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This lake has an astonishingly high mineral concentration due to a massive volcanic eruption that occurred in the vicinity over 7,000 years ago, covering the area with millions of tons of mineral ash. Seventeen streams and rivers deposit into the 140 square mile lake an annual average of 50,000 tons of the mineral-rich silt from the surrounding 4000 square mile volcanic basin, making Upper Klamath Lake one of the richest nutrient traps in the world (and part of the mineral-rich "Ring of Fire" region)
Much has been learned about this amazing food since it became available as a food source over 20 years ago. There are more benefits being discovered every day as this cyanophyta is introduced to the medical and scientific communities. AFA has been available in powders and capsules, but now, for the first time in history, AFA is available in its much more potent and vibrant frozen LIQUID form.
AFA Research - Brief Summaries
Recently there have been many scientifically-controlled studies analyzing the immune enhancing properties of Aphanizomenon flos-aquae (AFA) from Klamath Lake, Oregon. The following institutions have known research underway:
McGILL UNIVERSITY
BOSTON UNIVERSITY
THE UNIVERSITY OF NEW MEXICO
THE ROYAL VICTORIA HOSPITAL IN MONTREAL
THE RESEARCH INSTITUTE OF ONCOLOGY IN BELARUS, RUSSIA
In a recent double-blind, cross-over study at the Royal Victoria Hospital and led by Dr. Gette Jenson, they discovered that Blue Green Algae uniquely supports the healthy function of the immune system.
The following are brief summaries of other scientific studies:
Royal Victoria Hospital, affiliated with McGill University (Montreal) - Double-blind placebo-controlled study. Eating Aphanizomenon flos-aquae may help stimulate the circulatory system.
University of New Mexico - placebo controlled study. After eating Aphanizomenon flos-aquae for a period of one month, intestinal function can improve. Another placebo-contolled study suggests that eating Aphanizomenon flos-aquae can stimulate specific areas of the brain for increased mental alertness.
An Exciting New Discovery!
Recently the first stage of an extensive research project carried out at the Royal Victoria Hospital in Montreal, Canada produced some remarkable results. The project studies the effect of Aphanizomenon flos-aquae on the immune and endocrine systems, as well as on general blood physiology. It was discovered that eating AFA had a profound and unique effect on Natural Killer (NK) cells. The results were recently published under the title: Effects of the Blue Green Algae Aphanizomenon flos-aquae on Human Natural Killer Cells. It appears in Chapter 3.1 of the IBC Library Series, Volume 1911, Phytoceuticals: Examining the health benefit and pharmaceutical properties of natural antioxidants and phytochemicals.
NK cells have the ability to search for and recognize cells that are cancerous or have been infected by a virus, and kill them. The team of research scientists at the Royal Victoria Hospital, led by Dr. Gitte S. Jensen, discovered that eating Aphanizomenon flos-aquae triggers the movement of 40% of the circulating NK cells from the blood to the tissues where their main function is to perform immune surveillance and eliminate cancerous and virally-infected cells. Further research may prove that eating a small amount of AFA every day could assist in the prevention of cancer and viral infections. No other substance is known to trigger such a movement of NK cells in the body. This is very exciting news! We hope you will share it with everyone you know!
Other Scientific Research Findings Regarding AFA:
Study of AFA and the Immune System
Study of Chlorophyll
Study of Phycocyanin
Study of AFA as a Source of Polyunsaturated Fatty Acids
Current Research has discovered:
*Phenylethylamine (PEA) is known as the "molecule of love." Beside enhancing concentration and attention, PEA is a natural mood elevator and anti-depressant. *Phycocyanin, is the blue pigment in AFA, which is a natural selective COX-2 inhibitor with strong anti-inflammatory properties. *AFA contains a polysaccharide that stimulates the migration of immune cells in the body; the only natural compound known to stimulate immune cell migration. But the most extraordinary discover is the ability of AFA to stimulate stem cell release and migration, making AFA the first natural compound know to stimulate the natural innate phenomenon of healing, regeneration and repair in the human body. Order your copy of "Primordial Food" and read the complete research findings.
Study of Chlorophyll
Effect of dietary chlorophyll derivatives on mutagenesis and tumor cell growth
Chernomorsky S, Segelman A, Poretz RD. (1999). Teratog Carcinog Mutagen.19(5):313-22
Much attention in recent years has been given to the antigenotoxicity of chlorophyll. Chlorophyll, however, is known to be converted into pheophytin, pyropheophytin, and pheophorbide in processed vegetable food and following ingestion by humans. Studies were conducted on the antimutagenic and tumoricidal potencies of these compounds. All the chlorophyll derivatives tested exhibit identical antimutagenic effect towards 3-methylcholanthrene (3-MC), suggesting that the porphyrin nucleus may complex directly with the mutagen. It does not exclude, however, another mechanism of activity involving inactivation the enzymatic transformation of 3-MC. In contrast, the action of N'-nitro-N'-nitrosoguanidine (MNNG) depends upon structural differences between the chlorophyll derivatives. It is significantly lower when the phytol-containing pheophytin and pyropheophytin are tested as to that of the phytol-lacking pheophorbide. The higher concentrations of the chlorophyll derivatives were required to reduce the mutagenicity of MNNG than needed for 3-MC. The cytotoxicity of chlorophyll derivatives against tumor cells also was evaluated. The cellular uptake and inhibition of myeloma cell multiplicity were found to be greater for pheophorbide than for pheophytin. Calculated on the amount of cell associated chlorophyll derivative, however, pheophytin was more cytostatic/cytotoxic than pheophorbide. The results presented in this report indicate that food sources that yield chlorophyll derivatives may play a significant role in cancer prevention.
Study of Phycocyanin
Antioxidant and anti-inflammatory properties of C-phycocyanin from blue-green algae
Romay C, Armesto J, Remirez D, Gonzalez R, Ledon N, Garcia I Pharmacology Department, National Center for Scientific Research, CNIC, Havana, Cuba. ricardo@quimica.cneuro.cu
Objective: Phycocyanin is a pigment found in blue-green algae which contains open chain tetrapyrroles with possible scavenging properties. We have studied its antioxidant properties.
Materials and Methods: Phycocyanin was evaluated as a putative antioxidant in vitro by using: a) luminol-enhanced chemiluminescence (LCL) generated by three different radical species (O2-, OH., RO.) and by zymosan activated human polymorphonuclear leukocytes (PMNLs), b) deoxyribose assay and c) inhibition of liver microsomal lipid peroxidation induced by Feascorbic acid. The antioxidant activity was also assayed in vivo in glucose oxidase (GO)-induced inflammation in mouse paw.
Results: The results indicated that phycocyanin is able to scavenge OH. (IC50 = 0.91 mg/mL) and RO. (IC50 = 76 microg/mL) radicals, with activity equivalent to 0.125 mg/mL of dimethyl sulphoxide (DMSO) and 0.038 microg/mL of trolox, specific scavengers of those radicals respectively. In the deoxyribose assay the second-order rate constant was 3.56 x 10(11) M(-1) S(-1), similar to that obtained for some non-steroidal anti-inflammatory drugs. Phycocyanin also inhibits liver microsomal lipid peroxidation (IC50 = 12 mg/mL), the CL response of PMNLs (p < 0.05) as well as the edema index in GO-induced inflammation in mouse paw (p < 0.05).
Conclusions: To our knowledge this is the first report of the antioxidant and anti-inflammatory properties of c-phycocyanin.
Inflamm Res 1998 Jan;47(1):36-41
Study of AFA as a Source of Polyunsaturated Fatty Acids
Favorable Effects of Blue-Green Algae Aphanizomenon flos-aquae on Rat Plasma Lipids
Rafail 1. Kushak,1 Christian Drapeau,2,3 Elizabeth M. Van Cott,1 Harland H. Winter1 1Combined Program in Pediatric Gastroenterology and Nutrition and Division of Laboratory Medicine Massachusetts General Hospital, Harvard Medical School, Boston, MA; 2Cell Tech, Klamath Falls, or 3Current Address: Desert Lake Technologies, Klamath Falls, OR
ABSTRACT
Background: Polyunsaturated fatty acids (PUFA) are essential for human health. There are indications that the lipid fraction of blue-green algae Aphanizomenon flos-aquae contains about 50% of PUFA and may be a good dietary source of PUFA. The purpose of this study was to investigate the effect of diets supplemented with algae on blood plasma lipids.
Methods: Rats were fed with four different semisynthetic diets: i) standard, with 5% soybean oil; ii) PUFA-free with 5% coconut oil; iii) PUFA-free with 10% algae; iv) PUFA-free with 15% algae. After 32 days the levels of plasma fatty acids, triglycerides and cholesterol were studied.
Results: Rats fed the PUFA-free diet demonstrated an absence of linolenic acid (LNA) in plasma; however, supplementation with algae resulted in the same level of LNA as controls, an increased levels of eicosapentaenoic acid and docosahexaenoic acid, and a decreased level of arachidonic acid. Dietary supplementation with 10% and 15% algae decreased the plasma cholesterol to 54% and 25% of the control level, respectively (P<0.0005). Plasma triglyceride levels decreased significantly (P<0.005) after diet supplementation with 15% algae.
Conclusion: Algae Aphanizomenon flos-aquae is a good source of PUFA and because of potential hypocholesterolemic properties should be a valuable nutritional resource.
JANA, vol. 2, No. 3, 2000, pp. 59-65
Study of AFA and the Immune System
Consumption of Aphanizomenon flos-aquae Has Rapid Effects on the Circulation and Function of Immune Cells in Humans
A novel approach to nutritional mobilization of the immune system Gitte S. Jensen,1 Donald 1. Ginsberg,1 Patricia Huerta,1 Monica Citton,1 and Christian Drapeau 2,3 1Department of Surgery, McGill University, Montreal Quebec 2Cell Tech, Klamath Falls, or 3Current Address: Desert Lake Technologies, Klamath Falls, OR
Objective: To examine the short-term effects of consumption of a moderate amount (1.5 grams) of the blue green algae Aphanizomenon flos-aquae (AFA), on the immune system.
Methods: Using a crossover placebo-controlled, randomized, double-blinded design, 21 volunteers were studied, including 5 long-term AFA consumers.
Results: Consumption of a moderate amount (1.5 grams) of the blue-green algae Aphanizomenon flos-aquae results in rapid changes in immune cell trafficking. Two hours after AFA consumption, a generalized mobilization of lymphocytes and monocytes, but not polymorph nucleated cells was observed. This included increases in CD3+, CD4+, and CD8+ T cell subsets and CD19+ B cells. In addition, the relative proportions and absolute numbers of natural killer (NK) cells were reduced after AFA consumption. No changes were observed in the relative proportions of n6ve versus memory T cells, neither in the CD4 or the CD8 fractions. A mild, but significant reduction in phagocytic activity was observed for polymorph nucleated cells. When freshly purified lymphocytes were exposed to AFA extract in vitro, direct activation was not induced, as evaluated by tyrosine phosphorylation and proliferative activity.
Discussion: The changes in immune cell trafficking displayed high degree of cell specificity. Long-term consumers responded stronger, with respect to altered immune cell trafficking. In vitro, AFA did not induce a direct activation of lymphocytes. These data support a signaling pathway from gut-to-CNS-to-lymphoid tissue. The signals from CNS may be crucial for the rapid changes in the general distribution and specific recruitment we observed. Moderate anti-inflammatory modulation may account for the modification of phagocytic activity.
Conclusion: Consumption of AFA leads to rapid changes in immune cell trafficking, but not direct activation of lymphocytes. Thus, AFA increases the immune surveillance without directly stimulating the immune system.
JANA, vol. 2, No. 3, 2000, pp. 50-58
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