The effects of grape seed on apoptosis-related gene expression and oxidative stress in streptozotocin-induced diabetic rats

References

• Alberti KGMM, Aschner P, Benet PH. Definition, diagnosis and classification of diabetes mellitus and its complications. Report of WHO consultation. Geneva: World Health Organization; 1999: Part 1;2–3
   Google Scholar
• Calcutt NA, Cooper ME, Kern TS, Schmidt AM. Therapies for hyperglycaemia-induced diabetic complications: From animal models to clinical trials. Nat Rev Drug Discov. 2009;8:417–429
   PubMed Web of Science ®Google Scholar
• Lachin JM, Genuth S, Cleary P. Retinopathy and nephropathy in patients with type 1 diabetes four years after a trial of intensive therapy. N Engl J Med. 2000;342:381–389
   Google Scholar
• Paolisso G, D'Amore A, Galzerano D, et al. Daily vitamin E supplements improve metabolic control but not insulin secretion in elderly type II diabetic patients. Diabetes Care. 1993;16:1433–1437
   PubMed Web of Science ®Google Scholar
• Su J, Zhou L, Kong X, et al. Endoplasmic reticulum is at the crossroads of autophagy, inflammation, and apoptosis signaling pathways and participates in the pathogenesis of diabetes mellitus. J Diabetes Res. 2013;2013:193461
   PubMedGoogle Scholar
• Galluzzi L, Maiuri MC, Vitale I, et al. Cell death modalities: Classification and pathophysiological implications. Cell Death Differ. 2007;14:1237–1243
   PubMed Web of Science ®Google Scholar
• Ishii N, Patel KP, Lane PH, et al. Nitric oxide synthesis and oxidative stress in the renal cortex of rats with diabetes mellitus. J Am Soc Nephrol. 2001;12:1630–1639
   PubMed Web of Science ®Google Scholar
• Du X, Stocklauser-Farber K, 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. 1999;27:752–763
   PubMed Web of Science ®Google Scholar
• Zhuang S, Simon G. Peroxynitrite-induced apoptosis involves activation of multiple caspases in HL-60 cells. Am J Physiol Cell Physiol. 2000;279:341–351
   PubMedGoogle Scholar
• Nath KA. Tubulointerstitial changes as a major determinant in the progression of renal damage. Am J Kidney Dis. 1992;20:1–17
   PubMed Web of Science ®Google Scholar
• Tanaka S, Aida K, Nishida Y, Kobayashi T. Pathophysiological mechanisms involving aggressive islet cell destruction in fulminant type 1 diabetes. Endocr J. 2013;60:837–845
   PubMedGoogle Scholar
• Liu YN, Shen XN, Yao GY. Effects of grape seed proanthocyanidins extracts on experimental diabetic nephropathy in rats. Wei Sheng Yan Jiu. 2006;35:703–705
   PubMedGoogle Scholar
• Ibrahim HN, Hostetter TH. Diabetic nephropathy. J Am Soc Nephrol. 1997;8:487–493
   PubMed Web of Science ®Google Scholar
• Yan HD, Li XZ, Xie JM, Li M. Effects of advanced glycation end products on renal fibrosis and oxidative stress in cultured NRK-49F cells. Chin Med J (Engl). 2007;120:787–793
   PubMed Web of Science ®Google Scholar
• Erel O. A new automated colorimetric method for measuring total oxidant status. Clin Biochem. 2005;38:1103–1111
   PubMed Web of Science ®Google Scholar
• Erel O. A novel automated direct measurement method for total antioxidant capacity using a new generation, more stable ABTS radical cation. Clin Biochem. 2004;37:277–285
   PubMed Web of Science ®Google Scholar
• Rincon J, Pedreanez A, Viera N, Arcaya JL, Carrizo E, Mosquera J. Depressive status does not alter renal oxidative and immunological parameters during early diabetic nephropathy in rats. World J Biol Psychiatry. 2009;10:560–566
   PubMed Web of Science ®Google Scholar
• Anjaneyulu M, Chopra K. Diltiazem attenuates oxidative stress in diabetic rats. Ren Fail. 2005;27:335–344
   PubMed Web of Science ®Google Scholar
• Nishikawa T, Edelstein D, Du XL, et al. Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage. Nature. 2000;404:787–790
   PubMed Web of Science ®Google Scholar
• Ulusoy S, Ozkan G, Yucesan FB, et al. Anti-apoptotic and anti-oxidant effects of grape seed proanthocyanidin extract in preventing cyclosporine A-induced nephropathy. Nephrology (Carlton). 2012;17:372–379
   PubMed Web of Science ®Google Scholar
• Emrullah B, Ali BÇ, Esra E, et al. Changes of total antioxidant capacity and total oxidant status of aqueous humor in diabetes patients and correlations with diabetic retinopath. Int J Ophthalmol. 2013;6:531–536
   PubMedGoogle Scholar
• Anjaneyulu M, Tirkey N, Chopra K. Attenuation of cyclosporine-induced renal dysfunction by catechin: Possible antioxidant mechanism. Ren Fail. 2003;25:691–707
   PubMed Web of Science ®Google Scholar
• Li BY, Cheng M, Gao HQ, et al. Back-regulation of six oxidative stress proteins with grape seed proanthocyanidin extracts in rat diabetic nephropathy. J Cell Biochem. 2008;104:668–679
   PubMed Web of Science ®Google Scholar
• Pinent M, Blay M, Blade MC, Salvado MJ, Arola L, Ardevol A. Grape seed-derived procyanidins have an antihyperglycemic effect in streptozotocin-induced diabetic rats and insulinomimetic activity in insulin-sensitive cell lines. Endocrinology. 2004;145:4985–4990
   PubMed Web of Science ®Google Scholar
• Bagchi D, Bagchi M, Stohs SJ, et al. Free radicals and grape seed proanthocyanidin extract: importance in human health and disease prevention. Toxicology. 2000;148:187–197
   PubMed Web of Science ®Google Scholar
• Okouchi M, Okayama N, Aw TY. Preservation of cellular glutathione status and mitochondrial membrane potential by N-acetylcysteine and insulin sensitizers prevent carbonyl stress-induced human brain endothelial cell apoptosis. Curr Neurovasc Res. 2009;6:267–278
   PubMedGoogle Scholar
• Kumar D, Zimpelmann J, Robertson S, Burns KD. Tubular and interstitial cell apoptosis in the streptozotocin-diabetic rat kidney. Nephron Exp Nephrol. 2004;96:77–88
   PubMedGoogle Scholar
• Wong VY, Keller PM, Nuttall ME, et al. Role of caspases in human renal proximal tubular epithelial cell apoptosis. Eur J Pharm. 2001;433:135–140
   PubMedGoogle Scholar
• Alnemri E, Livingston DJ, Nicholson DW, et al. Human ICE/CED-3 protease nomenclature (Letter). Cell. 1996;87:171
   PubMed Web of Science ®Google Scholar
• Alnemri ES. Mammalian cell death proteases: A family of highly conserved aspartate specific cysteine proteases. J Cell Biochem. 1997;64:33–42
   PubMed Web of Science ®Google Scholar
• Cohen GM. Caspases: The executioners of apoptosis. Biochem J. 1997;326:1–16
   PubMed Web of Science ®Google Scholar
• Susanne M, Xia X, Jie T, Timothy SK. Caspase activation in retinas of diabetic and galactosemic mice and diabetic patients. Diabetes. 2002;51:1172–1179
   PubMedGoogle Scholar
• Koenen TB, Stienstra R, van Tits LJ, et al. Hyperglycemia activates caspase-1 and TXNIP-mediated IL-1β transcription in human adipose tissue. Diabetes. 2011;60:517–524
   PubMed Web of Science ®Google Scholar
• Cohen Z, Gonzales RF, Davis-Gorman GF, Copeland JG, McDonagh PF. Thrombin activity and platelet microparticle formation are increased in type 2 diabetic platelets: A potential correlation with caspase activation. Thromb Res. 2002;107:217–221
   PubMed Web of Science ®Google Scholar
• Ulusoy S, Ozkan G, Mungan S, et al. GSPE is superior to NAC in the prevention of contrast-induced nephropathy: Might this superiority be related to caspase 1 and calpain 1? Life Sci. 2014;103:101–110
   PubMed Web of Science ®Google Scholar
• Zha J, Harada H, Osipov K, Jockel J, Waksman G, Korsmeyer SJ. BH3 domain of BAD is required for heterodimerization with BCL-XL and pro-apoptotic activity. J Biol Chem. 1997;272:24101–24104
   PubMed Web of Science ®Google Scholar
• Inohara N, Koseki T, Chen S, Wu X, Nunez G. CIDE, a novel family of cell death activators with homology to the 45 kDa subunit of the DNA fragmentation factor. EMBO J. 1998;17:2526–2533
   PubMed Web of Science ®Google Scholar
• Du C, Fang M, Li Y, Li L, Wang X. Smac, a mitochondrial protein that promotes cytochrome c-dependent caspase activation by eliminating IAP inhibition. Cell. 2000;102:33–42
   PubMed Web of Science ®Google Scholar
• Verhagen A, Ekert PG, Silke J, et al. Identification of DIABLO, a mammalian protein that promotes apoptosis by binding to and antagonizing IAP proteins. Cell. 2000;102:43–53
   PubMed Web of Science ®Google Scholar
• Yeo SH, Noh JR, Kim YH, et al. Increased vulnerability to beta cell destruction and diabetes in mice lacking NAD(P)H: Quinone oxidoreductase 1. Toxicol Lett. 2013;219:35–41
   PubMedGoogle Scholar
• Hirata H, Takahashi A, Kobayashi S, et al. Caspases are activated in a branched protease cascade and control distinct downstream processin Fas-induced apoptosis. J Exp Med. 1998;187:587–600
   PubMed Web of Science ®Google Scholar
• Rytomaa M, Martin LM, Downward J. Involvement of FADD and Caspase 8 signalling in detachment-induced apoptosis. Curr Biol. 1999;9:587–600
   Google Scholar
• Scaffidi C, Medamma JP, Krammer PH, Peter ME. FLICE is predominantly expressed as two functionally active isoforms, caspas 8/a and caspase 8/b. J Biol Chem. 1997;272:1043–1046
   Google Scholar
• Sohn D, Schulze-Osthoff K, Janicke RU. Caspase 8 can be activated by interchain proteolysis without receptor-triggered dimerization during-induced apoptosis. J Biol Chem. 2005;280:5267–5273
   PubMedGoogle Scholar