Omega-3 EPA - for brain, cell membranes & connective tissueOmega-3 EPA - for brain, cell membranes & connective tissue

Nutritional supplements - Neways Health and Wellness

Omega-3 EPA - for brain, cell membranes & connective tissue
#2730
60.0 ct.
Price: $15.90
Quantity

Omega-3 EPA is an Essential Fatty Acid (EFA) supplement that supports the body's maintenance of blood lipids. Formulated with EPA (Eicosapentaenoic Acid), DHA (Docosahexaenoic Acid) and Vitamin E, Omega-3 EPA is a valuable brain nutrient supplement for growing children.

In spite of the current "antipathy toward fats," the body does need and use healthy types of fat, particularly the Essential Fatty Acids.

The fatty acids, EPA and DHA, in Omega-3 EPA are derived from fish oils. They support the body's maintenance of blood lipids, such as cholesterol. These Essential Fatty Acids are integral to total body health. They support the formation of healthy cell membranes, the maintenance of healthy muscles, the maintenance of healthy joints and the promotion of normal circulatory health.

Omega-3 EPA is formulated with Vitamin E, a natural antioxidant. Read clinical summary on Omega-3...

How to use

Take one softgel with a meal three times daily.

Storage

Refrigerate after opening.

Keep out of reach of children!

Caution

As with any nutritional supplement, consult a health care provider prior to use if you are pregnant or nursing, have a medical condition, or are taking any medication.

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Clinical Summary

A type of polyunsaturated fatty acid (PUFA) derived mainly from fish oil. Anecdotally, omega-3 fatty acids are used to treat depression, hypercholesterolemia and to reduce the risk of heart attack. A large survey of Finnish adults found that depressive symptoms were significantly higher among infrequent fish consumers 1 and other studies have shown that individuals with major depression have marked depletions in omega-3 fatty acids 2. Omega-3 fatty acid supplementation lowered triglyceride levels in people with type 2 diabetes mellitus, however, low density lipoprotein cholesterol levels were increased 3. Omega-3 fatty acids may also help patients with ulcerative colitis 4 and may reduce colon cancer risk 5 . Omega-3 may be useful as a perioperative supplement as it lowers the magnitude of the body's inflammatory response 6. It has been shown not to reduce coagulation and platelet function after surgery 7. Omega-3 fatty acids can reduce sunburn sensitivity 8. Reviews of trials using omega-3 fatty acids have shown possible benefits for patients with cystic fibrosis 9, but no benefit for patients with asthma 10. Only mixed results were seen in patients with schizophrenia 11. Results from a recent clinical trial suggest that dietary supplementation with fish oil may help reduce the symptoms of systemic lupus erythematosus 19 . The FDA recommended that the consumption of fish oils be limited to 3 grams or less per day as higher doses may increase the risk of bleeding. 18

Food Sources

  • Fish Oil
  • Cod Liver Oil
  • Flaxseed Oil
  • Linseed Oil

Purpoted Uses

  • Asthma
  • Atherosclerosis
  • Cancer prevention
  • Cardiovascular disease
  • Colitis
  • Cystic fibrosis
  • Depression
  • High cholesterol
  • Schizophrenia

Constituents

Fatty Acids including: Eicosapentaenoic (EPA), Docosahexaenoic (DHA), Myristic, Palmitric, Palmitoleic, Stearic, Oleic, Linoleic, Linolenic, Stearidonic, Eicosaenoic, Arachidonic, Docosaenoic and docosapentaenoic (DPA) 7.

Mechanism of Action

Omega-3 fatty acids are a type of polyunsaturated fatty acid containing two or more double bonds in their acyl chain and a double bond on carbon number 3 12. Changes in omega-3 fatty acid levels have been associated with cardiovascular disease and depression 13 . The cardioprotective effects of omega-3 likely come from its ability to be incorporated into and thereby enhance the stability of atherosclerotic plaques 12. Omega-3 fatty acid does not seem to affect platelet function or coagulation 7. Increasing the intake of polyunsaturated fatty acids has been shown to increase lipid peroxidation. Supplementation with omega-3 fatty acids, therefore, may increase the oxidative stress on the body. Studies have shown that mucosal alpha-tocopherol levels decrease upon omega-3 supplementation which researchers believe may result from the body's attempt to counteract the added oxidative burden 5. Besides reducing serum anti-oxidant levels, little is known about how this added oxidative stress affects the body. Omega-3 fatty acid supplementation has been shown to decrease IL-6 levels 6 and tumor necrosis factor-alpha 14 while leaving most other mononuclear cell functions unaffected 15. Omega-3 fatty acids may also reduce inflammation in patients with ulcerative colitis by reducing rectal dialysate leukotriene B4 4. Because of its anti-inflammatory effects, Omega-3 fatty acids have been thought to benefit patients with asthma 10 and cystic fibrosis 9, however studies are inconclusive. Increasing PUFA intake in pregnant women increases PUFA concentration but not cytokine concentration in human milk 16. Omega-3 fatty acid supplementation provides protection against ultra-violet radiation induced erythema and p53 expression, a biomarker of DNA damage 8.

Adverse Reactions

Reported: Fishy aftertaste 5, loose stools and nausea 17 after large doses.

Drug Interactions

May increase the effect of other anticoagulant/antiplatelet agents.

Lab Interactions

  • May reduce levels of alpha-tocopherol and beta-carotene 5 14.
  • High levels of omega-3 fatty acids may decrease triglyceride and increase LDL cholesterol levels 3.
  • Doses higher than 3 grams per day may increase bleeding time 18.

Literature Summary and Critique

Thies F, Garry JM, Yaqoob P, Rerkasem K, Williams J, Shearman CP et al. Association of n-3 polyunsaturated fatty acids with stability of atherosclerotic plaques: a randomised controlled trial. Lancet 2003;361:477-85.

A randomized controlled trial of polyunsaturated fatty acids and stability of atherosclerotic plaques. 188 patients awaiting carotid endarterectomy were randomized to receive sunflower oil (high omega-6 concentration), fish oil (high omega-3 concentration) or control oil until surgery. Each patient consumed six capsules per day each containing 1 g of oil and 1 mg alpha-tocopherol. Duration of treatment ranged from seven to 189 days with a median of 42 days. Patients receiving the fish oil supplementation were found to have readily incorporated omega-3 polyunsaturated fatty acids in their atherosclerotic plaques thereby enhancing the stability of the plaques. Patients receiving either sunflower oil or control had no change in fatty-acid composition or atherosclerotic stability during the course of treatment. Researchers believe that this stability of plaques may explain the reductions in cardiovascular events associated with omega-3 polyunsaturated fatty acid intake.

Stenson WF, Cort D, Rodgers J, Burakoff R, DeSchryver-Kecskemeti K, Gramlich TL et al. Dietary supplementation with fish oil in ulcerative colitis. Ann.Intern.Med 1992;116:609-14.

A multicenter, randomized, double-blind, placebo-controlled, crossover trial of fish oil and ulcerative colitis. 24 patients with ulcerative colitis were randomized to receive 18 Max-EPA capsules (3.24 g EPA and 2.6 g DHA) or 18 placebo capsules containing corn oil per day. Patients continued treatment for four months and after a washout period of one month, reversed treatment. Patients observed a statistically significant weight gain and reduction in acute histology index as well as rectal dialysate levels of leukotriene B4 during treatment.

Farmer A, Montori V, Dinneen S, Clar C. Fish oil in people with type 2 diabetes mellitus. Cochrane. Database.Syst.Rev. 2001;CD003205.

A systematic review of fish oil on cholesterol levels in people with type 2 diabetes mellitus including eighteen trials and 823 participants. Doses of fish oil ranged from 3 to 18 grams/day. Meta-analysis showed a statistically significant effect of fish oil in lowering triglycerides by 0.56 mmol/l and raising LDL cholesterol by 0.21 mmol/l. No statistically significant effect was observed for fasting glucose, HbA1c, total or HDL cholesterol. The effects on triglycerides and LDL cholesterol were more marked in recruited people with hypertriglyceridemia and in those trials using higher doses of fish oil. No adverse effects were reported. Researchers note that no trials with vascular or mortality defined endpoints were found.

Beckles WN, Elliott TM, Everard ML. Omega-3 fatty acids (from fish oils) for cystic fibrosis. Cochrane.Database.Syst.Rev. 2002;CD002201.

A systematic review of omega-3 fatty acids for cystic fibrosis including two trials and a total of 31 participants. Both trials compared omega-3 fatty acids to olive oil controls for six weeks. One study showed an improvement in FEV1, FVC, Schwachman score and reduction in sputum volume in the fish oil group. Larger, long-term, multi-center trials are needed to corroborate this evidence.

Woods RK, Thien FC, Abramson MJ. Dietary marine fatty acids (fish oil) for asthma in adults and children. Cochrane.Database.Syst.Rev. 2002;CD001283.

A systematic review of trials of omega-3 fatty acids for asthma in participants over two years of age that were at least four weeks in duration. The review included nine trials. No consistent effect on any of the following outcomes was observed: FEV1, peak flow rate, asthma symptoms, asthma medication use or bronchial hyper reactivity. One study which combined dietary manipulation with fish oil supplementation demonstrated improvement in peak flow and a reduction in asthma medication use, however the researchers concluded that there is little evidence to recommend omega-3 fatty acids to improve asthma control. No adverse effects were reported.

Joy CB, Mumby-Croft R, Joy LA. Polyunsaturated fatty acid supplementation for schizophrenia. Cochrane.Database.Syst.Rev. 2003;CD001257.

A systematic review of trials of polyunsaturated fatty acids for schizophrenia included including five small, short studies including 313 participants. One small study suggested that EPA enriched oil may have some antipsychotic properties when compared with placebo, however most trials were too small to show significant effect. Some of the trials included omega-6 fatty acid supplementation. Researchers conclude that larger, well designed studies are needed.

Duffy EM et al. The clinical effect of dietary supplementation with omega-3 fish oils and/or copper in systemic lupus erythematosus. J. Rheumatology. 2004;31(8):1551-6.

A double blind, double placebo controlled trial. 52 SLE patients were randomly assigned to 4 treatment groups that received 3 g fish oil and 3 g of copper, 3 g fish oil and placebo copper, 3 g copper and 3 g placebo fish oil, or both placebo capsules. Researchers found a significant reduction in symptoms of SLE in patients who took fish oil capsules compared to those on placebo. There was no measurable effect on symptoms in patients who took copper. Larger trials are needed to support this claim.

REFERENCES

1 Tanskanen A, Hibbeln JR, Tuomilehto J, Uutela A, Haukkala A, Viinamaki H et al. Fish consumption and depressive symptoms in the general population in Finland. Psychiatr.Serv. 2001;52:529-31.
2 Mischoulon D,.Fava M. Docosahexanoic acid and omega-3 fatty acids in depression. Psychiatr. Clin North Am 2000;23:785-94.
3 Farmer A, Montori V, Dinneen S, Clar C. Fish oil in people with type 2 diabetes mellitus. Cochrane.Database.Syst.Rev. 2001;CD003205.
4 Stenson WF, Cort D, Rodgers J, Burakoff R, DeSchryver-Kecskemeti K, Gramlich TL et al. Dietary supplementation with fish oil in ulcerative colitis. Ann.Intern.Med 1992;116:609-14.
5 Anti M, Armelao F, Marra G, Percesepe A, Bartoli GM, Palozza P et al. Effects of different doses of fish oil on rectal cell proliferation in patients with sporadic colonic adenomas. Gastroenterology 1994;107:1709-18.
6 Weiss G, Meyer F, Matthies B, Pross M, Koenig W, Lippert H. Immunomodulation by perioperative administration of n-3 fatty acids. Br J Nutr 2002;87 Suppl 1:S89-S94.
7 Heller AR, Fischer S, Rossel T, Geiger S, Siegert G, Ragaller M et al. Impact of n-3 fatty acid supplemented parenteral nutrition on haemostasis patterns after major abdominal surgery. Br J Nutr 2002;87 Suppl 1:S95-101.
8 Rhodes LE, Shahbakhti H, Azurdia RM, Moison RM, Steenwinkel MJ, Homburg MI et al. Effect of eicosapentaenoic acid, an omega-3 polyunsaturated fatty acid, on UVR-related cancer risk in humans. An assessment of early genotoxic markers. Carcinogenesis 2003;24:919-25.
9 Beckles WN, Elliott TM, Everard ML. Omega-3 fatty acids (from fish oils) for cystic fibrosis. Cochrane.Database.Syst.Rev. 2002;CD002201.
10 Woods RK, Thien FC, Abramson MJ. Dietary marine fatty acids (fish oil) for asthma in adults and children. Cochrane.Database.Syst.Rev. 2002;CD001283.
11 Joy CB, Mumby-Croft R, Joy LA. Polyunsaturated fatty acid supplementation for schizophrenia. Cochrane.Database.Syst.Rev. 2003;CD001257.
12 Thies F, Garry JM, Yaqoob P, Rerkasem K, Williams J, Shearman CP et al. Association of n-3 polyunsaturated fatty acids with stability of atherosclerotic plaques: a randomised controlled trial. Lancet 2003;361:477-85.
13 Severus WE, Littman AB, Stoll AL. Omega-3 fatty acids, homocysteine, and the increased risk of cardiovascular mortality in major depressive disorder. Harv.Rev.Psychiatry 2001;9:280-93.
14 Holm T, Berge RK, Andreassen AK, Ueland T, Kjekshus J, Simonsen S et al. Omega-3 fatty acids enhance tumor necrosis factor-alpha levels in heart transplant recipients. Transplantation 2001;72:706-11.
15 Wallace FA, Miles EA, Calder PC. Comparison of the effects of linseed oil and different doses of fish oil on mononuclear cell function in healthy human subjects. Br J Nutr 2003;89:679-89.
16 Hawkes JS, Bryan DL, Makrides M, Neumann MA, Gibson RA. A randomized trial of supplementation with docosahexaenoic acid-rich tuna oil and its effects on the human milk cytokines interleukin 1 beta, interleukin 6, and tumor necrosis factor alpha. Am J Clin Nutr 2002;75:754-60.
17 Fugh-Berman A,.Cott JM. Dietary supplements and natural products as psychotherapeutic agents. Psychosom.Med 1999;61:712-28.
18 Lewis, C. J. Letter Regarding Dietary Supplement Health Claim for Omega-3 Fatty Acids and Coronary Heart Disease. FDA Docket No. 91N-0103. 10-31-2000. U.S. Fooda nd Drug Administration. http://vm.cfsan.fda.gov/~dms/ds-ltr11.html
19 Duffy EM, et al. The Clinical effect of dietary supplementation with omega-3 fish oils and/or copper in systemic lupus erythematosus. J. Rheumatology 2004;31(8):1551-6.
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