Inhibitors of α-glucosidase and α-amylase from Cyperus rotundus

References

• Ali MS, Jahangir M, Hussan SS, Choudhary MI. (2002). Inhibition of alpha-glucosidase by oleanolic acid and its synthetic derivatives. Phytochemistry 60:295–9
   PubMed Web of Science ®Google Scholar
• Ardestani A, Yazdanparast R. (2007). Cyperus rotundus suppresses AGE formation and protein oxidation in a model of fructose-mediated protein glycoxidation. Int J Biol Macromol 41:572–8
   PubMed Web of Science ®Google Scholar
• Golbidi S, Ebadi SA, Laher I. (2011). Antioxidants in the treatment of diabetes. Curr Diabetes Rev 7:106–25
   PubMedGoogle Scholar
• Jin JH, Lee DU, Kim YS, Kim HP. (2011). Anti-allergic activity of sesquiterpenes from the rhizomes of Cyperus rotundus. Arch Pharm Res 34:223–8
   PubMed Web of Science ®Google Scholar
• Johansen JS, Harris AK, Rychly DJ, Ergul A. (2005). Oxidative stress and the use of antioxidants in diabetes: Linking basic science to clinical practice. Cardiovasc Diabetol 4:5–15
   PubMed Web of Science ®Google Scholar
• Karunakaran U, Park KG. (2013). A systematic review of oxidative stress and safety of antioxidants in diabetes: Focus on islets and their defense. Diabetes Metab J 37:106–12
   PubMedGoogle Scholar
• Kilani S, Ledauphin J, Bouhlel I, et al. (2008). Comparative study of Cyperus rotundus essential oil by a modified GC/MS analysis method. Evaluation of its antioxidant, cytotoxic, and apoptotic effects. Chem Biodivers 5:729–42
   PubMed Web of Science ®Google Scholar
• Kilani-Jaziri S, Neffati A, Limem I, et al. (2009). Relationship correlation of antioxidant and antiproliferative capacity of Cyperus rotundus products towards K562 erythroleukemia cells. Chem Biol Interact 181:85–94
   PubMed Web of Science ®Google Scholar
• Kobayashi K, Ishihara T, Khono E, et al. (2006). Constituents of stem bark of Callistemon rigidus showing inhibitory effects on mouse alpha-amylase activity. Biol Pharm Bull 29:1275–7
   PubMed Web of Science ®Google Scholar
• Kusano R, Ogawa S, Matsuo Y, et al. (2011). α-Amylase and lipase inhibitory activity and structural characterization of acacia bark proanthocyanidins. J Nat Prod 74:119–28
   PubMed Web of Science ®Google Scholar
• Lam SH, Chen JM, Kang CJ, et al. (2008). alpha-Glucosidase inhibitors from the seeds of Syagrus romanzoffiana. Phytochemistry 69:1173–8
   PubMed Web of Science ®Google Scholar
• Morikawa T, Xu F, Matsuda H, Yoshikawa M. (2010). Structures of novel norstilbene dimer, longusone A, and three new stilbene dimers, longusols A, B, and C, with antiallergic and radical scavenging activities from Egyptian natural medicine Cyperus longus. Chem Pharm Bull 58:1379–85
   PubMed Web of Science ®Google Scholar
• Priya-Rani M, Padmakumari KP. (2012). HPTLC and reverse phase HPLC methods for the simultaneous quantification and in vitro screening of antioxidant potential of isolated sesquiterpenoids from the rhizomes of Cyperus rotundus. J Chromatogr B 904:22–8
   PubMed Web of Science ®Google Scholar
• Psaltopoulou T, Panagiotakos DB, Pitsavos C, et al. (2011). Dietary antioxidant capacity is inversely associated with diabetes biomarkers: The ATTICA study. Nutr Metab Cardiovasc Dis 21:561–7
   PubMed Web of Science ®Google Scholar
• Raut NA, Gaikwad NJ. (2006). Antidiabetic activity of hydro-ethanolic extract of Cyperus rotundus in alloxan induced diabetes in rats. Fitoterapia 77:585–8
   PubMed Web of Science ®Google Scholar
• Richard T, Pawlus AD, Iglesias ML, et al. (2011). Neuroprotective properties of resveratrol and derivatives. Ann N Y Acad Sci 1215:103–8
   PubMed Web of Science ®Google Scholar
• Sabu MC, Kuttan R. (2002). Anti-diabetic activity of medicinal plants and its relationship with their antioxidant property. J Ethnopharmacol 81:155–60
   PubMed Web of Science ®Google Scholar
• Sang S, Cheng X, Stark RE, et al. (2002). Chemical studies on antioxidant mechanism of tea catechins: Analysis of radical reaction products of catechin and epicatechin with 2,2-diphenyl-1-picrylhydrazyl. Bioorg Med Chem 10:2233–7
   PubMed Web of Science ®Google Scholar
• Sayed HM, Mohamed MH, Farag SF, et al. (2007). A new steroid glycoside and furochromones from Cyperus rotundus L. Nat Prod Res 21:343–50
   PubMed Web of Science ®Google Scholar
• Sayed HM, Mohamed MH, Farag SF, et al. (2008). Fructose--amino acid conjugate and other constituents from Cyperus rotundus L. Nat Prod Res 22:1487–97
   PubMed Web of Science ®Google Scholar
• Seo EJ, Lee DU, Kwak JH, et al. (2011). Antiplatelet effects of Cyperus rotundus and its component (+)-nootkatone. J Ethnopharmacol 135:48–54
   PubMed Web of Science ®Google Scholar
• Souza PM, Sales PM, Simeoni LA, et al. (2012). Inhibitory activity of α-amylase and α-glucosidase by plant extracts from the Brazilian cerrado. Planta Med 78:393–9
   PubMed Web of Science ®Google Scholar
• Tang W, Eisenbrand G. (2011). Handbook of Chinese Medicinal Plants: Chemistry, Pharmacology, Toxicology. Vol. 1. Weinheim: Wiley-VCH
   Google Scholar
• Venkatasubramanian P, Kumar SK, Nair VS. (2010). Cyperus rotundus, a substitute for Aconitum heterophyllum: Studies on the Ayurvedic concept of Abhava Pratinidhi Dravya (drug substitution). J Ayurveda Integr Med 1:33–9
   PubMedGoogle Scholar
• Vo VC. (2004). Dictionary of Vietnamese Medicinal Plants. Hanoi, Vietnam: Medicine Publisher
   Google Scholar
• Wada S, Yasui Y, Tokuda H, Tanaka R. (2009). Anti-tumor-initiating effects of phenolic compounds isolated from the bark of Picea jezoensis var. jezoensis. Bioorg Med Chem 17:6414–21
   PubMed Web of Science ®Google Scholar
• Wan X, Wang XB, Yang MH, et al. (2011). Dimerization of piceatannol by Momordica charantia peroxidase and α-glucosidase inhibitory activity of the biotransformation products. Bioorg Med Chem 19:5085–92
   PubMed Web of Science ®Google Scholar
• Williams M, Hogg RE, Chakravarthy U. (2013). Antioxidants and diabetic retinopathy. Curr Diab Rep 13:481--7
   PubMed Web of Science ®Google Scholar
• Xiang T, Uno T, Ogino F, et al. (2005). Antioxidant constituents of Caragana tibetica. Chem Pharm Bull 53:1204–6
   PubMed Web of Science ®Google Scholar
• Yazdanparast R, Ardestani A. (2007). In vitro antioxidant and free radical scavenging activity of Cyperus rotundus. J Med Food 10:667–74
   PubMed Web of Science ®Google Scholar
• Zeng X, Qiu Q, Jiang C, et al. (2011). Antioxidant flavanes from Livistona chinensis. Fitoterapia 82:609–14
   PubMed Web of Science ®Google Scholar