References
- Yamagishi S, Imaizumi T. Diabetic vascular complications:Pathophysiology, biochemical basis, and potential therapeutic strategy. Curro Pharm. Design 11: 2279-2299 (2005) https://doi.org/10.2174/1381612054367300
- Bonnefont-Rousselot D. Glucose and reactive oxygen species. Curr. Opin. Clin. Nutr. 5: 561-568 (2002) https://doi.org/10.1097/00075197-200209000-00016
- Wen Y, Skidmore JC, Porter-Turner MM, Rea CA, Khokher MA, Singh BM. Relationship of glycation, antioxidant status, and oxidative stress to vascular endothelial damage in diabetes. Diabetes Obes. Metab. 4: 305-308 (2002) https://doi.org/10.1046/j.1463-1326.2002.00212.x
- Wolff SP, Jiang ZY, Hunt JV Protein glycation and oxidative stress in diabetes mellitus and aging. Free Radical Bio. Med. 10: 339-352 (1991) https://doi.org/10.1016/0891-5849(91)90040-A
- McCance DR, Dyer DG, Dunn JA, Baiue KE, Thorpe SR, Baynes JW, Lyons TJ. Maillard reaction products and their relation to complications in insulin-dependent diabetes mellitus. J. Clin. Invest. 91: 2470-2478 (1993) https://doi.org/10.1172/JCI116482
- Brownlee M, Cerami A, Viassara H. Advanced glycosylation end products in tissue and the biochemical basis of diabetic complications. New Engl. J. Med. 318: 1315-1321 (1988) https://doi.org/10.1056/NEJM198805193182007
- Ahmed N. Advanced glycation endproducts-role in pathology of diabetic complications. Diabetes Res. Clin. Pr. 67: 3-21 (2005) https://doi.org/10.1016/j.diabres.2004.09.004
- Vasan S, Zhang X, Kapurniotu A, Bernhagen J, Teichberg S, Basgen J, Wagle D, Slih D, Terlecky I, Bucala R, Cerami A, Egan J, Ulrich P. An agent cleaving glucose-derived protein crosslinks in vitro and in vivo. Nature 382: 275-278 (1996) https://doi.org/10.1038/382275a0
- Rahbar S, Figarola JL. Novel inhibitors of advanced glycation endproducts. Arch. Biochem. Biophys. 419: 63-79 (2003) https://doi.org/10.1016/j.abb.2003.08.009
- Kador PF. The role of aldose reductase in the development of diabetic complications. Med. Res. Rev. 8: 325-352 (1988) https://doi.org/10.1002/med.2610080302
- Enomoto S, Okada Y, Guvenc A, Erdurak CS, Coskun M, Okuyama T. Inhibitory effects of traditional Turkish folk medicines on aldose reductase (AR) and hematological activity, and on AR inhibitory activity of quercetin-3-0-methyl ether isolated from Cistus laurijolius L. BioI. Pharm. Bull. 27: 1140-1143 (2004) https://doi.org/10.1248/bpb.27.1140
-
Lee YS, Lee S, Lee HS, Kim BK, Ohuchi K, Shin KH. Inhibitory effects of isorhamnetin-3-O-
$\beta$ -D-glucoside from Salicornia herbacea on rat lens aldose reductase and sorbitol accumulation in streptozotocin-induced diabetic rat tissues. BioI. Pharm. Bull. 28:916-918 (2005) https://doi.org/10.1248/bpb.28.916 - Itokawa H, Morita H, Midorikawa I, Alyama R, Morita M. Diarylheptanoids from the rhizome of Alpinia officinarum Hance. Chem. Pharm. Bull. 33: 4889-4893 (1985) https://doi.org/10.1248/cpb.33.4889
- Itokawa H, Morita M, Mihashi S. The new diarylheptanoids from Alpinia officinarum Hance. Chem. Pharm. Bull. 29: 2383-2385 (1981) 15. Shin JE, Han MJ, Kim DH. 3-Methylethergalangin isolated from Alpinia officinarum inhibits pancreatic lipase. BioI. Pharm. Bull. 26:854-857 (2003) https://doi.org/10.1248/bpb.26.854
- Shin JE, Han MJ, Kim DH. 3-Methylethergalangin isolated from Alpinia officinarum inhibits pancreatic lipase. BioI. Pharm. Bull. 26:854-857 (2003) https://doi.org/10.1248/bpb.26.854
- Tao L, Wang ZT, Zhu EY, Lu YH, Wei DZ. HPLC analysis of bioactive flavonoids from the rhizome of Alpinia officinarum. S. Afr. J. Bot. 72: 163-166 (2006) https://doi.org/10.1016/j.sajb.2005.06.007
- Heo MY, Sohn SJ, Au WW. Anti-genotoxicity of galangin as a cancer chemopreventive agent candidate. Mutat. Res. 488: 135-150 (2001) https://doi.org/10.1016/S1383-5742(01)00054-0
- Wall ME, Wani MC, Manikumar G, Abraham P, Taylor H, Hughes TJ, Warner J, McGiveney R. Plant antimutagenic agents. 2. Flavonoids. J. Nat. Prod. 51: 1084-1091 (1988) https://doi.org/10.1021/np50060a006
- Imamura Y, Migita T, Uriu Y, Otagiri M, Okawara T. Inhibitory effects of flavonoids on rabbit heart carbonyl reductase. J. Biochem.-Tokyo 127: 653-658 (2000)
- Matsuda H, Ando S, Kato T, Morikawa T, Yoshikawa M. Inhibitors from the rhizomes of Alpinia officinarum on production of nitric oxide in lipopolysaccharide-activated macrophages and the structural requirements of diaryJheptanoids for the activity. Bioorgan. Med. Chem. 14: 138-142 (2006) https://doi.org/10.1016/j.bmc.2005.08.003
- De Monbrison F, Maitrejean M, Latour C, Bugnazet F, Peyron F, Barron D, Picot S. In vitro antimalarial activity of flavonoid derivatives dehydrosilybin and 8-(1;1)-DMA-kaempferide. Acta Trop. 97: 102-107 (2006) https://doi.org/10.1016/j.actatropica.2005.09.004
- Simoes LMC, Gregorio LE, Da Silva Filho AA, de Souza ML, Azzolini AECS, Bastos JK, Lucisano-Valim YM. Effect of Brazilian green propolis on the production of reactive oxygen species by stimulated neutrophils. J. Ethnopharmacol. 94: 59-65 (2004) https://doi.org/10.1016/j.jep.2004.04.026
- Curir P, Dolci M, Lanzotti, V, Taglialatela-Scafati O. Kaempferide triglycoside: A possible factor of resistance of carnation (Dianthus caryophyllus) to Fusarium oxysporum f. sp. dianthi. Phytochemistry 56: 717-721 (2001) https://doi.org/10.1016/S0031-9422(00)00488-X
- Ohkawa H, Ohishi N, Yagi, K. Assay for lipid peroxidation in animal tissues by thiobarbituric acid reaction. Anal. Biochem. 95:351-358 (1979) https://doi.org/10.1016/0003-2697(79)90738-3
- Popravko SA, Gurevich AI, Kolosov MN. Flavonoid components of propolis. Khim. Prir. Soedin+ 5: 476-482 (1969)
- Brownlee M, Vlassara H, Kooney A, Ulrich P, Cerami A. Aminoguanidine prevents diabetes-induced arterial wall protein cross-linking. Science 232: 1629-1632 (1986) https://doi.org/10.1126/science.3487117
- Hayman S, Kinoshita JH. Isolation and properties of Lens aldose reductase. J. BioI. Chem. 240: 877-882 (1965)
- Sato S, Kador PF. Inhibition of aldehyde reductase by aldose reductase inhibitors. Biochem. Pharmacol. 40: 1033-1042 (1990) https://doi.org/10.1016/0006-2952(90)90490-C
- Kim SJ, Kim GH. Quantification of quercetin in different parts of onion and its DPPH radical scavenging and antibacterial activity. Food Sci. Biotechnol. 15: 39-43 (2006)
- Wee JH, Moon JH, Eun JB, Chung JH, Kim YG, Park KH. Isolation and identification of antioxidants from peanut shells and the relationship between structure and antioxidant activity. Food Sci. Biotechnol. 16: 116-122 (2007)
- Gomez-Sanchez A, Maya I, Hermosin I. Reaction of amino sugars with malondialdehyde. Carbohyd. Res. 200: 167-180 (1990) https://doi.org/10.1016/0008-6215(90)84188-Z
- Monnier VM. Nonenzymatic glycosylation, the Maillard reaction and aging process. J. Gerontol. 45: 105-111 (1990) https://doi.org/10.1093/geronj/45.4.B105
- Shih CC, Wu YW, Lin WC. Antihyperglycemic and antioxidant properties of Anoectochilus formosanus in diabetic rats. Clin. Exp. Pharmacol. 29: 684-688 (2002) https://doi.org/10.1046/j.1440-1681.2002.03717.x
- Ryu JK, Lee T, Kim DJ. Free radical scavenging activity of Korean red ginseng for erectile dysfunction in non insulin dependent diabetes mellitus rats. Urology 65: 611-615 (2005) https://doi.org/10.1016/j.urology.2004.10.038
- Ravi K, Ramachandran B, Subramanian S. Effect of Eugenia jambolana seed kernel on antioxidant defense system in streptozotocin-induced diabetes in rats. Life Sci. 75: 2717-2731 (2004) https://doi.org/10.1016/j.lfs.2004.08.005