Fish Oil Capsules
Fish Oil Capsules
There is growing evidence increased consumption of fish may be beneficial to health. Recent studies have found an association between consumption of fish oil and reduced risk of cardiovascular disease, as well as improvements in other health conditions, such as psoriasis and rheumatoid arthritis.
Most current research on the benefits of consuming more fish is directed at the effects derived from omega-3 fatty acids in many fish species. However, studies of human dietary preferences reveal up to one-half of the population may not like to eat fish. Of those who do eat fish, many prefer fish only when it is deep-fried, or consume non-fatty fish species, which are poorer sources of fish oil. This is one reason fish oil capsules have become popular as an alternative source of fish oil.
Support for the use of fish oil capsules primarily comes from three well-known epidemiological studies, two of which were carried on outside of the United States. One study, conducted in the Netherlands, suggested ingestion of as little as 35 grams of fish per day (a single one-half pound meal of fish per week) might help prevent coronary heart disease, possibly significantly reducing mortality due to cardiovascular disease in a 20 year follow up. Further, it has been suggested a regular diet of fish may decrease levels of plasma triglycerides, plasma cholesterol, low density lipoprotein-cholesterol (LDL), and very low density lipoprotein-cholesterol (VLDL).
Conversely, two other epidemiological studies have shown no relationship between fish consumption and cardiovascular mortality. Yet it is important to note there is some conflicting evidence regarding the benefits of fish oil consumption on blood pressure and its relationship to the development of some types of cancer.
In general, fish oil capsules supply concentrations of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). The EPA-DHA rich fish oil is generally sold in soft gelatin capsules. The gelatin provides an oxygen barrier which prevents the development of toxic lipid peroxides (e.g. malondialdehyde). Liquid, non-encapsulated formulations generally do not have this protection, and therefore may contain some toxic lipid peroxides.
In most cases the fish oils come from cold water ocean fish. Encapsulated products contain fish oil, not fish liver oil. This distinction is important since fish liver oil contains fat-soluble vitamin A and vitamin D, which if taken excessively have the remote potential of being toxic. The literature contains reports of vitamin A and vitamin D toxicity when levels above 50,000 IU/day are consumed.
Method of Action
In general, dietary unsaturated fatty acids play an important role in reducing atherogenesis and thrombosis. Fish oils appear to reduce hyperlipidemia, while decreasing the production of the prothrombotic substance, thromboxane, by enhancing the production of the platelet antiaggregatory substance, prostacyclin.
Through the combined vasodilatory effects of prostacyclin (Pgl-2 and Pgl-3), fish oils may improve peripheral circulation and thereby facilitate the reduction of very low density lipoprotein-cholesterol (VLDL) removal. This may be due to a specific alteration of cell membrane fluidity, while also altering the activities of membrane-bound enzymes. This can result in change in receptor activity, specificity and signal transduction.
Fish oils also depress the synthesis of hepatic fatty acids and triglycerides and secretion of very low density lipoprotein-cholesterol (VLDL). One further benefit is fish oils displace arachidonic acid from tissue phospholipids, resulting in omega-3 essential fatty acid levels inhibiting thromboxane synthesis.
The effect of fish oils are very selective. Eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) components not only displace arachidonic acid and inhibit cyclo-oxygenase, but EPA becomes a substrate for cylco-oxygenase when the peroxide tone is high and is converted to the potent antiaggregatory Pgl-3. It has been suggested these findings may explain the increased bleeding time and the decreased incidence of coronary artery disease which has been reported in Japanese with high fish consumption and in some Eskimos.
EPA- and DHA-rich fish oil has also been found to suppress production of inflammatory agents found in rheumatoid arthritis and psoriasis. The anti-inflammatory effect of the omega-3 fatty acids might be mediated in part by their inhibitory effect on production of interleukin-1 and tumor necrosis factor, both principal mediators of inflammation. In cases of psoriasis vulgaris, fish oils produce symptomatic improvement by effecting changes in levels of the inflammatory leukotriene compounds, especially leukotriene B4. This leukotriene is a lipoxygenation product of the fatty acid arachidonic acid. The EPA in fish oil "replaces" the arachidonic acid in phospholipids, leading to the formation of leukotriene B5, rather than B4. Leukotriene B5 causes a much weaker inflammatory response. Neutrophils were isolated from the peripheral blood of patients given fish oil to treat their psoriasis. Patients whose symptoms improved with fish oil therapy had higher levels of leukotriene B5 than did those patients who showed no improvement.
Most fish oil capsules contain 300 or 500 milligrams of omega-3 fish oil per one gram capsule. Thus, patients therapeutically using fish oil at the levels discussed in this section, may require between 15 to 30 capsules to get the derived benefits described herein. This amount adds up to substantial calories in the total daily diet. Further, unless supplemented with vitamin E, there is a possibility of vitamin E deficiency developing from prolonged intake of high doses.
In a recent review of fish oil supplementation and coronary disease, it was concluded 10 capsules or 25 milliliters (1/2 teaspoon) of cod liver oil a day (providing 1.8 grams of EPA) appears "to be safe over a long term."
Caution should be taken when recommending fish oil supplementation to pregnant women, to individuals with known or suspected bleeding disorders or to persons taking aspirin therapeutically. These individuals should consult with their physician before beginning such supplementation.
Eleven preliminary animal studies have reported favorable anticancer activity by fish oil. These studies were reviewed in 1987. Considerably more research is going on at this time. However, it remains premature to recommend fish oil as an anticancer substance until additional studies are completed in humans.
In 1989, researchers studying the effects of fish oil on human mammary carcinoma growth discovered an important role for fish oil in altering tumor sensitivity to anticancer drugs. In that study, tumor growth in mice fed fish oil and inoculated with human mammary cancer was reduced.
As had been shown in prior research, measurements of mice mitochondrial enzymes involved in lipid metabolism showed the fish oil consumption caused increased oxidation of the polyunsaturated fatty acids. This would result in inhibition of tumor growth due to increased oxidation of fatty acids in tumor tissue. The result of such changes is increased lipid peroxidation causing increased susceptibility of the tumor to any pro-oxidant antitumor drug. So when the mice in this study were given two anticancer drugs, doxorubicin or mitomycin C, tumor growth was significantly inhibited.
Additional evidence of fish oil's potential inhibition of cancer growth comes from in vivo and in vitro work reported in 1989 examining the effect of EPA on metastasis of tumor cells. Researchers cultured malignant murine melanoma and human fibrosarcoma cells in a media supplemented with EPA. Production of collagenase IV by the tumor cells was significantly decreased. Collagenase IV is a critical substance found in cancer cells leading to metastatic activity. The same procedure was attempted with arachidonic acid metabolites without comparable results. These findings add further support to growing evidence indicating EPA may reduce the spontaneous metastases associated with some cancers, while also altering the progression of the cancer itself.
In general, dietary unsaturated fatty acids appear to reduce undesirable circulating fats (e.g. in hyperlipidemia) while decreasing the production of the prothrombotic substance thromboxane. In studies involving fish oil as an unsaturated fatty acid, data from clinical trials show a significant reduction of levels of very low density lipoprotein-cholesterol (VLDL), plasma triglycerides, plasma cholesterol, and low density lipoprotein-cholesterol (LDL).
These findings are important because they may explain the significant difference in mortality rate due to cardiovascular disease between certain Alaskan natives and mainland Americans. In an autopsy series of 339 Alaskan natives, Authaud found cardiovascular disease was a cause of death in only 35 (or 10.3%) of the cases, whereas it accounts for 50% for all deaths in the United States.
Recent evidence also suggests fish oil may prevent atherosclerosis in Rhesus monkeys and hyperlipidemic pigs, despite lack of improvement in serum cholesterol levels. These findings warrant consideration given the high mortality and morbidity associated with atherosclerosis.
For therapeutic dosages, intakes of 5 grams of fish oil a day may be advisable. However, there is sufficient evidence to consider fish oil supplementation, in the range of from 2 to 10 grams per day, for patients with elevated cholesterol (7.75 mmol/liter) or triglycerides (5.64 mmol/liter).
Kinsella has suggested for both prophylactic and therapeutic applications, the most benefit is derived from fish oil when total fat intake is lowered to least 30% of calories, saturated fatty acids to no more than 30% of total fat, and omega-6 fatty acids (vegetable oils) to a maximum of 10%.
Fish oil seems to have hypotensive effects ranging from small (with 5 grams per day) to substantial (6 grams per day). Yetiv has speculated fish oil depresses vascular reactivity to hormones involved in hypertension. Yetiv suggested fish oil acted by increasing vasodilatory prostaglandins Pgl-2 and Pgl-3, and this increase accounted for the observed reduction in blood pressure.
To test this hypothesis, a study was conducted to examined the ability of fish oil to lower blood pressure in men with mild essential hypertension. One group received 10 ml. of fish oil (3 grams of omega-3 fatty acids), a second group 50 ml. of fish oil (15 grams), a third group 50 ml. safflower oil (39 grams of omega-6 fatty acids) and a fourth group 50 ml. of a mixture of coconut, olive and safflower oils. The latter group represented the approximate amount of fatty acids consumed in the average American diet (39% saturated fat, 46% monounsaturated fat, and 15% polyunsaturated fat). Males who received the highest dose of fish oil (50 ml., equal to 9 grams of EPA and 6 grams of DHA) had an average reduction of 6.5mm Hg in systolic pressure and a 4.4mm Hg in diastolic pressure. None of the other three groups, including the 10 ml. fish oil group, saw this kind of reduction. The study did not find the expected association between the formation of Pgl-2 and Pgl-3 and a sustained reduction in blood pressure.
This indicates vasodilatory prostaglandins are not the primary mediators of blood pressure reduction by fish oil. What those mediators are remains unknown to date.
Lupus (Systemic Lupus Erythematosus)
SLE is a generalized connective tissue disorder tending to affect middle-aged females. It is characterized by skin eruptions, neurological manifestations, lymphadenopathy, fever and other symptoms, in addition, to a range of abnormal immunological phenomena, including hypocomplementemia and hypergammaglobulinemia.
In 1989, the first controlled study of fish oil's effects on SLE was reported. Prior to then a number of anecdotal reports suggested improvement of some patients following fish oil supplementation. The early clinical attempts were based on animal studies using inbred mice strains, which were criticized because of questionable generalization to human SLE patients.
The 1989 study tested 6 grams of EPA or 6 grams of DHA daily for five weeks in 12 patients having SLE. Thereafter, patients were taken off supplementation and continued without supplementation for a five week washout period. Then patients were returned to supplementation for another five weeks, but this time given 18 grams of EPA or DHA per day. At the higher EPA/DHA levels (18 grams a day) there was a 38% decrease in triglycerides, a 39% decrease in very low density lipoproteins (VLDL) cholesterol, and a 28% increase in high density lipoproteins (HDL).
Overall this resulted in significant improvements in inflammatory and atherosclerotic processes typically seen in SLE patients. These findings suggest some beneficial effects from fish oil supplementation. However, possible long-term benefits from fish oil supplementation in SLE patients have still not been studied. The first clinical trial of the benefits of fish oil's EPA in the alleviation of the symptoms of osteoarthritis was reported in 1989. Patients were given ibuprofen, an aspirin-like analgesic, with either 10 milliters of EPA a day or placebo for six months. Patients assessed the level of pain and interference they experienced in everyday activity. The average scores for these indexes "were strikingly lower in the EPA (group) than the placebo group." However, the differences were not as statistically significant as the researchers had hoped, meaning additional studies are suggested. This is the first report of fish oil being of benefit to patients with osteoarthritis.
Therapeutic Approaches cont'd
There are unsubstantiated reports that patients, given 15 grams of fish oil a day have significantly less frequent and/or intense migraines. This effect was particularly noticeable in male patients. These results might be due to changes in prostaglandin synthesis and/or reduction in platelet serotonin release, with a resultant reduction in cerebral vasospasms.
The first case of a human with omega-3 fatty acid deficiency was reported in 1988. The patient was a 7 year old girl with retarded growth who had been fed solely by gastric tube since age of 3 years. She began to experience normal growth after being supplemented with cod liver oil and linseed oil. This finding provides evidence omega-3 essential fatty acid is required by humans for normal growth.
Both hypertriglyceridemia and hypercholesterolemia are common in patients with nephrotic syndrome. These lipid disorders are associated with an increased risk of coronary heart disease. In one study completed in Canada, triglyceride levels decreased by 31% within nine days of fish oil supplementation. However, total or HDL-cholesterol levels did not change. Nine days after supplementation ceased, triglyceride levels showed a trend of returning back to their original levels.
Fish oils may also play a role in the treatment of autoimmune (e.g. lupus erythematosis, dermatomyositis, autoimmune nephritis) and inflammatory disorders, (e.g. rheumatoid arthritis, psoriasis), and atopic dermatitis.
Researchers in Denmark have successfully treated patients with psoriasis vulgaris with a low-fat diet supplemented with fish oil. Only 23% of such patients did not report either excellent, moderate or mild improvement in their condition. It was interesting to note in this study a number of patients did not show improvement until supplemented for at least four months. This may indicate the importance of allowing adequate time for clinical improvement after initiating fish oil therapy.
Fish oils may improve psoriasis due to changes in inflammatory leukotriene compounds, particularly leukotriene B4, which is a lipoxygentation product of the fatty acid arachidonic acid, and is believed to be involved in the inflammatory process associated with psoriasis. In essence, the fish oil replaces arachidonic acid in phospholipids resulting in the formation of leukotriene B5 rather than B4, hence the weaker inflammatory response.
A double-blind, placebo-controlled study of rheumatoid arthritis patients has been reported using 1.8 grams of EPA a day. Patients receiving EPA reported a decrease in morning stiffness and tenderness in the joints. This led to considerable popular press coverage on the possible benefits of fish oil for this condition. However, analysis of the study later showed any possible benefits of EPA were probably due to deterioration of the control group (placebo) rather than any real improvement in the fish oil group.
However, a more recent study of fish oil supplementation in patients with the inflammatory conditions of rheumatoid arthritis and psoriasis did show improvement. Patients taking 18 grams of fish oil concentrate (153 milligrams EPA and 103 milligrams DHA) for six weeks reported significant improvement in their condition. Samples of peripheral blood mononuclear cells from the patients showed suppressed synthesis of two principle mediators of inflammation, interleukin-1 and tumor necrosis factor. No such suppression was found in patients receiving placebo. Of interest was the finding that the anti-inflammatory effect of the fish oils remained strong up to four weeks after cessation of supplementation.
Raynaud's disease/Raynaud's phenomenon
In Raynaud's disease there is an intermittent bilateral attack of ischemia (periodic cessation of blood flow and blood pressure) of the fingers, toes, or even the ears and nose. The disease afflicts females more often than males. Raynaud's phenomenon is intermittent, often accompanied by paresthesia and pain, and brought on by cold or emotional stimuli. It can usually be relieved with heat. When the condition is idiopathic or primary, it is termed Raynaud's disease.
In 1989, researchers reported results from a double-blind placebo-controlled trial finding Raynaud's disease may benefit from fish oil (12 fish oil capsules containing nearly 4 grams of EPA and 2.64 grams of docosahenaenoic acid - DHA). The time interval before onset of Raynaud's phenomenon, especially in those with primary Raynaud's phenomenon, was significantly increased in those patients taking fish oil, versus those subjects taking placebo (olive oil). Even more impressive was finding 5 of 11 patients did not develop any Raynaud's symptoms at 6 or 12 weeks following fish oil after being exposed to cold water baths. By comparison, this favorable response was only seen in 1 of 9 patients receiving olive oil (placebo). Whether these findings will similarly benefit patients with secondary Raynaud's phenomenon requires further study.
Of particular concern has been the reports of prolonged bleeding time in populations having a proportionately high intake of fish. Several studies have shown this effect appears to be dose-dependent, although collagen-induced platelet aggregation is not inhibited. Many studies have shown fish oil supplements prolong bleeding time, inhibit platelet aggregation, and decrease Thromboxane 2 production. However, the concept of prolonged bleeding time is significant or potentially life-threatening is under review.Abstracts
Foran has pointed out there are some associated risks, in general, from increased consumption of fish. Some fish may be contaminated from industrial effluents and toxins. Many of these toxins are known to increase the risk of cancer. Animal experiments have demonstrated eating such contaminated fish as infrequently as once a week may increase the risk of developing cancer, in addition, to its risk to pregnant mothers and infants.
The potential adverse effects of long-term fish oil supplementation are unknown. However, this is also true of all other oils, such as vegetable oils and most hypolipidemic drugs currently prescribed.
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