Anti-oxidative and Anti-hyperglycemia Effects of Triticum aestivum Wheat Sprout Water Extracts on the Streptozotocin-induced Diabetic Mice

밀순 물추출물의 항산화 효과 및 Streptozotocin으로 유발한 당뇨 흰쥐에서 혈당강하에 미치는 영향

  • Lee, Sun-Hee (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) ;
  • Lee, Hoi-Seon (Faculty of Biotechnology and Center for Agricultural Science and Technology, College of Agriculture and Life Science, Chonbuk National University) ;
  • Kim, Dae-Ki (Department of Immunology and Institute of Medical Science, Chonbuk National University Medical School)
  • 이선희 (전북대학교 의과대학 및 의과학연구소) ;
  • 이영미 (원광대학교 약학대학 한약학과) ;
  • 이회선 (전북대학교 농업생명과학대학 응용생물공학부) ;
  • 김대기 (전북대학교 의과대학 및 의과학연구소)
  • Published : 2009.12.31

Abstract

This study was performed to investigate the anti-hyperglycemia effects of the Triticum aestivum wheat sprout (TAWS) water extracts in the diabetic mice. Diabetic experimental model was established by intraperitoneal injection of streptozotocin into male Balb/c mice. Mice were divided into five groups: normal (CON), diabetic control (DM), and three experimental groups (DM-100, diabetes with TAWS extracts 100mg/kg; DM-50, diabetes with TAWS extracts 50 mg/kg; DM-25, diabetes with TAWS extracts 25 mg/kg). TAWS extracts were administered orally in diabetic mice. Body weight, food intake, and blood glucose levels were recorded for 12 days and blood insulin levels were measured at the day 12. Oral administration of TAWS extracts reduced slightly food intake and induced a little body weight gain in DM-100 groups. The blood level of glucose was decreased in the dose-dependent manner; 55% in the DM-100 group and 39.7% in the DM-50 group. The blood level of insulin also was improved 10 folds in the DM-100 group and 3.6 folds in the DM-50 group compared to the DM group. The contents of total phenolic compounds and total flavonoids in 1 g dry mass of TAWS extracts were 6.6 mg of tannic acid equivalents and 1.0 mg of 8-hydroquinolline equivalents, respectively. In addition, the antioxidant and DPPH radical scavenging activity of TAWS extracts were 1.2 mM and 1.8 mM ascorbic acid equivalents, respectively. These results suggest that TAWS water extracts could contribute to attenuate clinical symptoms of diabetes mellitus.

Keywords

References

  1. Abrams, J. J., Ginsberg, H. and Grundy, S.M. (1982) Metabolism of cholesterol and plasma triglycerides in nonketotic diabetes mellitus. Diabetes 31: 903-910 https://doi.org/10.2337/diabetes.31.10.903
  2. Tisch, R. and Mcdevitt, H. (1966) Insulin-dependent diabetes mellitus. Cell 85: 291-297 https://doi.org/10.1016/S0092-8674(00)81106-X
  3. Giugliano, D., Ceriello, A. and Paolisso, G. (1996) Oxidative stress and diabetic vascular complications. Diabetes Care. 19: 257-267 https://doi.org/10.2337/diacare.19.3.257
  4. 김경래. (1994) 당뇨병 민간요법의 실태. 당뇨병. 18: 61-64
  5. H$\ddot{a}$nninen ,O., Rauma, A.L., Kaartinen, K. and Nenonen, M. (1999) Vegan diet in physiological health promotion. Acta Physiol Hung. 86: 171-180
  6. Nagaoka, H. (2005) Treatment of germinated wheat to increase levels of GABA and IP6 catalyzed by endogenous enzymes. Biotechnol. Prog. 21: 405-410 https://doi.org/10.1021/bp0496777
  7. Calzuola, I., Marsili, V. and Gianfranceschi, G.L. (2004) Synthesis of antioxidants in wheat sprouts. J. Agric. Food Chem. 52: 5201-5206 https://doi.org/10.1021/jf0307752
  8. Bar-Sela, G., Tsalic, M., Fried, G. and Goldberg, H. (2007) Wheat grass juice may improve hematological toxicity related to chemotherapy in breast cancer patients: a pilot study. Nutr. Cancer. 58: 43-48 https://doi.org/10.1080/01635580701308083
  9. Ben-Arye, E., Goldin, E., Wengrower, D., Stamper, A., Kohn, R. and Berry, E. (2002) Wheat grass juice in the treatment of active distal ulcerative colitis: a randomized double-blind placebo-controlled trial. Scand. J. Gastroenterol. 37: 444-449 https://doi.org/10.1080/003655202317316088
  10. Rakieten, N., Gordon, B.S., Cooney, D.A., Davis, R.D. and Schein, P.S. (1968) Renal tumorgenic action of streptozotocin (NSC-85998) in rats. Cancer Chemother. Rep. 52: 563-567
  11. Folin, O. and Denis, W. (1912) On phosphotungastic-phosphomolybdic conpounds as color reagents. J. Biol. Chem. 12: 239-249
  12. Moreno, M., Isla, M., Sampietro, A. and Vattuone, M. (2000) Comparison of the free radical-scavenging activity of propolis from several regions of Argentina. J. Ethnopharmacol. 71: 109-114 https://doi.org/10.1016/S0378-8741(99)00189-0
  13. Pellegrin, N., Roberta, R., Min, Y. and Catherine, R.E. (1998) Screening of dietary carotenoids and carotenoid-rich fruit extracts for antioxidant activites applying 2,2'-azinobis (3-ehylenebenzothiazoline-6-sulfonic acid) radical cation decolorization assay. Method Enzymol. 299: 379-389
  14. Blois, M. S. (1958) Antioxidant determination by the use of stable free radical. Nature 26: 1198-1199
  15. Sexton, W. L. (1994) Skeletal muscle vascular transport capacity in diabetic rats. Diabetes 43: 225-231 https://doi.org/10.2337/diabetes.43.2.225
  16. Raptis, S.A. and Dimitriadis, G.D. (2001) Oral hypoglycemic agents: insulin secretagogues, alpha-glucosidase inhibitors and insulin sensitizers. Exp. Clin. Endocrinol. Diabetes 109 Suppl: S265-S287
  17. Oneda, H., Lee, S. and Inouye, K. (2004) Inhibitory Effect of 0.19 {alpha}-Amylase Inhibitor from Wheat Kernel on the Activity of Porcine Pancreas {alpha}-Amylase and Its Thermal Stability. J. Biochem. 135: 421-427 https://doi.org/10.1093/jb/mvh050
  18. Asano, N., Oseki, K., Kaneko, E. and Matsui, K. (1994) Enzymic synthesis of alpha- and beta-D-glucosides of 1-deoxynojirimycin and their glycosidase inhibitory activities. Carbohydr. Res. 258: 255-266 https://doi.org/10.1016/0008-6215(94)84091-1
  19. Nojima, H., Kimura, I., Chen, F.J., Sugihara, Y., Haruno, M., Kato, A. and Asano, N. (1998) Antihyperglycemic effects of N-containing sugars from Xanthocercis zambesiaca, Morus bombycis, Aglaonema treubii, and Castanospermum australe in streptozotocin-diabetic mice. J. Nat. Prod. 61: 397-400 https://doi.org/10.1021/np970277l
  20. Forman, S., Estilow, M.L. and Vlienko, P. (1996) STZ diabetes alters immunoreactive b-endorphin levels and pain perception after 8wk in female rats. Diabetes 35: 1309-1313 https://doi.org/10.2337/diabetes.35.12.1309
  21. Furuse, M., Kimura, C., Mabayo, R.T. and Takahashi, H. (1993) Okumura J Dietary sorbose prevents and improves hyperglycemia in genetically diabetic mice. J. Nutri. 123: 59-65
  22. Fischer, K. J. and Stewart, J. K. (1986) Phenylethanolamine N-methyltransferase in the brains of streptozotocin diabetic rats. Endocrinology 119: 2586-2589 https://doi.org/10.1210/endo-119-6-2586
  23. Qa'dan, F., Verspohl, E.J., Nahrstedt, A., Petereit, F. and Matalka, K.Z. (2009) Cinchonain Ib isolated from Eriobotrya japonica induces insulin secretion in vitro and in vivo. J. Ethnopharmacol. 124: 224-227 https://doi.org/10.1016/j.jep.2009.04.023
  24. Li, C., Allen, A., Kwagh, J., Doliba, N.M., Qin, W., Najafi, H., Collins, H.W., Matschinsky, F.M., Stanley, C.A. and Smith, T.J. (2006) Green tea polyphenols modulate insulin secretion by inhibiting glutamate dehydrogenase. J. Biol. Chem. 281: 10214-10221 https://doi.org/10.1074/jbc.M512792200
  25. Dural, B. and Shetty, K. (2001) The stimulation of phenolics and antioxidant activity in pea (Pisum sativum) elicited by genetically transformed Anise root extract. J. Food Biochem. 25: 361-377 https://doi.org/10.1111/j.1745-4514.2001.tb00746.x
  26. Miyake, Y., Yamamoto, K. and Tsujihara, N. Osawa T. (1998) Protective effects of lemon flavonoids on oxidative stress in diabetic rats. Lipid 33: 689-695 https://doi.org/10.1007/s11745-998-0258-y
  27. Cavaliere, C., Foglia, P., Pastorini, E., Samperi, R. and Lagan$\grave{a}$, A. (2005) Identification and mass spectrometric characterization of glycosylated flavonoids in Triticum durum plants by high-performance liquid chromatography with tandem mass spectrometry. Rapid Commun. Mass Spectrom 19: 3143-3158 https://doi.org/10.1002/rcm.2185
  28. Hertog, M. G., Feskens, E. J., Hollman, P. C., Katan, M. B. and Kromhout, D. (1993) Dietary antioxidant flavonoids and risk of coronary heart disease: the Zutphen Elderly Study. Lancet 342: 1007-1011 https://doi.org/10.1016/0140-6736(93)92876-U
  29. Kulkarni, S. D., Tilak, J, C., Acharya, R., Rajurkar, N. S., Devasagayam, T. P. and Reddy, A. V. (2006) Evaluation of the antioxidant activity of wheatgrass (Triticum aestivum L.) as a function of growth under different conditions. Phytother. Res. 20: 218-227 https://doi.org/10.1002/ptr.1838
  30. Calzuola, I., Gianfranceschi, G.L. and Marsili, V. (2006) Comparative activity of antioxidants from wheat sprouts, Morinda citrifolia, fermented papaya and white tea. Int. J. Food Sci. Nutr. 57: 168-177 https://doi.org/10.1080/09637480600658328