxiredoxins to remove hydrogen peroxide generated in chloroplasts.[114][115][116]

Thioredoxin and glutathione systems

The thioredoxin system contains the 12-kDa protein thioredoxin and its companion thioredoxin reductase.[117] Proteins related to thioredoxin are present in all sequenced organisms. Plants, such as Arabidopsis thaliana, have a particularly great diversity of isoforms.[118] The active site of thioredoxin consists of two neighboring cysteines, as part of a highly conserved CXXC motif, that can cycle between an active dithiol form (reduced) and an oxidized disulfide form. In its active state, thioredoxin acts as an efficient reducing agent, scavenging reactive oxygen species and maintaining other proteins in their reduced state.[119] After being oxidized, the active thioredoxin is regenerated by the action of thioredoxin reductase, using NADPH as an electron donor.[120]

The glutathione system includes glutathione, glutathione reductase, glutathione peroxidases, and glutathione S-transferases.[76] This system is found in animals, plants and microorganisms.[76][121] Glutathione peroxidase is an enzyme containing four selenium-cofactors that catalyzes the breakdown of hydrogen peroxide and organic hydroperoxides. There are at least four different glutathione peroxidase isozymes in animals.[122] Glutathione peroxidase 1 is the most abundant and is a very efficient scavenger of hydrogen peroxide, while glutathione peroxidase 4 is most active with lipid hydroperoxides. Surprisingly, glutathione peroxidase 1 is dispensable, as mice lacking this enzyme have normal lifespans,[123] but they are hypersensitive to induced oxidative stress.[124] In addition, the glutathione S-transferases show high activity with lipid peroxides.[125] These enzymes are at particularly high levels in the liver and also serve in detoxification metabolism.[126]

Health research

Relation to diet

The dietary antioxidant vitamins A, C, and E are essential and required in specific daily amounts to prevent diseases.[3][127][128] Polyphenols, which have antioxidant properties in vitro due to their free hydroxy groups,[129] are extensively metabolized by catechol-O-methyltransferase which methylates free hydroxyl groups, and thereby prevents them from acting as antioxidants in vivo.[130][131]

Interactions

Common pharmaceuticals (and supplements) with antioxidant properties may interfere with the efficacy of certain anticancer medication and radiation therapy.[132] Pharmaceuticals and supplements that have antioxidant properties suppress the formation of free radicals by inhibiting oxidation processes. Radiation therapy induce oxidative stress that damages essential components of cancer cells, such as proteins, nucleic acids, and lipids that comprise cell membranes.[133]

Adverse effects

See also: Antioxidative stress
Structure of the metal chelator phytic acid

Relatively strong reducing acids can have antinutrient effects by binding to dietary minerals such as iron and zinc in the gastrointestinal tract and preventing them from being absorbed.[134] Examples are oxalic acid, tannins and phytic acid, which are high in plant-based diets.[135] Calcium and iron deficiencies are not uncommon in diets in developing countries where less meat is eaten and there is high consumption of phytic acid from beans and unleavened whole grain bread. However, germination, soaking, or microbial fermentation are all household strategies that reduce the phytate and polyphenol content of unrefined cereal. Increases in Fe, Zn and Ca absorption have been reported in adults fed dephytinized cereals compared with cereals containing their native phytate.[136]

Foods Reducing acid present
Cocoa bean and chocolate, spinach, turnip and rhubarb[137] Oxalic acid
Whole grains, maize, legumes[138] Phytic acid
Tea, beans, cabbage[137][139] Tannins

High doses of some antioxidants may have harmful long-term effects. The Beta-Carotene and Retinol Efficacy Trial (CARET) study of lung cancer patients found that smokers given supplements containing beta-carotene and vitamin A had increased rates of lung cancer.[140] Subsequent studies confirmed these adverse effects.[141] These harmful effects may also be seen in non-smokers, as one meta-analysis including data from approximately 230,000 patients showed that β-carotene, vitamin A or vitamin E supplementation is associated with increased mortality, but saw no significant effect from vitamin C.[142] No health risk was seen when all the randomized controlled studies were examined together, but an increase in mortality was detected when only high-quality and low-bias risk trials were examined separately.[143] As the majority of these low-bias trials dealt with either elderly people, or people with disease, these results may not apply to the general population.[144] This meta-analysis was later repeated and extended by the same authors, confirming the previous results.[143] These two publications are consistent with some previous meta-analyses that also suggested that vitamin E supplementation increased mortality,[145] and that antioxidant supplements increased the risk of colon cancer.[146] Beta-carotene may also increase lung cancer.[146][147] Overall, the large number of clinical trials carried out on antioxidant supplements suggest that either these products have no effect on health, or that they cause a small increase in mortality in elderly or vulnerable populations.[127][148][142]

Exercise and muscle soreness

A 2017 review showed that taking antioxidant dietary supplements before or after exercise is unlikely to produce a noticeable reduction in muscle soreness after a person exercises.[149]

Levels in food

Further information: List of antioxidants in food and Polyphenol antioxidant
Fruits and vegetables are good sources of antioxidant vitamins C and E.

Antioxidant vitamins are found in vegetables, fruits, eggs, legumes and nuts. Vitamins A, C, and E can be destroyed by long-term storage or prolonged cooking.[150] The effects of cooking and food processing are complex, as these processes can also increase the bioavailability of antioxidants, such as some carotenoids in vegetables.[151] Processed food contains fewer antioxidant vitamins than fresh and uncooked foods, as preparation exposes food to heat and oxygen.[152]

Antioxidant vitamins Foods containing high levels of antioxidant vitamins[139][153][154]
Vitamin C (ascorbic acid) Fresh or frozen fruits and vegetables
Vitamin E (tocopherols, tocotrienols) Vegetable oils, nuts, and seeds
Carotenoids (carotenes as provitamin A) Fruit, vegetables and eggs

Other antioxidants are not obtained from the diet, but instead are made in the body. For example, ubiquinol (coenzyme Q) is poorly absorbed from the gut and is made through the mevalonate pathway.[63] Another example is glutathione, which is made from amino acids. As any glutathione in the gut is broken down to free cysteine, glycine and glutamic acid before being absorbed, even large oral intake has little effect on the concentration of glutathione in the body.[155][156] Although large amounts of sulfur-containing amino acids such as acetylcysteine can increase glutathione,[157] no evidence exists that eating high levels of these glutathione precursors is beneficial for healthy adults.[158]

Measurement and invalidation of ORAC

Measurement of polyphenol and carotenoid content in food is not a straightforward process, as antioxidants collectively are a diverse group of compounds with different reactivities to various reactive oxygen species. In food science analyses in vitro, the oxygen radical absorbance capacity (ORAC) was once an industry standard for estimating antioxidant strength of whole foods, juices and food additives, mainly from the presence of polyphenols.[159][160] Earlier measurements and ratings by the United States Department of Agriculture were withdrawn in 2012 as biologically irrelevant to human health, referring to an absence of physiological evidence for polyphenols having antioxidant properties in vivo.[161] Consequently, the ORAC method, derived only from in vitro experiments, is no longer considered relevant to human diets or biology, as of 2010.[161]

Alternative in vitro measurements of antioxidant content in foods – also based on the presence of polyphenols – include the Folin-Ciocalteu reagent, and the Trolox equivalent antioxidant capacity assay.[162]

References

  1. ^ Klemchuk, Peter P. (2000). "Antioxidants". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a03_091. ISBN 3527306730.
  2. ^ a b Helberg, Julian; Pratt, Derek A. (2021). "Autoxidation vs. Antioxidants – the fight for forever". Chemical Society Reviews. 50 (13): 7343–7358. doi:10.1039/D1CS00265A. PMID 34037013. S2CID 235200305.
  3. ^ a b c "Antioxidants: In Depth". National Center for Complementary and Integrative Health, US National Institutes of Health. 1 November 2013. Retrieved 17 March 2023.
  4. ^ Fang, Yun-Zhong; Yang, Sheng; Wu, Guoyao (2002). "Free radicals, antioxidants, and nutrition". Nutrition. 18 (10): 872–879. doi:10.1016/s0899-9007(02)00916-4. PMID 12361782.
  5. ^ Benzie IF (September 2003). "Evolution of dietary antioxidants". Comparative Biochemistry and Physiology A. 136 (1): 113–26. doi:10.1016/S1095-6433(02)00368-9. hdl:10397/34754. PMID 14527634.
  6. ^ Mattill HA (1947). "Antioxidants". Annual Review of Biochemistry. 16: 177–92. doi:10.1146/annurev.bi.16.070147.001141. PMID 20259061.
  7. ^ German JB (1999). "Food Processing and Lipid Oxidation". Impact of Processing on Food Safety. Advances in Experimental Medicine and Biology. Vol. 459. pp. 23–50. doi:10.1007/978-1-4615-4853-9_3. ISBN 978-0-306-46051-7. PMID 10335367.
  8. ^ Jacob RA (1996). "Introduction: Three Eras of Vitamin C Discovery". Three eras of vitamin C discovery. Subcellular Biochemistry. Vol. 25. pp. 1–16. doi:10.1007/978-1-4613-0325-1_1. ISBN 978-1-4613-7998-0. PMID 8821966.
  9. ^ Knight JA (1998). "Free radicals: their history and current status in aging and disease". Annals of Clinical and Laboratory Science. 28 (6): 331–46. PMID 9846200.
  10. ^ Moureu C, Dufraisse C (1922). "Sur l'autoxydation: Les antioxygènes". Comptes Rendus des Séances et Mémoires de la Société de Biologie (in French). 86: 321–322.
  11. ^ Wolf G (March 2005). "The discovery of the antioxidant function of vitamin E: the contribution of Henry A. Mattill". The Journal of Nutrition. 135 (3): 363–6. doi:10.1093/jn/135.3.363. PMID 15735064.
  12. ^ Kader AA, Zagory D, Kerbel EL (1989). "Modified atmosphere packaging of fruits and vegetables". Critical Reviews in Food Science and Nutrition. 28 (1): 1–30. doi:10.1080/10408398909527490. PMID 2647417.
  13. ^ Zallen EM, Hitchcock MJ, Goertz GE (December 1975). "Chilled food systems. Effects of chilled holding on quality of beef loaves". Journal of the American Dietetic Association. 67 (6): 552–7. doi:10.1016/S0002-8223(21)14836-9. PMID 1184900.
  14. ^ Iverson F (June 1995). "Phenolic antioxidants: Health Protection Branch studies on butylated hydroxyanisole". Cancer Letters. 93 (1): 49–54. doi:10.1016/0304-3835(95)03787-W. PMID 7600543.
  15. ^ "E number index". UK food guide. Archived from the original on 4 March 2007. Retrieved 5 March 2007.
  16. ^ Robards K, Kerr AF, Patsalides E (February 1988). "Rancidity and its Measurement in Edible Oils and Snack Foods. A review". The Analyst. 113 (2): 213–24. Bibcode:1988Ana...113..213R. doi:10.1039/an9881300213. PMID 3288002.
  17. ^ Del Carlo M, Sacchetti G, Di Mattia C, Compagnone D, Mastrocola D, Liberatore L, Cichelli A (June 2004). "Contribution of the phenolic fraction to the antioxidant activity and oxidative stability of olive oil". Journal of Agricultural and Food Chemistry. 52 (13): 4072–9. doi:10.1021/jf049806z. PMID 15212450.
  18. ^ a b Frankel, Edwin N. (1 January 2012), Frankel, Edwin N. (ed.), "Chapter 3 - Photooxidation of unsaturated fats", Lipid Oxidation (Second Edition), Oily Press Lipid Library Series, Woodhead Publishing, pp. 51–66, ISBN 978-0-9531949-8-8, retrieved 15 April 2023
  19. ^ "Final report on the amended safety assessment of Propyl Gallate". International Journal of Toxicology. 26 (3_suppl): 89–118. 2007. doi:10.1080/10915810701663176. PMID 18080874. S2CID 39562131. Propyl Gallate is a generally recognized as safe (GRAS) antioxidant to protect fats, oils, and fat-containing food from rancidity that results from the formation of peroxides.
  20. ^ Débora, Jackeline; Cleide, Viviane; Luciana, Oliveira; Rosemeire, Aparecida (7 August 2019). "Polyphenols as natural antioxidants in cosmetics applications". Journal of Cosmetic Dermatology. 19 (1): 33–37. doi:10.1111/jocd.13093. PMID 31389656. S2CID 201156301.
  21. ^ Boozer CE, Hammond GS, Hamilton CE, Sen JN (1955). "Air Oxidation of Hydrocarbons.1II. The Stoichiometry and Fate of Inhibitors in Benzene and Chlorobenzene". Journal of the American Chemical Society. 77 (12): 3233–7. doi:10.1021/ja01617a026.
  22. ^ a b "Fuel antioxidants". Innospec Chemicals. Archived from the original on 15 October 2006. Retrieved 27 February 2007.
  23. ^ "Why use Antioxidants?". SpecialChem Adhesives. Archived from the original on 11 February 2007. Retrieved 27 February 2007.
  24. ^ Liu, Runzeng; Mabury, Scott A. (6 October 2020). "Synthetic Phenolic Antioxidants: A Review of Environmental Occurrence, Fate, Human Exposure, and Toxicity". Environmental Science & Technology. 54 (19): 11706–11719. Bibcode:2020EnST...5411706L. doi:10.1021/acs.est.0c05077. PMID 32915564. S2CID 221637214.
  25. ^ Xu, Jing; Hao, Yanfen; Yang, Zhiruo; Li, Wenjuan; Xie, Wenjing; Huang, Yani; Wang, Deliang; He, Yuqing; Liang, Yong; Matsiko, Julius; Wang, Pu (7 November 2022). "Rubber Antioxidants and Their Transformation Products: Environmental Occurrence and Potential Impact". International Journal of Environmental Research and Public Health. 19 (21): 14595. doi:10.3390/ijerph192114595. PMC 9657274. PMID 36361475.
  26. ^ a b Li, Chao; Cui, Xinyi; Chen, Yi; Liao, Chunyang; Ma, Lena Q (February 2019). "Synthetic phenolic antioxidants and their major metabolites in human fingernail". Environmental Research. 169: 308–314. Bibcode:2019ER....169..308L. doi:10.1016/j.envres.2018.11.020. PMID 30500685. S2CID 56486425.
  27. ^ Liu, Runzeng; Mabury, Scott A. (11 September 2020). "Synthetic Phenolic Antioxidants: A Review of Environmental Occurrence, Fate, Human Exposure, and Toxicity". Environ. Sci. Technol. 54 (19): 11706–11719. Bibcode:2020EnST...5411706L. doi:10.1021/acs.est.0c05077. PMID 32915564. S2CID 221637214.
  28. ^ Wang, Wanyi; Xiong, Ping; Zhang, He; Zhu, Qingqing; Liao, Chunyang; Jiang, Guibin (1 October 2021). "Analysis, occurrence, toxicity and environmental health risks of synthetic phenolic antioxidants: A review". Environmental Research. 201: 111531. Bibcode:2021ER....20111531W. doi:10.1016/j.envres.2021.111531. ISSN 0013-9351. PMID 34146526.
  29. ^ Zhang, Zi-Feng; Zhang, Xue; Sverko, Ed; Marvin, Christopher H.; Jobst, Karl J.; Smyth, Shirley Anne; Li, Yi-Fan (11 February 2020). "Determination of Diphenylamine Antioxidants in Wastewater/Biosolids and Sediment". Environmental Science & Technology Letters. 7 (2): 102–110. Bibcode:2020EnSTL...7..102Z. doi:10.1021/acs.estlett.9b00796. ISSN 2328-8930. S2CID 213719260.
  30. ^ a b c Davies KJ (1995). "Oxidative stress: the paradox of aerobic life". Biochemical Society Symposium. 61: 1–31. doi:10.1042/bss0610001. PMID 8660387.
  31. ^ a b c d e Sies H (March 1997). "Oxidative stress: oxidants and antioxidants". Experimental Physiology. 82 (2): 291–5. doi:10.1113/expphysiol.1997.sp004024. PMID 9129943. S2CID 20240552.
  32. ^ a b c d Vertuani S, Angusti A, Manfredini S (2004). "The Antioxidants and Pro-Antioxidants Network: an Overview". Current Pharmaceutical Design. 10 (14): 1677–94. doi:10.2174/1381612043384655. PMID 15134565.
  33. ^ Rhee SG (June 2006). "Cell signaling. H2O2, a necessary evil for cell signaling". Science. 312 (5782): 1882–3. doi:10.1126/science.1130481. PMID 16809515. S2CID 83598498.
  34. ^ Valko M, Leibfritz D, Moncol J, Cronin MT, Mazur M, Telser J (2007). "Free radicals and antioxidants in normal physiological functions and human disease". The International Journal of Biochemistry & Cell Biology. 39 (1): 44–84. doi:10.1016/j.biocel.2006.07.001. PMID 16978905.
  35. ^ a b Stohs SJ, Bagchi D (February 1995). "Oxidative mechanisms in the toxicity of metal ions" (PDF). Free Radical Biology & Medicine (Submitted manuscript). 18 (2): 321–36. CiteSeerX 10.1.1.461.6417. doi:10.1016/0891-5849(94)00159-H. PMID 7744317.
  36. ^ Nakabeppu Y, Sakumi K, Sakamoto K, Tsuchimoto D, Tsuzuki T, Nakatsu Y (April 2006). "Mutagenesis and carcinogenesis caused by the oxidation of nucleic acids". Biological Chemistry. 387 (4): 373–9. doi:10.1515/BC.2006.050. PMID 16606334. S2CID 20217256.
  37. ^ Valko M, Izakovic M, Mazur M, Rhodes CJ, Telser J (November 2004). "Role of oxygen radicals in DNA damage and cancer incidence". Molecular and Cellular Biochemistry. 266 (1–2): 37–56. doi:10.1023/B:MCBI.0000049134.69131.89. PMID 15646026. S2CID 207547763.
  38. ^ Stadtman ER (August 1992). "Protein oxidation and aging". Science. 257 (5074): 1220–4. Bibcode:1992Sci...257.1220S. doi:10.1126/science.1355616. PMID 1355616.
  39. ^ Raha S, Robinson BH (October 2000). "Mitochondria, oxygen free radicals, disease and ageing". Trends in Biochemical Sciences. 25 (10): 502–8. doi:10.1016/S0968-0004(00)01674-1. PMID 11050436.
  40. ^ Lenaz G (2001). "The mitochondrial production of reactive oxygen species: mechanisms and implications in human pathology". IUBMB Life. 52 (3–5): 159–64. doi:10.1080/15216540152845957. PMID 11798028. S2CID 45366190.
  41. ^ Finkel T, Holbrook NJ (November 2000). "Oxidants, oxidative stress and the biology of ageing". Nature. 408 (6809): 239–47. Bibcode:2000Natur.408..239F. doi:10.1038/35041687. PMID 11089981. S2CID 2502238.
  42. ^ Hirst J, King MS, Pryde KR (October 2008). "The production of reactive oxygen species by complex I". Biochemical Society Transactions. 36 (Pt 5): 976–80. doi:10.1042/BST0360976. PMID 18793173.
  43. ^ Seaver LC, Imlay JA (November 2004). "Are respiratory enzymes the primary sources of intracellular hydrogen peroxide?". The Journal of Biological Chemistry. 279 (47): 48742–50. doi:10.1074/jbc.M408754200. PMID 15361522.
  44. ^ a b Imlay JA (2003). "Pathways of oxidative damage". Annual Review of Microbiology. 57: 395–418. doi:10.1146/annurev.micro.57.030502.090938. PMID 14527285.
  45. ^ Demmig-Adams B, Adams WW (December 2002). "Antioxidants in photosynthesis and human nutrition". Science. 298 (5601): 2149–53. Bibcode:2002Sci...298.2149D. doi:10.1126/science.1078002. PMID 12481128. S2CID 27486669.
  46. ^ Krieger-Liszkay A (January 2005). "Singlet oxygen production in photosynthesis". Journal of Experimental Botany. 56 (411): 337–46. CiteSeerX 10.1.1.327.9651. doi:10.1093/jxb/erh237. PMID 15310815.
  47. ^ Kupper FC, Carpenter LJ, McFiggans GB, Palmer CJ, Waite TJ, Boneberg E-M, Woitsch S, Weiller M, Abela R, Grolimund D, Potin P, Butler A, Luther GW, Kroneck PMH, Meyer-Klaucke W, Feiters MC (2008). "Iodide accumulation provides kelp with an inorganic antioxidant impacting atmospheric chemistry". Proceedings of the National Academy of Sciences. 105 (19): 6954–6958. Bibcode:2008PNAS..105.6954K. doi:10.1073/pnas.0709959105. ISSN 0027-8424. PMC 2383960. PMID 18458346.
  48. ^ Szabó I, Bergantino E, Giacometti GM (July 2005). "Light and oxygenic photosynthesis: energy dissipation as a protection mechanism against photo-oxidation". EMBO Reports. 6 (7): 629–34. doi:10.1038/sj.embor.7400460. PMC 1369118. PMID 15995679.
  49. ^ Kerfeld CA (October 2004). "Water-soluble carotenoid proteins of cyanobacteria" (PDF). Archives of Biochemistry and Biophysics (Submitted manuscript). 430 (1): 2–9. doi:10.1016/j.abb.2004.03.018. PMID 15325905. S2CID 25306222.
  50. ^ Miller RA, Britigan BE (January 1997). "Role of oxidants in microbial pathophysiology". Clinical Microbiology Reviews. 10 (1): 1–18. doi:10.1128/CMR.10.1.1. PMC 172912. PMID 8993856.
  51. ^ Chaudière J, Ferrari-Iliou R (1999). "Intracellular antioxidants: from chemical to biochemical mechanisms". Food and Chemical Toxicology. 37 (9–10): 949–62. doi:10.1016/S0278-6915(99)00090-3. PMID 10541450.
  52. ^ Sies H (July 1993). "Strategies of antioxidant defense". European Journal of Biochemistry. 215 (2): 213–9. doi:10.1111/j.1432-1033.1993.tb18025.x. PMID 7688300.
  53. ^ Khaw KT, Woodhouse P (June 1995). "Interrelation of vitamin C, infection, haemostatic factors, and cardiovascular disease". BMJ. 310 (6994): 1559–63. doi:10.1136/bmj.310.6994.1559. PMC 2549940. PMID 7787643.
  54. ^ a b c d Evelson P, Travacio M, Repetto M, Escobar J, Llesuy S, Lissi EA (April 2001). "Evaluation of total reactive antioxidant potential (TRAP) of tissue homogenates and their cytosols". Archives of Biochemistry and Biophysics. 388 (2): 261–6. doi:10.1006/abbi.2001.2292. PMID 11368163.
  55. ^ Morrison JA, Jacobsen DW, Sprecher DL, Robinson K, Khoury P, Daniels SR (November 1999). "Serum glutathione in adolescent males predicts parental coronary heart disease". Circulation. 100 (22): 2244–7. doi:10.1161/01.CIR.100.22.2244. PMID 10577998.
  56. ^ Teichert J, Preiss R (November 1992). "HPLC-methods for determination of lipoic acid and its reduced form in human plasma". International Journal of Clinical Pharmacology, Therapy, and Toxicology. 30 (11): 511–2. PMID 1490813.
  57. ^ Akiba S, Matsugo S, Packer L, Konishi T (May 1998). "Assay of protein-bound lipoic acid in tissues by a new enzymatic method". Analytical Biochemistry. 258 (2): 299–304. doi:10.1006/abio.1998.2615. PMID 9570844.
  58. ^ a b Glantzounis GK, Tsimoyiannis EC, Kappas AM, Galaris DA (2005). "Uric acid and oxidative stress". Current Pharmaceutical Design. 11 (32): 4145–51. doi:10.2174/138161205774913255. PMID 16375736.
  59. ^ El-Sohemy A, Baylin A, Kabagambe E, Ascherio A, Spiegelman D, Campos H (July 2002). "Individual carotenoid concentrations in adipose tissue and plasma as biomarkers of dietary intake". The American Journal of Clinical Nutrition. 76 (1): 172–9. doi:10.1093/ajcn/76.1.172. PMID 12081831.
  60. ^ a b Sowell AL, Huff DL, Yeager PR, Caudill SP, Gunter EW (March 1994). "Retinol, alpha-tocopherol, lutein/zeaxanthin, beta-cryptoxanthin, lycopene, alpha-carotene, trans-beta-carotene, and four retinyl esters in serum determined simultaneously by reversed-phase HPLC with multiwavelength detection". Clinical Chemistry. 40 (3): 411–6. doi:10.1093/clinchem/40.3.411. PMID 8131277.
  61. ^ Stahl W, Schwarz W, Sundquist AR, Sies H (April 1992). "cis-trans isomers of lycopene and beta-carotene in human serum and tissues". Archives of Biochemistry and Biophysics. 294 (1): 173–7. doi:10.1016/0003-9861(92)90153-N. PMID 1550343.
  62. ^ Zita C, Overvad K, Mortensen SA, Sindberg CD, Moesgaard S, Hunter DA (2003). "Serum coenzyme Q10 concentrations in healthy men supplemented with 30 mg or 100 mg coenzyme Q10 for two months in a randomised controlled study". BioFactors. 18 (1–4): 185–93. doi:10.1002/biof.5520180221. PMID 14695934. S2CID 19895215.
  63. ^ a b Turunen M, Olsson J, Dallner G (January 2004). "Metabolism and function of coenzyme Q". Biochimica et Biophysica Acta (BBA) - Biomembranes. 1660 (1–2): 171–99. doi:10.1016/j.bbamem.2003.11.012. PMID 14757233.
  64. ^ Becker BF (June 1993). "Towards the physiological function of uric acid". Free Radical Biology & Medicine. 14 (6): 615–31. doi:10.1016/0891-5849(93)90143-I. PMID 8325534.
  65. ^ a b Sautin YY, Johnson RJ (June 2008). "Uric acid: the oxidant-antioxidant paradox". Nucleosides, Nucleotides & Nucleic Acids. 27 (6): 608–19. doi:10.1080/15257770802138558. PMC 2895915. PMID 18600514.
  66. ^ Enomoto A, Endou H (September 2005). "Roles of organic anion transporters (OATs) and a urate transporter (URAT1) in the pathophysiology of human disease". Clinical and Experimental Nephrology. 9 (3): 195–205. doi:10.1007/s10157-005-0368-5. PMID 16189627. S2CID 6145651.
  67. ^ Eggebeen AT (September 2007). "Gout: an update". American Family Physician. 76 (6): 801–8. PMID 17910294.
  68. ^ Campion EW, Glynn RJ, DeLabry LO (March 1987). "Asymptomatic hyperuricemia. Risks and consequences in the Normative Aging Study". The American Journal of Medicine. 82 (3): 421–6. doi:10.1016/0002-9343(87)90441-4. PMID 3826098.
  69. ^ Baillie JK, Bates MG, Thompson AA, Waring WS, Partridge RW, Schnopp MF, Simpson A, Gulliver-Sloan F, Maxwell SR, Webb DJ (May 2007). "Endogenous urate production augments plasma antioxidant capacity in healthy lowland subjects exposed to high altitude". Chest. 131 (5): 1473–8. doi:10.1378/chest.06-2235. PMID 17494796.
  70. ^ Nazarewicz RR, Ziolkowski W, Vaccaro PS, Ghafourifar P (December 2007). "Effect of short-term ketogenic diet on redox status of human blood". Rejuvenation Research. 10 (4): 435–40. doi:10.1089/rej.2007.0540. PMID 17663642.
  71. ^ a b "Vitamin C". Micronutrient Information Center, Linus Pauling Institute, Oregon State University, Corvallis, OR. 1 July 2018. Retrieved 19 June 2019.
  72. ^ Padayatty SJ, Katz A, Wang Y, Eck P, Kwon O, Lee JH, Chen S, Corpe C, Dutta A, Dutta SK, Levine M (February 2003). "Vitamin C as an antioxidant: evaluation of its role in disease prevention". Journal of the American College of Nutrition. 22 (1): 18–35. doi:10.1080/07315724.2003.10719272. PMID 12569111. S2CID 21196776.
  73. ^ Shigeoka S, Ishikawa T, Tamoi M, Miyagawa Y, Takeda T, Yabuta Y, Yoshimura K (May 2002). "Regulation and function of ascorbate peroxidase isoenzymes". Journal of Experimental Botany. 53 (372): 1305–19. doi:10.1093/jexbot/53.372.1305. PMID 11997377.
  74. ^ Smirnoff N, Wheeler GL (2000). "Ascorbic acid in plants: biosynthesis and function". Critical Reviews in Biochemistry and Molecular Biology. 35 (4): 291–314. doi:10.1080/10409230008984166. PMID 11005203. S2CID 85060539.
  75. ^ Meister A (April 1994). "Glutathione-ascorbic acid antioxidant system in animals". The Journal of Biological Chemistry. 269 (13): 9397–400. doi:10.1016/S0021-9258(17)36891-6. PMID 8144521.
  76. ^ a b c Meister A, Anderson ME (1983). "Glutathione". Annual Review of Biochemistry. 52: 711–60. doi:10.1146/annurev.bi.52.070183.003431. PMID 6137189.
  77. ^ Gaballa A, Newton GL, Antelmann H, Parsonage D, Upton H, Rawat M, Claiborne A, Fahey RC, Helmann JD (April 2010). "Biosynthesis and functions of bacillithiol, a major low-molecular-weight thiol in Bacilli". Proceedings of the National Academy of Sciences of the United States of America. 107 (14): 6482–6. Bibcode:2010PNAS..107.6482G. doi:10.1073/pnas.1000928107. PMC 2851989. PMID 20308541.
  78. ^ Newton GL, Rawat M, La Clair JJ, Jothivasan VK, Budiarto T, Hamilton CJ, Claiborne A, Helmann JD, Fahey RC (September 2009). "Bacillithiol is an antioxidant thiol produced in Bacilli". Nature Chemical Biology. 5 (9): 625–627. doi:10.1038/nchembio.189. PMC 3510479. PMID 19578333.
  79. ^ Fahey RC (2001). "Novel thiols of prokaryotes". Annual Review of Microbiology. 55: 333–56. doi:10.1146/annurev.micro.55.1.333. PMID 11544359.
  80. ^ Fairlamb AH, Cerami A (1992). "Metabolism and functions of trypanothione in the Kinetoplastida". Annual Review of Microbiology. 46: 695–729. doi:10.1146/annurev.mi.46.100192.003403. PMID 1444271.
  81. ^ a b Herrera E, Barbas C (March 2001). "Vitamin E: action, metabolism and perspectives". Journal of Physiology and Biochemistry. 57 (2): 43–56. doi:10.1007/BF03179812. hdl:10637/720. PMID 11579997. S2CID 7272312.
  82. ^ Packer L, Weber SU, Rimbach G (February 2001). "Molecular aspects of alpha-tocotrienol antioxidant action and cell signalling". The Journal of Nutrition. 131 (2): 369S–73S. doi:10.1093/jn/131.2.369S. PMID 11160563.
  83. ^ a b Brigelius-Flohé R, Traber MG (July 1999). "Vitamin E: function and metabolism". FASEB Journal. 13 (10): 1145–55. CiteSeerX 10.1.1.337.5276. doi:10.1096/fasebj.13.10.1145. PMID 10385606. S2CID 7031925.
  84. ^ Traber MG, Atkinson J (July 2007). "Vitamin E, antioxidant and nothing more". Free Radical Biology & Medicine. 43 (1): 4–15. doi:10.1016/j.freeradbiomed.2007.03.024. PMC 2040110. PMID 17561088.
  85. ^ Wang X, Quinn PJ (July 1999). "Vitamin E and its function in membranes". Progress in Lipid Research. 38 (4): 309–36. doi:10.1016/S0163-7827(99)00008-9. PMID 10793887.
  86. ^ Seiler A, Schneider M, Förster H, Roth S, Wirth EK, Culmsee C, Plesnila N, Kremmer E, Rådmark O, Wurst W, Bornkamm GW, Schweizer U, Conrad M (September 2008). "Glutathione peroxidase 4 senses and translates oxidative stress into 12/15-lipoxygenase dependent- and AIF-mediated cell death". Cell Metabolism. 8 (3): 237–48. doi:10.1016/j.cmet.2008.07.005. PMID 18762024.
  87. ^ Brigelius-Flohé R, Davies KJ (July 2007). "Is vitamin E an antioxidant, a regulator of signal transduction and gene expression, or a 'junk' food? Comments on the two accompanying papers: "Molecular mechanism of alpha-tocopherol action" by A. Azzi and "Vitamin E, antioxidant and nothing more" by M. Traber and J. Atkinson". Free Radical Biology & Medicine. 43 (1): 2–3. doi:10.1016/j.freeradbiomed.2007.05.016. PMID 17561087.
  88. ^ Atkinson J, Epand RF, Epand RM (March 2008). "Tocopherols and tocotrienols in membranes: a critical review". Free Radical Biology & Medicine. 44 (5): 739–64. doi:10.1016/j.freeradbiomed.2007.11.010. PMID 18160049.
  89. ^ Azzi A (July 2007). "Molecular mechanism of alpha-tocopherol action". Free Radical Biology & Medicine. 43 (1): 16–21. doi:10.1016/j.freeradbiomed.2007.03.013. PMID 17561089.
  90. ^ Zingg JM, Azzi A (May 2004). "Non-antioxidant activities of vitamin E". Current Medicinal Chemistry. 11 (9): 1113–33. doi:10.2174/0929867043365332. PMID 15134510. Archived from the original on 6 October 2011.
  91. ^ Sen CK, Khanna S, Roy S (March 2006). "Tocotrienols: Vitamin E beyond tocopherols". Life Sciences. 78 (18): 2088–98. doi:10.1016/j.lfs.2005.12.001. PMC 1790869. PMID 16458936.
  92. ^ Duarte TL, Lunec J (July 2005). "Review: When is an antioxidant not an antioxidant? A review of novel actions and reactions of vitamin C". Free Radical Research. 39 (7): 671–86. doi:10.1080/10715760500104025. PMID 16036346. S2CID 39962659.
  93. ^ a b Shen, Jiaqi; Griffiths, Paul T.; Campbell, Steven J.; Utinger, Battist; Kalberer, Markus; Paulson, Suzanne E. (1 April 2021). "Ascorbate oxidation by iron, copper and reactive oxygen species: review, model development, and derivation of key rate constants". Scientific Reports. 11 (1): 7417. Bibcode:2021NatSR..11.7417S. doi:10.1038/s41598-021-86477-8. ISSN 2045-2322. PMC 8016884. PMID 33795736.
  94. ^ a b Carr A, Frei B (June 1999). "Does vitamin C act as a pro-oxidant under physiological conditions?". FASEB Journal. 13 (9): 1007–24. doi:10.1096/fasebj.13.9.1007. PMID 10336883. S2CID 15426564.
  95. ^ a b Ho YS, Magnenat JL, Gargano M, Cao J (October 1998). "The nature of antioxidant defense mechanisms: a lesson from transgenic studies". Environmental Health Perspectives. 106 (Suppl 5): 1219–28. doi:10.2307/3433989. JSTOR 3433989. PMC 1533365. PMID 9788901.
  96. ^ Zelko IN, Mariani TJ, Folz RJ (August 2002). "Superoxide dismutase multigene family: a comparison of the CuZn-SOD (SOD1), Mn-SOD (SOD2), and EC-SOD (SOD3) gene structures, evolution, and expression". Free Radical Biology & Medicine. 33 (3): 337–49. doi:10.1016/S0891-5849(02)00905-X. PMID 12126755.
  97. ^ a b Bannister JV, Bannister WH, Rotilio G (1987). "Aspects of the structure, function, and applications of superoxide dismutase". CRC Critical Reviews in Biochemistry. 22 (2): 111–80. doi:10.3109/10409238709083738. PMID 3315461.
  98. ^ Johnson F, Giulivi C (2005). "Superoxide dismutases and their impact upon human health". Molecular Aspects of Medicine. 26 (4–5): 340–52. doi:10.1016/j.mam.2005.07.006. PMID 16099495.
  99. ^ Nozik-Grayck E, Suliman HB, Piantadosi CA (December 2005). "Extracellular superoxide dismutase". The International Journal of Biochemistry & Cell Biology. 37 (12): 2466–71. doi:10.1016/j.biocel.2005.06.012. PMID 16087389.
  100. ^ Melov S, Schneider JA, Day BJ, Hinerfeld D, Coskun P, Mirra SS, Crapo JD, Wallace DC (February 1998). "A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase". Nature Genetics. 18 (2): 159–63. doi:10.1038/ng0298-159. PMID 9462746. S2CID 20843002.
  101. ^ Reaume AG, Elliott JL, Hoffman EK, Kowall NW, Ferrante RJ, Siwek DF, Wilcox HM, Flood DG, Beal MF, Brown RH, Scott RW, Snider WD (May 1996). "Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury". Nature Genetics. 13 (1): 43–7. doi:10.1038/ng0596-43. PMID 8673102. S2CID 13070253.
  102. ^ Van Camp W, Inzé D, Van Montagu M (1997). "The regulation and function of tobacco superoxide dismutases". Free Radical Biology & Medicine. 23 (3): 515–20. doi:10.1016/S0891-5849(97)00112-3. PMID 9214590.
  103. ^ Chelikani P, Fita I, Loewen PC (January 2004). "Diversity of structures and properties among catalases" (PDF). Cellular and Molecular Life Sciences (Submitted manuscript). 61 (2): 192–208. doi:10.1007/s00018-003-3206-5. hdl:10261/111097. PMC 11138816. PMID 14745498. S2CID 4411482.
  104. ^ Zámocký M, Koller F (1999). "Understanding the structure and function of catalases: clues from molecular evolution and in vitro mutagenesis". Progress in Biophysics and Molecular Biology. 72 (1): 19–66. doi:10.1016/S0079-6107(98)00058-3. PMID 10446501.
  105. ^ del Río LA, Sandalio LM, Palma JM, Bueno P, Corpas FJ (November 1992). "Metabolism of oxygen radicals in peroxisomes and cellular implications". Free Radical Biology & Medicine. 13 (5): 557–80. doi:10.1016/0891-5849(92)90150-F. PMID 1334030.
  106. ^ Hiner AN, Raven EL, Thorneley RN, García-Cánovas F, Rodríguez-López JN (July 2002). "Mechanisms of compound I formation in heme peroxidases". Journal of Inorganic Biochemistry. 91 (1): 27–34. doi:10.1016/S0162-0134(02)00390-2. PMID 12121759.
  107. ^ Mueller S, Riedel HD, Stremmel W (December 1997). "Direct evidence for catalase as the predominant H2O2 -removing enzyme in human erythrocytes". Blood. 90 (12): 4973–8. doi:10.1182/blood.V90.12.4973. PMID 9389716.
  108. ^ Ogata M (February 1991). "Acatalasemia". Human Genetics. 86 (4): 331–40. doi:10.1007/BF00201829. PMID 1999334. S2CID 264033871.
  109. ^ Parsonage D, Youngblood D, Sarma G, Wood Z, Karplus P, Poole L (2005). "Analysis of the link between enzymatic activity and oligomeric state in AhpC, a bacterial peroxiredoxin". Biochemistry. 44 (31): 10583–92. doi:10.1021/bi050448i. PMC 3832347. PMID 16060667. PDB 1YEX
  110. ^ Rhee SG, Chae HZ, Kim K (June 2005). "Peroxiredoxins: a historical overview and speculative preview of novel mechanisms and emerging concepts in cell signaling". Free Radical Biology & Medicine. 38 (12): 1543–52. doi:10.1016/j.freeradbiomed.2005.02.026. PMID 15917183.
  111. ^ Wood ZA, Schröder E, Robin Harris J, Poole LB (January 2003). "Structure, mechanism and regulation of peroxiredoxins". Trends in Biochemical Sciences. 28 (1): 32–40. doi:10.1016/S0968-0004(02)00003-8. PMID 12517450.
  112. ^ Claiborne A, Yeh JI, Mallett TC, Luba J, Crane EJ, Charrier V, Parsonage D (November 1999). "Protein-sulfenic acids: diverse roles for an unlikely player in enzyme catalysis and redox regulation". Biochemistry. 38 (47): 15407–16. doi:10.1021/bi992025k. PMID 10569923. S2CID 29055779.
  113. ^ Jönsson TJ, Lowther WT (2007). "The peroxiredoxin repair proteins". Peroxiredoxin Systems. Subcellular Biochemistry. Vol. 44. pp. 115–41. doi:10.1007/978-1-4020-6051-9_6. ISBN 978-1-4020-6050-2. PMC 2391273. PMID 18084892.
  114. ^ Neumann CA, Krause DS, Carman CV, Das S, Dubey DP, Abraham JL, Bronson RT, Fujiwara Y, Orkin SH, Van Etten RA (July 2003). "Essential role for the peroxiredoxin Prdx1 in erythrocyte antioxidant defence and tumour suppression" (PDF). Nature. 424 (6948): 561–5. Bibcode:2003Natur.424..561N. doi:10.1038/nature01819. PMID 12891360. S2CID 3570549.
  115. ^ Lee TH, Kim SU, Yu SL, Kim SH, Park DS, Moon HB, Dho SH, Kwon KS, Kwon HJ, Han YH, Jeong S, Kang SW, Shin HS, Lee KK, Rhee SG, Yu DY (June 2003). "Peroxiredoxin II is essential for sustaining life span of erythrocytes in mice". Blood. 101 (12): 5033–8. doi:10.1182/blood-2002-08-2548. PMID 12586629.
  116. ^ Dietz KJ, Jacob S, Oelze ML, Laxa M, Tognetti V, de Miranda SM, Baier M, Finkemeier I (2006). "The function of peroxiredoxins in plant organelle redox metabolism". Journal of Experimental Botany. 57 (8): 1697–709. doi:10.1093/jxb/erj160. PMID 16606633.
  117. ^ Nordberg J, Arnér ES (December 2001). "Reactive oxygen species, antioxidants, and the mammalian thioredoxin system". Free Radical Biology & Medicine. 31 (11): 1287–312. doi:10.1016/S0891-5849(01)00724-9. PMID 11728801.
  118. ^ Vieira Dos Santos C, Rey P (July 2006). "Plant thioredoxins are key actors in the oxidative stress response". Trends in Plant Science. 11 (7): 329–34. Bibcode:2006TPS....11..329V. doi:10.1016/j.tplants.2006.05.005. PMID 16782394.
  119. ^ Arnér ES, Holmgren A (October 2000). "Physiological functions of thioredoxin and thioredoxin reductase". European Journal of Biochemistry. 267 (20): 6102–9. doi:10.1046/j.1432-1327.2000.01701.x. PMID 11012661.
  120. ^ Mustacich D, Powis G (February 2000). "Thioredoxin reductase". The Biochemical Journal. 346 (1): 1–8. doi:10.1042/0264-6021:3460001. PMC 1220815. PMID 10657232.
  121. ^ Creissen G, Broadbent P, Stevens R, Wellburn AR, Mullineaux P (May 1996). "Manipulation of glutathione metabolism in transgenic plants". Biochemical Society Transactions. 24 (2): 465–9. doi:10.1042/bst0240465. PMID 8736785.
  122. ^ Brigelius-Flohé R (November 1999). "Tissue-specific functions of individual glutathione peroxidases". Free Radical Biology & Medicine. 27 (9–10): 951–65. doi:10.1016/S0891-5849(99)00173-2. PMID 10569628.
  123. ^ Ho YS, Magnenat JL, Bronson RT, Cao J, Gargano M, Sugawara M, Funk CD (June 1997). "Mice deficient in cellular glutathione peroxidase develop normally and show no increased sensitivity to hyperoxia". The Journal of Biological Chemistry. 272 (26): 16644–51. doi:10.1074/jbc.272.26.16644. PMID 9195979.
  124. ^ de Haan JB, Bladier C, Griffiths P, Kelner M, O'Shea RD, Cheung NS, Bronson RT, Silvestro MJ, Wild S, Zheng SS, Beart PM, Hertzog PJ, Kola I (August 1998). "Mice with a homozygous null mutation for the most abundant glutathione peroxidase, Gpx1, show increased susceptibility to the oxidative stress-inducing agents paraquat and hydrogen peroxide". The Journal of Biological Chemistry. 273 (35): 22528–36. doi:10.1074/jbc.273.35.22528. hdl:10536/DRO/DU:30101410. PMID 9712879.
  125. ^ Sharma R, Yang Y, Sharma A, Awasthi S, Awasthi YC (April 2004). "Antioxidant role of glutathione S-transferases: protection against oxidant toxicity and regulation of stress-mediated apoptosis". Antioxidants & Redox Signaling. 6 (2): 289–300. doi:10.1089/152308604322899350. PMID 15025930.
  126. ^ Hayes JD, Flanagan JU, Jowsey IR (2005). "Glutathione transferases". Annual Review of Pharmacology and Toxicology. 45: 51–88. doi:10.1146/annurev.pharmtox.45.120403.095857. PMID 15822171.
  127. ^ a b Stanner SA, Hughes J, Kelly CN, Buttriss J (May 2004). "A review of the epidemiological evidence for the 'antioxidant hypothesis'". Public Health Nutrition. 7 (3): 407–22. doi:10.1079/PHN2003543. PMID 15153272.
  128. ^ Food, Nutrition, Physical Activity, and the Prevention of Cancer: a Global Perspective Archived 23 September 2015 at the Wayback Machine. World Cancer Research Fund (2007). ISBN 978-0-9722522-2-5.
  129. ^ Rice-Evans, Catherine A.; Miller, Nicholas J.; Paganga, George (1996). "Structure-antioxidant activity relationships of flavonoids and phenolic acids". Free Radical Biology and Medicine. 20 (7): 933–956. doi:10.1016/0891-5849(95)02227-9. PMID 8743980.
  130. ^ Del Rio D, Rodriguez-Mateos A, Spencer JP, Tognolini M, Borges G, Crozier A (May 2013). "Dietary (poly)phenolics in human health: structures, bioavailability, and evidence of protective effects against chronic diseases". Antioxidants & Redox Signaling. 18 (14): 1818–1892. doi:10.1089/ars.2012.4581. PMC 3619154. PMID 22794138.
  131. ^ "Flavonoids". Linus Pauling Institute, Oregon State University, Corvallis. 2016. Retrieved 24 July 2016.
  132. ^ Lemmo W (September 2014). "Potential interactions of prescription and over-the-counter medications having antioxidant capabilities with radiation and chemotherapy". International Journal of Cancer. 137 (11): 2525–33. doi:10.1002/ijc.29208. PMID 25220632. S2CID 205951215.
  133. ^ Forman, Henry Jay; Zhang, Hongqiao (30 June 2021). "Targeting oxidative stress in disease: promise and limitations of antioxidant therapy". Nature Reviews Drug Discovery. 20 (9): 689–709. doi:10.1038/s41573-021-00233-1. ISSN 1474-1784. PMC 8243062. PMID 34194012.
  134. ^ Hurrell RF (September 2003). "Influence of vegetable protein sources on trace element and mineral bioavailability". The Journal of Nutrition. 133 (9): 2973S–7S. doi:10.1093/jn/133.9.2973S. PMID 12949395.
  135. ^ Hunt JR (September 2003). "Bioavailability of iron, zinc, and other trace minerals from vegetarian diets". The American Journal of Clinical Nutrition. 78 (3 Suppl): 633S–639S. doi:10.1093/ajcn/78.3.633S. PMID 12936958.
  136. ^ Gibson RS, Perlas L, Hotz C (May 2006). "Improving the bioavailability of nutrients in plant foods at the household level". The Proceedings of the Nutrition Society. 65 (2): 160–8. doi:10.1079/PNS2006489. PMID 16672077.
  137. ^ a b Mosha TC, Gaga HE, Pace RD, Laswai HS, Mtebe K (June 1995). "Effect of blanching on the content of antinutritional factors in selected vegetables". Plant Foods for Human Nutrition. 47 (4): 361–7. doi:10.1007/BF01088275. PMID 8577655. S2CID 1118651.
  138. ^ Sandberg AS (December 2002). "Bioavailability of minerals in legumes". The British Journal of Nutrition. 88 (Suppl 3): S281–5. doi:10.1079/BJN/2002718. PMID 12498628.
  139. ^ a b Beecher GR (October 2003). "Overview of dietary flavonoids: nomenclature, occurrence and intake". The Journal of Nutrition. 133 (10): 3248S–3254S. doi:10.1093/jn/133.10.3248S. PMID 14519822.
  140. ^ Omenn GS, Goodman GE, Thornquist MD, Balmes J, Cullen MR, Glass A, Keogh JP, Meyskens FL, Valanis B, Williams JH, Barnhart S, Cherniack MG, Brodkin CA, Hammar S (November 1996). "Risk factors for lung cancer and for intervention effects in CARET, the Beta-Carotene and Retinol Efficacy Trial" (PDF). Journal of the National Cancer Institute. 88 (21): 1550–9. doi:10.1093/jnci/88.21.1550. PMID 8901853.
  141. ^ Albanes D (June 1999). "Beta-carotene and lung cancer: a case study". The American Journal of Clinical Nutrition. 69 (6): 1345S–50S. doi:10.1093/ajcn/69.6.1345S. PMID 10359235.
  142. ^ a b Bjelakovic G, Nikolova D, Gluud LL, Simonetti RG, Gluud C (February 2007). "Mortality in randomized trials of antioxidant supplements for primary and secondary prevention: systematic review and meta-analysis". JAMA. 297 (8): 842–57. doi:10.1001/jama.297.8.842. PMID 17327526.
  143. ^ a b Bjelakovic G, Nikolova D, Gluud LL, Simonetti RG, Gluud C (14 March 2012). "Antioxidant supplements for prevention of mortality in healthy participants and patients with various diseases". The Cochrane Database of Systematic Reviews. 2012 (3): CD007176. doi:10.1002/14651858.CD007176.pub2. hdl:10138/136201. PMC 8407395. PMID 22419320.
  144. ^ Study Citing Antioxidant Vitamin Risks Based On Flawed Methodology, Experts Argue News release from Oregon State University published on ScienceDaily. Retrieved 19 April 2007
  145. ^ Miller ER, Pastor-Barriuso R, Dalal D, Riemersma RA, Appel LJ, Guallar E (January 2005). "Meta-analysis: high-dosage vitamin E supplementation may increase all-cause mortality". Annals of Internal Medicine. 142 (1): 37–46. doi:10.7326/0003-4819-142-1-200501040-00110. PMID 15537682.
  146. ^ a b Bjelakovic G, Nagorni A, Nikolova D, Simonetti RG, Bjelakovic M, Gluud C (July 2006). "Meta-analysis: antioxidant supplements for primary and secondary prevention of colorectal adenoma". Alimentary Pharmacology & Therapeutics. 24 (2): 281–91. doi:10.1111/j.1365-2036.2006.02970.x. PMID 16842454. S2CID 20452618.
  147. ^ Cortés-Jofré M, Rueda JR, Asenjo-Lobos C, Madrid E, Bonfill Cosp X (March 2020). "Drugs for preventing lung cancer in healthy people". The Cochrane Database of Systematic Reviews. 2020 (3): CD002141. doi:10.1002/14651858.CD002141.pub3. PMC 7059884. PMID 32130738.
  148. ^ Shenkin A (February 2006). "The key role of micronutrients". Clinical Nutrition. 25 (1): 1–13. doi:10.1016/j.clnu.2005.11.006. PMID 16376462.
  149. ^ Ranchordas, Mayur K.; Rogerson, David; Soltani, Hora; Costello, Joseph T. (14 December 2017). "Antioxidants for preventing and reducing muscle soreness after exercise". The Cochrane Database of Systematic Reviews. 2017 (12): CD009789. doi:10.1002/14651858.CD009789.pub2. ISSN 1469-493X. PMC 6486214. PMID 29238948.
  150. ^ Rodriguez-Amaya DB (2003). "Food carotenoids: analysis, composition and alterations during storage and processing of foods". Forum of Nutrition. 56: 35–7. PMID 15806788.
  151. ^ Maiani G, Castón MJ, Catasta G, Toti E, Cambrodón IG, Bysted A, Granado-Lorencio F, Olmedilla-Alonso B, Knuthsen P, Valoti M, Böhm V, Mayer-Miebach E, Behsnilian D, Schlemmer U (September 2009). "Carotenoids: actual knowledge on food sources, intakes, stability and bioavailability and their protective role in humans". Molecular Nutrition & Food Research. 53 (Suppl 2): S194–218. doi:10.1002/mnfr.200800053. hdl:10261/77697. PMID 19035552. Archived from the original on 27 September 2018. Retrieved 18 April 2017.
  152. ^ Henry CJ, Heppell N (February 2002). "Nutritional losses and gains during processing: future problems and issues". The Proceedings of the Nutrition Society. 61 (1): 145–8. doi:10.1079/PNS2001142. PMID 12002789.
  153. ^ "Antioxidants and Cancer Prevention: Fact Sheet". National Cancer Institute. Archived from the original on 4 March 2007. Retrieved 27 February 2007.
  154. ^ Ortega R (December 2006). "Importance of functional foods in the Mediterranean diet". Public Health Nutrition. 9 (8A): 1136–40. doi:10.1017/S1368980007668530. PMID 17378953.
  155. ^ Witschi A, Reddy S, Stofer B, Lauterburg BH (1992). "The systemic availability of oral glutathione". European Journal of Clinical Pharmacology. 43 (6): 667–9. doi:10.1007/BF02284971. PMID 1362956. S2CID 27606314.
  156. ^ Flagg EW, Coates RJ, Eley JW, Jones DP, Gunter EW, Byers TE, Block GS, Greenberg RS (1994). "Dietary glutathione intake in humans and the relationship between intake and plasma total glutathione level". Nutrition and Cancer. 21 (1): 33–46. doi:10.1080/01635589409514302. PMID 8183721.
  157. ^ Dodd S, Dean O, Copolov DL, Malhi GS, Berk M (December 2008). "N-acetylcysteine for antioxidant therapy: pharmacology and clinical utility". Expert Opinion on Biological Therapy. 8 (12): 1955–62. doi:10.1517/14728220802517901. PMID 18990082. S2CID 74736842.
  158. ^ van de Poll MC, Dejong CH, Soeters PB (June 2006). "Adequate range for sulfur-containing amino acids and biomarkers for their excess: lessons from enteral and parenteral nutrition". The Journal of Nutrition. 136 (6 Suppl): 1694S–1700S. doi:10.1093/jn/136.6.1694S. PMID 16702341.
  159. ^ Cao G, Alessio HM, Cutler RG (March 1993). "Oxygen-radical absorbance capacity assay for antioxidants". Free Radical Biology & Medicine. 14 (3): 303–11. doi:10.1016/0891-5849(93)90027-R. PMID 8458588.
  160. ^ Ou B, Hampsch-Woodill M, Prior RL (October 2001). "Development and validation of an improved oxygen radical absorbance capacity assay using fluorescein as the fluorescent probe". Journal of Agricultural and Food Chemistry. 49 (10): 4619–26. doi:10.1021/jf010586o. PMID 11599998.
  161. ^ a b "Withdrawn: Oxygen Radical Absorbance Capacity (ORAC) of Selected Foods, Release 2 (2010)". United States Department of Agriculture, Agricultural Research Service. 16 May 2012. Retrieved 13 June 2012.
  162. ^ Prior RL, Wu X, Schaich K (May 2005). "Standardized methods for the determination of antioxidant capacity and phenolics in foods and dietary supplements" (PDF). Journal of Agricultural and Food Chemistry. 53 (10): 4290–302. doi:10.1021/jf0502698. PMID 15884874. Archived from the original (PDF) on 29 December 2016. Retrieved 24 October 2017.

Further reading

  • Halliwell B, Gutteridge JM (2015). Free Radicals in Biology and Medicine (5th ed.). Oxford University Press. ISBN 978-0-19-856869-8.
  • Lane N (2003). Oxygen: The Molecule That Made the World. Oxford University Press. ISBN 978-0-19-860783-0.
  • Pokorny J, Yanishlieva N, Gordon MH (2001). Antioxidants in Food: Practical Applications. CRC Press. ISBN 978-0-8493-1222-9.
Quelle: https://en.wikipedia.org/wiki/Antioxidants