DOI QR코드

DOI QR Code

Antioxidative Action of Corni Fructus Aqueous Extract on Kidneys of Diabetic Mice

  • Received : 2011.01.05
  • Accepted : 2011.01.28
  • Published : 2011.03.01

Abstract

This study investigated the antioxidative action of Corni Fructus aqueous extract on kidneys of diabetic mice. The electron donating abilities of Corni Fructus aqueous extract and its antioxidant activities (XO, SOD, CAT, GST, eNOS) in kidneys of C57BL/6 or db/db mice were evaluated. For in vivo study, seven week-old male mice were divided into normal control group (NC, C57BL/6 mice), diabetic control group (DC, db/db mice) and Corni Fructus (500 mg/kg/day for 8 weeks) treated diabetic group (DCF, db/db mice). The electron donating abilities of Corni Fructus aqueous extract exhibited 7%, 24.4%, and 42.7% at concentrations of 100, 500, and $1000\;{\mu}g/ml$, respectively. The activity of XO in the DCF group was significantly lower than the DC group by 35% (p < 0.05). The SOD activity was significantly higher in the DCF group than the DC group by 26% (p < 0.05). The activities of CAT and GST were lowered in the DCF group than the DC group by 26% (p < 0.05) and 7.6%, respectively. The mRNA expression of eNOS in kidneys was lower in the DCF group than the DC group by 24%. These results indicate that Corni Fructus reduced oxidation stress as evidenced by the restoration of the enzymatic antioxidative defense system in renal tissues of db/db mice. It is suggested that these antioxidative actions of Corni Fructus on renal tissues in db/db mice could contribute to its renoprotective effects on diabetic nephropathy.

Keywords

References

  1. Aebi, H. (1984). Catalase in vitro. Methods Enzymol., 105, 121-126. https://doi.org/10.1016/S0076-6879(84)05016-3
  2. Baynes, J.W. (1991). Role of oxidative stress in development of complications in diabetes. Diabetes, 40, 405-412. https://doi.org/10.2337/diabetes.40.4.405
  3. Blois, M.S. (1958). Antioxidant determination by the use of a stable free radical. Nature, 181, 1199-1200. https://doi.org/10.1038/1811199a0
  4. Butler, R., Morris, A.D., Belch, J.J.F., Hill, A. and Struthers, A.D. (2000). Allopurinol normalizes endothelial dysfunction in type 2 diabetics with mild hypertension. Hypertension, 35, 746-751. https://doi.org/10.1161/01.HYP.35.3.746
  5. Del Maestro, R.F. (1980). An approach to free radicals in medicine and biology. Acta Physiol. Scand. Suppl., 492, 153-168.
  6. Habig, W.H., Pabst, M.J. and Jakoby, W.B. (1974). Glutathione Stransferase. The first enzymatic step in mercapturic acid formation. J. Biol. Chem., 249, 7130-7139.
  7. Hunt, J.V., Dean, R.T. and Wolff, S.P. (1988). Hydroxyl radical production and autoxidative glycosylation. Glucose autoxidation as the cause of protein damage in the experimental glycation model of diabetes and aging. Biochem. J., 256, 205-212.
  8. Jin, U.H., Kim, D.I., Lee, T.K., Lee, D.N., Kim, J.K., Lee, I.S. and Kim, C.H. (2006). Herbal formulation, Yukmi-jihang-tang-Jahage, regulates bone resorption by inhibition of phosphorylation mediated by tyrosine kinase Src and cyclooxygenase expression. J. Ethnopharmacol., 106, 333-343. https://doi.org/10.1016/j.jep.2006.01.012
  9. Karasu, C. (2010). Glycoxidative stress and cardiovascular complications in experimentally-induced diabetes: effects of antioxidant treatment. Open Cardiovasc. Med. J., 4, 240-256. https://doi.org/10.2174/1874192401004010240
  10. Kim, H.J. and Kim, Y.C. (2010). Antidiabetic and renoprotective effects of Corni Fructus extract in db/db mice. Mol. Cell Toxicol.,6, 135-142. https://doi.org/10.1007/s13273-010-0020-7
  11. Kim, H.J., Kim, K.S., Lee, T.J. and Kim, Y.C. (2009). Antidiabetic effects of Corni Fructus extract on blood glucose and insulin resistance in db/db mice. Toxicol. Res., 25, 93-99. https://doi.org/10.5487/TR.2009.25.2.093
  12. Larkins, R.G. and Dunlop, M.E. (1992). The link between hyperglycemia and diabetic nephropathy. Diabetologia, 35, 499-504. https://doi.org/10.1007/BF00400475
  13. Latha, M. and Pari, L. (2003). Preventive effects of Cassia auriculata L. flowers on brain lipid peroxidation in rats treated with streptozotocin. Mol. Cell. Biochem., 243, 23-28. https://doi.org/10.1023/A:1021697311150
  14. Lawrence, J.C., Jill, S.G., Eric, P.D., Joyce, A.D., Donald, D.L. and Mark, A.Y. (2001). Effect of antioxidant treatment of streptozotocin-induced diabetic rats on endoneurial blood flow, motor nerve conduction velocity and vascular reactivity of epineurial arterioles of the sciatic nerve. Diabetes, 50, 1927-1937. https://doi.org/10.2337/diabetes.50.8.1927
  15. Li, K.M., Yang, X.J., Yu, M.Q., Xie, C. and Xu, L.Z. (1994). Determination of loganin in Cornus officinalis Sieb. et Zucc. by TLC scanner. Zhongguo Zhong Yao Za Zhi, 19, 738-763.
  16. Lowenstein, C.J. and Snyder, S.J. (1992). Nitric oxide, a novel biologic messenger. Cell, 70, 705-707. https://doi.org/10.1016/0092-8674(92)90301-R
  17. Lowry, O.H., Rosenbrough, N.J., Far, A.L. and Randall, R.J. (1951). Protein measurement with the folin phenol reagent. J. Biol. Chem., 193, 265-275.
  18. Maritim, A.C., Sanders, R.A. and Watkins, J.B. (2003). Effect of alpha lipoic acid on biomarkers of oxidative stress in streptozotocin- induced diabetic rats. J. Nutr. Biochem., 14, 288-294. https://doi.org/10.1016/S0955-2863(03)00036-6
  19. Martin, J.P., Dailey, M. and Sugarman, E. (1987). Negative and positive assays of superoxide dismutase based on hematoxylin autoxidation. Arch. Biochem. Biophys., 255, 329-336. https://doi.org/10.1016/0003-9861(87)90400-0
  20. Morel, D.W. and Chisolm, G.M. (1989). Antioxidative treatment of diabetic rats inhibits lipoprotein oxidation and cytotoxicity. J. Lipid Res., 30, 1827-1834.
  21. Rong, Y., Li, L., Shah, V. and Lau, B.H.S. (1995). Pycnogenol protects vascular endothelial cells from t-butyl hydroperoxideinduced oxidant injury. Biotechnol. Ther., 5, 117-126.
  22. Stirpe, F. and Della, C.E. (1969). The regulation of rat liver xanthine oxidase. Conversion in vitro of the enzyme activity from dehydrogenase (type D) to oxidase (type O). J. Biol. Chem., 244, 3855-3863.
  23. Taghizadeh Afshari, A., Shirpoor, A., Farshid, A., Saadatian, R., Rasmi, Y., Saboory, E., Ilkhanizadeh, B. and Allameh, A. (2007). The effect of ginger on diabetic nephropathy, plasma antioxidant capacity and lipid peroxidation in rats. Food Chem., 101, 148-153. https://doi.org/10.1016/j.foodchem.2006.01.013
  24. Venkateswaran, S. and Pari, L. (2002). Antioxidant effect of Phaseolus vulgaris in streptozotocin-induced diabetic rats. Asia Pac. J. Clin. Nutr., 11, 206-209. https://doi.org/10.1046/j.1440-6047.2002.00292.x
  25. Xia, Y., Dawson, V.L., Dawson, T.M., Snyder, S.H. and Zweier, J.L. (1996). Nitric oxide synthase generates superoxide and nitric oxide in arginine-depleted cells leading to peroxynitritemediated cellular injury. Proc. Natl. Acad. Sci. USA, 93, 6770-6774. https://doi.org/10.1073/pnas.93.13.6770
  26. Yamabe, N., Kang, K.S., Goto, E., Tanaka, T. and Yokozawa, T. (2007). Beneficial effect of Corni Fructus, a constituent of Hachimi-jio-gan, on advanced glycation end-product-mediated renal injury in streptozotocin-treated diabetic rats. Biol. Pharm. Bull., 30, 520-526. https://doi.org/10.1248/bpb.30.520

Cited by

  1. The Altered Renal and Hepatic Expression of Solute Carrier Transporters (SLCs) in Type 1 Diabetic Mice vol.10, pp.3, 2015, https://doi.org/10.1371/journal.pone.0120760
  2. Tang-Luo-Ning Improves Mitochondrial Antioxidase Activity in Dorsal Root Ganglia of Diabetic Rats: A Proteomics Study vol.2017, pp.2314-6141, 2017, https://doi.org/10.1155/2017/8176089
  3. Improvement of Persistent Detrusor Overactivity through Treatment with a Phytotherapeutic Agent (WSY-1075) after Relief of Bladder Outlet Obstruction vol.35, pp.2287-4690, 2017, https://doi.org/10.5534/wjmh.17010
  4. Cornus mas and Cornus Officinalis—Analogies and Differences of Two Medicinal Plants Traditionally Used vol.9, pp.1663-9812, 2018, https://doi.org/10.3389/fphar.2018.00894