Glyconutrients
 

Red Algae

Many claims have been made for the effectiveness of seaweeds on human health. It has been suggested, amongst other things, that seaweeds have curative powers for tuberculosis, arthritis, colds and influenza, worm infestations, and may even improve one's attractiveness to the opposite sex. Red marine algae, referred to as 'superfood', is noted to be a source of nutrients and botanically based medicines.

Research on antiviral carbohydrates from marine red algae indicate a high potential for low-cost, broad spectrum antiviral agents. Further research in the family of Dumontiaceae produced two patents where clinical efficacy for herpes I and II was clearly shown. The treatment was effective for treating subjects (e.g. human patients) both prior to and subsequent to herpes infection. It was used topically to alleviate symptoms associated with herpes infections or preferably systemic, by oral administration, to eradicate the virus and thereby prevent symptom recurrence. No side effects or toxicity were noted. This treatment, which now must be considered alternative, suggests a breakthrough in the discovery of natural immunomodulatory and antiviral agents.

Recent research and gathering of anecdotal evidence on the health benefits and antiherpetic action of the red marine alga, Dumontiaceae, has yielded much promise. Its use as a topical has been further documented and thought superior to acyclovir. It was shown to be clinically effective against herpes zoster infections as well. Anecdotal reports from patients suffering from Epstein Barr (another herpes virus) and Candida have shown marked improvement in a short period of time through oral administration (systemic).

General health benefits show red marine algae useful in weight-loss programs and for lowering cholesterol and fat in the blood. It contains soothing, mucilaginous gels such as algin, carregeenan, and agar, which specifically rejuvenate the lungs and gastrointestinal tract. Once thought of as a liability that blocked assimilation, the tough cell wall in Dumontiaceae has been found to be invaluable. It binds with heavy metal, pesticides, and carcinogens, and carries these toxins safely out of the body. Contained within the cell walls are polysaccharides, which are a complex of simple sugars. These long chained complex sugars stimulate interferon production as well as other anti-tumor and immune- enhancing activity (improving activity of T- and B-cells). Other compounds in the cell wall are related to those found in friendly bacteria which fortify and

According to Elson Haas, M.D., co-author of Vitamins for Dummies (IDG, 1999), algin-rich kelp binds lead and other heavy metals and removes them from the body. Kelp's high calcium content may also reduce the amount of toxic metals that are absorbed. But kelp isn't the only seaweed capable of combating heavy metals. The polysaccharides found in red marine algae, particularly Irish moss (Chondrus crispus), are also thought to bind and eliminate heavy metals. Better yet, red marine algae has antibiotic and immune-boosting properties, which help protect our bodies from invading toxins. strengthen our immune systems to fight against invading organisms and toxins.

One variety of red seaweed, Porcheria hornaminyahae, was tested in the mid-1980s by the National Cancer Institute and was found to contain a chemical that killed cancer cells. An in vitro study conducted at the Sapporo Medical University School of Medicine in Japan found that the holdfasts of kelp contain L-tryptophan, an essential amino acid. Although L-tryptohphan is not normally thought of as a cancer cure, the researchers found that the L-tryptophan derived from kelp inhibited breast cancer.

What's more, seaweed has been found to inhibit the formation of tumors. A test of 306 species of marine algae at Saga University in Karatsu, Japan, found forty-seven varieties that demonstrated strong anti-tumor activity. And a French study found that one of the sea lettuces, green laver (Ulva lactuca), provides oligosaccharides, which may stop the multiplication of cancerous cells. Although the study of seaweed's anti-tumor activity is in its infancy, there are a few commonly eaten seaweeds that show potential. Japanese researchers have discovered that hijiki (Hijikia fusiformis) seems to stimulate T cells, the body's natural killer cells. And other Japanese studies show that non and wakame may have the ability to suppress chemically induced tumors. According to Alfred A. Bushway, Ph.D., professor of food science at the University of Maine, seaweed's potential cancer fighting abilities may be due to its high concentration of sodium alginate, "but this is a research area that needs to be more fully explored," he says.

Showing Anticancer Promise

William Gerwick’s (a professor of Pharmacy at Oregon State University) work has helped identify and patent at least four new anticancer-type substances from blue-green algae:

  • Curacin A inhibits cancer by binding to certain cell receptors so that the cancer cells cannot replicate themselves.
  • Dolastatin 10 is undergoing National Cancer Institute-supported trials against a variety of solid tumors. Dolastatin 10 was judged to be “one of the most potent anticancer agents in vitro;” initial reports of phase I clinical testing showed that the compound “has potent activity” against small-cell lung cancer, and other research has found that the chemical has potential for treatment of leukemia and non-Hodgkins lymphoma.
  • Cryptophycin is a by-product of algae metabolism that was first described as an antifungal compound and later shown to possess phenomenal anticancer properties. It is currently in phase II clinical trials against several common tumor types. One study, reported in The Journal of Cancer Chemotherapy and Pharmacology, found cryptophycin to be “significantly more potent and less sensitive to multidrug resistance mechanisms than other antimitotic antitumor agents currently used in cancer therapy.”
  • Tolytoxin and related scytophycins are substances which inhibit cancer cell proliferation by novel mechanisms. One of several new algal-based compounds, Curacin A is showing promise as a possible cancer treatment. May 2000

Although the effects of long term use of an alternative treatment such as the red marine alga, Dumontiaceae, has not been clinically substantiated, edible seaweeds have been consumed for thousands of years and are considered safe, nutritious, and beneficial. The added dimension that science has uncovered surrounding its antiviral and immunomodulatory potential; opens up a whole new source of food that could serve to palliate or even hopefully cure virally caused diseases. Since most life derived from the sea, the novel idea that the ocean lies untapped as perhaps our greatest medicinal resource is entirely possible and may be critical to our human survival.

References:

1. Baba et. al., "Mechanism of inhibitory effect of dextran sulfate and heparin in replication of human immunodeficiency virus in vitro." Proc Natl. Acad. Sci 85:6132-6136. 1988

2. Barbul, A. et al., "Arginine stimulates lymphocyte immune response in healthy human beings. Surgery 90: pp 244-251. 1984
3. Cole and Sheath, (Ed.), Biology of the Red Algae, Cambridge University Press, Cambridge, 1990.

4. Dieg et. al., "Inhibition of herpes virus replication by marine algae extracts," Anitimicrb. Ag. Chemother. 6:524-525. 1974

5. Dieg et. al., "Evaluation of extracts of marine algae for antiviral activity in experimental herpes simplex infections of infant mice." In Fifty-second Technical Progress Report, Section 4, Naval Biosciences Laboratory, School of Public Health, University of California, Berkeley. 1977

6. Dieg et. al., "Development of dermal lesions in adult mice infected with herpes simplex virus: application of the model in the evaluation of antiherpesvirus substance from marine algae." Office of Naval Research, University of California Sea Grant Program. Unpublished.

7. Ehresmann et al., "Antiviral properties of algal polysaccharides and related compounds," In H. A. Hoppe et. al., (ed.), Marine Algae in Pharmaceutical Science, W. de Gruyter, N. Y.: 293-302. 1979 8. Ehresmann, et. al, "Antiviral substances from California marine algae," J. Phycol. 13: 37-40. 1979

9. Gonzales et. al., "Polysaccharides as antiviral agents: antiviral activity of carrageenan," Antimicrobial Agents and Chemotherapy. 31: 1388-1393. 1987

10. Hallinan et. al., "Inhibition of reverse transcriptase by polyvinyl sulfate (PVS)," Cancer Biochem. Biophys. 98:97-101. 1981

11. Hatch et. al., "Chemical characterization and therapeutic evaluation of anti Herpes virus polysaccharides from species of Dumontiaceae," In H. A. Hoppe et. al., (ed.) Marine Algae in Pharmaceutical Science W. de Gruyter, N. Y. 346-363. 1979

12. Mitsuya et. al., 1988 "Dextran sulfate suppression of viruses in the HIV family: inhibition of virion binding to CD4 and cells," Science 240:646-649. 1988

13. Nakashima et. al., "Antiretroviral activity in a marine red alga: reverse transcriptase inhibition by an aqueous extract of Schizymenia pacifica" Journal Cancer Res. Clin Oncol 113: 413-16. 1987

14. Neushul, "Antiviral carbohydrates from marine red algae." Hydrobiologia 204/205:99-104. 1990

15. Pitchford, Paul, Healing with Whole Foods, North Atlantic Books, Berkeley, California, 1993

16. Richards et. al., "Antiviral activity of extracts from marine algae," Antimicrob. Agents Chemother. 14: 24-3-. 1978

17. Schaffrath et. al., "Interactions of glycosaminoglycans with DNA and RNA synthesizing enzymes invitro," Z. Physiol Chem. 357:499-508. 1976

16. Solomon et. al., "Inhibitory effect of heparin on Rous Sarcoma virus," J. Bact. 92:1855-56. 1966

18. Straus et al.,, "Suppression of frequently recurring gential herpes" N Eng J of Medicine, Vol 310 No. 24 pg. 1545-50. 1984

19. Douglas et al., "Acyclovir and Genital Herpes" N Eng J of Medicine, Vol. 310 No. 24 pg. 1551-56. 1984

20. Thomson and Fowler, "Carrageenan: a review of its effects on the immune system,: Agents and Actions. 11: 265-273. 1981

21. Ueno and Kuno, "Dextran sulphate, a potent anti-HIV agent in vitro having synergism with sidovudine," Lancet 1:1379. 1987


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