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Evidence-Based Complementary and Alternative Medicine
Volume 2016, Article ID 6385850, 10 pages
http://dx.doi.org/10.1155/2016/6385850
Research Article

Dendrobium officinale Prevents Early Complications in Streptozotocin-Induced Diabetic Rats

School of Chinese Pharmaceutical Science, Guangzhou University of Chinese Medicine, Guangzhou Higher Education Mega Center, Guangzhou 510006, China

Received 18 August 2015; Revised 2 February 2016; Accepted 3 February 2016

Academic Editor: Vincenzo De Feo

Copyright © 2016 Shao-zhen Hou et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. K. K. M. Yue, S.-N. Leung, P.-M. Man et al., “Alterations in antioxidant enzyme activities in the eyes, aorta and kidneys of diabetic rats relevant to the onset of oxidative stress,” Life Sciences, vol. 77, no. 7, pp. 721–734, 2005. View at Publisher · View at Google Scholar · View at Scopus
  2. N. H. Ugochukwu and N. E. Babady, “Antioxidant effects of Gongronema latifolium in hepatocytes of rat models of non-insulin dependent diabetes mellitus,” Fitoterapia, vol. 73, no. 7-8, pp. 612–618, 2002. View at Publisher · View at Google Scholar · View at Scopus
  3. M. Makni, H. Fetoui, N. K. Gargouri, E. M. Garoui, and N. Zeghal, “Antidiabetic effect of flax and pumpkin seed mixture powder: effect on hyperlipidemia and antioxidant status in alloxan diabetic rats,” Journal of Diabetes and Its Complications, vol. 25, no. 5, pp. 339–345, 2011. View at Publisher · View at Google Scholar · View at Scopus
  4. R. Srivatsan, S. Das, R. Gadde et al., “Antioxidants and lipid peroxidation status in diabetic patients with and without complications,” Archives of Iranian Medicine, vol. 12, no. 2, pp. 121–127, 2009. View at Google Scholar · View at Scopus
  5. I. Juranek, L. Horakova, L. Rackova, and M. Stefek, “Antioxidants in treating pathologies involving oxidative damage: an update on medicinal chemistry and biological activity of stobadine and related pyridoindoles,” Current Medicinal Chemistry, vol. 17, no. 6, pp. 552–570, 2010. View at Publisher · View at Google Scholar · View at Scopus
  6. N.-Y. Park, S.-K. Park, and Y. Lim, “Long-term dietary antioxidant cocktail supplementation effectively reduces renal inflammation in diabetic mice,” British Journal of Nutrition, vol. 106, no. 10, pp. 1514–1521, 2011. View at Publisher · View at Google Scholar · View at Scopus
  7. I. Aladag, A. Eyibilen, M. Güven, U. Erkokmaz, and U. Erkokmaz, “Role of oxidative stress in hearing impairment in patients with type two diabetes mellitus,” Journal of Laryngology and Otology, vol. 123, no. 9, pp. 957–963, 2009. View at Publisher · View at Google Scholar · View at Scopus
  8. C. Day, “Traditional plant treatments for diabetes mellitus: pharmaceutical foods,” British Journal of Nutrition, vol. 80, no. 1, pp. 5–6, 1998. View at Publisher · View at Google Scholar · View at Scopus
  9. X. Lin, P.-C. Shaw, S. C.-W. Sze, Y. Tong, and Y. Zhang, “Dendrobium officinale polysaccharides ameliorate the abnormality of aquaporin 5, pro-inflammatory cytokines and inhibit apoptosis in the experimental Sjögren's syndrome mice,” International Immunopharmacology, vol. 11, no. 12, pp. 2025–2032, 2011. View at Publisher · View at Google Scholar · View at Scopus
  10. X.-F. Liu, J. Zhu, S.-Y. Ge et al., “Orally administered Dendrobium officinale and its polysaccharides enhance immune functions in BALB/c mice,” Natural Product Communications, vol. 6, no. 6, pp. 867–870, 2011. View at Google Scholar · View at Scopus
  11. H. Dong, H. Sun, E. Magal et al., “Inflammatory pain in the rabbit: a new, efficient method for measuring mechanical hyperalgesia in the hind paw,” Journal of Neuroscience Methods, vol. 168, no. 1, pp. 76–87, 2008. View at Publisher · View at Google Scholar · View at Scopus
  12. T. Sugiyama, T. Okuno, M. Fukuhara et al., “Angiotensin II receptor blocker inhibits abnormal accumulation of advanced glycation end products and retinal damage in a rat model of type 2 diabetes,” Experimental Eye Research, vol. 85, no. 3, pp. 406–412, 2007. View at Publisher · View at Google Scholar · View at Scopus
  13. A. Vielma, L. Delgado, C. Elgueta, R. Osorio, A. G. Palacios, and O. Schmachtenberg, “Nitric oxide amplifies the rat electroretinogram,” Experimental Eye Research, vol. 91, no. 5, pp. 700–709, 2010. View at Publisher · View at Google Scholar · View at Scopus
  14. B.-Q. Lin, J.-Y. Zhou, Y. Ma, Y.-J. Deng, C.-J. Zheng, and J.-L. Lin, “Preventive effect of danhong huayu koufuye on diabetic retinopathy in rats,” International Journal of Ophthalmology, vol. 4, no. 6, pp. 599–604, 2011. View at Publisher · View at Google Scholar · View at Scopus
  15. E. M. Salido, N. de Zavalía, L. Schreier et al., “Retinal changes in an experimental model of early type 2 diabetes in rats characterized by non-fasting hyperglycemia,” Experimental Neurology, vol. 236, no. 1, pp. 151–160, 2012. View at Publisher · View at Google Scholar · View at Scopus
  16. P. T. Campbell, C. C. Newton, A. V. Patel, E. J. Jacobs, and S. M. Gapstur, “Diabetes and cause-specific mortality in a prospective cohort of one million U.S. adults,” Diabetes Care, vol. 35, no. 9, pp. 1835–1844, 2012. View at Publisher · View at Google Scholar · View at Scopus
  17. Q. Li, E. Zemel, B. Miller, and I. Perlman, “Early retinal damage in experimental diabetes: electroretinographical and morphological observations,” Experimental Eye Research, vol. 74, no. 5, pp. 615–625, 2002. View at Publisher · View at Google Scholar · View at Scopus
  18. H. Heynen, L. Wachtmeister, and D. van Norren, “Origin of the oscillatory potentials in the primate retina,” Vision Research, vol. 25, no. 10, pp. 1365–1373, 1985. View at Publisher · View at Google Scholar · View at Scopus
  19. P. Witkovsky, S. Stone, and H. Ripps, “Pharmacological modification of the light-induced responses of Müller (glial) cells in the amphibian retina,” Brain Research, vol. 328, no. 1, pp. 111–120, 1985. View at Publisher · View at Google Scholar · View at Scopus
  20. A. J. M. Boulton, A. I. Vinik, J. C. Arezzo et al., “Diabetic neuropathies: a statement by the American Diabetes Association,” Diabetes Care, vol. 28, no. 4, pp. 956–962, 2005. View at Publisher · View at Google Scholar · View at Scopus
  21. T. P. Almdal and H. Vilstrup, “Exogenous hyperglucagonaemia in insulin controlled diabetic rats increases urea excretion and nitrogen loss from organs,” Diabetologia, vol. 31, no. 11, pp. 836–841, 1988. View at Publisher · View at Google Scholar · View at Scopus
  22. C. Depre, M. E. Young, J. Ying et al., “Streptozotocin-induced changes in cardiac gene expression in the absence of severe contractile dysfunction,” Journal of Molecular and Cellular Cardiology, vol. 32, no. 6, pp. 985–996, 2000. View at Publisher · View at Google Scholar · View at Scopus
  23. F. Franconi, M. A. S. Di Leo, F. Bennardini, and G. Ghirlanda, “Is taurine beneficial in reducing risk factors for diabetes mellitus?” Neurochemical Research, vol. 29, no. 1, pp. 143–150, 2004. View at Publisher · View at Google Scholar · View at Scopus
  24. N. Alvarado-Vásquez, R. Lascurain, E. Cerón et al., “Oral glycine administration attenuates diabetic complications in streptozotocin-induced diabetic rats,” Life Sciences, vol. 79, no. 3, pp. 225–232, 2006. View at Publisher · View at Google Scholar · View at Scopus