Abstract
Mitochondrial disease (MD) generally refers to a group of disorders that are attributable to malfunctioning mitochondria that are unable to efficiently or effectively generate energy. Some of the most profound effects of MD are seen in the brain and the muscles, while other commonly affected organs include heart, liver, nervous system, eyes, ears, and kidneys. One of the promising nutritional components which may play crucial role in the management of MD is omega-3 polyunsaturated fatty acids (n-3 PUFAs). Animal studies concluded that the omega-3 PUFAs, i.e., ALA and especially EPA and DHA, have some positive effects on functional parameters of mitochondria in various mitochondrial dysfunction-related pathological conditions such as neurodegenerative diseases: Parkinson’s disease, Alzheimer’s disease, aging, cardiovascular diseases, diabetes, and ROS-induced damages. Supplementation with n-3 PUFAs from fish oil (FO) has shown mitochondrial neuroprotective effect in animal models of Parkinson’s disease and aging while clinical trials with patients have shown equivocal results. n-3 PUFAs protected cardiac mitochondria from Ca2+-induced swelling in isoproterenol-treated rats. In animal studies, DHA supplementation brought about significant changes in mitochondria membrane phospholipid components. Similar pattern was noted in cardiac mitochondria from diabetic animal model.
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References
Vitols E, Linnane AW. Studies on the oxidative metabolism of Saccharomyces cerevisiae II. Morphology and Oxidative Phosphorylation Capacity of Mitochondria and Derived Particles from Baker’s Yeast. J Biophy Biochem Cytol. 1961;9(3):701–10.
Bellamy D. The endogenous citric acid-cycle intermediates and amino acids of mitochondria. Biochem J. 1962;82(1):218–24.
Campbell NA, Williamson B, Heyden RJ. Biology: Exploring Life: Boston. Massachusetts: Pearson Prentice Hall; 2006. p. 492.
McBride HM, Neuspiel M, Wasiak S. Mitochondria: more than just a powerhouse. Cur Biol. 2006;16(14):551–60.
Naviaux RK. The spectrum of mitochondrial disease. A primary care physicians guide. 1997;3–10.
Poyton RO, McEwen JE. Crosstalk between nuclear and mitochondrial genomes. Annu Rev Biochem. 1996;65:563–607.
DiMauro S, Schon EA. Mitochondrial respiratory-chain diseases. New Engl J Med. 2003;348(26):2656–68.
DiMauro S, Andreu AL, Musumeci O, Bonilla E. Diseases of oxidative phosphorylation due to mtDNA mutations. Semin Neurol. 2001;21(3):251–60.
Sirrs S, O’Riley M, Lorne Clarke MDCM, AM FCCMG. Primer on mitochondrial disease: Biochemistry, genetics, and epidemiology. Depression. 2011;500:70s.
McInnes J. Mitochondrial-associated metabolic disorders: foundations, pathologies and recent progress. Nutr Metab. 2013;10(1):1–13.
Gvozdjáková A, Pella D, Kucharská J, Otsuka K, Singh RB. Omega-3-PUFA, Omega-6-PUFA and Mitochondria. Mitochondrial Med. 2008;343–56.
Eckert GP, Lipka U, Muller WE. Omega-3 fatty acids in neurodegenerative diseases: focus on mitochondria. Prostaglandins Leukot Essent Fatty Acids. 2013;88(1):105–14.
Eckert A, et al. Mitochondrial dysfunction—a pharmacological target in Alzheimer’s disease. Mol Neurobiol. 2012;46(1):136–50.
Kidd PM. Neurodegeneration from mitochondrial insufficiency: nutrients, stem cells, growth factors, and prospects for brain rebuilding using integrative management. Alter Med Rev. 2005;10(4):268.
Galli C, White HB Jr, Paoletti R. Lipid alterations and their reversion in the central nervous system of growing rats deficient in essential fatty acids. Lipids. 1971;6(6):378–87.
Bourre, JM. Effects of nutrients (in food) on the structure and function of the nervous system: update on dietary requirements for brain. Part 2: macronutrients. J Nutr Health Aging. 2006;10(5), 386.
Afshordel S, Hagl S, Werner D, Röhner N, Kögel D, Bazan NG, Eckert GP. Omega-3 polyunsaturated fatty acids improve mitochondrial dysfunction in brain aging–Impact of Bcl-2 and NPD-1 like metabolites. Prostaglandins Leukot Essent Fatty Acids. 2015;92:23–31.
Lee LK, Shahar S, Rajab N, Yusoff NAM, Jamal RA, Then SM. The role of long chain omega-3 polyunsaturated fatty acids in reducing lipid peroxidation among elderly patients with mild cognitive impairment: a case-control study. J Nutr Biochem. 2013;24(5):803–8.
Dyall SC, Michael-Titus AT. Neurological benefits of omega-3 fatty acids. NeuroMol Med. 2008;10(4):219–35.
Pagano G, Aiello Talamanca A, Castello G, Cordero MD, d’Ischia M, Gadaleta MN, et al. Oxidative stress and mitochondrial dysfunction across broad-ranging pathologies: toward mitochondria-targeted clinical strategies. Oxidative Med Cell Longev. 2014; 2014.
Di Lisa F, Kaludercic N, Carpi A, Menabò R, Giorgio M. Mitochondria and vascular pathology. Pharmacol Reports. 2009;61(1):123–30.
Perrotta I, Perrotta E, Sesti S, Cassese M, Mazzulla S. MnSOD expression in human atherosclerotic plaques: an immunohistochemical and ultrastructural study. Cardiovas Pathol. 2013;22(6):428–37.
Sobenin IA, Sazonova MA, Postnov AY, Bobryshev YV, Orekhov AN. Changes of mitochondria in atherosclerosis: possible determinant in the pathogenesis of the disease. Atherosclerosis. 2013;227(2):283–8.
Guzik B, Sagan A, Ludew D, Mrowiecki W, Chwała M, Bujak-Gizycka B, et al. Mechanisms of oxidative stress in human aortic aneurysms—association with clinical risk factors for atherosclerosis and disease severity. Inter J Cardiol. 2013;168(3):2389–96.
Stanley WC, Hoppel CL. Mitochondrial dysfunction in heart failure: potential for therapeutic interventions? Cardiovas Res. 2000;45(4):805–6.
Jarreta D, Orús J, Barrientos A, Miró O, Roig E, Heras M, et al. Mitochondrial function in heart muscle from patients with idiopathic dilated cardiomyopathy. Cardiovas Res. 2000;45(4):860–5.
McInnes J. Mitochondrial-associated metabolic disorders: foundations, pathologies and recent progress. Nutr and Metab. 2013;10(1):1–13.
Guzy RD, Hoyos B, Robin E, Chen H, Liu L, Mansfield KD, et al. Mitochondrial complex III is required for hypoxia-induced ROS production and cellular oxygen sensing. Cell Metab. 2005;1(6):401–8.
Murray AJ, Edwards LM, Clarke K. Mitochondria and heart failure. Curr Opin Clin Nutr Metab Care. 2007;10(6):704–11.
Panasiuk OS, Shysh AM, Moĭbenko OO. The influence of dietary omega-3 polyunsaturated fatty acids on functional parameters of myocardial mitochondria during isoproterenol-induced heart injury. FiziolZh (Kiev, Ukraine: 1994). 2013;60(1):18–24.
Panasiuk O, Shysh A, Bondarenko A, Moibenko O. Omega-3 polyunsaturated fatty acid-enriched diet differentially protects two subpopulations of myocardial mitochondria against Ca2 + -induced injury. Expt Clin Cardiol. 2013;18(1):e60.
Pepe S. Effect of dietary polyunsaturated fatty acids on age-related changes in cardiac mitochondrial membranes. Expt Gerontol. 2005;40(5):369–76.
Dabkowski ER, O’Connell KA, Xu W, Ribeiro Jr RF, Hecker PA, Shekar KC, et al. Docosahexaenoic acid supplementation alters key properties of cardiac mitochondria and modestly attenuates development of left ventricular dysfunction in pressure overload-induced heart failure. Cardiovas Drugs Ther. 2013; 27(6):499–510.
Galvao TF, Khairallah RJ, Dabkowski ER, Brown BH, Hecker PA, O’Connell KA, et al. Marine n3 polyunsaturated fatty acids enhance resistance to mitochondrial permeability transition in heart failure but do not improve survival. Physiol-Heart Circulatory Physiol. 2013;304(1):H12–21.
Khairallah RJ, Sparagna GC, Khanna N, O’Shea KM, Hecker PA, Kristian T, et al. Dietary supplementation with docosahexaenoic acid, but not eicosapentaenoic acid, dramatically alters cardiac mitochondrial phospholipid fatty acid composition and prevents permeability transition. Biochima et Biophysica Acta-Bioenergetics. 2010; 1797(8):1555–62.
Stanley WC, Khairallah RJ, Dabkowski ER. Update on lipids and mitochondrial function: impact of dietary n-3 polyunsaturated fatty acids. Curr Opin Clin Nutr Metabol care. 2012; 15(2):122.
Chen L, Magliano DJ, Zimmet PZ. The worldwide epidemiology of type 2 diabetes mellitus—present and future perspectives. Nat Rev Endocrinol. 2012;8(4):228–36.
Khan S, Raghuram GV, Bhargava A, Pathak N, Chandra DH, Jain SK, et al. Role and clinical significance of lymphocyte mitochondrial dysfunction in type 2 diabetes mellitus. Translational Res. 2011;158(6):344–59.
Michikawa Y, Mazzucchelli F, Bresolin N, Scarlato G, Attardi G. Aging-dependent large accumulation of point mutations in the human mtDNA control region for replication. Science. 1999;286(5440):774–9.
Petersen KF, Befroy D, Dufour S, Dziura J, Ariyan C, Rothman DL, et al. Mitochondrial dysfunction in the elderly: possible role in insulin resistance. Science. 2003;300(5622):1140–2.
Leloup C, Tourrel-Cuzin C, Magnan C, Karaca M, Castel J, Carneiro L, et al. Mitochondrial reactive oxygen species are obligatory signals for glucose-induced insulin secretion. Diabetes. 2009;58(3):673–81.
Zhukovs’ka AS, ShyshAM Moĭbenko OO. Study of the impact of omega-3 PUFA on fatty acid composition of heart, respiration and swelling of mitochondria of the heart in diabetes. FiziolZh. 2012;58(2):16–26.
Taneda S, Honda K, Tomidokoro K, Uto K, Nitta K, Oda H. Eicosapentaenoic acid restores diabetic tubular injury through regulating oxidative stress and mitochondrial apoptosis. Am J Physiol Renal Physiol. 2010;299(6):F1451–61.
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Katyare, S.S., Mali, A.V. (2016). Omega-3 Fatty Acids and Mitochondrial Functions. In: Hegde, M., Zanwar, A., Adekar, S. (eds) Omega-3 Fatty Acids. Springer, Cham. https://doi.org/10.1007/978-3-319-40458-5_17
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DOI: https://doi.org/10.1007/978-3-319-40458-5_17
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