J. Chronic Fatigue Syndr. 2004 Lipid Replacement and Antioxidant Nutritional Therapy for Restoring Mitochondrial Function and Reducing Fatigue in Chronic Fatigue Syndrome and other Fatiguing Illnesses Garth L. Nicolson, PhD The Institute for Molecular Medicine, Huntington Beach, California, USA
ABSTRACT. Evidence in the literature indicates that diminished mitochondrial function through loss of efficiency in the electron transport chain caused by oxidation occurs during aging and in fatiguing illnesses. Lipid Replacement Therapy (LRT) administered as a nutritional supplement with antioxidants can prevent oxidative membrane damage, and LRT can be used to restore mitochondrial and other cellular membrane functions via delivery of undamaged replacement lipids to cellular organelles. Recent clinical trials have shown the benefit of LRT plus antioxidants in restoring mitochondrial electron transport function and reducing moderate to severe chronic fatigue. These studies indicate the benefits of LRT plus antioxidants in preventing loss of mitochondrial function, most likely by protecting mitochondrial and other cellular membranes from oxidative and other damage and removing damaged lipids by lipid replacement.
In one clinical study we determined if mitochondrial function is reduced in subjects with mild to severe chronic fatigue, and if this can be reversed with NTFactor®, a nutritional supplement that replaces damaged cellular lipids.
Using the Piper Fatigue Scale there was a significant time-dependent reduction in overall fatigue in moderately or severely fatigued subjects while on the dietary supplement for 4-8 weeks. Analysis of mitochrondrial function indicated that four and eight weeks of the dietary supplement in moderately or severely fatigued subjects significantly increased mitochondrial function.
The results indicate that LRT plus antioxidants can significantly reduce moderate to severe chronic fatigue and restore mitochondrial function. Dietary use of unoxidized membrane lipids plus antioxidants is recommended for patients with moderate to severe fatigue.
KEYWORDS. lipids, antioxidants, therapy, dietary supplement, fatigue, mitochondria, chronic fatigue syndrome Address correspondence to: Professor Garth L. Nicolson, Department of Molecular Pathology, The Institute for Molecular Medicine, 16371 Gothard St. H, Huntington Beach, California 92647 Tel: +1-714-596-6636 Email: email@example.com, Website: www.immed.org
INTRODUCTION One of the most important changes in tissues and cells that occurs during aging and chronic degenerative disease is accumulated oxidative damage due to cellular reactive oxygen species (ROS). ROS are oxidative and free radical oxygen- and nitrogen-containing molecules, such as nitric oxide, oxygen and hydroxide radicals and other molecules . Critical targets of ROS are the genetic apparatus and cellular membranes [1,2], and in the latter case oxidation can affect lipid fluidity, permeability and membrane function [3,4]. Similar changes occur in fatiguing illnesses, such as chronic fatigue syndrome (CFS), where patients show increased susceptibility to peroxidation . One of the most important changes caused by accumulated ROS damage during aging and in fatigue is loss of electron transport function, and this appears to be directly related to mitochondrial membrane lipid peroxidation , which can induce permeability changes in mitochondria and loss of transmembrane potential and oxidative phosphorylation [1,2]. I will concentrate this brief review on recent clinical trials that have shown the effectiveness of lipid replacement therapy (LRT) plus antioxidants in the treatment of certain clinical disorders and conditions, such as chronic fatigue . LRT is not just the dietary substitution of certain lipids with proposed health benefits; it is the actual replacement of damaged cellular lipids with undamaged lipids to ensure proper structure and function of cellular structures, mainly cellular and organelle membranes . Damage to membrane lipids can impair fluidity, electrical properties, enzymatic activities and transport functions of cellular and organelle membranes [1-5]. During LRT lipids must be protected from oxidative and other damage, and this is also necessary during storage as well as during ingestion, digestion, and absorption in vivo. LRT must result in delivery of high concentrations of unoxidized, undamaged membrane lipids in order to reverse the damage and restore function to oxidized cellular membranes. Combined with antioxidant supplements, LTR has proven to be an effective method to prevent ROS-associated changes in certain cellular activities and functions and for use in the treatment of certain clinical conditions .
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HEALTH BENEFITS OF LIPID SUPPLEMENTS Mixtures of lipids introduced as dietary supplements have been used to improve general health [7,8], and they have also been used as an adjunct therapy in the treatment of various clinical conditions, for example, the use of n-3 fatty acids in cardiovascular diseases and inflammatory disorders [8-11]. Although not every clinical study has found health benefits from lipid dietary supplementation , most studies have documented the value of dietary supplements that favor certain types of lipids over others, such as when n-3 polyunsaturated fatty acids (mainly fish- or flaxseed-derived) are favored relative to n-6 lipids [7-11]. Cellular lipids are in dynamic equilibrium in the body, and this is why LRT is possible . Orally ingested lipids diffuse to the gut epithelium and are bound and eventually transported into the blood and lymph using specific carrier alipoproteins and also by nonspecific partitioning and diffusion mechanisms [13,14]. Within minutes, lipid molecules are transported from gut epithelial cells to endothelial cells, then excreted into and transported in the circulation bound to lipoproteins and blood cells where they are generally protected from oxidation [15,16]. Once in the circulation, specific lipoprotein carriers and red blood cells protect lipids throughout their passage and eventual deposition onto specific cell membrane receptors where they can be taken into cells via endosomes and by diffusion . After binding to specific cell surface receptors that bring the lipids into cells, lipid transporters in the cytoplasm deliver specific lipids to cell organelles where they are taken in by specific transport proteins, partitioning, and diffusion . The concentration gradients that exist from the gut during the digestion of lipids to their absorption by gut epithelial cells and their transfer to blood and then tissues are important in driving lipids into cells. Similarly, damaged lipids can be removed by a similar reverse process that may be driven by lipid transfer proteins and by enzymes that recognize and degrade damaged lipids and remove them .
CHRONIC FATIGUE AND OXIDATIVE DAMAGE TO MITOCHONDRIA Intractable or chronic fatigue lasting more than 6 months that is not reversed by sleep is the most common complaint of patients seeking medical care [18,19]. It is also an important secondary condition in many clinical diagnoses and occurs naturally during aging [19,20]. The phenomenon of fatigue has only recently been defined as a multidimensional sensation, and attempts have been made to determine the extent of fatigue and its possible causes [20-22]. Most patients understand fatigue as a loss of energy and inability to perform even simple tasks without exertion. Many medical conditions are associated with fatigue, including respiratory, coronary, musculoskeletal, and bowel conditions as well as infections and cancer [6,19-22]. Fatigue is related to cellular energy systems found primarily in the cells’ mitochondria. Damage to mitochondrial components, mainly by ROS oxidation, can impair their ability to produce high-energy molecules such as ATP and NADH. This occurs naturally with aging and during chronic illnesses, where the production of ROS can cause oxidative stress and cellular damage, resulting in oxidation of lipids, proteins and DNA [23,24]. When oxidized, these molecules are structurally and sometimes functionally changed. Important targets of ROS damage are mitochondria, mainly their phospholipid-containing membranes, and cellular and mitochondrial DNA [1,23,24]. Excess ROS production throughout our lifetimes can result in accumulation of mitochondrial and nuclear damage [1,23-25]. Opposed to this, cellular free-radical scavenging enzymes neutralize excess ROS and repair the enzymes that reverse ROS-mediated damage [25,26]. Although some ROS production is important in triggering cell proliferation, gene expression and destruction of invading microbes [26,27], with aging ROS damage accumulates [1,22,23]. When this occurs, antioxidant enzymes and enzyme repair mechanisms along with biosynthesis cannot restore or replace enough ROS-damaged molecules [1,23,28-30]. Disease and infection can result in oxidative damage that exceeds the abilities of cellular systems to repair and replace damaged molecules [6,23,26], and this is also the situation in fatiguing illnesses .
PREVENTING ROS-MEDIATED DAMAGE WITH ANTIOXIDANTS Reversal of damage of cellular and mitochondrial membranes as well as DNA are important in preventing loss of cellular energy [28-30]. This can be accomplished, in part, by neutralizing ROS with various antioxidants or increasing free-radical scavenging systems that neutralize ROS. Thus dietary antioxidants and some accessory molecules, such as zinc and certain vitamins, are important in maintaining antioxidant and free-radical scavenging systems. In addition to zinc and vitamins, there are at least 40 micronutrients required in the human diet , and aging increases the need to supplement these to prevent age-associated damage to mitochondria and other cellular elements. Antioxidant use alone, however, may not be sufficient to maintain cellular components free of ROS damage. Therefore, LRT is important in replacing ROS-damaged membrane lipids . In animal studies dietary antioxidant supplementation has partially reversed the age-related declines in cellular antioxidants and mitochondrial enzyme activities and prevented mitochondria from most age-associated functional decline. For example, in rodents fed diets supplemented with antioxidants the antioxidants were found to inhibit the progression of certain age-associated changes in cerebral mitochondrial electron transport chain enzyme activities [32,33]. Thus animal studies have shown that antioxidants can partially prevent age-associated changes in mitochondrial function. However, antioxidants alone cannot completely eliminate ROS damage to mitochondria, and this is why LRT is an important addition to antioxidant dietary supplementation . Dietary antioxidants may also modify the pathogenic processes of certain diseases [6,34]. For example, antioxidant administration has been shown to have certain neuroprotective effects . The dietary use of antioxidants has been shown to prevent age-associated mitochondrial dysfunction and damage, inhibit the age-associated decline in immune and other functions and prolong the lifespan of laboratory animals [6,35-37].
PRECLINICAL STUDIES USING LIPID REPLACEMENT THERAPY LTR replaces damaged cellular and mitochondrial membrane phospholipids and other lipids that are essential structural and functional components of all biological membranes . One such LRT dietary supplement is NTFactor®, and this supplement has been used successfully in animal and clinical lipid replacement studies [38,39]. NTFactor’s encapsulated lipids are protected from oxidation in the gut and can be absorbed and transported into tissues without undue damage. NTFactor® contains a variety of components, including glycophospholipids and other lipids, nutrients, probiotics, vitamins, minerals and plant extracts (Table 1). NTFactor® has also been used for studies in laboratory animals. In aged rodents, Seidman et al.  found that NTFactor prevented hearing loss associated with aging and shifted the threshold hearing from 35-40 dB in control aged animals to 13-17 dB in the treatment group (P<0.005). They also found that NTFactor preserved cochlear mitochondrial function as measured in a Rhodamine-123 transport assay , increasing mitochondrial function by 34%. NTFactor also prevented aging-related mitochondrial DNA deletions found in the cochlear . Thus LRT was successful in preventing age-associated hearing loss and mitochondrial damage in rodents.
CLINICAL STUDIES USING LIPID REPLACEMENT THERAPY LRT has been successfully used in clinical studies to reduce fatigue and protect cellular and mitochondrial membranes from damage by ROS [39,40]. For example, NTFactor has been used in a vitamin and mineral mixture (Propax®) in cancer patients to reduce the effects of cancer therapy, such as chemotherapy-induced fatigue, nausea, vomiting and other side effects associated with chemotherapy . This double-blinded, cross-over, placebo-controlled, randomized trial on cancer patients receiving chemotherapy Propax® supplementation showed LRT improvement from fatigue, nausea, diarrhea, impaired taste, constipation, insomnia and other quality of life indicators . Following cross-over to the Propax® supplement, patients reported rapid improvement in nausea, impaired taste, tiredness, appetite, sick feeling and other quality of life indicators . Propax® plus NTFactor has been used in an dietary LRT study with severe chronic fatigued patients to reduce their fatigue . Using the Piper Fatigue Scale  we found that fatigue was reduced approximately 40% (P<0.0001), from severe to moderate fatigue, after eight weeks of supplementation with Propax®. Recently we examine the effects of NTFactor on fatigue in moderately and mildly fatigued subjects and to determine if their mitochondrial function, as measured by the transport and reduction of Rhodamine-123 and fatigue scores, improved with administration of NTFactor . Use of NTFactor for 8 or 12 weeks resulted in a 33% or 35.5% reduction in fatigue, respectively (P<0.001) . In this clinical trial there was good correspondence between reductions in fatigue and gains in mitochondrial function. After only 8 weeks of LRT with NTFactor, mitochondrial function was significantly improved (P<0.001), and after 12 weeks of NTFactor supplementation, mitochondrial function was found to be similar to that of young healthy adults . After 12 weeks of supplement use, subjects discontinued the supplement for an additional 12 weeks, and their fatigue and mitochondrial function were again measured. After the 12-week wash-out period fatigue and mitochondrial function were intermediate between the initial starting values and those found after eight or 12 weeks on supplement, indicating that continued dietary LTR is probably required to show improvements in mitochondrial function and maintain lower fatigue scores . The results indicate that in moderately to severely fatigued subjects dietary LRT can significantly improve and even restore mitochondrial function and significantly improve fatigue.
SUMMARY When mitochondrial function is impaired, such as during moderate to severe fatigue, the net energy available to cells is limited to the Krebs Cycle and anaerobic metabolism. There are a number of conditions and substances that can impair mitochondrial function, but peroxidation and damage of mitochondrial membrane lipids are probably among the most important effects [29,43]. Mitochondrial function appears to be directly related to fatigue, and when patients experience moderate to severe fatigue their mitochondrial function is inevitably impaired. Fatigue is a complex phenomenon determined by several factors, including psychological health [21,22], but at the biochemical level fatigue is related to the metabolic energy available to tissues and cells, mainly through mitochondrial electron transport. Thus the integrity of mitochondrial membranes is critical to cell function and energy metabolism. When mitochondrial membrane lipids are damaged by oxidation, they must be repaired or replaced in order to maintain the production of cellular energy to alleviate fatigue. During aging and in many diseases, including fatiguing illnesses, ROS-mediated accumulation of oxidized mitochondrial lipid occurs. The failure to repair or replace these damaged molecules at a rate that exceeds their damage results in impaired mitochondrial function. Mitochondrial membrane damage and subsequent dysfunction by ROS can also lead to an increased rate of mitochondrial DNA modifications (especially mutations and deletions). The mitochondrial theory of aging proposes that the development of chronic degenerative diseases is the result, in part, of accumulated oxidative damage to mitochondrial membranes and DNA over time [28,29,34,36]. The damage to mitochondrial membranes and DNA seems to also be involved in the etiology of age-associated degenerative diseases [34,44]. Restoration of mitochondrial membrane integrity, fluidity and other properties are essential for the optimal functioning of the electron transport chain. The ability to control membrane lipid peroxidation and DNA damage will likely play an important role in attenuating the development of age-related degenerative diseases [34,44,45]. Dietary LRT plus antioxidants has proven to be a valuable tool in maintaining mitochondrial function and preventing fatigue, and it should be an important part of CFS treatment strategies .
1. Huang H, Manton KG. The role of oxidative damage in mitochondria during aging: a review. Front Biosci 2004; 9:1100-1117.
2. Kanno T, Sato EE, Muranaka S, Fujita H, Fujiwara T, Utsumi T, Inoue M, Utsumi K. Oxidative stress underlies the mechanism for Ca(2+)-induced permeability transition of mitochondria. Free Radical Res 2004; 38(1):27-35.
3. Nicolson GL, Poste G, Ji T. Dynamic aspects of cell membrane organization. Cell Surface Rev 1977; 3:1-73.
4. Subczynski WK, Wisniewska A. Physical properties of lipid bilayer membranes: relevance to membrane biological functions. Acta Biochim Pol 2000; 47:613-625.
5. Manuel y Keenoy B, Moorkens G, Vertommen J, De leeuw I. Antioxidant status and lipoprotein peroxidation in chronic fatigue syndrome. Life Sci 2001; 68: 2037-2049.
6. Nicolson GL. Lipid replacement as an adjunct to therapy for chronic fatigue, anti-aging and restoration of mitochondrial function. J Am Nutraceut Assoc 2003; 6(3): 22-28.
7. Harris WS. n-3 fatty acids and lipoproteins: comparison of results from human and animal studies. Lipids 1996; 31:243-252. 8
. Connor WE. Importance of n-3 fatty acids in health and disease. Am J Clin Nutr 2000; 71:S171-S178.
9. Butcher G, Hengstler HC, Schindler P, Meier C. n-3 polyunsaturated fatty acids in coronary heart disease: a meta-analysis of randomized controlled trials. Am J Med 2002; 112:298-304.
10. Belluzzi A. n-3 fatty acids for the treatment of inflammatory bowel diseases. Proc Nutr Soc 2002; 61:391-393.
11. Calder PC. Dietary modification of inflammation with lipids. Proc Nutr Soc 2002; 61:345-358.
12. Grimble RF. Nutritional modulation of immune function. Proc Nutr Soc 2001; 60:389-397.
13. Hajri T, Abumrad NA. Fatty acid transport across membranes: relevance to nutrition and metabolic pathology. Annu Rev Nutr 2002; 22:383-415.
14. Hamilton JA. Fatty acid transport: difficult or easy? J Lipid Res 1998; 39(3):467-481.
15. Fellmann P, Herve P, Pomorski T, Muller P, et al. Transmembrane movement of diether phospholipids in human erythrocytes and human fibroblasts. Biochem 2000; 39: 4994-5003.
16. Conner SD, Schmid SL. Regulated portals of entry into the cell. Nature 2003; 422:37-44.
17. Mansbach CM, Dowell R. Effect of increasing lipid loads on the ability of the endoplasmic reticulum to transport lipid to the Golgi. J Lipid Res 2000; 41: 605-612.
18. Kroenke K, Wood DR, Mangelsdorff AD, et al. Chronic fatigue in primary care. Prevalence, patient characteristics, and outcome. JAMA 1988; 260:929-934.
19. Morrison JD. Fatigue as a presenting complaint in family practice. J Family Pract 1980; 10:795-801.
20. Piper BF, Dribble SL, Dodd MJ, et al. The revised Piper Fatigue Scale: psychometric evaluation in women with breast cancer. Oncol Nursing Forum 1998; 25:667-684.
21. McDonald E, David AS, Pelosi AJ, Mann AH. Chronic fatigue in primary care attendees. Psychol Med 1993; 23:987-998.
22. Piper BF, Linsey AM, Dodd MJ. Fatigue mechanism in cancer. Oncol Nursing Forum 1987; 14:17-23.
23. Richter C, Par JW, Ames B. Normal oxidative damage to mitochondrial and nuclear DNA is extensive. Proc Nat Acad Sci USA 1998; 85:6465-6467.
24. Wei YH, Lee HC. Oxidative stress, mitochondrial DNA mutation and impairment of antioxidant enzymes in aging. Exp Biol Med 2002; 227:671-682.
25. Harman D. Aging: A theory based on free radical and radiation chemistry. J Gerontol 1956; 2:298-300.
26. Halliwell B. Role of free radicals in the neurodegenerative diseases: therapeutic implications for antioxidant treatment. Drugs Aging 2001; 18:685-716.
27. Tan, NSS, Vinckenbosch NS, Liu N, Yasmin P, Desvergne R, et al. Selective cooperation between fatty acid binding proteins and peroxisome proliferator-activated receptors in regulating transcription. Mol Cell Biol 2002; 22:5114-51127.
28. Chen D, Cao G, Hastings T et al. Age-dependent decline of DNA repair activity for oxidative lesions in rat brain mitochondria. J Neurochem 2002; 81:1273-1284.
29. Xu D, Finkel T. A role for mitochondria as potential regulators of cellular life span. Biochem Biophysics Res Commun 2002; 294:245-248.
30. De AK, Darad R. Age-associated changes in antioxidants and antioxidative enzymes in rats. Mech Ageing Dev 1991; 59: 123-128.
31. Ames BM. Micronutrients prevent cancer and delay aging. Toxicol Lett 1998; 102:1035-1038.
32. Sharman EH, Bondy SC. Effects of age and dietary antioxidants on cerebral electron transport chain activity. Neurobiol Aging 2001; 22: 629-634.
33. Sugiyama S, Yamada K, Ozawa T. Preservation of mitochondrial respiratory function by coenzyme Q10 in aged rat skeletal muscle. Biochem Mol Biol Int 1995; 37:1111-1120.
34. Lin M, Simon D, Ahn C, Lauren K, Beal MF. High aggregrate burden of somatic mtDNA point mutations in aging and Alzheimer’s disease brain. Human Mol Genet 2002; 11:133-145.
35. Matthews RT, Yang L, Browne S, et al. Coenzyme Q10 administration increases brain mitochondrial concentrations and exerts neuroprotective effects. Proc Natl Acad Sci USA 1998; 95: 8892-8897.
36. Miquel, J. Can antioxidant diet supplementation protect against age-related mitochondrial damage? Ann NY Acad Sci 2002; 959:317-347.
37. De AK, Darad R. Age-associated changes in antioxidants and antioxidative enzymes in rats. Mech Ageing Dev 1991; 59: 123-128.
38. Ellithorpe RR, Settineri R, Nicolson GL. Pilot Study: Reduction of fatigue by use of a dietary supplement containing glycophospholipids. J Am Nutraceut Assoc 2003; 6(1):23-28.
39. Agadjanyan, M., Vasilevko, V., Ghochikyan, et al. Nutritional supplement (NTFactor) restores mitochondrial function and reduces moderately severe fatigue in aged subjects. J Chronic Fatigue Syndr 2003; 11(3): 23-26.
40. Seidman M, Khan MJ, Tang WX, Quirk WS. Influence of lecithin on mitochondrial DNA and age-related hearing loss. Otolaryngol Head Neck Surg 2002; 127:138-144.
41. Kim MJ, Cooper DD, Hayes SF, Spangrude GJ. Rhodamine-123 staining in hematopoietic stem cells of young mice indicates mitochondrial activation rather than dye efflux. Blood 1998; 91: 4106-4117.
42. Colodny L, Lynch K, Farber C, Papish S, et al. Results of a study to evaluate the use of Propax to reduce adverse effects of chemotherapy. J Am Nutraceut Assoc 2000; 2:17-25.
43. Paradies G, Petrosillo G, Pistolese M, Ruggiero F. Reactive oxygen species affect mitochondrial electron transport complex I activity through oxidative cardiolipin damage. Gene 2002; 286:135-141.
44. Kowald A. The mitochondrial theory of aging: do damaged mitochondria accumulate by delayed degradation? Exp Gerontol 1999; 34:605-612.
45. Johns DR. 1995. Seminars in medicine of Beth Israel Hospital, Boston: Mitochondrial DNA and Disease. New Engl J Med 1995; 333: 638-44.
Table 1. Components of NTFactor® , a dietary LRT supplement. NT Factor® is a nutrient complex that is extracted and prepared using a proprietary process. In addition, nutrients, vitamins and probiotic microorganisms are added to the preparation. It contains the following ingredients: Glycophospholipids: polyunsaturated phosphatidylcholine, other polyunsaturated phosphatidyl lipids and glycolipids. Probiotics: Bifido bacterium, Lactobacillus acidophilus and Lactobacillus bacillus in a freeze-dried, microencapsulated form with appropriate growth nutrients. Food Supplements, Vitamins and Growth Media: bacterial growth factors to support probiotic growth, including defatted rice bran, arginine, beet root fiber extract, black strap molasses, glycine, magnesium sulfate, para-amino-benzoate, leek extract, pantethine (bifidus growth factor), taurine, garlic extract, calcium borogluconate, artichoke extract, potassium citrate, calcium sulfate, spirulina, bromelain, natural vitamin E, calcium ascorbate, alpha-lipoic acid, oligosaccharides, vitamin B-6, niacinamide, riboflavin, inositol, niacin, calcium pantothenate, thiamin, vitamin B-12, folic acid, chromium picolinate. NT Factor is a registered trademark of Nutritional Therapeutics, Inc., PO Box 5963 Hauppauge NY 11788 (tel: +1-800-982-9158)