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Topical Review Article

Journal of Evidence-Based
Complementary & Alternative Medicine
Vitamin C: Overview and Update 16(1) 49-57
ª The Author(s) 2011
Reprints and permission:
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DOI: 10.1177/1533210110392951
http://cam.sagepub.com
Amanda K. Schlueter, MS1 and Carol S. Johnston, PhD1

Abstract
Vitamin C functions in enzyme activation, oxidative stress reduction, and immune function. There is considerable evidence that
vitamin C protects against respiratory tract infections and reduces risk for cardiovascular disease and some cancers. Current
trials are examining the efficacy of intravenous vitamin C as cancer therapy. Many experts believe that the recommended intakes
for vitamin C (45 to 90 mg daily) are several orders of magnitude too low to support optimal vitamin C functionality. Also, there is
a misperception that vitamin C deficiency disease (scurvy) is largely historical and rarely observed in developed nations. Physical
symptoms of scurvy include swelling of the lower extremities, bleeding gums, fatigue, and hemorrhaging, as well as psychological
problems, including depression, hysteria, and social introversion. The long-term safety of vitamin C supplementation seems evi-
dent as large investigations have noted reduced risk of mortality in vitamin C supplementing populations and in those with elevated
plasma vitamin C concentrations.

Keywords
vitamin C, scurvy, metabolism, disease states, ascorbic acid, dehydroascorbic acid, cancer

Received September 24, 2010. Accepted for publication October 16, 2010.

History and that fresh fruits and vegetables were the cure. Although a
cure was known for the disease, the agent responsible was not.
Cases of ascorbic acid (vitamin C) deficiency disease (scurvy),
In 1912, Casimir Funk working at the Lister Institute in the
are well documented throughout history. Although it is prob-
United Kingdom recognized scurvy, as well as beriberi and
able that many have suffered from the disease for centuries
rickets, as diseases of dietary deficiencies. The lacking ingre-
while on land, scurvy is most commonly associated with the
dients responsible for these diseases he termed vital amines
extended sea travels in the 16th, 17th, and 18th centuries.1
or vitamins.4 In 1928, while studying the oxidation reduction
A Dutch fleet sailed to the East Indies in 1595 with 249 men,
reactions in plants and animals, the Hungarian scientist,
returning in 1597 with only 88; presumably, scurvy was a Albert Szent-Györgyi isolated a powerful reducing agent he
major cause for this loss.2 In 1620, the Mayflower lost 50 of its
termed hexuronic acid.5 In 1932, hexuronic acid was revealed
102 men aboard, many because of scurvy. At the time, treat-
to be the antiscorbutic factor, vitamin C, in independent
ments for the disease were ineffective and ranged from
reports by Szent-Györgyi and Glen King of the University of
molasses and cider to sweating and purges.1
Pittsburgh.6,7
Scurvy symptoms include bleeding gums, swollen and pain-
ful legs, bruising, skin hemorrhages, weakness, and apathy.
James Lind is widely recognized as the first to identify an
effective treatment for scurvy through the use of a clinical trial.
Biochemistry and Function
While aboard the HMS Salisbury in 1747 as a surgeon, he Vitamin C represents a redox system consisting of 2 L-isomers:
selected 12 men with similar cases of scurvy. After placing the ascorbic acid (vitamin C) in the reduced state and dehydroascor-
men into 6 pairs, he proceeded to carry out 6 different treat- bic acid (DHA) in the oxidized state (Figure 1). Most of
ments for their maladies: a quart of cider a day, 25 drops of the vitamin’s functionality in the human body is related to the
vitriol a day, 2 spoonfuls of vinegar 3 times a day, half a pint role of vitamin C as an electron donor; hence, vitamin C is the
of sea water a day, or a purgative electuary a day. The final pair active, stable form of vitamin C in tissues. When used as a cofac-
received 2 oranges and 1 lemon a day for 6 days. The final pair tor or antioxidant, vitamin C is oxidized to the more unstable
recovered whereas the other pairs did not. Lind recorded his
trial in Treatise of the Scurvy in 1753.3 1
By 1796, British ships were instructed to include lemon Arizona State University, Phoenix, AZ, USA
juice in their crew cargo in order to prevent scurvy.1 As a result, Corresponding Author:
deaths due to scurvy decreased. By the late 1800s, it was widely Carol S. Johnston, PhD, 6950 E. Williams Field Road, Mesa, AZ 85212, USA
accepted around the world that scurvy was a nutritional disease, Email: carol.johnston@asu.edu
50 Journal of Evidence-Based Complementary & Alternative Medicine 16(1)

Dopamine b-hydroxylase catalyzes the conversion of dopamine


VEO. VEOH to norepinephrine, requiring vitamin C for the process.13 In addi-
tion, peptidyl-glycine a-amidating monooxygenase catalyzes
OH . H2O
many reactions through the amidation of peptides. This enzyme
enzyme-Fe(III) enzyme-Fe(II) is responsible for the synthesis of neurotransmitters and hor-
enzyme-Cu(II) enzyme-Cu(I)
mones, including calcitonin, oxytocin, vasopressin, cholecystoki-
nin, and gastrin-releasing peptide.14
As an effective reducing agent, vitamin C also serves as a
REDUCTION ROLE powerful antioxidant, scavenging reactive oxygen and nitrogen
species in the body. Reactive species are generated by normal
cell processes as well as environmental stressors and can cause
oxidative damage to lipids, cell proteins, and nucleic acids in
DNA. Vitamin C supplementation has been shown to reduce
ASCORBIC
ASCORBYL
DEHYDROASCORBIC
levels of oxidative stress, thereby reducing potential damage
ACID
RADICAL
ACID to tissues.15
REGENERATION Although the direct antioxidant protection afforded by
vitamin C is limited to water-soluble environments, vitamin
GSSG 2GSH
C does play an antioxidant role in lipids through its regenera-
tion of fat-soluble vitamin E. Vitamin C readily donates an
+
NADP NADPH
electron to the vitamin E radical to regenerate the active form
of vitamin E, a-tocopherol. The antioxidant function of a-toco-
Figure 1. Relationships between the vitamin C redox system and pherol limits lipid peroxidation in the membranes of cells,
other compounds mitochondria, and endoplasmic reticulum, and thereby maintains
Abbreviations: VEOH, vitamin E; VEO., tocopheroxyl radical; cell integrity.8
OH. ¼ hydroxyl radical; GSH, reduced glutathione. Histamine promotes blood flow and healing in times of
physiological stress. However, excess histamine is noted
dehydroascorbic acid, which is readily ‘‘recycled’’ back to during periods of chronic stress, inflammation, or allergy, and
vitamin C by several enzyme systems, including glutathione- negatively affects immunity and respiration. Vitamin C
dependent systems or reduced nicotinamide adenine dinucleo- destroys the imidole ring of the histamine molecule, and an
tide phosphate (NADPH)-dependent systems.8 One report cal- inverse relationship has been demonstrated between plasma
culated that these enzyme systems can regenerate the amount vitamin C concentrations and blood histamine.16 This result
of vitamin C typically in blood (35 mmol/L) every 3 minutes could be of importance, as histamine can aggravate the respira-
suggesting a remarkable ability of the human system to tory tract and impair neutrophil chemotaxis, resulting in
conserve vitamin C.9 allergy-like symptoms and weakened immunity.
Vitamin C functions as an enzyme cofactor in a number of In the intestinal tract, vitamin C enhances iron bioavailabil-
hydroxylation reactions in vivo; specifically, vitamin C maintains ity by maintaining non-heme iron in the ferrous state. Vitamin
metal ions within these enzymes in a reduced state which is C also promotes duodenal ferric reductase activity further con-
required for enzyme activity. Although alternate electron donors tributing to the absorption potential of dietary iron.17 Hallberg
can function in these roles, vitamin C is the most effective cofac- et al18 showed that iron absorption increased in a dose–
tor for these enzymes as indicated by the development of disease response manner when vitamin C was ingested with a meal.
states when vitamin C status is poor.10 Three of these enzymes These investigators recommended a dose of 50 mg vitamin C
function in collagen biosynthesis: prolyl 4-hydroxylase, prolyl per meal to maximize non-heme iron absorption; natural or
3-hydroxylase, and lysyl hydroxylase enzymes. In these enzymes, synthetic sources of ascorbic acid both have the ability to per-
vitamin C maintains the iron ion in the reduced ferrous (Fe2þ) form this function. In tissues, vitamin C upregulates ferritin
state required for enzyme activity.11 messenger ribonucleic acid (messenger RNA) translation
Carnitine, tyrosine, and certain neurotransmitter and hormone thereby increasing intracellular iron storage and preventing
synthesis is aided by vitamin C as well. Trimethyllysine dioxy- iron-induced oxidative damage within cells.19,20 These data
genase and 4-g-butyrobetaine dioxygenase are both enzymes provide strong evidence that vitamin C has a potent regulatory
used in the production of carnitine. In these enzymes, vitamin C influence on iron metabolism.
again serves as a reducing agent, reducing iron to its ferrous
state.12 In tyrosine synthesis, vitamin C is thought to maintain fer-
rous iron in the homogentisate dioxygenase enzyme and cuprous Metabolism and Deficiency
copper (Cu1þ) in p-hydroxyphenylpyruvate. Both enzymes are Vitamin C is ingested in both its reduced and oxidized forms
essential in the conversion of phenylalanine to tyrosine. The pro- throughout the length of the human small intestine, albeit
duction of certain neurotransmitters and hormones require vita- through different mechanisms.21 Vitamin C is absorbed via the
min C to maintain cuprous copper for enzyme activity. sodium-dependent active transporter, SVCT1, largely in the
Schlueter and Johnston 51

ileum and jejunum; whereas, dehydroascorbic acid is excretion. Massey et al29 demonstrated that 40% of subjects
absorbed, with lesser frequency, by facilitated diffusion with supplemented with high-dose vitamin C (2000 mg/day as
higher concentration in the more proximal portions of the divided doses) exhibited a 10% or greater increase in oxalate
intestines, the duodenum, and jejunum.22 When glucose is excretion, whereas the remaining 60% of supplemented sub-
added to in vitro systems, dehydroascorbic acid, but not vita- jects showed no change in urinary oxalate. In addition, these
min C, uptake by brush border cells is inhibited, implying same 40% showed an increased risk of developing oxalate kid-
that dehydroascorbic acid, is mainly absorbed with the aid ney stones, because of increased endogenous oxalate synthesis
of glucose transporters.23 and absorption. Thus, it would be prudent for those individuals
The absorption efficiency of vitamin C is highly dependent susceptible to oxalate stones to limit vitamin C supplementa-
on the amount ingested, and can vary widely. At low doses tion to 500 mg daily.30
(20 mg), absorption can reach nearly 100%, whereas at higher Plasma vitamin C concentration <11 mmol/L (0.2 mg/dL),
doses (12 g), only 16% is absorbed.24 The bioavailability of is indicative of scurvy.31 Common physical symptoms
vitamin C can be represented by a curve with a steep incline of scurvy include swelling of the lower extremities, bleed-
between 30 mg and 100 mg daily intake. At a single 100 mg/d ing gums, malaise or fatigue, bruising, petechiae, corkscrew
dose, tissue saturation is achieved; however, higher intakes hairs, dry skin, and hemorrhaging.32,33 Although less appre-
(>500 mg/d) are required to achieve plasma saturation and to ciated, psychological symptoms accompany scurvy, includ-
maximize antioxidant protection.25 Single doses >1000 mg/d ing depression, hysteria, and social introversion.34-37 These
can cause gastrointestinal distress, nausea, and osmotic diar- personality changes occur at higher body pools of vitamin
rhea, as the body attempts to rid itself of the high intraluminal C (761 to 561 mg) than do psychomotor alterations (190
concentration of vitamin C. The tolerable upper intake level to 63 mg); furthermore, after the initiation of vitamin C
(UL) for vitamin C, 2000 mg daily, is based on likely obser- therapy in deficient individuals, depression was alleviated
vance of osmotic diarrhea and related gastrointestinal more rapidly than was the physical pain of swollen legs.34
disturbances. Hence, mental affect appears to be very sensitive to vitamin
Vitamin C circulates mainly as unbound vitamin C and is C status.
available as a reductant in blood and interstitial fluids. Vitamin Although scurvy is easily detected through detailed diet
C oxidation forms the transient ascorbyl radical, monodehydro- recalls and blood tests, symptoms of the disease are often
L-ascorbic acid, which is either quickly recycled to vitamin C nonspecific or masquerade as other diseases such as celluli-
or, when oxidative stress is high, oxidized to form dehydroas- tis,36 vasculitis, or arthritis.38 The misperception that scurvy
corbic acid. Dehydroascorbic acid is rapidly transported into is largely a historical disease and rarely observed in devel-
bystander cells (eg, erythrocytes, leukocytes, and many oped nations where fruits and vegetables are abundant fur-
insulin-sensitive tissues) on glucose transporters;26 once inside ther complicates diagnoses. This is evident in the recent
cells, dehydroascorbic acid is rapidly recycled to vitamin C, an medical literature, as many scurvy cases were first misdiag-
important source of intracellular vitamin C. Because these nosed and mistreated before the root of the problem is dis-
transporters are also responsible for glucose absorption, glu- covered and treated. In affluent societies, those at risk of
cose is a competitive inhibitor of dehydroascorbic acid trans- developing vitamin C deficiency typically have diets lack-
port. In fact, hyperglycemia, which can be caused by ing in fresh fruits and vegetables (often associated with poor
diabetes, sepsis, or stress, results in decreased uptake of dehy- diet choices or imposed restrictive diet plans). Also, cigar-
droascorbic acid, and therefore, lower concentrations of intra- ette smokers exhibit decreased plasma vitamin C concentra-
cellular vitamin C.27 dehydroascorbic acid has a short half- tions despite adequate dietary intakes39 as do individuals
life (<2 minutes) and if not taken up by cells, it is metabolized with chronic hyperglycemia due to diabetes, sepsis, or
to excretory products, mainly oxalic acid. stress.27 Additionally, adult males consistently exhibit lower
Vitamin C is directly transported into tissues via the sodium- plasma vitamin C concentrations across the life cycle than
dependent transporter, SVCT2.28 SVCT2 can in part account do their female counterparts.
for gender differences in vitamin C status with lower plasma
vitamin C concentrations consistently demonstrated for males
versus females. In female mice, SVCT2 in the spleen had
Vitamin C and Disease States
decreased uptake of vitamin C in comparison with male mice,
decreasing the amount of vitamin C that was cleared from Vitamin C supplementation has a protective influence on sev-
plasma.28 In addition, female mice showed a decrease in urin- eral disease states, most notably the common cold, cardiovas-
ary vitamin C excretion, resulting in higher plasma vitamin C cular disease, and some cancers (Figure 2). Many other
concentrations in female mice in comparison to male mice. disease states have been studied in relationship to vitamin C,
Vitamin C excretory products include vitamin C, dehydroas- including age-related macular degeneration, cataract, diabetes,
corbic acid, and oxalic acid. At high intakes (>500 mg), 50% of and rheumatoid arthritis; however, the link between vitamin C
the absorbed dosage is excreted unmetabolized as vitamin C and these conditions has not been clearly established.40 More
after several hours. With typical intakes, approximately 1.5% research is warranted to determine if vitamin C can play a pro-
of ingested vitamin C is converted to oxalate for urinary tective or therapeutic role in these conditions.
52 Journal of Evidence-Based Complementary & Alternative Medicine 16(1)

The Common Cold 50% for individuals in the top quartile for plasma vitamin C
levels as compared with that observed for those in the lowest
Vitamin C is thought to reduce the duration and severity of
quartile.54 A later analysis from EPIC-Norfolk study indicated
common cold symptoms by enhancing immune responses and
that risk for incident stroke was reduced 42% for individuals in
by functioning as an antihistamine. In vitro, vitamin C destroys
the top quartile for plasma vitamin C as compared with that
histamine by breaking the imizadole ring structure of the mole-
observed for those in the lowest quartile.55 National survey data
cule,41 and, in vivo, plasma histamine concentrations are
collected in the United States from 1976 to 1980 (the NHANES
reduced 40% in healthy adults after 2 weeks of vitamin C sup-
data set) showed similar results: For every 0.5 mg/dL rise in
plementation (2 g/d).42 Since histamine is a mediator for the
serum vitamin C, there was an 11% decrease in the prevalence
common symptoms of colds and allergy, this antihistamine
of cardiovascular disease and stroke incidence.56 However,
property of vitamin C could function to reduce cold severity.
analysis of a later NHANES data set (1989-1994) by these same
Reduced leukocyte motility, for example, chemotaxis, is also
investigators showed an inverse relationship between serum
associated with severity of cold symptoms,43 and several stud-
vitamin C concentrations and risk for cardiovascular disease
ies demonstrated that vitamin C supplementation enhances leu-
only for participants who consumed alcohol.57 The authors
kocyte chemotaxis.44,45 Furthermore, acute vitamin C
speculated that the lack of an inverse relationship between vita-
supplementation (1 g) is associated with a rapid, but transient,
min C status and cardiovascular disease risk in the general pop-
rise in vitamin C concentrations in respiratory tract lining
ulation could be explained by survivor bias; that is, those who
fluids, which could provide immediate antioxidant protection
survived a cardiovascular event could have made dietary
to lung tissues and temporarily attenuate oxidative stress in
changes resulting in an increased plasma vitamin C status, or
airways.46
those with low serum vitamin C could have perished by a stroke
In elderly patients hospitalized with acute respiratory infec-
or heart attack.
tions, patients randomized to receive 200 mg of vitamin C daily
A pooled analysis of 9 cohorts (293 172 total participants;
recovered more rapidly than patients receiving placebo, and the
4647 major incident coronary heart disease events) revealed
vitamin C supplemented patients experienced lower death rates
that dietary vitamin C was not related to incident coronary
compared with the placebo group (4% vs 17%).47 In a Japanese
heart disease when supplement users were excluded from the
population (439 patients with atrophic gastritis), chronic vita-
analyses.58 However, in this pooled analysis, supplemental
min C supplementation (500 mg/d) reduced the number of
vitamin C (400 mg/d) was associated with a 25% reduction
common colds by 20% over a 3-year period compared with pla-
in incident coronary heart disease in comparison with that noted
cebo ingestion.48 In a randomized clinical trial conducted in the
for nonusers of vitamin C supplements (P < .001). Adjustments
United Kingdom (168 healthy adults), vitamin C supplementation
for ‘‘healthy’’ lifestyle and potential dietary confounders did not
(1 g/d for 60 days) was associated with shorter cold dura-
weaken this association. Hence, the heart-protective effects of
tions (1.8 vs 3.1 days) and fewer reported colds (0.4 vs 0.6
vitamin C appear to be most pronounced with supplemental
colds/person).49 Recent meta-analyses show modest beneficial
intakes >400 mg/d.
effects of vitamin C supplementation for reducing common
Clinical trial results are mixed regarding a role for supple-
cold duration (8% to 14%) and severity (as indicated by days
mental vitamin C in reducing cardiovascular disease risk.
confined to home and off work or school).50,51
A large-scale randomized trial in more than 14 000 men did not
The most pronounced benefit of vitamin C supplementation
show a beneficial effect of supplemental vitamin C (500 mg/d
for reducing cold incidence and severity has been demonstrated
for 8 years) for any cardiovascular end point, including myo-
in populations experiencing extreme physical stress. Vitamin C
cardial infarction, total stroke, or cardiovascular mortality.59
supplementation (600 mg/d) markedly reduced the incidence of
Yet in smaller randomized clinical trials, vitamin C supplemen-
upper respiratory tract infections in ultramarathon runners for
tation (500 to 1000 mg/d for up to 8 weeks) was associated
the 14-day period following a competitive 42-km race when
with reduced systolic and diastolic blood pressure, reduced
compared with placebo treatment (33% vs 68%, respec-
systemic arterial stiffness, and reduced elevated C-reactive pro-
tively).52 In military recruits, vitamin C supplementation
tein.60-62 Moreover, both oral and intravenous injection of vita-
(range 300 to 3000 mg/d) was associated with significant
min C enhanced flow-mediated endothelium-dependent
reductions in cold severity in 4 of 5 controlled trials; but a sig-
dilation 40% to 180%.63,64 These latter investigations provide
nificant reduction in cold episodes associated with vitamin C
theoretical mechanisms for the reported beneficial effects of
supplementation was noted in only 1 of these trials.53
supplemental vitamin C for reducing cardiovascular disease risk.

Cardiovascular Disease Cancer


Data from a prospective population study encompassing more High intakes of vitamin C have been associated with decreased
than 25 000 men and women (40 to 79 years old) living in the risk of certain cancers, particularly cancers of the pharynx, oral
United Kingdom (the European Prospective Investigation into cavity, esophagus, lung, and stomach.65 Although the antican-
Cancer [EPIC]-Norfolk study) indicated that risk of dying from cer actions of vitamin C are not well defined, it is thought that
cardiovascular disease or ischemic heart disease was reduced the antioxidant properties of vitamin C protect against
Schlueter and Johnston 53

Vitamin C and Health

Cardiovascular
Health
Common Cold Hypotensive acon GI tract Cancers
Anhistamine acon Endothelial compliance Gastric juice anoxidant
Chemotaxis promoon CRP reducon Luminal anoxidant
Respiratory tract anoxidant
Reduced reacve oxygen species

Figure 2. Protective influence of vitamin C supplementation on disease states

molecular damage that is associated with carcinogenesis and/or Plasma vitamin C is tightly controlled and concentrations do
that vitamin C may modulate signal transduction and gene not generally exceed about 100 mM even with oral dosages
expression.66 as high as 2500 mg because of saturation of the mucosal
In the stomach, vitamin C is present in high concentrations vitamin C transporter, SVCT1, and increased renal losses.24
in gastric juice (10-fold higher concentrations than in plasma) However, pharmacologic concentrations (0.3 to 20 mmol/L)
and protects the gastric mucosa from reactive oxygen are achieved in blood with intravenous infusions of vitamin
species and N-nitroso compounds. Patients with gastritis and C, and there is much research in vitro suggesting that, at phar-
Helicobacter pylori infections have decreased amounts of macologic concentrations, vitamin C is highly effective at
vitamin C in gastric juice, a factor that could contribute to risk selectively destroying a wide variety of cancer cells.77-79
for gastric cancer.67 Vitamin C supplementation in these Recently, several small uncontrolled trials have examined the
patients increased vitamin C concentrations in gastric juice and efficacy of intravenous vitamin C as cancer therapy with mixed
decreased cancer biomarkers.65 Using a case–control study results.80-82 However, the observation that patient well-being
design nested within a large, 10-country prospective investiga- and quality of life assessments were improved with vitamin C
tion, gastric cancer risk was reduced 45% for individuals in the infusions is encouraging.83
highest versus the lowest quartile of plasma vitamin C levels.68 Intravenous vitamin C is widely used by complementary and
Risk for gastric cancer was particularly strong in subjects alternative medicine practitioners for a variety of conditions
consuming high amounts of red and processed meats, which including infection and fatigue.84 Apart from the known
elevate endogenous levels of N-nitroso compounds. These data adverse effects of vitamin C (the potential for renal stone
suggest that this specific population (those with high intakes of formation and for hemolysis in glucose-6-phosphate
red and processed meats) would particularly benefit from dehydrogenase deficiency), intravenous administration of
vitamin C supplementation. vitamin C by these practitioners, which averaged 28 g every
Meta-analyses indicate that individuals with high intakes of 4 days for 22 treatments, was evidently safe and well tolerated.
vitamin C are at reduced risk for esophageal cancer,69 lung can- Well-designed trials are needed to assess the role vitamin C
cer,70 and breast cancer.71 However, these analyses examined infusions have in cancer treatment.
only relationships between diet and cancer risk and cannot
distinguish if the relationship is specific to dietary vitamin C
or related to other components in vitamin C–rich fruits and Maintaining Adequate Vitamin C Status
vegetables. Vitamin C is found in a variety of fruits, juices, and vegetables
Randomized clinical trials have not demonstrated a benefit (Table 1). Natural and synthetic sources of vitamin C appear to
for supplemental vitamin C in cancer prevention72-74 leading be equally bioavailable and provide similar antioxidant protec-
many to conclude that high oral dosages of vitamin C should tion after ingestion.85,86 However, the stability of vitamin C in
not be promoted as an anticancer therapy. Importantly, some foods is precarious and readily influenced by oxygen, heat, pH,
evidence suggests that vitamin C can reduce the effectiveness and metallic ions, resulting in the oxidation of vitamin C.87
of anticancer therapies by preserving tumor cell integrity dur- Vitamin C is well preserved in frozen foods; hence, orange
ing chemotherapy.75 Yet a recent meta-analysis was unable juice reconstituted from frozen concentrate is a better
to demonstrate a reduction in chemotherapy efficacy associated source of vitamin C as compared with ready-to-drink orange
with the use of vitamin C supplements; in fact, the analysis juice (86 mg/serving vs 39-46 mg/serving).88 Cooking reduces
suggested a possible benefit of antioxidant supplementation the vitamin C content of vegetables by 40% to 60%,89 and pro-
during chemotherapy on survival times and tumor responses.76 longed warming of foods (150 F for 4 hours) reduces vitamin
Although controversial, interest in intravenous vitamin C C content >75%.90 Vitamin C losses during vegetable storage
injection to treat cancer patients has resurfaced in recent years. are as high as 70%; hence, if vegetables are not purchased
54 Journal of Evidence-Based Complementary & Alternative Medicine 16(1)

Table 1. Dietary Sources of Vitamin C Academy of Sciences is quite high, 2000 mg/d. Osmotic diar-
rhea was the main concern cited by the National Academy of
Food, Standard Amount Vitamin C Content (mg)
Sciences; however, risk for kidney stones does increase in
Guava, raw, 1=2 cup 188 individuals supplementing vitamin C, and renal experts sug-
Red sweet pepper, raw, 1=2 cup 142 gest that 500 mg vitamin C per day is the maximum dose that
Red sweet pepper, cooked, 1=2 cup 116 can be considered safe.30 Many forms of vitamin C are mar-
Kiwi fruit, 1 medium 70 keted to consumers across a broad price range; yet research
Orange, raw, 1 medium 70
suggests that the forms commonly available (vitamin C with
Orange juice, 3=4 cup 61-93
Grapefruit juice, 3=4 cup 50-70 rose hips, Ester-C, and generic vitamin C) have similar
Vegetable juice cocktail, 3=4 cup 50 bioavailability.97
Strawberries, raw, 1=2 cup 49 Individuals who supplement vitamin C regularly maintain
Brussels sprouts, cooked, 1=2 cup 48 higher plasma concentrations of the vitamin,98 and the long-
Cantaloupe, 1=4 medium 47 term safety of vitamin C supplementation seems evident as sev-
Papaya, raw, 1=4 medium 47 eral large investigations have noted reduced risk of mortality in
Kohlrabi, cooked, 1=2 cup 45
vitamin C supplementing populations99,100 and in populations
Broccoli, raw, 1=2 cup 39
Edible pod peas, cooked, 1=2 cup 38 with elevated plasma vitamin C concentrations.54,101
Broccoli, cooked, 1=2 cup 37
Sweet potato, canned, 1=2 cup 34 Author Contributions
Tomato juice, 3=4 cup 33 Both the authors have contributed in this article.
Cauliflower, cooked, 1=2 cup 28
Pineapple, raw, 1=2 cup 28
Declaration of Conflicting Interests
Kale, cooked, 1=2 cup 27
Mango,1=2 cup 23 The authors declared no conflicts of interest with respect to the authorship
and/or publication of this article.

frozen, storage time should be minimized, and items should


Funding
be served fresh or steamed with minimal exposure to heat
The authors received no financial support for the research and/or
and air.91 Orange juice that was refrigerated after reconstitu-
authorship of this article.
tion from frozen concentrate had significantly less bioavail-
able vitamin C at day 8 compared with baseline, and the
antioxidant protection to plasma was lost at day 8 compared References
with baseline.92 The lability of vitamin C in foods is an impor- 1. Baron JH. Sailors’ scurvy before and after James Lind—a
tant consideration since many populations world-wide consume reassessment. Nutr Rev. 2009;67:315-332.
produce that is transported, stored, and processed prior to 2. Tickner FJ, Medvei VC. Scurvy and the health of European crews
purchase. in the Indian Ocean in the 17th century. Med Hist. 1958;2:36-46.
Recommended intakes for vitamin C range from 45 mg/d 3. James Lind: bicentenary of the publication of the first edition of
(World Health Organization) to 90 mg/d (National Academy his treatise on scurvy. J R Nav Med Serv. 1953;39:198-203.
of Sciences).93 Since vitamin C is not prevalent in all fruits and 4. Funk C. The etiology of the deficiency diseases. Beriberi, poly-
vegetables, foods should be carefully selected to ensure the neuritis in birds, epidemic dropsy, scurvy, experimental scurvy
inclusion of several vitamin C–rich foods daily, and care in animals, infantile scurvy, ship beriberi, pellagra. J State Med.
should be taken regarding the storage and handling of these 1912;20:341-368.
food items. Although 45 to 90 mg vitamin C daily will protect 5. Szent-Györgyi A. Observations on the function of peroxidase
against vitamin C deficiency, higher intakes are needed to satu- systems and the chemistry of the adrenal cortex: description of
rate tissues (100 mg/d) or plasma (e500 mg/d).24 Many experts a new carbohydrate derivative. Biochem J. 1928;22:1387-q409.
believe that the current recommended intakes for vitamin C are 6. King CG, Waugh WA. The chemical nature of vitamin C.
several orders of magnitude too low to support optimal vitamin Science. 1932;75:357-358.
C functionality in vivo.94-96 7. Svirbely JL, Szent-Györgyi A. Hexuronic acid as the antiscorbutic
Given the important roles vitamin C plays in enzyme factor. Nature. 1932;129:576.
activation, oxidative stress reduction, immune function, and 8. Mandl A, Szarka A, Banhegyi G. Vitamin C: update on physiology
carcinogen abatement, daily supplementation of the vitamin and pharmacology. Br J Pharmacol. 2009;157:1097-1110.
can be considered prudent for maintaining optimal vitamin 9. Mendiratta S, Qu ZC, May JM. Erythrocyte ascorbate recycling:
C concentrations in plasma and tissues since food sources can antioxidant effects in blood. Free Radic Biol Med. 1998;24:
be unreliable. Vitamin C bioavailability is nearly 100% for 789-797.
vitamin C dosages up to 200 mg and drops to 75% and to 10. Levine M. New concepts in the biology and biochemistry of
49% for dosages of 500 mg and 1250 mg, respectively.24 ascorbic acid. N Eng J Med. 1986;314:892-902.
There are few toxicity concerns with vitamin C supplementa- 11. Englard S, Seifter S. The biochemical functions of ascorbic acid.
tion, and the tolerable upper limit set by the National Annu Rev Nutr. 1986;6:365-406.
Schlueter and Johnston 55

12. Rebouche C. Ascorbic acid and carnitine biosynthesis. Am J Clin 31. Gropper SS, Smith JL, Groff JL. Vitamin C (ascorbic acid). In:
Nutr. 1991;54:1147-1152. Howe E, Feldman E, eds. Advanced Nutrition and Human Meta-
13. Wimalasena K, Wimalasena DS. The reduction of membrane- bolism. Belmont, CA: Thomson Wadsworth; 2005:259-275.
bound dopamine beta-monooxygenase in resealed chromaffin 32. Hodges RE, Baker EM, Hood J, Sauberlich HE, March SC.
granule ghosts. Is intragranular ascorbic acid a mediator for Experimental scurvy in man. Am J Clin Nutr. 1969;22:535-548.
extragranular reducing equivalents? J Biol Chem. 1995;270: 33. Crandon JH, Lund CG, Dill DB. Experimental human scurvy.
27516-27524. N Engl J Med. 1940;223:353.
14. Oldham CD, Girard PR, Nerem RM, May SW. Peptide amidating 34. Walker A. Chronic scurvy. Br J Dermatol. 1968;80:625-630.
enzymes are present in cultured endothelial cells. Biochem Bio- 35. Kinsman RA, Hood J. Some behavioral effects of ascorbic acid
phys Res Commun. 1992;184:323-329. deficiency. Am J Clin Nutr. 1971;24:455-464.
15. Halliwell B, Whiteman M. Antioxidant and prooxidant properties 36. Patrazou E, Opal S. Scurvy masquerading as infectious cellulitis.
of vitamin C. In: Packer L, Fuchs J, eds. Vitamin C in Health and Intern Med J. 2008;38:452-453.
Disease. New York, NY: Marcel Dekker; 1997:25-94. 37. De Santis J. Scurvy and psychiatric symptoms. Perspect
16. Johnston CD, Solomon RE, Corte C. Vitamin C depletion is Psychiatr Care. 1993;29:18-22.
associated with alterations in blood histamine and plasma free 38. Kumar V, Choudhury B. Scurvy—a forgotten disease with an
carnitine in adults. J Am Coll Nutr. 1996;15:586-591. unusual presentation. Trop Doct. 2009;39:190-192.
17. Atanasova BD, Li AC, Bjarnason I, Tzatchev KN, Simpson RJ. 39. Wei W, Kim Y, Boudreau N. Association of smoking with serum
Duodenal ascorbate and ferric reductase in human iron and dietary levels of antioxidants in adults: NHANES III, 1988-
deficiency. Am J Clin Nutr. 2005;81:130-133. 1994. Am J Public Health. 2001;91:258-264.
18. Hallberg L, Brune M, Rossander L. Effect of ascorbic acid on iron 40. Diplock AT, Charleux JL, Crozier-Willi G, et al. Functional food
absorption from different types of meals. Studies with ascorbic science and defence against reactive oxidative species. Br J Nutr.
acid-rich foods and synthetic ascorbic acid given in different amounts 1998;80(suppl 1):S77-S112.
with different meals. Human Nutr: Appl Nutr. 1986;40A:97-113. 41. Uchida K, Mitsui M, Kawakishi S. Monooxygenation of N-acetyl-
19. Hoffman KE, Yanelli K, Bridges KR. Ascorbic acid and iron histamine mediated by l-ascorbate. Biochim Biophys Acta. 1989;
metabolism: alterations in lysosomal function. Am J Clin Nutr. 991:377-379.
1991;54:1188-1192. 42. Johnston CS, Retrum KR, Srilakshmi JC. Antihistamine effects
20. Toth I, Bridges KR. Ascorbic acid enhances ferritin mRNA trans- and complications of supplemental vitamin C. J Am Diet Assoc.
lation by an IRP/aconitase switch. J Biol Chem. 1995;270: 1992;92:988-989.
19540-19544. 43. Onerci M, Hasçelik G, Sener B, Sennaroğlu L. The effect of
21. Goldenberg H, Schweinzer E. Transport of vitamin C in animal tonsillectomy on neutrophil chemotaxis in adults with chronic
and human cells. J Bioenerg Biomembr. 1994;26:359-367. tonsillitis. Eur Arch Otorhinolaryngol. 1995;252:488-490.
22. Malo C, Wilson JX. Glucose modulates vitamin C transport in 44. Stadler N, Eggermann J, Vöö S, Kranz A, Waltenberger J.
adult human small intestinal brush border membrane vesicles. Smoking-induced monocyte dysfunction is reversed by vitamin
J Nutr. 2000;130:63-69. C supplementation in vivo. Arterioscler Thromb Vasc Biol.
23. Fujita I, Akagi Y, Hirano J, et al. Distinct mechanisms of transport 2007;27:120-126.
of ascorbic acid and dehydroascorbic acid in intestinal epithelial 45. Johnston CS, Huang S. Effect of ascorbic acid nutriture on blood
cells (IEC-6). Res Commun Mol Pathol Pharmacol. 2000;107: histamine and neutraphil chemotaxis in guinea pigs. J Nutr. 1991;
219-231. 121:126-130.
24. Levine M, Conry-Cantilena C, Wang Y, et al. Vitamin C 46. Behndig AF, Blomberg A, Helleday R, Kelly FJ, Mudway IS.
pharmacokinetics in healthy volunteers: evidence for a recom- Augmentation of respiratory tract lining fluid ascorbate concen-
mended dietary allowance. Proc Natl Acad Sci U S A. 1996; trations through supplementation with vitamin C. Inhal Toxicol.
93:3704-3709. 2009;21:250-258.
25. Johnston CS, Cox SK. Plasma-saturating intakes of vitamin C 47. Hunt C, Chakravorty NK, Annan G, Habibzadeh N, Schorah CJ.
confer maximal antioxidant protection to plasma. J Am Coll Nutr. The clinical effects of vitamin C supplementation in elderly hos-
2001;20:623-627. pitalized patients with acute respiratory infections. Int J Vitam
26. Paddayatty SJ, Levine M. New insights into the physiology and Nutr Res. 1994;64:212-219.
pharmacology of vitamin C. CMAJ. 2001;164:353-355. 48. Sasazuki S, Sasaki S, Tsubono Y, Okubo S, Hayashi M,
27. Wilson JX. Regulation of vitamin C transport. Annu Rev Nutr. Tsugane S. Effect of vitamin C on common cold: randomized
2005;25:105-125. controlled trial. Eur J Clin Nutr. 2006;60:9-17.
28. Kuo SM, MacLean ME, McCormick K, Wilson JX. Gender and 49. Van Straten M, Josling P. Preventing the common cold with a
sodium-ascorbate isoforms determine ascorbate concentrations vitamin C supplement: a double-blind, placebo-controlled survey.
in mice. J Nutr. 2004;134:2216-2221. Adv Ther. 2002;19:151-159.
29. Massey LK, Liebman M, Kynast-Gales SA. Ascorbate increases 50. Douglas RM, Hemilä H, Chalker E, Treacy B. Vitamin C
human oxaluria and kidney stone risk. J Nutr. 2005;135: for preventing and treating the common cold. Cochrane
1673-1677. Database Syst Rev. 2007;(3):CD000980. doi:10.1002/
30. Massey L. Safety of vitamin C. Am J Clin Nutr. 2005;82:488. 14651858.CD000980.pub3.
56 Journal of Evidence-Based Complementary & Alternative Medicine 16(1)

51. Douglas RM, Hemilä H, D’Souza R, Chalker EB, Treacy B. Vita- Investigation into Cancer and Nutrition (EPIC-EURGAST). Car-
min C for preventing and treating the common cold. Cochrane cinogenesis. 2006;27:2250-2257.
Database Syst Rev. 2004;(4):CD000980.. 69. Kubo A, Corley DA. Meta-analysis of antioxidant intake and the
52. Peters EM, Goetzsche JM, Grobbelaar B, Noakes TD. Vitamin C risk of esophageal and gastric cardia adenocarcinoma. Am J Gas-
supplementation reduces the incidence of postrace symptoms of troenterol. 2007;102:2323-2330.
upper-respiratory-tract infection in ultramarathon runners. Am 70. Cho E, Hunter DJ, Spiegelman D, et al. Intakes of vitamins A, C
J Clin Nutr. 1993;57:170-174. and E and folate and multivitamins and lung cancer: a pooled
53. Hemilä H. Vitamin C supplementation and respiratory infections: analysis of 8 prospective studies. Int J Cancer. 2006;118:970-978.
a systematic review. Mil Med. 2004;169:920-925. 71. Howe GR, Hirohata T, Hislop TG, et al. Dietary factors and risk
54. Khaw KT, Bingham S, Welch A, et al. Relation between plasma of breast cancer: combined analysis of 12 case-control studies.
ascorbic acid and mortality in men and women in EPIC-Norfolk J Natl Cancer Inst. 1990;82:561-569.
prospective study: a prospective population study. European Pro- 72. Bjelakovic G, Nikolova D, Simonetti RG, Gluud C. Antioxidant
spective Investigation into Cancer and Nutrition. Lancet. 2001; supplements for preventing gastrointestinal cancers. Cochrane
357:657-663. Database Syst Rev. 2004;(4):CD004183.
55. Myint PK, Sinha S, Luben RN, Bingham SA, Wareham NJ, 73. Jiang L, Yang KH, Tian JH, et al. Efficacy of antioxidant vitamins
Khaw KT. Risk factors for first-ever stroke in the EPIC-Norfolk and selenium supplement in prostate cancer prevention: a meta-
prospective population-based study. Eur J Cardiovasc Prev analysis of randomized controlled trials. Nutr Cancer. 2010;62:
Rehabil. 2008;15:663-669. 719-727.
56. Simon JA, Hudes ES, Browner WS. Serum ascorbic acid and car- 74. Lin J, Cook NR, Albert C, et al. Vitamins C and E and beta car-
diovascular disease prevalence in U.S. adults. Epidemiology. otene supplementation and cancer risk: a randomized controlled
1998;9:316-321. trial. J Natl Cancer Inst. 2009;101:14-23.
57. Simon JA, Hudes ES. Serum ascorbic acid and cardiovascular dis- 75. Perrone G, Hideshima T, Ikeda H, et al. Ascorbic acid inhibits
ease prevalence in U.S. adults: the Third National Health and antitumor activity of bortezomib in vivo. Leukemia. 2009;23:
Nutrition Examination Survey (NHANES III). Ann Epidemiol. 1679-1686.
1999;9:358-365. 76. Block KI, Koch AC, Mead MN, Tothy PK, Newman RA,
58. Knekt P, Ritz J, Pereira MA, et al. Antioxidant vitamins and Gyllenhaal C. Impact of antioxidant supplementation on che-
coronary heart disease risk: a pooled analysis of 9 cohorts. Am motherapeutic efficacy: a systematic review of the evidence from
J Clin Nutr. 2004;80:1508-1520. randomized controlled trials. Cancer Treat Rev. 2007;33:
59. Sesso HD, Buring JE, Christen WG, et al. Vitamins E and C in the 407-418.
prevention of cardiovascular disease in men: the Physicians’ Health 77. Verrax J, Delvaux M, Beghein N, Taper H, Gallez B, Buc
Study II randomized controlled trial. JAMA. 2008;300:2123-2133. Calderon P Enhancement of quinone redox cycling by ascorbate
60. Mullan BA, Young IS, Fee H, McCance DR. Ascorbic acid induces a caspase-3 independent cell death in human leukaemia
reduces blood pressure and arterial stiffness in type 2 diabetes. cells. An in vitro comparative study. Free Radic Res. 2005;39:
Hypertension. 2002;40:804-809. 649-657.
61. Block G, Jensen CD, Dalvi TB, et al. Vitamin C treatment 78. Du J, Martin SM, Levine M, et al. Mechanisms of ascorbate-
reduces elevated C-reactive protein. Free Radic Biol Med. induced cytotoxicity in pancreatic cancer. Clin Cancer Res.
2009;46:70-77. 2010;16:509-520.
62. Hajjar IM, George V, Sasse EA, Kochar MS. A randomized, 79. Chen Q, Espey MG, Sun AY, et al. Pharmacologic doses of ascor-
double-blind, controlled trial of vitamin C in the management bate act as a prooxidant and decrease growth of aggressive tumor
of hypertension and lipids. Am J Ther. 2002;9:289-293. xenografts in mice. Proc Natl Acad Sci U S A. 2008;105:
63. Williams MJ, Sutherland WH, McCormick MP, de Jong SA, 11105-11109.
McDonald JR, Walker RJ. Vitamin C improves endothelial dys- 80. Bael TE, Peterson BL, Gollob JA. Phase II trial of arsenic trioxide
function in renal allograft recipients. Nephrol Dial Transplant. and ascorbic acid with temozolomide in patients with metastatic
2001;16:1251-1255. melanoma with or without central nervous system metastases.
64. Grebe M, Eisele HJ, Weissmann N, et al. Antioxidant vitamin C Melanoma Res. 2008;18:147-151.
improves endothelial function in obstructive sleep apnea. Am 81. Padayatty SJ, Riordan HD, Hewitt SM, Katz A, Hoffer LJ,
J Respir Crit Care Med. 2006;173:897-901. Levine M. Intravenously administered vitamin C as cancer
65. Jacob RA, Sotoudeh G. Vitamin C function and status in chronic therapy: three cases. CMAJ. 2006;174:937-942.
disease. Nutr Clin Care. 2002;5:66-74. 82. Hoffer LJ, Levine M, Assouline S, et al. Phase I clinical trial of
66. Li Y, Schellhorn HE. New developments and novel therapeutic i.v. ascorbic acid in advanced malignancy. Ann Oncol. 2008;19:
perspectives for vitamin C. J Nutr. 2007;137:2171-2184. 1969-1974.
67. Zhang ZW, Abdullahi M, Farthing MJ. Effect of physiological 83. Yeom CH, Jung GC, Song KJ. Changes of terminal cancer
concentrations of vitamin C on gastric cancer cells and Helicobacter patients’ health-related quality of life after high dose vitamin C
pylori. Gut. 2002;50:165-169. administration. J Korean Med Sci. 2007;22:7-11.
68. Jenab M, Riboli E, Ferrari P, et al. Plasma and dietary vitamin C 84. Padayatty SJ, Sun AY, Chen Q, Espey MG, Drisko J, Levine M.
levels and risk of gastric cancer in the European Prospective Vitamin C: intravenous use by complementary and alternative
Schlueter and Johnston 57

medicine practitioners and adverse effects. PLoS One. 2010;5(7): Academies Press; 2000. http://www.nap.edu/ openbook/
e11414. 0309069351/html/index.html. Accessed September 23, 2010.
85. Mangels AR, Block G, Frey CM, et al. The bioavailability to 94. Ausman LM. Criteria and recommendations for vitamin C
humans of ascorbic acid from oranges, orange juice and cooked intake. Nutr Rev. 1999;57:222-224.
broccoli is similar to that of synthetic ascorbic acid. J Nutr. 95. Krajcovicova-Kudlackova M, Babinska K, Valachovicova M,
1993;123:1054-1061. Paukova V, Dusinska M, Blazicek P. Vitamin C protective
86. Johnston CS, Dancho CL, Strong GM. Orange juice ingestion and plasma value. Bratisl Lek Listy. 2007;108:265-268.
supplemental vitamin C are equally effective at reducing plasma 96. Levine M, Rumsey SC, Daruwala R, Park JB, Wang Y. Criteria
lipid peroxidation in healthy adult women. J Am Coll Nutr. 2003; and recommendations for vitamin C intake. JAMA. 1999;281:
22:519-523. 1415-1423.
87. Lopez A, Krehl WA, Good E. Influence of time and temperature 97. Johnston CS, Luo B. Comparison of the absorption and excretion
on ascorbic acid stability. J Am Diet Assoc. 1967;50:308-310. of three commercially available sources of vitamin C. J Am Diet
88. Johnston CS, Bowling DL. Stability of ascorbic acid in commer- Assoc. 1994;94:779-781.
cially available orange juices. J Am Diet Assoc. 2002;102:525-529. 98. Schleicher RL, Carroll MD, Ford ES, Lacher DA. Serum
89. Nursal B, Yücecan S. Vitamin C losses in some frozen vegetables vitamin C and the prevalence of vitamin C deficiency in the
due to various cooking methods. Nahrung. 2000;44:451-453. United States: 2003-2004 National Health and Nutrition
90. Hallberg L, Rossander L, Persson H, Svahn E. Deleterious effects Examination Survey (NHANES). Am J Clin Nutr. 2009;90:
of prolonged warming of meals on ascorbic acid content and iron 1252-1263.
absorption. Am J Clin Nutr. 1982;36:846-850. 99. Pocobelli G, Peters U, Kristal AR, White E. Use of supplements
91. Moraes FA, Cota AM, Campos FM, Pinheiro-Sant’Ana HM. of multivitamins, vitamin C, and vitamin E in relation to mortal-
Vitamin C loss in vegetables during storage, preparation and dis- ity. Am J Epidemiol. 2009;170:472-483.
tribution in restaurants [in Portuguese]. Cien Saude Colet. 2010; 100. Watkins ML, Erickson JD, Thun MJ, Mulinare J, Heath CW.
15:51-62. Multivitamin use and mortality in a large prospective study.
92. Johnston CS, Hale JC. Oxidation of ascorbic acid in stored Am J Epidemiol. 2000;152:149-162.
orange juice is associated with reduced plasma vitamin C con- 101. Fletcher AE, Breeze E, Shetty PS. Antioxidant vitamins and
centrations and elevated lipid peroxides. J Am Diet Assoc. mortality in older persons: findings from the nutrition add-on
2005;105:106-109. study to the Medical Research Council Trial of Assessment and
93. Institute of Medicine. Dietary Reference Intakes for Vitamin C, Management of Older People in the Community. Am J Clin Nutr.
Vitamin E, Selenium, and Carotenoids. Washington, DC: National 2003;78:999-1010.

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