Effects of Triticum aestivum sprout on Blood Glucose and Lipid Levels in the Streptozotocin-Induced Diabetic Mice

소맥엽의 섭취가 Streptozotocin 유발 당뇨 흰쥐에서 혈중 포도당 및 지질에 미치는 영향

  • Lee, Sun-Hee (Department of Immunology and Institute of Medical Science, Chonbuk National University Medical School) ;
  • Lim, Sung-Won (Department of Immunology and Institute of Medical Science, Chonbuk National University Medical School) ;
  • Lee, Young-Mi (Department of Oriental Pharmacy, College of Pharmacy, Wonkwang University) ;
  • Kang, Chun-Sik (Department of Rice and Winter Cereal Crop, NICS, RDA) ;
  • Cheong, Young-Keun (Department of Rice and Winter Cereal Crop, NICS, RDA) ;
  • Park, Chul-Soo (Department of Rice and Winter Cereal Crop, NICS, RDA) ;
  • Song, Bong-Joon (Chong Kun Dang Healthcare Corp. Research Center) ;
  • Kim, Dae-Ki (Department of Immunology and Institute of Medical Science, Chonbuk National University Medical School)
  • 이선희 (전북대학교 의과대학 및 의과학연구소) ;
  • 임성원 (전북대학교 의과대학 및 의과학연구소) ;
  • 이영미 (원광대학교 약학대학 한약학과) ;
  • 강천식 (농촌진흥청 국립식량과학원) ;
  • 정연근 (농촌진흥청 국립식량과학원) ;
  • 박철수 (농촌진흥청 국립식량과학원) ;
  • 송봉준 (종근당 건강(주)) ;
  • 김대기 (전북대학교 의과대학 및 의과학연구소)
  • Received : 2010.09.10
  • Accepted : 2010.11.02
  • Published : 2010.12.25

Abstract

This study investigated the functional effect by diets of Triticum aestivum sprout (TA) on the levels of blood glucose and lipid profiles in streptozotocin(STZ)-induced diabetic mice. Diabetes mellitus were induced by STZ intraperitoneal injection (50 mg/kg) into the male Balb/c mice. All mice fed AIN-93 diet for 3 weeks. Mice were divided to 4 groups: normal, diabetic control and two experimental groups (TA 5.0, diet with Triticum aestivum sprout 5.0% w/w; TA 2.5, diet with Triticum aestivum 2.5% w/w). The blood glucose level was decreased by TA intake in diabetic mice in the dose-dependant manner; 21.34% and 35.77% in TA 2.5 and TA 5.0 groups. The weight gain and feed efficiency ratio also were improved by TA intake compared with DM group. The weight gain was increased 1.28 and 1.09 folds in TA 5.0 and TA 2.5 groups, respectively. The weight of organs, including liver and kidney, was reduced but that of spleen and abdominal fat was increased by TA intake. Moreover, TA treatment increased the level of HDL but decreased the level of total cholesterol and triglycerides in the blood of diabetic mice. The blood of HbA1c also was significantly decreased without changing hematocrit by TA treatment compared with DM group. These results indicate the TA intake has the functional effects attenuating blood glucose and plasma lipid levels in insulin-dependent diabetes.

Keywords

References

  1. Mokdad, A.H., Ford, E.S., Bowman, B.A., Nelson, D.E., Engelgau, M.M., Victor, F., Marks, J.S. Diabetes trends in the U.S: 1990-1998. Diabetes Care 23: 1278-1283, 2000. https://doi.org/10.2337/diacare.23.9.1278
  2. Lim, H.S., Chyun, J.H., Kim, Y.S., Nam, M.S. Effect of Nutrition Education on Diabetic Management in Diabetic Patients. Korean J Nutrition 34: 69-78, 2001.
  3. Saudek, C.D., Eder, H.A. Lipid metabolism in diabetes mellitus. Am J Med 66: 843-852, 1979. https://doi.org/10.1016/0002-9343(79)91126-4
  4. Baynes, J.W. Role of oxidative stress in development of complications in diabetes. Diabetes 40: 405-412, 1991. https://doi.org/10.2337/diabetes.40.4.405
  5. Strachan, M.W.J., Deary, I.J., Ewing, F.M.E., Frier, B.M. Is type 2 (non-insulin dependent) diabetes mellitus associated with an increased risk of cognitive dysfunction?. Diabetes Care 20: 438-445, 1997. https://doi.org/10.2337/diacare.20.3.438
  6. Yusuf, S., Hawken, S., Ounpuu, S., Dans, T., Avezum, A., Lanas, F., McQueen, M., Budaj, A., Pais, P., Varigos, J., Lisheng, L. Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study. Lancet 364: 937-952, 2004. https://doi.org/10.1016/S0140-6736(04)17018-9
  7. Abrams, J.J., Ginberg, H., Grundy, S.M. Metabolism of cholesterol and plasma triglycerides in non-ketotic diabetes mellitus. Diabetes 31: 903-910, 1982. https://doi.org/10.2337/diabetes.31.10.903
  8. MacLennan, A.H., Wilson, D.H., Taylor, A.W. Prevalence and cost of alternative medicine in Australia. Lancet 347: 569-573, 1996. https://doi.org/10.1016/S0140-6736(96)91271-4
  9. Tapsell, L.C., Hemphill, I., Cobiac, L., Patch, C.S., Sullivan, D.R., Fenech, M., Roodenrys, S., Keogh, J.B., Clifton, P.M., Williams, P.G., Fazio, V.A., Inge, K.E. Health benefits of herbs and spices: the past, the present, the future. Med J Austria 185: S4-24, 2006.
  10. Nagaoka, H. Treatment of Germinated Wheat to Increase Levels of GABA and IP6 Catalyzed by Endogenous Enzymes. Biotechnol Progr 21: 405-410, 2005.
  11. Kulkarni, S.D., Tilak, J.C., Acharya, R., Rajurkar, N.S., Devasagayam, T.P., Reddy, A.V. Evaluation of the antioxidant activity of wheat grass (Triticum aestivum L.) as a function of growth under different conditions. Phytotherapy Research 203: 218-227, 2006.
  12. Marawaha, R.K., Bansal, D., Kaur, S., Trehan, A. Wheat grass juice reduces transfusion requirement in patients with thalassemia major: a pilot study. Indian Pediatr 41: 716-720, 2004.
  13. Ben-Arye, E., Goldin, E., Wengrower, D., Stamper, A., Kohn, R., Berry, E. Wheat grass juice in the treatment of active distal ulcerative colitis: a randomized double-blind placebo-controlled trial. Scand J Gastroenterol 37: 444-449, 2002. https://doi.org/10.1080/003655202317316088
  14. Bar-Sela, G., Tsalic, M., Fried, G., Goldberg, H. Wheat Grass Juice May Improve Hematological Toxicity Related to Chemotherapy in Breast Cancer Patients: A Pilot Study. Nutrition and Cancer 58: 43-48, 2007. https://doi.org/10.1080/01635580701308083
  15. Lai, C.N. Chlorophyll: The active factor in wheat sprout extract inhibiting the metabolic activation of carcinogens in vitro. Nutrition and Cancer 3: 19-21, 1979.
  16. Ahmed, I., Adeghate, E., Cummings, E., Sharma, A.K., Singh, J. Beneficial effects and mechanism of action of Momordica charantia juice in the treatment of streptozotocininduced diabetes mellitus in rat. Mol Cell Biochem 261: 63-70, 2004. https://doi.org/10.1023/B:MCBI.0000028738.95518.90
  17. Kahn, C.R. The molecular mechanism of insulin action. Ann Rev Med 36: 249-251, 1985.
  18. Best, J.D., O'Neal. D.N. Diabetic dyslipidaemia-current treatment recommen-dations. Drugs 59: 1101-1111, 2000. https://doi.org/10.2165/00003495-200059050-00006
  19. Sexton, W.S. Skeletal muscle vascular transport capacity in diabetic rats. Diabetes 43: 225-231, 1994. https://doi.org/10.2337/diabetes.43.2.225
  20. Malabu, U.H., Dryden, S., Mccarthy, H.D., Kilpatrick, A., Williams, G. Effects of chronic vanadate administration in the STZ-induced diabetic rats. The antihyperglycemic action of vanadate is attributable entirely to its suppression of feeding. Diabetes 43: 9-15, 1994. https://doi.org/10.2337/diabetes.43.1.9
  21. Lee, J.S., Son, H.S., Maeng, Y.S., Chang, Y.K., Ju, J.S. Effect of buckwheat on organ weight, glucose and lipid metabolism in streptozotocin-induced diabetic rats. Korean J Nutr 27: 819-827, 1994.
  22. O'Meara, N.M.G., Devery, R.A.M., Owens, D., Collins, P.B., Johnson, A.H., Tomkin, G.H. Cholesterol metabolism in alloxan-induced diabetic rabbit. Diabetes 39: 626-633, 1990. https://doi.org/10.2337/diabetes.39.5.626
  23. Nikkila, E.A., Kekki, M. Plasma triglyceride transport kinetics in diabetes mellitus. Metabolism 22: 1-22, 1973. https://doi.org/10.1016/0026-0495(73)90024-3
  24. Yoon, J.A., Son, Y.S. Effects of fruits and stems of Opuntia ficus-indica on blood glucose and lipid metabolism in streptozotocin-induced diabetic rats. J Korean Soc Food Sci Nutr 38: 146-153, 2009. https://doi.org/10.3746/jkfn.2009.38.2.146
  25. Goldberg, R.B. Lipid disorders in diabetes. Diabetes Care 4: 561-572, 1981. https://doi.org/10.2337/diacare.4.5.561
  26. Brooks, D.P., Nutting, D.F., Crofton, J.T., Share, L. Vasopressin in rats with genetic and streptozocin-induced diabetes. Diabetes 38: 54-57, 1989. https://doi.org/10.2337/diabetes.38.1.54
  27. Kim, K.R., Choi, J.H., Woo, M.H., Kim, Y.H., Choi, S.W. Effects of Enzymatic Hydrolysates from Hamcho (Salicornia herbacea L.) on Blood Glucose and Serum Lipid Composition in Streptozotocin-Induced Diabetic Rats. J Korean Soc Food Sci Nutri 37: 170-176, 2008. https://doi.org/10.3746/jkfn.2008.37.2.170
  28. Safeer, R.S., Ugalat, P.S. Cholesterol treatment guidelines update. Am Fam Physician 65: 871-880, 2002.
  29. Dobiasova, M. Atherogenic index of plasma [Log(TG/HDL-C)]: Theoretical and practical implications. Clin Chem 50: 1113-1115, 2004. https://doi.org/10.1373/clinchem.2004.033175
  30. Dai, S., Thompson, K.H., McNeill, J.H. One-year treatment of streptozotocin-induced diabetic rats with vanadyl sulphate. Pharmacol Toxicol 74: 101-109, 1994. https://doi.org/10.1111/j.1600-0773.1994.tb01083.x
  31. Koh, J.B., Choi, M.A., Kim, J.Y., Rho, M.H., Kim, D.J. Effects of tea fungus/kombucha beverage on serum protein levels and enzyme activity in streptozotocin-induced diabetic rats. J Korean Soc Food Sci Nutr 28: 1137-1143, 1999.
  32. Wannamethee, S.G., Perry, I.J., Shaper, A.G. Hematocrit and risk of NIDDM. Diabetes 45: 576-579, 1996. https://doi.org/10.2337/diabetes.45.5.576
  33. Rahbar, S. An abnormal hemoglobin in red cells of diabetes. Clin Chim Acta 22: 296-298, 1968. https://doi.org/10.1016/0009-8981(68)90372-0