Blue Ice Unheated Cod Liver Oil, Oslo Orange Flavor 8 oz. by Green Pasture
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Oslo Orange Flavor 8 oz. (237 ml)
Item Number: O-A
Weight (shipping): 1.00 lbs.
In a scientific review article published in the International Journal of Ophthalmology, Dr. Huang and his team concluded that cod liver oil should be beneficial for the treatment of glaucoma. See the full article below.
Dr. David Levi, ND, says that this fermented cod liver oil is different from all the other fish oils because it is raw and has never been exposed to heat. All the other fish oils have been heated and a lot of the nutrients have therefore been denatured. Cod liver oil is a powerful anti-inflammatory. Among its numerous benefits it can even help diabetics regulate blood sugar. Fermented cod liver oil is the best bioavailable source of vitamin D. The video below contains more of Dr. Levi's comments.
Premium quality fermented raw cod liver oil from Green Pasture is made of cod exclusively caught in and around the Arctic region. (In contrast, the largest population of farmed raised cod/ salmon in the world is found in Norway. Keep that in mind when looking at other brands of cod liver oil!)
It is naturally high in vitamin and essential nutrients content. It is indeed the gold standard in pure fish fat/oil from the liver of the cod fish extracted through fermentation rather then cold/hot temps or chemical extraction as the rest of the industry uses. Deep dark rich color equals real life giving nutrients.
Naturally occurring cod liver oil (not synthetic, man-made oils) provides fat soluble vitamins A and D and when extracted properly also provides a healthy dose of other naturally occurring acids like DHA, EPA and several of the Omega vitamins. EPA is an important link in the chain of fatty acids which regulate tissue hormones and DHA is important for brain and nervous system function and in conditions such as glaucoma.
Unlike other cod liver oils that are distilled (using high heat), Green Pasture's Cod Liver Oil is raw! It is the result of months of fermenting. This unique extraction process yields an oil that is drastically richer in nutrients. In fact, it contains many nutrients that have no presence at all in other oils and is 2.5 times more nutrient dense in vitamins A and D. It contains a very healthy ratio of the two to each other, which is important in working together. The cod used in this product has yielded a high purity level due to the lack of environmental contaminates and the manufacturer, Green Pastures Products, is a family-owned business dedicated to providing high-quality sacred-food oils, just as they were made prior to the industrialized food and farming revolution.
Green Pasture's Fermented Cod Liver Oil stands out from other similar products due to its unique nutrient profile, small serving size, variety of enzymes/nutrients absent in industrialized products and the fact that it doesn't contain any added vitamin E. Every bottle of Blue Ice Fermented Cod Liver Oil will vary as this is an artisan food and not a mass produced fish oil product. This product is rich in pigments unlike the clear yellowish consistency of refined oils. Taste, color, and nutrient levels will vary from season to season so don’t be surprised when your first bottle is different than the second. Because this oil retains all of the original nutrients, you might like a flavored or encapsulated version if you are a first timer since the unflavored can be strong. Enjoy the benefits of healthy fats (EPA/DHA), loads of vitamins, and rare nutrient metabolites just like the Vikings of old!
Statement from manufacturer regarding contamination:
Every lot is tested for PCB's, metals etc... And every small run is tested three times for pathogens (standard food screens). Plus we direct other standard tests not required that we accumulate for understanding and discussion. All testing is done by third party labs as we do not have any in-house lab capabilities. The testing is done per FDA regulations for food safety and our products meet the requirements 100%+. The testing we do is beyond what you will typically find within the food industry.Go to top
All our fish are wild caught.
We do publish random test data on the web site. I do not always update this list so it is not always current. This does not mean that we do not test as this is standard procedure as described above, part of SSOP, GMP plus it is regulated by the FDA.
Cod liver oil: a potential protective supplement for human glaucoma
Wen-Bin Huang, Qian Fan, and Xiu-Lan Zhang
Glaucoma is one of the leading causes of visual impairment and blindness. Improved knowledge of the pathogenesis of this disease has allowed the exploration of new therapeutic methods. In general, elevated intraocular pressure (IOP), oxidative stress, and vascular insufficiency are accepted as the major risk factors for the progression of glaucoma. Many natural compounds have been found beneficial for glaucoma. Nutritional therapies are now emerging as potentially effective in glaucomatous therapy. One nutritional supplement with potential therapeutic value is cod liver oil, a dietary supplement that contains vitamin A and omega-3 polyunsaturated fatty acids (PUFAs). Vitamin A is important for preserving normal vision and it is a well-known antioxidant that prevents the oxidative damage that contributes to the etiology and progression of glaucoma. Vitamin A is also a crucial factor for maintaining the integrity of conjunctival and corneal ocular surfaces, and preventing the impairment of ocular epithelium caused by topical antiglaucomatous drugs. Omega-3 fatty acids are beneficial for glaucoma patients as they decrease IOP, increase ocular blood flow, and improve optic neuroprotective function. In this article, we propose that cod liver oil, as a combination of vitamin A and omega-3 fatty acids, should be beneficial for the treatment of glaucoma. However, further studies are needed to explore the relationship between cod liver oil and glaucoma.
Keywords: cod liver oil, glaucoma, omega-3 fatty acids, vitamin A
Glaucoma is the second leading cause of blindness in the world. According to Quigley,, by the year 2000, the number of people in the world with primary glaucoma was estimated at nearly 66.8 million, with 6.7 million suffering from bilateral blindness. This number is expected to increase to 79.6 million by 2020, and of these, 74% will have open angle glaucoma (OAG). The treatments available for glaucoma are still far from satisfactory; therefore, new therapeutic approaches continue to be sought.
Glaucoma is an optical neuropathy characterized by a specific structural alteration of the optic nerve head that leads to progressive deterioration of the visual field. Although increased intraocular pressure (IOP) is a major risk factor for primary open angle glaucoma (POAG), other factors also play important roles, including vascular insufficiency, glutamate-mediated toxicity, excess production of nitric oxide(NO), and oxidative stress. Improved knowledge of the pathogenesis of the disease is now opening up new therapeutic strategies. Nutrition, a subject of interest in many fields of medicine, is also being viewed as a potential therapeutic path and ophthalmologists are beginning to seek possible ways to preserve vision through diet and supplements. For example, Mozaffarieh et al- have found that gingko, dark chocolate, tea, coffee, red wine, the anthocyanosides found in bilberries, ubiquinone, and melatonin are potential neuroprotective agents for glaucoma. Other avenues of treatment, such as magnesium, salt and udrocortisone, are already used by some physicians. Nutritional therapies are therefore emerging as potentially effective methods for preventing the progression of glaucoma.
Cod liver oil is used widely as a dietary supplement. It is a rich source of vitamin A, vitamin D, and essential omega-3 fatty acids, especially eicosapentaenoic acid (EPA) and docosahexanoic acid (DHA). Because of its special components, cod liver oil is generally accepted as good for human health. In previous studies, cod liver oil supplementation has been suggested to reduce cardio-metabolic risk factors, have anticancer effects, and ameliorate cognitive impairment induced by chronic stress. To our knowledge, no study has yet investigated the potential beneficial effects of cod liver oil in preventing the progression of glaucoma. The aim of this article is to consider the hypothesis that cod liver oil is a potential protective compound for the treatment of human glaucoma. In the following, we present a body of evidence in support of a role for cod liver oil, as a source of vitamin A and omega-3 fatty acids, in glaucomatous therapy.
The Role of Vitamin A in Glaucoma
Vitamin A is an essential fat-soluble vitamin. It is required for normal functioning of growth, vision, epithelial differentiation, immunity, and reproduction. Vitamin A also has a vital role in ocular metabolism: it is essential for conjunctival and corneal epithelial maintenance, retinal phototransduction, and retinal pigment epithelial cell viability. A deficiency of vitamin A will lead to vision loss, keratomalacia, Bitot's spot, and dry eye. Night blindness results when the vitamin A pool in the eye becomes depleted, and the concentration in the rod cells is lowered. This condition is reversible with increased vitamin A intake or supplementation. In short, vitamin A is important for maintaining normal vision.
An association between oxidative stress and POAG has already been reported-. Tezel found that oxidative stress takes part in the neurodegenerative process. Welge-Lussen and Birke concluded that oxidative stress can induce characteristic glaucomatous trabecular meshwork (TM) changes, and speculated that the prevention of oxidative stress exposure to the TM may help to reduce the progression of POAG. According to Feilchenfeld et al oxidative injury also occurs in blood vessels and astrocytes in the pre-laminar optic nerve head in human POAG. Further studies have concluded that oxidative stress may contribute to the etiology and progression of POAG. Therefore, the potential is great for antioxidant supplementation to minimize TM changes, protect the optic nerve and the ocular vessels,,. If increasing total dietary antioxidant intake is to succeed as an effective therapeutic strategy, this would be a promising means of primary prevention for POAG.
Vitamin A, provitamin A, and carotenoids are well-known antioxidants. However, humans cannot synthesize vitamin A and must obtain it from their diets. Cod liver oil is a good source of vitamin A supplementation, as the dose of vitamin A is moderate and the quality of vitamin A is excellent. The antioxidant activity of vitamin A and related carotenoids is conferred by the hydrophobic chain of polyene units that can quench singlet oxygen, neutralize thiyl radicals, and combine with and stabilize peroxyl radicals. The majority of research performed to date has examined the antioxidant effects of vitamin A and carotenoids. The observation by Das et al suggested that vitamin A and its metabolites exhibited an antioxidant effect even greater than that produced by vitamin E. It is extensively suggested that vitamin A supplementation can exert protective effects against neurodegenerative and cardiovascular diseases, since oxidative stress play a major role in the pathogenesis of such conditions,. However, using data from two large prospective cohorts, Kang et al found little evidence that an increase total intake of vitamin A substantially reduced the risks of POAG. Further research, experiments, and clinical trials are still necessary to investigate the potential association between the antioxidant properties of vitamin A and their effects on glaucoma.
Topical IOP lowering drugs for glaucoma must penetrate across the tissues of the eye to reach their therapeutic targets. Frequently, these tissues are the first to show signs and symptoms of drug toxicity and adverse effects such as eyelid dermatitis, malpositions, lacrimal system scarring, ocular discomfort upon instillation, tear film instability, conjunctival inflammation, subconjunctival fibrosis, conjunctival epithelium changes, and corneal surface and endothelial impirment. Many studies have demonstrated that long-term use of ocular hypotensive medications can cause significant changes to the ocular surface,. Vitamin A is essential for conjunctival and corneal epithelial maintenance and it plays a vital role in ocular epithelial growth and differentiation. It is a crucial factor for regulating mucin production of the ocular surface epithelium, which is known to be an important part of the ocular surface defense. A randomized controlled experimental study in rabbits concluded that vitamin A palmitate could promote the repair of mechanical defects in the corneal epithelium and the development of intracellular conjunction; and it also could promote regeneration of conjunctival goblet cells and re-establish intracellular conjunction of the conjunctival epithelium. Base on this evidence, vitamin A not only can maintain ocular surface integrity, but it also can prevent impairment of the ocular epithelium caused by antiglaucomatous drugs.
However, the intake of large doses of vitamin A can cause nausea, vomiting, headache, and dry scaly skin. More severe health problems can arise from storing excess vitamin A in the body, including liver damage, osteoporosis, and nervous system disorders. For these reasons, the total vitamin A intake is recommended as less than 3000µg per day from retinol. Supplementation of moderate amounts of cod liver oil appears to be relatively safe.
The Role of Omega-3 Fatty Acids in Glaucoma
Not all fatty acids can be synthesized by the human body. Those that cannot be synthesized and must be obtained from the diet are known as “essential fatty acids.” There are two known families of “essential fatty acids”: omega-3 and omega-6 fatty acids. Of these, two long-chain omega-3 fatty acids, EPA and DHA, are particularly important nutritional components. Both EPA and DHA are concentrated in the phospholipids of cell membranes throughout the human body, but especially in the brain, heart, retina, and testes.
Previous reviews have discussed the role of omega-3 fatty acids in prevention and therapy of various diseases (cardiovascular diseases, cancer, depression, neurological diseases, etc.) as well as their mechanisms of action,. Dietary omega-3 fatty acids have also been shown to be beneficial to the outcome of ocular diseases such as decreasing risk for age-related maculopathy (ARM). According to Ren et al, patients with POAG have an abnormal blood fatty acid composition that is characterized by a reduction in EPA, DHA, and omega-3 fatty acids. Therefore, we predict that omega-3 fatty acids should display potential beneficial effects on glaucoma.
Among the factors involved in the pathogenesis of glaucoma, elevated IOP is the major risk factor. The final consequence of IOP elevation is retinal cell loss, which leads to a specific structural alteration of the optic nerve head and progressive deterioration of the visual field. Results of a large-scale and long-term clinical trial have provided convincing evidence that lowering IOP prevents progression at both the early and late stages of glaucoma. The IOP is determined by the balance between aqueous humor production and outflow.Nguyen et al demonstrated that an increased consumption of omega-3 fatty acids leads to decreased IOP through an increased aqueous outflow facility. The exact mechanism of the aqueous outflow increase is via prostaglandins (PGs), which are metabolites of omega-3 fatty acids. These reduce IOP by enhancing uveoscleral and trabecular outflow via direct effects on ciliary muscle relaxation and remodeling of extracellular matrix. The PGs are powerful ocular hypotensive agents that can be used for the treatment of elevated IOP. Cod liver oil that contains both EPA and DHA has been demonstrated to lower IOP in experimental animals.
Vascular insufficiency is also recognized as another important risk factor, in addition to IOP. Circumstantial evidence points to an association between vascular insufficiency and glaucoma. Recent findings indicate a role for vascular deficits in the pathogenesis of glaucoma, suggesting that treatments designed to improve ocular blood flow may be of benefit to glaucoma patients. A study done by Hamard et al on POAG patients and normal tension glaucoma (NTG) patients showed that the optic nerve blood flow velocity was reduced and the ability of the red blood cells (RBCs) to aggregate was increased, leading to increases in the local viscosity within the papillary capillary network. Decreased blood flow velocity and increased blood viscosity will lead to vascular insufficiency. Evidence has been shown that blood viscosity is significantly and uniformly lowered in subjects who receive omega-3 fatty acids. The potential mechanism is thought to relate to the ability of omega-3 fatty acids to enhance cell membrane fluidity, decrease platelet aggregation, and reduce serum cholesterol concentrations by decreasing the synthesis of very low density lipoprotein and low-density lipoprotein. Omega-3 fatty acids appear to increase blood fluidity by at least two independent mechanisms: changing red cell deformability possibly by altering the cell membrane composition, and lowering plasma viscosity possibly by altering the protein pattern of the plasma. However, the therapeutic potential of omega-3 fatty acids for improving ocular circulation needs to be explored more thoroughly.
Previous studies have found that omega-3 fatty acids are beneficial for the treatment of glaucomatous optic neuropathy (GON). Omege-3 fatty acids function in the treatment of GON by preventing retinal cell structural degradation and by decreasing glial cell activation induced by the elevation of IOP. Caramazza et al also demonstrated that polyunsaturated fatty acids, acting on nerve cell trophism, helped to preserve nerve fiber function in GON. Omega-3 fatty acids are considered an efficacious supportive therapy in the prevention and treatment of GON.
Base on the above literature review, we find evidence to support the idea that vitamin A and omega-3 fatty acids can play a protective role in the treatment of glaucoma. Cod liver oil, as a combined supplement of vitamin A and omega-3 fatty acids, should be more effective than single supplement formulations. However, the true efficacy of cod liver oil has not yet been solidly determined and further studies are needed to clarify its true benefits. Properly controlled, long-term clinical trials are needed to determine whether supplementation with cod liver oil would be therapeutically beneficial as a treatment for glaucoma. We hope that this study will encourage others to investigate the effects of cod liver oil on glaucoma.
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Foundation items: Supported by National Natural Science Foundation of China (81170849); Guangdong Provincial Natural Science Foundation, China (No.S2011020002401); Research Fund for the Doctoral Program of Higher Education of China (No. 20100171110077)
Int J Ophthalmol. 2011; 4(6): 648–651.
Published online Dec 18, 2011. doi: 10.3980/j.issn.2222-3959.2011.06.15
Wen-Bin Huang, Qian Fan, and Xiu-Lan Zhang
Zhongshan Ophthalmic Center, State Key Laboratory of Ophthalmology, Sun Yat-sen University, Guangzhou 510060, Guangdong Province, China
Correspondence to: Xiu-Lan Zhang. Zhongshan Ophthalmic Center, State Key Laboratory of Ophthalmology, Sun Yat-sen University, Guangzhou 510060, Guangdong Province, China. Email: nc.ude.usys.liam@2lxgnahz
Received October 16, 2011; Accepted November 24, 2011.
Copyright International Journal of Ophthalmology Press
Articles from International Journal of Ophthalmology are provided here courtesy of Press of International Journal of Ophthalmology
1. Quigley HA. Number of people with glaucoma worldwide. Br J Ophthalmol. 1996;80(5):389–393. [PMC free article] [PubMed]
2. Quigley HA, Broman AT. The number of people with glaucoma worldwide in 2010 and 2020. Br J Ophthalmol. 2006;90(3):262–267. [PMC free article] [PubMed]
3. Agarwal R, Gupta SK, Agarwal P, Saxena R, Agrawal S. Current concepts in the pathophysiology of glaucoma. Indian J Ophthalmol. 2009;57(4):257–266. [PMC free article] [PubMed]
4. Mozaffarieh M, Flammer J. Is there more to glaucoma treatment than lowering IOP? Surv Ophthalmol. 2007;52:S174–179. [PubMed]
5. Mozaffarieh M, Grieshaber MC, Orgül S, Flammer J. The Potential Value of Natural Antioxidative Treatment in Glaucoma. Surv Ophthalmol. 2008;53(5):479–505. [PubMed]
6. Mozaffarieh M, Fraenkl S, Konieczka K, Flammer J. Targeted preventive measures and advanced approaches in personalised treatment of glaucoma neuropathy. EPMA J. 2010;1(2):229–235. [PMC free article] [PubMed]
7. Trofimiuk E, Braszko JJ. Long-term administration of cod liver oil ameliorates cognitive impairment induced by chronic stress in rats. Lipids. 2011;46(5):417–423. [PubMed]
8. Abeywardena MY, Patten GS. Role of omega3 Longchain polyunsaturated fatty acids in reducing cardio-metabolic risk factors. Endocr Metab Immune Disord Drug Targets. 2011;11(3):232–246. [PubMed]
9. Dyck MC, Ma DW, Meckling KA. The anticancer effects of Vitamin D and omega-3 PUFAs in combination via cod-liver oil: One plus one may equal more than two. Med Hypotheses. 2011;77(3):326–332. [PubMed]
10. Trofimiuk E, Braszko JJ. Long-term administration of cod liver oil ameliorates cognitive impairment induced by chronic stress in rats. Lipids. 2011;46(5):417–423. [PubMed]
11. Ross SA, McCaffery PJ, Drager UC, De Luca LM. Retinoids in embryonal development. Physiol Rev. 2000;80:1021–1054. [PubMed]
12. Tanumihardjo SA. Vitamin A: Biomarkers of nutrition for development. Am J Clin Nutr. 2011;94(2):658S–665S. [PMC free article] [PubMed]
13. Tezel G. Oxidative stress in glaucomatous neurodegeneration: Mechanisms and consequences. Prog Retin Eye Res. 2006;25(5):490–513. [PMC free article] [PubMed]
14. Welge-Lussen U, Birke k. Oxidative stress in the trabecular meshwork of POAG. Klin Monbl Augenheilkd. 2010;227(2):99–107. [PubMed]
15. Feilchenfeld Z, Yücel YH, Gupta N. Oxidative injury to blood vessels and glia of the pre-laminar optic nerve head in human glaucoma. Exp Eye Res. 2008;87(5):409–414. [PubMed]
16. Das NP. Effect of vitamin A on lipid peroxidation in rat brain mitochondria. J Neurochem. 1989;52:585–588. [PubMed]
17. Lee HP, Casadesus G, Zhu X, Lee HG, Perry G, Smith MA, Gustaw-Rothenberg K, Lerner A. All-trans retinoic acid as a novel therapeutic strategy for Alzheimer's disease. Expert Rev Neurother. 2009;9(11):1615–1621. [PMC free article] [PubMed]
18. Palace VP, Khaper N, Qin Q, Singal PK. Antioxidant potentials of vitamin A and carotenoids and their relevance to heart disease. Free Radical Bio Med. 1999;26(5-6):746–761. [PubMed]
19. Kang JH, Pasquale LR, Willett W, Rosner B, Egan KM, Faberowski N, Hankinson SE. Antioxidant intake and primary open-angle glaucoma: A prospective study. Am J Epidemiol. 2003;158(4):337–346. [PubMed]
20. Servat JJ, Bernardino CR. Effects of common topical antiglaucoma medications on the ocular surface, eyelids and periorbital tissue. Drug Aging. 2011;28(4):267–282. [PubMed]
21. Noecker RJ, Herrygers LA, Anwaruddin R. Corneal and conjunctival changes caused by commonly used glaucoma medications. Cornea. 2004;23(5):490–496. [PubMed]
22. Stewart WC, Stewart JA, Nelson LA. Ocular surface disease in patients with ocular hypertension and glaucoma. Curr Eye Res. 2011;36(5):391–398. [PubMed]
23. Heinz C, Steuhl KP, Meller D. Corneal perforation associated with vitamin A deficiency. Ophthalmologe. 2004;101(6):614–617. [PubMed]
24. Qiu XD, Gong L, Chen MJ. Research on effects of vitamin A palmitate on repair of mechanical corneal epithelial defects and conjunctival goblet cells in rabbits. Chin J Ophthalmol. 2010;46(2):151–160. [PubMed]
25. Nan C, Linda B. Facts about vitamin A (University of Florida, Institute of Food and Agricultural Sciences) Available fr0m: http://edis.ifas.ufl.edu/fy206. Last retrieved on 2011 Sep 28.
26. Moyad MA. An introduction to dietary/supplemental omega-3 fatty acids for general health and prevention: part I. Urol Oncol. 2005;23:28–35. [PubMed]
27. Moyad MA. An introduction to dietary/supplemental omega-3 fatty acids for general health and prevention: part II. Urol Oncol. 2005;23:36–48. [PubMed]
28. Merle B, Delyfer MN, Korobelnik JF, Rougier MB, Colin J, Malet F, Féart C, Le Goff M, Dartigues JF, Barberger-Gateau P, Delcourt C. Dietary omega-3 fatty acids and the risk for age-related maculopathy: the Alienor Study. Invest Ophthalmol Vis Sci. 2011;52(8):6004–6011. [PubMed]
29. Ren H, Magulike N, Ghebremeskel K, Crawford M. Primary open-angle glaucoma patients have reduced levels of blood docosahexaenoic and eicosapentaenoic acids. Prostag Leukotr Ess. 2006;74(3):157–163. [PubMed]
30. Kass MA, Heuer DK, Higginbotham EJ, Johnson CA, Keltner JL, Miller JP, Parrish RK, 2nd, Wilson MR, Gordon MO. The Ocular Hypertension Treatment Study: a randomized trial determines that topical ocular hypotensive medication delays or prevents the onset of primary open-angle glaucoma. Arch Ophthalmol. 2002;120:701–713. [PubMed]
31. Nguyen CTO, Bui BV, Sinclair AJ, Vingrys AJ. Dietary omega 3 fatty acids decrease intraocular pressure with age by increasing aqueous outflow. Invest Ophthalmol Vis Sci. 2007;48(2):756–762. [PubMed]
32. Lands WEM. Biochemistry and physiology of n-3 fatty acids. FASEB J. 1992;6(8):2530–2536. [PubMed]
33. Schwartz K, Budenz D. Current management of glaucoma. Curr Opin Ophthalmol. 2004;15(2):119–126. [PubMed]
34. Mancino M, Ohia E, Kulkarni P. A comparative study between cod liver oil and liquid lard int on intraocular pressure on rabbits. Prostag Leukotr Ess. 1992;45(3):239–243. [PubMed]
35. Yanagi M, Kawasaki R, Wang JJ, Wong TY, FRANZCO CJ, Kiuchi Y. Vascular risk factors in glaucoma: a review. Clin Experiment Ophthalmol. 2011;39(3):252–258. [PubMed]
36. Hamard P, Hamard H, Dufaux J, Quesnot S. Optic nerve head blood flow using a laser Doppler velocimeter and haemorheology in primary open angle glaucoma and normal pressure glaucoma. Br J Ophthalmol. 1994;78(6):449–453. [PMC free article] [PubMed]
37. Mueller BA, Talbert RL. Biological mechanisms and cardiovascular effects of omega-3 fatty acids. Clin Pharm. 1988;7(11):795–807. [PubMed]
38. Ernst E. Effects of n-3 fatty acids on blood rheology. J Intern Med Suppl. 1989;225(731):129–132. [PubMed]
39. Schnebelen C, Pasquis B, Salinas-Navarro M, Joffre C, Creuzot-Garcher CP, Vidal-Sanz M, Bron AM, Bretillon L, Acar N. A dietary combination of omega-3 and omega-6 polyunsaturated fatty acids is more efficient than single supplementations in the prevention of retinal damage induced by elevation of intraocular pressure in rats. Graef Arch Clin Exp Ophthalmol. 2009;247(9):1191–1203. [PubMed]
40. Caramazza N, Damele M, Parente G, Alessandrini A, Cellini M. Use of polyunsatured fatty acids in the treatment of glaucomatous optic neuropathy (GON) Ann Ottalmol Clin Ocul. 1999;125(11-12):329–338.
41. Cellini M, Rossi A, Moretti M. The use of polyunsaturated fatty acids in ocular hypertension. A study with blue-on-yellow perimetry. Acta Ophthalmol Scand Suppl. 1999;77(229):54–55.