Abstract
Plants and minerals have been used since ancient times for the treatment of many ailments and diseases. Most were used for mystical reasons and others relied on the “doctrine of signatures”, which stated that the shape of the plant reflected its potential medicinal use. The root of the mandrake or ginseng, for instance, is shaped like that of the human body and has been used as a general tonic for a variety of illnesses [1]. It is claimed by herbalists to have immunostimulant properties. Siberian ginseng or Taiga root (Eleutherococcus senticosus) is also used as a tonic and has been reported to exhibit immunostimulatory properties. The pharmacological bases of these actions are unclear, so these plant medicines cannot be considered unequivocally as immunostimulants.
Final manuscript submitted on December 09, 2016.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Selected Readings
Barrett B. Medicinal properties of Echinacea: a critical review. Phytomedicine. 2003;10:66–86.
Firuzi O, Miri R, Tavakkoli M, Saso L. Antioxidant therapy: current status and future prospects. Curr Med Chem. 2011;18(25):3871–88.
Garcıa-Lafuente A, Guillamon E, Villares A, Rostagno MA, Martınez JA. Flavonoids as anti-inflammatory agents: implications in cancer and cardiovascular disease. Inflamm Res. 2009;58:537–52.
Kotsirilos V, Vitetta L, Sali A. A guide to evidence-based integrative and complementary medicine. Australia: Churchill Livingstone - Elsevier; 2011.
Maggini S, Wintergerst ES, Beveridge S, Hornig DH. Selected vitamins and trace elements support immune function by strengthening epithelial barriers and cellular and humoral immune responses. Br J Nutr. 2007;98(Suppl 1):S29–35.
Roxas M, Jurenka J. Colds and influenza: a review of diagnosis and conventional, botanical, and nutritional considerations. Altern Med Rev. 2007;12:25–48.
Saso L, Firuzi O. Pharmacological applications of antioxidants: lights and shadows. Curr Drug Targets. 2014;15(13):1177–99.
Important Websites
American Dietetic Association. www.eatright.org.
Memorial Sloan-Kettering Cancer Center. About herbs, botanicals and other products. www.mskcc.org/aboutherbs.
Natural Standard. US database containing evidence-based information about complementary and alternative therapies. www.naturalstandard.com.
Positive Health. Complementary Medicine Magazine. www.positivehealth.com/permit/Articles/Nutrition.
World Health Organization. Vitamin and mineral nutrition information system. www.who.int/vmnis/en/.
References
Leake CD. An historical account of pharmacology to the twentieth century. Springfield, IL: Charles C. Thomas; 1975.
Bast A. Ten misconceptions about antioxidants. Trends Pharmacol Sci. 2013;34(8):430–6.
Samadi AK, Bilsland A, Georgakilas AG, Amedei A, Amin A, Bishayee A, et al. A multi-targeted approach to suppress tumor-promoting inflammation. Semin Cancer Biol. 2015;35(Suppl):S151–84.
Foster S. Echinacea. Nature’s immune enhancer. Rochester: Healing Arts Press; 1991.
Gilroy CM, Steiner JF, Byers T, Shapiro H, Georgian W. Echinacea and truth in labeling. Arch Intern Med. 2003;163(6):699.
Bauer R, Wagner H. Echinacea. Handbuch fur Ärzte, Apotheker und andere Naturwissenschaftler. Stuttgart: Wissenschaftliche; 1990.
Woelkart K, Bauer R. The role of alkamides as an active principle of echinacea. Planta Med. 2007;73(7):615–23.
Zhai Z, Liu Y, Wu L, Senchina DS, Wurtele ES, Murphy PA, et al. Enhancement of innate and adaptive immune functions by multiple Echinacea species. J Med Food. 2007;10(3):423–34.
Dong G-C, Chuang P-H, Chang K, Jan P, Hwang P-I, Wu H-B, et al. Blocking effect of an immuno-suppressive agent, cynarin, on CD28 of T-cell receptor. Pharm Res. 2009;26(2):375–81.
Jager H, Meinel L, Dietz B, Lapke C, Bauer R, Merkle HP, et al. Transport of alkamides from Echinacea species through Caco-2 monolayers. Planta Med. 2002;68(5):469–71.
Guiotto P, Woelkart K, Grabnar I, Voinovich D, Perissutti B, Invernizzi S, et al. Pharmacokinetics and immunomodulatory effects of phytotherapeutic lozenges (bonbons) with Echinacea purpurea extract. Phytomedicine. 2008;15(8):547–54.
Dall’Acqua S, Perissutti B, Grabnar I, Farra R, Comar M, Agostinis C, et al. Pharmacokinetics and immunomodulatory effect of lipophilic Echinacea extract formulated in softgel capsules. Eur J Pharm Biopharm. 2015;97(Pt A):8–14.
Parnham MJ. Benefit-risk assessment of the squeezed sap of the purple coneflower (Echinacea purpurea) for long-term oral immunostimulation. Phytomedicine. 1996;3(1):95–102.
Hoheisel O, Sandberg M, Bertram S, Bulitta M, Schafer M. Echinagard® treatment shortens the course of the common cold: a double-blind, placebo-controlled clinical trial. Eur J Clin Res. 1997;9:261–8.
Roxas M, Jurenka J. Colds and influenza: a review of diagnosis and conventional, botanical, and nutritional considerations. Altern Med Rev. 2007;12(1):25–48.
Karsch-Völk M, Barrett B, Kiefer D, Bauer R, Ardjomand-Woelkart K, Linde K. Echinacea for preventing and treating the common cold. Cochrane Database Syst Rev. 2014;(2):CD000530.
Brendler T, van Wyk B-E. A historical, scientific and commercial perspective on the medicinal use of Pelargonium sidoides (Geraniaceae). J Ethnopharmacol. 2008;119(3):420–33.
Kolodziej H. Fascinating metabolic pools of Pelargonium sidoides and Pelargonium reniforme, traditional and phytomedicinal sources of the herbal medicine Umckaloabo. Phytomedicine. 2007;14(Suppl 6):9–17.
Kolodziej H, Kayser O, Radtke OA, Kiderlen AF, Koch E. Pharmacological profile of extracts of Pelargonium sidoides and their constituents. Phytomedicine. 2003;10(Suppl 4):18–24.
Kolodziej H, Kiderlen AF. In vitro evaluation of antibacterial and immunomodulatory activities of Pelargonium reniforme, Pelargonium sidoides and the related herbal drug preparation EPs 7630. Phytomedicine. 2007;14(Suppl 6):18–26.
Thäle C, Kiderlen A, Kolodziej H. Anti-infective mode of action of EPs 7630 at the molecular level. Planta Med. 2008;74(6):675–81.
Conrad A, Hansmann C, Engels I, Daschner FD, Frank U. Extract of Pelargonium sidoides (EPs 7630) improves phagocytosis, oxidative burst, and intracellular killing of human peripheral blood phagocytes in vitro. Phytomedicine. 2007;14(Suppl 6):46–51.
Dickersin K, Li T. Surgery for nonarteritic anterior ischemic optic neuropathy. Cochrane Database Syst Rev. 2015;(3):CD001538.
Koch E, Biber A. Treatment of rats with the Pelargonium sidoides extract EPs 7630 has no effect on blood coagulation parameters or on the pharmacokinetics of warfarin. Phytomedicine. 2007;14(Suppl 6):40–5.
Holtskog R, Sandvig K, Olsnes S. Characterization of a toxic lectin in Iscador, a mistletoe preparation with alleged cancerostatic properties. Oncology. 1988;45(3):172–9.
Eck J, Langer M, Möckel B, Witthohn K, Zinke H, Lentzen H. Characterization of recombinant and plant-derived mistletoe lectin and their B-chains. Eur J Biochem. 1999;265(2):788–97.
Joller PW, Menrad JM, Schwarz T, Pfüller U, Parnham MJ, Weyhenmeyer R, et al. Stimulation of cytokine production via a special standardized mistletoe preparation in an in vitro human skin bioassay. Arzneimittelforschung. 1996;46(6):649–53.
Beuth J, Ko HL, Gabius HJ, Burrichter H, Oette K, Pulverer G. Behavior of lymphocyte subsets and expression of activation markers in response to immunotherapy with galactoside-specific lectin from mistletoe in breast cancer patients. Clin Investig. 1992;70(8):658–61.
Kienle GS, Glockmann A, Schink M, Kiene H. Viscum album L. extracts in breast and gynaecological cancers: a systematic review of clinical and preclinical research. J Exp Clin Cancer Res. 2009;28:79.
Zwierzina H, Bergmann L, Fiebig H, Aamdal S, Schöffski P, Witthohn K, et al. The preclinical and clinical activity of aviscumine: a potential anticancer drug. Eur J Cancer. 2011;47(10):1450–7.
Walzel H, Jonas L, Rosin T, Brock J. Relationship between internalization kinetics and cytotoxicity of mistletoe lectin I to L1210 leukaemia cells. Folia Biol (Praha). 1990;36(3–4):181–8.
Mulsow K, Enzlein T, Delebinski C, Jaeger S, Seifert G, Melzig MF. Impact of mistletoe triterpene acids on the uptake of mistletoe lectin by cultured tumor cells. PLoS One. 2016;11(4):e0153825.
Bergmann L, Aamdal S, Marreaud S, Lacombe D, Herold M, Yamaguchi T, et al. Phase I trial of r viscumin (INN: aviscumine) given subcutaneously in patients with advanced cancer: a study of the European Organisation for Research and Treatment of Cancer (EORTC protocol number 13001). Eur J Cancer. 2008;44(12):1657–62.
Horneber MA, Bueschel G, Huber R, Linde K, Rostock M. Mistletoe therapy in oncology. Cochrane Database Syst Rev. 2008;(2):CD003297.
Mistletoe Extracts (PDQ®): Complementary and alternative medicine - Patient Information [NCI]-Questions and Answers About Mistletoe. 2016. http://www.webmd.com/cancer/tc/mistletoe-extracts-pdq-complementary-and-alternative-medicine%2D%2D-patient-information-nci-questions-and-answers-about-mistletoe.
Habeck M. Mistletoe compound enters clinical trials. Drug Discov Today. 2003;8(2):52–3.
Sandstead HH. Understanding zinc: recent observations and interpretations. J Lab Clin Med. 1994;124(3):322–7.
Institute of Medicine, Food and Nutrition Board. Dietary reference intakes for vitamin A, vitamin K, arsenic, boron, chromium, copper, iodine, iron, manganese, molybdenum, nickel, silicon, vanadium, and zinc. Washington, DC: National Academies Press; 2001.
Shankar AH, Prasad AS. Zinc and immune function: the biological basis of altered resistance to infection. Am J Clin Nutr. 1998;68(2 Suppl):447S–63S.
Reinhold D, Ansorge S, Grüngreiff K. Immunobiology of zinc and zinc therapy. Immunol Today. 1999;20(2):102–3.
Lin RS, Rodriguez C, Veillette A, Lodish HF. Zinc is essential for binding of p56(lck) to CD4 and CD8alpha. J Biol Chem. 1998;273(49):32878–82.
Black RE. Therapeutic and preventive effects of zinc on serious childhood infectious diseases in developing countries. Am J Clin Nutr. 1998;68(2 Suppl):476S–9S.
Mocchegiani E, Verbanac D, Santarelli L, Tibaldi A, Muzzioli M, Radosevic-Stasic B, et al. Zinc and metallothioneins on cellular immune effectiveness during liver regeneration in young and old mice. Life Sci. 1997;61(12):1125–45.
Mocchegiani E, Muzzioli M, Cipriano C, Giacconi R. Zinc, T-cell pathways, aging: role of metallothioneins. Mech Ageing Dev. 1998;106(1–2):183–204.
Sandstead HH. Requirements and toxicity of essential trace elements, illustrated by zinc and copper. Am J Clin Nutr. 1995;61(3 Suppl):621S–4S.
Sharif R, Thomas P, Zalewski P, Fenech M. Zinc deficiency or excess within the physiological range increases genome instability and cytotoxicity, respectively, in human oral keratinocyte cells. Genes Nutr. 2012;7(2):139–54.
Haase H, Rink L. The immune system and the impact of zinc during aging. Immun Ageing. 2009;6:9.
Mocchegiani E, Giacconi R, Cipriano C, Malavolta M. NK and NKT cells in aging and longevity: role of zinc and metallothioneins. J Clin Immunol. 2009;29(4):416–25.
Mocchegiani E, Costarelli L, Giacconi R, Malavolta M, Basso A, Piacenza F, et al. Micronutrient-gene interactions related to inflammatory/immune response and antioxidant activity in ageing and inflammation. A systematic review. Mech Ageing Dev. 2014;136–137:29–49.
Hooper PL, Visconti L, Garry PJ, Johnson GE. Zinc lowers high-density lipoprotein-cholesterol levels. JAMA. 1980;244(17):1960–1.
Reeves MA, Hoffmann PR. The human selenoproteome: recent insights into functions and regulation. Cell Mol Life Sci. 2009;66(15):2457–78.
Brown KM, Arthur JR. Selenium, selenoproteins and human health: a review. Public Health Nutr. 2001;4(2B):593–9.
Finch JM, Turner RJ. Effects of selenium and vitamin E on the immune responses of domestic animals. Res Vet Sci. 1996;60(2):97–106.
Bosschaerts T, Guilliams M, Noel W, Hérin M, Burk RF, Hill KE, et al. Alternatively activated myeloid cells limit pathogenicity associated with African trypanosomiasis through the IL-10 inducible gene selenoprotein P. J Immunol. 2008;180(9):6168–75.
Barrett CW, Short SP, Williams CS. Selenoproteins and oxidative stress-induced inflammatory tumorigenesis in the gut. Cell Mol Life Sci. 2017;74(4):607–16. http://www.ncbi.nlm.nih.gov/pubmed/27563706
Urban T, Jarstrand C. Selenium effects on human neutrophilic granulocyte function in vitro. Immunopharmacology. 1986;12(2):167–72.
Reinhold U, Pawelec G, Enczmann J, Wernet P. Class-specific effects of selenium on PWM-driven human antibody synthesis in vitro. Biol Trace Elem Res. 1989;20(1–2):45–58.
Bonomini M, Forster S, De Risio F, Rychly J, Nebe B, Manfrini V, et al. Effects of selenium supplementation on immune parameters in chronic uraemic patients on haemodialysis. Nephrol Dial Transplant. 1995;10(9):1654–61.
Broome CS, McArdle F, Kyle JAM, Andrews F, Lowe NM, Hart CA, et al. An increase in selenium intake improves immune function and poliovirus handling in adults with marginal selenium status. Am J Clin Nutr. 2004;80(1):154–62.
Leist M, Maurer S, Schultz M, Elsner A, Gawlik D, Brigelius-Flohé R. Cytoprotection against lipid hydroperoxides correlates with increased glutathione peroxidase activities, but not selenium uptake from different selenocompounds. Biol Trace Elem Res. 1999;68(2):159–74.
Suzuki KT, Ishiwata K, Ogra Y. Incorporation of selenium into selenoprotein P and extracellular glutathione peroxidase: HPLC-ICPMS data with enriched selenite. Analyst. 1999;124(12):1749–53.
Bügel S, Larsen EH, Sloth JJ, Flytlie K, Overvad K, Steenberg LC, et al. Absorption, excretion, and retention of selenium from a high selenium yeast in men with a high intake of selenium. Food Nutr Res 2008;52. https://doi.org/10.3402/fnr.v52i0.1642
Hoffmann PR, Berry MJ. The influence of selenium on immune responses. Mol Nutr Food Res. 2008;52(11):1273–80.
Peretz A, Nève J, Desmedt J, Duchateau J, Dramaix M, Famaey JP. Lymphocyte response is enhanced by supplementation of elderly subjects with selenium-enriched yeast. Am J Clin Nutr. 1991;53(5):1323–8.
Bendich A. Antioxidant vitamins and their functions in immune responses. Adv Exp Med Biol. 1990;262:35–55.
Basu TK. Vitamins in human health and disease. Wallingford: CAB International; 1996.
Schwager J, Schulze J. Modulation of interleukin production by ascorbic acid. Vet Immunol Immunopathol. 1998;64(1):45–57.
Campbell JD, Cole M, Bunditrutavorn B, Vella AT. Ascorbic acid is a potent inhibitor of various forms of T cell apoptosis. Cell Immunol. 1999;194(1):1–5.
Nualart FJ, Rivas CI, Montecinos VP, Godoy AS, Guaiquil VH, Golde DW, et al. Recycling of vitamin C by a bystander effect. J Biol Chem. 2003;278(12):10128–33.
Maggini S, Wintergerst ES, Beveridge S, Hornig DH. Selected vitamins and trace elements support immune function by strengthening epithelial barriers and cellular and humoral immune responses. Br J Nutr. 2007;98(Suppl 1):S29–35.
Servili M, Esposto S, Fabiani R, Urbani S, Taticchi A, Mariucci F, et al. Phenolic compounds in olive oil: antioxidant, health and organoleptic activities according to their chemical structure. Inflammopharmacology. 2009;17(2):76–84.
Wang Y, Huang DS, Eskelson CD, Watson RR. Long-term dietary vitamin E retards development of retrovirus-induced disregulation in cytokine production. Clin Immunol Immunopathol. 1994;72(1):70–5.
Kirmizis D, Chatzidimitriou D. Antiatherogenic effects of vitamin E: the search for the Holy Grail. Vasc Health Risk Manag. 2009;5:767–74.
Boxer LA, Oliver JM, Spielberg SP, Allen JM, Schulman JD. Protection of granulocytes by vitamin E in glutathione synthetase deficiency. N Engl J Med. 1979;301(17):901–5.
Meydani SN, Meydani M, Blumberg JB, Leka LS, Siber G, Loszewski R, et al. Vitamin E supplementation and in vivo immune response in healthy elderly subjects. A randomized controlled trial. JAMA. 1997;277(17):1380–6.
Meydani M. Nutrition interventions in aging and age-associated disease. Ann N Y Acad Sci. 2001;928:226–35.
Prasad JS. Effect of vitamin E supplementation on leukocyte function. Am J Clin Nutr. 1980;33(3):606–8.
Stepanić V, Kujundžić RN, Trošelj KG. Epigenetics and epigenomics. In: Payne CJ, editor. InTech; 2014.
Walle T. Bioavailability of resveratrol. Ann N Y Acad Sci. 2011;1215:9–15.
Rastmanesh R. High polyphenol, low probiotic diet for weight loss because of intestinal microbiota interaction. Chem Biol Interact. 2011;189(1–2):1–8.
Wang S, Moustaid-Moussa N, Chen L, Mo H, Shastri A, Su R, et al. Novel insights of dietary polyphenols and obesity. J Nutr Biochem. 2014;25(1):1–18.
Sears B, Ricordi C. Anti-inflammatory nutrition as a pharmacological approach to treat obesity. J Obes. 2011;2011:431985.
Portillo P. Beneficial effects of quercetin on obesity and diabetes. Open Nutraceuticals J. 2011;4(1):189–98.
Stepanic V, Gasparovic AC, Troselj KG, Amic D, Zarkovic N. Selected attributes of polyphenols in targeting oxidative stress in cancer. Curr Top Med Chem. 2015;15(5):496–509.
Kim H-S, Quon MJ, Kim J-A. New insights into the mechanisms of polyphenols beyond antioxidant properties; lessons from the green tea polyphenol, epigallocatechin 3-gallate. Redox Biol. 2014;2:187–95.
da-Silva WS, Harney JW, Kim BW, Li J, Bianco SDC, Crescenzi A, et al. The small polyphenolic molecule kaempferol increases cellular energy expenditure and thyroid hormone activation. Diabetes. 2007;56(3):767–76.
Parish J, Perić M, Čipčić Paljetak H, Matijašić M, Verbanac D. Translating the Mediterranean diet: from chemistry to kitchen. Period Biol. 2011;113(3):303–10.
Bazzano LA, Serdula MK, Liu S. Dietary intake of fruits and vegetables and risk of cardiovascular disease. Curr Atheroscler Rep. 2003;5(6):492–9.
Benelli R, Venè R, Bisacchi D, Garbisa S, Albini A. Anti-invasive effects of green tea polyphenol epigallocatechin-3-gallate (EGCG), a natural inhibitor of metallo and serine proteases. Biol Chem. 2002;383(1):101–5.
Weisburger JH. Tea and health: the underlying mechanisms. Proc Soc Exp Biol Med. 1999;220(4):271–5.
Bushman JL. Green tea and cancer in humans: a review of the literature. Nutr Cancer. 1998;31(3):151–9.
Naasani I, Oh-Hashi F, Oh-Hara T, Feng WY, Johnston J, Chan K, et al. Blocking telomerase by dietary polyphenols is a major mechanism for limiting the growth of human cancer cells in vitro and in vivo. Cancer Res. 2003;63(4):824–30.
Zvetkova E, Wirleitner B, Tram NT, Schennach H, Fuchs D. Aqueous extracts of Crinum latifolium (L.) and Camellia sinensis show immunomodulatory properties in human peripheral blood mononuclear cells. Int Immunopharmacol. 2001;1(12):2143–50.
Lu Y-P, Lou Y-R, Xie J-G, Peng Q-Y, Liao J, Yang CS, et al. Topical applications of caffeine or (−)-epigallocatechin gallate (EGCG) inhibit carcinogenesis and selectively increase apoptosis in UVB-induced skin tumors in mice. Proc Natl Acad Sci U S A. 2002;99(19):12455–60.
Jatoi A, Ellison N, Burch PA, Sloan JA, Dakhil SR, Novotny P, et al. A phase II trial of green tea in the treatment of patients with androgen independent metastatic prostate carcinoma. Cancer. 2003;97(6):1442–6.
Senior K. Tea: a rich brew of anti-cancer magic bullets? Drug Discov Today. 2001;6(21):1079–80.
Lamy S, Gingras D, Béliveau R. Green tea catechins inhibit vascular endothelial growth factor receptor phosphorylation. Cancer Res. 2002;62(2):381–5.
Bae M-J, Ishii T, Minoda K, Kawada Y, Ichikawa T, Mori T, et al. Albumin stabilizes (−)-epigallocatechin gallate in human serum: binding capacity and antioxidant property. Mol Nutr Food Res. 2009;53(6):709–15.
Suzuki J, Isobe M, Morishita R, Nagai R. Tea polyphenols regulate key mediators on inflammatory cardiovascular diseases. Mediat Inflamm. 2009;2009:494928.
Wu L, Wang X, Xu W, Farzaneh F, Xu R. The structure and pharmacological functions of coumarins and their derivatives. Curr Med Chem. 2009;16(32):4236–60.
Huang W-Y, Cai Y-Z, Zhang Y. Natural phenolic compounds from medicinal herbs and dietary plants: potential use for cancer prevention. Nutr Cancer. 2010;62(1):1–20.
Sardari S, Mori Y, Horita K, Micetich RG, Nishibe S, Daneshtalab M. Synthesis and antifungal activity of coumarins and angular furanocoumarins. Bioorg Med Chem. 1999;7(9):1933–40.
Kayser O, Kolodziej H. Antibacterial activity of simple coumarins: structural requirements for biological activity. Zeitschrift für Naturforschung C J Biosci. 1999;54(3–4):169–74.
Park H, Lee C-M, Jung ID, Lee JS, Jeong Y, Chang JH, et al. Quercetin regulates Th1/Th2 balance in a murine model of asthma. Int Immunopharmacol. 2009;9(3):261–7.
Lugli E, Ferraresi R, Roat E, Troiano L, Pinti M, Nasi M, et al. Quercetin inhibits lymphocyte activation and proliferation without inducing apoptosis in peripheral mononuclear cells. Leuk Res. 2009;33(1):140–50.
Boots AW, Haenen GRMM, Bast A. Health effects of quercetin: from antioxidant to nutraceutical. Eur J Pharmacol. 2008;585(2–3):325–37.
Kawai Y. β-Glucuronidase activity and mitochondrial dysfunction: the sites where flavonoid glucuronides act as anti-inflammatory agents. J Clin Biochem Nutr. 2014;54(3):145–50.
Erlund I, Kosonen T, Alfthan G, Mäenpää J, Perttunen K, Kenraali J, et al. Pharmacokinetics of quercetin from quercetin aglycone and rutin in healthy volunteers. Eur J Clin Pharmacol. 2000;56(8):545–53.
D’Andrea G. Quercetin: a flavonol with multifaceted therapeutic applications? Fitoterapia. 2015;106:256–71.
Zinsmeister HD, Becker H, Eicher T. Moose, eine Quelle biologisch aktiver Naturstoffe? Angew Chemie. 1991;103(2):134–51.
Parnham MJ, Kesselring K. Rosmarinic acid. Drugs Future. 1985;10:756–7.
Jelić D, Mildner B, Kostrun S, Nujić K, Verbanac D, Culić O, et al. Homology modeling of human Fyn kinase structure: discovery of rosmarinic acid as a new Fyn kinase inhibitor and in silico study of its possible binding modes. J Med Chem. 2007;50(6):1090–100.
Halpern GM. A celebration of wine: wine IS medicine. Inflammopharmacology. 2008;16(5):240–4.
Bertelli AAA, Das DK. Grapes, wines, resveratrol, and heart health. J Cardiovasc Pharmacol. 2009;54(6):468–76.
Marques FZ, Markus MA, Morris BJ. Resveratrol: cellular actions of a potent natural chemical that confers a diversity of health benefits. Int J Biochem Cell Biol. 2009;41(11):2125–8.
Beher D, Wu J, Cumine S, Kim KW, Lu S-C, Atangan L, et al. Resveratrol is not a direct activator of SIRT1 enzyme activity. Chem Biol Drug Des. 2009;74(6):619–24.
Hubbard BP, Gomes AP, Dai H, Li J, Case AW, Considine T, et al. Evidence for a common mechanism of SIRT1 regulation by allosteric activators. Science. 2013;339(6124):1216–9.
Fitó M, Cladellas M, de la Torre R, Martí J, Muñoz D, Schröder H, et al. Anti-inflammatory effect of virgin olive oil in stable coronary disease patients: a randomized, crossover, controlled trial. Eur J Clin Nutr. 2008;62(4):570–4.
Beauchamp GK, Keast RSJ, Morel D, Lin J, Pika J, Han Q, et al. Phytochemistry: ibuprofen-like activity in extra-virgin olive oil. Nature. 2005;437(7055):45–6.
Visioli F, Bernardini E. Extra virgin olive oil’s polyphenols: biological activities. Curr Pharm Des. 2011;17(8):786–804.
Cicerale S, Lucas L, Keast R. Biological activities of phenolic compounds present in virgin olive oil. Int J Mol Sci. 2010;11(2):458–79.
De la Torre-Carbot K, Chávez-Servín JL, Jaúregui O, Castellote AI, Lamuela-Raventós RM, Nurmi T, et al. Elevated circulating LDL phenol levels in men who consumed virgin rather than refined olive oil are associated with less oxidation of plasma LDL. J Nutr. 2010;140(3):501–8.
Rodríguez-Morató J, Xicota L, Fitó M, Farré M, Dierssen M, de la Torre R. Potential role of olive oil phenolic compounds in the prevention of neurodegenerative diseases. Molecules. 2015;20(3):4655–80.
Parnham MJ. The pharmaceutical potential of seleno-organic compounds. Expert Opin Invest Drugs. 1996;5:861–70.
Inglot AD, Młochowski J, Zielińska-Jenczylik J, Piasecki E, Ledwoń TK, Kloc K. Seleno-organic compounds as immunostimulants: an approach to the structure-activity relationship. Arch Immunol Ther Exp. 1996;44(1):67–75.
Acknowledgements
Co-authors D.V. and M.P. fully acknowledge the Croatian Science Foundation for the support of this work under the project MINUTE for IBD (HRZZ grant no IP-11-2013-5467).
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2019 Springer International Publishing AG
About this chapter
Cite this chapter
Parnham, M.J., Stepanić, V., Tafferner, N., Panek, M., Verbanac, D. (2019). Mild Plant and Dietary Immunomodulators. In: Parnham, M., Nijkamp, F., Rossi, A. (eds) Nijkamp and Parnham's Principles of Immunopharmacology. Springer, Cham. https://doi.org/10.1007/978-3-030-10811-3_28
Download citation
DOI: https://doi.org/10.1007/978-3-030-10811-3_28
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-030-10809-0
Online ISBN: 978-3-030-10811-3
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)