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| CLINICAL STUDIES WITH ESSENTIAL PHOSPHOLIPIDS REFERENCES (click here)
consists of essential phospholipids from soya that are specially formulated for intravenous administration. Phospholipids are extremely important components of cell membranes. The integrity of the cell membrane is critical to the proper functioning of the cell. As the cell ages the phospholipid composition of the membrane changes and the cell's functions deteriorate and it loses its normal shape and elasticity. Eventually the cell dies and is destroyed by the immune system. Damage to the cell membrane, and thereby aging, is thought to be mediated by the actions of highly reactive chemicals referred to as free radicals. The damage caused by free radicals must be repaired in order to preserve normal cell function, and in order to do so, the cells need an abundant supply of the essential phospholipids phosphatidylcholine and deoxycholic acid. Lipostabil Phosphatidylcholine contains these important phospholipids and other essential nutrients that allow cells to repair damage and restore youthful function. Phosphatidylcholine is a phospholipid that is a major constituent of cell membranes. Phosphatidylcholine is also known as 1, 2-diacyl-:ussn:ue-glycero-3-phosphocholine, PtdCho and lecithin. It is represented by the following chemical structure:
Lecithin is regarded as a well tolerated and non-toxic emulsifier. It is approved by the United States Food and Drug Administration for human consumption with the status "Generally Recognized As Safe". It is an integral part of cell membranes, and can be totally metabolised. Lecithin is used commercially for anything requiring a natural emulsifier and/or lubricant, from pharmaceuticals to protective coverings. For example, lecithin is the emulsifier that keeps chocolate and cocoa butter in a confectionery bar from separating. Lecithins containing phosphatidylcholine are produced from vegetable, animal and microbial sources, but mainly from vegetable sources. Soybean, sunflower and rapeseed are the major plant sources of commercial lecithin. Soybean is the most common source. Plant lecithins are considered to be GRAS (generally regarded as safe). Egg yolk lecithin is not a major source of lecithin in nutritional supplements. Eggs themselves naturally contain from 68 to 72% phosphatidylcholine, while soya contains from 20 to 22% phosphatidylcholine. The fatty acid makeups of phosphatidylcholine from plant and animal sources differ. Saturated fatty acids, such as palmitic and stearic, make up 19 to 24% of soya lecithin; the monounsaturated oleic acid contributes 9 to 11%; linoleic acid provides 56 to 60%; and alpha-linolenic acid makes up 6 to 9%. In egg yolk lecithin, the saturated fatty acids, palmitic and stearic, make up 41 to 46% of egg lecithin, oleic acid 35 to 38%, linoleic acid 15 to 18% and alpha-linolenic 0 to 1%. Soya lecithin is clearly richer in polyunsaturated fatty acids than egg lecithin. Unsaturated fatty acids are mainly bound to the second or middle carbon of glycerol. Choline comprises about 15% of the weight of phosphatidylcholine.
Pharmacokinetics Phosphatidylcholine is also metabolized to choline, fatty acids and glycerol. The fatty acids and glycerol either get oxidized to produce energy or become involved in lipogenesis. Choline is a precursor of acetylcholine. Serum choline levels peak between 2 to 6 hours after oral intake.
RESEARCH SUMMARY Clinical studies have demonstrated that choline is essential for normal liver function. Phosphatidylcholine is a better delivery form and is also more tolerable than choline. But, in addition, research has shown that phosphatidylcholine, independent of its choline content, has striking hepatoprotective effects. In two animal studies using baboons fed diets high in alcohol, some supplemented with a soy-derived polyunsaturated lecithin (60% phosphatidylcholine) and some unsupplemented, both fibrosis and cirrhosis were largely prevented in the phosphatidylcholine group. Most of the unsupplemented animals in these studies, which continued for up to eight years, developed fibrosis or cirrhosis. Because these researchers had previously found that choline, equal in amounts contained in the phosphatidylcholine-rich lecithin they subsequently used, had no comparable protective effects on the liver, they concluded that the polyunsaturated phospholipids themselves may have been responsible for the benefits observed. In vitro studies have shown that these phospholipids increase hepatic collagenase activity and may thus help prevent fibrosis and cirrhosis by encouraging collagen breakdown. Several other mechanisms under investigation may also contribute. Others have reported similarly encouraging results in animal models. Clearly, human trials are warranted. In addition, phosphatidylcholine has demonstrated other protective effects in non-alcoholic liver disorders, including protection against various other toxic substances. Its benefits in viral hepatitis were reported some years ago by several different research groups in Europe and elsewhere. In one of these studies, individuals suffering from hepatitis type A and B were given 1.8 grams of phosphatidylcholine daily. Compared with unsupplemented controls, the phosphatidylcholine group enjoyed quicker recoveries, fewer relapses and quicker normalization of liver function tests. Researchers in Great Britain treated chronic active hepatitis C patients with 3 grams daily of phosphatidylcholine in double-blind fashion. The phosphatidylcholine patients had significantly reduced symptoms, compared with controls. All histologic evidence of the disease disappeared in some cases. These researchers, like others, have hypothesized that phosphatidylcholine's possible antiviral effects are related to the supplement's apparent ability to increase cellular membrane fluidity and repair the membranes of liver cells. Detoxification Hypercholesterolemia and Atherosclerosis: Phosphatidylcholine and weight reduction The treatment with phosphatidylcholine in the context of injection lipolysis (fat dissolving injections). It has primarily been used clinically for intravenous treatment of fat embolism, for lowering cholesterol levels and as a liverprotective substance. For some years now, phosphatidylcholine has also been used for subcutaneous treatments of circumscribed fat deposits at eyelids, abdominal folds, flanks, upper and lower limbs and other body areas; and the clinical results have been excellent. Phosphatidylcholine exerts an important influence on the regulation of lipid homeostasis by producing essential components of lipoproteins.. It activates L-CAT (lecithin-cholesterol acyltransferase) which in turn initiates the transportation of excess cholesterol found in the tissue, to the liver and their transformation into bile acids. In the lungs, phosphatidylcholine is active as a surfactant preventing the alveolar breakdown at the end of the expiration. As from the 35th week of pregnancy, a mix consisting of 90% phosphatidylcholine and 10% proteins (surfactant proteins SP-A and surfactant proteins D) is produced in the pneumocytes in the course of the foetal lung development. This spreads like a ilm on the alveolar surface and can be detected in bronchial secretion and amniotic fluid. It facilitates the development of the collapsed alveoli of the newborn and forms a part of the protection and self-cleaning mechanism of the bronchial system. In case of a surfactant deficiency syndrome, it is – in addition to other measures - set into the bronchial system. Also in connection with the body’s inflammatory process, phosphatidylcholine fulfils important physiological tasks, namely by means of the biosynthesis of prostaglandins, leukotrienes and thromboxanes of the arachidonic acid. Phospholilpase-A2 releases arachidonic acid from the membrane lipids. Through the action of cyclooxygenase, it is turned into prostaglandin H2, the precursor of all physiological prostaglandins and thromboxanes. Due to cyclooxygenase inhibition, phosphatidyl has a prostaglandin-antagonistic effect. Phosphatidylcholine is hydrolyzed in the fatty tissue by phospholipase D and produces apolar phosphoric acid and polar cholines. Cholines have lipotropic properties and work as emulsifiers; and are components of the phospholipids. At the end of the 80s, phosphatidylcholine was used for infiltration in xanhelasmata, and this with satisfactory success. In the 90s, some physicians in Brazil started with subcutaneous injections into fat deposits under the eyelids, in the abdomen, hip and flanks. The results of these treatments of localised adiposities to improve body contours were outstanding. Scientific research of the lipolysis mechanism of phosphatidylcholine on to human adipocytes revealed that phosphatidylcholine penetrates the adipocytes and is then, due to the impact of phospholipase D, hydrolyzed to phosphoric acid and choline. Cholines act as emulsifiers, and phosphoric acid triggers the activation of protein kinase C (PKC). The latter has the effect that lipolytic lipases – assisted by HSL (hormone sensitive lipases) hydrolyze triglycerides to become fatty acids and glycerine. With the help of lipoproteins – e.g. phosphatidylcholine is the major component of HDL - these are now transported to the liver and eliminated as bile acids. Lipostabil® is the tradename for an injectable preparation of phosphatidycholine manufactured by Aventis. It is approved for cardiological (to reduce cholesterol) use in some countries in Europe, though not including the United Kingdom.
According to the American Medical Association, one in five American adults, or about 47 million, are afflicted with the syndrome, which can more than double one’s risk of heart attack, stroke, and diabetes. One study of people with NAFLD found that 88% of those with nonalcoholic steatohepatitis had metabolic syndrome, compared to 55% of patients with simple fatty liver. The researchers concluded that the presence of the syndrome increased the risk of a person with benign fatty liver disease progressing to nonalcoholic steatohepatitis. No cure and no single specific treatment are available for metabolic syndrome; today doctors can only treat the various conditions—such as obesity, hypertension, high cholesterol, and diabetes—that are components of the disease.Even more important than the fact that a person is obese is where excess fat is stored on the body. Research has shown that people who carry excess weight around their middle (abdomen or waist) are most prone to developing insulin resistance. And recent studies have revealed that the majority of people with nonalcoholic fatty liver disease have central (abdominal) obesity. Phosphatidylcholine, should be an essential part of any sensible weight reduction programme, when weight reduction is large and side effects are to be kept to the bare minimum. For any weight reduction regime to be permanent it is strongly advised for drug therapt to be combined with diet (calorie) redcution and a regular exercise programme.
Alzheimer's Disease: Recently it has been suggested that phosphatidylcholine might eventually have some therapeutic role in some cancers. There is no evidence of this to date, but animal studies indicate that deficiencies in choline and phosphatidylcholine may disrupt cell membrane signal transduction in ways that could lead to various cancers. There is ample evidence that liver cancer is promoted in various animals by choline-deficient diets, and it has been shown that excess choline can protect against liver cancer in a mouse model. Those with malabsorption problems may develop diarrhea or steatorrhea when using phosphatidylcholine supplements. Those with the antiphospholipid-antibody syndrome should exercise caution in the use. Those with malabsorption problems may develop diarrhea or steatorrhea when using phosphatidylcholine supplements. Those with the antiphospholipid-antibody syndrome should exercise caution in the use of phosphatidylcholine supplements. Dosage By i.v injection: carefully inject by slow i.v. injection (duration of injection 3-4min). It is suggested to dilute with patient's own blood with a 1:1 ratio. Do not mix any other substance or electrolitic solution into the same syringe. Recommended dosage is 1-2 amps daily. It can be increased according to doctor's advice, to 3-4 amps daily. It is possible to inject 2 amps at the same time, with the same syringe, always very slowly. By phleboclysis: the amps content must be diluted only in glucidic solutions (such as glucose or levulose). The solution must be clear for the whole duration of phleboclysis. In acid environments, some fine flocculation episodes could occur. For the same reason electrolitic solutions cannot be used for dilution. The final solution Ph should be close to 7.5. The suggested dosage is 4-8 amps daily in 250-1000ml sugary solution. It can be increased according to doctor's advice, to 12-16 amps daily, especially in the total parenteral nutrition. Tolerability can be increased, by adjustment of phleboclysis speed in those patients particularly sensitive from a neurovegetative point of view. If phleboclysis injections are not given daily, intravenous injections are suggested between intervals. Parenteral treatment should be completed, as soon as possible, by oral treatment with Essentiale forte caps. • Using lecithin, the most common form of choline supplementation, with 90 percent phosphatidylcholine, the dosage (three times daily with meals) is:
* For Lipodissolve treatment please refer previous section for details ADVERSE REACTIONS INTERACTIONS OVERDOSAGE Atoba MA, Ayoola EA, Ogunseyinde O. Effects of essential phospholipid choline on the course of acute hepatitis-B infection. Trop Gastroenterol. 1985; 6:96-9. Buko V, Lukivskaya O, Nikitin V, et al. Hepatic and pancreatic effects of polyenoylphosphatidylcholine in rats with alloxan-induced diabetes. Cell Biochem Funct. 1996; 14:131-137. Canty DJ, Zeisel SH. Lecithin and choline in human health and disease. Nutr Rev. 1994; 52:327-339. Cohen BM, Lipinski JF, Altesman RI. Lecithin in the treatment of mania: double-blind, placebo-controlled trials. Am J Psychiatry. 1982; 139:1162-1164. Gelenberg AJ, Dorer DJ, Wojcik JD, et al. A crossover study of lecithin treatment of tardive dyskinesia. J Clin Psychiatry. 1990; 51:149-153. Growdon JH, Gelenberg AJ, Doller J, et al. Lecithin can suppress tardive dyskinesia. N Engl J Med. 1978; 298:1029-1030. Hanin I, Ansell GB, eds. Lecithin. Technological, Biological and Therapeutic Aspects. New York and London: Plenum Press; 1987. Hirsch MJ, Growdon JH, Wurtman RJ. Relations between dietary choline or lecithin intake, serum choline levels, and various metabolic indices. Metabolism. 1978; 27:953-960. Jackson IV, Nuttall EA, Ibe IO, Perez-Cruet J. Treatment of tardive dyskinesia with lecithin. Am J Psychiatry. 1979; 136:1458-1460. Jenkins PJ, Portmann BP, Eddleston AL, Williams R. Use of polyunsaturated phosphatidylcholine in HBsAg negative chronic active hepatitis: results of prospective double-blind controlled trial. Liver. 1982; 2:7-81. Kosina F, Budka K, Kolouch Z, et al. Essential cholinephospholipids in the treatment of virus hepatitis. Cas Lek Cesk. 1981; 120:957-960. Lieber CS, Leo MA, Aleynik SI, et al. Alcohol Clin Exp Res. 1997; 21:375-379. Lieber CS, De Carl LM, Mak KM, et al. Attenuation of alcohol-induced hepatic fibrosis by polyunsaturated lecithin. Hepatol. 1990; 12:1390-1398. Little A, Levy R, Chuaqui-Kidd P, Hand D. A double-blind, placebo-controlled trial of high-dose lecithin in Alzheimer's disease. J Neur Neurosurg Psych. 1985; 48:736-742. Visco G. Polyunsaturated phosphatidylcholine in association with vitamin B complex in the treatment of acute viral hepatitis B. results of a randomized double-blind clinical study. Clin Ter. 1985; 114:183-188. Wurtman RJ, Hefti F, Melamed E. Precursor control of neurotransmitter synthesis. Pharmac Rev. 1981; 32:315-335. Wurtman RJ, Hirsch MJ, Growdon JH. Lecithin consumption raises serum-free-choline levels. Lancet. 1977; 2(8028):68-69. As a licensed Pharmacy and Wholesaler we strictly observe legal requirements in both our and your country. Information provided on this site is for informational purposes only and is not a substitute for professional medical advice.We do not 'prescribe' nor 'proscribe' the information given which is only for uptodate information purposes only! You should not use this information for diagnosing or treating a health problem or disease or prescribing any medication. Only your healthcare provider should diagnose your healthcare problems and prescribe.
General & Medical Disclaimer
Information contained in this website does NOT constitute legal or medical advice. All information contained herein is solely for educational purposes. All items contained in this website are to be considered advertisements. Furthermore, any electronic or other means of communication sent to this website will not constitute a doctor-patient relationship, nor any other legal relationship of any kind. Phosphatidylcholine and any of our other advertised medical techniques or aesthetic substances, are sold under the condition that their application and use is provided under supervision and monitoring by a licensed physician in the country, where the order originates. Refund Policy: All sales are final due to the perishable nature of the products.
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