Differences between α-linolenic and linoleic acid supplementation on the redox status and cardiodynamic parameters of male and female Wistar albino rats
Keywords:
α-linolenic acid, linoleic acid, redox status, cardiac contractility, ratAbstract
The aim of present study was to investigate the difference between α-linolenic acid (ALA, omega-3) and linoleic acid (LA, n-6) on the redox status and cardiac function of the isolated rat heart. ALA or LA were administered for 6 weeks by gavage to all animals, which were randomly divided into 4 groups: male rats treated with a linoleic acid (M-LA), dose of 7.3 mg/kg/day; female rats treated with a linoleic acid (F-LA), dose of 7.3 mg/kg/day; male rats treated with an α-linolenic acid (M-ALA), dose of 165 mg/kg/day; female rats treated with α-linolenic acid (F-ALA), dose of 165 mg/kg/day. Using the Langendorff technique, markers of heart function were evaluated: the maximum and minimum rates of pressure development in the left ventricle (LV; dp/dt max, dp/dt min), systolic and diastolic left ventricle pressure (SLVP, DLVP, respectively), heart rate (HR) and coronary flow (CF). We measured the concentrations of prooxidative markers: nitrites (NO2-), superoxide anion radicals (O2-) and hydrogen peroxide (H2O2), as well as the index of lipid peroxidation (TBARS) in the plasma and effluent. In the lysate, we measured the concentrations of reduced glutathione (GSH), catalase (CAT) and superoxide dismutase (SOD). ALA more negatively influenced the isolated rat heart, especially in females. In contrast, the administration of LA was linked to more prominent oxidative stress, while the application of ALA was associated with improved activity of the antioxidative defense system (with better values in males).
https://doi.org/10.2298/ABS170810038R
Received: August 10, 2017; Revised: September 24, 2017; Accepted: October 6, 2017; Published online: October 16, 2017
How to cite this article: Radoman K, Živković V, Nikolić T, Stojić I, Raičević D, Jeremić J, Srejović I, Jakovljević V. Differences between α-linolenic and linoleic acid supplementation on the redox status and cardiodynamic parameters of male and female Wistar albino rats. Arch Bio Sci. 2018;70(2):223-31.
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References
Spector A, Kim H. Discovery of essential fatty acids. J Lipid Res. 2015;56:11-21.
Das U. Biological significance of essential fatty acids. J Assoc Physicians India. 2006;54:309-19.
Mele M, Cannelli G, Carta G, Cordeddu L, Melis M, Murru E, Stanton C, Banni S. Metabolism of c9,t11-conjugated linoleic acid (CLA) in humans. Prostaglandins Leukot Essent Fatty Acids. 2013;89:115-9.
Lunn J, Theobald H. The health effects of dietary unsaturated fatty acids. Nutr Bull. 2006;31:178-224.
Simopoulos A. The importance of the omega-6/omega-3 fatty acid ratio in cardiovascular disease and other chronic diseases. Exp Biol Med. 2008;233:674-88.
Patterson E, Wall R, Fitzgerald G, Ross R, Stanton C. Health implications of high dietary omega-6 polyunsaturated fatty acids. J Nutr Metab. 2012;53:942-6.
Arsić A, Prekajski N, Vučić V, Tepšić J, Popović T, Vrvić M, Glibetić M. Milk in human nutrition: comparison of fatty acid profiles. Acta Vet (Beogr). 2009;59:569-78.
Du R, Zhong T, Zhang W, Song P, Song W, Zhao Y, Wang C, Tang Y, Zhang X, Zhang Q. Antitumor effect of iRGD-modified liposomes containing conjugated linoleic acid-paclitaxel (CLA-PTX) on B16-F10 melanoma. Int J Nanomedicine. 2014;9:3091-105.
Farvid M, Ding M, Pan A, Sun Q, Chiuve S, Steffen L, Willett W, Hu F. Dietary linoleic acid and risk of coronary heart disease: A systematic review and meta-analysis of prospective cohort studies. Circulation. 2014;130:1568-78.
Chowdhury R, Warnakula S, Kunutsor S, Crowe F, Ward H, Johnson L, Franco O, Butterworth A, Forouhi N, Thompson S, Khaw K, Mozaffarian D, Danesh J, Di Angelantonio E. Association of dietary, circulating, and supplement fatty acids with coronary risk: A systematic review and meta-analysis. Ann Intern Med. 2014;160:398-06.
Blasbalg T, Hibbeln J, Ramsden C, Majchrzak S, Rawlings R. Changes in consumption of omega-3 and omega-6 fatty acids in the United States during the 20th century. Am J Clin Nutr. 2011;93:950-62.
Ramsden C, Zamora D, Majchrzak-Hong S, Faurot K, Broste S, Frantz R, Davis J, Ringel A, Suchindran C, Hibbeln J. Re-evaluation of the traditional diet-heart hypothesis: Analysis of recovered data from Minnesota Coronary Experiment (1968-1973). BMJ. 2016;353:1246-8.
Miyashita K. Paradox of omega-3 PUFA oxidation. Eur J Lipid Sci Technol. 2014;116:1268-79.
Di Nunzio M, Valli V, Bordoni A. PUFA and oxidative stress. Differential modulation of the cell response by DHA. Int J Food Sci Nutr. 2016;67:834-43.
Espinosa-Diez C, Miguel V, Mennerich D, Kietzmann T, Sánchez-Pérez P, Cadenas S, Lamas S. Antioxidant responses and cellular adjustments to oxidative stress. Redox Biol. 2015;6:183-97.
Chinnadurai K, Kanwal K, Tyagi A, Stanton C, Ross P. High conjugated linoleic acid enriched ghee (clarified butter) increases the antioxidant and antiatherogenic potency in female Wistar rats. Lipids Health Dis. 2016;12:121-25.
Kukoba T, Shysh A, Moĭbenko O, Kotsiuruba A, Kharchenko O. The effects of alpha-linolenic acid on the functioning of the isolated heart during acute myocardial ischemia/reperfusion. Fiziol Zh. 2006;52:12-20.
Hassan A, Ibrahim A, Mbodji K, Coëffier M, Ziegler F, Bounoure F, Chardigny M, Skiba M, Savoye G, Déchelotte P, Marion-Letellier R. An α-linolenic acid-rich formula reduces oxidative stress and inflammation by regulating NF-κB in rats with TNBS-induced colitis. J Nutr. 2010;140:1714-21.
Sikorska-Wiśniewska M, Mika A, Śledziński T, Małgorzewicz S, Stepnowski P, Rutkowski B, Chmielewski M. Disorders of serum omega-3 fatty acid composition in dialyzed patients, and their associations with fat mass. Ren Fail. 2017;39:406-12.
Folino A, Sprio E, Di Scipio F, Berta N, Rastaldo R. Alpha-linolenic acid protects against cardiac injury and remodelling induced by beta-adrenergic overstimulation. Food Funct. 2015;6:2231-9.
Mitchell L, Grant F, Melchert B, Petty M, Kennedy R. Linoleic acid metabolites act to increase contractility in isolated rat heart. Cardiovasc Toxicol. 2002;2:219-30.
McCord M, Fridovich I. SOD enzyme function for erythrocuprein. J Biol Chem. 1969;224:6049-55.
Auclair C, Voisin E. Nitroblue tetrazolium reduction. In: Greenwald RA, editor. CRC handbook of methods for oxygen radical research. CRC Press Boca Raton; 1985. p. 123-32.
Green L, Wagnwr D, Glogowski J, Skipper P, Wishnok J, Tannenbaum S. Analysis of nitrate, nitrite and (15 N) nitrate in biological fluids. Anal Biochem. 1982;126:131-8.
Pick E, Keisari Y. A simple colorimetric method for the measurement of hydrogen peroxide produced by cells in culture. J Immunol Methods.1980;38:161-70.
Ohkawa H, Ohishi N. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979;95:351-8.
Beutler E. Catalase. In: Beutler E, editor. Red cell metabolism: A manual of biochemical methods. New York: Grune and Stratton; 1982. p. 105-6.
Beutler E, Duron O, Kelly B. Improved method for the determination of blood glutathione. J Lab Clin Med. 1963;61:882-8.
Bačová B, Seč P, Radošinská J, Certík M, Vachulová A, Tribulová N. Lower omega-3 index is a marker of increased propensity of hypertensive rat heart to malignant arrhythmias. Physiol Res. 2013;62:201-8.
Ristic-Medic D, Suzic S, Vucic V, Takic M, Tepsic J, Glibetic M. Serum and erythrocyte membrane phospholipids fatty acid composition in hyperlipidemia: effects of dietary intervention and combined diet and fibrate therapy. Gen Physiol Biophys. 2009;28:190-9.
Berecki G, Den Ruijter H, Verkerk A, Schumacher C, Baartscheer A, Bakker D. Dietary fish oil reduces the incidence of triggered arrhythmias in pig ventricular myocytes. Heart Rhythm. 2007;4:1452-60.
Blanchard H, Pédrono F, Boulier-Monthéan N, Catheline D, Rioux V, Legrand P. Comparative effects of well-balanced diets enriched in α-linolenic or linoleic acids on LC-PUFA metabolism in rat tissues. Prostaglandins Leukot Essent Fatty Acids. 2013;88:383-9.
Salem N, Lin Y, Moriguchi T, Lim S, Salem Jr N, Hibbeln J. Distribution of omega-6 and omega-3 polyunsaturated fatty acids in the whole rat body and 25 compartments. Prostaglandins Leukot Essent Fatty Acids. 2010;100:13-20.
Popović T, Borozan S, Arsić A, Martačić J, Vučić V, Trbović A, Mandić L, Glibetić M. Fish oil supplementation improved liver phospholipids fatty acid composition and parameters of oxidative stress in male Wistar rats. J Anim Phys Anim Nutr. 2012;96:1020-9.
Komatsu W, Ishihara K, Murata M, Saito H, Shinohara K. Docosahexaenoic acid suppresses nitric oxide production and inducible nitric oxide synthase expression in interferon-gamma plus lipopolysaccharide-stimulated murine macrophages by inhibiting the oxidative stress. Free Radic Biol Med. 2003;34:1006-16.
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