References
- Roper NA, Bilous RW, Kelly WF, Unwin NC, Connolly VM. 2002. Cause-specific mortality in a population with diabetes. Diabetes Care 25: 43-48. https://doi.org/10.2337/diacare.25.1.43
- Fos CS, Coady S, Sorlie PD, D'Agostino Sr RB, Pencina MJ, Vasan RS, Meigs JB, Levy D, Savage PJ. 2007. Increasing cardiovascular disease burden due to diabetes mellitus: the framingham heart study. Circulation 115: 1544-1150. https://doi.org/10.1161/CIRCULATIONAHA.106.658948
- Baron AD. 1998. Postprandial hyperglycaemia and a-glucosidase inhibitors. Diabetes Res Clin Pract 40(suppl): S51-S55. https://doi.org/10.1016/S0168-8227(98)00043-6
- Ratner RE. 2001. Controlling postprandial hyperglycemia. Am J Cardiol 8(suppl): 26H-31H.
- Lebovitz HE. 1997. Alpha-glucosidase inhibitors. Endocrinol Metabol Clin North Am 26: 539-551. https://doi.org/10.1016/S0889-8529(05)70266-8
- Fernando MR, Wickramasingle N, Thabrew MI, Ariyananda PL, Karunanayake EH. 1991. Effect of Artocarpus heterophyllus and Asteracanthus longifolia on glucose tolerance in normal human subjects and inmaturity-onset diabetic patients. J Ethnopharmacol 31: 277-282. https://doi.org/10.1016/0378-8741(91)90012-3
-
Welsh PA, Lachance CA, Wasserman BP. 1989. Dietary phenolic compounds: inhibition of
$Na^{+}$ -dependent D-glucose uptake in rat intestinal brush border membrane vesicles. J Nutr 119: 1698-1704. https://doi.org/10.1093/jn/119.11.1698 -
Bhandari MR, Anurakkun NJ, Hong G, Kawabata J. 2008.
$\alpha$ -Glucosidase and$\alpha$ --amylase inhibitory activities of Nepalese medicinal herb Pakhanbhed (Bergenia ciliata, Haw.). Food Chem 106: 247-252. https://doi.org/10.1016/j.foodchem.2007.05.077 - Hanefeld M. 1998. The role of acarbose in the treatment of non-insulindependent diabetes mellitus. J Diabetes Complicat 12: 228-237. https://doi.org/10.1016/S1056-8727(97)00123-2
- Yuan YV, Walsh NA. 2006. Antioxidant and antiproliferative activities of extracts from a variety of edible seaweeds. Food Chem Toxicol 44: 1144-1150. https://doi.org/10.1016/j.fct.2006.02.002
- Chandini SK, Ganesan P, Bhaskar N. 2008. In vitro antioxidant activities of three selected brown seaweeds of India. Food Chem 107: 707-713. https://doi.org/10.1016/j.foodchem.2007.08.081
- Kang JY, Khan MNA, Park NH, Cho JY, Lee MC, Fujii H, Hong YK. 2008. Antipyretic, analgesic, and anti-inflammatory activities of the seaweed Sargassum fulvellum and Sargassum thunbergii in mice. J Ethnopharmacol 116: 187-190. https://doi.org/10.1016/j.jep.2007.10.032
- Pushpamali WA, Nikapitiya C, De Zoysa M, Whang I, Kim SJ, Lee J. 2008. Isolation and purification of an anticoagulant from fermented red seaweed Lomentaria catenata. Carbohydr Polym 73: 274-279. https://doi.org/10.1016/j.carbpol.2007.11.029
- Kwon MJ, Nam TJ. 2006. Porphyran induces apoptosis related signal pathway in AGS gastric cancer cell lines. Life Sci 79: 1956-1962. https://doi.org/10.1016/j.lfs.2006.06.031
- Kuda T, Ikemori T. 2009. Minerals, polysaccharides and antioxidant properties of aqueous solutions obtained from macroalgal beach-casts in the Noto Peninsula, Ishikawa, Japan. Food Chem 112: 575-581. https://doi.org/10.1016/j.foodchem.2008.06.008
- Nakai M, Kageyama N, Nakahara K, Miki W. 2006. Phlorotannins as radical scavengers from the extract of Sargassum ringgoldianum. Marine Biotechnology 8: 409-414. https://doi.org/10.1007/s10126-005-6168-9
- Heo SJ, Park EJ, Lee KW, Jeon YJ. 2005. Antioxidant activities of enzymatic extracts from brown seaweeds. Bioresour Technol 96: 1613-1623.
- Yang HP. 2007. Antioxidant and antitumor activities of enzymatic extracts from Sargassum coreanum. PhD Dissertation, Cheju National University, Jeju, Korea.
- Athukorala Y, Lee KW, Kim SK, Jeon YJ. 2007. Anticoagulant activity of marine green and brown algae collected from Jeju Island in Korea. Bioresour Technol 98: 1711-1716. https://doi.org/10.1016/j.biortech.2006.07.034
- Athukorala Y, Jeon YJ. 2005. Screening for angiotensin 1-converting enzyme inhibitory activity of Ecklonia cava. J Food Sci Nutr 10: 134-139. https://doi.org/10.3746/jfn.2005.10.2.134
- Ren D, Noda H, Amano H, Nishino T, Nishizawa K. 1994. Study on antihypertensive and antihyperlipidemic effects of marine algae. Fisheries Science 60: 83-88. https://doi.org/10.2331/fishsci.60.83
- Min KH, Kim HJ, Jeon YJ, Han JS. 2011. Ishige okamurae ameliorates hyperglycemia and insulin resistance in C57BL/ KsJ-db/db mice. Diabetes Res Clin Pract 93: 70-76. https://doi.org/10.1016/j.diabres.2011.03.018
- Watanabe J, Kawabata J, Kurihara H, Niki R. 1997. Isolation and identification of alpha-glucosidase inhibitors from tochucha (Eucommia ulmoides). Biosci Biotechnol Biochem 61: 177-178. https://doi.org/10.1271/bbb.61.177
- Kim JS. 2004. Effect of Rhemanniae radix on the hyperglycemic mice induced with streptozotocin. J Korean Soc Food Sci Nutr 33: 1133-1138. https://doi.org/10.3746/jkfn.2004.33.7.1133
-
Hasenah A, Houghton PJ, Soumyanath A. 2006.
$\alpha$ -Amylase inhibitory activity of some Malaysian plants used to treat diabetes: with particular reference to Phyllanthus amarus. J Ethnopharmacol 107: 449-455. https://doi.org/10.1016/j.jep.2006.04.004 -
Kim KY, Nama KA, Kurihara H, Kim SM. 2008. Potent
$\alpha$ -glucosidase inhibitors purified from the red alga Grateloupia elliptica. Phytochemistry 69: 2820-2825. https://doi.org/10.1016/j.phytochem.2008.09.007 -
Lee SH, Li Y, Karadeniz F, Kim MM, Kim SK. 2009.
$\alpha$ -Glucosidase and$\alpha$ -amylase inhibitory activities of phloroglucinol derivatives from edible marine brown alga, Ecklonia cava. J Sci Food Agric 89: 1552-1558. https://doi.org/10.1002/jsfa.3623 - Abrahamson MJ. 2004. Optimal glycemic control in type 2 diabetes mellitus: fasting and postprandial glucose in context. Arch Intern Med 164: 486-491. https://doi.org/10.1001/archinte.164.5.486
- Haller H. 1998. The clinical importance of postprandial glucose. Diabetes Res Clin Pract 40: S43-49. https://doi.org/10.1016/S0168-8227(98)00042-4
- Inoue I, Takahashi K, Noji S, Awata T, Negishi K, Katayama S. 1997. Acarbose controls postprandial hyper-proinsulinemia in non-insulin-dependent diabetes mellitus. Diabetes Res Clin Pract 36: 143-151. https://doi.org/10.1016/S0168-8227(97)00045-4
- Duckworth W, Abraira C, Moritz T, Reda D, Emanuele N, Reaven PD, Zieve FJ, Marks J, Davis SN, Hayward R, Warren SR, Goldman S, McCarren M, Vitek ME, Henderson WG, Huang GD. 2009. Glucose control and vascular complications in veterans with type 2 diabetes. N Engl J Med 360: 129-139. https://doi.org/10.1056/NEJMoa0808431
- Stettler C, Allemann S, Jü ni P, Cull CA, Holman RR, Egger M, Krähenbühl S, Diem P. 2006. Glycemic control and macrovascular disease in types 1 and 2 diabetes mellitus: meta-analysis of randomized trials. Am Heart J 152: 27-38. https://doi.org/10.1016/j.ahj.2005.09.015
- Holman RR, Paul SK, Bethel MA, Matthews DR, Neil HA. 2008. 10-year follow-up of intensive glucose control in type 2 diabetes. N Engl J Med 359: 1577-1589. https://doi.org/10.1056/NEJMoa0806470
- Nam JS, Lee WJ, Yoon IS, Kang MW, Jang HS, Youn JH, Kim BR, Kong HJ, Kim KH, Kim YH, Lee DS, Choi HJ. 2007. Effect of a brown algae extract on postprandial glucose control in neonatal diabetic and obese rats. J FASEB 21: 845.2.
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