Advanced search
Publication Cover
Bioscience, Biotechnology, and Biochemistry Volume 70, 2006 - Issue 9
Journal homepage
381
Views
41
CrossRef citations to date
0
Altmetric
Original Articles

Protective Effect of Grape Seed Polyphenols against High Glucose-Induced Oxidative Stress

Hajime FUJIIInstitute of Natural Medicine, University of Toyama
,
Takako YOKOZAWAInstitute of Natural Medicine, University of Toyama
,
Young Ae KIMInstitute of Natural Medicine, University of Toyama
,
Chihiro TOHDAInstitute of Natural Medicine, University of Toyama
&
Gen-ichiro NONAKAUsaien Pharmaceutical Co., Ltd.
Pages 2104-2111 | Received 31 Jan 2006, Accepted 04 May 2006, Published online: 22 May 2014

  • 1) Allen, D. A., Harwood, S., Varagunam, M., Raftery, M. J., and Yaqoob, M. M., High glucose-induced oxidative stress causes apoptosis in proximal tubular epithelial cells and is mediated by multiple caspases. FASEB J., 17, 908–910 (2003).
  • 2) Fiordaliso, F., Bianchi, R., Staszewsky, L., Cuccovillo, I., Doni, M., Laragione, T., Salio, M., Savino, C., Melucci, S., Santangelo, F., Scanziani, E., Masson, S., Ghezzi, P., and Latini, R., Antioxidant treatment attenuates hyperglycemia-induced cardiomyocyte death in rats. J. Mol. Cell. Cardiol., 37, 959–968 (2004).
  • 3) Liu, B., Bhat, M., and Nagaraj, R. H., AlphaB-crystallin inhibits glucose-induced apoptosis in vascular endothelial cells. Biochem. Biophys. Res. Commun., 321, 254–258 (2004).
  • 4) Surh, Y. J., Molecular mechanisms of chemopreventive effects of selected dietary and medicinal phenolic substances. Mutat. Res., 428, 305–327 (1999).
  • 5) Kim, Y. A., Lee, W. H., Choi, T. H., Rhee, S. H., Park, K. Y., and Choi, Y. H., Involvement of p21WAF1/CIP1, pRB, bax and NF-kappaB in induction of growth arrest and apoptosis by resveratrol in human lung carcinoma A549 cells. Int. J. Oncol., 23, 1143–1149 (2003).
  • 6) Cao, Y., Fu, Z. D., Wang, F., Liu, H. Y., and Han, R., Anti-angiogenic activity of resveratrol, a natural compound from medicinal plants. J. Asian Nat. Prod. Res., 7, 205–213 (2005).
  • 7) Kim, Y. A., Rhee, S. H., Park, K. Y., and Choi, Y. H., Antiproliferative effect of resveratrol in human prostate carcinoma cells. J. Med. Food, 6, 273–280 (2003).
  • 8) Kim, Y. A., Choi, B. T., Lee, Y. T., Park, D. I., Rhee, S. H., Park, K. Y., and Choi, Y. H., Resveratrol inhibits cell proliferation and induces apoptosis of human breast carcinoma MCF-7 cells. Oncol. Rep., 11, 441–446 (2004).
  • 9) Natella, F., Belelli, F., Gentili, V., Ursini, F., and Scaccini, C., Grape seed proanthocyanidins prevent plasma postprandial oxidative stress in humans. J. Agric. Food Chem., 50, 7720–7725 (2002).
  • 10) Bagchi, D., Bagchi, M., Stohs, S. J., Das, D. K., Ray, S. D., Kuszynski, C. A., Joshi, S. S., and Pruess, H. G., Free radicals and grape seed proanthocyanidin extract: importance in human health and disease prevention. Toxicology, 148, 187–197 (2000).
  • 11) Park, J. B., Inhibition of glucose and dehydroascorbic acid uptakes by resveratrol in human transformed myelocytic cells. J. Nat. Prod., 64, 381–384 (2001).
  • 12) Kashiwada, Y., Iizuka, H., Yoshioka, K., Chen, R. F., Nonaka, G., and Nishioka, I., Tannins and related compounds. XCIII. Occurrence of enantiomeric proanthocyanidins in the Leguminosae plants, Cassia fistula L. and C. javanica L. Chem. Pharm. Bull., 38, 888–893 (1990).
  • 13) Nonaka, G., Hsu, F. L., and Nishioka, I., Structures of dimeric, trimeric, and tetrameric procyanidins from Areca catechu L. J. Chem. Soc. Chem. Commun., 781–783 (1981).
  • 14) Nonaka, G., Kawahara, O., and Nishioka, I., Tannins and related compounds. XV. A new class of dimeric flavan-3-ols gallates, theasinensins A and B, and proanthocyanidin gallates from green tea leaf (1). Chem. Pharm. Bull., 31, 1906–1914 (1982).
  • 15) Carmichael, J., DeGraff, W. G., Gazdar, A. F., Minna, J. D., and Mitchell, J. B., Evaluation of a tetrazolium-based semiautomated colorimetric assay: assessment of chemosensitivity testing. Cancer Res., 47, 936–942 (1987).
  • 16) Wang, H., and Joseph, J. A., Quantifying cellular oxidative stress by dichlorofluorescein assay using microplate reader. Free Radic. Biol. Med., 27, 612–616 (1999).
  • 17) Cho, K. J., Han, S. H., Kim, B. Y., Hwang, S. G., Park, K. K., Yang, K. H., and Chung, A. S., Chlorophyllin suppression of lipopolysaccharide-induced nitric oxide production in RAW 264.7 cells. Toxicol. Appl. Pharmacol., 166, 120–127 (2000).
  • 18) Asahina, T., Kashiwagi, A., Nishio, Y., Ikebuchi, M., Harada, N., Tanaka, Y., Takagi, Y., Saeki, Y., Kikkawa, R., and Shigeta, Y., Impaired activation of glucose oxidation and NADPH supply in human endothelial cells exposed to H2O2 in high-glucose medium. Diabetes, 44, 520–526 (1995).
  • 19) Wu, Q. D., Wang, J. H., Fennessy, F., Redmond, H. P., and Bouchier-Hayes, D., Taurine prevents high-glucose-induced human vascular endothelial cell apoptosis. Am. J. Physiol., 277, C1229–C1238 (1999).
  • 20) Romeo, G., Liu, W. H., Asnaghi, V., Kern, T. S., and Lorenzi, M., Activation of nuclear factor-kappaB induced by diabetes and high glucose regulates a proapoptotic program in retinal pericytes. Diabetes, 51, 2241–2248 (2002).
  • 21) Ceriello, A., Quagliaro, L., Piconi, L., Assaloni, R., Da Ros, R., Maier, A., Esposito, K., and Giugliano, D., Effect of postprandial hypertriglyceridemia and hyperglycemia on circulating adhesion molecules and oxidative stress generation and the possible role of simvastatin treatment. Diabetes, 53, 701–710 (2004).
  • 22) Vincent, A. M., Olzmann, J. A., Brownlee, M., Sivitz, W. I., and Russell, J. W., Uncoupling proteins prevent glucose-induced neuronal oxidative stress and programmed cell death. Diabetes, 53, 726–734 (2004).
  • 23) Yokozawa, T., and Nakagawa, T., Inhibitory effects of Luobuma tea and its components against glucose-mediated protein damage. Food Chem. Toxicol., 42, 975–981 (2004).
  • 24) Jimenez-Ramsey, L. M., Rogler, J. C., Housley, T. L., Butler, L. G., and Elkin, R. G., Absorption and distribution of C-labeled condensed tannins and related sorghum phenolic in chickens. J. Agric. Food Chem., 42, 963–967 (1994).
  • 25) Bravo, L., Polyphenols: chemistry, dietary sources, metabolism, and nutritional significance. Nutr. Rev., 56, 317–333 (1998).
  • 26) Baba, S., Osakabe, N., Natsume, M., and Terao, J., Absorption and urinary excretion of procyanidin B2 [epicatechin-(4β-8)-epicatechin] in rats. Free Radic. Biol. Med., 33, 142–148 (2002).
  • 27) Donovan, J. L., Manach, C., Rios, L., Morand, C., Scalbert, A., and Rémésy, C., Procyanidins are not bioavailable in rats fed a single meal containing a grapeseed extract or the procyanidin dimer B3. Br. J. Nutr., 87, 299–306 (2002).
  • 28) Sano, A., Yamakoshi, J., Tokutake, S., Tobe, K., Kubota, Y., and Kikuchi, M., Procyanidin B1 is detected in human serum after intake of proanthocyanidin-rich grape seed extract. Biosci. Biotechnol. Biochem., 67, 1140–1143 (2003).
  • 29) Roychowdhury, S., Wolf, G., Keilhoff, G., Bagchi, D., and Horn, T., Protection of primary glial cells by grape seed proanthocyanidin extract against nitrosative/oxidative stress. Nitric Oxide, 5, 137–149 (2001).
  • 30) Halliwell, B., and Gutteridge, J. M. C., Consequences of oxidative stress: cell death. In “Free Radicals in Biology and Medicine,” Oxford University Press, New York, pp. 337–341 (2001).
  • 31) Zanetti, M., Zwacka, R., Engelhardt, J., Katusic, Z., and O’Brien, T., Superoxide anions and endothelial cell proliferation in normoglycemia and hyperglycemia. Arterioscler. Thromb. Vasc. Biol., 21, 195–200 (2001).
  • 32) Chen, K., and Keaney, J., Reactive oxygen species-mediated signal transduction in the endothelium. Endothelium, 11, 109–121 (2004).
  • 33) Usui, T., Shizuuchi, S., Watanabe, H., and Hayase, F., Cytotoxicity and oxidative stress induced by the glyceraldehyde-related Maillard reaction products for HL-60 cells. Biosci. Biotechnol. Biochem., 68, 333–340 (2004).
  • 34) Li, M. H., Jang, J. H., Sun, B., and Surh, Y. J., Protective effects of oligomers of grape seed polyphenols against {beta}-amyloid-induced oxidative cell death. Ann. NY Acad. Sci., 1030, 317–329 (2004).
  • 35) Du, X., Stocklauser-Farber, K., and Rosen, P., Generation of reactive oxygen intermediates, activation of NF-kappaB, and induction of apoptosis in human endothelial cells by glucose: role of nitric oxide synthase? Free Radic. Biol. Med., 27, 752–763 (1999).
  • 36) Ishii, N., Patel, K. P., Lane, P. H., Taylor, T., Bian, K., Murad, F., Pollock, J. S., and Carmines, P. K., Nitric oxide synthesis and oxidative stress in the renal cortex of rats with diabetes mellitus. J. Am. Soc. Nephrol., 12, 1630–1639 (2001).
  • 37) Walker, L. M., Walker, P. D., Imam, S. Z., Ali, S. F., and Mayeux, P. R., Evidence for peroxynitrite formation in renal ischemia-reperfusion injury: studies with the inducible nitric oxide synthase inhibitor L -N(6)-(1-Iminoethyl)lysine. J. Pharmacol. Exp. Ther., 295, 417–422 (2000).
  • 38) Surh, Y. J., Chun, K. S., Cha, H. H., Han, S. S., Keum, Y. S., Park, K. K., and Lee, S. S., Molecular mechanisms underlying chemopreventive activities of anti-inflammatory phytochemicals: down-regulation of COX-2 and iNOS through suppression of NF-kappa B activation. Mutat. Res., 480–481, 243–268 (2001).
  • 39) Simonian, N. A., and Coyle, J. T., Oxidative stress in neurodegenerative diseases. Annu. Rev. Pharmacol. Toxicol., 36, 83–106 (1996).
  • 40) Cheng, H. F., Wang, C. J., Moeckel, G. W., Zhang, M. Z., McKanna, J. A., and Harris, R. C., Cyclooxygenase-2 inhibitor blocks expression of mediators of renal injury in a model of diabetes and hypertension. Kidney Int., 62, 929–939 (2002).
  • 41) Minghetti, L., Cyclooxygenase-2 (COX-2) in inflammatory and degenerative brain diseases. J. Neuropathol. Exp. Neurol., 63, 901–910 (2004).
  • 42) Zha, S., Yegnasubramanian, V., Nelson, W. G., Isaacs, W. B., and De Marzo, A. M., Cyclooxygenases in cancer: progress and perspective. Cancer Lett., 215, 1–20 (2004).
  • 43) Koliopanos, A., Friess, H., Kleeff, J., Roggo, A., Zimmermann, A., and Buchler, M. W., Cyclooxygenase 2 expression in chronic pancreatitis: correlation with stage of the disease and diabetes mellitus. Digestion, 64, 240–247 (2001).
  • 44) Melk, A., Schmidt, B. M., Takeuchi, O., Sawitzki, B., Rayner, D. C., and Halloran, P. F., Expression of p16INK4a and other cell cycle regulator and senescence associated genes in aging human kidney. Kidney Int., 65, 510–520 (2004).
  • 45) Zang, X., and Morrison, D. C., Lipopolysaccharide-induced selective priming effects on tumor necrosis factor alpha and nitric oxide production in mouse peritoneal macrophages. J. Exp. Med., 177, 511–516 (1993).
  • 46) Horton, J. W., Free radicals and lipid peroxidation mediated injury in burn trauma: the role of antioxidant therapy. Toxicology, 189, 75–88 (2003).

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.