Food as Medicine in Context of COVID 19: Concept of Rainbow Diet
DOI:
https://doi.org/10.21048/IJND.2021.58.2.25908Keywords:
Food, Immunity, Herbs, Nutraceuticals, Functional Food, Rainbow DietAbstract
Food is like fuel for our body. It is said that if we eat proper food no medicine will be required. If we don't eat proper food no medicine will act. A close relationship exists between the immune state and occurrences of diseases. Low immune function of an individual results in poor health but also prevents recovery. The enhancement of host immune response has been recognised as a possible means of defence against pathogen attack. Immunomodulation through natural substances, i.e. our food and food supplement through herbs may be considered as complimentary for the prevention and cure of diseases as food after all is the best medicine for our body. Traditionally, our food includes a large number of immunity boosters such as milk, spices like garlic, onion, turmeric, ginger and black pepper, vegetables such as drum stick, cucumber, carrot and red capsicum, mushroom, cabbage, cauliflower, spinach, peas, fruits like pine apple, watermelon and other with vitamin C, herbs like tulsi, amla, lemon, etc. Grains and seeds such as pumpkin and flaxseed which are enriched with immunity booster minerals like zinc and selenium and omega-3 fatty acids have been parts of our traditional food. Pulses such as lentil and soybean, egg and cheese are also good source of immunomodulating substances. Herbs under the category "Rasayana” in Ayurveda such as Ashwagandha, Giloe, Shatavari, etc. are being prescribed as immunomodulator since ancient time.
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Accepted 2021-04-12
Published 2021-05-18
References
Delwart, E. Scientist, 2016. https://www.the-scientist.com/features/virusesof the humanbody. Accessed on April 27, 2020.
Howard, C.R. and Fletcher, N.F. Emerging virus diseases: Can we ever expect the unexpected? Em. Microb. Infect., 2012, 1, 1-11. DOI: 10.1038/emi.2012.47 DOI: https://doi.org/10.1038/emi.2012.47
Woolhouse, M.E. and Gowtage-Sequeria, S. Host range and emerging and reemerging pathogens. Emerg. Infect. Dis., 2005, 11, 1842-1847. doi: 10.3201/eid1112.050997 DOI: https://doi.org/10.3201/eid1112.050997
Watanabe, K., Takatsuki, H., Sonoda, M., Tamura, S., Murakami, N. and Kobayashi, N. Antiinfluenza viral effects of novel nuclear export inhibitors from Valerianae Radix and Alpinia galangal. Drug Discoveries & Therapeutics, 2011, 5, 26-31. DOI: 10.5582/ddt.v5.1.26 DOI: https://doi.org/10.5582/ddt.v5.1.26
Nanjan, M.J. The Role of Natural Products In Drug Discover. In: Souvenier and Abstracts International Symposium on Medicinal Plants and Herbal Drugs in Human and Livestock Wealth A Global Prospective.2016, Chennai, pp. 13-14.
Sultan, M.T., Butt, M.S., Qayyum, M.M.N and Suleria, H.A.R. Immunity: Plants as effective mediators. Cric Rev. Fd. Sci. Nutr., 2014, 54, 1298-1308. https://doi.org/10.1080/10408398.20 11.633249 DOI: https://doi.org/10.1080/10408398.2011.633249
Bourgeon, S., Raclot, T., Le Maho, Y., Ricquier, D. and Criscuolo, F. Innate immunity, assessed by plasma NO measurements, is not suppressed during the incubation fast in eiders. Dev. Comp. Immunol., 2007, 31, 720-728. https://doi.org/10.1016/j.dci.2006.11.009 DOI: https://doi.org/10.1016/j.dci.2006.11.009
Butt, M.S. and Sultan, M.T. Green tea: Nature's defense against malignancies. Cri. Rev. Fd. Sci. Nutr., 2009, 49, 463-473.doi: 10.1080/10408390802145310 DOI: https://doi.org/10.1080/10408390802145310
Chaouat, G., Ledee-Bataille, N. and Dubanchet, S. Immune cells in uteroplacental tissues throughout pregnancy: A brief review. Reprod. Biomed. Online., 2007, 14, 256-266. DOI: 10.1016/s1472-6483(10)60796-1 DOI: https://doi.org/10.1016/S1472-6483(10)60796-1
Chanana, V., Majumdar, S. and Rishi, P. Involvement of caspase-3, lipid peroxidation and TNF-α in causing apoptosis of macrophages by coordinately expressed Salmonella phenotype under stress conditions. Mol. Immunol., 2007, 44, 1551-1558. https://doi.org/10.1016/j.molimm.2006.08.022 DOI: https://doi.org/10.1016/j.molimm.2006.08.022
Zhang, T., Li, Y., Wang, Y-J., Wang, X., Young, M, Douglas, S.D., Ho, W-Z. Natural killer cell inhibits human immunodeficiency virus replication in chronically infected immune cells. Antiviral Res., 73, 2007, 132-139. https://doi.org/10.1016/j.antiviral.2006.08.006 DOI: https://doi.org/10.1016/j.antiviral.2006.08.006
Cooper, M.D. and Alder, M.N. The evolution of adaptive immune systems. Cell, 2006, 124, 815822. DOI: 10.1016/j.cell.2006.02.001 DOI: https://doi.org/10.1016/j.cell.2006.02.001
Li, S., Yao, X., Liu, H., Li, J. and Fan, B. Prediction of T-cell epitopes based on least squares support vector machines and amino acid properties. Analytica Chimica Acta, 2007,584, 37-42. https://doi.org/10.1016/j.aca.2006.11.037 DOI: https://doi.org/10.1016/j.aca.2006.11.037
Currier, N.L. and Miller, S.C. The effect of immunization with killed tumor cells, with/without feeding of Echinacea purpurea in an erythroleukemic mouse model. J. Alter. Complem. Med., 2002, 8, 49-58.https://doi.org/10.1089/107555302753507177 DOI: https://doi.org/10.1089/107555302753507177
Fauci, A.S., Mavilio, D. and Kottilil, S. NK cells in HIV infection: Paradigm for protection or targets for ambush. Nat. Rev. Immunol., 2005, 5, 835-843. DOI: 10.1038/nri1711 DOI: https://doi.org/10.1038/nri1711
Timar, K.K., Dallos, A., Kiss, M., Huzz, S., Bos, J.D. and Asghar, S.S. Expression of terminal complement components by human keratinocytes. Mol. Immunol., 2007, 44, 2578-2586. https:// doi.org/10.1016/j.molimm.2006.12.014 DOI: https://doi.org/10.1016/j.molimm.2006.12.014
Childs, C.E., Calder, P.C. and Miles, E.A. Diet and immune function. Nutr., 2019, 11, 1933. doi: 10.3390/nu11081933 DOI: https://doi.org/10.3390/nu11081933
London, C., Functional foods that boost the immune system. Functional Food Product Development (Ed. Jim Smith and Edward Charter), Blackwell Publishing, 2010, pp. 295-325. DOI: https://doi.org/10.1002/9781444323351.ch14
Akrami, R., Gharaei, A., Mansour, M.R. and Galeshi, A. Effects of dietary onion (Allium cepa) powder on growth, innate immune response and hemato-biochemical parameters of beluga (Huso huso Linnaeus, 1754) juvenile. Fish and Selfish Immunol., 2015, 45, 828-834. https://doi.org/10.1016/j.fsi.2015.06.005. DOI: https://doi.org/10.1016/j.fsi.2015.06.005
Wilson, E.A. and Demmig-Adams, B. Antioxidant, anti-inflammatory and antimicrobial properties of garlic and onions. Nutr. Fd. Sci, 2007, 37, 178-183. DOI: 10.1108/00346650710749071 DOI: https://doi.org/10.1108/00346650710749071
Bhattacharya, M., Girish, G.V., Karmohapatra, S.K., Samad, S.A. and Sinha, A.K. Systemic production of IFN-α by Garlic (Allium Sativum) in humans. J. Interfer. Cytok. Res., 27, 377-382. https://doi.org/10.1089/jir.2006.0124 DOI: https://doi.org/10.1089/jir.2006.0124
Podlogar, J.A. and Verspohl, E.J. Antiinflammatory effects of ginger and some of its components in human bronchial epithelial (BEAS-2B) cells. Phytother. Res., 2012, 26, 333-336. https://doi.org/10.1002/ptr.3558 DOI: https://doi.org/10.1002/ptr.3558
King, J.C. Zinc: an essential but elusive nutrient. Am. J. Clin. Nutr., 2011, 94, 679S-84S. doi:10.3945/ajcn.110.005744 DOI: https://doi.org/10.3945/ajcn.110.005744
Haase, H., Mocchegiani, E. and Rink, L. Correlation between zinc status and immune function in the elderly. Biogerontol., 2006, 7, 421-428. DOI: 10.1007/s10522-006-9057-3. DOI: https://doi.org/10.1007/s10522-006-9057-3
Saunders, A.V., Craig, W.J. and Baines, S.K. Zinc and vegetarian diets. Med. J. Aust., 2013, 199, 17-21. doi: 10.5694/mja11.11493 DOI: https://doi.org/10.5694/mjao11.11493
Rose, T. Vitamins and Minerals (How to get the nutrients Your Body Needs). Bounty Books, London.
Suresh, K. and Vasudevan, D.M. Augmentation of murine natural killer cell and antibody dependent cellular cytotoxicity activities by Phyllanthus emblica, a new immunomodulator. J. Ethnopharmacol., 1994, 44, 55-60. DOI: 10.1016/0378-8741(94)90099-x DOI: https://doi.org/10.1016/0378-8741(94)90099-X
Liu, X., Zhao, M., Wu, K, Chai, X., Yu, H., Tao, Z. and Wang, J. Immunomodulatory and anticancer activities of phenolics from emblica fruit (Phyllanthus emblica L.). Fd. Chem., 2012, 131, 685-690. DOI: 10.1016/j.foodchem.2011.09.063 DOI: https://doi.org/10.1016/j.foodchem.2011.09.063
Kim, H. Glutamine as an immunonutrient. Yonsei. Med. J., 2011, 52, 892-897. doi: 10.3349/ ymj.2011.52.6.892 DOI: https://doi.org/10.3349/ymj.2011.52.6.892
Lacey, J.M. and Wilmore, D.W. Is glutamine a conditionally essential amino acid? Nutr. Rev., 1990, 48, 297-309. https://doi.org/10.1111/j.1753-4887.1990.tb02967.x DOI: https://doi.org/10.1111/j.1753-4887.1990.tb02967.x
Calder, P.C. and Yaqoob, P. Glutamine and the immune system. Amino Acids, 1999, 17, 227241. https://doi.org/10.1007/BF01366922 DOI: https://doi.org/10.1007/BF01366922
Huang, Y., Shao, X.M. and Neu, J. Immunonutrients and neonates. Eur. J. Ped., 2003, 162,122128. https://doi.org/10.1007/s00431-002-1128-0 DOI: https://doi.org/10.1007/s00431-002-1128-0
Lenders, C.M., Liu, S., Wilmore, D.W., Sampson, L., Dougherty, L.W., Spiegelman, D. and Willett, W.C. Evaluation of a novel food composition database that includes glutamine and other amino acids derived from gene sequencing data. Eur. J. Clin. Nutr., 2009, 63, 1433-1439. https://doi.org/10.1038/ejcn.2009.110 DOI: https://doi.org/10.1038/ejcn.2009.110
Efron, D.T., Kirk, S.J., Regan, M.C., Wasserkrug, H.L. and Barbul, A. Nitric oxide generation from L-arginine is required for optimal human peripheral blood lymphocyte DNA synthesis. Surgery, 1991, 110, 327-334.
Tong, B.C. and Barbul, A. Cellular and physiological effects of arginine. Mini. Rev. Med. Chem., 2004, 4, 823-832. DOI: 10.2174/1389557043403305 DOI: https://doi.org/10.2174/1389557043403305
Ros, E. Nuts and CVD. Br. J. Nutr., 2015, 113, 111-120. DOI: 10.1017/S0007114514003924 DOI: https://doi.org/10.1017/S0007114514003924
Albaugh, V.L. and Barbul, A. Reference Module in Life Science 2017.
Carver, J.D. The role of nucleotides in human nutrition. J. Nutr., 1994, 124, 144-148. https://doi.org/10.1016/0955-2863(94)00019-I DOI: https://doi.org/10.1016/0955-2863(94)00019-I
Schloerb, P.R. Immune-enhancing diets: products, components, and their rationales. J. Parent. Enteral Nutr., 2001, 25, 3-7. DOI: 10.1177/014860710102500202 DOI: https://doi.org/10.1177/014860710102500202
Bagwe, S., Tharappel, L.J.P., Kaur, G. and Buttar, H.S. Bovine colostrum: an emerging nutraceutical. J. Compl. Integr. Med., 2015, 12, 175-185. doi:10.1515/jcim-2014-0039 DOI: https://doi.org/10.1515/jcim-2014-0039
Vanderpool, C., Yan, F. and Polk, D.B. Mechanisms of probiotic action: Implications for therapeutic applications in inflammatory bowel diseases. Inflamm. Bowel Dis., 2008, 14, 15851596. DOI: 10.1002/ibd.20525. DOI: https://doi.org/10.1002/ibd.20525
Yan, F. and Polk, D.B. Probiotics: progress toward novel therapies for intestinal diseases. Curr. Opin. Gastroenterol., 2010, 26, 95-101. doi: 10.1097/MOG.0b013e328335239a DOI: https://doi.org/10.1097/MOG.0b013e328335239a
Nakashima, Yamada, K., Iwata, O., Sugimoto, R., Atsuji, K., Ogawa, T., Ohgo, N.I. and Suzuki, K. β-Glucan in foods and its physiological functions. J. Nutr. Sci. Vitaminol., 2018, 64, 8-17. DOI: 10.3177/jnsv.64.8 DOI: https://doi.org/10.3177/jnsv.64.8
Patwardhan, B., Kalbag, D., Patki, P.S. and Nagsampagi, B.A. Search of immunomodulatory agents: a review. Ind. Drugs, 1990, 28, 56-63.
Sharma, U., Bala, B., Kumar, N., Singh, B., Munshi, R.K. and Bhalerao, S. Immunomodulatory active compounds from Tinospora cordifolia. J. Ethnopharmacol., 2012, 141, 918-926. https://doi.org/10.1016/j.jep.2012.03.027 DOI: https://doi.org/10.1016/j.jep.2012.03.027
Chauhan, N.S., Saraf, D.K. and Dixit, V.K. Effect of vajikaran rasayana herbs on pituitary– gonadal axis. Eur. J. Integr. Med., 2010, 2, 89-91. doi:10.1016/j.eujim.2010.03.002 DOI: https://doi.org/10.1016/j.eujim.2010.03.002
Galloway, T.S. and Depledge, M.H. Immunotoxicity in invertebrates: Measurement and ecotoxicological relevance. Ecotoxicol., 2001, 10, 5-23. DOI: 10.1023/a:1008939520263 DOI: https://doi.org/10.1023/A:1008939520263
Harikrishnan, R., Balasundaram, C., Jawahar, S. and Heo, M.S. Immunomodulatory effect of Withania somnifera supplementation diet in the giant freshwater prawn Macrobrachium rosenbergii (de Man) against Aeromonas hydrophila. Fish Shellfish Immunol., 2012, 32, 94100. DOI: 10.1016/j.fsi.2011.10.027 DOI: https://doi.org/10.1016/j.fsi.2011.10.027
Rasool, M. and Varalakshmi, P. Immunomodulatory role of Withania somnifera root powder on experimental induced inflammation: An in vivo and in vitro study. Vasc. Pharmacol., 2006, 44, 406-410. https://doi.org/10.1016/j.vph.2006.01.015 DOI: https://doi.org/10.1016/j.vph.2006.01.015
Gautam, M., Saha, S., Bani, S., Kaul, A., Mishra, S., Patil, D., Satti, N.K., Suri, K.A., Gairola, S., Suresh, K., Jadhav, S., Qazi, G.N. and Patwardhan, B. Immunomodulatory activity of Asparagus racemosus on systemic Th1/Th2 immunity: Implications for immunoadjuvant potential. J. Ethnopharmacol, 2009, 121, 241-247. doi:10.1016/j.jep.2008.10.028 DOI: https://doi.org/10.1016/j.jep.2008.10.028
Abbas, A.K., Murphy, K.M. and Sher, A. Functional diversity of helper T lymphocytes. Nature, 1996, 383, 787-793. https://doi.org/10.1038/383787a0 DOI: https://doi.org/10.1038/383787a0
Warren, H.S., Vogel, F.R. and Chedid, L.A. Current status of immunological adjuvants. Ann. Rev. Immunol., 1986, 4, 369-388. DOI: https://doi.org/10.1146/annurev.iy.04.040186.002101
Zeinalian, M., Eshaghi, M., Hadian, M., Naji, H., Marandi, S.M.M.M and Asgary, S., Personalized nutrition: an ancient concept in Iranian traditional medicine. Int. J. Preven. Med., 2017
Ramaswamy, J. https://www.thehindu.com/sci-tech/health/diet-and-nutrition/try-therainbowdiet/article3527256.
Roller, M., Clune, Y., Collins, K., Rechkemmer, G and Watzl, B. Consumption of prebiotic inulin enriched with oligofructose in combination with the probiotics Lactobacillus rhamnosus and Bifidobacterium lactis has minor effects on selected immune parameters in polypectomised and colon cancer patients. Br. J. Nur., 2007, 97, 676-684. DOI: 10.1017/S0007114507450292. DOI: https://doi.org/10.1017/S0007114507450292