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Year : 2009  |  Volume : 75  |  Issue : 2  |  Page : 116-118

Vitiligo and diet: A theoretical molecular approach with practical implications


1 Shiraz University of Medical Sciences, Shiraz, Iran
2 National Skin Center, Singapore

Correspondence Address:
M R Namazi
Dermatology Department, Faghihi Hospital, Shiraz
Iran
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0378-6323.48654

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How to cite this article:
Namazi M R, Chee Leok G. Vitiligo and diet: A theoretical molecular approach with practical implications. Indian J Dermatol Venereol Leprol 2009;75:116-8

How to cite this URL:
Namazi M R, Chee Leok G. Vitiligo and diet: A theoretical molecular approach with practical implications. Indian J Dermatol Venereol Leprol [serial online] 2009 [cited 2015 Jul 28];75:116-8. Available from: http://www.ijdvl.com/text.asp?2009/75/2/116/48654


The psychologically devastating disorder vitiligo affects 1% of the world's population. [1] Over the years, the neurological, biochemical, immunological and genetic aspects of the pathobiology of this enigmatic disorder have been explored. Vitiligo has a multifactorial, multistep etiology, always characterized by an increase of external or internal phenol/catechol concentrations and reactive oxygen species. [2],[3] It is recently suggested that reactive oxygen species can alter melanocyte-specific factors to produce neo-antigens and can also amplify antigen presentation and autoimmune destruction of melanocytes. [3] It is also proposed that phenol-containing chemicals can compete with tyrosine to produce reactive quinones. This conversion is reinforced by a disturbed redox balance seen in vitiligo (increased hydrogen peroxide). Such reactive quinones can be covalently bound to the catalytic center of tyrosinase to give a neo-antigen. Micromolar (non-cytotoxic) quantities of O -quinones may be sufficient in this haptenation to mount an immune response. O -quinones derived from estrogen can serve as surrogate substrates of tyrosinase and cause haptenation. [2] Furthermore, estrogen is implicated to play an important role in the development of autoimmunity. [4] Given the important contribution of reactive oxygen species, estrogen and phenol-containing agents to the pathophysiology of vitiligo, this article tries to draw attention to the potential link between nutrition and vitiligo.

Given the pivotal role of oxidative stress in the pathobiology of vitiligo, α-tochopherol was used in combination with psoralen with ultraviolet A (PUVA) in order to shorten the duration of the treatment. [5] Also, α-tochopherol cream combined with weak to moderate topical corticosteroids or PUVA was proposed and used with success. [6] Some patients with active or stable vitiligo were treated with an antioxidant pool (tochopherol acetate, ubiquinone, selenomethionine, methionine) in order to increase both the enzymatic and the non-enzymatic antioxidant pattern. After 3 months of therapy, the progression of the vitiligo was stopped and, in some cases, repigmentation of the most recent lesions was observed. [7]

Given the pivotal role of oxidative stress in the pathogenesis of vitiligo, food contaminants/additives/preservatives and cosmetic products could aggravate vitiligo because they produce oxidative stress in the skin. [8] Increased consumption of omega-6 or a vegetable source of oils and decreased omega-3 intake may increase, in vivo , the production of free radicals and pro-inflammatory cytokines. Vegetable oil could exacerbate autoimmune disease by increasing the free radical formation through decreasing the antioxidant enzyme mRNA levels. In contrast, omega-3 lipid intake in the presence of an antioxidant supplement appears to exert protection against autoimmunity by enhancing antioxidant enzymes and transforming growth factor-β mRNA levels. [9] Omega-3 fatty acids and eicosapentaenoic acid, in particular, are well-documented inhibitors of pro-inflammatory cytokines such as tumor necrosis factor-α (TNF-α). [10] In most human nutritional studies, the enrichment of cell membranes with omega-3 polyunsaturated fatty acids has been reported to increase the glutathione (GSH) peroxidase activity. [11] Moreover, the organic compound indole-3-carbinol, found in omega-3 fatty acids, induces CYP1A1, which hydroxylates estrogens into 2-hydroxyestrone. [12] It is advisable, therefore, that vitiligo patients avoid omega-6 lipids and use omega-3 lipids. Moreover, omega-3 fatty acids play a critical role in the development and function of the central nervous system and evidence from epidemiological, laboratory and clinical studies suggest that omega-3 fatty acids may favorably influence the vulnerability and outcome in depressive disorders. [10] This fact points further to the beneficial effect of these lipids against vitiligo, as 20% of the vitiligo patients are reported to be depressed about their illness. [12]

Mango, cashew, pistaschio, oak, cassava, areca nut, red chillies, cherry, raspberry, cranberry, blackberry and tea contain naturally occurring plant phenol and polyphenolic compounds (tannins), which may aggravate vitiligo by the mechanism outlined above. Moreover, it is reported that phenol molecules induce the release of interleukin-1α (IL-1α) and TNF-α from keratinocytes. Increased TNF-α and IL1-α levels in the lesional skin of patients with non-segmental vitiligo has been recently reported and it is suggested that these cytokines play important roles in the pathophysiology of vitiligo. [13] Additionally, tannins induce apoptosis in vitro , inhibit cellular enzymes, bind to cell membrane and make it fragile and chelate metal ions. [14] All these effects can aggravate vitiligo. The high phenol and tannin content of the foods widely consumed in India could explain why the highest incidence of vitiligo is seen in this country. [1]

Are there any beneficial foodstuffs for vitiligo patients?

As mentioned above, omega-3 fatty acids could be helpful for vitiligo patients. The potent free radical scavenging properties of carotenoids could also be harnessed to treat vitiligo.

Quercetin has been found to have strong cytoprotective effects on H 2 O 2 -induced cell death. [15] Onion and apple, the richest sources of quercetin, [16] are thus beneficial for vitiligo patients. Moreover, thiols, which are abundant in onion, exert an antioxidant activity toward superoxide anion, hydrogen peroxide and singlet oxygen. Thiols also block electrophilic metabolites and modulate several xenobiotic-metabolizing pathways. [17]

Crimini mushrooms are coffee colored and richer in flavor and nutrients than the more common white button mushroom. The range of traditional nutrients found in crimini mushrooms is impressive. Crimini mushrooms are an excellent source of selenium, riboflavin (vitamin B2), pantothenic acid (vitamin B5), niacin (vitamin B3) and copper. Five ounces of raw crimini mushrooms provide 52.6% of the daily value (DV) for selenium, 35.5% of the DV for copper, 10.0% of the DV for manganese, 40.6% of the DV for riboflavin, 21.3% of the DV for pantothenic acid and 10.4% of the DV for zinc. Selenium is a necessary cofactor of GSH peroxidase. Copper, along with manganese, is an essential cofactor of superoxide dismutase. Vitamin B2 is a cofactor for the enzyme GSH reductase, which reduces the oxidized form of GSH back to its reduced version. Notably, L-ergothioneine, a sulfur-containing amino acid synthesized by soil bacteria in fungal substrates and functioning as a powerful antioxidant, has been discovered in mushrooms. [18] L-ergothioneine scavenges superoxide and singlet oxygen and suppresses TNF-α. [19] Of the most commonly consumed mushrooms, portabellas and crimini have the most L-ergothioneine, followed by white buttons. L-ergothioneine is not destroyed when mushrooms are cooked. In a research presented at the 2005 American Chemical Society meeting in Washington, DC, an American research team revealed that mushrooms contain higher concentrations of L-ergothioneine than either of the two dietary sources previously believed to contain the most,: chicken liver and wheat germ. Mushrooms prevent circulating levels of estrogen in the body from becoming excessive. This effect appears to be accomplished through inhibition of aromatase (estrogen synthase) that is necessary for the production of estrogen. Mushrooms thus afford protection against breast cancer. [18] Crimini mushrooms could benefit vitiligo patients.

Whey, a protein complex derived from milk, is being touted as a functional food with a number of health benefits. Whey has potent antioxidant activity, mainly by contributing cysteine-rich proteins that aid in the synthesis of GSH. Cysteine contains a thiol (sulfhydryl) group that serves as an active reducing agent in preventing oxidation and tissue damage. Lactoferrin, an iron-binding glycoprotein found in whey, is a non-enzymatic antioxidant and anti-inflammatory agent. A mouse study revealed the ability of lactoferrin to downregulate levels of TNF-α and IL-6, [20] which are supposed to be involved in the pathogenesis of vitiligo. [21] Lactoperoxidase, an important enzyme in the whey fraction of milk, has the ability to catalyze certain molecules, including the reduction of hydrogen peroxide. Alpha-lactalbumin, also found in whey, can chelate heavy metals and reduce oxidative stress because of its iron-chelating properties. Whey also has GSH peroxidase activity. [20] Given these facts, vitiligo patents can gain benefit by consuming whey. Interestingly, human studies demonstrated that whey protein improved cognitive function and coping ability in highly stressed individuals. A rise in serotonin is thought to improve adaptation to stress and the authors proposed that tryptophan available in whey provides a substrate to increase brain serotonin levels.[22] This fact points further to the benefit of whey for vitiligo patients, given the important role of stress in the exacerbation of vitiligo and the stress produced by the disorder itself.

 
  References Top

1.Sehgal VN, Srivastava G. Vitiligo: Compendium of clinico-epidemiological features. Indian J Dermatol Venereol Leprol 2007;73:149-56.  Back to cited text no. 1  [PUBMED]  Medknow Journal
2.Westerhof W, d′Ischia M. Vitiligo puzzle: The pieces fall in place. Pigment Cell Res 2007;20:345-59.  Back to cited text no. 2  [PUBMED]  [FULLTEXT]
3.Namazi MR. Neurogenic dysregulation, oxidative stress, autoimmunity, and melanocytorrhagy in vitiligo: Can they be interconnected? Pigment Cell Res 2007;20:360-3.  Back to cited text no. 3  [PUBMED]  [FULLTEXT]
4.Ackerman LS. Sex hormones and the genesis of autoimmunity. Arch Dermatol 2006;142:371-6.  Back to cited text no. 4  [PUBMED]  [FULLTEXT]
5.Koshevenko IN. Alpha-tocopherol in the combined treatment of vitiligo. Vestnik Dermatologii I Venerologii (Moskva) 1989;10:70-2.  Back to cited text no. 5    
6.Mandel ASH, Haberman HF, Powlowski D, Goldstein E. Non PUVA non surgical therapies for vitiligo. Clin Dermatol 1997;15:907-19.  Back to cited text no. 6    
7.Picardo M, Camera E, Maresca V, Pittarello A, Feonetti F, Passi S. Antioxidant treatment in vitiligo? Pigment Cell Res 1997;10:360.  Back to cited text no. 7    
8.Bickers RD, Athar M. Oxidative stress in the pathogenesis of skin disease. J Invest Dermatol 2006;126:2565-75.  Back to cited text no. 8    
9.Fernandez G. Dietary lipids and risk of autoimmune disease. Clin Immunol Immunopathol 1994;72:193-7.  Back to cited text no. 9    
10.Logan AC. Omega-3 fatty acids and major depression: A primer for the mental health professional. Lipids Health Dis 2004;3:25.  Back to cited text no. 10  [PUBMED]  [FULLTEXT]
11.Joulain C, Prigent AF, Nιmoz G, Lagarde M. Increased glutathione peroxidase activity in human blood mononuclear cells upon in vitro incubation with n-3 fatty acids. Biochem Pharmacol 1994;47:1315-23.  Back to cited text no. 11    
12.Namazi MR. Prescribing cyclic antidepressants for vitiligo patents, which agenrs are superior, which are not? Psychether Psychosom 2003;72:361-2.  Back to cited text no. 12    
13.Birol A, Kisa U, Kurtipek GS, Kara F, Kocak M, Erkek E, Caglayan O. Increased tumor necrosis factor alpha (TNF-alpha) and interleukin 1 alpha (IL1-alpha) levels in the lesional skin of patients with nonsegmental vitiligo. Int J Dermatol. 2006;45:992-3.  Back to cited text no. 13    
14.Tur E, Brenner S. The role of the water system as an exogenous factor in pemphigus. Int J Dermatol 1997;36:810-6.  Back to cited text no. 14    
15.Jeong YM, Choi YG, Kim DS, Park SH, Yoon JA, Kwon SB, et al . Cytoprotective effect of green tea extract and quercetin against hydrogen peroxide-induced oxidative stress. Arch Pharm Res 2005;28:1251-6  Back to cited text no. 15  [PUBMED]  
16.Kakar AK, Shahzad M, Haroon TS. Keloids: Clinical features and management. J Pak Assoc Dermatol 2006;16:163-73.  Back to cited text no. 16    
17.De Flora S, Izzotti A, D′Agostini F, Cesarone CF. Antioxidant activity and other mechanisms of thiols involved in chemoprevention of mutation and cancer. Am J Med 1991;91:122S-30S.  Back to cited text no. 17  [PUBMED]  
18.George Mateljan Foundation. Mushrooms, Crimini. Available from: http://www.whfoods.com/genpage.php?tname=foodspice&dbid=97. [Last accessed on January 31, 2009]  Back to cited text no. 18    
19.Obayashi K, Kurihara K, Okano Y, Masaki H, Yarosh DB. L-Ergothioneine scavenges superoxide and singlet oxygen and suppresses TNF-alpha and MMP-1 expression in UV-irradiated human dermal fibroblasts. J Cosmet Sci 2005;56:17-27.  Back to cited text no. 19  [PUBMED]  
20.Marshal K. Therapeutic applications of Whey protein. Altern Med Rev 2004;2:136-56.  Back to cited text no. 20    
21.Tu CX, Gu JS, Lin XR. Increased interleukin-6 and granulocyte-macrophage colony stimulating factor levels in the sera of patients with non-segmental vitiligo. J Dermatol Sci 2003;31:73-8.  Back to cited text no. 21  [PUBMED]  [FULLTEXT]
22.Marcus CR, Olivier B, de Haan EH. Whey protein rich in alpha-lactalbumin increases the ratio of plasma tryptophan to the sum of the other large neutral amino acids and improves cognitive performance in stress-vulnerable subjects. Am J Clin Nutr 2002;75:1051-6.  Back to cited text no. 22    



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