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The role of vitamin C in the treatment of pain: new insights


The vitamin C deficiency disease scurvy is characterised by musculoskeletal pain and recent epidemiological evidence has indicated an association between suboptimal vitamin C status and spinal pain. Furthermore, accumulating evidence indicates that vitamin C administration can exhibit analgesic properties in some clinical conditions. The prevalence of hypovitaminosis C and vitamin C deficiency is high in various patient groups, such as surgical/trauma, infectious diseases and cancer patients. A number of recent clinical studies have shown that vitamin C administration to patients with chronic regional pain syndrome decreases their symptoms. Acute herpetic and post-herpetic neuralgia is also diminished with high dose vitamin C administration. Furthermore, cancer-related pain is decreased with high dose vitamin C, contributing to enhanced patient quality of life. A number of mechanisms have been proposed for vitamin C’s analgesic properties. Herein we propose a novel analgesic mechanism for vitamin C; as a cofactor for the biosynthesis of amidated opioid peptides. It is well established that vitamin C participates in the amidation of peptides, through acting as a cofactor for peptidyl-glycine α-amidating monooxygenase, the only enzyme known to amidate the carboxy terminal residue of neuropeptides and peptide hormones. Support for our proposed mechanism comes from studies which show a decreased requirement for opioid analgesics in surgical and cancer patients administered high dose vitamin C. Overall, vitamin C appears to be a safe and effective adjunctive therapy for acute and chronic pain relief in specific patient groups.


Pain is defined as ‘an unpleasant sensory and emotional experience associated with actual or potential tissue damage, or described in terms of such damage’ [1]. The taxonomy of pain has developed through the work of the International Association for the Study of Pain and encompasses broad classifications that relate to the aetiology of pain, such as nociceptive (pain in response to injury) and neuropathic (nerve pain or pain in response to nerve damage), as well as particular pain features, such as allodynia (increased sensitization of neurons) and hyperalgesia (increased sensitivity to pain). Time course influences, such as chronic and acute, are also taken into consideration. The principal organ of pain is the brain. Noxious stimuli, once transduced, are conducted as nociceptive signals to the central nervous system via the spinal cord and ascend to the higher centres. It is here that the experience of pain is perceived and experienced in a complex and dynamic interaction between cerebral areas both sophisticated and primal. Pain is a transdiagnostic symptom and while somatic pathology plays a role in activating pain pathways, psychosocial, cultural and environmental factors influence the experience of pain over time [2].

In the absence of empirical evidence to validate the presence of pain measurement relies largely on eliciting the experience of the patient through self-report. It is understood that pain is an individual and subjective experience and may or may not be associated with evident tissue damage or disease. Furthermore, there are many influencing factors, such as mental state (both organic and psychological), coping strategies, social/cultural context, experience, and co-symptoms. The patient self-report can be validated using multiple outcome measurement tools designed to capture the complexity of the pain experience, for example, the visual analogue and numerical pain rating scales [3], the McGill pain questionnaire [4], and the Brief Pain Inventory [5].

Recent epidemiological evidence has indicated an association between spinal pain and suboptimal vitamin C status [6]. Musculoskeletal pain is also a symptom of the vitamin C deficiency disease scurvy [7]. Furthermore, accumulating evidence indicates that vitamin C administration can exhibit analgesic properties in some clinical conditions. In this review we focus on human studies investigating the role of vitamin C in orthopedic, virus-associated, cancer-related, and post-surgical pain. Preclinical models of pain are not always directly comparable to clinical scenarios of pain [8]. Nevertheless, we discuss some preclinical studies, although these have been carried out in animals that can synthesise their own vitamin C and, as such, are not ideal models for the human vitamin C-requiring situation. Vitamin C has a number of important functions in the body, primarily through acting as a cofactor for a family of biosynthetic and regulatory metallo-enzymes. These functions include synthesis of neurotransmitters and peptide hormones, and regulation of transcription factors and gene expression [9, 10]. We cover the potential analgesic mechanisms of vitamin C and propose a novel analgesic mechanism involving the biosynthesis of amidated opioid peptides. We also discuss study limitations, highlighting the need for an improved understanding of the pharmacokinetics of oral and intravenous vitamin C in future studies.

Vitamin C deficiency and pain

Pain is a symptom of the vitamin C deficiency disease scurvy, presenting primarily within the musculoskeletal system as arthralgia in the knees, ankles and wrists, as well as myalgia [7, 11]. Children in particular suffer from severe lower limb pain, as evidenced by numerous case reports in the literature [1216]. There have also been reports of adults and the elderly experiencing musculoskeletal pain due to severe vitamin C deficiency [17, 18]. Scurvy-related pain appears to be primarily due to bleeding into the musculoskeletal tissues, which can become so debilitating that patients are unable to walk [7]. Bleeding into the muscles and other soft tissues results in swelling and tenderness in the affected area, whilst bleeding into the hip, knee and ankle joints results in hemarthroses, and bleeding into the periosteum results in severe bone pain. Pain due to vitamin C deficiency can be completely resolved within a week or two following supplementation with intakes of vitamin C that will eventually result in plasma saturation (i.e. ≥200 mg/day, see examples cited in [12]).

It is interesting to note that Duggan et al. reported that a child’s painful scurvy symptoms began after an upper respiratory infection and that “possibly the increased metabolic needs associated with this infection unmasked a subclinical vitamin C deficiency [14].” Khalid also reported three cases of children suffering from respiratory infections or gastrointestinal dysfunction who concurrently developed painful swellings of their joints [16]. The author stated that “scurvy occurred as a result of their increased requirement of vitamin C due to stress of illness combined with poor dietary intake. It is therefore recommended that during illness one should be careful about the intake of vitamin C, keeping in mind that acute illness rapidly depletes stores of ascorbic acid. Those already malnourished are more prone to this development [14].” Similarly, others have reported painful scurvy symptoms following confirmed or suspected respiratory infection [18, 19], stating that “sepsis of either digestive or pulmonary origin, leading to sustained metabolic demand, might have acted as a precipitating factor [18].” As such, it is possible that other hospital-associated pain may be partly due to vitamin C deficiency, which is relatively prevalent in hospital settings [2023].

Vitamin C deficiency and enhanced requirements in patients

Vitamin C deficiency (defined as plasma vitamin C concentrations <11 µmol/L) is relatively rare in the general population of developed countries, with a prevalence of 6% reported in the United States [24]. However, vitamin C deficiency and scurvy has been reported to occur in elderly hospitalized patients [25, 26], critically ill patients [18, 27, 28], and cancer patients [29]. Hospitalized patients, in general, are more likely to present with hypovitaminosis C (defined as plasma vitamin C concentrations <23 µmol/L), and a higher proportion of hospital patients exhibit deficiency compared with the general population [20, 21]. Trauma and surgery are known to significantly deplete vitamin C concentrations [22], and patients with severe infections and sepsis also have significant depletion of vitamin C [23]. Cancer patients typically have lower vitamin C status than healthy controls [30, 31], with a large proportion of them presenting with hypovitaminosis C and outright deficiency [32].

It is interesting to note that animals, which can synthesise their own vitamin C, will increase their synthesis of the vitamin if they become stressed, are under a disease burden, or are administered drugs, including analgesics [3335]. Therefore, it seems likely that hospitalised patients, who are under enhanced physiological stress, often presenting with a disease burden, and being administered multiple drugs, will have enhanced requirements for vitamin C. In support of this premise, vitamin C intakes of 100–200 mg/day provide adequate to saturating plasma status in healthy individuals [36], however, much higher gram doses are required to normalize plasma vitamin C status in surgical and critically ill patients [22, 23]. Administration of vitamin C to cancer patients results in lower plasma concentrations compared with healthy controls [37], suggesting a depleted body pool. Furthermore, administration of some anti-cancer therapies has been shown to significantly decrease patient vitamin C concentrations and scurvy-like symptoms have been reported [3840]. Other drugs, such as aspirin, may also interfere with vitamin C uptake and could potentially result in hypovitaminosis C in individuals with low vitamin C intake [41]. Overall, these studies indicate an increased utilisation of and requirement for vitamin C in different patient cohorts.

Vitamin C and orthopedic pain

Persistent musculoskeletal pain and associated complex regional pain syndrome (CRPS) present particular features underpinned by complex dynamic neural plasticity [3]. Features such as allodynia and hyperalgesia allude to sensitization of the nociceptive neurons, both peripheral and central, which invokes a cascade of effects experienced as pain that is both difficult to predict and manage. Vitamin C deficiency has been associated with spinal pain, primarily neck, lower back and arthritis/rheumatism [6]. The vitamin has been shown to exert a number of regulatory effects on cells of the skeletal system, including osteogenic, chondrogenic and osteoblastogenic [42]. Mechanisms of vitamin C action in bone cells primarily involve up- or downregulation of the expression of specific genes through regulation of transcription factors and epigenetic marks.

A number of randomized controlled trials have investigated the effect of vitamin C supplementation on the incidence of CRPS in wrist and ankle surgery patients (Table 1) [4347]. Doses of vitamin C used in these studies ranged from 0.2 to 1.5 g/day for 45–50 days post-surgery. All studies, but one [43], showed a decreased incidence of CRPS in the patients receiving vitamin C, with vitamin C doses ≥0.5 g/day being the most efficacious [44]. Previous research has indicated that surgical patients have high vitamin C requirements and supplementation with >0.5 g/day vitamin C is required to restore normal vitamin C status in these patients [22]. The results of these studies have been pooled in various combinations in a number of recent meta-analyses [4852] and all, but one [50], concluded that the evidence indicates that daily administration of vitamin C can decrease the incidence of CRPS following distal fracture surgery.

Table 1 The effect of vitamin C on complex regional pain syndrome (CRPS) and other orthopedic pain

Patients undergoing joint replacement surgery for osteoarthritis were administered 0.5 g/day prophylactic vitamin C for 50 days post-surgery (Table 1) [53, 54]. Although osteoarthritis of the carpometacarpo joint can be complicated by CRPS, no cases of CRPS were observed under vitamin C prophylaxis. A randomized placebo-controlled crossover trial carried out with 133 patients with osteoarthritis of the hip or knee joint showed reduced pain following consumption of 1 g/day calcium ascorbate for 2 weeks as determined by the visual analogue scale (P < 0.008) [55]. The observed decrease in pain was less than half that reported for non-steroidal anti-inflammatories. We have shown a complete decrease in pain in a patient with rheumatoid arthritis following administration of twice weekly infusions of high-dose vitamin C [56]. This data suggests that vitamin C may be more effective for the pain associated with rheumatoid arthritis than osteoarthritis, or that intravenous administration of the vitamin may be more effective than oral administration in patients with arthritis. It is noteworthy that the average vitamin C status of patients with rheumatoid arthritis is less than half that of healthy controls (i.e. 27 ± 13 versus 70 ± 21 µmol/L, respectively) [57].

Paget’s disease of bone is a chronic disorder caused by the excessive breakdown and formation of bone and disorganized bone remodeling which results in bone weakening, misshapen bones, fractures, arthritis, and pain. An early study in 16 patients with Paget’s disease of bone showed that oral doses of 3 g/day vitamin C for 2 weeks decreased pain in 50% of the patients and resulted in a complete elimination of pain in 20% of the patients [58]. Excretion of hydroxyproline was elevated following administration of vitamin C, and was highest in those patients who experienced complete relief of pain. This suggests that vitamin C is acting as a cofactor for the hydroxylase enzymes responsible for collagen synthesis [10]. When 3 g/day vitamin C was administered to Piaget’s patients in combination with normal calcitonin treatment, there was no additional attenuation of pain above calcitonin alone, although normalization of hydroxyproline excretion was observed, in contrast to calcitonin treatment, which decreases hydroxyproline excretion [59].

Vitamin C and virus-associated pain

Infection with viral pathogens is commonly associated with myalgia, arthralgia or neuralgia [60]. Herpes zoster infection (shingles) results in a painful skin rash which generally lasts 2–4 weeks. However, some people develop ongoing nerve pain, a condition known as postherpetic neuralgia, which may last for months or years and is due to nerve damage or alterations caused by the virus in discrete dermatomes. Pain can be mild to extreme in the affected dermatome, and can include sensations of burning pain, itching, hyperesthesia (oversensitivity), or paresthesia (tingling, pricking, or numbness, ‘pins and needles’) [61, 62]. Analysis of the nutrient status of 50 patients with postherpetic neuralgia indicated significantly lower circulating concentrations of vitamin C compared with 50 healthy controls (i.e. 30 ± 21 versus 76 ± 31 µmol/L, respectively) [63]. More than 50% of the patients had hypovitaminosis C (i.e. <23 µmol/L) and vitamin C concentrations ≤45 µmol/L were found to independently increase the risk of post-herpetic neuralgia (adjusted OR 21; 95% CI 6, 76; P < 0.001).

A number of case studies have indicated that both acute and postherpetic neuralgia can be dramatically decreased following intravenous vitamin C infusions (2.5–15 g daily or every other day for 5–14 days) [6467]. In an uncontrolled follow-up study, Schencking et al. recruited 64 patients with Herpes Zoster who were subsequently administered 7.5 g intravenous vitamin C two to four times a week for a total of 2 weeks [68]. Baseline pain was reported to be 58% (as determined by VAS), which decreased to 22% within 2 weeks and this had decreased to 6% at 12 week follow-up. Overall, there was a decrease in pain for 92% of the patients. The lack of a control group is a major limitation of this study.

Two placebo-controlled trials have investigated the effect of intravenous vitamin C on acute and post-herpetic neuralgia (Table 2) [69, 70]. Chen et al. carried out a trial in 41 patients with postherpetic neuralgia randomized to receive intravenously 50 mg vitamin C/kg body weight three times over 5 days, or placebo infusion [69]. Patients receiving vitamin C reported a larger decrease in numeric rating scale for pain, and a greater global impression of change. Another recent RCT in 87 herpes zoster patients, randomized to receive 5 g intravenous vitamin C or placebo three times over 5 days, found no effect on acute pain within the first 4 weeks of hospitalization, but did show a decreased incidence of postherpetic neuralgia and significantly decreased pain at 8 and 16 weeks follow up [70].

Table 2 The effect of vitamin C on acute and chronic viral-associated pain

Chikunguya virus infection is characterized by severe joint pain, which typically lasts weeks or months, and sometimes years [71]. Parvovirus B19 infection (also known as fifth disease) may also present with acute or persistent arthropathy, painful swelling of the joints that feels similar to arthritis [72]. Two cases of severe arthralgia associated with Chikungunya and parovirus B19 reportedly responded to high dose oral (10 g/day) and intravenous vitamin C treatments (Table 2) [73, 74]. Despite one case having 100 g/day vitamin C infusions, no adverse side effects were reported [73]. An uncontrolled prospective study carried out in 56 patients with Chikungunya virus indicated that a single infusion of 25–50 g intravenous vitamin C (administered with a 3% hydrogen peroxide solution) provided a 60% decrease in pain and completely eliminated pain in 9% of the patients [75].

Vitamin C and cancer-related pain

Pain is one of the most common symptoms reported by cancer patients, and can seriously affect their quality of life [76]. Pain associated with cancer can be related to the primary tumour, cancer treatment, associated procedures and as a consequences of disease progression and metastasis. Furthermore, cancer pain may include several types of pain and pain features occurring concurrently as mixed pain, such as nociceptive, neuropathic, and bone pain [3]. Cancer-associated pain resulting from metastasis to bone is a severe and complex condition comprising neuropathic, nociceptive and inflammatory pain [77, 78]. As mentioned above, cancer patients typically have depleted vitamin C status [3032] as well as higher requirements than healthy controls [37], which could potentially be exacerbated by anti-cancer therapies [3840].

High dose oral and intravenous vitamin C has been administered to cancer patients for many decades as a complementary and alternative therapy [79]. Although the efficacy of vitamin C as a cancer treatment is questionable, recent research has indicated a positive impact of high dose vitamin C on cancer- and chemotherapy-related quality of life, including pain [80]. Early studies of high dose vitamin C in patients with advanced cancer indicated that many patients experienced some improvement in subjective symptoms, including decreased pain and the need for analgesics [81, 82]. Cameron and Campbell [81] reported a number of cases of dramatic to complete amelioration of bone pain in patients with severe cancer-related pain given both high dose oral and intravenous vitamin C (Table 3). Retrospective studies of patients with bone metastases receiving 2.5 g intravenous vitamin C once weekly or during intensifying pain reported a range of responses, including 0–100% decreases in pain [83, 84]. These, and the earlier case studies [81], indicate that vitamin C can potentially provide dramatic improvements in pain relief in cancer patients with bone metastases.

Table 3 The effect of vitamin C on cancer-related pain

Over the last decade a number of studies have attempted to quantify the effect of high dose vitamin C on cancer-related symptoms such as pain (Table 3). These studies have typically used the European Organisation for the Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ) [85]. The EORTC QLQ assesses the typical cancer-related symptoms of pain, fatigue, nausea/vomiting, dyspnea, appetite loss, sleep disturbance, constipation, and diarrhea using a 4 point Likert scale. A difference of 10–20% represents a medium change in quality of life [86]. Most quality of life studies have reported decreases of >30% pain as assessed by the EORTC pain scale in patients with cancer receiving intravenous vitamin C (Table 3). A retrospective study of patients with breast cancer receiving 7.5 g intravenous vitamin C once a week showed decreases in a number of cancer-associated symptoms using a 3 point Likert scale, including a 30% decrease in pain during adjuvant therapy in the vitamin C group compared with the control group [87].

Two prospective studies of patients with advanced cancer who were administered intravenous vitamin C at doses of 10–100 g vitamin C (twice a week) have shown 30–44% decreases in pain using the EORTC pain scale within 1–4 weeks [88, 89]. Yeom et al. [88] recruited 39 patients with terminal cancer who subsequently received 10 g intravenous vitamin C twice weekly for 1 week, followed by 4 g/day oral vitamin C for 1 week. Patients exhibited 30% pain at baseline (as measured by the EORTC-QLQ) and this decreased by one-third following vitamin C infusion (P = 0.013). Takahashi et al. [89] recruited 60 patients with advanced cancer who received 25–100 g intravenous vitamin C twice weekly for 4 weeks. Baseline pain in this cohort was 18% and this decreased by 44% following vitamin C infusion (P < 0.05, using the EORTC-QLQ). A Phase I RCT designed to assess the safety, tolerability and pharmacokinetics of high dose intravenous vitamin C in patients with advanced cancer also assessed quality of life as a secondary outcome [90]. This showed a decrease in pain for the few patients who completed the EORTC-QLQ at 3 and 4 weeks follow-up (Table 3).

Vitamin C and opioid analgesic requirements

The use of opioid analgesia is widely considered an essential component in the management of moderate to severe pain, however, opioid use is associated with a well-documented side effect profile. Opioid effects, both therapeutic and adverse, are dose dependent and subject to significant inter-individual variability with bearing on symptoms including nausea and vomiting, constipation, and sedation and respiratory depression [91]. Co-analgesic agents and interventions that are opioid sparing may improve the analgesic effect and reduce adverse effects.

Cancer-related pain is typically managed with opioids [92]. In the early 1970s Cameron and Pauling [93] described dramatic decreases in opiate dependence in five patients with advanced cancer following high dose vitamin C administration. These patients were in considerable pain due to skeletal metastases and were receiving large regular doses of opiate analgesics (morphine or diamorphine). Within five to seven days of commencing vitamin C, four of the five patients became completely free from pain, and the fifth required only mild analgesics [81]. Several of these cases are summarized in Table 4. Interestingly, none of the patients experienced any withdrawal symptoms despite having received opiate analgesia for periods of weeks or months, nor did they request that their opiate regime be continued. It is interesting to note that vitamin C (at a dose of 300 mg/kg body weight/day for 4 weeks) has been shown to dramatically decrease the major withdrawal symptoms of heroin addicts compared with a control group who were treated with conventional medication only [94]. A complete decrease in morphine requirement was also observed in a patient with terminal cancer undergoing 30 g/day vitamin C infusion for palliative care [95]. Murata et al. [82] reported a dose-dependent decrease in opioid requirement in patients with terminal cancer who received vitamin C. In those who received 0.5–3 g/day vitamin C, 50% of the patients required opioid drugs, whereas only 17% of those who received 5–30 g/day vitamin C required opioids, compared with 79% in the control group (Table 4). A recent study failed to confirm a decrease in opioid requirement in 17 patients with a range of malignancies [96], however, the study lasted for only 3 days and the vitamin C dose was lower than in studies that reported positive findings (Table 4).

Table 4 The effect of vitamin C on opioid analgesic requirements

Three recent placebo-controlled trials have been carried out to investigate the effect of vitamin C on opioid requirement for postoperative pain, two using intravenous vitamin C [97, 98] and one using oral vitamin C [99]. In the most recent, 97 patients undergoing laparoscopic colectomy for colon cancer were randomized to receive intravenously 50 mg vitamin C per kg body weight or placebo infused immediately after induction of anaesthesia (Table 4). A decrease in postoperative morphine consumption was observed at 2 h (P < 0.05) in the vitamin C group, as well as a decreased frequency of rescue analgesia (P < 0.01), and decreased pain at 2, 6 and 24 h post-surgery as assessed by the numeric pain rating scale (P < 0.05). In the other study, 40 patients undergoing uvulopalatopharyngoplasty with tonsillectomy, which is normally associated with intense postoperative pain, were randomized to receive intravenously either 3 g vitamin C or placebo 30 min into the surgery (Table 4). A decrease in post-operative pethidine dose was recorded for the vitamin C group compared with the placebo group (5 vs 46 mg, P = 0.0001), as well as a delay in the time of first dose of pethidine use (12 vs 3 h, P = 0.003), and a decline in the total number of times pethidine requested was requested (0.2 vs 1.3 times, P = 0.001). Visual analogue scale scores were also lower in the vitamin C group at all time points assessed (recovery, 6, 12, 24 h, P = 0.001). Opioid-based analgesics are typically used for postoperative analgesia, however these may complicate care by causing excessive sedation and respiratory depression. In contrast, no side effects were observed with the vitamin C treatment.

In an earlier study, a single oral dose of 2 g vitamin C or placebo was given to 80 randomised cholecystectomy patients 1 h prior to anesthesia (Table 4). Postoperative morphine consumption and verbal numerical rating scale scores for incisional pain were recorded for 24 h. Morphine consumption was lower in the vitamin C group versus the placebo group (16 vs 23 mg, P = 0.02) and, despite the lower opioid usage in the vitamin C group, there was no difference in reported pain intensity or side effects between the two groups [99]. Although baseline plasma vitamin C concentrations were not determined, blood samples were collected approximately 1 h post-randomisation for vitamin C analysis. The placebo group had marginal vitamin C status (23 ± 17 µmol/L) and the vitamin C group had 57 ± 28 µmol/L, although this is possibly an underestimate as oral vitamin C uptake typically takes more than 1 h to peak [100].

Support for the opioid-sparing effects of vitamin C has come from murine studies. Co-administration of 1 g/kg vitamin C with morphine prevented the development of morphine tolerance and physical dependence in mice [101]. Intraperitoneal administration of 400 mg/kg vitamin C significantly decreased self-administration of morphine and withdrawal syndrome signs in rats [102]. Vitamin C itself was shown to have antinociceptive effects in mice (ED50 of 206 mg/kg). Furthermore, it exhibited not only additive effects, but also synergistic effects, in combination with the opioids morphine and tramadol [103]. Thus, vitamin C administration appears to have potential application as an adjunctive therapy to decrease opioid requirements and dependence.

Vitamin C and pain study design limitations

A major limitation of many of the vitamin C and pain studies is inappropriate study design due to a general lack of understanding around the pharmacokinetics of vitamin C. Oral vitamin C is transported through the intestinal epithelium via sodium-dependent vitamin C transporters (SVCT-1) [104]. Levine and coworkers have shown that oral vitamin C uptake becomes less efficient as the dose increases due to saturation of the transporters. Although an oral dose of 200 mg vitamin C is completely absorbed, at doses of 500 mg and 1250 mg vitamin C, <75% and <50% of the vitamin dose is absorbed [36]. Furthermore, steady state plasma vitamin C concentrations rarely exceed 80 µmol/L due to rapid renal clearance. In contrast, intravenously administered vitamin C, which bypasses the intestinally regulated uptake of oral vitamin C, can provide plasma concentrations that are 250 fold higher [36]. However, it should be noted that because vitamin C has a short half-life in plasma of approximately 2 h [90], the high (millimolar) plasma concentrations provided by intravenous administration are relatively transient. Therefore, to maximise uptake and plasma concentrations of vitamin C, the chosen intravenous (or oral) dose should ideally be administered in several smaller doses over the day [100].

Few of the cited pain studies have measured vitamin C concentrations in their patients either before or after administration of the vitamin C intervention. Administration of vitamin C to patients who already have adequate vitamin C status (i.e. ≥50 µmol/L) is unlikely to have a significant effect and is a limitation of many previous vitamin C studies [105]. Although many patient cohorts are likely to have less than adequate vitamin C status (i.e. <50 µmol/L) and hypovitaminosis C (<23 µmol/L), baseline measures should still be collected to allow stratification and/or sub-group analysis of the patient cohorts. For example, we have shown that volunteers with marginal vitamin C status (hypovitaminosis C) have an attenuated response to recommended daily intakes of vitamin C (i.e. 50 mg/day), likely due to suboptimal tissue status, and as such need higher intakes to reach adequate plasma concentrations [106]. This phenomenon is likely to be even more pronounced in hospitalized patients due to increased metabolic demands for vitamin C due to surgery, trauma, infection or other disease processes. Both surgical and infectious disease patients have significantly lower than normal vitamin C status and much higher vitamin C concentrations (0.5–3 g/day) are required for restoration to normal status [22, 23]. Similar trends are observed with patients with cancer [37].

Although a number of placebo-controlled studies have been carried out, primarily for CRPS, postherpetic neuralgia and post-surgical pain, none of the cancer quality of life studies have included placebo controls (Table 3). As such, it is not possible to determine the relative contribution of the placebo effect in these studies, particularly as this effect tends to be more prevalent with subjective measures such as pain [107]. Finally, a major limitation of many vitamin C and pain studies is the lack of mechanistic underpinnings.

Potential analgesic mechanisms of vitamin C

As yet, there is no consensus as to the analgesic mechanism(s) by which vitamin C could be acting. Oxidative stress and inflammation have been implicated in the sequelae of many pathologies, including arthritis, CRPS, infection, cancer and surgical trauma. Vitamin C is a potent antioxidant [108] which can scavenge a wide range of reactive oxygen species and, thus, is capable of protecting cells and tissues from oxidative damage [109]. Because of its well-known antioxidant properties, this is the mechanism by which vitamin C is often assumed to act in conditions where oxidative stress has been implicated. This is, however, an overly simplistic assumption due to the numerous enzymatic reactions in which vitamin C acts as a cofactor in the body [9]. Vitamin C also exhibits anti-inflammatory properties, providing marked decreases in markers of inflammation such as C-reactive protein and pro-inflammatory cytokines, e.g. tumor necrosis factor, interferon, and interleukins [110]. The biochemical mechanisms underlying vitamin C’s ability to decrease pro-inflammatory mediators are currently unknown.

Vitamin C has a well-established role as a cofactor for the synthesis of catecholamine neurotransmitters, and hence is involved in neuromodulation [111]. Vitamin C is a cofactor for the enzyme dopamine β-hydroxylase, which converts dopamine into norepinephrine [112, 113]. Vitamin C may also facilitate the synthesis of dopamine through recycling the cofactor tetrahydrobiopterin, which is required for optimal activity of the rate-limiting enzyme tyrosine hydroxylase [114]. A similar tetrahydrobiopterin recycling mechanism has been proposed for vitamin C in the biosynthesis of the monoamine neurotransmitter serotonin [115]. It is noteworthy that both serotonin and norepinephrine reuptake inhibitors show efficacy in control of pain [116]. Ascorbate-deficient animal models exhibit decreased norepinephrine concentrations compared with controls [117119]. Thus, administration of vitamin C to depleted patients may enhance endogenous synthesis of these neurotransmitters which may in turn contribute to the vitamin C-dependent analgesia observed in some patients.

One currently unexplored analgesic mechanism involves the potential role of vitamin C in the synthesis of amidated opioid peptides. Vitamin C is a cofactor for the enzyme peptidylglycine α-amidating mono-oxygenase (PAM) [120]. PAM is the only known enzyme in humans capable of amidating the carboxy-terminus of peptide hormone precursors, a post-translational modification which is essential for their subsequent stability and/or biological activities [121]. A number of amidated neuropeptides have potent opioid activity. Endomorphin-1 and -2 are amidated tetrapeptides which have the highest known selectivity and affinity for the µ-opioid receptor of all known mammalian opioids [122]. Like other opioid peptides, it is presumed that the endomorphins are generated via post-translational cleavage of a larger precursor protein. For example, another amidated opioid peptide with analgesic properties, which was first identified in human adrenal medulla (adrenorphin or metorphamide) [123, 124], is derived from the proteolytic cleavage of proenkephalin A. A glycine-extended precursor of the opioid peptide would then act as the substrate for post-translational amidation by the ascorbate-dependent enzyme PAM to generate the active carboxy-amidated hormone (Fig. 1).

Fig. 1
figure 1

Proposed synthesis of endomorphin-1 by the vitamin C-dependent enzyme peptidylglycine α-amidating monooxygenase (PAM). The enzyme comprises a peptidylglycine α-hydroxylating monooxygenase (PHM) domain, which converts glycine-extended peptides into a hydroxyglycine intermediate, and a peptidyl α-hydroxyglycine α-amidating lyase (PAL) domain, which converts the hydroxyglycine intermediate into an amidated product. AA ascorbic acid, DHA dehydroascorbic acid

The endomorphins are widely expressed in the central nervous system and immune tissues [125]. They have well known analgesic properties, particularly for neuropathic pain, but also have anti-inflammatory activity, and have been proposed as potential therapeutic agents in the treatment of chronic inflammatory diseases such as rheumatoid arthritis and osteoarthritis [126]. As such, it is tempting to speculate that some of the observed anti-inflammatory effects of vitamin C could be due to enhanced synthesis of endomorphins. It is noteworthy that nervous and neuroendocrine tissues, where monoamine neurotransmitters and amidated neuropeptide hormones are synthesised, contain the highest concentrations of vitamin C in the body [127]. Depletion of amidated neuropeptide hormones has been demonstrated in humans during severe infection [128], which is known to significantly deplete vitamin C concentrations [23], and administration of vitamin C to animal models enhances the synthesis of these PAM-derived hormones [129]. Therefore, it is possible that depletion of vitamin C during acute or chronic disease or trauma could contribute to pain symptoms due to sub-optimal biosynthesis of analgesic neurotransmitters and neuropeptide hormones. The observation that vitamin C administration significantly decreases the requirement for opioid analgesics (Table 4) lends support to this hypothesis.

Calcitonin has been used for decades as a treatment for osteoporosis and other diseases involving accelerated bone turnover [130]. Calcitonin also has a direct analgesic effect on bone pain and has been utilised for improving the pain of acute vertebral fractures, malignant bone metastases, Paget’s disease, and complex regional pain syndrome [130]. It is interesting to note that calcitonin is an amidated peptide hormone, requiring post-translational amidation by PAM for full activity of the mature hormone [131]. Thus, vitamin C is likely to be also required as a cofactor for the synthesis of calcitonin. The analgesic properties of calcitonin appear to be independent of its effects on bone resorption and are possibly mediated through enhanced release of the potent analgesic β-endorphin [130]. Therefore, vitamin C may exhibit analgesia both indirectly, through calcitonin-dependent modulation of endorphins, and directly through enhanced synthesis of endomorphins.


Acute and chronic pain can be debilitating for patients, particularly if not adequately managed by conventional analgesics. Accumulating evidence indicates that vitamin C can exhibit analgesic properties in some clinical conditions, thus potentially mitigating suffering and improving patient quality of life. Pain is costly because it requires medical treatment, complicates treatment of other conditions and results in lost productivity. In the USA the annual cost of pain was greater than the annual costs of heart disease, cancer, and diabetes [132]. Vitamin C is cost effective and appears to be a safe and effective adjunctive therapy for specific pain relief. Notably, it decreases the requirement for opioid analgesics, particularly post surgically and for bone metastasis, thus potentially diminishing the deleterious side effects of opioids. Future high quality studies are required to confirm these findings. Inclusion of placebo controls is preferred due to the subjective nature of pain, however, this can sometimes be difficult to justify in certain patient groups, hence the paucity of placebo-controlled trials for intravenous vitamin C and cancer quality of life. Ideally, studies should also include patients who have less than adequate vitamin C status at baseline (i.e. <50 µmol/L) to ensure that their concentrations are able to increase following supplementation. Overall, future studies should endeavor to ascertain the following aspects: measurement of vitamin C concentrations at baseline and following intervention to determine if specific patient groups respond, determination of the optimal rout of administration (i.e. enteral or parenteral), the optimal dose and frequency of vitamin C administration (which will likely differ depending upon the type of pain and associated conditions), and the potential mechanisms of action of vitamin C.



ascorbic acid


chronic regional pain syndrome


dehydroascorbic acid


European Organisation for the Research and Treatment of Cancer




numerical analogue scale


numeric rating scale


peptidyl α-hydroxyglycine α-amidating lyase domain


peptidylglycine α-amidating mono-oxygenase


patient global impression of change


peptidylglycine α-hydroxylating monooxygenase domain


postherpetic neuralgia


quality of life questionnaire


randomized controlled trial


visual analog scale


  1. 1.

    International Association for the Study of Pain. IASP taxonomy by task force on taxonomy. 2014. Accessed 1 Nov 2016.

  2. 2.

    Crowe M, Whitehead L, Seaton P, Jordan J, McCall C, Maskill V, Tripp H. Qualitative meta-synthesis: the experience of chronic pain across conditions. J Adv Nurs. 2016. doi:10.1111/jan.13174.

    Article  PubMed  Google Scholar 

  3. 3.

    Schug SA, Palmer GM, Scott DA, Halliwell R, Trinca J. Acute pain management: scientific evidence. 4th ed. Melbourne: Australian and New Zealand College of Anaesthetists and Faculty of Pain Medicine; 2015.

    Google Scholar 

  4. 4.

    Ngamkham S, Vincent C, Finnegan L, Holden JE, Wang ZJ, Wilkie DJ. The McGill Pain Questionnaire as a multidimensional measure in people with cancer: an integrative review. Pain Manag Nurs. 2012;13(1):27–51.

    PubMed  Google Scholar 

  5. 5.

    Cleeland CS. The measurement of pain from metastatic bone disease: capturing the patient’s experience. Clin Cancer Res. 2006;12(20 Pt 2):6236s–42s.

    PubMed  Google Scholar 

  6. 6.

    Dionne CE, Laurin D, Desrosiers T, Abdous B, Le Sage N, Frenette J, Mondor M, Pelletier S. Serum vitamin C and spinal pain: a nationwide study. Pain. 2016;157(11):2527–35.

    CAS  PubMed  Google Scholar 

  7. 7.

    Fain O. Musculoskeletal manifestations of scurvy. Joint Bone Spine. 2005;72(2):124–8.

    PubMed  Google Scholar 

  8. 8.

    Cohen SP, Mao J. Neuropathic pain: mechanisms and their clinical implications. BMJ. 2014;348:f7656.

    PubMed  Google Scholar 

  9. 9.

    Du J, Cullen JJ, Buettner GR. Ascorbic acid: chemistry, biology and the treatment of cancer. Biochim Biophys Acta. 2012;1826(2):443–57.

    CAS  PubMed  PubMed Central  Google Scholar 

  10. 10.

    Englard S, Seifter S. The biochemical functions of ascorbic acid. Annu Rev Nutr. 1986;6:365–406.

    CAS  PubMed  Google Scholar 

  11. 11.

    Hodges RE, Hood J, Canham JE, Sauberlich HE, Baker EM. Clinical manifestations of ascorbic acid deficiency in man. Am J Clin Nutr. 1971;24(4):432–43.

    CAS  PubMed  Google Scholar 

  12. 12.

    Popovich D, McAlhany A, Adewumi AO, Barnes MM. Scurvy: forgotten but definitely not gone. J Pediatr Health Care. 2009;23(6):405–15.

    PubMed  Google Scholar 

  13. 13.

    Ghedira Besbes L, Haddad S, Ben Meriem C, Golli M, Najjar MF, Guediche MN. Infantile scurvy: two case reports. Int J Pediatr. 2010;2010:717518.

    PubMed  PubMed Central  Google Scholar 

  14. 14.

    Duggan CP, Westra SJ, Rosenberg AE. Case records of the Massachusetts General Hospital. Case 23-2007. A 9-year-old boy with bone pain, rash, and gingival hypertrophy. N Engl J Med. 2007;357(4):392–400.

    CAS  PubMed  Google Scholar 

  15. 15.

    Kumar R, Aggarwal A, Faridi MM. Complex regional pain syndrome type 1 and scurvy. Indian Pediatr. 2009;46(6):529–31.

    PubMed  Google Scholar 

  16. 16.

    Khalid MM. Scurvy; radiological diagnosis. Prof Med J. 2009;16(3):466–8.

    Google Scholar 

  17. 17.

    Cutforth RH. Adult scurvy. Lancet. 1958;1(7018):454–6.

    CAS  PubMed  Google Scholar 

  18. 18.

    Doll S, Ricou B. Severe vitamin C deficiency in a critically ill adult: a case report. Eur J Clin Nutr. 2013;67(8):881–2.

    CAS  PubMed  Google Scholar 

  19. 19.

    Ramar S, Sivaramakrishnan V, Manoharan K. Scurvy–a forgotten disease. Arch Phys Med Rehabil. 1993;74(1):92–5.

    CAS  PubMed  Google Scholar 

  20. 20.

    Fain O, Paries J, Jacquart B, Le Moel G, Kettaneh A, Stirnemann J, Heron C, Sitbon M, Taleb C, Letellier E, Betari B, Gattegno L, Thomas M. Hypovitaminosis C in hospitalized patients. Eur J Intern Med. 2003;14(7):419–25.

    PubMed  Google Scholar 

  21. 21.

    Gan R, Eintracht S, Hoffer LJ. Vitamin C deficiency in a university teaching hospital. J Am Coll Nutr. 2008;27(3):428–33.

    CAS  PubMed  Google Scholar 

  22. 22.

    Fukushima R, Yamazaki E. Vitamin C requirement in surgical patients. Curr Opin Clin Nutr Metab Care. 2010;13(6):669–76.

    CAS  PubMed  Google Scholar 

  23. 23.

    Carr AC, Shaw GM, Fowler AA, Natarajan R. Ascorbate-dependent vasopressor synthesis: a rationale for vitamin C administration in severe sepsis and septic shock? Crit Care. 2015;19:e418.

    Google Scholar 

  24. 24.

    Schleicher RL, Carroll MD, Ford ES, Lacher DA. Serum vitamin C and the prevalence of vitamin C deficiency in the United States: 2003–2004 National Health and Nutrition Examination Survey (NHANES). Am J Clin Nutr. 2009;90(5):1252–63.

    CAS  PubMed  Google Scholar 

  25. 25.

    Raynaud-Simon A, Cohen-Bittan J, Gouronnec A, Pautas E, Senet P, Verny M, Boddaert J. Scurvy in hospitalized elderly patients. J Nutr Health Aging. 2010;14(6):407–10.

    CAS  PubMed  Google Scholar 

  26. 26.

    Teixeira A, Carrie AS, Genereau T, Herson S, Cherin P. Vitamin C deficiency in elderly hospitalized patients. Am J Med. 2001;111(6):502.

    CAS  PubMed  Google Scholar 

  27. 27.

    Holley AD, Osland E, Barnes J, Krishnan A, Fraser JF. Scurvy: historically a plague of the sailor that remains a consideration in the modern intensive care unit. Intern Med J. 2011;41(3):283–5.

    CAS  PubMed  Google Scholar 

  28. 28.

    Kieffer P, Thannberger P, Wilhelm JM, Kieffer C, Schneider F. Multiple organ dysfunction dramatically improving with the infusion of vitamin C: more support for the persistence of scurvy in our “welfare” society. Intensive Care Med. 2001;27(2):448.

    CAS  PubMed  Google Scholar 

  29. 29.

    Fain O, Mathieu E, Thomas M. Scurvy in patients with cancer. BMJ. 1998;316(7145):1661–2.

    CAS  PubMed  PubMed Central  Google Scholar 

  30. 30.

    Torun M, Yardim S, Gonenc A, Sargin H, Menevse A, Simsek B. Serum beta-carotene, vitamin E, vitamin C and malondialdehyde levels in several types of cancer. J Clin Pharm Ther. 1995;20(5):259–63.

    CAS  PubMed  Google Scholar 

  31. 31.

    Mahdavi R, Faramarzi E, Seyedrezazadeh E, Mohammad-Zadeh M, Pourmoghaddam M. Evaluation of oxidative stress, antioxidant status and serum vitamin C levels in cancer patients. Biol Trace Elem Res. 2009;130(1):1–6.

    CAS  PubMed  Google Scholar 

  32. 32.

    Mayland CR, Bennett MI, Allan K. Vitamin C deficiency in cancer patients. Palliat Med. 2005;19(1):17–20.

    PubMed  Google Scholar 

  33. 33.

    Nakano K, Suzuki S. Stress-induced change in tissue levels of ascorbic acid and histamine in rats. J Nutr. 1984;114(9):1602–8.

    CAS  PubMed  Google Scholar 

  34. 34.

    Campbell EJ, Vissers MC, Bozonet S, Dyer A, Robinson BA, Dachs GU. Restoring physiological levels of ascorbate slows tumor growth and moderates HIF-1 pathway activity in Gulo(−/−) mice. Cancer Med. 2015;4(2):303–14.

    CAS  PubMed  Google Scholar 

  35. 35.

    Burns JJ, Mosbach EH, Schulenberg S. Ascorbic acid synthesis in normal and drug-treated rats, studied with L-ascorbic-1-C14 acid. J Biol Chem. 1954;207(2):679–87.

    CAS  PubMed  PubMed Central  Google Scholar 

  36. 36.

    Levine M, Conry-Cantilena C, Wang Y, Welch RW, Washko PW, Dhariwal KR, Park JB, Lazarev A, Graumlich JF, King J, Cantilena LR. Vitamin C pharmacokinetics in healthy volunteers: evidence for a recommended dietary allowance. Proc Natl Acad Sci USA. 1996;93(8):3704–9.

    CAS  PubMed  Google Scholar 

  37. 37.

    Mikirova N, Casciari J, Riordan N, Hunninghake R. Clinical experience with intravenous administration of ascorbic acid: achievable levels in blood for different states of inflammation and disease in cancer patients. J Transl Med. 2013;11(1):191.

    CAS  PubMed  PubMed Central  Google Scholar 

  38. 38.

    Marcus SL, Dutcher JP, Paietta E, Ciobanu N, Strauman J, Wiernik PH, Hutner SH, Frank O, Baker H. Severe hypovitaminosis C occurring as the result of adoptive immunotherapy with high-dose interleukin 2 and lymphokine-activated killer cells. Cancer Res. 1987;47(15):4208–12.

    CAS  PubMed  Google Scholar 

  39. 39.

    Alexandrescu DT, Dasanu CA, Kauffman CL. Acute scurvy during treatment with interleukin-2. Clin Exp Dermatol. 2009;34(7):811–4.

    CAS  PubMed  Google Scholar 

  40. 40.

    Oak AS, Jaleel T, Fening K, Pavlidakey PG, Sami N. A case of scurvy associated with nilotinib. J Cutan Pathol. 2016;43(8):725–6.

    PubMed  Google Scholar 

  41. 41.

    Basu TK. Vitamin C-aspirin interactions. Int J Vitam Nutr Res Suppl. 1982;23:83–90.

    CAS  PubMed  PubMed Central  Google Scholar 

  42. 42.

    Aghajanian P, Hall S, Wongworawat MD, Mohan S. The roles and mechanisms of actions of vitamin C in bone: new developments. J Bone Miner Res. 2015;30(11):1945–55.

    CAS  PubMed  PubMed Central  Google Scholar 

  43. 43.

    Ekrol I, Duckworth AD, Ralston SH, Court-Brown CM, McQueen MM. The influence of vitamin C on the outcome of distal radial fractures: a double-blind, randomized controlled trial. J Bone Joint Surg Am. 2014;96(17):1451–9.

    PubMed  Google Scholar 

  44. 44.

    Zollinger PE, Tuinebreijer WE, Breederveld RS, Kreis RW. Can vitamin C prevent complex regional pain syndrome in patients with wrist fractures? A randomized, controlled, multicenter dose-response study. J Bone Joint Surg Am. 2007;89(7):1424–31.

    CAS  PubMed  PubMed Central  Google Scholar 

  45. 45.

    Zollinger PE, Tuinebreijer WE, Kreis RW, Breederveld RS. Effect of vitamin C on frequency of reflex sympathetic dystrophy in wrist fractures: a randomised trial. Lancet. 1999;354(9195):2025–8.

    CAS  PubMed  Google Scholar 

  46. 46.

    Besse JL, Gadeyne S, Galand-Desme S, Lerat JL, Moyen B. Effect of vitamin C on prevention of complex regional pain syndrome type I in foot and ankle surgery. Foot Ankle Surg. 2009;15(4):179–82.

    PubMed  Google Scholar 

  47. 47.

    Cazeneuve JF, Leborgne JM, Kermad K, Hassan Y. Vitamin C and prevention of reflex sympathetic dystrophy following surgical management of distal radius fractures. Acta Orthop Belg. 2002;68(5):481–4.

    CAS  PubMed  PubMed Central  Google Scholar 

  48. 48.

    Shibuya N, Humphers JM, Agarwal MR, Jupiter DC. Efficacy and safety of high-dose vitamin C on complex regional pain syndrome in extremity trauma and surgery–systematic review and meta-analysis. J Foot Ankle Surg. 2013;52(1):62–6.

    PubMed  Google Scholar 

  49. 49.

    Meena S, Sharma P, Gangary SK, Chowdhury B. Role of vitamin C in prevention of complex regional pain syndrome after distal radius fractures: a meta-analysis. Eur J Orthop Surg Traumatol. 2015;25(4):637–41.

    PubMed  Google Scholar 

  50. 50.

    Evaniew N, McCarthy C, Kleinlugtenbelt YV, Ghert M, Bhandari M. Vitamin C to prevent complex regional pain syndrome in patients with distal radius fractures: a meta-analysis of randomized controlled trials. J Orthop Trauma. 2015;29(8):e235–41.

    PubMed  Google Scholar 

  51. 51.

    Chen S, Roffey DM, Dion CA, Arab A, Wai EK. Effect of perioperative vitamin C supplementation on postoperative pain and the incidence of chronic regional pain syndrome: a systematic review and meta-analysis. Clin J Pain. 2016;32(2):179–85.

    PubMed  Google Scholar 

  52. 52.

    Aim F, Klouche S, Frison A, Bauer T, Hardy P. Efficacy of vitamin C in preventing complex regional pain syndrome after wrist fracture: a systematic review and meta-analysis. Orthop Traumatol Surg Res. 2017. doi:10.1016/j.otsr.2016.12.021.

    Article  PubMed  PubMed Central  Google Scholar 

  53. 53.

    Zollinger PE, Ellis ML, Unal H, Tuinebreijer WE. Clinical outcome of cementless semi-constrained trapeziometacarpal arthroplasty, and possible effect of vitamin C on the occurrence of complex regional pain syndrome. Acta Orthop Belg. 2008;74(3):317–22.

    PubMed  PubMed Central  Google Scholar 

  54. 54.

    Zollinger PE, Unal H, Ellis ML, Tuinebreijer WE. Clinical results of 40 consecutive basal thumb prostheses and No CRPS type I after vitamin C prophylaxis. Open Orthop J. 2010;4:62–6.

    PubMed  PubMed Central  Google Scholar 

  55. 55.

    Jensen NH. Reduced pain from osteoarthritis in hip joint or knee joint during treatment with calcium ascorbate. A randomized, placebo-controlled cross-over trial in general practice. Ugeskr Laeger. 2003;165(25):2563–6.

    PubMed  PubMed Central  Google Scholar 

  56. 56.

    Carr AC, Vissers MCM, Cook J. Parenteral vitamin C relieves chronic fatigue and pain in a patient presenting with rheumatoid arthritis and mononeuritis multiplex secondary to CNS vasculitis. Case Rep Clin Path. 2015;2(2):57–61.

    Google Scholar 

  57. 57.

    Lunec J, Blake DR. The determination of dehydroascorbic acid and ascorbic acid in the serum and synovial fluid of patients with rheumatoid arthritis (RA). Free Radic Res Commun. 1985;1(1):31–9.

    CAS  PubMed  Google Scholar 

  58. 58.

    Basu TK, Smethurst M, Gillett MB, Donaldson D, Jordan SJ, Williams DC, Hicklin JA. Ascorbic acid therapy for the relief of bone pain in Paget’s disease. Acta Vitaminol Enzymol. 1978;32(1–4):45–9.

    CAS  PubMed  PubMed Central  Google Scholar 

  59. 59.

    Smethurst M, Basu TK, Gillett MB, Donaldson D, Jordan SJ, Williams DC, Hicklin JA. Combined therapy with ascorbic acid and calcitonin for the relief of bone pain in Paget’s disease. Acta Vitaminol Enzymol. 1981;3(1):8–11.

    CAS  PubMed  PubMed Central  Google Scholar 

  60. 60.

    Opstelten W, McElhaney J, Weinberger B, Oaklander AL, Johnson RW. The impact of varicella zoster virus: chronic pain. J Clin Virol. 2010;48(Suppl 1):S8–13.

    PubMed  Google Scholar 

  61. 61.

    Stankus SJ, Dlugopolski M, Packer D. Management of herpes zoster (shingles) and postherpetic neuralgia. Am Fam Physician. 2000;61(8):2437–44.

    CAS  PubMed  PubMed Central  Google Scholar 

  62. 62.

    Katz J, Cooper EM, Walther RR, Sweeney EW, Dworkin RH. Acute pain in herpes zoster and its impact on health-related quality of life. Clin Infect Dis. 2004;39(3):342–8.

    PubMed  Google Scholar 

  63. 63.

    Chen JY, Chu CC, Lin YS, So EC, Shieh JP, Hu ML. Nutrient deficiencies as a risk factor in Taiwanese patients with postherpetic neuralgia. Br J Nutr. 2011;106(5):700–7.

    CAS  PubMed  Google Scholar 

  64. 64.

    Chen JY, Chu CC, So EC, Hsing CH, Hu ML. Treatment of postherpetic neuralgia with intravenous administration of vitamin C. Anesth Analg. 2006;103(6):1616–7.

    PubMed  Google Scholar 

  65. 65.

    Schencking M, Sandholzer H, Frese T. Intravenous administration of vitamin C in the treatment of herpetic neuralgia: two case reports. Med Sci Monit. 2010;16(5):CS58–61.

    PubMed  PubMed Central  Google Scholar 

  66. 66.

    Schencking M, Kraft K. Cantharidin patches and intravenous administration of vitamin C in the concomitant treatment of herpes zoster: a case report. J Chinese Integrative Med. 2011;9(4):410–3.

    Google Scholar 

  67. 67.

    Byun SH, Jeon Y. Administration of vitamin C in a patient with Herpes Zoster—a case report. Korean J Pain. 2011;24(2):108–11.

    CAS  PubMed  PubMed Central  Google Scholar 

  68. 68.

    Schencking M, Vollbracht C, Weiss G, Lebert J, Biller A, Goyvaerts B, Kraft K. Intravenous vitamin C in the treatment of shingles: results of a multicenter prospective cohort study. Med Sci Monit. 2012;18(4):CR215–24.

    CAS  PubMed  PubMed Central  Google Scholar 

  69. 69.

    Chen JY, Chang CY, Feng PH, Chu CC, So EC, Hu ML. Plasma vitamin C is lower in postherpetic neuralgia patients and administration of vitamin C reduces spontaneous pain but not brush-evoked pain. Clin J Pain. 2009;25(7):562–9.

    PubMed  Google Scholar 

  70. 70.

    Kim MS, Kim DJ, Na CH, Shin BS. A study of intravenous administration of vitamin C in the treatment of acute herpetic pain and postherpetic neuralgia. Ann Dermatol. 2016;28(6):677–83.

    CAS  PubMed  PubMed Central  Google Scholar 

  71. 71.

    Schilte C, Staikowsky F, Couderc T, Madec Y, Carpentier F, Kassab S, Albert ML, Lecuit M, Michault A. Chikungunya virus-associated long-term arthralgia: a 36-month prospective longitudinal study. PLoS Negl Trop Dis. 2013;7(3):e2137.

    PubMed  PubMed Central  Google Scholar 

  72. 72.

    Servey JT, Reamy BV, Hodge J. Clinical presentations of parvovirus B19 infection. Am Fam Physician. 2007;75(3):373–6.

    PubMed  Google Scholar 

  73. 73.

    Gonzalez MJ, Miranda-Massari JR, Berdiel MJ, Duconge J, Rodriguez-Lopez JL, Hunninghake R, Cobas-Rosario VJ. High dose intraveneous vitamin C and chikungunya fever: a case report. J Orthomol Med. 2014;29(4):154–6.

    PubMed  PubMed Central  Google Scholar 

  74. 74.

    Lallement A, Zandotti C, Brouqui P. Persistent parvovirus B19 viremia with chronic arthralgia treated with ascorbic acid: a case report. J Med Case Rep. 2015;9:1.

    PubMed  PubMed Central  Google Scholar 

  75. 75.

    Marcial-Vega V, Idxian Gonzalez-Terron G, Levy TE. Intravenous ascorbic acid and hydrogen peroxide in the management of patients with chikungunya. Bol Asoc Med Puerto R. 2015;107(1):20–4.

    Google Scholar 

  76. 76.

    Buga S, Sarria JE. The management of pain in metastatic bone disease. Cancer Control. 2012;19(2):154–66.

    CAS  PubMed  Google Scholar 

  77. 77.

    Falk S, Dickenson AH. Pain and nociception: mechanisms of cancer-induced bone pain. J Clin Oncol. 2014;32(16):1647–54.

    CAS  PubMed  Google Scholar 

  78. 78.

    Mantyh PW. Bone cancer pain: from mechanism to therapy. Curr Opin Support Palliat Care. 2014;8(2):83–90.

    PubMed  PubMed Central  Google Scholar 

  79. 79.

    Padayatty SJ, Sun AY, Chen Q, Espey MG, Drisko J, Levine M. Vitamin C: intravenous use by complementary and alternative medicine practitioners and adverse effects. PLoS ONE. 2010;5(7):e11414.

    PubMed  PubMed Central  Google Scholar 

  80. 80.

    Carr AC, Vissers MCM, Cook JS. The effect of intravenous vitamin C on cancer- and chemotherapy-related fatigue and quality of life. Front Oncol. 2014;4(283):1–7.

    Google Scholar 

  81. 81.

    Cameron E, Campbell A. The orthomolecular treatment of cancer. II. Clinical trial of high-dose ascorbic acid supplements in advanced human cancer. Chem Biol Interact. 1974;9(4):285–315.

    CAS  PubMed  Google Scholar 

  82. 82.

    Murata A, Morishige F, Yamaguchi H. Prolongation of survival times of terminal cancer patients by administration of large doses of ascorbate. Int J Vitam Nutr Res Suppl. 1982;23:103–13.

    CAS  PubMed  Google Scholar 

  83. 83.

    Kiziltan HS, Bayir AG, Demirtas M, Meral I, Taspinar O, Eris AH, Aydin T, Mayadagli A. Ascorbic-acid treatment for progressive bone metastases after radiotherapy: a pilot study. Altern Ther Health Med. 2014;20(Suppl 2):16–20.

    PubMed  Google Scholar 

  84. 84.

    Gunes-Bayir A, Kiziltan HS. Palliative vitamin C application in patients with radiotherapy-resistant bone metastases: a retrospective study. Nutr Cancer. 2015;67(6):921–5.

    CAS  PubMed  Google Scholar 

  85. 85.

    Aaronson NK, Ahmedzai S, Bergman B, Bullinger M, Cull A, Duez NJ, Filiberti A, Flechtner H, Fleishman SB, de Haes JC, et al. The European Organization for Research and Treatment of Cancer QLQ-C30: a quality-of-life instrument for use in international clinical trials in oncology. J Natl Cancer Inst. 1993;85(5):365–76.

    CAS  PubMed  Google Scholar 

  86. 86.

    Cocks K, King MT, Velikova G, de Castro G Jr., Martyn St-James M, Fayers PM, Brown JM. Evidence-based guidelines for interpreting change scores for the European Organisation for the Research and Treatment of Cancer Quality of Life Questionnaire Core 30. Eur J Cancer. 2012;48(11):1713–21.

    CAS  PubMed  Google Scholar 

  87. 87.

    Vollbracht C, Schneider B, Leendert V, Weiss G, Auerbach L, Beuth J. Intravenous vitamin C administration improves quality of life in breast cancer patients during chemo-/radiotherapy and aftercare: results of a retrospective, multicentre, epidemiological cohort study in Germany. Vivo. 2011;25(6):983–90.

    CAS  Google Scholar 

  88. 88.

    Yeom CH, Jung GC, Song KJ. Changes of terminal cancer patients’ health-related quality of life after high dose vitamin C administration. J Korean Med Sci. 2007;22(1):7–11.

    CAS  PubMed  PubMed Central  Google Scholar 

  89. 89.

    Takahashi H, Mizuno H, Yanagisawa A. High-dose intravenous vitamin C improves quality of life in cancer patients. Personalized Med Universe. 2012;2(1):49–53.

    Google Scholar 

  90. 90.

    Stephenson CM, Levin RD, Spector T, Lis CG. Phase I clinical trial to evaluate the safety, tolerability, and pharmacokinetics of high-dose intravenous ascorbic acid in patients with advanced cancer. Cancer Chemother Pharmacol. 2013;72(1):139–46.

    CAS  PubMed  PubMed Central  Google Scholar 

  91. 91.

    Gammaitoni AR, Fine P, Alvarez N, McPherson ML, Bergmark S. Clinical application of opioid equianalgesic data. Clin J Pain. 2003;19(5):286–97.

    PubMed  Google Scholar 

  92. 92.

    Mercadante S, Fulfaro F. World Health Organization guidelines for cancer pain: a reappraisal. Ann Oncol. 2005;16(Suppl 4):iv32–5.

    Google Scholar 

  93. 93.

    Cameron E, Baird GM. Ascorbic acid and dependence on opiates in patients with advanced disseminated cancer. Intern Res Commun Syst. 1973;1:33.

    Google Scholar 

  94. 94.

    Evangelou A, Kalfakakou V, Georgakas P, Koutras V, Vezyraki P, Iliopoulou L, Vadalouka A. Ascorbic acid (vitamin C) effects on withdrawal syndrome of heroin abusers. Vivo. 2000;14(2):363–6.

    CAS  Google Scholar 

  95. 95.

    Carr AC, Vissers MCM, Cook J. Parenteral vitamin C for palliative care of terminal cancer patients. NZ Med J. 2014;127(1396):84–6.

    Google Scholar 

  96. 96.

    Pinkerton E, Good P, Gibbons K, Hardy J. An open-label pilot study of oral vitamin C as an opioid-sparing agent in patients with chronic pain secondary to cancer. Support Care Cancer. 2017;25(2):341–3.

    CAS  PubMed  Google Scholar 

  97. 97.

    Jeon Y, Park JS, Moon S, Yeo J. Effect of intravenous high dose vitamin C on postoperative pain and morphine use after laparoscopic colectomy: a randomized controlled trial. Pain Res Manag. 2016. doi:10.1155/2016/9147279.

    Article  PubMed  PubMed Central  Google Scholar 

  98. 98.

    Ayatollahi V, Dehghanpoor-Farashah S, Behdad S, Vaziribozorg S, Rabbani Anari M. Effect of intravenous vitamin C on post-operative pain in uvulopalatopharyngoplasty with tonsillectomy. Clin Otolaryngol. 2017;42(1):139–43.

    CAS  PubMed  Google Scholar 

  99. 99.

    Kanazi GE, El-Khatib MF, Yazbeck-Karam VG, Hanna JE, Masri B, Aouad MT. Effect of vitamin C on morphine use after laparoscopic cholecystectomy: a randomized controlled trial. Can J Anaesth. 2012;59(6):538–43.

    PubMed  Google Scholar 

  100. 100.

    Padayatty SJ, Sun H, Wang Y, Riordan HD, Hewitt SM, Katz A, Wesley RA, Levine M. Vitamin C pharmacokinetics: implications for oral and intravenous use. Ann Intern Med. 2004;140(7):533–7.

    CAS  PubMed  Google Scholar 

  101. 101.

    Khanna NC, Sharma SK. Megadoses of vitamin C prevent the development of tolerance and physical dependence on morphine in mice. Life Sci. 1983;33(Suppl 1):401–4.

    CAS  PubMed  Google Scholar 

  102. 102.

    Talkhooncheh M, Alaei HA, Ramshini E, Shahidani S. The effect of vitamin C on morphine self-administration in rats. Adv Biomed Res. 2014;3:178.

    PubMed  PubMed Central  Google Scholar 

  103. 103.

    Zeraati F, Araghchian M, Farjoo MH. Ascorbic Acid interaction with analgesic effect of morphine and tramadol in mice. Anesthesiol Pain Med. 2014;4(3):e19529.

    Google Scholar 

  104. 104.

    Savini I, Rossi A, Pierro C, Avigliano L, Catani MV. SVCT1 and SVCT2: key proteins for vitamin C uptake. Amino Acids. 2008;34(3):347–55.

    CAS  PubMed  Google Scholar 

  105. 105.

    Lykkesfeldt J, Poulsen HE. Is vitamin C supplementation beneficial? Lessons learned from randomised controlled trials. Br J Nutr. 2010;103(9):1251–9.

    CAS  PubMed  Google Scholar 

  106. 106.

    Carr AC, Pullar JM, Bozonet SM, Vissers MC. Marginal ascorbate status (hypovitaminosis C) results in an attenuated response to vitamin C supplementation. Nutrients. 2016;8(6):E341.

    PubMed  Google Scholar 

  107. 107.

    Hrobjartsson A, Gotzsche PC. Placebo interventions for all clinical conditions. Cochrane Database Syst Rev. 2010;1:CD003974.

    Google Scholar 

  108. 108.

    Buettner GR. The pecking order of free radicals and antioxidants: lipid peroxidation, alpha-tocopherol, and ascorbate. Arch Biochem Biophys. 1993;300(2):535–43.

    CAS  PubMed  Google Scholar 

  109. 109.

    Carr A, Frei B. Does vitamin C act as a pro-oxidant under physiological conditions? FASEB J. 1999;13(9):1007–24.

    CAS  PubMed  Google Scholar 

  110. 110.

    Mikirova N, Casciari J, Rogers A, Taylor P. Effect of high-dose intravenous vitamin C on inflammation in cancer patients. J Transl Med. 2012;10:189.

    CAS  PubMed  PubMed Central  Google Scholar 

  111. 111.

    Harrison FE, May JM. Vitamin C function in the brain: vital role of the ascorbate transporter SVCT2. Free Radic Biol Med. 2009;46(6):719–30.

    CAS  PubMed  PubMed Central  Google Scholar 

  112. 112.

    Levine M. Ascorbic acid specifically enhances dopamine beta-monooxygenase activity in resting and stimulated chromaffin cells. J Biol Chem. 1986;261(16):7347–56.

    CAS  PubMed  Google Scholar 

  113. 113.

    May JM, Qu ZC, Nazarewicz R, Dikalov S. Ascorbic acid efficiently enhances neuronal synthesis of norepinephrine from dopamine. Brain Res Bull. 2013;90:35–42.

    CAS  PubMed  Google Scholar 

  114. 114.

    May JM, Qu ZC, Meredith ME. Mechanisms of ascorbic acid stimulation of norepinephrine synthesis in neuronal cells. Biochem Biophys Res Commun. 2012;426(1):148–52.

    CAS  PubMed  PubMed Central  Google Scholar 

  115. 115.

    Ward MS, Lamb J, May JM, Harrison FE. Behavioral and monoamine changes following severe vitamin C deficiency. J Neurochem. 2013;124(3):363–75.

    CAS  PubMed  Google Scholar 

  116. 116.

    Mochizucki D. Serotonin and noradrenaline reuptake inhibitors in animal models of pain. Hum Psychopharmacol. 2004;19(Suppl 1):S15–9.

    CAS  PubMed  Google Scholar 

  117. 117.

    Hoehn SK, Kanfer JN. Effects of chronic ascorbic acid deficiency on guinea pig lysosomal hydrolase activities. J Nutr. 1980;110(10):2085–94.

    CAS  PubMed  Google Scholar 

  118. 118.

    Deana R, Bharaj BS, Verjee ZH, Galzigna L. Changes relevant to catecholamine metabolism in liver and brain of ascorbic acid deficient guinea-pigs. Int J Vitam Nutr Res. 1975;45(2):175–82.

    CAS  PubMed  Google Scholar 

  119. 119.

    Bornstein SR, Yoshida-Hiroi M, Sotiriou S, Levine M, Hartwig HG, Nussbaum RL, Eisenhofer G. Impaired adrenal catecholamine system function in mice with deficiency of the ascorbic acid transporter (SVCT2). FASEB J. 2003;17(13):1928–30.

    CAS  PubMed  Google Scholar 

  120. 120.

    Prigge ST, Mains RE, Eipper BA, Amzel LM. New insights into copper monooxygenases and peptide amidation: structure, mechanism and function. Cell Mol Life Sci. 2000;57(8–9):1236–59.

    CAS  PubMed  Google Scholar 

  121. 121.

    Merkler DJ. C-terminal amidated peptides: production by the in vitro enzymatic amidation of glycine-extended peptides and the importance of the amide to bioactivity. Enzyme Microb Technol. 1994;16(6):450–6.

    CAS  PubMed  Google Scholar 

  122. 122.

    Okada Y, Tsuda Y, Bryant SD, Lazarus LH. Endomorphins and related opioid peptides. Vitam Horm. 2002;65:257–79.

    CAS  PubMed  Google Scholar 

  123. 123.

    Boarder MR, Contractor H, Marriott D, McArdle W. Metorphamide, a C-terminally amidated opioid peptide, in human adrenal and human phaeochromocytoma. Regul Pept. 1985;12(1):35–42.

    CAS  PubMed  Google Scholar 

  124. 124.

    Matsuo H, Miyata A, Mizuno K. Novel C-terminally amidated opioid peptide in human phaeochromocytoma tumour. Nature. 1983;305(5936):721–3.

    CAS  PubMed  Google Scholar 

  125. 125.

    Fichna J, Janecka A, Costentin J, Do Rego JC. The endomorphin system and its evolving neurophysiological role. Pharmacol Rev. 2007;59(1):88–123.

    CAS  PubMed  Google Scholar 

  126. 126.

    Jessop DS, Fassold A, Wolff C, Hofbauer R, Chover-Gonzalez A, Richards LJ, Straub RH. Endomorphins in rheumatoid arthritis, osteoarthritis, and experimental arthritis. Ann NY Acad Sci. 2010;1193:117–22.

    PubMed  Google Scholar 

  127. 127.

    Hornig D. Distribution of ascorbic acid, metabolites and analogues in man and animals. Ann NY Acad Sci. 1975;258:103–18.

    CAS  PubMed  Google Scholar 

  128. 128.

    Sharshar T, Carlier R, Blanchard A, Feydy A, Gray F, Paillard M, Raphael JC, Gajdos P, Annane D. Depletion of neurohypophyseal content of vasopressin in septic shock. Crit Care Med. 2002;30(3):497–500.

    CAS  PubMed  Google Scholar 

  129. 129.

    Giusti-Paiva A, Domingues VG. Centrally administered ascorbic acid induces antidiuresis, natriuresis and neurohypophyseal hormone release in rats. Neuro Endocrinol Lett. 2010;31(1):87–91.

    CAS  PubMed  Google Scholar 

  130. 130.

    Mehta NM, Malootian A, Gilligan JP. Calcitonin for osteoporosis and bone pain. Curr Pharm Des. 2003;9(32):2659–76.

    CAS  PubMed  Google Scholar 

  131. 131.

    Yabuta M, Suzuki Y, Magota K, Tsuruoka N, Matsukura S, Tanaka S, Ohshima T, Ohsuye K. Production of recombinant human calcitonin in Escherichia coli. Ann NY Acad Sci. 1994;721:82–4.

    CAS  PubMed  Google Scholar 

  132. 132.

    Gaskin DJ, Richard P. The economic costs of pain in the United States. J Pain. 2012;13(8):715–24.

    PubMed  Google Scholar 

  133. 133.

    Carr AC, Vissers MC, Cook J. Relief from cancer chemotherapy side effects with pharmacologic vitamin C. NZ Med J. 2014;127(1388):66–70.

    Google Scholar 

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Authors’ contributions

AC conceived the novel vitamin C-dependent opioid synthesis mechanism and the review topic, and wrote the vitamin C-related sections; CM wrote the general pain-related sections. Both authors read and approved the final manuscript.

Authors’ information

AC is a biomedical researcher with many years’ experience running human intervention studies investigating the bioavailability and health effects of vitamin C. CM is a clinician with many years’ experience working to improve the experience of patients with pain.


We thank Professors Harri Hemilä and Marie Crowe for critically reviewing the manuscript and providing helpful suggestions. A.C. is the recipient of a Sir Charles Hercus Health Research Fellowship from the Health Research Council of New Zealand.

Competing interests

The authors declare that they have no competing interests.

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Data sharing not applicable to this review as no datasets were generated or analysed for the review.

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Correspondence to Anitra C. Carr.

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Carr, A.C., McCall, C. The role of vitamin C in the treatment of pain: new insights. J Transl Med 15, 77 (2017).

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  • Vitamin C
  • Chronic regional pain syndrome
  • Post-herpetic neuralgia
  • Cancer quality of life
  • Opioid requirements