References
- Laclaustra M, Corella D, Ordovas J. Metabolic syndrome pathophysiology: the role of adipose tissue. Nutr Metab Cardiovasc Dis 2007;17:125-39. https://doi.org/10.1016/j.numecd.2006.10.005
- Trayhurn P. Endocrine and signaling role of adipose tissue: new perspectives on fat. Acta Physiol Scand 2005;184:285-93. https://doi.org/10.1111/j.1365-201X.2005.01468.x
- Fantuzzi G. Adipose tissue, adipokines, and inflammation. J Allergy Clin Immunol 2005;115:911-9. https://doi.org/10.1016/j.jaci.2005.02.023
- Wang CC, Galstone ML, Drazin B. Molecular mechanism of insulin resistance that impact cardiovascular biology. Diabetes 2004;53:2735-40. https://doi.org/10.2337/diabetes.53.11.2735
- Kahn BB, Flier JS. Obesity and insulin resistance. J Clin Invest 2000;106:473-81. https://doi.org/10.1172/JCI10842
- Hae J. DongEuBoGam. Seoul: Namsangdang; 1990. p.140-2.
- Lu B, Wu X, Tie X, Zhang Y, Zhang Y. Toxicology and safty of anti-oxidant of bamboo leaves. Part 1: Acute and subchronic toxicity studies on anti-oxidant of bamboo leaves. Food Chem Toxicol 2005;43:783-92. https://doi.org/10.1016/j.fct.2005.01.019
- Lu B, Wu X, Shi J, Dong Y, Zhang Y. Toxicology and safty of anti-oxidant of bamboo leaves. Part 2: Developmental toxicity test in rat with antioxidant of bamboo leaves. Food Chem Toxicol 2006;44:1739-43. https://doi.org/10.1016/j.fct.2006.05.012
- Jung EY. Effect of the Sasa Borealis leaves extract on metabolic syndrome in C57/BL6j mice fed a high fat diet [master's thesis]. Gwanju: Chonnam National University; 2006.
- Kim EY, Jung EY, Lim HS, Heo YR. The effects of the Sasa Borealis leaves extract on plsma adiponectin, resistin, C-reactive protein and homocyteine levels in high fat diet-induced obese C57/BL6J mice. The Korean Journal of Nutrition 2007;40: 303-11.
- Ko BS, Jun DW, Jang JS, Kim JH, Park S. Effect of Sasa borealis and white lotus root and leaves on insulin action and secretion In Vitro. Korean Journal of Food Science and Technology 2006;38:114-20.
- Oh HK. Development of the hamburger patties containing Sasa Borealis bamboo leaves, Laminaria japonica or rice [doctor's thesis]. Gwangju: Chonnam National University; 2008.
- Park YO. Antioxidant activities of extracts of Sasa Borealis leaves [doctor's thesis]. Gwangju: Chonnam National University; 2008.
- Yun EK. Effects of Sasa Borealis leaves extract on glucose tolerance of major contributing foods to carbohydrate intake [master's thesis]. Gwanju: Chonnam National University; 2009.
- Choi YJ, Choi JS, Shin SY, Bae JY, Kang SW, Kang IJ, Kang YH. Blocked of chronic high glucose-induced endotherial apoptosis by Sasa borealis bamboo extract. Exp Biol Med 2008;233:580-91. https://doi.org/10.3181/0707-RM-205
- Hwang JY, Han JS. Inhibitory effects of Sasa borealis leaves extracts on carbohydrate digestive enzyme and postprandial hyperglycemia. Journal of the Korean Society of Food Science and Nutrition 2007;36:989-94. https://doi.org/10.3746/jkfn.2007.36.8.989
-
Lee MJ, Park WH, Song YS, Lee YW, Song YO, Moon GS. Effect of bamboo culm extract on oxidative stress and genetic expression: Bamboo culm extract ameliorates cell adhesion molecule expression and NF
$\kappa$ B activity through the suppression of the oxidative stress. Clin Nutr 2008;27:755-63. https://doi.org/10.1016/j.clnu.2008.06.002 - Park EJ, Jhon DY. The antioxidant, angiotensin converting enzyme inhibition activity, and phenolic compounds of bamboo shoot extracts. LWT-Food Science and Technology 2010;43:655-9. https://doi.org/10.1016/j.lwt.2009.11.005
- Zang Y, Yao X, Bao B, Zhang Y. Anti-fatigue activity of a triterpenoid-rich extract from Chinese bamboo shavings (Caulis bamfusae in taeniam). Phytother Res 2006;20:872-8. https://doi.org/10.1002/ptr.1965
- Choi DB, Cho KA, Na MS, Choi HS, Kim YO, Lim DH, Cho SJ, Cho H. Effect of bamboo oil on antioxidative activity and nitrite scavenging activity. Journal of Industrial and Engineering Chemistry 2008;14:765-70. https://doi.org/10.1016/j.jiec.2008.06.005
- Cho H, Cho KA, Jia S, Cho SJ, Choi DB. Influence of bamboo oil supplementation on blood lipid concentration in serum. Journal of Industrial and Engineering Chemistry 2009;15:281-4. https://doi.org/10.1016/j.jiec.2008.12.002
- Pham B, Cranney A, Boers M, Verhoeven AC, Wells G, Tugwell P. Validity of area-under-the-curve analysis to summarize effect in rheumatoid arthritis clinical trials. J Rheumatol 1999;26:712-6.
- Hosker JP, Matthews DR, Rudenski AS, Burnett MA, Darling P, Bown EG, Turner RC. Continuous infusion of glucose with model assessment: measurement of insulin resistance and beta-cell function in men. Diabetologia 1985;28:401-11. https://doi.org/10.1007/BF00280882
- Kim S, Moustaid-Mossa N. Secretory, endocrine and autocrine/paracrine function of adipocyte. J Nutr 2000;130:3110S-3115S.
- Urs S, Heo YR, Kim S, Kim JH, Jones BH, Moustaid-Moussa N. Genomics, proteomics and nutrition: Applications to obesity research. Nutritional Sciences 2002;5:129-33.
- Xu H, Barnes GT, Yang Q, Tan G, Yang D, Chou CJ, Sole J, Nichols A, Ross JS, Tartaglia LA, Chen H. Chronic inflammation in fat plays a crucial role in the development of obesity-related insulin resistance. J Clin Invest 2003;112:1821-30. https://doi.org/10.1172/JCI19451
- Hotamisligil GS, Sharigill NS, Spiegelman BM. Adipose expression of tumor necrosis factor-alpha: direct role in obesity-linked insulin resistance. Science 1993;259:87-91. https://doi.org/10.1126/science.7678183
- Moller DE. Potential role of TNF-alpha in the pathogenesis of insulin resistance and type 2 diabetes. Trends Endocrinol Metab 2000;46:1526-31.
- Christiansen T, Richelsen B, Bruun JM. Monocyte chemoattractant protein-1 is produced in isolated adipocyte, associated with adiposity and reduced after weight loss in morbid obese subjects. Int J Obes (Lond) 2005;29:146-50. https://doi.org/10.1038/sj.ijo.0802839
- Sartipy P, Loskutoff DJ. Monocyte chemoattractant protein 1 in obesity and insulin resistance. Proc Natl Acad Sci U S A 2003; 100:7265-70. https://doi.org/10.1073/pnas.1133870100
-
Wang B, Jenkins JR, Trayhurn P. Expression and secretion of inflammation-related adipokines by human adipocytes differentiated in culture: integrated response to TNF-
$\alpha$ . Am J Physiol Endocrinol Metab 2005;288:E731-40. - German AJ, Hervera M, Hunter L, Holden SL, Morris PJ, Biourge V, Trayhurn. Improvement in insulin resistance and reduction in plsma inflammatory adipokines after weight loss in obese dogs. Domest Animal Endocrinol 2009;37:214-26. https://doi.org/10.1016/j.domaniend.2009.07.001
- Panee J. Bamboo extract in the prevention of diabetes and breast cancer. In: Watson RR, editors. Complementary and Alternative Therapies and the Aging Population: An Evidence-Based Approach. San Diego, ELSEVIER; 2008. p.159-77.
- Yoon KD, Kim CY, Huh H. The flavone glycosides of Sasa Borealis. Korean Journal of Pharmacognosy 2000;31:224-7.
- Mahato SB, Nandy AK, Roy G. Triterpenoids. Phytochemistry 1992;31:2199-249. https://doi.org/10.1016/0031-9422(92)83257-Y
-
Jung HJ, Nam JH, Choi J, Lee KT, Park HJ. 19
$\alpha$ -hydroxyursane-type triterpenoids: antinociceptive anti-inflammatory principles of the roots of Rosa rugosa. Biol Pharm Bull 2005;28:101-4. https://doi.org/10.1248/bpb.28.101
Cited by
- extract exerts an antidiabetic effect via activation of the AMP-activated protein kinase vol.7, pp.1, 2013, https://doi.org/10.4162/nrp.2013.7.1.15
- Nakai Leaf Extract and Cisplatin Suppresses the Cancer Stemness and Invasion of Human Lung Cancer Cells vol.13, pp.6, 2014, https://doi.org/10.1177/1534735414534462
- Anti-diabetic potential of a Sasa quelpaertensis Nakai extract in L6 skeletal muscle cells vol.23, pp.4, 2014, https://doi.org/10.1007/s10068-014-0183-4
- Oral Administration of Oleuropein and Its Semisynthetic Peracetylated Derivative Prevents Hepatic Steatosis, Hyperinsulinemia, and Weight Gain in Mice Fed with High Fat Cafeteria Diet vol.2015, pp.1687-8345, 2015, https://doi.org/10.1155/2015/431453
- vol.5, pp.3, 2016, https://doi.org/10.1002/fsn3.416
- Sasa borealis leaf extract-mediated green synthesis of silver–silver chloride nanoparticles and their antibacterial and anticancer activities vol.41, pp.3, 2017, https://doi.org/10.1039/C6NJ03454C
- leaf extract-mediated gold nanoparticles pp.2169-141X, 2017, https://doi.org/10.1080/21691401.2017.1293675
- Diet-Induced Obesity in Mice Reduces the Maintenance of Influenza-Specific CD8+ Memory T Cells vol.140, pp.9, 2010, https://doi.org/10.3945/jn.110.123653
- Sasa quelpaertensis Leaf Extract Inhibits Colon Cancer by Regulating Cancer Cell Stemness in Vitro and in Vivo vol.16, pp.12, 2015, https://doi.org/10.3390/ijms16059976
- Effects of Oleacein on High-Fat Diet-Dependent Steatosis, Weight Gain, and Insulin Resistance in Mice vol.9, pp.1664-2392, 2018, https://doi.org/10.3389/fendo.2018.00116
- Regulation by chronic-mild stress of glucocorticoids, monocyte chemoattractant protein-1 and adiposity in rats fed on a high-fat diet vol.103, pp.2, 2010, https://doi.org/10.1016/j.physbeh.2011.01.017
- Hyperleptinemia is associated with parameters of low-grade systemic inflammation and metabolic dysfunction in obese human beings vol.7, pp.None, 2010, https://doi.org/10.3389/fnint.2013.00062
- 식물화합물 다량 함유 제주조릿대 잎 추출물의 제조와 특성 vol.26, pp.11, 2016, https://doi.org/10.5352/jls.2016.26.11.1330
- Suppressive effect of Sasa veitchii extract on obesity induced by a high-fat diet through modulation of adipose differentiation in mice vol.4, pp.6, 2010, https://doi.org/10.2131/fts.4.261
- Enhancement of Immune Activities of Mixtures with Sasa quelpaertensis Nakai and Ficus erecta var. sieboldii vol.9, pp.7, 2010, https://doi.org/10.3390/foods9070868
- 좁은잎천선과 및 조릿대 혼합 추출물의 항산화 성분과 항산화 활성 vol.52, pp.4, 2010, https://doi.org/10.9721/kjfst.2020.52.4.369
- Immunomodulatory Effect of Sasa quelpaertensis Leaves Fermentation Products in Mice vol.7, pp.3, 2010, https://doi.org/10.3390/fermentation7030142