Effects of Walnut on Lipid Profile as Well as the Expression of Sterol-Regulatory Element Binding Protein-1c(SREBP-1c) and Peroxisome Proliferator Activated Receptors α (PPARα) in Diabetic Rat

Abstract

Diabetes Mellitus has appeared as a universal burden. Studies have reported that mortality from Coronary Heart Disease (CHD) in diabetic patients is 2 - 4 times higher than nondiabetics. In this respect, walnut is a treatment which has beneficial effects on CHD risk factors. PPARα and SREBP-1c play an important role in the regulation of lipid metabolism. This study was aimed to evaluate the effects of walnut on lipid profile as well as SREBP-1c and PPARα protein levels in rats. Animals were randomly divided into 3 groups (n = 6); Group 1: Received chow only (control), Group 2: Diabetic rats + chow, Group 3: Diabetic rats + chow supplemented with 4% of whole walnuts. After four weeks rats were sacrificed, blood was collected; lipid profiles as well as SREBP-1c and PPARα protein levels were determined. Compared with diabetic rats walnut significantly decreased serum cholesterol (P < 0.01), LDL-c (P < 0.01), triglyceride (P < 0.001) and VLDL-c (P < 0.001) and also increased HDL-c (P < 0.05) compared with diabetic. Moreover, SREBP-1c protein level significantly decreased (P < 0.05) and PPARα significantly increased in walnut group compared with diabetic group (P < 0.05). The findings showed that walnut administration in diet clinically decreases atherosclerosis risk factors. Lipid profile reduction might be due to the rise of PPARα and the reduction of SREBP-1c by this medical treatment in liver.

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E. Oshaghi, A. Sorkhani and A. Rezaei, "Effects of Walnut on Lipid Profile as Well as the Expression of Sterol-Regulatory Element Binding Protein-1c(SREBP-1c) and Peroxisome Proliferator Activated Receptors α (PPARα) in Diabetic Rat," Food and Nutrition Sciences, Vol. 3 No. 2, 2012, pp. 255-259. doi: 10.4236/fns.2012.32037.

Conflicts of Interest

The authors declare no conflicts of interest.

References

[1] J. Stamler, O. Vaccaro, J. Neaton and D. Wentworth, “For the Multiple Risk Factor Intervention Trial Research Group: Diabetes, Other Risk Factors, and 12-Year Cardiovascular Mortality for Men Screened in the Multiple Risk Factor Intervention Trial,” Diabetes Care, Vol. 16, No. 2, 1993, pp. 434-444. doi:10.2337/diacare.16.2.434
[2] J. Sabate, E. G. Fraser, K. Burke, S. F. Knutsen, H. Bennett and K. D. Lindsted, “Effects of Walnut on Serum Lipid Levels and Blood Pressure in Normal Men,” New England Journal of Medicine, Vol. 328, No. 9, 1993, pp. 605-607. doi:10.1056/NEJM199303043280902
[3] P. A. Edwards, H. R. Kast and A. M. Anisfeld, “Bareing It all: The Adoption of LXR and FXR and Their Roles in Lipid Homeostasis,” Journal of Lipid Research, Vol. 43, No. 1, 2002, pp. 2-12.
[4] Z. Huang, X. Zhou, A. C. Nicholson, J. A. M. Gotto, D. P. Hajjar and J. Han, “Activation of Peroxisome Proliferator-Activated Receptor α in Mice Induces Expression of the Hepatic Low-Density Lipoprotein Receptor,” British Journal of Pharmacology, Vol. 155, No. 4, 2008, pp. 596-605. doi:10.1038/bjp.2008.331
[5] W. Friedewald and K. Leseg and D. Fredrickson, “Estimation of the Concentration of Low Density Lipoprotein Cholesterol in Plasma without Use of Preparative Centrifuge,” Clinical Chemistry, Vol. 18, 1972, pp. 499-502.
[6] M. A. Montanaro, A. M. Bernasconi, M. S. Gonzalez, O. J. Rimoldi and R. R. Brenner, “Effects of Feno?brate and Insulin on the Biosynthesis of Unsaturated Fatty Acids in Streptozotocin Diabetic Rats,” Prostaglandins, Leukotrienes and Essential Fatty Acids, Vol. 73, No. 5, 2005, pp. 369-378. doi:10.1016/j.plefa.2005.06.004
[7] S. J. Thornton, E. Wong, D. S. Lee and K. M. Wasan, “Effect of Dietary Fat on Hepatic Liver X Receptor Expression in P-Glycoprotein Deficient Mice: Implications for Cholesterol Metabolism,” Lipids in Health and Disease, Vol. 7, 2008, p. 21.
[8] A. P. Simopoulos, “The Importance of the Ratio of Omega-6/Omega-3 Essential Fatty Acids,” Biomed Pharmacother, Vol. 56, No. 8, 2002, pp. 365-379. doi:10.1016/S0753-3322(02)00253-6
[9] C. Crews, P. Hough, J. Godward, P. Brereton, M. Lees, S. Guiet and W. Winkelmann, “Study of the Main Constituents of Some Authentic Walnut Oils,” Journal of Agriculture and Food Chemistry, Vol. 53, No. 12, 2005, pp. 4853-4860. doi:10.1021/jf0478354
[10] T. Fukuda, H. Ito and T. Yoshida, “Antioxidative Polyphenols from Walnuts (Juglans regia L),” Phytochemistry, Vol. 63, No. 7, 2003, pp. 795-801. doi:10.1016/S0031-9422(03)00333-9
[11] R. J. Reiter, L. C. Manchester and D. X. Tan, “Melatonin in Walnuts: Influence on Levels of Melatonin and Total Antioxidant Capacity of Blood,” Nutrition, Vol. 21, No. 9, 2005, pp. 920-924. doi:10.1016/j.nut.2005.02.005
[12] R. Mushtaq and Z. T. Khan, “Effect of Walnut on Lipid Profile in Obese Female in Different Ethnic Groups of Quetta, Pakistan,” Pakistan Journal of Nutrition, Vol. 8, No. 10, 2009, pp. 1617-1622. doi:10.3923/pjn.2009.1617.1622
[13] R. J. K. Srivastava, S. He and R. S. Newton, “Differential Regulation of Human Apolipoprotein AI and High-Density Lipoprotein by Fenofibrate in HapoAI and HapoAICIII-AIV Transgenic Mice,” Biochimica et Biophysica Acta, Vol. 1811, No. 2, 2011, pp. 76-83.
[14] Y. Koohsoltani, Y. A. Esfahani, M. Shayesteh and S. Datgiri, “Effect of Pulp Walnut Administration on Blood Lipids in Normo Lipidemic and Hyper Lipidemic People,” Journal of Tabriz University of Medical Sciences, Vol. 62, 2004, pp. 55-60.
[15] S. M. Ulven, K. T. Dalen, J. Gustafsson and H. I. Nebb, “LXR Is Crucial in Lipid Metabolism,” Prostaglandins, Leukotrienes and Essential Fatty Acids, Vol. 73, No. 1, 2005, pp. 59-63. doi:10.1016/j.plefa.2005.04.009
[16] I. Shimomura, H. Shimano, B. S. Korn, Y. Bashmakov and J. D. Horton. “Nuclear Sterol Regulatory ElementBinding Proteins Activate Genes Responsible for the Entire Program of Unsaturated Fatty Acid Biosynthesis in Transgenic Mouse Liver,” Journal of Biological Chemistry, Vol. 273, 1998, pp. 35299-35306. doi:10.1074/jbc.273.52.35299
[17] J. Ou, H. Tu, B. Shan, A. Luk, R. A. De Bose-Boyd, Y. Bashmakov, J. L. Goldstein and M. S. Brown, “Unsaturated Fatty Acids Inhibit Transcription of the Sterol Regulatory Element-Binding Protein-1c (SREBP-1c) Gene by Antagonizing Ligand-Dependent Activation of the LXR,” Proceedings of the National Academy of Sciences of the United States of America, Vol. 98, No. 11, 2001, pp. 6027-6032. doi:10.1073/pnas.111138698
[18] N. Zaima, T. Sugawara, D. Goto and T. Hirata, “Trans Geometric Isomers of EPA Decrease LXRa-Induced Cellular Triacylglycerol via Suppression of SREBP-1c and PGC-1b,” Journal of Lipid Research, Vol. 47, No. 12, 2006, pp. 2712-2717. doi:10.1194/jlr.M600273-JLR200
[19] R. Kallwitz, A. M. Lachlan and S. J. Cotler, “Role of Peroxisome Proliferators-Activated Receptors in the Pathogenesis and Treatment of Nonalcoholic Fatty Liver Disease,” World Journal of Gastroenterology, Vol. 14, No. 1, 2008, pp. 22-28.
[20] H. Shu, B. Wong, G. Zhou, Y. Li, J. Berger, J. W. Woods, S. D. Wright and T. Q. Cai, “Activation of PPAR Alpha or Gamma Reduces Secretion of Matrix Metalloproteinase 9 but Not Interleukin 8 from Human Monocytic THP-1 Cells,” Biochemical and Biophysical Research Communications, Vol. 267, No. 1, 2000, pp. 345-349. doi:10.1006/bbrc.1999.1968
[21] A. Keech, R. J. Simes and P. Barter, “Effects of LongTerm Fenofibrate Therapy on Cardiovascular Events in 9795 People with Type 2 Diabetes Mellitus (the FIELD Study): Randomized Controlled Trial,” Lancet, Vol. 366, No. 9500, 2005, pp. 1849-1861. doi:10.1016/S0140-6736(05)67667-2

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