Scientific Name: Spirulina Who is this for?
Uses
Note: Although spirulina species are only a few of the many types of blue-green algae, the name spirulina is often used to identify the whole group of edible blue-green algae. Spirulina has many potential medicinal uses. It contains antioxidants such as beta carotene and zeaxanthin. Antioxidants are thought to protect body cells from damage caused by a chemical process called oxidation. Oxygen free radicals, natural chemicals that may suppress immune function and damage body cells, are the result of oxidation. Both beta carotene and zeaxanthin decrease the activity of oxygen free radicals. In addition, zeaxanthin is thought to strengthen the retina of the eyes, helping to prevent macular degeneration – a condition that distorts or destroys sight as parts of the eye deteriorate. Early results from ongoing animal studies indicate that antioxidants in spirulina may also help to prevent a type of kidney stones that are caused by chemicals known as oxalates. Spirulina may also help to protect against damage that certain prescription drugs may cause to body organs. Furthermore, in laboratory, animal, and human studies, spirulina has shown the ability to enhance immune function. In a study of middle-aged men, increased immune system function persisted up to 6 months after the study participants stopped taking spirulina. Results of animal studies appear to show that spirulina may increase the production of anti-inflammatory chemicals known as interferons and interleukins. Therefore, it may decrease or prevent some allergic responses. Spirulina may also block the release of histamine from mast cells during an allergic reaction. By blocking histamine release, spirulina may prevent or lessen histamine’s effects, which include blood vessel expansion, muscle contraction, and stomach acid production. In one small study of children who had high levels of an antibody known as immunoglobulin E (IgE), dietary supplementation with spirulina seemed to help their IgE return to near normal levels. IgE may be one indicator of an allergic response. Both the antioxidant and immune-enhancing effects of spirulina may give it some anticancer properties. Spirulina appears to have additional anticancer effects, as well – possibly by promoting the release of tumor necrosis factor (TNF) alpha, a chemical in the body that attacks tumor cells. In several studies of laboratory animals, spirulina prevented the development and spread of experimentally-produced cancers. In other animal studies, when extracts of spirulina were injected into already existing cancerous tumors, the tumors stopped spreading and some disappeared completely. One human study involved individuals who had oral leukoplakia, a condition of the mouth that usually develops into cancer if it is not treated. Oral use of spirulina for one year prevented the progression to cancer in 45% of the study participants. More human studies are underway to confirm the exact anticancer effects that spirulina might have. Additionally, spirulina has shown antiviral effects in laboratory and animal studies. In several of the published studies, it appeared to block the entrance of viral cells into host cells. Spirulina may also prevent, delay, or decrease viral cell division through actions that are not yet understood. In some studies, several viruses, including HIV – the virus that causes AIDS — were apparently killed or damaged by spirulina or chemicals derived from it. At least one group of researchers suggests that regular consumption of algae may help prevent or lessen infections by viruses including cytomegalovirus, herpes, and influenza. Laboratory and animal studies support these antiviral effects, but much more study is needed to prove spirulina’s possible role in the treatment and prevention of viral diseases. Early results from animal studies and a few human studies suggest that spirulina supplementation may also prevent or treat numerous other conditions, but all of these potential uses for spirulina need much more research. When should I be careful taking it? Precautions
In a very few individuals, taking spirulina may have caused sudden worsening of relatively rare autoimmune conditions known as pemphigus vulgaris and dermatomyositis. Therefore, individuals who have these conditions should take spirulina carefully and discontinue taking it if their conditions seem to be getting worse. Spirulina contains all the amino acids, including phenylalanine. Individuals with a genetic disorder known as phenylketonuria do not produce an enzyme that digests phenylalanine. As a result, phenylalanine may build up in the body, possibly causing eczema, seizures, and brain damage. Individuals with phenylketonuria should not take spirulina. Spirulina may be contaminated with other types of blue-green algae that are harmful when ingested. Additionally, in the past, some spirulina products have been found to contain lead, mercury, or other heavy metal pollutants. Individuals who decide to take spirulina should purchase a product certified as pure from a reliable commercial source. What side effects should I watch for?
Pure spirulina has not been reported to cause any side effects. However, other types of blue-green algae may be mixed with it, especially if it is harvested from wild algae. If algae from the genus Microcystis are included, liver damage may result. Symptoms of liver damage, which may be apparent between one-half hour and 24 hours after ingesting Microcystis, include:
What interactions should I watch for?
No interactions are known to occur between spirulina and prescription drugs, non-prescription drugs, other herbal products, or foods. However, because few reliable studies of spirulina have been conducted in humans, its possible interactions may not be understood completely. Some interactions between herbal products and medications can be more severe than others. The best way for you to avoid harmful interactions is to tell your doctor and/or pharmacist what medications you are currently taking, including any over-the-counter products, vitamins, and herbals. For specific information on how spirulina interacts with drugs, other herbals, and foods and the severity of those interactions, please use our Drug Interactions Checker to check for possible interactions. Should I take it? Spirulina species include a few of the hundreds of species collectively known as blue-green algae. Algae are tiny organisms that usually grow in water. Because so many different kinds of algae exist, they are grouped by their general color – blue-green, green, yellow-green, red, and brown. Algae do not have leaves, stems, or roots like plants, but most of them contain chlorophyll, the pigment needed by plants to turn sunlight into food energy. Like plants, they also remove carbon dioxide from the air and release oxygen. Like animals, however, algae make proteins and sugars. They multiply rapidly, sometimes making them a nuisance on ponds where they are not wanted. Unlike other algae which may be flat or round, spirulina are shaped like springs or corkscrews. Wild algae provide food for fish, birds, and water animals. Humans have also collected them for both animal and human food at various times and in various parts of the world. Records left by the Spanish explorers of South America, for example, show that Aztec people were harvesting what appears to be some type of blue-green algae from lakes as early as the 16th century. Spirulina’s popularity as a food source has been inconsistent, though, with most use in cultures that have few field crops. During the 1970s, researchers rediscovered spirulina as a plentiful and economical source of minerals, proteins, and vitamins. It also contains a polyunsaturated omega-6 fatty acid known as gamma-linolenic acid (GLA). Fatty acids such as GLA are known as essential fatty acids because the body needs them to regulate activities that include heart function, insulin utilization, and mood balance. The body cannot produce essential fatty acids, so they must be taken in the diet or as supplements. Now, commercial cultivation of spirulina and other types of algae is well-established in several parts of the world. Farmers in warm weather areas of Africa, Japan, North America, and South America cultivate several types of algae, including spirulina, in artificial ponds that have controlled nutrient supplies. In cool countries such as Belgium, Britain, and the Netherlands, algae are grown in large, flooded greenhouses warmed by waste heat produced by power generation. Insects do not usually attack algae, so pesticides are not needed and most algae can be grown organically – even outside. Harvested essentially all year, spirulina is collected and cleaned. It is then blended into a thick bluish green liquid, which is fast-dried into a powder. Spirulina powder may then be made into capsules or tablets, or it may be left as a powder to be added to foods. In a closed environment such as a space station, spirulina and other types of algae may serve as both a food source and an air purification system. Because they are rich sources of nutrients, algae are used extensively for poultry and animal feed in some countries and they have also been used to fertilize crops. Some evidence from recent studies shows that they can be used to remove lead and other contaminants from polluted water. Commercially pure spirulina and other algae provide coloring agents that are used in manufacturing and pharmaceuticals. As an antioxidant, spirulina may be added to cosmetics for potential anti-aging effects or to foods and chemicals as a preservative. Dosage and Administration
Typically, supplemental spirulina is available in oral dosage forms – most commonly tablets. Powdered spirulina is also available. One tablespoon of spirulina powder is about 7,000 mg (7 grams) and directions for taking it usually indicate that it can be mixed into liquids or soft foods. Doses used in the few human studies that have been conducted varied from about 1,000 mg (one gram) per day to more than 5,000 mg (5 grams) per day. If spirulina is taken, the directions on the package that is bought should be followed for the condition being treated. Summary A source of protein for human or animal diets, spirulina also contains antioxidants and chemicals that may increase immune function. Therefore, spirulina may be useful for preventing and treating allergies and cancer. It may have antiviral effects and it may help to lower the amounts of sugar and cholesterol in the blood. Risks Phenylketonuria may be worsened by taking spirulina. Its possible contamination with other types of blue-green algae has resulted in liver damage. Side Effects Although no side effects have been identified for spirulina, other types of blue-green algae may cause liver damage. Interactions Spirulina is not known to interfere with drugs, other dietary supplements, herbals, or foods. Last Revised September 21, 2006 References
Annapurna VV, Deosthale YG, Bamji MS. Spirulina as a source of vitamin A. Plant Foods in Human Nutrition. 1991;41(2):125-134. Anon: Spirulina. In: DerMarderosian A, Beutler JA, eds. Facts and Comparisons: The Review of Natural Products. St. Louis, MO, Facts and Comparisons. February 1998. Ayehunie S, Belay A, Baba TW, Ruprecht RM. Inhibition of HIV-1 replication by an aqueous extract of Spirulina platensis (Arthrospira platensis). Journal of Acquired Immune Deficiency Syndrome and Human Retrovirology. 1998;18(1):7-12. Belay A. The potential application of Spirulina (arthrospira) as a nutritional and therapeutic supplement in health management. Journal of the American Naprapathic Association. 2002;5(2):27-47. Bhat VB, Madyastha KM. C-phycocyanin: a potent peroxyl radical scavenger in vivo and in vitro. Biochemistry and Biophysics Research Communication. 2000;275(1):20-25. Ble-Castillo JL, Rodriguez-Hernandez A, Miranda-Zamora R, Juarez-Oropeza MA, Diaz-Zagoya JC. Arthrospira maxima prevents the acute fatty liver induced by the administration of simvastatin, ethanol and a hypercholesterolemic diet to mice. Life Sciences. 2002;70(22):2665-2673. Chamorro G, Salazar M, Araujo KG, dos Santos CP, Ceballos G, Castillo LF. Update on the pharmacology of Spirulina (Arthrospira), an unconventional food. [Article in Spanish] Archivo Latinoamericano Nutrition. 2002;52(3):232-240. Chamorro G, Salazar M, Favila L, Bourges H. Pharmacology and toxicology of Spirulina alga. [Article in Spanish] La Revista de Investigacion Clinica. 1996;48(5):389-399. Chen H, Pan SS. Bioremediation potential of spirulina: toxicity and biosorption studies of lead. J Zhejiang Univ Sci B. 2005;6(3):171-174. Chiu HF, Yang SP, Kuo YL, Lai YS, Chou TC. Mechanisms involved in the antiplatelet effect of C-phycocyanin. British Journal of Nutrition. 2006;95(2):435-440. Converti A, Scapazzoni S, Lodi A, Carvalho JC. Ammonium and urea removal by Spirulina platensis. Journal of Indian Microbiology and Biotechnology. 2006;33(1):8-16. Dagnelie PC, van Staveren WA, van den Berg H. Vitamin B-12 from algae appears not to be bioavailable. American Journal of Clinical Nutrition. 1991;53:695-697. Dasgupta T, Banejee S, Yadav PK, Rao AR. Chemomodulation of carcinogen metabolising enzymes, antioxidant profiles and skin and forestomach papillomagenesis by Spirulina platensis. Molecular and Cellular Biochemistry. 2001;226(1-2):27-38. Egorova EA, Gmoshinskii IV, Zorin SN, Mazo VK. Studies of immunomodulation caused by selenium-enriched phycocyanin. [Article in Russian] Vopr Pitan. 2006;75(2):19-21. Farooq SM, Asokan D, Kalaiselvi P, Sakthivel R, Varalakshmi P. Prophylactic role of phycocyanin: a study of oxalate mediated renal cell injury. Chemico-Biological Interactions. 2004;149(1):1-7. Farooq SM, Asokan D, Sakthivel R, Kalaiselvi P, Varalakshmi P. Salubrious effect of C-phycocyanin against oxalate-mediated renal cell injury. Clinica Chimica Acta. 2004;348(1-2):199-205. Farooq SM, Ebrahim AS, Subramhanya KH, Sakthivel R, Rajesh NG, Varalakshmi P. Oxalate mediated nephronal impairment and its inhibition by c-phycocyanin: a study on urolithic rats. Molecular and Cellular Biochemistry. 2006;284(1-2):95-101. Gilroy DJ, Kauffman KW, Hall RA, Huang X, Chu FS. Assessing potential health risks from microcystin toxins in blue-green algae dietary supplements. Environmental Health Perspectives. 2000;108(5):435-439. Godia F, Albiol J, Montesinos JL, et al. MELISSA: a loop of interconnected bioreactors to develop life support in space. Journal of Biotechnology. 2002;99(3):319-330. Gonzalez de Rivera C, Miranda-Zamora R, Diaz-Zagoya JC, Juarez-Oropeza MA. Preventive effect of Spirulina maxima on the fatty liver induced by a fructose-rich diet in the rat, a preliminary report. Life Sciences. 1993;53(1):57-61. Grzanna R, Polotsky A, Phan PV, Pugh N, Pasco D, Frondoza CG. Immolina, a high-molecular-weight polysaccharide fraction of spirulina, enhances chemokine expression in human monocytic THP-1 cells. Journal of Alternative and Complementary Medicine. 2006;12(5):429-435. Han LK, Li DX, Xiang L, et al. Isolation of pancreatic lipase activity-inhibitory component of spirulina platensis and it reduce postprandial triacylglycerolemia. [Article in Japanese] Yakugaku Zasshi. 2006;126(1):43-49. Hayashi K, Hayashi T, Kojima I. A natural sulfated polysaccharide, calcium spirulan, isolated from Spirulina platensis: in vitro and ex vivo evaluation of anti-herpes simplex virus and anti-human immunodeficiency virus activities. AIDS Research and Human Retroviruses. 1996;12(15):1463-1471. Hayashi T, Hayashi K, Maeda M, Kojima I. Calcium spirulan, an inhibitor of enveloped virus replication, from a blue-green alga Spirulina platensis. Journal of Natural Products. 1996;59(1):83-87. Hayashi O, Hirahashi T, Katoh T, Miyajima H, Hirano T, Okuwaki Y. Class specific influence of dietary Spirulina platensis on antibody production in mice. Journal of Nutritional Science and Vitaminology (Tokyo). 1998;44(6):841-851. Hayashi O, Katoh T, Okuwaki Y. Enhancement of antibody production in mice by dietary Spirulina platensis. Journal of Nutritional Science and Vitaminology (Tokyo). 1994;40(5):431-441. Hernandez-Corona A, Nieves I, Meckes M, Chamorro G, Barron BL. Antiviral activity of Spirulina maxima against herpes simplex virus type 2. Antiviral Research. 2002;56(3):279-285. Hirahashi T, Matsumoto M, Hazeki K, Saeki Y, Ui M, Seya T. Activation of the human innate immune system by Spirulina: augmentation of interferon production and NK cytotoxicity by oral administration of hot water extract of Spirulina platensis. International Immunopharmacology. 2002;2(4):423-434. Hsiao G, Chou PH, Shen MY, Chou DS, Lin CH, Sheu JR. C-phycocyanin, a very potent and novel platelet aggregation inhibitor from Spirulina platensis. Journal of Agricultural and Food Chemistry. 2005;53(20):7734-7740. Huang JM, Bai SM, Hu ZX, Yang CL, Zhu DB, Shi JP. Effects of spirulina on serum lipids, erythrocyte membrane fluidity and vascular endothelial cells in tail-suspended rats [Article in Chinese] Space Medicine and Medical Engineering (Beijing). 2003;16(3):184-186. Ishimi Y, Sugiyama F, Ezaki J, Fujioka M, Wu J. Effects of spirulina, a blue-green alga, on bone metabolism in ovariectomized rats and hindlimb-unloaded mice. Bioscience, Biotechnology and Biochemistry. 2006;70(2):363-368. Iwata K, Inayama T, Kato T. Effects of Spirulina platensis on plasma lipoprotein lipase activity in fructose-induced hyperlipidemic rats. Journal of Nutritional Science and Vitaminology (Tokyo). 1990;36(2):165-171. Jellin JM, Gregory P, Batz F, Hitchens K, et al, eds. Pharmacist's Letter/Prescriber's Letter. Natural Medicines Comprehensive Database, 3rd Edition. Stockton CA: Therapeutic Research Facility, 2000. Kapoor R, Mehta U. Supplementary effect of spirulina on hematological status of rats during pregnancy and lactation. Plant Foods and Human Nutrition. 1998;52(4):315-324. Kay RA. Microalgae as food and supplement. Critical Reviews in Food Science and Nutrition. 1991;30(6):555-573. Khan M, Shobha JC, Mohan IK, et al. Protective effect of Spirulina against doxorubicin-induced cardiotoxicity. Phytotherapy Research. 2005;19(12):1030-1037. Khan M, Shobha JC, Mohan IK, et al. Spirulina attenuates cyclosporine-induced nephrotoxicity in rats. Journal of Applied Toxicology. 2006;26(5):444-451. Khan M, Varadharaj S, Ganesan LP, et al. C-phycocyanin protects against ischemia-reperfusion injury of heart through involvement of p38 MAPK and ERK signaling. American Journal of Physiology and Heart Circulation Physiology. 2006;290(5):H2136-H2145. Khan M, Varadharaj S, Shobha JC, et al. C-phycocyanin ameliorates doxorubicin-induced oxidative stress and apoptosis in adult rat cardiomyocytes. Journal of Cardiovascular Pharmacology. 2006;47(1):9-20. Khan Z, Bhadouria P, Bisen PS. Nutritional and therapeutic potential of Spirulina. Current Pharmaceutcal Biotechnology. 2005;6(5):373-379. Kim HM, Lee EH, Cho HH, Moon YH. Inhibitory effect of mast cell-mediated immediate-type allergic reactions in rats by spirulina. Biochemistry and Pharmacology. 1998;55(7):1071-1076. Kuhad A, Tirkey N, Pilkhwal S, Chopra K. Effect of Spirulina, a blue green algae, on gentamicin-induced oxidative stress and renal dysfunction in rats. Fundamental Clinical Pharmacology. 2006;20(2):121-128. Kuhad A, Tirkey N, Pilkhwal S, Chopra K. Renoprotective effect of Spirulina fusiformis on cisplatin-induced oxidative stress and renal dysfunction in rats. Renal Failure. 2006;28(3):247-254. Kushak RI, Drapeau C, Van Cott EM, Winter HH. Favorable effects of blue-green algae Aphanizomenon flos-aquae on rat plasma lipids. Journal of the American Naprapathic Association. 2000;2(3):50;59-65. Kushak RI, Drapeau C, Winter HS. The effect of blue-green algae Aphanizomenon flos-Aquae on nutrient assimilation in rats. Journal of the American Naprapathic Association. 2001;3(1):35-39. Lee AN, Werth VP. Activation of autoimmunity following use of immunostimulatory herbal supplements. Archives Dermatology. 2004;140(6):723-727. Li B, Gao MH, Zhang XC, Chu XM. Molecular immune mechanism of C-phycocyanin from Spirulina platensis induces apoptosis in HeLa cells in vitro. Biotechnology and Applied Biochemistry. 2006;43(Pt 3):155-164. Liu XM, Zhang HQ. Effect of polysaccharide from Spirulina platensis on hematopoietic cells proliferation, apoptosis and Bcl-2 expression in mice bearing tumor treated with chemotherapy. [Article in Chinese] Yao Xue Xue Bao. 2002;37(8):616-20. Lu HK, Hsieh CC, Hsu JJ, Yang YK, Chou HN. Preventive effects of Spirulina platensis on skeletal muscle damage under exercise-induced oxidative stress. European Journal of Applied Physiology. 2006;98(2):220-226. Mao TK, Van de Water J, Gershwin ME. Effects of a Spirulina-based dietary supplement on cytokine production from allergic rhinitis patients. Journal of Medical Food. 2005;8(1):27-30. Mathew B, Sankaranarayanan R, Nair PP, et al. Evaluation of chemoprevention of oral cancer with Spirulina fusiformis. Nutrition and Cancer. 1995;24(2):197-202. Mazo VK, Gmoshinskii IV, Zilova IS. Microalgae Spirulina in human nutrition. [Article in Russian] Vopr Pitan. 2004;73(1):45-53. Miranda MS, Cintra RG, Barros SB, Mancini Filho J. Antioxidant activity of the microalga Spirulina maxima. Brazilian Journal of Medical and Biological Research. 1998;31(8):1075-1079. Misbahuddin M, Islam AZ, Khandker S, Ifthaker-Al-Mahmud, Islam N, Anjumanara. Efficacy of spirulina extract plus zinc in patients of chronic arsenic poisoning: a randomized placebo-controlled study. Clinical Toxicology (Philadelphia). 2006;44(2):135-141. Mishima T, Murata J, Toyoshima M, et al. Inhibition of tumor invasion and metastasis by calcium spirulan (Ca-SP), a novel sulfated polysaccharide derived from a blue-green alga, Spirulina platensis. Clinical Experience in Metastasis. 1998;16(6):541-550. Mohan IK, Khan M, Shobha J, et al. Protection against cisplatin-induced nephrotoxicity by Spirulina in rats. Cancer Chemotherapy and Pharmacology. 2006;58(6):802-808. Mosulishvili LM, Kirkesali EI, Belokobylsky AI, et al. Experimental substantiation of the possibility of developing selenium- and iodine-containing pharmaceuticals based on blue-green algae Spirulina platensis. Journal of Pharmaceutical and Biomedical Analysis. 2002;30(1):87-97. Nagaoka S, Shimizu K, Kaneko H, et al. A novel protein C-phycocyanin plays a crucial role in the hypocholesterolemic action of Spirulina platensis concentrate in rats. Journal of Nutrition. 2005;135(10):2425-2430. Nakhost Z, Karel M. Potential utilization of algal protein concentrate as a food ingredient in space habitats. Sci Aliments. 1989;9:491-506. Oguchi M, Otsubo K, Nitta K, Hatayama S. Food production and gas exchange system using blue-green alga (Spirulina) for CELSS. Advances in Space Research. 1987;7(4):7-10. Oguchi M, Otsubo K, Nitta K, Shimada A, Fujii S, Koyano T, Miki K. Closed and continuous algae cultivation system for food production and gas exchange in CELSS. Advances in Space Research. 1989;9(8):169-177. Otles S, Pire R. Fatty acid composition of Chlorella and Spirulina microalgae species. Journal of AOAC International. 2001;84(6):1708-1714. Parikh P, Mani U, Iyer U. Role of Spirulina in the control of glycemia and lipidemia in type 2 diabetes mellitus. Journal of Medical Foods. 2001;4(4):193-199. Petrus A. Algae-a blooming success? FAIR, Cooperative Research Measures. July 2000. Available at: http://europa.eu.int/comm/research/agriculture/pdf/p33.pdf. Accessed December 1, 2003. Pinero Estrada JE, Bermejo Bescos P, Villar del Fresno AM. Antioxidant activity of different fractions of Spirulina platensis protean extract. Farmacologia. 2001l;56(5-7):497-500. Premkumar K, Abraham SK, Santhiya ST, Ramesh A. Protective effect of Spirulina fusiformis on chemical-induced genotoxicity in mice. Fitoterapia. 2004;75(1):24-31. Pugh N, Ross SA, ElSohly HN, ElSohly MA, Pasco DS. Isolation of three high molecular weight polysaccharide preparations with potent immunostimulatory activity from Spirulina platensis, aphanizomenon flos-aquae and Chlorella pyrenoidosa. Planta Medica. 2001;67(8):737-742. Reddy CM, Bhat VB, Kiranmai G, Reddy MN, Reddanna P, Madyastha KM. Selective inhibition of cyclooxygenase-2 by C-phycocyanin, a biliprotein from Spirulina platensis. Biochemistry and Biophysics Research Communications. 2000;277(3):599-603. Remirez D, Gonzalez R, Merino N, Rodriguez S, Ancheta O. Inhibitory effects of Spirulina in zymosan-induced arthritis in mice. Mediators of Inflammation. 2002;11(2):75-79. Remirez D, Ledon N, Gonzalez R. Role of histamine in the inhibitory effects of phycocyanin in experimental models of allergic inflammatory response. Mediators of Inflammation. 2002;11(2):81-85. Rodriguez-Hernandez A, Ble-Castillo JL, Juarez-Oropeza MA, Diaz-Zagoya JC. Spirulina maxima prevents fatty liver formation in CD-1 male and female mice with experimental diabetes. Life Sciences. 2001;69(9):1029-1037. Romay C, Armesto J, Remirez D, Gonzalez R, Ledon N, Garcia I. Antioxidant and anti-inflammatory properties of C-phycocyanin from blue-green algae. Inflammation Research. 1998;47(1):36-41. Romay C, Gonzalez R, Ledon N, Remirez D, Rimbau V. C-phycocyanin: a biliprotein with antioxidant, anti-inflammatory and neuroprotective effects. Current Protein and Peptide Science. 2003;4(3):207-216. Romay C, Ledon N, Gonzalez R. Further studies on anti-inflammatory activity of phycocyanin in some animal models of inflammation. Inflammation Research. 1998;47(8):334-338. Salazar M, Chamorro GA, Salazar S, Steele CE. Effect of Spirulina maxima consumption on reproduction and peri- and postnatal development in rats. Food Chemistry and Toxicology. 1996;34(4):353-359. Salazar M, Martinez E, Madrigal E, Ruiz LE, Chamorro GA. Subchronic toxicity study in mice fed Spirulina maxima. Journal of Ethnopharmacology. 1998;62(3):235-241. Samuels R, Mani UV, Iyer UM, Nayak US. Hypocholesterolemic effect of spirulina in patients with hyperlipidemic nephrotic syndrome. Journal of Medical Food. 2002;5(2):91-96. Schwartz J, Shklar G. Regression of experimental hamster cancer by beta carotene and algae extracts. Journal of Oral and Maxillofacial Surgery. 1987;45(6):510-515. Schwartz J, Shklar G, Reid S, Trickler D. Prevention of experimental oral cancer by extracts of Spirulina-Dunaliella algae. Nutrition and Cancer. 1988;11(2):127-134. Shastri D, Kumar M, Kumar A. Modulation of lead toxicity by Spirulina fusiformis. Phytotherapy Research. 1999;13(3):258-260. Shklar G, Schwartz J. Tumor necrosis factor in experimental cancer regression with alphatocopherol, beta-carotene, canthaxanthin and algae extract. European Journal of Cancer and Clinical Oncology. 1988;24(5):839-850. Simpore J, Zongo F, Kabore F, et al. Nutrition rehabilitation of HIV-infected and HIV-negative undernourished children utilizing spirulina. Annals of Nutrition and Metabolism. 2005;49(6):373-380. Stromberg I, Gemma C, Vila J, Bickford PC. Blueberry- and spirulina-enriched diets enhance striatal dopamine recovery and induce a rapid, transient microglia activation after injury of the rat nigrostriatal dopamine system. Experimental Neurology. 2005;196(2):298-307. Subhashini J, Mahipal SV, Reddy MC, Mallikarjuna Reddy M, Rachamallu A, Reddanna P. Molecular mechanisms in C-Phycocyanin induced apoptosis in human chronic myeloid leukemia cell line-K562. Biochemistry and Pharmacology. 2004;68(3):453-462. Teas J, Hebert JR, Fitton JH, Zimba PV. Algae -- a poor man's HAART? Medical Hypotheses. 2004;62(4):507-510. Torres-Duran PV, Miranda-Zamora R, Paredes-Carbajal MC, Mascher D, Ble-Castillo J, Diaz-Zagoya JC, Juarez-Oropeza MA. Studies on the preventive effect of Spirulina maxima on fatty liver development induced by carbon tetrachloride, in the rat. Journal of Ethnopharmacology. 1999;64(2):141-147. Torres-Duran PV, Miranda-Zamora R, Paredes-Carbajal MC, Mascher D, Diaz-Zagoya JC, Juarez-Oropeza MA. Spirulina maxima prevents induction of fatty liver by carbon tetrachloride in the rat. Biochemistry and Molecular Biology International. 1998;44(4):787-793. Upasani CD, Balaraman R. Protective effects of Spirulina on lead induced deleterious changes in the lipid peroxidatin and endogenous antioxidants in rats. Phytotherapy Research. 2003;17(4):330-334. Vadiraja BB, Gaikwad NW, Madyastha KM. Hepatoprotective effect of C-phycocyanin: protection for carbon tetrachloride and R-(+)-pulegone-mediated hepatotoxicty [sic] in rats. Biochemistry and Biophysics Research Communications. 1998;249(2):428-431. Wang Y, Chang CF, Chou J, et al. Dietary supplementation with blueberries, spinach, or spirulina reduces ischemic brain damage. Experimental Neurology. 2005;193(1):75-84. Watanabe F, Katsura H, Takenaka S, Fujita T, Abe K, Tamura Y, Nakatsuka T, Nakano Y. Pseudovitamin B(12) is the predominant cobamide of an algal health food, spirulina tablets. Journal of Agricultural and Food Chemistry. 1999;47(11):4736-4741. Watanabe F, Takenaka S, Kittaka-Katsura H, Ebara S, Miyamoto E. Characterization and bioavailability of vitamin B12-compounds from edible algae. Journal of Nutrition Science and Vitaminology (Tokyo). 2002 ;48(5):325-331. Wu LC, Ho JA, Shieh MC, Lu IW. Antioxidant and antiproliferative activities of Spirulina and Chlorella water extracts. Journal of Agricultural and Food Chemistry. 2005;53(10):4207-4212. Yang HN, Lee EH, Kim HM. Spirulina platensis inhibits anaphylactic reaction. Life Sciences. 1997;61(13):1237-1244. Last Revised September 21, 2006 Note: The above information is not intended to replace the advice of your physician, pharmacist, or other healthcare professional. It is not meant to indicate that the use of the product is safe, appropriate, or effective for you. In general, herbal products are not subject to review or approval by the U.S. Food and Drug Administration (FDA). They are not required to be standardized, meaning that the amounts of active ingredients or contaminants they contain may vary between brands or between different batches of the same brand. Not all of the risks, side effects, or interactions associated with the use of herbal products are known because few reliable studies of their use in humans have been done. This information is provided for your education only. Please share this information with your healthcare provider and be sure that you talk to your doctor and pharmacist about all the prescription and non-prescription medicines you take before you begin to use any herbal product. |