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Protective Effect of Dietary Buchu (Allium tuberosum Rottler) on Oxidative Stress and Lipofuscin Formation in Streptozotocin-Induced Diabetic Rats

Streptozotocin-유발 당뇨쥐에서 부추식이의 산화적 스트레스 및 Lipofuscin 생성 억제 효과

  • 이점옥 (인제대학교 바이오헬스 소재 연구센터, 식품과학연구소 및 식품생명과학부) ;
  • 류승희 (인제대학교 바이오헬스 소재 연구센터, 식품과학연구소 및 식품생명과학부) ;
  • 이유순 (경북과학대학 향장공업과) ;
  • 김정인 (인제대학교 바이오헬스 소재 연구센터, 식품과학연구소 및 식품생명과학부) ;
  • 문갑순 (인제대학교 바이오헬스 소재 연구센터, 식품과학연구소 및 식품생명과학부)
  • Published : 2003.12.01

Abstract

Diabetes mellitus has been known to be a state of increased oxidative stress. Free radical formation and lipid peroxidation are accelerated in this metabolic disorder. Buchu (Allium tuberosum Rottler) contains lots of antioxidative nutrients such as chlorophyll, vitamin C, $\beta$-carotene, phenolic compounds and sulfur compounds. To investigate the protective effects of buchu, 10% lyophilized buchu diet was fed to streptozotocin (STZ)-induced diabetic rats for 14 weeks and lipid peroxidation, protein oxidation, contents of reactive oxygen species, activities of antioxidative enzymes and contents of accumulated lipofuscin were measured as indicators of oxidative stress. Hepatic MDA and carbonyl contents tended to decrease in 10% buchu diet group compared with control group. Dietary buchu significantly suppressed lipid and protein oxidation in the skin of rats (p<0.05). Contents of hepatic hydroxyl radicals, which exert the highest toxicity among the reactive oxygen species, were significantly decreased in rats fed 10% buchu diet (P<0.05). Activities of antioxidative enzyme, such as superoxide dismutase, catalase, and glutathione peroxidase, tended to increase in liver and skin of rats fed 10% buchu diet, while hepatic catalase activity was significantly increased in buchu group compared with control group. Buchu supplementation significantly inhibited the accumulation of lipofuscin, an end-product of lipid peroxidation reactions induced by reactive oxygen radicals, in eye tissues compared with control diet (p<0.001). In conclusion, buchu supplementation diminished the oxidative stress, so dietary buchu could help to attenuate diabetes complications.

산화적 스트레스를 많이 받는 당뇨상태에서 항산화활성이 높은 부추의 섭취가 지질 및 단백질 산화, 활성산소종의 생성, 항산화 효소계 활성 변화 및 lipofuscin생성에 미치는 영향을 조사하고자 S.D.계 쥐에게 streptozotocin을 복강투여하여 당뇨병을 유발시킨 후 대조군 식이와 10% 부추식이를 14주간 섭취시켰다. 부추의 섭취는 대조군식이에 비해 간보다는 피부조직에서 지질 및 단백질 산화를 유의적으로 감소 시켰고(p<0.05), 반응성이 큰 활성산소종인 hydroxyl radical의 생성도 당뇨군에 비해 유의적으로 감소된 것으로 나타났다(p<0.05).부추의 섭취는 간과 피부조직의 항산화 효소계 활성을 증가시키는 것으로 나타났으며 심장과 눈 조직에서 노화색소인 lipofuscin을 측정한 결과 당뇨군에 비해 당뇨부추군에서 감소하였고 특히 눈에서 유의적으로 감소하였다(p<0.001). 이상의 결과로 부추의 섭취는 당뇨 합병증을 일으키는 주요 원인인 산화적 스트레스를 억제하는 효과를 나타내었고, 당뇨 합병증의 증상완화에 도움을 줄 것으로 기대되어 진다.

Keywords

References

  1. Abrams JJ, Ginsberg H, Grundy SM. 1982. Metabolism of cholesterol and plasma triglycerides in non ketoic diabetes mellitus. Diabetes 31: 903-910. https://doi.org/10.2337/diabetes.31.10.903
  2. Park SH, Lee YK, Lee HS. 1994. The effect of dietary fiber feeding on gastrointestinal functions and lipid and glucose metabolism in streptozotocin-induced diabetic rats. Korean J Nutr 27: 311-322.
  3. Tai ES, Lim SC, Tan BY, Chew SK, Heng D, Tan CE. 2000. Screening for diabetes mellitus-a two-step approach in individuals with impaired fasting glucose improves detection of those at risk of complications. Diabet Med 17: 771-775. https://doi.org/10.1046/j.1464-5491.2000.00382.x
  4. Lalla E, Lamster IB, Drury S, Fu C, Schmidt AM. 2000. Hyperglycemia, glycoxidation and receptor for advanced glycation endproducts: potential mechanisms underlying diabetic complications, including diabetes-associated periodontitis. Periodontol 23: 50-62. https://doi.org/10.1034/j.1600-0757.2000.2230104.x
  5. Aust SD, Chignell CF, Bray TM, Kalyanaraman B, Mason RP. 1993. Free radicals in toxicology. Toxicology and Applied Pharmacology 120: 168-178. https://doi.org/10.1006/taap.1993.1100
  6. Yoo SO, Bae JH. 1993. Investigation of Korean native Chinese chives on flower bud differentiation. J Kor Soc Hort Sci 34: 395-401.
  7. Kim SJ, Park KH. 1995. Retardation of kimchi fermentation by the extracts of Allium tuberosum and growth inhibition of related microorganism. Korean J Food Sci Technol 27: 813-818.
  8. Shanhai Science and Technological publisher. 1985. The dictionary of Chinese drugs. Shougakukan, Tokyo. Vol 1, p 449.
  9. Kwak YJ, Jun HJ, Lee MJ, Kwon TW, Kim JS. 1998. Modulation of anticarcinogenic enzyme and plasma testosterone level in male mouse fed leek-supplemented diet. J Korean Soc Food Sci Nutr 27: 968-972.
  10. Hwang CW, Shin HK, Do MS, Kim YJ, Park JH, Choi YS, Joo WH. 2001. The various biofunctional effects (anticarcinogenic, antioxidative and lypolytic activity) of Pohang buchu. Korean J Food Sci Technol 33: 279-281.
  11. Park YJ, Kim MH, Bae SJ. 2002. Anticarcinogenic effects of Allium tuberosum on human cancer cells. Korean J Food Sci Technol 34: 688-693.
  12. Hong JH Lee MH Kang MC, Hur SH. 2000. Separation and identification of antimicrobial compounds from Korean leek (Allium tuberosum). J Food Hyg Safety 15: 235-240.
  13. Lee MK, Lee HA, Park IS. 2001. Growth retardation of Escherichia coli and Staphylococcus aureus by leek extract. J Korean Soc Food Sci Nutr 30: 196-198.
  14. Moon GS, Ryu BM, Lee MJ. 2003. Components and antioxidative activities of buchu (Chinese chives) harvested at different times. Korean J Food Sci Technol 35: 493-498.
  15. Lee MJ, Ryu BM, Lee YS, Moon GS. 2002. Effect of long term buchu (Chinese chives) diet on antioxidative system of ICR mice. J Korean Soc Food Sci Nutr 31: 834-839. https://doi.org/10.3746/jkfn.2002.31.5.834
  16. Lee MJ, Ryu BM, Kim MH, Lee YS, Moon GS. 2002. Protective effect of dietary buchu (chinese chives) against oxidative damage from aging and ultraviolet irradiation in ICR mice skin. Nutraceuticals & Food 7: 238-244.
  17. Moon GS, Lee MJ. 2003. The long term effect of buchu (Chinese chives) diet on ROS formation in the liver and skin tissue of ICR mice. J Korean Soc Food Sci Nutr 32: 444- 449. https://doi.org/10.3746/jkfn.2003.32.3.444
  18. Ohkawa H, Ohishi N, Yagi K. 1979. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem 95: 351-358. https://doi.org/10.1016/0003-2697(79)90738-3
  19. Oliver CN, Ahn B, Moerman EJ, Goldstein S, Stadtman ER. 1987. Age-related changes in oxidized proteins. J Biol Chem 262: 5483-5492.
  20. Marklund S, Marklund G. 1974. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur J Biochem 47: 469-474. https://doi.org/10.1111/j.1432-1033.1974.tb03714.x
  21. Aebi H. 1984. Catalase in vitro. Methods in Enzymol 105: 121-126. https://doi.org/10.1016/S0076-6879(84)05016-3
  22. Lawrence RA, Burk F. 1976. Glutathione peroxidase activity in selenium-deficient rat liver. Biochem Biophys Res Comm 71: 952-958. https://doi.org/10.1016/0006-291X(76)90747-6
  23. Peterson GL. 1977. A simplification of the protein assay method of Lowry et al. which is more generally applicable. Analy Biochem 83: 346-356. https://doi.org/10.1016/0003-2697(77)90043-4
  24. Choi JH, Kim DI, Park SH, Kim DW, Lee JS, Kim HS. 1999. Investigation of anti-aging effect and determination of chemical structures of pine needle extract (PNE) through the animal experiments. 1. Effects of PNE on oxygen raticals and their scavenger enzymes in liver of SD rats. Korean J Life Science 9: 466-472.
  25. Fletcher BL, Dillard CJ, Tappel AL. 1973. Measurement of fluorescent lipid peroxidation products in biological systems and tissues. Analytical Biochemistry 52: 1-9. https://doi.org/10.1016/0003-2697(73)90327-8
  26. Turk J, Corbett JA, Ramanadham S, Bohrer A, McDaniel ML. 1993. Biochemical evidence for nitric oxide formation from streptozotocin in isolated pancreatic islets. Biochem Biophys Res Commun 197: 1458-1464. https://doi.org/10.1006/bbrc.1993.2641
  27. Liu K, Paterson AJ, Chin E, Kudlow JE. 2000. Glucose stimulates protein modification by O-linked GlcNAc in pancreatic beta cells: linkage of O-linked GlcNAc to beta cell death. Proc Natl Acad Sci USA 97: 2820-2825. https://doi.org/10.1073/pnas.97.6.2820
  28. Roos MD, Xie W, Su K, Clark JA, Yang X, Chin E, Paterson AJ, Kudlow JE. 1998. Streptozotocin, an analog of N-acetylglucosamine, blocks the removal of O-GlcNAc from intracellular proteins. Proc Assoc Am Phys 110: 422-432.
  29. Jung HS, Noh KH, Cho HY, Park JY, Choi CY, Kwon TW, Song YS. 2003. Effect of buchu (Allium tuberosum) on lipid peroxidation and antioxidative defense system in streptozotocin- induced diabetic rats. Korean J Life Sci 13: 333-342. https://doi.org/10.5352/JLS.2003.13.3.333
  30. Baynes JW. 1991. Role of oxidative stress in development of complications in diabetes. Diabetes 40: 405-412. https://doi.org/10.2337/diabetes.40.4.405
  31. Obrosova IG, Fathallah L, Greene DA. 2000. Early changes in lipid peroxidation and antioxidative defense in diabetic rat retina: effect of DL-alpha-lipoic acid. Eur J Pharmacol 398: 139-146. https://doi.org/10.1016/S0014-2999(00)00286-7
  32. Maytin M, Leopold J, Loscalzo J. 1999. Oxidant stress in the vasculature. Curr Atheroscler Rep 1: 156-164. https://doi.org/10.1007/s11883-999-0012-z
  33. Lee SZ, Park SH, Lee HS. 2001. Changes in in vivo lipid peroxidation and antioxidant defense system in streptozotocininduced diabetic rats: a time course study. Korean J Nutr 34: 253-264.
  34. Rhee SJ, Yang JA, Kim SO, Choe JH, Shin JY, Chai YM, Cha BK. 1997. Changes of physiological antioxidative system according to the period in streptozotocin-induced diabetic rats. HSJAS 5: 117-125.
  35. Hunt JV, Smith CCT, Wolff SP. 1990. Autoxidative glycosylation and possible involvement of peroxides and free radicals in LDL modification by glucose. Diabetes 39: 1420-1424. https://doi.org/10.2337/diabetes.39.11.1420
  36. Wolff SP, Dean RT. 1987. Glucose autoxidation and protein modification: the potential role “antioxidative glycosylation” in diabetes mellitus. Biochem J 245: 243-250.
  37. Takasu N, Komiya I, Asasa T, Nagasawa Y, Yamada T. 1991. Streptozotocin and alloxan induced $H_2O_2$ generation and DNA fragmentation in pancreatic islets. Diabetes 40: 1141-1145.
  38. Verrotti A, Chiarelli F, Amerio PL, Morgese G. 1995. Skin diseases in children with type 1 diabetes mellitus. J Eur Acad Dermatol Venereol 4: 41-43. https://doi.org/10.1016/0926-9959(94)00062-5
  39. Han JB, Kim KS, Son SJ, Yoo HJ. 1986. Statistical study of cutaneous manifestations and systemic complications in diabetes mellitus. Korean J Dermatol 24: 271-277.
  40. Romano G, Moretti G, Di Benedetto A, Giofre C, Di Cesare E, Russo G, Califano L, Cucinotta D. 1998. Skin lesions in diabetes mellitus: prevalence and clinical correlations. Diabetes Research and Clinical Practice 39: 101-106. https://doi.org/10.1016/S0168-8227(97)00119-8
  41. Chithra P, Sajithlal GB, Chandrakasan G. 1998. Influence of aloe vera on the healing of dermal wounds in diabetic rats. Journal of Ethnopharmacology 59: 195-201. https://doi.org/10.1016/S0378-8741(97)00124-4
  42. Goodson WH, Hunt TK. 1979. Wound healing and the diabetic patient. Surgery, Genecology and Ovstetrics 149: 600- 608.
  43. Park ER, Jo JO, Kim SM, Lee MY, Kim KS. 1998. Volatile flavor components of leek (Allium tuberosum Rottler). J Korean Soc Food Sci Nutr 27: 563-567.
  44. Ahn RM, Kim WT, Lee HS. 1991. Protective effect of leek (Allium odorum L.) on the cadmium poisoning in rats. Kor J Env Hlth 17: 102-113.
  45. Saleh AW, David VG. 1987. Alteration in free radical tissue defense mechanism in streptozotocin-induced diabetic rats. Diabetes 36: 1014-1018. https://doi.org/10.2337/diabetes.36.9.1014
  46. Kesavulu MM, Giri R, Kameswara RB, Apparao C. 2000. Lipid peroxidation and antioxidnat enzyme levels in type 2 diabetics with microvascular complications. Diabetes Metab 26: 387-392.
  47. Kakkar R, Kalra J, Mantha SV, Prasod K. 1995. Lipid peroxidation and activity of antioxidant enzymes in diabetic rats. Molecular and Cellular Biochemistry 151: 113-119. https://doi.org/10.1007/BF01322333
  48. Kwak YJ, Chun HJ, Kim JS. 1998. Chlorophyll, mineral contents and SOD-like activities of leeks harvested at different times. Korean J Soc Food Sci 14: 513-515.
  49. Yarat A, Tunali T, Yanardag R, Gursoy F, Sacan O, Emekli N, Ustuner A, Ergenekon G. 2001. The effect of glurenorm (gliquidone) on lenses and skin in experimental diabetes. Free Rad Biol Med 31: 1038-1042. https://doi.org/10.1016/S0891-5849(01)00693-1
  50. Choi JS, Kim JY, Lee JH, Young HS, Lee TW. 1992. Isolation of adenosin and free amino acid composition from the leaves of Allium tuberosum. J Korean Soc Food Nutr 21: 286-290.
  51. Trachtman H, Cel Pizzo R, Futterweit S, Levine D, Rao PS, Valderrama E, Sturman JA. 1992. Taurine attenuates renal disease in chronic puromycin aminonucleoside nephropathy. Am J Physiol 262: 117-123.
  52. Kilic F, Bhardwaj R, Caulfeild J, Trevithick JR. 1999. Modelling cortical cataractogenesis 22: Is in vitro reduction of damage in model diabetic rat cataract by taurine due to its antioxidant activity? Exp Eye Res 69: 291-300. https://doi.org/10.1006/exer.1999.0697

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