Vitamin C

| Main Article
| Discussion
| Related Articles  [?]
| Bibliography  [?]
| External Links  [?]
| Citable Version  [?]
| Catalogs [?]

|
|
|
|
|
|
|
|
|

This editable, developed Main Article is subject to a disclaimer.

[edit intro]

## Contents

* 1 Description
* 1.1 Role as enzyme cofactor
* 1.2 Antioxidant functions
* 1.3 Action on receptors
* 1.4 Biosynthesis
* 1.4.1 Is uric acid an antioxidant for vitamin C?
* 1.5 Transport
* 1.6 Distribution
* 1.7 Food sources
* 1.8 History
* 2 Recommended daily requirements
* 2.1 Scurvy
* 2.2 Based on pharmacokinetics
* 2.3 Based on evolutionary biology
* 3 Therapeutic uses
* 3.1 Critical care
* 3.2 Post-operative complications
* 3.3 Anemia
* 3.4 Viral diseases
* 3.5 Toxics
* 3.6 Medications (reduction of adverse effects)
* 3.7 Cardiovascular disease and fat intake
* 3.8 Cardiovascular disease as a long latency collagen disease
* 3.9 Cancer
* 3.9.1 Biochemistry
* 3.9.2 Trials of cancer treatment in humans
* 3.9.3 Trials of cancer prevention in humans
* 3.10 Cataracts
* 3.11 Obstetrics and gynaecology
* 4 Side effects and contraindications
* 5 References

Vitamin C is a water-soluble vitamin required by several mammalian species, including humans and higher primates, who mainly get it by eating fresh fruits and vegetables. It has many physiological effects and, at present, eight different well characterized roles, but it is not specifically required for any enzyme.[1] As research advances, it appears that its first name, ignose, meaning "I don't know", or "godnose," describes it best.[2]

Vitamin C

This article is about the biochemistry of vitamin C, or ascorbic acid. For the chemical properties, see Ascorbic acid.

First known as the vitamin that prevents scurvy (hence its chemical name, ascorbic acid), vitamin C is an important factor in * the maintenance of good health. Vitamin C is:

* the most widely sold dietary supplement in the world;
* required for the maintenance of the most abundant protein in the body,
* the most "luminously controversial of all biological, alternative cancer therapies",[3]
* the vitamin which intake has declined the most drastically in the course of human evolution, and
* the vitamin which requirements have been debated for the most time and with the most intensity.

This article describes the debates about vitamin C, and presents the state-of-the-art in vitamin C therapeutics and the context in which knowledge on this nutrient has been produced.

## Description[edit]

The evolution of vertebrates can be viewed as the history of how they responded to the "the call for oxygen"[4] \-- for "the fire of life".[5] Most important is the need to use this fire without being "burnt" by it.[6] The development of antioxidant machineries is closely intertwined with the development of species. An analysis of the evolutionary record suggests that the aquatic animals that were ancestors of amphibians did not significantly increase their concentrations of superoxide dismutase (SOD), the first line of defense against oxygen toxicity, instead, to cope with the sharp, 30-fold, increase in oxygen exposure, they developed a machinery to transform glucose into ascorbic acid.[7] The further evolution from reptiles to mammals was marked by a gradual increase in GULO, the fourth and last step in the vitamin C-producing machinery, and of SOD. In reptiles, about 9.4 mg/kg body weight of ascorbate is produced each day, whereas 184.2 mg/kg is produced each day in mammals (9.2 g for a 50 kg mammal).[8] Nonetheless, SOD tended to be favoured to the expense of GULO.

In exceptional cases, a complete loss of vitamin C production occurred during evolution: Old World higher primates do without endogenous vitamin C, and express roughly twice as much SOD as other mammals. Amongst those species, humans have the best SOD defense.[7] It is thought that the loss of the ability to produce vitamin C occurred some 25 to 45 million years ago, when the natural environment of the common ancestor of primates was abundant in vitamin C.[9] Higher primates, who still live in vitamin-C rich environments, consume 2000 to 6000 mg of vitamin C per day,[10] much more than the recommended doses for modern man, which are at least 20 times lower.

According to the Online Mendeleian Inheritance in Man database, hypoascorbemia is a "public" inborn error of metabolism, as it affects all members of the human race.[9]

Vitamin C (chemical names ascorbic acid and ascorbate) is produced from glucose in the liver of most mammals and in the kidneys of most birds and reptiles. Mammals that are unable to synthesize vitamin C include humans and other primates, guinea pigs, Indian fruit bats, rainbow trouts and Nepalese red-vented bulbols. As usually defined, a vitamin is a nutrient present in the diet that is required in small amounts for normal health; because most vertebrate species produce it in large amounts, it cannot be considered as a vitamin in these species, but a dietary intake of small amounts of vitamin C is indeed required for normal health in humans. By contrast, other vitamins are indeed required in small amounts in the diet by most mammals, including humans. Vitamin C is present in foods (particularly plants) at much higher concentrations than any other vitamin (by several orders of magnitude; from 10 to 100 mg/100g).[11]

Vitamin C (Ascorbic acid)

General
Chemical formula | C6H8O6
Molecular weight | 176.13 g/mol
Vitamin properties
Solubility | Water
RDA (adult male)  | 90 mg/day (US)
RDA (adult female)  | 75 mg/day (US)
Tolerable Upper Intake Level (UL) (adult male)  | 10000 mg/day
Tolerable Upper Intake Level (UL)t (adult female)  | 10000 mg/day
Deficiency symptoms

* Scurvy

Excess symptoms

* diarrhea
* indigestion

Common sources

* fruits
* Leafy vegetables
* Ascorbic Acid Supplements

### Role as enzyme cofactor[edit]

Vitamin C is an electron donor (reducing agent, or antioxidant), and in this role it is required by several enzymes, including eight in humans. These eight enzymes are either iron-dependent dioxygenases or copper-dependent monooxygenases, which catalyze the incorporation of oxygen into organic substrates. Many other dioxygenases and monooxygenases probably use ascorbate as a co-substrate to reduce iron or copper, oxygen, and 2-oxo-glutarate, a Krebs cycle intermediate, in the case of dioxygenases.[12][11] It is at present difficult, for this reason, to characterize this pleiotropic molecule. Three of these enzymes are involved in collagen hydroxylation, and two in carnitine synthesis.

Collagen is the most abundant protein in the human body. The key enzyme in collagen synthesis is prolyl-4-hydroxylase (P4H). It consumes a large part of the whole vitamin C pool, and, conversely, its rate of activity reflects vitamin C availability in cells. The role of vitamin C in animal physiology and disease cannot be explored independently from collagen's role. (IN PROGRESS: DEVELOP COLLAGEN ARTICLE IN PARALLEL)

More recently, a new form of the dioxygenase P4H was discovered. As opposed to the collagen P4H, the hypoxia-inducible factor-α P4H (HIFα-P4H), does not bind and transform the prolines from collagen, but prolines on sites (or residues) of proteins with a certain sequence of amino acids[13] It is required for the regulation of hypoxia-inducible factor, a protein that functions as an oxygen sensor[14] and a physiological defense against cancer formation.[15][16]

Tyrosine hydroxylase is rate limiting in the synthesis of all catecholamines (dopamine, epinephrine (aka adrenaline), norepineprine, (aka noradrenaline).[12] Norepinephrine is a neurotransmitter in the central nervous system involved in many different functions, and is released into the blood as a hormone from the adrenal medulla.

Carnitine is the molecule that allows most fat molecules to be carried in the mitochondria where they will be transformed into energy. Carnitine is also required to carry excess organic acids out of mitochondria, where they would otherwise impair energy production. The metabolic pathway that leads from the amino acid lysine to carnitine requires vitamin C twice. The steps are the enzymes gamma-butyrobetaine hydroxylase and epsilon-N-trimethyl-lysine hydroxylase. Low vitamin C causes a decreases in carnitine production, which contributes to fat deposition and overweight. At present, whether low levels of vitamin C might contribute to obesity is not known, but the normalisation of vitamin C levels in people with low vitamin C status was shown to raise their ability to burn fat 4-fold during submaximal exercise.[17]

### Antioxidant functions[edit]

(in progress)

Vitamin C is also a major water phase low-molecular weight antioxidant.

In oxidation process the molecule of vitamin C step by step oxidazed with built up some active prooxidant substances. [18].

### Action on receptors[edit]

At physiological concentrations, Vitamin C interacts with some receptors in a manner that should be distinguished from its antioxidant effects. Vitamin C binds to (and inhibits) the NMDA receptor \- an important receptor for the neurotransmitter glutamate[19][20]. It also binds to (and enhances signalling through) adrenergic receptors[21] and some histamine receptors.[22] Interestingly, considering the widespread expression of histamine and adrenergic receptors, by binding vitamin C they might be important in protecting it from oxidation.[22] In this case, the receptors and the antioxidant could be said to have a privileged relationship in which they enhance each other's specific function. For the NMDA receptor, the status of vitamin C might be relatively privileged as well. The NMDA receptor is involved in memory and learning, as well as anxiety, epilepsy, and neurodegeneration, and signalling though it is enhanced when it is reduced (not oxidized) at the so-called NMDA redox site.[23] However, somewhat paradoxically, signalling through the NMDA receptor is inhibited, notably, by the antioxidant ascorbate.[20] In comparison, lipoic acid and glutathione, in their reduced forms, enhance receptor function and may be involved in vivo in epileptogenesis, while their oxidized forms act oppositely.[23] The inhibitory binding of ascorbate, hydroquinone and the redox cofactor pyrroloquinoline quinone, are abolished if the NMDA receptor redox site is oxidized into a disulfide.[23]

### Biosynthesis[edit]

Yeasts do not synthesize vitamin C, but produce another antioxidant, erythorbic acid.[24] However, metabolic engineering of yeasts such as Saccharomyces cerevisiae can be used for the industrial production of vitamin C.[25]

Plants, humans' main source of vitamin C, produce it in large amounts as a defense against viruses, bacteria and other environmental challenges and to cope with the internal challenges associated with photosynthesis.[26]

In animals, vitamin C is synthesised through four enzyme-driven steps, which convert glucose to ascorbic acid. The last enzyme in the process, l-gulonolactone oxidase, cannot be made by humans because the gene for this enzyme is defective (Pseudogene ΨGULO). The loss of an enzyme concerned with ascorbic acid synthesis has occurred quite frequently in evolution and has affected most fish; many birds; some bats; guinea pigs; and most primates, including humans. The mutations have not been lethal because ascorbic acid is so prevalent in the environment.

In addition to those species who lost vitamin C synthesis during evolution, it is worth mentioning the Shionogi rat, which is used in laboratories (much like the guinea pig) to study the inability to produce vitamin C and its consequences.

The ODS rat

The newly developed model of hypoascorbemia, the Osteogenic Disorder Shionogi rat (ODS rat), provides a unique occasion to analyze the early adaptative changes occurring when a species loses endogenous vitamin C synthesis. Contrary to the long-held belief that the high vitamin C intake of early anthropoideans was alone sufficient to compensate for the mutation,[9] ODS rats compensate this metabolic disease through several different mechanisms, some of which are not well characterized yet.

#### Is uric acid an antioxidant for vitamin C?[edit]

It was noted in 1970 that the inability of higher primates to break down uric acid, due to a mutation in the enzyme uricase, parallels the well-known metabolic disease of higher primates.[27] Uric acid and ascorbate are both strong reducing agents (electron-donors): uric acid scavenges oxygen radicals, singlet oxygen, oxo-haem oxidants and hydroperoxyl radicals. In addition, uric acid can form complexes with iron and inhibit the  oxidation of lipids and vitamin C by the Fe3+ ion. Uric acid concentrations are so high in human plasma that they almost reach saturation; they are 5 to 10 times higher than those of vitamin C and several orders of magnitude higher than the concentrations of the potentially deleterious ion.[28]

The hypothesis by Proctor that uric acid has taken over some of the functions of ascorbic acid received experimental support thirty years later, when it was shown that ODS rats spontaneously develop high plasma uric acid (without the help of a mutation in the uricase gene), amongst many other compensatory mechanisms. In further support of this hypothesis, uric acid was shown to protect different superoxide dismutases against peroxide-mediated inactivation.[29][30] Hence, uric acid further improves the expression of SODs, that already tend to greater expression with the evolution of heavier animals.

Overall, one fundamental component of the multifaceted antioxidant protection afforded by uric acid is the formation of complexes with iron. The University of Southern California group who studied extensively the relative role of uric acid in humans, recall: "During the course of our studies we found that urate was able to inhibit a number of oxidative reactions without itself being consumed. This observation deviated from the classical mechanism for antioxidant action and was characteristically seen in radical reactions involving redox active metals, such as iron."[31] Any antioxidant molecule that can perform this function without being used up in the process is advantageous. Uric acid is strongly correlated with cardiovascular events as well as mortality in type 2 diabetes.[32] Future intervention studies will allow to tell if the rise in uric acid is pathogenic or, on the contrary, adaptative and if so, whether it behaves as an "antioxidant for ascorbate," by protecting it from iron-mediated oxidation.

Linus Pauling specified that the machinery for producing vitamin C was a burden that handicapped vitamin C-synthesizing individuals. In times of stress, the synthesis of vitamin C from glycogen can raise sharply: an adult goat, who manufactures more than 13,000 mg of vitamin C per day in normal health, will produce as much as 100,000 mg daily when faced with life-threatening disease, trauma or stress.[33]

When vitamin C-synthesizing species are exposed to high dietary levels of vitamin C, vitamin C concentrations decrease disproportionately in various organs, suggesting that endogenous synthesis of the vitamin is downregulated (it responds by decreasing) and/or that catabolism (destruction) or elimination of the vitamin are increased.[34] Whether this "overreaction", in an environment providing large amounts of vitamin C, contributed to the selection of individuals with low or absent vitamin C synthesis is an open question.

Another possible compensatory mechanism is the synthesis of lipoprotein(a). Lipoprotein(a), which is almost exclusively present in primates, might strengthen the extracellular matrix and compensate to some extent the relative lack of collagen and elastin synthesis. In addition, evidence suggests that, in some circumstances, lp(a), like vitamin C, delays lipid oxidation (peroxidation).[35]

Amongst higher primates, those who became omnivores (humans, chimpanzees, and orangutans, but not gorillas) apparently developed ways to cope with periods of vitamin C shortages. In these species, alterations in osteocalcin vitamin C-dependent hydroxylation appear to be responses to a "selective pressure to limit hydroxylation."[36]

### Transport[edit]

Vitamin C, being water soluble, does not cross lipid-rich membranes easily: it must follow specific paths through plasma membranes to enter and leave cells. It is thus important to understand the transport of vitamin C in the various cells of the body to comprehend its role in health and disease. Another molecule must also be taken into account: dehydroascorbic acid (DHAA; vitamin C which has undergone oxidation).

Active transport requires energy. Two transporters with extreme specificity for vitamin C, sodium-dependent vitamin C transporters 1 and 2 (SVCT1 and SVCT2) have been characterized. Recently, the sodium dependence of SVCT2 has been questioned. It appears that at least this transporter subtype is calcium/magnesium dependent.[37] Intracellular and extracellular concentrations of both divalent ions thus condition the transport of vitamin C through these transporters. The presence of sodium at a certain threshold makes SVCT2 more efficient: vitamin C and sodium work cooperatively to achieve a high rate of transport of both molecules. The SVCTs have limited capacities, as they tend to decrease in number the more vitamin C is accumulated in cells, and with increasing concentrations of the vitamin in circulation.[38] SVCT1 is mostly found in the liver and the kidneys (worthy of note, these are the two sites for vitamin C synthesis in the animal kingdom); SVCT2 dominates in the brain, skeletal muscles, and the spleen.

A lesser known, but important, mode of transport of vitamin C is exocytosis. In this process, vesicles filled with vitamin C are secreted from cells, allowing vitamin C to influence neighboring cells. This secretion appears to be coordinated with the secretion of biologically active polypeptides from various glands, notably the pituitary gland; the metabolism of those polypeptides requires vitamin C as a cofactor (peptidyl-glycine α-amidating mono-oxygenase, vitamin C-requiring).[39]

Facilitated diffusion is the process whereby molecules move from a compartment where there is more of the molecule to a compartment where there is less of it. Facilitated diffusion lets DHAA (but not vitamin C) enter cells, and lets vitamin C (but not DHAA) leave cells. The latter process is less understood than the former, but is essential in cells which deliver and keep vitamin C in the blood, i.e. the enterocytes (intestinal cells) and renal tubular cells (kidney cells). Once DHAA has entered a cell, it is recycled back to vitamin C.

The fact that glucose transporters also transport the glucose derivative DHAA explains a paradoxical finding made my James Lind in his Treatise of the Scurvy:

(Victims of scurvy had) ravaged bodies (but) what was very surprising, the brains of those poor creatures were always sound and entire (...)[40]

It thus appears that the glucose transporters, by transporting oxidized vitamin C, allow organs to quickly store vitamin C at times of increased oxidative stress.[41] Once dehydroascorbic acid has crossed the blood-brain barrier and is in the brain, it is recycled (reduced) back to vitamin C, and retained in this compartment.[41] Conversely, conditions associated with low insulin, insulin resistance, high glucose and/or inflammation (diabetes, type 1 and 2, trauma, sepsis) impact on DHAA uptake and intracellular vitamin C status (also see Therapeutic uses). Adipocytes, astrocytes, endothelial cells, erythrocytes, granulosa cells, hepatocytes, neutrophils, osteoblasts and smooth muscle cells accumulate DHAA for the accumulation of vitamin C.

(in progress:) The pro-inflammatory shift seen in vitamin C deficient species (see The Shionogi rat) may enhance the compensatory transport and recycling of vitamin C, as shown in a mouse model of sublethal endotoxin exposure (in which GULO, the final step in vitamin C biosynthesis, was inhibited).[42]

### Distribution[edit]

In the blood

Vitamin C concentrations in the blood are usually between 10 and 160 micromol/L,[43] and seldom exceed 80 micromol/L after most meals[44] Oral supplementation can raise levels to 220 micromol/L, while intravenous infusion can raise concentrations to 13 400 micromol/L.[45]

Leukocytes (white blood cells) use oxidants to destroy microbes.[46]; they can tolerate high levels of oxidative stress and have transport systems that allow large amounts of vitamin C to be mobilized quickly (concentrations of the vitamin can reach 50 times those found in the blood).[47] Although lymphocytes are used to evaluate the body's need for vitamin C, they are not especially representative of the needs of organs and tissues.

In urine and feces

Determining the concentrations of vitamin C in urine and feces allows for a basic evaluation of the amounts that were absorbed by the body. However, vitamin C-synthecizing species continually excrete vitamin C in their urine. The mere urinary excretion of vitamin is a normal part of its metabolism and not a sign of excess consumption, and the relationship between the intake of the vitamin and its excretion varies widely.

In organs and tissues

Some glands, organs and tissues contain 100 times more vitamin C than the blood, including the adrenal glands, pituitary gland, thymus, retina, corpus luteum, and various types of neurons.[43]

High concentrations of vitamin C are required for the adequate synthesis of catecholamines and steroids in the adrenal gland (adrenal cortex and adrenal medulla).[48] In response to stress, the adrenals secrete vitamin C locally, creating high concentrations that act at the adrenal gland in a paracrine manner.[44]

In the ovaries, the corpus luteum produces the steroid hormone progesterone, which is particularly important for maintaining pregnancy. Different enzymes involved in progesterone synthesis are enhanced by vitamin C at concentrations of 100 micromol/L (in the higher nutritional range).[49] Also see Therapeutic uses - Pregnancy. Conversely, prostaglandin PGF2 alpha, which is important for the initiation of parturition at the end of a normal pregnancy, increases the secretion of vitamin C by the corpus luteum.[50]

The brain contains on average 10 times more vitamin C than the blood, and species that are exceptionally tolerant to oxygen deprivation concentrate even higher amounts of vitamin C.[51] In animal models of diabetes, where blood glucose levels are abnormally high, a drastic inhibition of vitamin C transport to the brain (through its oxidized form) is observed.[52]

The retina, like the brain, accumulates high concentrations of vitamin C using GLUT1 glucose transporters, on the blood-retinal barrier. An experimental model of diabetes showed vitamin C concentrations in the retina to be drastically reduced by the high concentrations of glucose seen in diabetes, as a result of the competition of glucose with dehydroascorbic acid for entry in the retina (in this study, the transport of DHA was decreased by two thirds).[52]

### Food sources[edit]

The richest natural sources are fruits and vegetables, and of those, the camu camu fruit , the billygoat plum and the Indian gooseberry or amla (Emblica officinalis) contain the highest concentration of the vitamin (about 30 times more than oranges). Vitamin C is the most widely taken nutritional supplement.

Plants

There is an enormous difference in vitamin C content between cultivated fruits and fruits found in the wild, especially those that Human's ancestors consumed when they got rid of endogenous capacity. Amongst fruits commonly found on the market, citrus fruits and small fruits (such as strawberries or blueberries) are relatively good sources of vitamin C. The amount of vitamin C in foods of plant origin depends on the variety of the plant, the soil condition and the climate in which it grew, the length of time since it was picked and the storage conditions, and the method of preparation. Cooking in particular is often said to destroy vitamin C -- but see Food preparation, below.

With the gradual recognition that vitamin C prevents more than the sailor's disease, and in response to the general trends in consumer demands, the biotechnological industry has realized the commercial possibilities of new, patented, plant species with an enhanced ability to make vitamin C.[53]

Animals

Some cuts of meat are sources of vitamin C for humans. The muscle and fat that make up the modern western diet are, however, poor sources. As with fruit and vegetables, cooking degrades the vitamin C content.

Vitamin C is present in mother's milk and in less amounts in raw cow's milk (but pasteurized milk contains only trace amounts of the vitamin). [54]

Food preparation

Recent observations suggest that the impact of temperature and cooking on vitamin C may have been overestimated, since it decomposes around 190–192°C, well above the boiling point of water:

* Since it is water soluble, vitamin C will strongly leach into the cooking water, but this doesn't necessarily mean the vitamin is destroyed.
* Contrary to what is commonly assumed, it can take much longer than 2-3 min to destroy vitamin C at boiling point.
* Cooking doesn't leach vitamin C in all vegetables at the same rate; for instance, it has been suggested that the vitamin is not destroyed when boiling broccoli.[55] This may be a result of vitamin C leaching into the cooking water at a slower rate from this vegetable.

Consistent with the interaction of vitamin C with copper metals in physiology, pots made with alloys of this metal will destroy the vitamin.[56]

Fresh-cut fruit may not lose much of its nutrients when stored in the refrigerator for a few days.[57]

Supplements

Vitamin C is the most widely taken dietary supplement.[58] It is available in many forms including caplets, tablets, capsules, drink mix packets, in multi-vitamin formulations, in multiple anti-oxidant formulations, as chemically pure crystalline powder, time release versions, and also including bioflavonoids such as quercetin, hesperidin and rutin. Tablet and capsule sizes range from 25 mg to 1500 mg. Vitamin C (ascorbic acid) crystals are typically available in bottles containing 300 g to 1 kg of powder (a teaspoon of vitamin C crystals equals 5,000 mg). Other forms of Vitamin C as sodium ascorbate, magnesium ascorbate, calcium ascorbate, mixed mineral ascorbates (e.g. Na, K, Mg, Ca, Zn), and Ester-C are also available, though less popular.

Vitamin C-enriched teas and infusions are increasingly appearing in markets. If boiling temperatures did indeed destroy vitamin C at the rate that had previously been suggested, using such products would be nonsensical. As note above, boiling is not as potently detrimental to the integrity of the vitamin C as was previously assumed.

### History[edit]

For more information, see: History of vitamin C.

Scurvy is a disease resulting from a deficiency of vitamin C that leads to spots on the skin, spongy gums, and bleeding from the mucous membranes. Those afflicted are pale, feel depressed, and are partially immobilized; in serious cases there can be open wounds and loss of teeth. Scurvy was once common among sailors, when at sea for longer than fresh fruit and vegetables could then be stored.

James Lind (1716-1794) was a Scottish doctor and a pioneer of naval hygiene. In 1747, while serving as surgeon on HMS Salisbury in the Channel Fleet, he carried out experiments to find a rational treatment for scurvy; he already knew of the benefits of lime juice; John Woodall (1556-1643) in his book The Surgeon's Mate had written of "the scurvy called in Latine Scorbutum" and noted that natural remedies included "the Lemmons, Limes, Tamarinds, Oranges, and other choices of good helps from the Indies....", but Lind did not know why these were effective or whether they were any more effective than other "remedies" of the time. He speculated that limes might be effective because of their acidity, and so in his experiment he treated two of the patients with vinegar. He chose 12 men from the ship, all suffering from scurvy, and divided them into pairs, giving each pair different additions to their basic diet - cider; seawater; a mixture of garlic, mustard and horseradish; vinegar, and oranges and lemons. Those fed citrus fruits experienced a remarkable recovery. By this test Lind had, in a carefully controlled manner, established the superiority of citrus fruits above all other 'remedies'.

Vitamin C was first isolated in 1928, and in 1932 it was shown to prevent scurvy. Both Charles Glen King at the University of Pittsburgh and Albert Szent-Györgyi (working with ex-Pittsburgh researcher Joseph Svirbely) came to discover what is now known as vitamin C around April of 1932. Although Szent-Györgyi was awarded the 1937 Nobel Prize in Medicine, many feel King is as responsible for its development. [59]

## Recommended daily requirements[edit]

The Food and Nutrition Board at the Institute of Medicine advise that he best way to get the daily requirement of essential vitamins, including vitamin C, is to eat a balanced diet. A healthy diet should contain the following amounts of vitamin C:

Infants and Children

* 0 - 6 months: 40 mg/day
* 7 - 12 months: 50 mg/day
* 1 - 3 years: 15 mg/day
* 4 - 8 years: 25 mg/day
* 9 - 13 years: 45 mg/day

Adolescents

* Girls 14 - 18 years: 65 mg/day
* Boys 14 - 18 years: 75 mg/day

Adults

* Men age 19 and older: 90 mg/day
* Women age 19 and older: 75 mg/day
* Women who are pregnant or breastfeeding and those who smoke need higher amounts.

As emphasised above, the optimum daily dose of vitamin C has been debated for decades. There was an upward trend in the recommendations issued by public health advisory boards and a growing tendency to distinguish between vitamin C as the anti-scorbutic vitamin and vitamin C as a nutrient required to prevent or delay a range of diseases unrelated to scurvy. Most scientists now agree that scurvy is not a proper framework to study the role of this molecule in health, but the implications of the 10 to 20-fold decrease in ascorbate intake during evolution are still under scrutiny, 60 years after its discovery.

Also see evolutionary medicine and evolutionary biology

Different health advisory bodies offer different advice regarding the daily requirement for vitamin C, and the USA and Canada recommend about twice the amount that the World Health Organization (WHO)recommends.

The Linus Pauling Institute recommends more than four times the amount that the USA and Canada recommend, or ten times what the WHO recommends. However, after the death of Pauling, the Linus Pauling Institute came to diverge from Linus Pauling himself, who recommended doses in the same range as what other primates consume in the wild (also see Biosynthesis, above).

| Guinea pigs  | UK  | USA  | WHO  | Linus Pauling Institute  | Vitamin C Foundation  | Linus Pauling  | Other primates

|
|
|
|
|
|
|
|

Daily vitamin C intake (mg)  | 10-30[60] | 40  | 95  | 45[61] | 400  | 3000 [62] | 6000-18000  | 2000-6000[63]

### Scurvy[edit]

Scurvy is a potentially serious condition that results from inadequate consumption of fresh fruit and vegetables, usually because of ignorance about proper nutrition, psychiatric disorders, alcoholism, or social isolation. It was once a common disease of sailors on long voyages, who had to subsist for long periods on dried beef and biscuits, and was a feature of the Irish famine in the 19th century. The symptoms of scurvy first appear only after many weeks of low intake. The first symptom is fatigue, followed by a wide variety of cutaneous symptoms, including follicular hyperkeratosis, perifollicular hemorrhages, ecchymoses, xerosis, leg edema, and bent or coiled body hairs. Scurvy is associated with generally poor wound healing. Gum abnormalities include gingival swelling, purplish discoloration, and hemorrhages. The patient with scurvy commonly reports pain in the back and joints, that is sometimes accompanied by hemorrhage into the soft tissue and joints. Anemia is a common symptom, and leukopenia an occasional symptom. Scurvy is life-threatening; syncope and sudden death may occur. However, treatment with vitamin C results in rapid, often dramatic, improvement. [2]

While Hippocrates described a case of scurvy in about 400 BCE, the cause of this disease was first clearly established by a surgeon in the British Royal Navy, James Lind, in 1747. In one of the earliest "controlled experiments", Lind gave some of the crew two oranges and one lemon per day, in addition to normal rations, while others (the control group) continued with their normal rations. The results showed that citrus fruits prevented scurvy, and Lind published his work in 1753 as his Treatise on the Scurvy.

This disease is still the basis of some recommended dietary allowances throughout the world. The studies of Krebs et al. [64] and later studies in Iowa were the first attempts to quantify vitamin C requirements, and led to the conclusion that between 6.5 and 10 mg per day is needed to prevent or cure early signs of deficiency. The Iowa studies showed that, at tissue saturation, the body contains a total of about 20 mg/kg vitamin C (about 1.5 g in total), and that vitamin C is lost at a rate of about 3% per day. Symptoms of scurvy appear when the whole body content falls below about 300 mg. In 1999,the WHO and the UK recommended 30 mg as a safeguard for most of the population.[2] RDAs have been slightly raised since.

In 1974, Linus Pauling pointed out that amounts of recommended vitamin C in the range of 45 mg per day (for adults) should be renamed Minimum Dietary Allowances to reflect the fact that they were only intended to prevent a deficiency disease.[65] Although this suggestion was not accepted by health authorities, more recent recommendations reflect the notion that vitamin C not only prevents scurvy but contributes to the attainment of the "best of health".

### Based on pharmacokinetics[edit]

Some authors have argued that many studies of vitamin C are methodologically flawed, for a variety of reasons, and argue that more studies are needed to determine physiological daily requirements [66] In line with Pauling's suggestion, Levine et al. pioneered the use of pharmacokinetic studies to base recommended dietary allowances on physiological requirements.[67] This approach gave solid support to the 5 servings of fruits and vegetables a day recommandation[67][68] made by the World Health Organization.

Vitamin C intake recommendations are now set to levels necessary to attain the "best state of physical and mental health,"[69]. The international consensus is that increasing fruit and vegetable consumption is an essential part of the prevention and management of chronic diseases (cardiovascular diseases, cancer, diabetes and obesity)[70]

### Based on evolutionary biology[edit]

The notion that the genome of Man has not evolved as rapidly as his methods to produce food is commonly recognized, in particular in evolutionary biology and evolutionary medicine. The thrifty gene hypothesis is an example of an evolutionary biology theory that is based on the discrepancies between genetic evolution and historical evolution.

As early as 1949, Bourne[71] pointed out the magnitude of the decrease in vitamin C intake that occurred as the human lineage left the environment in which the vitamin C machinery had been lost. Most recent data confirm the initial statements by Bourne, Stone[72] and Pauling[73] that the environment in which vitamin C production was lost provided gram amounts of vitamin C (between 2 and 6 g).[10]

Stone called hypoascorbemia, the inability to produce vitamin C, an inborn error of metabolism, comparable to lactose intolerance, for example. The Online Mendeleian Inheritance in Man database (National Center for Biotechnology Information)[9] considers this analysis to be valid, and adds that it could be called a "public inborn error of metabolism". Although the basic postulate of Stone, which was later strongly supported by Pauling, is now accepted by OMIM, the implications of the evolutionary discordance remain to be explored.

For a discussion on the latency time between the formulation of evolutionary biology hypotheses and their testing, see Older evolutionary hypotheses, in evolutionary medicine.

## Therapeutic uses[edit]

### Critical care[edit]

"RECENT FINDINGS: In critically ill patients and after severe burns, the rapid restoration of depleted ascorbate levels with high-dose parenteral vitamin C may reduce circulatory shock, fluid requirements and oedema. ... The rapid replenishment of ascorbate is of special clinical significance in critically ill patients who experience drastic reductions in ascorbate levels, which may be a causal factor in the development of circulatory shock. Supraphysiological levels of ascorbate, which can only be achieved by the parenteral and not by the oral administration of vitamin C, may facilitate the restoration of vascular function in the critically ill patient."[74]

### Post-operative complications[edit]

A reduction of plasma ascorbic acid concentration in the post-operative period has been well documented and is associated with an increase in post-operative complications ... Doses of approximately 1150 mg ascorbic acid would be necessary to compensate for the observed loss and to raise plasma ascorbic acid to high normal values. CONCLUSIONS: There is a significantly increased post-operative metabolic clearance of ascorbic acid that might be considered when framing future dose recommendations in post-operative patients.[75]

### Anemia[edit]

The present study also demonstrated that for populations receiving an abundant supply of non-heme iron, it is possible to control anemia in a simple, safe, and inexpensive manner by adding ascorbic acid to drinking water.[76]

### Viral diseases[edit]

Vitamin C has a very interesting therapeutic index in viral infections, and has been claimed to be effective against a very broad variety of viruses, including  herpes simplex, vaccinia,  rabies,  herpes zoster (shingles),  measles , influenza,  foot-and-mouth,  hepatitis, HIV,  polio virus and so forth [77].

Vitamin C acts in conjunction with copper (and perhaps other transition metals such as iron) and oxygen to produce hydroxyl radicals, which are the most toxic free radicals.[78] As emphacized above (see Description -- Antioxidant properties of vitamin C), most of the enzymatic and non-enzymatic effects of vitamin C are due to its antioxidant properties, and in particular to its ability to reduce iron and copper. In viruses, transition metal chemistry is not regulated in the same way as in mammalian cells. Concentrations of vitamin C that will lead to viral DNA damage (through copper reduction and subsequent generation of hydroxyl radical from hydrogen peroxide) can be attained in the body through supplementation.[79]

(WP content under revision: Ascorbate usage in studies of up to several grams per day, have been associated with decreased cold duration and severity of symptoms, possibly as a result of an antihistamine effect [80].

In 2002 a meta-study into all the published research on effectiveness of ascorbic acid in the treatment of infectious disease and toxins was conducted, by Thomas Levy, Medical Director of the Colorado Integrative Medical Centre in Denver. He claimed that evidence exists for its therapeutic role in a wide range of viral infections and for the treatment of snake bites.

Colds A recent 55-study review [81] found little positive effect of a vitamin C intake on common cold at low doses, but indication of prophylaxis benefits at higher doses especially where the subjects were in stressful situations.

At least 29 controlled clinical trials (many double-blind and placebo-controlled) involving a total of over 11,000 participants have been conducted into vitamin C and the Common cold. These trials were reviewed in the 1990s[82][83] and again more recently.[84] The trials show that vitamin C reduces the duration and severity of colds but not the frequency. The data indicate that there is a normal dose-response relationship. Vitamin C is more effective the higher the dose. [85] The controlled trials and clinical experience show that vitamin C in doses ranging from 0.1 to 2 g/day have little effect. The vast majority of the trials were limited to doses below 1 g/day. As doses rise, it becomes increasingly difficult to keep the trials double blind because of the obvious gastro-intestinal side effects of heavy doses of vitamin C. So, the most effective trials at doses between 2 and 10 g/day are generally met with skepticism.

Hepatitis C virus infection A phase I clinical trial was conducted to determine whether antioxidants could be beneficial in hepatitis C virus infection (HCV infection). This infection leads to a lack of antiviral defenses and to oxidative stress in the liver. Ultimately, oxidative stress, notably lipid-mediated oxidative stress (lipid peroxidation), causes liver cells to degenerate and die. Vitamin C was part of the protocol. The trial yielded favourable changes : normalization of liver enzymes (ALT returned to normal in 44 % of those who had abnormal ALT); decrease in viral load (25 % of patients); tissue changes (36.1 % had improvements histologic parameters); and 58 % of patients saw their quality of life improve with the antioxidant treatment (increase in the SF-36[86] score).[87]

### Toxics[edit]

Lead

(in progress)

There is also evidence that vitamin C is useful in preventing lead poisoning, possibly helping to chelate the toxic heavy metal from the body. [5]

Common pesticides and contaminants

There exists great concern about the impact of pesticides and other contaminants on the reproductive capabilities on animals, including humans.[88] The toxicity of pesticides and contaminants can occur, notably, through endocrine disruption and/or oxidative stress.

The oxidative toxicity of bisphenol A to the epididymis and its effect on sperm motility and sperm count have been shown to be lessened by vitamin C.[89] The oxidative toxicities of endosulfan, phosphamidon,mancozeb and PCB (Aroclor 1254) were also neutralized by vitamin C.[90][91] It is important to note that the protective effects occurred irrespective of the chemical structure of the toxics, but rather addressed a common pathway of injury, i.e. oxidative stress, considering the very broad variety of chemical properties of toxics commonly encountered in the environment and in humans.

### Medications (reduction of adverse effects)[edit]

Reduction of gentamicin nephrotoxicity

Vitamin C has been found to be effective in reducing or protecting against nephrotoxicity caused by the aminoglycoside antibiotic gentamicin.[92]

### Cardiovascular disease and fat intake[edit]

After a high-fat meal, triglycerides raise and the flow of blood through the arteries is impaired. Two grams of vitamin C largely suppress the impairment in flow-mediated dilatation in people with coronary heart disease as well as in healhty persons.[93] In persons using a high-fat, low carbohydrate diet to lose weight, 1 g of vitamin C combined to 800 IU of vitamin E was successfully used to lower C-reactive protein, a confirmation of previous studies on the acute CRP-lowering effect of high, but physiological post-meal intakes of vitamin C.

Overall, these finding indicate that previous trials of vitamin C must be reinterpreted in function of the timing of the supplementation and in function of the amount of fat consumed.

### Cardiovascular disease as a long latency collagen disease[edit]

(Under revision: Nobel laureate chemist Linus Pauling stated that "chronic scurvy" or "subclinical scurvy" is a condition of vitamin C deficiency which is not as easily noticeable as acute scurvy (because chronic scurvy is mostly internal), characterized by micro lesions of tissues (such as that caused by blood pulsing through arteries, which stretches the arterial walls causing them to tear slightly), due to suboptimal collagen synthesis (see Collagen synthesis, above). Pauling and Rath stated that cardiovascular disease is primarily a collagen defect in the vasculature, and that plaque deposits were consequences. In support of this notion, the Proceedings of the National Academy of Sciences published in 2000 evidence that Shionogi rats (see Biosynthesis, above), a scurvy-prone species like Man, had a tendency to develop damage to the aorta, low HDL cholesterol and high total cholesterol, in a manner akin to typical human heart disease, under suboptimal vitamin C nutriture.[94]

Vitamin C is the main component of the three ingredients in Pauling and Rath's patented preventive cure for Lp(a)[95] related heart disease, the other two being the amino acid lysine and nicotinic acid (a form of Vitamin B3). Lp(a) as an atherosclerotic, evolutionary substitute for ascorbate[96] is still discussed as a hypothesis by mainstream medical science[97] and the Rath-Pauling related protocols[98] have not been rigorously tested and evaluated as conventional medical treatment by the FDA. )

### Cancer[edit]

Although abundant biochemical reasons exist why vitamin C may help prevent and treat cancer, randomized controlled trials of supplementation in humans have not found benefit.

#### Biochemistry[edit]

As noted above, at physiologically attainable concentrations, vitamin C suppresses the deleterious effects of oxidative stress. As oxidative stress is thought to increase the risk of several cancers, it has been suggested that vitamin C might help prevent such cancers (see Toxics -- Common pesticides and contaminants). There is evidence that a diet rich in fresh fruit and vegetables - prominent sources of antioxidants - can reduce the risk of some cancers, but no clear evidence that taking vitamin C supplements is protective.

In 2005 in vitro (test tube) research by the National Institutes of Health indicated that, at high concentrations, vitamin C was preferentially toxic to several strains of cancer cells, supporting Linus Pauling's claims that vitamin C can be used to fight cancer.[99]

Vitamin C does inhibit some intracellular signalling pathways that are important in the proliferation of cancer cells, including the PI3K/AKT pathway [100] Vitamin C inhibits this pathway in vitro as well as in vivo.[101] The form of vitamin C used to demonstrate these effects is ascorbyl stearate, a lipophilic, vitamin C derivative, which is termed a nutraceutical.

Hypoxia-inducible factor-1 (HIF-1) is another well known protein involved in carcinogenisis. Vitamin C inhibits its expression, leading researchers to question whether it is the antioxidant and DNA-protective effect of vitamin C that really explains its anticancer effects. [15]

#### Trials of cancer treatment in humans[edit]

In 1979 and 1985, two randomized controlled trials found no beneficial effect of vitamin C supplementation in cancer patients[102][103], as a result, interest for vitamin C in cancer declined markedly, although there have since been occasional case reports suggesting that there might be benefits in some cases [104]

#### Trials of cancer prevention in humans[edit]

Vitamin C cannot prevent cancer in men according to randomized controlled trials.[105][106][107] Although analysis of secondary outcomes in the earliest trial suggested a reduction in prostate cancer and colorectal cancer [107], this was not confirmed in prespecified analyses in the latter trials.[105][106]

### Cataracts[edit]

A decrease in lens vitamin C concentrations in the course of cataract progression was shown.[108]

The 'Jean Mayer USDA Human Nutrition Research Center on Aging' showed that, in the 'Nurses' Health Study' cohort, practically all older women who consumed vitamin C supplements for more than 10 years were protected from lense opacities,[109] thus confirming earlier epidemiological evidence on the benefits of vitamin C supplementation in the prevention of cataracts.[110]

The finding, made in 1998, that cataract is associated with lens vitamin C deficiency[108] received support in 2004. While concentrations of vitamin C in the healthy aqueous humour are between 60 and 85 mg/dL (about 20 to 30 times those in plasma), they average just 4.3 mg/dL in people with cataract.[111] This, together with the fact that the transport of vitamin C from the aqueous humour to the lens is rather slow in humans,[112] indicates that the lens is a tissue that needs high intakes of vitamin C.

### Obstetrics and gynaecology[edit]

Recent studies into the use of a combination of Vitamin E ("natural" source isomer moiety, d-alpha tocopheryl ester) and vitamin C in preventing oxidative stress leading to pre-eclampsia failed to show significant benefit at the dosage tested, [113] In another study the same dosage did decrease average gestational time resulting in a higher incidence of low birthweight babies in one study.[114] Studies into antioxidants for pre-eclampsia are continuing.[115]

## Side effects and contraindications[edit]

Contraindications A Contraindication is a condition which makes an individual more likely to be harmed by a dose of vitamin C than an average person.

* A primary concern is people with unusual or unaddressed iron overload conditions, including hemochromatosis. Vitamin C enhances iron absorption. If sufferers of iron overload conditions take gram sized doses of vitamin C, they may worsen the iron overload due to enhanced iron absorption.

* Inadequate Glucose-6-phosphate dehydrogenase enzyme (G6PD) levels, a genetic condition, may predispose some individuals to hemolytic anemia after intake of specific oxidizing substances present in some food and drugs. This includes repeated, very large intravenous or oral dosages of vitamin C. There is a test available for G6PD deficiency [6].

Side-effects

* Vitamin C causes diarrhea if taken in quantities beyond a certain limit, which varies by individual. The diarrhea will cease as soon as the dose is reduced.

* Large doses of vitamin C may cause acid indigestion, particularly when taken on an empty stomach.

Toxicity

Vitamin C exhibits remarkably low toxicity. For example, in a rat, the LD50 (the dose that will kill 50% of a population) has been reported as 11900 mg/kg,[116] or, for a 70 kg (155 pound) human, 833 grams of vitamin C would need to be ingested to stand a 50% chance of killing the person.

Harmful effects

Reports of harmful effects of vitamin C tend to receive prominent media coverage. As such, these reports tend to generate much debate and more research into vitamin C. Some of the harmful effects described below were proven invalid in later studies, while other effects are still being analyzed.

* In April 1998, the journal Nature reported carcinogenic and teratogenic effects of excessive doses of vitamin C. The effects were noted in test tube experiments. [117]

The authors later clarified their position, stating that their results "show a definite increase in 8-oxoadenine after supplementation with vitamin C. This lesion is at least ten times less mutagenic than 8-oxoguanine, and hence our study shows an overall profound protective effect of this vitamin".[118]

* In April 2000, University of Southern California researchers reported a thickening of the arteries of the neck in persons taking high vitamin C doses. (ref.[119] para 10)

* A speculated increased risk of kidney stones may be a side effect of taking vitamin C in larger than normal amounts (>1 g). The potential mechanism of action is through the metabolism of vitamin C (ascorbic acid) to dehydroascorbic acid, which is then metabolized to oxalic acid,[120] a known constituent of kidney stones.

* "Rebound scurvy" is a theoretical condition that could occur when daily intake of vitamin C is rapidly reduced from a very large amount to a relatively low amount. Advocates suggest this is an exaggeration of the rebound effect which occurs because ascorbate-dependent enzyme reactions continue for 24–48 hours after intake is lowered, and use up vitamin C which is not being replenished. The effect is to lower one's serum vitamin C blood concentration to less than normal for a short amount of time. During this period of time there is a slight risk of cold or flu infection through reduced resistance. Within a couple of days the enzyme reactions shut down and blood serum returns to the normal level of someone not taking large supplements. This is not scurvy, which takes weeks of zero vitamin C consumption to produce symptoms. It is something people who take large vitamin C supplements need to be aware of in order to gradually reduce dosage rather than quit taking vitamin C suddenly.

* Some writers[121] have identified a theoretical risk of poor copper absorption from high doses of vitamin C. However, ceruloplasmin levels seem specifically lowered by high vitamin C intake. In one study, 600 mg of vitamin C daily did not decrease copper absorption or overall body copper status in young men, but led to lower ceruloplasmin levels similar to those caused by copper deficiency.[122] In another, ceruloplasmin levels were significantly reduced.[123]

Conflicts with prescription drugs

Pharmaceuticals designed to reduce stomach acid such as the proton pump inhibitors (PPIs), are among the most widely-sold drugs in the world. One PPI, omeprazole, lowers the bioavailability of vitamin C by 12%, independent of dietary intake. This means that one would have to consume 14% more vitamin C to counteract the use of 40 mg/day of omeprazole. The probable mechanism of vitamin C reduction, intragastric pH elevated into alkalinity, would apply to all other PPI drugs, though not necessarily to doses of PPIs low enough to keep the stomach slightly acidic. [124]

## References[edit]

1. ↑ Barja, G (1996) Ascorbic acid and aging. In Harris, James W. (1996). Ascorbic acid: biochemistry and biomedical cell biology. New York: Plenum Press. ISBN 0-306-45148-4.
2. ↑ 2.0 2.1 2.2 Hirschmann JV & al. (1999). "Adult scurvy". J Am Acad Dermatol 41: 895–906; quiz 907–10. PMID 10570371.
3. ↑ Hoffer LJ (2001). "Proof versus plausibility: rules of engagement for the struggle to evaluate alternative cancer therapies". CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne 164: 351–3. PMID 11232135. [e]
4. ↑ Krogh A (1941) The Comparative Physiology of Respiratory Mechanisms. Philadelphia: University of Pennsylvania Press
5. ↑ Kleiber M (1961) The Fire of Life. New York: Wiley.
6. ↑ Maina JN (2002). "Structure, function and evolution of the gas exchangers: comparative perspectives". J Anat 201: 281–304. PMID 12430953.
7. ↑ 7.0 7.1 Nandi A et al. (1997). "Evolutionary significance of vitamin C biosynthesis in terrestrial vertebrates". Free Radic Biol Med 22: 1047–54. PMID 9034244. [e]
8. ↑ Chatterjee IB (1973). "Evolution and the biosynthesis of ascorbic acid". Science 182: 1271–2. PMID 4752221.
9. ↑ 9.0 9.1 9.2 9.3 OMIM - HYPOASCORBEMIA. Retrieved on 2007-11-13.
10. ↑ 10.0 10.1 Milton K (1999). "Nutritional characteristics of wild primate foods: do the diets of our closest living relatives have lessons for us?". Nutrition 15: 488–98. PMID 10378206. [e]
11. ↑ 11.0 11.1 Linster CL, Van Schaftingen E (2007). "Vitamin C. Biosynthesis, recycling and degradation in mammals". FEBS J. 274: 1–22. PMID 17222174.
12. ↑ 12.0 12.1 Arrigoni O, De Tullio MC (2002). "Ascorbic acid: much more than just an antioxidant". Biochim. Biophys. Acta 1569: 1–9. PMID 11853951.
13. ↑ The sequence is -Leu-X-X-Leu-Ala-Pro-. For more details, see Hieta R (2003) Prolyl 4-hydroxylase: Structural and functional characterization of the peptide-substrate-binding domain of the human enzyme, and cloning and characterization of a plant enzyme with unique properties \- 2.2.6. HIF prolyl 4-hydroxylases. Department of Medical Biochemistry and Molecular Biology, University of Oulu
14. ↑ Nytko KJ et al (2007). "Regulated function of the prolyl-4-hydroxylase domain (PHD) oxygen sensor proteins". Antioxid. Redox Signal. 9: 1329–38. PMID 17627474.
15. ↑ 15.0 15.1 Gao P et al (2007). "HIF-dependent antitumorigenic effect of antioxidants in vivo". Cancer Cell 12: 230–8. PMID 17785204.
16. ↑ Knowles HJ et al (2003). "Effect of ascorbate on the activity of hypoxia-inducible factor in cancer cells". Cancer Res. 63: 1764–8. PMID 12702559.
17. ↑ Johnston CS et al. (2006). "Marginal vitamin C status is associated with reduced fat oxidation during submaximal exercise in young adults". Nutrition & metabolism 3: 35. DOI:10.1186/1743-7075-3-35. PMID 16945143. Research Blogging.
18. ↑ ‘’The pro-oxidant chemistry of the natural antioxidants vitamin C, vitamin E, carotenoids and flavonoids’’ (Rietjens IMCM et al. )
19. ↑ Majewska MD, Bell JA (1990). "Ascorbic acid protects neurons from injury induced by glutamate and NMDA". Neuroreport 1: 194–6. PMID 1983355.
20. ↑ 20.0 20.1 Majewska MD et al. (1990). "Regulation of the NMDA receptor by redox phenomena: inhibitory role of ascorbate". Brain Res 537: 328–32. PMID 1964838.
21. ↑ Dillon PF  et al. (2004). "Antioxidant-independent ascorbate enhancement of catecholamine-induced contractions of vascular smooth muscle". Am J Physiol 286: H2353–60. PMID 14975930.
22. ↑ 22.0 22.1 {{cite journal |author=Dillon PF & al.|title=Ascorbate enhancement of H1 histamine receptor sensitivity coincides with ascorbate oxidation inhibition by histamine receptors |journal=Am J Physiol |volume=291 |pages=C977–84 |year=2006 |pmid=16760260
23. ↑ 23.0 23.1 23.2 Sanchez RM et al (2000). "Novel role for the NMDA receptor redox modulatory site in the pathophysiology of seizures". J Neurosci 20: 2409–17. PMID 10704515.
24. ↑ Huh WK et al. (1998). "D-Erythroascorbic acid is an important antioxidant molecule in Saccharomyces cerevisiae". Mol Microbiol 30: 895–903. PMID 10094636. [e]
25. ↑ Sauer M et al. (2004). "Production of L-ascorbic acid by metabolically engineered Saccharomyces cerevisiae and Zygosaccharomyces bailii". Appl Environ Microbiol 70: 6086–91. DOI:10.1128/AEM.70.10.6086-6091.2004. PMID 15466554. Research Blogging.
26. ↑ Giovannoni JJ (2007). "Completing a pathway to plant vitamin C synthesis". Proc Natl Acad Sci USA 104: 9109–10. DOI:10.1073/pnas.0703222104. PMID 17517613. Research Blogging.
27. ↑ Ascorbic Acid and Uric Acid, Similar Functions ?.
28. ↑ Davies KJ & al. (1986). "Uric acid-iron ion complexes. A new aspect of the antioxidant functions of uric acid". Biochem. J. 235: 747–54. PMID 3753442.
29. ↑ Landmesser U, Drexler H (2002). "Toward understanding of extracellular superoxide dismutase regulation in atherosclerosis: a novel role of uric acid?". Arterioscler Thromb Vasc Biol 22: 1367–8. PMID 12231552. [e]
30. ↑ Hink HU et al. (2002). "Peroxidase properties of extracellular superoxide dismutase: role of uric acid in modulating in vivo activity". Arterioscler Thromb Vasc Biol 22: 1402–8. PMID 12231557. [e]
31. ↑ Sevanian A, Davies KJ, Hochstein P (1991). "Serum urate as an antioxidant for ascorbic acid". Am. J. Clin. Nutr. 54: 1129S–1134S. PMID 1962559.
32. ↑ Ioachimescu AG, Brennan DM, Hoar BM, Kashyap SR, Hoogwerf BJ (2007). "Serum uric acid, mortality and glucose control in patients with Type 2 diabetes mellitus: a PreCIS database study". Diabet. Med. 24 (12): 1369–74. DOI:10.1111/j.1464-5491.2007.02302.x. PMID 17976199. Research Blogging.
33. ↑ Vitamins and Minerals M. Ellert, Southern Illinois University, School of Medicine. 1998 - "However, if the ability of a 70-kg goat to synthesize endogenous ascorbate is compared with the RDA of a 70-kg human, there is a 300-fold difference (13,000 mg vs. 45 mg)." To be more accurate, the difference is much greater, since those 13,000 mg are amounts directly released in the circulation, and are thus equivalent to intravenous, and not oral, doses.
34. ↑ Tsao CS et al. (1987). "Effect of dietary ascorbic acid intake on tissue vitamin C in mice". J Nutr 117: 291–7. PMID 3559744. [e]
35. ↑ Lippi G, Guidi G (2000). "Lipoprotein(a): from ancestral benefit to modern pathogen?". QJM 93: 75–84. PMID 10700477. [e]
36. ↑ Nielsen-Marsh CM & al. (2005). "Osteocalcin protein sequences of Neanderthals and modern primates". Proc. Natl. Acad. Sci. U.S.A. 102: 4409–13. PMID 15753298.
37. ↑ Godoy A et al. (2007). "Mechanistic insights and functional determinants of the transport cycle of the ascorbic acid transporter SVCT2. Activation by sodium and absolute dependence on bivalent cations". J Biol Chem 282: 615–24. DOI:10.1074/jbc.M608300200. PMID 17012227. Research Blogging.
38. ↑ Wilson JX (2005). "Regulation of vitamin C transport". Annu Rev Nutr 25: 105–25. DOI:10.1146/annurev.nutr.25.050304.092647. PMID 16011461. Research Blogging.
39. ↑ von Zastrow M et al. (1986). "Exocrine secretion granules contain peptide amidation activity". Proc Natl Acad Sci USA 83: 3297–301. PMID 3458183. [e]
40. ↑ Stewart CP, Guthrie D (1953) Lind's Treatise on Scurvy. Edinburgh University Press, Edinburgh. 227-231.
41. ↑ 41.0 41.1 Agus DB et al. (1997). "Vitamin C crosses the blood-brain barrier in the oxidized form through the glucose transporters". J Clin Invest 100: 2842–8. PMID 9389750. [e]
42. ↑ Kuo SM et al. (2005). "Endotoxin increases ascorbate recycling and concentration in mouse liver". J Nutr 135: 2411–6. PMID 16177205.
43. ↑ 43.0 43.1 Hediger MA (2002). "New view at C". Nat Med 8: 445–6. PMID 11984580.
44. ↑ 44.0 44.1 Padayatty SJ et al. (2007). "Human adrenal glands secrete vitamin C in response to adrenocorticotrophic hormone". Am J Clin Nutr 86: 145–9. PMID 17616774.
45. ↑ Levine M et al. (1996). "Vitamin C pharmacokinetics in healthy volunteers: evidence for a recommended dietary allowance". Proc Natl Acad Sci USA 93: 3704–9. PMID 8623000. [e]
46. ↑ Park MK et al. (1992). "Oxygen tensions and infections: modulation of microbial growth, activity of antimicrobial agents, and immunologic responses". Clin Infect Dis 14: 720–40. PMID 1562664. [e]
47. ↑ Washko P et al. (1989). "Ascorbic acid transport and accumulation in human neutrophils". J Biol Chem 264: 18996–9002. PMID 2681206. [e]
48. ↑ Patak Pet al. (2004). "Vitamin C is an important cofactor for both adrenal cortex and adrenal medulla". Endocr Res 30: 871–5. PMID 15666839. [e]
49. ↑ Wu X et al. (2007). "Ascorbic acid transported by sodium-dependent vitamin C transporter 2 stimulates steroidogenesis in human choriocarcinoma cells". Endocrinology. DOI:10.1210/en.2007-0262. PMID 17901237. Research Blogging.
50. ↑ Petroff BK et al. (1998). "Depletion of vitamin C from pig corpora lutea by prostaglandin F2 alpha-induced secretion of the vitamin". J Reprod Fertil 112: 243–7. PMID 9640263. [e]
51. ↑ Rice ME et al. (2002). "Brain antioxidant regulation in mammals and anoxia-tolerant reptiles: balanced for neuroprotection and neuromodulation". Comp Biochem Physiol C 133: 515–25. PMID 12458180. [e]
52. ↑ 52.0 52.1 Minamizono A et al. (2006). "Inhibition of dehydroascorbic acid transport across the rat blood-retinal and -brain barriers in experimental diabetes". Biol Pharm Bull 29: 2148–50. PMID 17015969. [e]
53. ↑ Chen Z et al. (2003). "Increasing vitamin C content of plants through enhanced ascorbate recycling". Proc Natl Acad Sci USA 100 (6): 3525–30. DOI:10.1073/pnas.0635176100. PMID 12624189. Research Blogging.
54. ↑ Comparing Milk: Human, Cow, Goat & Commercial Infant Formula Compiled and referenced by Associate Professor Stephanie Clark, Ph.D Assistant Professor, Dept. of Food Science and Human Nutrition, Washington State University. Accessed January 2007.
55. ↑ Combs GF. The Vitamins, Fundamental Aspects in Nutrition and Health. 2nd ed. San Diego, CA: Academic Press, 2001:245–272
56. ↑ Safety data University of Oxford Physical & Theoretical Chemistry Lab. Safety home page.
57. ↑ WebMD Medical News Fresh-Cut Fruit May Keep Its Vitamins, Miranda Hitti
58. ↑ The Diet Channel Vitamin C might be the most widely known and most popular vitamin purchased as a supplement.
59. ↑ University of Pittsburgh"In recognition of this medical breakthrough, some scientists believe that King deserved a Nobel Prize." Accessed February 2007
60. ↑ Guinea Lynx :: Scurvy -- Vitamin C Deficiency. Retrieved on 2007-12-22.
61. ↑ Vitamin and mineral requirements in human nutrition, 2nd edition World Health Organization and Food and Agriculture Organization, 2004 - Retrieved January 2007
62. ↑ [http://www.vitamincfoundation.org/vitcrda.htm Vitamin C Foundation's RDA -
63. ↑ Milton K (1999). "Nutritional characteristics of wild primate foods: do the diets of our closest living relatives have lessons for us?". Nutrition 15: 488–98. PMID 10378206. [e]
64. ↑ Krebs NA (1948) Vitamin C requirements of human adults: experimental studies of vitamin C deprivation in man. Lancet 254:853-6
65. ↑ Pauling L (1974). "Are recommended daily allowances for vitamin C adequate?". Proc Natl Acad Sci USA 71: 4442–6. PMID 4612519.
66. ↑ e.g. Padayatty SJ, Levine M (2006). "Vitamin C and E and the Prevention of Preeclampsia -- Letter". NEJM 355: 1065–6.
67. ↑ 67.0 67.1 Mark Levine, NIDDK, National Institutes of Health. Retrieved on 2007-11-19. “"Recommended dietary allowances (RDAs) for vitamin C (ascorbate) have been based on preventing the deficiency disease scurvy. We proposed that new RDAs for vitamin C and other vitamins could be determined using in situ kinetics, a concept developed by this laboratory."”
68. ↑ Wannamethee SG et al. (2006). "Associations of vitamin C status, fruit and vegetable intakes, and markers of inflammation and hemostasis". Am J Clin Nutr 83: 567–74; quiz 726–7. PMID 16522902. [e]
69. ↑ Article 12, International Covenant on Economic, Social and Cultural Rights, United Nations, resolution 2200A (XXI), 16 December 1966 [1]
70. ↑ WHO/FAO release independent Expert Report on diet and chronic disease. March 3rd, 2003. World Health Organization [2]
71. ↑ Bourne, GH (1949) Brit J Nutr 2:346 quoted in Pauling L (1970). "Evolution and the need for ascorbic acid". Proc Natl Acad Sci USA 67: 1643–8. PMID 5275366. [e]
72. ↑ Stone I (1967). "The genetic disease, Hypoascorbemia. A fresh approach to an ancient disease and some of its medical implications". Acta geneticae medicae et gemellologiae 16 (1): 52–62. PMID 6063937.
73. ↑ Pauling L (1970). "Evolution and the need for ascorbic acid". Proc Natl Acad Sci USA 67: 1643–8. PMID 5275366. [e]
74. ↑ McGregor GP et al. (2006). "Rationale and impact of vitamin C in clinical nutrition". Curr Opin Clin Nutr Metab Care 9: 697–703. DOI:10.1097/01.mco.0000247478.79779.8f. PMID 17053422. Research Blogging.
75. ↑ Rümelin A et al. (2005). "Metabolic clearance of the antioxidant ascorbic acid in surgical patients". J. Surg. Res. 129: 46–51. DOI:10.1016/j.jss.2005.03.017. PMID 16085104. Research Blogging.
76. ↑ de Almeida CA et al (2005). "Effect of fortification of drinking water with iron plus ascorbic acid or with ascorbic acid alone on hemoglobin values and anthropometric indicators in preschool children in day-care centers in Southeast Brazil". Food Nutr Bull 26: 259–65. PMID 16222916. [e]
77. ↑ Jariwalla RJ, Harakeh, S. "Mechanisms underlying the action of vitamin C in viral and immunodeficiency diseases"Fuchs, Jurgen; Packer, Lester; Fuchs, Jürgen (1997). Vitamin C in health and disease. New York: M. Dekker, 309-10. ISBN 0-8247-9313-7.
78. ↑ Samuni A et al. (1983). "On the cytotoxicity of vitamin C and metal ions. A site-specific Fenton mechanism". Eur J Biochem 137: 119–24. PMID 6317379. [e]
79. ↑ Harakeh and Jariwalla. (1996) "Antiviral and Immunomodulatory Activities of Ascorbic Acid" in Harris, James W. (1996). Ascorbic acid: biochemistry and biomedical cell biology. New York: Plenum Press. ISBN 0-306-45148-4.
80. ↑ [3]
81. ↑ Douglas RM, Hemilä H (2005) Vitamin C for Preventing and Treating the Common Cold. PLoS Med 2(6): e168
82. ↑ H. Hemilia, Does Vitamin C Alleviate the Symptoms of the Common Cold?, Scand J Infect Dis: 26:1 (1996)
83. ↑ H. Hemilia H (1996) Vitamin C supplementation and common cold symptoms: problems with inaccurate reviews. Nutrition, 12: 804
84. ↑ Douglas RM et al. "Vitamin C for preventing and treating the common cold," National Centre for Epidemiology and Population Health, Australian National University, 2000, URL accessed Jan 25, 2006]
85. ↑ Supplementwatch.com Vitamin C - Scientific Support Section - "At least 3 controlled studies have shown an 80% reduction in the incidence of pneumonia among vitamin C users. In one large study (over 700 students), vitamin C (1 g per hour for the first 6 hours followed by 3 g per day), reduced cold and flu symptoms by 85%."
86. ↑ International Quality of Life Assessment - The SF Instruments. Retrieved on 2007-11-19.
87. ↑ Melhem A et al. (2005). "Treatment of chronic hepatitis C virus infection via antioxidants: results of a phase I clinical trial". J Clin Gastroenterol 39: 737–42. PMID 16082287. [e]
88. ↑ Myers, John E. B.; Colborn, Theo; Dumanoski, Dianne (1996). Our stolen future: are we threatening our fertility, intelligence, and survival?: a scientific detective story. New York: Dutton. ISBN 0-525-93982-2).
89. ↑ Chitra KC, Rao KR, Mathur PP (2003). "Effect of experimental varicocele on structure and function of epididymis in adolescent rats: a histological and biochemical study". Asian J. Androl. 5 (3): 203–8. PMID 12937802. [e]
90. ↑ Khan PK, Sinha SP (1996). "Ameliorating effect of vitamin C on murine sperm toxicity induced by three pesticides (endosulfan, phosphamidon and mancozeb)". Mutagenesis 11 (1): 33–6. PMID 8671712. [e]
91. ↑ Krishnamoorthy G, Venkataraman P, Arunkumar A, Vignesh RC, Aruldhas MM, Arunakaran J (2007). "Ameliorative effect of vitamins (alpha-tocopherol and ascorbic acid) on PCB (Aroclor 1254) induced oxidative stress in rat epididymal sperm". Reprod. Toxicol. 23 (2): 239–45. DOI:10.1016/j.reprotox.2006.12.004. PMID 17267175. Research Blogging.
92. ↑ Ali BH (2003). "Agents ameliorating or augmenting experimental gentamicin nephrotoxicity: some recent research". Food Chem. Toxicol. 41 (11): 1447–52. PMID 12962996. [e]
93. ↑ Ling L, Zhao SP, Gao M, Zhou QC, Li YL, Xia B (2002). "Vitamin C preserves endothelial function in patients with coronary heart disease after a high-fat meal". Clinical cardiology 25 (5): 219–24. PMID 12018880. [e]
94. ↑ Maeda N, Hagihara H, Nakata Y, Hiller S, Wilder J, Reddick R (2000). "Aortic wall damage in mice unable to synthesize ascorbic acid". Proc. Natl. Acad. Sci. U.S.A. 97 (2): 841–6. PMID 10639167. [e]
95. ↑ Rath MW, Pauling LC. US Patent 5,278,189. Prevention and treatment of occlusive cardiovascular disease with ascorbate and substances that inhibit the binding of lipoprotein(a). USPTO. 11 Jan 1994.
96. ↑ Rath M, Linus P. Hypothesis: Lipoprotein (a) is a surrogate for ascorbate. Proc Natl Acad Sci USA. Vol 87, 6204–6207, Aug 1990.
97. ↑ Kniffin CL, McKusick VA, Brennan P. APOLIPOPROTEIN(a); LPA. OMIMTM - Online Mendelian Inheritance in Man, Johns Hopkins University. 1986–2006
98. ↑ [4]
99. ↑ Qi Chen et al. Pharmacologic ascorbic acid concentrations selectively kill cancer cells: Action as a pro-drug to deliver hydrogen peroxide to tissues. Proc Natl Acad Sci USA | 2005 | vol. 102 | 13604–13609 "These findings give plausibility to intravenous ascorbic acid in cancer treatment, and have unexpected implications for treatment of infections where H2O2 may be beneficial."
100. ↑ Zhao Y et al. (2007). "Cancer resistance in transgenic mice expressing the SAC module of Par-4". Cancer Res 67: 9276–85. DOI:10.1158/0008-5472.CAN-07-2124. PMID 17909035. Research Blogging.
101. ↑ Fang Q et al. (2006). "Ascorbyl stearate inhibits cell proliferation and tumor growth in human ovarian carcinoma cells by targeting the PI3K/AKT pathway". Anticancer Res. 26 (1A): 203–9. PMID 16475700. [e]
102. ↑ Creagan ET, Moertel CG, O'Fallon JR, et al (September 1979). "Failure of high-dose vitamin C (ascorbic acid) therapy to benefit patients with advanced cancer. A controlled trial". N. Engl. J. Med. 301 (13): 687–90. PMID 384241. [e]
103. ↑ Moertel CG, Fleming TR, Creagan ET, Rubin J, O'Connell MJ, Ames MM (January 1985). "High-dose vitamin C versus placebo in the treatment of patients with advanced cancer who have had no prior chemotherapy. A randomized double-blind comparison". N. Engl. J. Med. 312 (3): 137–41. PMID 3880867. [e]
104. ↑ Sebastian J et al. Vitamin C documented to quell advanced-stage cancer in three cases involving bladder, lung, kidney and lymphoma tumors. Can Med Assn J 174: 937–42, 2006
105. ↑ 105.0 105.1 Gaziano JM, Glynn RJ, Christen WG, et al (January 2009). "Vitamins E and C in the prevention of prostate and total cancer in men: the Physicians' Health Study II randomized controlled trial". JAMA 301 (1): 52–62. DOI:10.1001/jama.2008.862. PMID 19066368. Research Blogging.
106. ↑ 106.0 106.1 Lippman SM, Klein EA, Goodman PJ, et al (January 2009). "Effect of selenium and vitamin E on risk of prostate cancer and other cancers: the Selenium and Vitamin E Cancer Prevention Trial (SELECT)". JAMA 301 (1): 39–51. DOI:10.1001/jama.2008.864. PMID 19066370. Research Blogging.
107. ↑ 107.0 107.1 (April 1994) "The effect of vitamin E and beta carotene on the incidence of lung cancer and other cancers in male smokers. The Alpha-Tocopherol, Beta Carotene Cancer Prevention Study Group". N. Engl. J. Med. 330 (15): 1029–35. PMID 8127329. [e]
108. ↑ 108.0 108.1 Tessier F et al. (1998). "Decrease in vitamin C concentration in human lenses during cataract progression". Int J Vitam Nutr Res 68: 309–15. PMID 9789763. [e]
109. ↑ Jacques PF et al (1997). "Long-term vitamin C supplement use and prevalence of early age-related lens opacities". Am J Clin Nutr 66 (4): 911–6. PMID 9322567. [e]
110. ↑ Robertson JM et al. (1991). "A possible role for vitamins C and E in cataract prevention". Am J Clin Nutr 53 (1 Suppl): 346S–351S. PMID 1985408. [e]
111. ↑ Miratashi SAM (2004) Vitamin C concentration of aqueous humour and plasma in patients with senile cataract. Asian J Ophtalmol 6:6-9.
112. ↑ Taylor A et al (1997). "Vitamin C in human and guinea pig aqueous, lens and plasma in relation to intake". Curr Eye Res 16: 857–64. PMID 9288446. [e]
113. ↑ Rumbold A et al. (2006). "Vitamins C and E and the risks of preeclampsia and perinatal complications.". N Engl J Med 354: 1796-806. PMID 16641396.
114. ↑ Poston L et al. (2006). "Vitamin C and vitamin E in pregnant women at risk for pre-eclampsia (VIP trial): randomised placebo-controlled trial.". Lancet 367: 1145–54. PMID 16616557.
115. ↑ Rumbold A et al. Antioxidants for preventing pre-eclampsia, The Cochrane Database of Systematic Reviews, 2006 Issue 4
116. ↑ Safety (MSDS) data for ascorbic acid.
117. ↑ Oregon State University - Vitamin C and cancer
118. ↑ [Nature; Volume 395; Page 232; 17 September 1998]
119. ↑ FAQ provided by The Vitamin C Foundation.
120. ↑ Hokama S et al. (2000) Ascorbate conversion to oxalate in alkaline milieu and Proteus mirabilis culture. Mol Urol 4:321–8. Massey LK et al. (2005) Ascorbate increases human oxaluria and kidney stone risk J Nutr 135:1673–7.
121. ↑ acu-cell
122. ↑ NCBI
123. ↑ NCBI
124. ↑ E. B. Henry, and others Proton pump inhibitors reduce the bioavailability of dietary vitamin C "The gastric juice concentration of vitamin C is reduced in subjects with elevated intragastric pH. This is probably because of the fact that the vitamin is unstable at non-acidic pH and undergoes irreversible denaturation.
.... After 28 days of 40 mg/day of omeprazole the mean plasma vitamin C level had fallen by 12.3% (P = 0.04)." Alimentary Pharmacology & Therapeutics Volume 22 Page 539 - September 2005 doi:10.1111/j.1365-2036.2005.02568.x Accessed Nov 2006