DOI QR코드

DOI QR Code

Alterations in the blood glucose, serum lipids and renal oxidative stress in diabetic rats by supplementation of onion (Allium cepa. Linn)

  • Bang, Mi-Ae (Solar Salt Biotechnology Research Center, Mokpo National University) ;
  • Kim, Hyeon-A (Food and Nutrition, Mokpo National University) ;
  • Cho, Young-Ja (Food and Nutrition, Mokpo National University)
  • Published : 2009.09.30

Abstract

This study examined the anti-diabetic effect of onion (Allium cepa. Linn) in the streptozotocin (STZ)-induced diabetic rats. Male Sprague-Dawley rats were divided into normal rats fed control diet or supplemented with onion powder (7% w/w) and diabetic rats fed control diet or supplemented with onion powder. Diabetes was induced by a single injection of STZ (60 mg/kg, ip) in citrate buffer. The animals were fed each of the experimental diet for 5 weeks. Blood glucose levels of rats supplemented with onion were lower than those of rats fed control diet in the diabetic rats. Onion also decreased the total serum lipid, triglyceride, and atherogenic index and increased HDL-cholesterol/total cholesterol ratio in the diabetic rats. Glutathione peroxidase, glutathione reductase and glutathione S-transferase activities were high in the diabetic rats compared to normal rats and reverted to near-control values by onion. These results indicate that onion decreased blood glucose, serum lipid levels and reduced renal oxidative stress in STZ-induced diabetic rats and this effect might exert the anti-diabetic effect of onion.

Keywords

References

  1. Babu PS & Srinivasan K (1999). Renal lesions in streptozotocininduced diabetic rats maintained on onion and capsaicin containing diets. J Nutr Biochem 10:477-483 https://doi.org/10.1016/S0955-2863(99)00031-5
  2. Banginski ES, Foa PP & Zak B (1983). In Methods of Enzymatic Analysis 2, p.876-80. Academic Press, New York. USA
  3. Bordia A, Bansal HC, Arora SK & Singh SV (1975). Effect of essential oils of garlic and onion on alimentary hyperlipidemia. Atherosclerosis 21:15-19 https://doi.org/10.1016/0021-9150(75)90091-X
  4. Bordia A, Verma SK & Vyas AK (1977). Effect of essential oils of onion and garlic on experimental atherosclerosis in rabbits. Atherosclerosis 26:375-386
  5. Carlberg I & Mannervick B (1985). Glutathione reductase. Methods Enzymol 113:484-499 https://doi.org/10.1016/S0076-6879(85)13062-4
  6. Carson JF (1987). Chemistry and biological properties of onion and garlic. Food Reviews Internationl 3:71-103 https://doi.org/10.1080/87559128709540808
  7. Dincer Y, Alademir Z, Ilkova H & Akcay T (2002). Susceptibility of gluathione and glutathione-related antioxidant activity to hydrogen peroxide in patients with type 2 diabetes: effect of glycemic control. Clin Biochem 35:297-301 https://doi.org/10.1016/S0009-9120(02)00317-X
  8. Feldt-Rasmussen B, Mathiesen ER & Deckert T (1986). Effect of 2 years of strict metabolic control on progression of incipient nephropathy in insulin dependent diabetes. Lancet 2:1300-1304 https://doi.org/10.1016/S0140-6736(86)91433-9
  9. Ghosh R, Mukherjee B & Chatterjee M (1994). A novel effect of selenium on streptozotocin-induced diabetic mice. Diabetes Res 25:165-171
  10. Habig WH, Pabst MJ & Jakoby WB (1974). Glutathione S-transferase. J Biol Chem 249:7130-7139
  11. Hartnett ME, Stratton RD, Browne RW, Rosner BA, Lanham RJ & Armstrong D (2000). Serum markers of oxidative stress and severity of diabetic retinopathy. Diabetes Care 23:234-240 https://doi.org/10.2337/diacare.23.2.234
  12. Haygaard N (1968). Cellular mechanisms of oxygen toxicity. Physiological Reviews 48:311-373 https://doi.org/10.1152/physrev.1968.48.2.311
  13. Howard BV, Savage PJ, Bennion LJ & Bennett PH (1978). Lipoprotein composition in diabetes mellitus. Atherosclerosis 30:153-162 https://doi.org/10.1016/0021-9150(78)90058-8
  14. Irizar A & Ioannides C (1995). Extrahepatic expression of P450 proteins in insulin-dependent diabetes mellitus. Xenobiotica 25:941-949 https://doi.org/10.3109/00498259509046665
  15. Jung YS, Kim MH, Lee SH, Baik EJ, Park SW & Moon CH (2002). Antithrombotic effect of onion in streptozotocin-induced diabetic rat. Prostaglandins 66:453-458 https://doi.org/10.1054/plef.2002.0373
  16. Kakkar R, Mantha SV, Radhi J, Prasad K & Kalra J (1997). Antioxidant defense system in diabetic kidney: a time course study. Life Sci 60:667-679 https://doi.org/10.1016/S0024-3205(96)00702-3
  17. Kesavulu M., Rao BK, Giri R, Vijaya J, Subramanyam G & Apparao Ch (2001). Lipid peroxidation and antioxidant enzyme status in Type 2 diabetic with coronary heart disease. Diabetes Res Clin Pract 53:33 https://doi.org/10.1016/S0168-8227(01)00238-8
  18. Lowry OH, Rosebrough NJ, Farr AL & Randall RT (1951). Protein measurement with the folin phenol reagent. J Biol Chem 193:265-275
  19. Mak DH, Ip SP, Li PC, Poon MK & Ko KM (1996). Alterations in tissue glutathione antioxidant system in streptozotocin-induced diabetic rats. Mol Cell Biochem 162:153-158 https://doi.org/10.1007/BF00227543
  20. Medvedeva IV, Pufacheva TA & Dorodneva EF (2002). Influence of glucose control on the main parameters of serum lipid profile and platelet membranes in patients with metabolic syndrome and type 2 diabetes mellitus. Atheroscler Suppl 3:163 https://doi.org/10.1016/S1567-5688(02)80452-4
  21. Miranda M, Muriach M, Almansa I, Arnal E, Messeguer A, Diaz-Llopis M, Romero FJ & Bosch-Morell F (2007). CR-6 protects glutathione peroxidase activity in experimental diabetes. Free Radic Biol Med 43:1494-1498 https://doi.org/10.1016/j.freeradbiomed.2007.08.001
  22. Moorhead JF (1991). Lipids and progressive kidney disease. Kidney Int Suppl 31:S35-40
  23. Mulec H, Johnson SA & Bjorck S (1990). Relationship between serum cholesterol and diabetic nephropathy. Lancet 335:1537-1538 https://doi.org/10.1016/0140-6736(90)93090-C
  24. Nikkila EA & Kekki M (1973). Plasma triglyceride transport in diabetes mellitus. Metabolism 22:1-22 https://doi.org/10.1016/0026-0495(73)90024-3
  25. Nourooz-Zadeh J, Rahini A & Tajaddini-Sarmadi J (1997). Relationships between plasma measures of oxidative stress and metabolic controls in NIDDM. Diabetologia 40:647-653 https://doi.org/10.1007/s001250050729
  26. Nuutila AM, Puupponen-Pimia R, Aarni M, Marja K & Caldentey O (2003). Comparison of antioxidant activities of onion and garlic extracts by inhibition of lipid peroxidation and radical scavenging activity. Food Chem 81:485-493 https://doi.org/10.1016/S0308-8146(02)00476-4
  27. Obrosova I, Cao X, Greene DA & Stevens MJ (1998). Diabetes-induced changes in lens antioxidant status, glucose utilization and energy metabolism: effect of DL-alpha-lipoic acid. Diabetologia 41:1442-1450 https://doi.org/10.1007/s001250051090
  28. Qureshi AA, Sami SA & Khan FA (2002). Effects of stabilized rice bran, its soluble and fiber fractions on blood glucose levels and serum lipid parameters in human with diabetes mellitus type I and II. J Nutr Biochem 13:175-187 https://doi.org/10.1016/S0955-2863(01)00211-X
  29. Reddy AS, Rao CV, Rivenson A & Kelloff G (1993). Chemoprevention of colon carcinogenesis by organosulfur compounds. Cancer Res 53:3493-3498
  30. Tapple AL (1978). Glutathione peroxidase and hydroperoxides. Meth Enzymol 52:506-513 https://doi.org/10.1016/S0076-6879(78)52055-7
  31. Wohaieb SA & Godin DV (1987). Alterations in free radical tissue-defense mechanisms in streptozotocin-induced diabetes in rat: effects of insulin treatment. Diabetes 36:1014-1018 https://doi.org/10.2337/diabetes.36.9.1014
  32. Zhang SL, Chen X, Hsieh TJ, Leclerc M, Henley N, Allidina A, Halle JP, Brunette MG, Filep JC, Tang SS, Ingelfinger JR & Chan JS (2000). Hyperglycemia includes insulin resistance on angiotensinogen gene expression in diabetic rat kidney proximal tubular cells. J Endocrinol 172:333-344 https://doi.org/10.1677/joe.0.1720333

Cited by

  1. Onion — Allium cepa, bulb vol.11, pp.1, 2013, https://doi.org/10.1007/s10298-012-0747-5
  2. Effects of raw red onion consumption on metabolic features in overweight or obese women with polycystic ovary syndrome: A randomized controlled clinical trial vol.40, pp.4, 2014, https://doi.org/10.1111/jog.12311
  3. Dietary Phytochemicals: Natural Swords Combating Inflammation and Oxidation-Mediated Degenerative Diseases vol.2016, pp.1942-0994, 2016, https://doi.org/10.1155/2016/5137431
  4. White Vegetables: Glycemia and Satiety vol.4, pp.3, 2013, https://doi.org/10.3945/an.112.003509
  5. Phytotherapy in the Management of Diabetes: A Review vol.23, pp.1, 2018, https://doi.org/10.3390/molecules23010105
  6. The potential of pigeon pea (Cajanus cajan) beverage as an anti-diabetic functional drink vol.102, pp.1755-1315, 2018, https://doi.org/10.1088/1755-1315/102/1/012054
  7. The Effects of Onion Consumption on Prevention of Nonalcoholic Fatty Liver Disease vol.33, pp.1, 2018, https://doi.org/10.1007/s12291-017-0636-7
  8. Hypocholesterolemic activity of onion is mediated by enhancing excretion of fecal sterols in hamsters vol.1, pp.1, 2009, https://doi.org/10.1039/c0fo00036a
  9. 양파의 고지혈증 효과에 대한 메타분석 vol.23, pp.6, 2012, https://doi.org/10.7465/jkdi.2012.23.6.1103
  10. The Mechanism Underlying the Spasmolytic and Bronchodilatory Activities of the Flavonoid-rich Red Onion “Allium cepa L.” Peel Extract vol.10, pp.2, 2009, https://doi.org/10.3923/ijp.2014.82.89
  11. Effect of Steamed Onion (ONIRO) Consumption on Body Fat and Metabolic Profiles in Overweight Subjects: A 12-Week Randomized, Double-Blind, Placebo-Controlled Clinical Trial vol.39, pp.3, 2009, https://doi.org/10.1080/07315724.2019.1635052
  12. Investigation of the anti-hyperglycemic and antioxidant effects of wheat bread supplemented with onion peel extract and onion powder in diabetic rats vol.20, pp.1, 2009, https://doi.org/10.1007/s40200-021-00770-x