Abstract
Background
Dietary fatty acids can alter membrane fatty acid composition with the consequent change in the action of various receptors. Incorporation of mustard oil was found to increase insulin secretion, reduce blood glucose levels, and increase the expression of glucose transporter gene 4 (Glut4).
Methods
Three-week-old male Wistar rats were fed with 8% lipid-inclusive isocaloric mash diet. There were non-diabetic control (NDC) and diabetic control (DC) groups fed with ghee, and similarly non-diabetic (NDT) and diabetic treatment (DT) groups fed with mustard oil. Streptozotocin (STZ) was administered intraperitoneally once at a dose rate of 40 mg/kg bodyweight for the induction of diabetes. Blood glucose was estimated using glucometer periodically. Lipids were extracted from mustard oil and in tissue samples, and fatty acid estimation was done using gas chromatography (GC). Gene expression of 84 genes related to diabetes was measured in muscle tissue using Qiagen™ RT2 polymerase chain reaction (PCR) profiler array. The real-time PCR data obtained as threshold cycle (Ct) values were analyzed using Ingenuity Pathway Analysis® (IPA®) software.
Results
After induction of diabetes by day 30, the average glucose levels were above 500 mg/dL in diabetic groups, but for the mustard oil treatment group, they were reduced to 337 mg/dL by the 60 days of treatment. Significantly higher levels of unsaturated fatty acids particularly linoleic acid and linolenic acid were found in mustard oil treatment groups. Insulin receptor signaling was prominent in both ghee-fed normal and mustard oil–fed diabetic treatment groups. Glucose was found to be the major upstream regulator in all the groups except for ghee-fed diabetic control group.
Conclusions
Mustard oil inclusion in the diet reduces blood glucose levels by increased insulin receptor signaling, thereby partially reversing diabetic state in experimentally induced diabetic rats.
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References
Liu S, Baracos VE, Quinney HA, Clandinin MT, et al. Dietary omega-3 and polyunsaturated fatty acids modify fatty acyl composition and insulin binding in skeletal-muscle sarcolemma. Biochem J. 1994;299:831–7.
Ayre KJ, Hulbert AJ. Dietary fatty acid profile influences the composition of skeletal muscle phospholipids in rats. J Nutr. 1996;126:653–62.
Olomu JM, Baracos VE. Prostaglandin synthesis and fatty acid composition of phospholipids and triglycerides in skeletal muscle of chicks fed combinations of flaxseed oil and animal tallow. Lipids. 1991;26:743–9.
Mann JI. Nutrition recommendations for the treatment and prevention of type 2 diabetes and the metabolic syndrome: an evidence-based review. Nutr Rev. 2006;64:422–7.
Kinsell LW, Walker G, Michaels GD, Olson FE, Coelho M, McBride Y, et al. Dietary fats and the diabetic patient. N Engl J Med. 1959;261:431–4.
Abbott SK, Else PL, Hulbert AJ, et al. Membrane fatty acid composition of rat skeletal muscle is most responsive to the balance of dietary n−3 and n−6 PUFA. Br J Nutr. 2010;103:522–9.
Ginsberg BH, Brown TJ, Simon I, Spector AA, et al. Effect of the membrane lipid environment on the properties of insulin receptors. Diabetes. 1981;30:773–80.
Storlien LH, Baur LA, Kriketos AD, Pan DA, Cooney GJ, Jenkins AB, et al. Dietary fats and insulin action. Diabetologia. 1996a;39:621–31.
Russo LG. Dietary n-6 and n-3 polyunsaturated fatty acids: from biochemistry to clinical implications in cardiovascular prevention. Biochem Pharmacol. 2009;77(6):937–46.
Gould RJ, Ginsberg BH, Spector AA, et al. Lipid effects on the binding properties of a reconstituted insulin receptor. J Biol Chem. 1982;257(1):477–84.
Cheema SK, Clandinin MT. Diet- and diabetes-induced change in insulin binding to the nuclear membrane in spontaneously diabetic rats is associated with change in the fatty acid composition of phosphatidylinositol. J Nutr Biochem. 2001;12:213–8. https://doi.org/10.1016/S0955-2863(00)00135-2.
Borkman M, Storlien LH, Pan DA, Jenkins AB, Chisholm DJ, Campbell LV, et al. The regulation between insulin sensitivity and fatty acid composition of skeletal muscle phospholipids. N Engl J Med. 1993;328(4):238–44.
Storlien LH, Pan DA, Kriketos AD, Connor JO, Caterson ID, Cooney GJ, et al. Skeletal muscle membrane lipids and insulin resistance. Lipids. 1996b;31:S261–5.
Simonikova P, Wein S, Gasperikova D, Ukropec J, Certik M, Klimes I, et al. Comparison of the extrapancreatic action of γ-linolenic acid and n-3 PUFAs in the fat diet-induced insulin resistance. Endocr Regul. 2002;36:143–9.
Paniagua JA, de la Sacristana AG, Sánchez E, Romero I, Vidal-Puig A, Berral FJ, et al. A MUFA-rich diet improves posprandial glucose, lipid and GLP-1 responses in insulin-resistant subjects. J Am Coll Nutr. 2007;26(5):434–44.
Kumar A, Sharma A, Upadhyaya KC, et al. Vegetable oil: nutritional and industrial perspective. Curr Genomics. 2016;17(3):230–40.
Vassiliou EK, Gonzalez A, Garcia C, Tadros JH, Charakborty G, Toney JH, et al. Oleic acid and peanut oil high in oleic acid reverse the inhibitory effect of insulin production of the inflammatory cytokine TNF-a both in vitro and in vivo systems. Lipids Health Dis. 2009;26:8–25.
Perez-Rosales R, Villanueva-Rodrıguez S, Cosıo-Ramırez R, et al. El aceite de aguacate y sus propiedades nutricionales (Avocado oil and its nutritional properties). e-Gnosis. 2015;3:10.
Rama T, Padmanath K, Valli C, Pandian V, et al. Influence of sunflower oil supplementation in streptozotocin induced diabetic rats. Res J Pharm, Biol Chem Sci. 2018;9(2):510–21.
Dinesh Kumar B, Mukherjee S, Pradhan R, Mitra A, Chakraborty C. Effects of edible oils in type 2 diabetes mellitus. J Clin Diagn Res. 2009;3:1389–94.
Hamdan A, Haji Idrus R, Mokhtar MH. Effects of Nigella sativa on type-2 diabetes mellitus: a systematic review. Int J Environ Res Public Health. 2019;16(24):4911. https://doi.org/10.3390/ijerph16244911.
Jurado-Ruiz E, Álvarez-Amor L, Varela LM, Berná G, Parra-Camacho MS, María J, et al. Extra virgin olive oil diet intervention improves insulin resistance and islet performance in diet-induced diabetes in mice. Sci Rep. 2019;9:1311.
Rasmussen OW, Thomsen CH, Hansen KW, Winther E, Hermansen K, et al. Favourable effect of olive oil in patients with non-insulin-dependent diabetes. The effect on blood pressure, blood glucose and lipid levels of a high-fat diet rich in monounsaturated fat compared with a carbohydrate-rich diet. Ugeskr Laeger. 1995;157(8):1028–32.
Girón MD, Salto R, Hortelano P, Periago JL, Vargas AM, Suárez MD, et al. Increased diaphragm expression of GLUT4 in control and streptozotocin-diabetic rats by fish oil-supplemented diets. Lipids. 1999;34:801–7. https://doi.org/10.1007/s11745-999-0426-0.
Peyron-Caso E, Fluteau-Nadler S, Kabir M, Guerre-Millo M, Quignard-Boulangé A, Slama G, et al. Regulation of glucose transport and transporter 4 (GLUT-4) in muscle and adipocytes of sucrose-fed rats: effects of N-3 poly- and monounsaturated fatty acids. Horm Metab Res. 2002;34:360–6. https://doi.org/10.1055/s-2002-33467.
Sukanya V, Pandiyan V, Vijayarani K, Padmanath K, et al. A study on insulin levels and the expression of Glut4 in streptozotocin (STZ) induced diabetic rats treated with mustard oil diet. Indian J Clin Biochem. 2019. https://doi.org/10.1007/s12291-019-00852-x.
Ikemoto S, Takahashi M, Tsunoda N, Maruyama K, Itakura H, Ezaki O, et al. High-fat diet-induced hyperglycemia and obesity in mice: differential effects of dietary oils. Metabolism. 1996;45(12):1539–46.
Picinato MC, Curi R, Machado UF, Carpinelli AR, et al. Soybean- and olive-oils-enriched diets increase insulin secretion to glucose stimulus in isolated pancreatic rat islets. Physiol Behav. 1998;65:289–94. https://doi.org/10.1016/s0031-9384(98)00157-7.
Maidin NQH, Ahmad N. Protective and antidiabetic effects of virgin coconut oil (Vco) on blood glucose concentrations in alloxan induced diabetic rats. Int J Pharm Pharm Sci. 2013;7(10):57–60.
Poletto AC, Anhe GF, Eichler P, Takahashi HK, Furuya DT, Okamoto MM, et al. Soybean and sunflower oil-induced insulin resistance correlates with impaired GLUT4 protein expression and translocation specifically in white adipose tissue. Cell Biochem Funct. 2010;28(2):114–21.
Clarke SD. Polyunsaturated fatty acid regulation of gene transcription: a mechanism to improve energy balance and insulin resistance. Br J Nutr. 2000;83(1):S59–66.
Shepherd PR, Kahn BB. Glucose transporters and insulin action--implications for insulin resistance and diabetes mellitus. N Engl J Med. 1999;341(4):248–57.
Bryant NJ, Govers R, James DE, et al. Regulated transport of the glucose transporter GLUT4. Nat Rev Mol Cell Biol. 2002;3(4):267–77.
Folch J, Lees M, Sloane-Stanley GH, et al. A simple method for the isolation and purification of total lipides from animal tissues. J Biol Chem. 1957;226(1):497–509.
Pfaffl MW. Mathematical modelling of prefermenters-I. Model development and verification. Nucleic Acids Res. 2001. https://doi.org/10.1016/S0043-1354(98)00516-8.
Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-delta delta C(T)) method. Methods. 2001;25(4):402–8.
Ming Z, Xiao-Yan L, Jing L, Zhi-Gang X, Li C, et al. The characterization of high-fat diet and multiple low-dose streptozotocin induced type 2 diabetes rat model. Exp Diabetes Res. 2009:1–9.
Kitukale MD, Chandewar AV. An overview on some recent herbs having antidiabetic potential. Res J Pharm, Biol Chem Sci. 2014;5(6):190.
Jayasri MA, Radha A, Mathew TL, et al. A Amylase and a glucosidase inhibitory activity of Costus pictus in the management of diabetes. J Herb Med Toxicol. 2009;3:91–4.
Guyton AC, Hall JE. Textbook of medical physiology. 10th ed. Philadelphia: Saunders WB; 2000. p. 810–8.
Gerling CJ, Mukai K, Chabowski A, Heigenhauser GJF, Holloway GP, Spriet LL, et al. Incorporation of omega-3 fatty acids into human skeletal muscle sarcolemmal and mitochondrial membranes following 12 weeks of fish oil supplementation. Front Physiol. 2019. https://doi.org/10.3389/fphys.2019.00348.
Kumar V, Ahmed D, Gupta PS, Anwar F, Mujeeb M, et al. Anti-diabetic, anti-oxidant and antihyperlipidemic activities of Melastoma malabathricum Linn leaves in streptozotocin induced diabetic rats. BMC Compl Altern Med. 2013;13(222):1–19.
Murray RR, Granner DK, Mayes PA, Rodwell VW, et al. Harper’s biochemistry. 25th ed. Stamford: Appleton and Lange; 1999. p. 610–7.
Campbell PJ, Carlson MG, Hill JO, Nurjhan N, et al. Regulation of free fatty acid metabolism by insulin in humans: role of lipolysis and reesterification. Am J Phys. 1992;263(6):E1063–9.
Boone DR, Micci MA, Taglialatela IG, Hellmich JL, Weisz HA, Bi M, et al. Pathway-focused PCR array profiling of enriched populations of laser capture microdissected hippocampal cells after traumatic brain injury. PLoS ONE. 2015;10(5):0127287.
Abel ED, Peroni O, Kim JK, Kim YB, Boss O, Hadro E, et al. Adipose-selective targeting of the GLUT4 gene impairs insulin action in muscle and liver. Nature. 2001;409(6821):729–33.
Carvalho E, Schellhorn SE, Zabolotny JM, Tozzo SME, Peroni OD, Houseknecht KL, et al. GLUT4 overexpression or deficiency in adipocytes of transgenic mice alters the composition of GLUT4 vesicles and the subcellular localization of GLUT4 and insulin-responsive aminopeptidase. J Biol Chem. 2004;279(20):21598–605.
Charron MJ, Katz EB, Olson AL, et al. GLUT4 gene regulation and manipulation. J Biol Chem. 1999;274(6):3253–6.
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Devi, P.A., Pandiyan, V., Kumar, T.M.A.S. et al. Dietary supplementation of mustard oil reduces blood glucose levels by triggering insulin receptor signaling pathway. Int J Diabetes Dev Ctries 42, 126–137 (2022). https://doi.org/10.1007/s13410-021-00952-6
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DOI: https://doi.org/10.1007/s13410-021-00952-6