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Of the Phospholipids, more than 78% is Phosphatidylcholine..
Phospholipids
It is reported that Phosphatidylcholine's role in the maintenance of cell-membrane integrity is vital. From the growth and maintenance of DNA and RNA as proteins to energy and intracellular communication Phosphatidylcholine is integral to all of the basic biological processes. Low levels of it are associated with a number of disorders. e.g., liver disease, neurological diseases, various cancers and cell death.
Phosphatidylcholine is absorbed into the mucosal cells of the small intestine. Phosphatidylcholine may be indicated to help restore liver function. It may also have an application for the treatment of some manic conditions
Phosphatidylcholine (derived from lecithin), a primary dietary source of choline, is composed of a phosphate group, 2 fatty acids, and choline. The composition of essential fatty acids in phosphatidylcholine determines its value in promoting health. When phosphatidylcholine is ingested, most of it is broken down into choline, glycerol free fatty acids, and the phosphate group, rather than being incorporated intact into cellular membranes.
Although choline can be manufactured in humans from either methionine or serine, it has recently been designated an essential nutrient.
Choline is required for the proper metabolism of fats; it facilitates the movement of fats in and out of cells. Like Vitamin B12, 5-adenosylmethionine, and Folic Acid, choline acts in the human body as a methyl donor. As such, choline is essential for proper liver function due to its key role in the lipotropic effect, i.e., the export of fat from the liver. In the absence of adequate choline, fats become trapped in the liver, where they block metabolism. Stagnation of fat and bile eventually leads to the development of more serious liver disorders such as cirrhosis.
Choline is needed for cell membrane integrity because of the critical role it plays in the manufacture of primary components of cell membranes, such as phosphatidylcholine and sphingomyelin.
Choline is essential in the synthesis of acetylcholine. Choline supplementation increases the accumulation of acetylcholine which plays a crucial role in many brain processes, including memory. (Canty, DJ and Zeisel, SH. Nutr Reviews. 52;327-339, 1994)
Choline
Choline has recently been designated as an essential nutrient.
RDA:
Infants and children: 125 to 375 mg/day
Women: 425 mg/day; Pregnant women: 450 mg/day; Breast-feeding women: 500 mg/day
Men: 500 mg/day
Choline is a dietary supplement used to treat high cholesterol, improve memory, and protect the liver.

Other names for Choline include: CDP-choline, Citicoline, Phosphatidylcholine, Polyenylphosphatidylcholine (PPC), and Tetra-methylglycine.
Phosphatidylcholine increases the solubility of cholesterol and thereby decreases cholesterol‘s ability to induce atherosclerosis. Phosphatidylcholine aids in lowering cholesterol levels, removing cholesterol from tissue deposits, and inhibiting platelet aggregation. (Brook, JG, Linn, S, and Aviram, M. Biochem Med Metabol Biol. 35;31-39, 1986.) The high content of linoleic acid in phosphatidylcholine may be responsible for much of the benefit derived from supplementation.
Phosphatidylcholine is found in soy lecithin. It can be taken as dietary lecithin or as a supplement for high cholesterol, atherosclerosis (fat deposits on arteries), high blood pressure, liver problems, bipolar depression, dementia, dyskinesias (difficulty making movements), gallbladder disease, headache, and multiple sclerosis. It is used on the skin for acne and psoriasis.

Other names for Phosphatidylcholine include: Lecithin, Phosphatidylethanolamine, Phosphatidyl, Phosphatidylinositol, PC-55, Ethanolamine, and Serine.
Lecithin is found in all living cells. The highest amount of Lecithin is found in the brain, heart, liver, and kidney. Lecithin can also be prepared from soybeans. It is commonly used as a supplement for atherosclerosis (hardening and narrowing of the arteries), Alzheimer's disease, depression, dementia, gallbladder disease, gallstones, liver disease, headache, multiple sclerosis, acne (pimples), psoriasis, and high cholesterol. Its use in the treatment of depression, dementia, gallbladder disease, headache, multiple sclerosis, and psoriasis may not be effective. Lecithin that is available at health food stores is usually a combination of fats (including phosphatidylcholine), oil, and carbohydrates.

Other names for Lecithin include: Phosphatidylcholine, Phosphatidylethanolamine, Phosphatidylinositol, PC-55, Ethanolamine, and Serine.
Antioxidant
Astaxanthin, unlike some carotenoids, does not convert to Vitamin A (retinol) in the human body. Too much Vitamin A is toxic for a human, but astaxanthin is not. However, it is a powerful antioxidant; it is 10 times more capable than other carotenoids.[3]
While astaxanthin is a natural nutritional component, it can be found as a food supplement. The supplement is intended for human, animal, and aquaculture consumption. The commercial production of astaxanthin comes from both natural and synthetic sources
Astaxanthin, a naturally occurring carotenoid pigment, is a powerful biological antioxidant. Astaxanthin exhibits strong free radical scavenging activity and protects against lipid peroxidation and oxidative damage of LDL-cholesterol, cell membranes, cells, and tissues. Astaxanthin has been the focus of a large and growing number of peer-reviewed scientific publications.
Significant research and discoveries on the possible roles of antioxidants in our health, in the aging process, and on specific diseases, have been made in the recent years and published in peer-reviewed scientific journals. Astaxanthin is one of the most potent and bio-active biological antioxidants found in nature.
Several studies have shown the effectiveness of astaxanthin as a cancer preventive in rats and mice. For example, Tanaka et al. (1994b) showed that astaxanthin protected mice from urinary bladder carcinogenesis. (Tanaka et al. 1995b) the investigators showed that astaxanthin prevents oral carcinogenesis in rats. (Tanaka et al. 1994a). A further study by this group (Tanaka et al. 1995a) explored the effect of astaxanthin on colon cancer in male rats.
Astaxanthin has been shown to significantly influence immune function in a number of in vitro and in vivo assays using animal models. The majority of this work has been carried out by Harumi Jyonouchi and colleagues at the University of Minnesota.
There is abundant evidence that certain carotenoids can help protect the retina from oxidative damage (Snodderly 1995). A recent study with rats indicates that astaxanthin is effective at ameliorating retinal injury, and that it is also effective at protecting photoreceptors from degeneration (Tso and Lam 1996). The results of this study suggest that astaxanthin could be useful for prevention and treatment of neuronal damage associated with age-related macular degeneration, and that it may also be effective at treating ischemic reperfusion injury, Alzheimer's disease, Parkinson's disease, spinal cord injuries, and other types of central nervous system injuries (Tso and Lam 1996). In this study, astaxanthin was found to easily cross the blood-brain barrier (unlike beta-carotene), and did not form crystals in the eye (unlike canthaxanthin; Tso and Lam 1996).
The astaxanthin molecule is similar to that of the familiar carotenoid beta-carotene (Fig. 1), but the small differences in structure confer large differences in the chemical and biological properties of the two molecules. In particular, astaxanthin exhibits superior antioxidant properties to beta-carotene in a number of in vitro studies (Terao 1989; Miki 1991; Palozza and Krinsky 1992; Lawlor and O'Brien 1995). While the positive effects of astaxanthin on farmed fish and crustaceans have been recognized for years, the potential benefits of this powerful antioxidant to human health are only now being revealed.
As is the case with other carotenoids, astaxanthin is a potent quencher of singlet oxygen. One comprehensive study found astaxanthin to be twice as effective as beta-carotene (and about 80 times more effective than vitamin E) in quenching singlet oxygen in chemical solution (Di Mascio et al . 1991);
Antioxidant role of carotenoids is in the scavenging of free radicals. An elegant study of carotenoid-radical reactions in chemical solution clearly demonstrated that reactivity rates depend not only on the carotenoid but also on the nature of the radical (Mortensen et al. 1997). In one study, astaxanthin was approximately as effective as canthaxanthin (a xanthophyll structurally similar to astaxanthin), and about 50% more effective than beta-carotene and zeaxanthin, in preventing fatty acid peroxidation in chemical solution (Terao 1989). In a membrane model, astaxanthin was found to be more effective at scavenging peroxyl radicals than was beta-carotene (Palozza and Krinsky 1992). Another study using membrane models found similar results, with astaxanthin better at delaying lipid peroxidation than zeaxanthin, canthaxanthin, or beta-carotene (Lim et al. 1992). A tissue culture model demonstrated that astaxanthin was superior to beta-carotene or vitamin E in protecting the cells from herbicide-induced oxidative stress (Lawlor and O'Brien 1995).
Many human diseases and degenerative processes have been linked in some way to the action of free radicals. Free radicals are not necessarily the only cause for these conditions, but may well make the human body more susceptible to other disease-initiating factors, may enhance the progression of diseases, and may inhibit the body's own defenses and repair processes. The following conditions involving multiple organs have all been linked to free radicals (Cross et al. 1987):
  • Cancer
  • Aging (including immune deficiency with aging and premature aging disorders)
  • Radiation injury
  • Alcohol damage
  • Ischemia-reperfusion injuries
  • Inflammatory-immune injuries (including vasculitis from drugs and hepatitis B virus, idiopathic and membranous glomerulonephritis, and autoimmune diseases)
  • Reactions induced by drugs and toxins
  • Iron overload (including idiopathic hemochromatosis, dietary iron overload, thalassemia and other chronic anemias)
  • Amyloid diseases

In addition, a number of single-organ conditions have been related to free radicals (Cross et al. 1987):
  • Affecting the brain--senile dementia, neurotoxin reactions, hyperbaric oxygen effects, Parkinson's disease, cerebral trauma, hypertensive cerebrovascular injury, allergic encephalomyelitis and other demyelinating diseases, neuronal ceroid lipofuscinoses, ataxia-telangiectasia syndrome, potentiation of traumatic injury, aluminum overload
  • Affecting erythrocytes (red blood cells)--lead poisoning, protoporphyrin photo-oxidation, malaria, sickle-cell anemia, favism, Fanconi anemia
  • Affecting the lungs--emphysema, hyperoxia, cigarette-smoke effects, oxidant pollutant effects, acute respiratory distress syndrome, bronchopulmonary dysplasia, mineral dust pneumoconiosis, bleomycin toxicity, paraquat toxicity
  • Affecting the heart and cardiovascular system--atherosclerosis, stroke, doxorubicin toxicity, peripheral circulation problems, Keshan disease (selenium deficiency), alcohol cardiomyopathy
  • Affecting the kidney--renal graft rejection, nephritic antiglomerular basement membrane disease, heavy metal nephrotoxicity, aminoglycoside nephrotoxicity
  • Affecting joints--rheumatoid arthritis
  • Affecting the gastrointestinal tract and liver--endotoxin liver injury, carbon tetrachloride liver injury, diabetogenic action of alloxan, free fatty acid-induced pancreatitis, abetalipoproteinemia, nonsteroidal anti-inflammatory drug-induced lesions
  • Affecting the skin--sunburn and solar radiation injury, thermal injury, porphyria, contact dermatitis, Bloom syndrome, effects of photosensitive dyes
  • Affecting the eyes--age-related macular degeneration, ocular hemorrhage, degenerative retinal damage, cataractogenesis, retinopathy of prematurity, photic retinopathy

It is quite clear that human health depends to a large extent on the body's ability to control free radicals and thus reduce oxidative damage to tissues, cells, and DNA. To that end, antioxidants play an essential role in disease prevention, in longevity, and in overall well-being.

Omega 3’s

DHA acts by reducing white blood cell accumulation...
Docosahexanoic acid (DHA), an omega-3 fatty acid found in fish oils, has been shown to reduce the size of tumours and enhance the positive effects of the chemotherapy drug cisplatin, while limiting its harmful side effects. The rat experiments, described in BioMed Central's open access journal Cell Division, provide some support for the plethora of health benefits often ascribed to omega-3 acids.

Professor A. M. El-Mowafy led a team of researchers from Mansoura University, Egypt, who studied DHA's effects on solid tumours growing in mice, as well as investigating how this fatty acid interacts with cisplatin, a chemotherapy drug that is known to cause kidney damage. El-Mowafy said, "DHA elicited prominent chemopreventive effects on its own, and appreciably augmented those of cisplatin as well. Furthermore, this study is the first to reveal that DHA can obliterate lethal cisplatin-induced nephrotoxicity and renal tissue injury."

DHA is an omega-3 fatty acid that is commonly found in cold-water fish oil, and some vegetable oils. It is a major component of brain gray matter and of the retina in most mammalian species and is considered essential for normal neurological and cellular developments. According to the authors, "While DHA has been tentatively linked with protection against cardiovascular, neurological and neoplastic diseases, there exists a paucity of research information, in particular regarding its interactions with existing chemotherapy drugs". The researchers found that, at the molecular level, DHA acts by reducing leukocytosis (white blood cell accumulation), systemic inflammation, and oxidative stress - all processes that have been linked with tumour growth.

El-Mowafy and his colleagues have called for greater deployment of omega-3 in the fight against cancer. They write, "Our results suggest a new, fruitful drug regimen in the management of solid tumors based on combining cisplatin, and possibly other chemotherapeutics, with DHA".

Notes:

1. Chemopreventive and renal protective effects for docosahexaenoic acid (DHA): implications of CRP and lipid peroxides
M E Elmesery, M M Algayyar, H A Salem, M M Darweish and A M El-Mowafy
Cell Division (in press)
Article available at the journal website: http://www.celldiv.com/
All articles are available free of charge, according to BioMed Central's open access policy.

2. Cell Division is an Open Access, peer-reviewed online journal that will encompass all aspects of cell cycle control in eukaryotes. Cell Division is an online forum for and from the cell-cycle community that aims to publish articles on all exciting aspects of cell-cycle research and to bridge the gap between models of cell cycle regulation, development, and cancer biology. This forum will be driven by specialized and timely research articles, reviews and commentaries focused on this fast moving field, providing an invaluable tool for cell-cycle biologists.

3. BioMed Central (http://www.biomedcentral.com/) is an STM (Science, Technology and Medicine) publisher which has pioneered the open access publishing model. All peer-reviewed research articles published by BioMed Central are made immediately and freely accessible online, and are licensed to allow redistribution and reuse. BioMed Central is part of Springer Science+Business Media, a leading global publisher in the STM sector.

Source:
Graeme Baldwin
BioMed Central


Omega-3 fatty acids could help protect men against advanced prostate cancer...


For the study, Witte's team studied 466 men with aggressive prostate cancer and 478 healthy men. The researchers collected data on the men's diet and genetically assessed nine cox-2 single nucleotide polymorphisms.
"We detected strong protective associations between increasing intake of long-chain omega-3 polyunsaturated fatty acids and more advanced prostate cancer," Witte said. "These fatty acids are primarily from dark fish such as salmon."
This association held even if men had a high-risk genetic variant in the cox-2 gene, Witte said. "In contrast, men with low intake of dark fish and the high-risk variant had a substantially increased risk of more advanced prostate cancer," he noted.
The researchers found that men who had the highest intake of omega-3 fatty acids had a 63 percent lower risk of aggressive prostate cancer compared with men with the lowest intake of omega-3 fatty acids.
Then the researchers looked at the effect of omega-3 fatty acid in men with a cox-2 variant called rs4647310, a known inflammatory gene. Among men with low omega-3 fatty acid intake and this variant, the risk of developing advanced prostate cancer increased fivefold. However, men who had a high intake of omega-3 fatty acids had a significantly lower risk, even if they had the cox-2 variant.
These findings suggest that eating fish or other sources of long-chain omega-3 polyunsaturated fatty acids may decrease a man's risk of being diagnosed with more advanced prostate cancer, Witte said. "And the decrease in risk may be even more pronounced if one has a high-risk genetic variant in the cox-2 gene."
Focusing on more advanced tumors is important, since these tumors are most likely to take an aggressive course and thus impact a man's survival, he added. "Moreover, our results further support the hypothesis that long-chain omega-3 polyunsaturated fatty acids may modify prostate inflammation through the cyclooxygenase (cox) pathway," Witte said.
Eric Jacobs, strategic director of pharmacoepidemiology at the American Cancer Society, thinks the jury is still out on connecting omega-3 fatty acids with a reduced risk of advanced prostate cancer.
"In this study, a diet high in long-chain omega-3 fatty acids was associated with lower risk of developing advanced prostate cancer," Jacobs said. "However, some previous studies did not find similar results."
Indeed, other research has proved fruitless when it comes to using supplements
to help prevent prostate cancer. Two studies released in January in the Journal of the American Medical Association found no evidence of benefit from supplemental selenium, vitamin E or vitamin C on prostate cancer and other cancers. Other recent studies have suggested that vitamins, B, C, D, E, folic acid and calcium taken alone, or in various combinations, aren't effective for cancer prevention either.
Nevertheless, more research into omega-3s role in prostate cancer prevention is needed, Jacobs said.


CAUTION: People with seafood allergies, coagulopathy, or taking anticoagulants or other related medications should notify their physician and be tested prior to taking this dietary supplement.

These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.
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